Variant report

Variant	nsv834633
Chromosome Location	chr3:21918264-22088338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr3:21953424-21953558	K562	blood:	n/a	n/a
2	CEBPB	chr3:22038225-22038503	IMR90	lung:	n/a	chr3:22038377-22038388
3	CEBPB	chr3:22021993-22022316	HepG2	liver:	n/a	n/a
4	CEBPB	chr3:22038218-22038531	HepG2	liver:	n/a	chr3:22038377-22038388
5	CEBPB	chr3:21955973-21956275	HepG2	liver:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
6	CEBPB	chr3:21961843-21962449	IMR90	lung:	n/a	n/a
7	CEBPB	chr3:22053597-22053883	A549	lung:	n/a	chr3:22053728-22053739 chr3:22053726-22053739 chr3:22053726-22053737
8	CEBPB	chr3:21943011-21943293	MCF-7	breast:	n/a	n/a
9	CEBPB	chr3:21996134-21996664	IMR90	lung:	n/a	n/a
10	CEBPB	chr3:21996174-21996533	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr3:22053569-22053879	K562	blood:	n/a	chr3:22053728-22053739 chr3:22053726-22053739 chr3:22053726-22053737
12	CEBPB	chr3:21955978-21956313	Hela-S3	cervix:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
13	CEBPB	chr3:21942814-21943369	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:22048917-22049238	A549	lung:	n/a	n/a
15	CEBPB	chr3:21942912-21943334	A549	lung:	n/a	n/a
16	CEBPB	chr3:22038239-22038536	A549	lung:	n/a	chr3:22038377-22038388
17	CEBPB	chr3:22030902-22031215	HepG2	liver:	n/a	chr3:22031068-22031085 chr3:22031049-22031060
18	CEBPB	chr3:21919524-21919825	HepG2	liver:	n/a	chr3:21919625-21919636
19	CEBPB	chr3:22053600-22053821	HepG2	liver:	n/a	chr3:22053728-22053739 chr3:22053726-22053739 chr3:22053726-22053737
20	CEBPB	chr3:22048817-22049249	HepG2	liver:	n/a	n/a
21	CEBPB	chr3:21942972-21943348	IMR90	lung:	n/a	n/a
22	CEBPB	chr3:22048834-22049295	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr3:21961852-21962386	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:21942958-21943298	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:22030956-22031213	A549	lung:	n/a	chr3:22031068-22031085 chr3:22031049-22031060
26	CEBPB	chr3:21943081-21943297	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr3:21956051-21956262	A549	lung:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
28	CEBPB	chr3:22030829-22031267	Hela-S3	cervix:	n/a	chr3:22031068-22031085 chr3:22031049-22031060
29	CEBPB	chr3:21919524-21919848	IMR90	lung:	n/a	chr3:21919625-21919636
30	CEBPB	chr3:21983754-21984218	IMR90	lung:	n/a	chr3:21984197-21984210
31	CEBPB	chr3:22053532-22054406	Hela-S3	cervix:	n/a	chr3:22053728-22053739 chr3:22053726-22053739 chr3:22053726-22053737
32	CEBPB	chr3:21955980-21956311	IMR90	lung:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
33	CEBPB	chr3:22048734-22049247	IMR90	lung:	n/a	n/a
34	CHD2	chr3:21962058-21962212	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr3:21936054-21936200	SK-N-SH_RA	brain:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
36	CTCF	chr3:21998853-21998886	GM13976	blood:	n/a	n/a
37	CTCF	chr3:21935947-21936308	SK-N-SH_RA	brain:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
38	CTCF	chr3:21936060-21936210	HCT-116	colon:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
39	CTCF	chr3:21936120-21936270	GM12871	blood:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
40	CTCF	chr3:21936118-21936262	MCF-7	breast:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
41	CTCF	chr3:21936040-21936190	HepG2	liver:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
42	CTCF	chr3:21936460-21936610	AG04450	lung:	n/a	n/a
43	CTCF	chr3:21936146-21936202	MCF-7	breast:	n/a	chr3:21936150-21936163 chr3:21936148-21936166
44	CTCF	chr3:21936038-21936286	Spleen_OC	spleen:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
45	CTCF	chr3:21936100-21936250	GM12866	blood:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
46	CTCF	chr3:22071463-22071492	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr3:21950720-21950870	HPF	lung:	n/a	n/a
48	CTCF	chr3:21936320-21936470	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr3:21936040-21936190	GM06990	blood:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
50	CTCF	chr3:21936100-21936250	AG09319	gingival:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:22030381-22030431	Jurkat	blood:	n/a
2	chr3:21960904-21960954	A549	lung:	n/a
3	chr3:21960904-21960954	HIPEpiC	eye:	n/a
4	chr3:21960904-21960954	HRE	kidney:	n/a
5	chr3:21960904-21960954	GM12878	blood:	n/a
6	chr3:21960904-21960954	HUVEC	blood vessel:	n/a
7	chr3:22030381-22030431	HEEpiC	esophagus:	n/a
8	chr3:21960904-21960954	PFSK-1	brain:	n/a
9	chr3:22030381-22030431	GM12892	blood:	n/a
10	chr3:22030381-22030431	GM12891	blood:	n/a
11	chr3:21960904-21960954	HPAEpiC	pulmonary alveolar:	n/a
12	chr3:22030381-22030431	Caco-2	colon:	n/a
13	chr3:22030381-22030431	HCM	heart:	n/a
14	chr3:22030381-22030431	NH-A	brain:	n/a
15	chr3:21960904-21960954	HCT-116	colon:	n/a
16	chr3:21960904-21960954	LNCaP	prostate:	n/a
17	chr3:22030381-22030431	SK-N-MC	brain:	n/a
18	chr3:21960904-21960954	HMEC	breast:	n/a
19	chr3:22030381-22030431	H1-hESC	embryonic stem cell:	embryo
20	chr3:22030381-22030431	IMR90	lung:	fetal
21	chr3:21960904-21960954	SK-N-SH_RA	brain:	n/a
22	chr3:22030381-22030431	PANC-1	pancreas:	n/a
23	chr3:21960904-21960954	GM12892	blood:	n/a
24	chr3:21960904-21960954	HCM	heart:	n/a
25	chr3:21960904-21960954	Caco-2	colon:	n/a
26	chr3:22030381-22030431	AG09319	gingival:	n/a
27	chr3:22030381-22030431	Hepatocyte	liver:	n/a
28	chr3:21960904-21960954	NHDF-neo	bronchial:	n/a
29	chr3:22030381-22030431	HUVEC	blood vessel:	n/a
30	chr3:22030381-22030431	SKMC	muscle:	n/a
31	chr3:22030381-22030431	U87	brain:	n/a
32	chr3:21960904-21960954	GM12891	blood:	n/a
33	chr3:21960904-21960954	AoSMC	blood vessel:	n/a
34	chr3:21960904-21960954	Hela-S3	cervix:	n/a
35	chr3:21960904-21960954	PANC-1	pancreas:	n/a
36	chr3:21960904-21960954	GM19239	blood:	n/a
37	chr3:21960904-21960954	HCF	heart:	n/a
38	chr3:22030381-22030431	BJ	skin:	n/a
39	chr3:22030381-22030431	ovcar-3	ovarian:	n/a
40	chr3:22030381-22030431	GM12878	blood:	n/a
41	chr3:22030381-22030431	SK-N-SH_RA	brain:	n/a
42	chr3:22030381-22030431	T-47D	breast:	n/a
43	chr3:22030381-22030431	LNCaP	prostate:	n/a
44	chr3:21960904-21960954	AG09309	skin:	n/a
45	chr3:22030381-22030431	RPTEC	kidney:	n/a
46	chr3:22030381-22030431	HEK293	kidney:	embryo
47	chr3:22030381-22030431	SAEC	small airway:	n/a
48	chr3:22030381-22030431	NHBE	bronchial:	n/a
49	chr3:21960904-21960954	SK-N-SH	brain:	n/a
50	chr3:21960904-21960954	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:21939959..21942443-chr3:21956783..21959351,2	K562	blood:
2	chr3:22060147..22061903-chr3:22064159..22066026,2	K562	blood:
3	chr3:21927265..21931115-chr3:21931720..21934482,3	K562	blood:
4	chr3:21922639..21924964-chr3:21928274..21929966,2	K562	blood:
5	chr3:21946123..21950317-chr3:21950645..21954305,3	K562	blood:
6	chr3:21525568..21526468-chr3:21935899..21936657,2	MCF-7	breast:
7	chr3:21922639..21924964-chr3:21928274..21929966,2	K562	blood:
8	chr3:21942258..21944994-chr3:21945829..21948153,2	K562	blood:
9	chr3:21919005..21921576-chr3:21924260..21925811,2	K562	blood:
10	chr3:21948578..21950299-chr3:21951052..21953875,2	MCF-7	breast:
11	chr3:21948578..21950299-chr3:21951052..21953875,2	MCF-7	breast:
12	chr3:22056493..22058211-chr3:22060114..22061974,2	K562	blood:
13	chr3:21919005..21921576-chr3:21924260..21925811,2	K562	blood:
14	chr3:21927265..21931115-chr3:21931720..21934482,3	K562	blood:
15	chr3:22060147..22061903-chr3:22064159..22066026,2	K562	blood:
16	chr3:21942258..21944994-chr3:21945829..21948153,2	K562	blood:
17	chr3:22042480..22044020-chr3:22057123..22059814,2	K562	blood:
18	chr3:21954020..21955585-chr3:21957563..21959846,2	MCF-7	breast:
19	chr3:20266881..20267830-chr3:21935770..21936618,4	MCF-7	breast:
20	chr3:21954020..21955585-chr3:21957563..21959846,2	MCF-7	breast:
21	chr3:20381543..20382061-chr3:21935726..21936559,2	MCF-7	breast:
22	chr3:22051906..22054873-chr3:22056499..22059265,2	K562	blood:
23	chr11:126141332..126144254-chr3:22001697..22003217,2	K562	blood:
24	chr3:21793981..21794891-chr3:21935742..21936689,4	MCF-7	breast:
25	chr3:22042480..22044020-chr3:22057123..22059814,2	K562	blood:
26	chr3:21946123..21950317-chr3:21950645..21954305,3	K562	blood:
27	chr3:22051906..22054873-chr3:22056499..22059265,2	K562	blood:
28	chr3:21939959..21942443-chr3:21956783..21959351,2	K562	blood:
29	chr3:22056493..22058211-chr3:22060114..22061974,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2E2-7	chr3:21975327-21975419	l_2330_chr3:21975326-21982219_testes
2	lnc-UBE2E2-2	chr3:22002908-22003032	ENSG00000223351
3	lnc-UBE2E2-2	chr3:21984058-21984156	ENSG00000223351
4	lnc-UBE2E2-2	chr3:22019707-22019783	ENSG00000223351
5	lnc-UBE2E2-2	chr3:21998631-21998684	ENSG00000223351
6	lnc-UBE2E2-2	chr3:22000324-22000415	ENSG00000223351
7	lnc-UBE2E2-2	chr3:22000324-22000415	ENSG00000223351
8	lnc-SGOL1-3	chr3:21919332-21919650	NONHSAT088650
9	lnc-UBE2E2-7	chr3:21982020-21982219	l_2330_chr3:21975326-21982219_testes
10	lnc-UBE2E2-2	chr3:22021123-22021320	ENSG00000223351
11	lnc-UBE2E2-2	chr3:21998628-21998684	ENSG00000223351

Variant related genes	Relation type
ZNF385D-AS2	TF binding region
ZNF385D-AS2	CpG island
ENSG00000110074	chromatin interactions

Extended variants
information (count: 5956 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:5956 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562925755	chr3:21918299-21918300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533513752	chr3:21918334-21918335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138989773	chr3:21918336-21918337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569698938	chr3:21918339-21918340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377612188	chr3:21918340-21918341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs812393	chr3:21918407-21918408	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs527644752	chr3:21918422-21918423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149891604	chr3:21918430-21918431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568039287	chr3:21918444-21918445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529133948	chr3:21918450-21918451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184387564	chr3:21918464-21918465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144942330	chr3:21918493-21918494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs57613290	chr3:21918551-21918552	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs557531400	chr3:21918552-21918553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566481261	chr3:21918589-21918590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533742267	chr3:21918590-21918591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140941943	chr3:21918593-21918594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565854277	chr3:21918643-21918644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574421976	chr3:21918670-21918671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189480313	chr3:21918686-21918687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374222750	chr3:21918715-21918716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs3912213	chr3:21918745-21918746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs578080616	chr3:21918748-21918749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545499481	chr3:21918749-21918750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558346748	chr3:21918753-21918754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs117731420	chr3:21918789-21918790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542645435	chr3:21918815-21918816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73146841	chr3:21918818-21918819	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs181835515	chr3:21918856-21918857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs17009894	chr3:21918863-21918864	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs572178624	chr3:21918904-21918905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184541927	chr3:21918909-21918910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554557494	chr3:21918945-21918946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140322538	chr3:21918976-21918977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs532951188	chr3:21918987-21918988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551476626	chr3:21918991-21918992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566601114	chr3:21919001-21919002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533858566	chr3:21919031-21919032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs779036	chr3:21919039-21919040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs567222884	chr3:21919043-21919044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534615611	chr3:21919047-21919048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189316591	chr3:21919056-21919057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78814206	chr3:21919061-21919062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs578139668	chr3:21919067-21919068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545298701	chr3:21919145-21919146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554325415	chr3:21919167-21919168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs180796875	chr3:21919171-21919172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556821139	chr3:21919188-21919189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114917397	chr3:21919203-21919204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35148863	chr3:21919205-21919206	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21918200-21919000	Enhancers	Fetal Lung	lung
2	chr3:21918400-21918800	Enhancers	Fetal Stomach	stomach
3	chr3:21918400-21919000	Enhancers	Fetal Kidney	kidney
4	chr3:21918600-21919000	Enhancers	Aorta	Aorta
5	chr3:21919000-21920400	Weak transcription	Fetal Lung	lung
6	chr3:21919000-21920800	Weak transcription	Fetal Kidney	kidney
7	chr3:21920400-21923000	Enhancers	Fetal Lung	lung
8	chr3:21920800-21921200	Enhancers	Fetal Kidney	kidney
9	chr3:21922000-21927800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr3:21923000-21923600	Weak transcription	Fetal Lung	lung
11	chr3:21923600-21923800	Enhancers	Fetal Lung	lung
12	chr3:21929800-21931000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr3:21930400-21930800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:21930800-21940000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:21932800-21933200	Enhancers	Fetal Lung	lung
16	chr3:21933000-21933200	Enhancers	Fetal Kidney	kidney
17	chr3:21933200-21935800	Weak transcription	Fetal Kidney	kidney
18	chr3:21933200-21936200	Weak transcription	Fetal Lung	lung
19	chr3:21934000-21934400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr3:21934400-21934800	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr3:21934400-21935200	Enhancers	Fetal Heart	heart
22	chr3:21934600-21934800	Enhancers	NHLF	lung
23	chr3:21934600-21935000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:21934600-21935200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr3:21934600-21935200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr3:21934600-21935200	Enhancers	HSMM	muscle
27	chr3:21934600-21935200	Enhancers	HSMMtube	muscle
28	chr3:21934600-21935400	Enhancers	Muscle Satellite Cultured Cells	--
29	chr3:21934600-21936000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr3:21934800-21935000	Enhancers	NHDF-Ad	bronchial
31	chr3:21935200-21936200	Weak transcription	Fetal Heart	heart
32	chr3:21935200-21936200	Weak transcription	HSMMtube	muscle
33	chr3:21935800-21936400	Enhancers	Fetal Kidney	kidney
34	chr3:21936200-21936400	Enhancers	Fetal Lung	lung
35	chr3:21936200-21936400	Enhancers	HSMMtube	muscle
36	chr3:21936200-21936600	Enhancers	Fetal Brain Female	brain
37	chr3:21936200-21936800	Enhancers	Fetal Heart	heart
38	chr3:21937600-21937800	Enhancers	NHDF-Ad	bronchial
39	chr3:21938000-21938800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr3:21940000-21940600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:21940200-21940600	Enhancers	Fetal Stomach	stomach
42	chr3:21940600-21941200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr3:21942800-21943400	Enhancers	Liver	Liver
44	chr3:21943000-21943600	Enhancers	Hela-S3	cervix
45	chr3:21947000-21947200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr3:21947200-21948000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr3:21948000-21948400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr3:21948400-21950000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr3:21950000-21950800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr3:21950600-21951400	Enhancers	Fetal Lung	lung

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