Variant report

Variant	esv3510798
Chromosome Location	chr5:16966764-17125849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:973)
CpG islands
(count:915)
Chromatin interactive
region (count:34)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:973 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:17118841-17118886	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:16983216-16983715	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:17118878-17119132	K562	blood:	n/a	n/a
4	ATF1	chr5:17118791-17119097	K562	blood:	n/a	n/a
5	ATF1	chr5:17012523-17012700	K562	blood:	n/a	n/a
6	ATF3	chr5:17113357-17113905	A549	lung:	n/a	n/a
7	ATF3	chr5:17118709-17119111	K562	blood:	n/a	n/a
8	ATF3	chr5:17113541-17114004	A549	lung:	n/a	n/a
9	BACH1	chr5:17006327-17006386	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr5:17070065-17070739	A549	lung:	n/a	n/a
11	BCL3	chr5:17055971-17056633	A549	lung:	n/a	chr5:17056280-17056289
12	BCL3	chr5:17113364-17114023	A549	lung:	n/a	n/a
13	BCL3	chr5:17055970-17056696	A549	lung:	n/a	chr5:17056280-17056289
14	BCL3	chr5:17058477-17059019	A549	lung:	n/a	n/a
15	BCL3	chr5:17013122-17013511	A549	lung:	n/a	n/a
16	BCL3	chr5:17113349-17114305	A549	lung:	n/a	n/a
17	BCL3	chr5:17062157-17062626	A549	lung:	n/a	n/a
18	BHLHE40	chr5:17070833-17070947	K562	blood:	n/a	n/a
19	BHLHE40	chr5:16970304-16970653	K562	blood:	n/a	n/a
20	BHLHE40	chr5:16970479-16970499	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:17079653-17079697	A549	lung:	n/a	n/a
22	BHLHE40	chr5:17118767-17119102	K562	blood:	n/a	n/a
23	BHLHE40	chr5:17070151-17070417	K562	blood:	n/a	n/a
24	BHLHE40	chr5:17079984-17080037	K562	blood:	n/a	n/a
25	CBX3	chr5:17118637-17119124	HCT-116	colon:	n/a	n/a
26	CBX3	chr5:17118620-17119301	HCT-116	colon:	n/a	n/a
27	CBX3	chr5:17118695-17119050	K562	blood:	n/a	n/a
28	CCNT2	chr5:17118784-17119145	K562	blood:	n/a	n/a
29	CEBPB	chr5:17013250-17013503	MCF-7	breast:	n/a	chr5:17013356-17013367
30	CEBPB	chr5:17019477-17019975	IMR90	lung:	n/a	chr5:17019649-17019660
31	CEBPB	chr5:17088234-17088508	Hela-S3	cervix:	n/a	chr5:17088363-17088374 chr5:17088386-17088397
32	CEBPB	chr5:17113041-17114245	A549	lung:	n/a	n/a
33	CEBPB	chr5:17088212-17088556	A549	lung:	n/a	chr5:17088363-17088374 chr5:17088386-17088397
34	CEBPB	chr5:17088230-17088451	K562	blood:	n/a	chr5:17088363-17088374 chr5:17088386-17088397
35	CEBPB	chr5:17016664-17016800	Hela-S3	cervix:	n/a	chr5:17016733-17016744
36	CEBPB	chr5:17013301-17013385	K562	blood:	n/a	chr5:17013356-17013367
37	CEBPB	chr5:17054583-17054733	A549	lung:	n/a	chr5:17054649-17054660
38	CEBPB	chr5:16972221-16972410	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:17113355-17113775	A549	lung:	n/a	n/a
40	CEBPB	chr5:17013195-17013576	Hela-S3	cervix:	n/a	chr5:17013356-17013367
41	CEBPB	chr5:17113344-17113881	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:17113361-17113899	A549	lung:	n/a	n/a
43	CEBPB	chr5:17012465-17012896	A549	lung:	n/a	n/a
44	CEBPB	chr5:16987969-16988251	H1-hESC	embryonic stem cell:	n/a	chr5:16988108-16988119
45	CEBPB	chr5:17070070-17070714	A549	lung:	n/a	n/a
46	CEBPB	chr5:17013136-17013597	A549	lung:	n/a	chr5:17013356-17013367
47	CEBPB	chr5:16999251-16999475	IMR90	lung:	n/a	n/a
48	CEBPB	chr5:16987950-16988215	HepG2	liver:	n/a	chr5:16988108-16988119
49	CEBPB	chr5:17054560-17054787	K562	blood:	n/a	chr5:17054649-17054660
50	CEBPB	chr5:16986137-16986208	IMR90	lung:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17115565-17115615	HRCEpiC	kidney:	n/a
2	chr5:17115565-17115615	GM12878	blood:	n/a
3	chr5:17031869-17031919	HRPEpiC	eye:	n/a
4	chr5:17057446-17057496	HRE	kidney:	n/a
5	chr5:17031953-17032003	GM12878	blood:	n/a
6	chr5:17001489-17001539	PFSK-1	brain:	n/a
7	chr5:17115565-17115615	CMK	blood:	n/a
8	chr5:17031953-17032003	AG09309	skin:	n/a
9	chr5:16994665-16994715	HRCEpiC	kidney:	n/a
10	chr5:17113616-17113666	SK-N-MC	brain:	n/a
11	chr5:17023042-17023092	GM12892	blood:	n/a
12	chr5:16994665-16994715	NHBE	bronchial:	n/a
13	chr5:17062511-17062561	HCM	heart:	n/a
14	chr5:17057446-17057496	SKMC	muscle:	n/a
15	chr5:17023042-17023092	HL-60	blood:	n/a
16	chr5:17120060-17120110	HEK293	kidney:	embryo
17	chr5:17057446-17057496	PANC-1	pancreas:	n/a
18	chr5:17031869-17031919	GM12878	blood:	n/a
19	chr5:16994665-16994715	LNCaP	prostate:	n/a
20	chr5:17001489-17001539	PrEC	prostate:	n/a
21	chr5:17113616-17113666	GM12892	blood:	n/a
22	chr5:17113616-17113666	ProgFib	skin:	n/a
23	chr5:17001489-17001539	AG04449	skin:	fetal
24	chr5:17115565-17115615	LNCaP	prostate:	n/a
25	chr5:17115565-17115615	MCF-7	breast:	n/a
26	chr5:17119012-17119062	Caco-2	colon:	n/a
27	chr5:17019007-17019057	HCT-116	colon:	n/a
28	chr5:16990305-16990355	HRCEpiC	kidney:	n/a
29	chr5:17031869-17031919	HCPEpiC	choroid plexus:	n/a
30	chr5:17120060-17120110	Hepatocyte	liver:	n/a
31	chr5:17019007-17019057	A549	lung:	n/a
32	chr5:17023042-17023092	HNPCEpiC	eye:	n/a
33	chr5:17119012-17119062	HEEpiC	esophagus:	n/a
34	chr5:17120060-17120110	NHBE	bronchial:	n/a
35	chr5:16994665-16994715	SK-N-SH	brain:	n/a
36	chr5:17019007-17019057	NHDF-neo	bronchial:	n/a
37	chr5:17031869-17031919	PrEC	prostate:	n/a
38	chr5:16994665-16994715	GM06990	blood:	n/a
39	chr5:17062511-17062561	SKMC	muscle:	n/a
40	chr5:17119012-17119062	HCM	heart:	n/a
41	chr5:17031953-17032003	NHBE	bronchial:	n/a
42	chr5:17001489-17001539	IMR90	lung:	fetal
43	chr5:17119012-17119062	HRE	kidney:	n/a
44	chr5:17019007-17019057	ovcar-3	ovarian:	n/a
45	chr5:17057446-17057496	ECC-1	luminal epithelium:	n/a
46	chr5:17031953-17032003	HNPCEpiC	eye:	n/a
47	chr5:17062511-17062561	A549	lung:	n/a
48	chr5:17119012-17119062	PANC-1	pancreas:	n/a
49	chr5:17032596-17032646	HEK293	kidney:	embryo
50	chr5:17115565-17115615	HAEpiC	amniotic membrane:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:17072245..17074328-chr5:17081355..17083029,2	MCF-7	breast:
2	chr5:16995098..16996958-chr5:17000346..17002199,2	MCF-7	breast:
3	chr5:17017463..17019806-chr5:17023489..17025073,2	MCF-7	breast:
4	chr20:52740441..52742261-chr5:17072460..17075149,2	MCF-7	breast:
5	chr5:17055618..17058211-chr5:17065724..17068403,2	K562	blood:
6	chr5:17119510..17121601-chr5:17125768..17127398,2	MCF-7	breast:
7	chr5:16935309..16937325-chr5:17118507..17120513,2	MCF-7	breast:
8	chr5:17076577..17078375-chr5:17096009..17098566,2	MCF-7	breast:
9	chr5:16934582..16937209-chr5:17122711..17127017,4	MCF-7	breast:
10	chr5:17068695..17071363-chr5:17076784..17079484,2	MCF-7	breast:
11	chr5:16934373..16937606-chr5:17013930..17017066,4	MCF-7	breast:
12	chr5:16934962..16937579-chr5:17059842..17062235,2	MCF-7	breast:
13	chr5:17072245..17074328-chr5:17081355..17083029,2	MCF-7	breast:
14	chr5:17005526..17008394-chr5:17011075..17012616,2	MCF-7	breast:
15	chr5:16986508..16989410-chr5:17147317..17149449,2	MCF-7	breast:
16	chr5:16999937..17003903-chr5:17005517..17010107,4	MCF-7	breast:
17	chr5:17076577..17078375-chr5:17096009..17098566,2	MCF-7	breast:
18	chr5:17004434..17006256-chr5:17007845..17010404,2	K562	blood:
19	chr15:31658493..31659133-chr5:17069697..17070202,2	MCF-7	breast:
20	chr5:17004434..17006256-chr5:17007845..17010404,2	K562	blood:
21	chr5:16934978..16936561-chr5:16972825..16974430,2	MCF-7	breast:
22	chr5:17017463..17019806-chr5:17023489..17025073,2	MCF-7	breast:
23	chr5:17055618..17058211-chr5:17065724..17068403,2	K562	blood:
24	chr5:17119510..17121601-chr5:17125768..17127398,2	MCF-7	breast:
25	chr5:16935759..16937605-chr5:17023658..17025231,2	MCF-7	breast:
26	chr5:17005526..17008394-chr5:17011075..17012616,2	MCF-7	breast:
27	chr5:16935045..16937109-chr5:17037395..17039614,2	MCF-7	breast:
28	chr5:16999937..17003903-chr5:17005517..17010107,4	MCF-7	breast:
29	chr5:16935331..16937898-chr5:17010889..17014144,4	MCF-7	breast:
30	chr5:16934770..16937849-chr5:17124311..17128019,3	MCF-7	breast:
31	chr5:16995098..16996958-chr5:17000346..17002199,2	MCF-7	breast:
32	chr5:16934690..16937466-chr5:17114616..17116389,3	MCF-7	breast:
33	chr5:16883490..16885617-chr5:17011887..17014186,2	MCF-7	breast:
34	chr5:17068695..17071363-chr5:17076784..17079484,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-2	chr5:17065660-17065809	XLOC_004306
2	lnc-BASP1-2	chr5:17065660-17065809	XLOC_004306
3	lnc-BASP1-2	chr5:17089182-17089310	XLOC_004306
4	lnc-BASP1-2	chr5:17063337-17063762	XLOC_004306
5	lnc-MYO10-5	chr5:17107469-17107898	ENSG00000271892.1
6	lnc-BASP1-2	chr5:17063337-17063762	XLOC_004306

No data

Variant related genes	Relation type
BASP1	TF binding region
ENSG00000271892	TF binding region
ENSG00000206814	TF binding region
BASP1	CpG island
ENSG00000271892	CpG island
ENSG00000206814	CpG island
ENSG00000145555	chromatin interactions

Extended variants
information (count: 7262 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:7262 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369517912	chr5:16966768-16966769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557100050	chr5:16966772-16966773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186223919	chr5:16966776-16966777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535889965	chr5:16966826-16966827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77512080	chr5:16966853-16966854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532020876	chr5:16966855-16966856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566452212	chr5:16966870-16966871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372377647	chr5:16966957-16966958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146658862	chr5:16966963-16966964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550449987	chr5:16966986-16966987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553246006	chr5:16966992-16966993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376638131	chr5:16967030-16967031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369191306	chr5:16967083-16967084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200715309	chr5:16967167-16967168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181360449	chr5:16967168-16967169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79531649	chr5:16967169-16967170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs71672431	chr5:16967170-16967171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs61457214	chr5:16967172-16967173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6866906	chr5:16967173-16967174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200366330	chr5:16967178-16967179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201061291	chr5:16967180-16967181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62371047	chr5:16967265-16967266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190696049	chr5:16967271-16967272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201527679	chr5:16967296-16967297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs118105375	chr5:16967315-16967316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78639288	chr5:16967337-16967338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375244825	chr5:16967341-16967342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372483685	chr5:16967366-16967367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200116915	chr5:16967371-16967372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372058320	chr5:16967386-16967387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112173996	chr5:16967400-16967401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs398108642	chr5:16967412-16967413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114819582	chr5:16967413-16967414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542740629	chr5:16967416-16967417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550632437	chr5:16967436-16967437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182729739	chr5:16967469-16967470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561375273	chr5:16967521-16967522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74464337	chr5:16967522-16967523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386685881	chr5:16967534-16967535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111887417	chr5:16967539-16967540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116364360	chr5:16967540-16967541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550766675	chr5:16967577-16967578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534041951	chr5:16967596-16967597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs60550726	chr5:16967604-16967605	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs188051972	chr5:16967628-16967629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573853670	chr5:16967636-16967637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190091319	chr5:16967665-16967666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533496262	chr5:16967667-16967668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553270194	chr5:16967671-16967672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577890073	chr5:16967679-16967680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1534 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16962600-16970400	Weak transcription	Right Atrium	heart
2	chr5:16964800-16970000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr5:16965200-16970400	Weak transcription	NHEK	skin
4	chr5:16965400-16970400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:16965400-16970800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr5:16966000-16970200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr5:16966000-16973000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:16968400-16968800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:16968800-16970200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:16970000-16970600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:16970200-16971000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr5:16970200-16971200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:16970200-16972400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr5:16970200-16973800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:16970400-16970600	ZNF genes & repeats	Right Atrium	heart
16	chr5:16970400-16970800	Enhancers	NHEK	skin
17	chr5:16970400-16971000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr5:16970600-16971200	Enhancers	HMEC	breast
19	chr5:16970600-16972000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr5:16970600-16975000	Weak transcription	Right Atrium	heart
21	chr5:16970800-16971400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr5:16970800-16971800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr5:16971000-16972000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr5:16971000-16983200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr5:16971800-16976200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr5:16972400-16976000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr5:16973000-16973200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:16973000-16974400	Enhancers	Fetal Brain Male	brain
29	chr5:16973400-16974000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr5:16973400-16974400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr5:16973800-16976000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:16974600-16975600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr5:16975800-16977000	Enhancers	GM12878-XiMat	blood
34	chr5:16976000-16977000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr5:16976000-16977000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:16976200-16977000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr5:16976400-16977000	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr5:16977000-16980600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:16977000-16982000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr5:16977000-16983200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr5:16978600-16991400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:16980600-16983000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr5:16980800-16981000	Enhancers	A549	lung
44	chr5:16980800-16981600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr5:16980800-16981600	Enhancers	NH-A	brain
46	chr5:16980800-16982600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr5:16980800-16983200	Enhancers	HUVEC	blood vessel
48	chr5:16981000-16981200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr5:16981000-16981200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr5:16981000-16981600	Enhancers	Muscle Satellite Cultured Cells	--

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