Variant report

Variant	nsv876614
Chromosome Location	chr3:21919039-21994022
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	chr3:21955980-21956311	IMR90	lung:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
3	CEBPB	chr3:21942958-21943298	HepG2	liver:	n/a	n/a
4	CEBPB	chr3:21956051-21956262	A549	lung:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
5	CEBPB	chr3:21955978-21956313	Hela-S3	cervix:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
6	CEBPB	chr3:21943011-21943293	MCF-7	breast:	n/a	n/a
7	CEBPB	chr3:21955973-21956275	HepG2	liver:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
8	CEBPB	chr3:21943081-21943297	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:21961843-21962449	IMR90	lung:	n/a	n/a
10	CEBPB	chr3:21919524-21919848	IMR90	lung:	n/a	chr3:21919625-21919636
11	CEBPB	chr3:21942912-21943334	A549	lung:	n/a	n/a
12	CEBPB	chr3:21961852-21962386	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:21942814-21943369	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:21983754-21984218	IMR90	lung:	n/a	chr3:21984197-21984210
15	CEBPB	chr3:21919524-21919825	HepG2	liver:	n/a	chr3:21919625-21919636
16	CEBPB	chr3:21942972-21943348	IMR90	lung:	n/a	n/a
17	CHD2	chr3:21962058-21962212	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr3:21936060-21936210	NHLF	lung:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
19	CTCF	chr3:21935988-21936295	A549	lung:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
20	CTCF	chr3:21936020-21936170	HCT-116	colon:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
21	CTCF	chr3:21936060-21936210	HCT-116	colon:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
22	CTCF	chr3:21936078-21936221	GM10248	blood:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
23	CTCF	chr3:21936120-21936270	HMEC	breast:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
24	CTCF	chr3:21936100-21936250	MCF-7	breast:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
25	CTCF	chr3:21936080-21936230	Hela-S3	cervix:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
26	CTCF	chr3:21935749-21936689	SK-N-SH	brain:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
27	CTCF	chr3:21936040-21936190	MCF-7	breast:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
28	CTCF	chr3:21936061-21936271	LNCaP	prostate:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
29	CTCF	chr3:21980128-21980180	MCF-7	breast:	n/a	n/a
30	CTCF	chr3:21936038-21936286	Spleen_OC	spleen:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
31	CTCF	chr3:21936100-21936250	AG04449	skin:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
32	CTCF	chr3:21936140-21936290	NHDF-neo	bronchial:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
33	CTCF	chr3:21936118-21936262	MCF-7	breast:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
34	CTCF	chr3:21935928-21936527	A549	lung:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
35	CTCF	chr3:21935911-21936346	MCF-7	breast:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
36	CTCF	chr3:21936060-21936210	NHDF-neo	bronchial:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
37	CTCF	chr3:21921140-21921290	BJ	skin:	n/a	n/a
38	CTCF	chr3:21936080-21936230	AG09309	skin:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
39	CTCF	chr3:21936760-21936910	AG10803	skin:	n/a	n/a
40	CTCF	chr3:21936040-21936190	SAEC	small airway:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
41	CTCF	chr3:21950720-21950870	HPF	lung:	n/a	n/a
42	CTCF	chr3:21936054-21936200	SK-N-SH_RA	brain:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
43	CTCF	chr3:21936060-21936210	GM12872	blood:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
44	CTCF	chr3:21936100-21936250	HMF	breast:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
45	CTCF	chr3:21936020-21936170	HCM	heart:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
46	CTCF	chr3:21936080-21936230	AG09319	gingival:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
47	CTCF	chr3:21936080-21936230	NB4	blood:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
48	CTCF	chr3:21936118-21936220	K562	blood:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
49	CTCF	chr3:21936040-21936190	HVMF	connective:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166
50	CTCF	chr3:21936070-21936285	Hela-S3	cervix:	n/a	chr3:21936143-21936164 chr3:21936150-21936163 chr3:21936148-21936166

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:21960904-21960954	H1-hESC	embryonic stem cell:	embryo
2	chr3:21960904-21960954	SKMC	muscle:	n/a
3	chr3:21960904-21960954	GM19239	blood:	n/a
4	chr3:21960904-21960954	MCF10A-Er-Src	breast:	n/a
5	chr3:21960904-21960954	ProgFib	skin:	n/a
6	chr3:21960904-21960954	HNPCEpiC	eye:	n/a
7	chr3:21960904-21960954	HEEpiC	esophagus:	n/a
8	chr3:21960904-21960954	GM12892	blood:	n/a
9	chr3:21960904-21960954	U87	brain:	n/a
10	chr3:21960904-21960954	HUVEC	blood vessel:	n/a
11	chr3:21960904-21960954	AoSMC	blood vessel:	n/a
12	chr3:21960904-21960954	AG09309	skin:	n/a
13	chr3:21960904-21960954	SK-N-SH_RA	brain:	n/a
14	chr3:21960904-21960954	BE2_C	brain:	n/a
15	chr3:21960904-21960954	HepG2	liver:	n/a
16	chr3:21960904-21960954	NHBE	bronchial:	n/a
17	chr3:21960904-21960954	NT2-D1	testis:	n/a
18	chr3:21960904-21960954	AG04449	skin:	fetal
19	chr3:21960904-21960954	HCT-116	colon:	n/a
20	chr3:21960904-21960954	HCF	heart:	n/a
21	chr3:21960904-21960954	A549	lung:	n/a
22	chr3:21960904-21960954	HIPEpiC	eye:	n/a
23	chr3:21960904-21960954	BJ	skin:	n/a
24	chr3:21960904-21960954	AG09319	gingival:	n/a
25	chr3:21960904-21960954	ovcar-3	ovarian:	n/a
26	chr3:21960904-21960954	HRPEpiC	eye:	n/a
27	chr3:21960904-21960954	SK-N-SH	brain:	n/a
28	chr3:21960904-21960954	LNCaP	prostate:	n/a
29	chr3:21960904-21960954	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:21960904-21960954	IMR90	lung:	fetal
31	chr3:21960904-21960954	K562	blood:	n/a
32	chr3:21960904-21960954	ECC-1	luminal epithelium:	n/a
33	chr3:21960904-21960954	PrEC	prostate:	n/a
34	chr3:21960904-21960954	Hepatocyte	liver:	n/a
35	chr3:21960904-21960954	T-47D	breast:	n/a
36	chr3:21960904-21960954	HEK293	kidney:	embryo
37	chr3:21960904-21960954	CMK	blood:	n/a
38	chr3:21960904-21960954	GM12891	blood:	n/a
39	chr3:21960904-21960954	SK-N-MC	brain:	n/a
40	chr3:21960904-21960954	Jurkat	blood:	n/a
41	chr3:21960904-21960954	AG10803	skin:	n/a
42	chr3:21960904-21960954	PANC-1	pancreas:	n/a
43	chr3:21960904-21960954	HMEC	breast:	n/a
44	chr3:21960904-21960954	Caco-2	colon:	n/a
45	chr3:21960904-21960954	AG04450	lung:	fetal
46	chr3:21960904-21960954	PFSK-1	brain:	n/a
47	chr3:21960904-21960954	HAEpiC	amniotic membrane:	n/a
48	chr3:21960904-21960954	Hela-S3	cervix:	n/a
49	chr3:21960904-21960954	HCPEpiC	choroid plexus:	n/a
50	chr3:21960904-21960954	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:21948578..21950299-chr3:21951052..21953875,2	MCF-7	breast:
2	chr3:21942258..21944994-chr3:21945829..21948153,2	K562	blood:
3	chr3:21525568..21526468-chr3:21935899..21936657,2	MCF-7	breast:
4	chr3:21954020..21955585-chr3:21957563..21959846,2	MCF-7	breast:
5	chr3:20381543..20382061-chr3:21935726..21936559,2	MCF-7	breast:
6	chr3:21919005..21921576-chr3:21924260..21925811,2	K562	blood:
7	chr3:21927265..21931115-chr3:21931720..21934482,3	K562	blood:
8	chr3:21927265..21931115-chr3:21931720..21934482,3	K562	blood:
9	chr3:21948578..21950299-chr3:21951052..21953875,2	MCF-7	breast:
10	chr3:21922639..21924964-chr3:21928274..21929966,2	K562	blood:
11	chr3:21954020..21955585-chr3:21957563..21959846,2	MCF-7	breast:
12	chr3:21922639..21924964-chr3:21928274..21929966,2	K562	blood:
13	chr3:20266881..20267830-chr3:21935770..21936618,4	MCF-7	breast:
14	chr3:21942258..21944994-chr3:21945829..21948153,2	K562	blood:
15	chr3:21946123..21950317-chr3:21950645..21954305,3	K562	blood:
16	chr3:21919005..21921576-chr3:21924260..21925811,2	K562	blood:
17	chr3:21939959..21942443-chr3:21956783..21959351,2	K562	blood:
18	chr3:21939959..21942443-chr3:21956783..21959351,2	K562	blood:
19	chr3:21946123..21950317-chr3:21950645..21954305,3	K562	blood:
20	chr3:21793981..21794891-chr3:21935742..21936689,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2E2-7	chr3:21975327-21975419	l_2330_chr3:21975326-21982219_testes
2	lnc-UBE2E2-7	chr3:21982020-21982219	l_2330_chr3:21975326-21982219_testes
3	lnc-UBE2E2-2	chr3:21984058-21984156	ENSG00000223351
4	lnc-SGOL1-3	chr3:21919332-21919650	NONHSAT088650

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

Extended variants
information (count: 3932 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3932 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs779036	chr3:21919039-21919040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567222884	chr3:21919043-21919044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534615611	chr3:21919047-21919048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189316591	chr3:21919056-21919057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78814206	chr3:21919061-21919062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs578139668	chr3:21919067-21919068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545298701	chr3:21919145-21919146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554325415	chr3:21919167-21919168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs180796875	chr3:21919171-21919172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556821139	chr3:21919188-21919189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114917397	chr3:21919203-21919204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35148863	chr3:21919205-21919206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560951913	chr3:21919214-21919215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575989891	chr3:21919228-21919229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76520254	chr3:21919229-21919230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556505495	chr3:21919249-21919250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553433321	chr3:21919288-21919289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562615478	chr3:21919301-21919302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533233779	chr3:21919307-21919308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs779035	chr3:21919327-21919328	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs372249080	chr3:21919337-21919338	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs372400919	chr3:21919436-21919437	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs186525210	chr3:21919439-21919440	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs143353222	chr3:21919486-21919487	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs375309936	chr3:21919511-21919512	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs191382562	chr3:21919534-21919535	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs114613867	chr3:21919546-21919547	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs113616022	chr3:21919601-21919602	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs77711928	chr3:21919619-21919620	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs171829	chr3:21919620-21919621	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs531106004	chr3:21919634-21919635	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs571878979	chr3:21919671-21919672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs809647	chr3:21919672-21919673	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs553989838	chr3:21919673-21919674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181576142	chr3:21919680-21919681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536358770	chr3:21919685-21919686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530397349	chr3:21919697-21919698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542371528	chr3:21919706-21919707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1684518	chr3:21919711-21919712	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs116216097	chr3:21919731-21919732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548655803	chr3:21919733-21919734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116866072	chr3:21919758-21919759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369581471	chr3:21919764-21919765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577901078	chr3:21919809-21919810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545286849	chr3:21919865-21919866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559291112	chr3:21919888-21919889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372734112	chr3:21919891-21919892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs17009897	chr3:21919895-21919896	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs531206730	chr3:21919903-21919904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527446735	chr3:21919904-21919905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21919000-21920400	Weak transcription	Fetal Lung	lung
2	chr3:21919000-21920800	Weak transcription	Fetal Kidney	kidney
3	chr3:21920400-21923000	Enhancers	Fetal Lung	lung
4	chr3:21920800-21921200	Enhancers	Fetal Kidney	kidney
5	chr3:21922000-21927800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:21923000-21923600	Weak transcription	Fetal Lung	lung
7	chr3:21923600-21923800	Enhancers	Fetal Lung	lung
8	chr3:21929800-21931000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr3:21930400-21930800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:21930800-21940000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:21932800-21933200	Enhancers	Fetal Lung	lung
12	chr3:21933000-21933200	Enhancers	Fetal Kidney	kidney
13	chr3:21933200-21935800	Weak transcription	Fetal Kidney	kidney
14	chr3:21933200-21936200	Weak transcription	Fetal Lung	lung
15	chr3:21934000-21934400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr3:21934400-21934800	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr3:21934400-21935200	Enhancers	Fetal Heart	heart
18	chr3:21934600-21934800	Enhancers	NHLF	lung
19	chr3:21934600-21935000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr3:21934600-21935200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr3:21934600-21935200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr3:21934600-21935200	Enhancers	HSMM	muscle
23	chr3:21934600-21935200	Enhancers	HSMMtube	muscle
24	chr3:21934600-21935400	Enhancers	Muscle Satellite Cultured Cells	--
25	chr3:21934600-21936000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr3:21934800-21935000	Enhancers	NHDF-Ad	bronchial
27	chr3:21935200-21936200	Weak transcription	Fetal Heart	heart
28	chr3:21935200-21936200	Weak transcription	HSMMtube	muscle
29	chr3:21935800-21936400	Enhancers	Fetal Kidney	kidney
30	chr3:21936200-21936400	Enhancers	Fetal Lung	lung
31	chr3:21936200-21936400	Enhancers	HSMMtube	muscle
32	chr3:21936200-21936600	Enhancers	Fetal Brain Female	brain
33	chr3:21936200-21936800	Enhancers	Fetal Heart	heart
34	chr3:21937600-21937800	Enhancers	NHDF-Ad	bronchial
35	chr3:21938000-21938800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr3:21940000-21940600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:21940200-21940600	Enhancers	Fetal Stomach	stomach
38	chr3:21940600-21941200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr3:21942800-21943400	Enhancers	Liver	Liver
40	chr3:21943000-21943600	Enhancers	Hela-S3	cervix
41	chr3:21947000-21947200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr3:21947200-21948000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr3:21948000-21948400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr3:21948400-21950000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr3:21950000-21950800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr3:21950600-21951400	Enhancers	Fetal Lung	lung
47	chr3:21951400-21953800	Weak transcription	Fetal Lung	lung
48	chr3:21953800-21955400	Enhancers	Colon Smooth Muscle	Colon
49	chr3:21953800-21956800	Enhancers	Fetal Lung	lung
50	chr3:21954000-21954200	Enhancers	Placenta Amnion	Placenta Amnion

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