Variant report

Variant	nsv876936
Chromosome Location	chr3:70304538-70352489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:193)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:193 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:70313397-70314038	HepG2	liver:	n/a	n/a
2	ATF3	chr3:70330643-70331286	A549	lung:	n/a	n/a
3	BCL3	chr3:70313284-70313962	A549	lung:	n/a	n/a
4	BCL3	chr3:70330602-70331311	A549	lung:	n/a	n/a
5	BCL3	chr3:70330686-70331249	A549	lung:	n/a	n/a
6	BHLHE40	chr3:70313367-70313809	HepG2	liver:	n/a	n/a
7	BHLHE40	chr3:70345132-70345162	GM12878	blood:	n/a	n/a
8	CBX3	chr3:70340237-70340430	K562	blood:	n/a	n/a
9	CEBPB	chr3:70313339-70313888	A549	lung:	n/a	n/a
10	CEBPB	chr3:70313188-70314071	A549	lung:	n/a	n/a
11	CEBPB	chr3:70330850-70331283	A549	lung:	n/a	n/a
12	CEBPB	chr3:70348297-70348536	IMR90	lung:	n/a	n/a
13	CEBPB	chr3:70348318-70348533	A549	lung:	n/a	n/a
14	CEBPB	chr3:70330783-70331335	A549	lung:	n/a	n/a
15	CEBPB	chr3:70330700-70331346	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:70330602-70331397	A549	lung:	n/a	n/a
17	CEBPB	chr3:70347482-70347867	Hela-S3	cervix:	n/a	chr3:70347639-70347652
18	CTCF	chr3:70314837-70314910	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr3:70334033-70334120	GM20000	blood:	n/a	n/a
20	CTCF	chr3:70331020-70331170	A549	lung:	n/a	n/a
21	E2F4	chr3:70349384-70349494	MCF10A-Er-Src	breast:	n/a	chr3:70349434-70349443
22	E2F6	chr3:70305536-70306113	A549	lung:	n/a	n/a
23	E2F6	chr3:70330727-70331378	A549	lung:	n/a	n/a
24	EGR1	chr3:70339754-70339979	K562	blood:	n/a	n/a
25	EGR1	chr3:70324685-70324861	K562	blood:	n/a	n/a
26	EP300	chr3:70326136-70327099	SK-N-SH	brain:	n/a	chr3:70326749-70326756 chr3:70326570-70326580 chr3:70326443-70326453
27	EP300	chr3:70313160-70314085	A549	lung:	n/a	n/a
28	EP300	chr3:70313151-70314175	A549	lung:	n/a	n/a
29	EP300	chr3:70330541-70331322	A549	lung:	n/a	chr3:70330718-70330728
30	EP300	chr3:70330602-70331150	Hela-S3	cervix:	n/a	chr3:70330718-70330728
31	EP300	chr3:70330174-70331400	A549	lung:	n/a	chr3:70330718-70330728
32	EP300	chr3:70313465-70313838	HepG2	liver:	n/a	n/a
33	EP300	chr3:70326215-70326948	A549	lung:	n/a	chr3:70326749-70326756 chr3:70326570-70326580 chr3:70326443-70326453
34	EP300	chr3:70326129-70327123	A549	lung:	n/a	chr3:70326749-70326756 chr3:70326570-70326580 chr3:70326443-70326453
35	FOS	chr3:70330881-70331023	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr3:70330730-70331152	Hela-S3	cervix:	n/a	n/a
37	FOS	chr3:70310285-70311223	HUVEC	blood vessel:	n/a	chr3:70310681-70310691 chr3:70310682-70310691 chr3:70310681-70310691 chr3:70310680-70310691 chr3:70310682-70310689
38	FOS	chr3:70313600-70313822	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr3:70330865-70331086	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr3:70313482-70313921	HUVEC	blood vessel:	n/a	n/a
41	FOSL2	chr3:70313520-70313839	HepG2	liver:	n/a	n/a
42	FOSL2	chr3:70330732-70331204	A549	lung:	n/a	n/a
43	FOSL2	chr3:70313216-70314190	A549	lung:	n/a	n/a
44	FOSL2	chr3:70330751-70331201	MCF-7	breast:	n/a	n/a
45	FOSL2	chr3:70310450-70310846	A549	lung:	n/a	chr3:70310681-70310691 chr3:70310682-70310691 chr3:70310681-70310691 chr3:70310682-70310689
46	FOSL2	chr3:70330380-70331486	A549	lung:	n/a	n/a
47	FOSL2	chr3:70313486-70313899	HepG2	liver:	n/a	n/a
48	FOSL2	chr3:70313517-70313985	A549	lung:	n/a	n/a
49	FOSL2	chr3:70310301-70310973	A549	lung:	n/a	chr3:70310681-70310691 chr3:70310682-70310691 chr3:70310681-70310691 chr3:70310682-70310689
50	FOXA1	chr3:70313341-70313944	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:70339967-70340017	NT2-D1	testis:	n/a
2	chr3:70339935-70339985	ProgFib	skin:	n/a
3	chr3:70339935-70339985	SK-N-SH_RA	brain:	n/a
4	chr3:70339967-70340017	CMK	blood:	n/a
5	chr3:70339935-70339985	HCPEpiC	choroid plexus:	n/a
6	chr3:70339935-70339985	HCT-116	colon:	n/a
7	chr3:70339967-70340017	HCT-116	colon:	n/a
8	chr3:70339935-70339985	U87	brain:	n/a
9	chr3:70339935-70339985	AG09319	gingival:	n/a
10	chr3:70339967-70340017	HCF	heart:	n/a
11	chr3:70339967-70340017	HAEpiC	amniotic membrane:	n/a
12	chr3:70339935-70339985	GM06990	blood:	n/a
13	chr3:70339935-70339985	AG04449	skin:	fetal
14	chr3:70339967-70340017	AG09319	gingival:	n/a
15	chr3:70339967-70340017	GM12892	blood:	n/a
16	chr3:70339935-70339985	AG09309	skin:	n/a
17	chr3:70339967-70340017	BE2_C	brain:	n/a
18	chr3:70339935-70339985	PFSK-1	brain:	n/a
19	chr3:70339967-70340017	ovcar-3	ovarian:	n/a
20	chr3:70339967-70340017	SK-N-SH	brain:	n/a
21	chr3:70339935-70339985	NHDF-neo	bronchial:	n/a
22	chr3:70339967-70340017	Hepatocyte	liver:	n/a
23	chr3:70339935-70339985	HPAEpiC	pulmonary alveolar:	n/a
24	chr3:70339967-70340017	T-47D	breast:	n/a
25	chr3:70339935-70339985	A549	lung:	n/a
26	chr3:70339967-70340017	HCPEpiC	choroid plexus:	n/a
27	chr3:70339935-70339985	BJ	skin:	n/a
28	chr3:70339967-70340017	MCF10A-Er-Src	breast:	n/a
29	chr3:70339935-70339985	ovcar-3	ovarian:	n/a
30	chr3:70339935-70339985	MCF-7	breast:	n/a
31	chr3:70339935-70339985	HNPCEpiC	eye:	n/a
32	chr3:70339967-70340017	HUVEC	blood vessel:	n/a
33	chr3:70339967-70340017	HRE	kidney:	n/a
34	chr3:70339935-70339985	SK-N-MC	brain:	n/a
35	chr3:70339935-70339985	AoSMC	blood vessel:	n/a
36	chr3:70339935-70339985	HL-60	blood:	n/a
37	chr3:70339967-70340017	H1-hESC	embryonic stem cell:	embryo
38	chr3:70339935-70339985	GM12891	blood:	n/a
39	chr3:70339967-70340017	A549	lung:	n/a
40	chr3:70339935-70339985	SK-N-SH	brain:	n/a
41	chr3:70339967-70340017	GM12878	blood:	n/a
42	chr3:70339935-70339985	HIPEpiC	eye:	n/a
43	chr3:70339967-70340017	PANC-1	pancreas:	n/a
44	chr3:70339935-70339985	K562	blood:	n/a
45	chr3:70339967-70340017	Caco-2	colon:	n/a
46	chr3:70339967-70340017	AG09309	skin:	n/a
47	chr3:70339935-70339985	NT2-D1	testis:	n/a
48	chr3:70339935-70339985	HEK293	kidney:	embryo
49	chr3:70339967-70340017	ECC-1	luminal epithelium:	n/a
50	chr3:70339935-70339985	HCF	heart:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:70339740..70342430-chr3:70343681..70346313,2	K562	blood:
2	chr3:70348474..70350327-chr3:70352138..70355044,2	K562	blood:
3	chr3:70348474..70350327-chr3:70352138..70355044,2	K562	blood:
4	chr3:70339740..70342430-chr3:70343681..70346313,2	K562	blood:
5	chr3:70322866..70326501-chr3:70330007..70332995,3	MCF-7	breast:
6	chr3:70322866..70326501-chr3:70330007..70332995,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000222615	TF binding region
ENSG00000222615	CpG island

Extended variants
information (count: 1553 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1553 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1357268	chr3:70304538-70304539	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs5849942	chr3:70304577-70304578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532865127	chr3:70304585-70304586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562983322	chr3:70304696-70304697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371517743	chr3:70304700-70304701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576486590	chr3:70304710-70304711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545577437	chr3:70304712-70304713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374166116	chr3:70304718-70304719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569564761	chr3:70304724-70304725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565376052	chr3:70304766-70304767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554991855	chr3:70304772-70304773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117886786	chr3:70304783-70304784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147704557	chr3:70304818-70304819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374457656	chr3:70304848-70304849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192096152	chr3:70304859-70304860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116713811	chr3:70304882-70304883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183532028	chr3:70304898-70304899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6419771	chr3:70304927-70304928	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs527942984	chr3:70304928-70304929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563081172	chr3:70304946-70304947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115599816	chr3:70304960-70304961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148876361	chr3:70304964-70304965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527590984	chr3:70304982-70304983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9884082	chr3:70305040-70305041	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs143554189	chr3:70305054-70305055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532828133	chr3:70305060-70305061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs151000139	chr3:70305092-70305093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188529852	chr3:70305110-70305111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532762510	chr3:70305139-70305140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528929258	chr3:70305167-70305168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560081793	chr3:70305176-70305177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548973306	chr3:70305210-70305211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549405622	chr3:70305248-70305249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144585289	chr3:70305256-70305257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200961451	chr3:70305284-70305285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534520274	chr3:70305299-70305300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192873774	chr3:70305303-70305304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115594670	chr3:70305319-70305320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112933649	chr3:70305346-70305347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182788577	chr3:70305380-70305381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114523852	chr3:70305423-70305424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547707813	chr3:70305424-70305425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150179112	chr3:70305432-70305433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138517891	chr3:70305442-70305443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141569008	chr3:70305459-70305460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114869942	chr3:70305503-70305504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571979940	chr3:70305563-70305564	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs374272450	chr3:70305585-70305586	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs549527982	chr3:70305630-70305631	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs145342263	chr3:70305669-70305670	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	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
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	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
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Mental retardation	17847001	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70300400-70305800	Weak transcription	HUVEC	blood vessel
2	chr3:70304600-70304800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:70304800-70306000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:70305400-70306200	Enhancers	A549	lung
5	chr3:70305800-70306400	Enhancers	HUVEC	blood vessel
6	chr3:70306000-70306200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:70306400-70308200	Weak transcription	HUVEC	blood vessel
8	chr3:70308200-70311200	Enhancers	HUVEC	blood vessel
9	chr3:70309800-70310200	Enhancers	A549	lung
10	chr3:70310200-70311200	Flanking Active TSS	A549	lung
11	chr3:70310800-70311200	Enhancers	Duodenum Mucosa	Duodenum
12	chr3:70311000-70311200	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr3:70311200-70311600	Enhancers	A549	lung
14	chr3:70311200-70312600	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr3:70311200-70313000	Weak transcription	Duodenum Mucosa	Duodenum
16	chr3:70311200-70313400	Weak transcription	HUVEC	blood vessel
17	chr3:70311600-70312800	Weak transcription	A549	lung
18	chr3:70312600-70312800	Enhancers	Fetal Intestine Small	intestine
19	chr3:70312600-70313200	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr3:70312800-70313400	Enhancers	A549	lung
21	chr3:70312800-70314200	Weak transcription	Fetal Intestine Small	intestine
22	chr3:70312800-70314400	Enhancers	Liver	Liver
23	chr3:70312800-70315000	Enhancers	Fetal Intestine Large	intestine
24	chr3:70313000-70313200	Enhancers	Duodenum Mucosa	Duodenum
25	chr3:70313000-70314200	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr3:70313000-70314600	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr3:70313200-70313600	Weak transcription	Duodenum Mucosa	Duodenum
28	chr3:70313200-70314200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr3:70313400-70314000	Enhancers	Fetal Heart	heart
30	chr3:70313400-70314000	Flanking Active TSS	A549	lung
31	chr3:70313400-70314000	Enhancers	HUVEC	blood vessel
32	chr3:70313400-70314400	Enhancers	HepG2	liver
33	chr3:70313600-70315200	Enhancers	Duodenum Mucosa	Duodenum
34	chr3:70314000-70314200	Enhancers	A549	lung
35	chr3:70314200-70314400	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr3:70314200-70314600	Enhancers	Fetal Intestine Small	intestine
37	chr3:70314200-70314800	Flanking Active TSS	A549	lung
38	chr3:70314800-70315200	Enhancers	A549	lung
39	chr3:70321800-70322000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr3:70321800-70322400	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr3:70322000-70322600	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr3:70322400-70322800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:70322400-70322800	Enhancers	Colon Smooth Muscle	Colon
44	chr3:70322400-70323000	Enhancers	A549	lung
45	chr3:70322400-70326600	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr3:70322600-70322800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr3:70322800-70325800	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr3:70323000-70325600	Weak transcription	A549	lung
49	chr3:70325600-70326200	Enhancers	A549	lung
50	chr3:70325800-70326000	Enhancers	Duodenum Mucosa	Duodenum

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