Variant report

Variant	nsv537745
Chromosome Location	chr5:45264656-45872829
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	ATF1	chr5:45384259-45384430	K562	blood:	n/a	n/a
2	ATF1	chr5:45779869-45779893	K562	blood:	n/a	n/a
3	ATF1	chr5:45520472-45520538	K562	blood:	n/a	n/a
4	ATF2	chr5:45793733-45794112	GM12878	blood:	n/a	n/a
5	ATF2	chr5:45793625-45794610	GM12878	blood:	n/a	n/a
6	BACH1	chr5:45695045-45695509	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr5:45622469-45623083	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:45694432-45694821	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:45622547-45622743	K562	blood:	n/a	n/a
10	BACH1	chr5:45696406-45696585	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr5:45794116-45794419	GM12878	blood:	n/a	n/a
12	BATF	chr5:45793691-45794568	GM12878	blood:	n/a	n/a
13	BATF	chr5:45793742-45794099	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:45793739-45794103	GM12878	blood:	n/a	n/a
15	BCL11A	chr5:45794121-45794555	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:45793646-45794647	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:45848140-45848326	H1-hESC	embryonic stem cell:	n/a	n/a
18	BHLHE40	chr5:45799491-45799496	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:45793537-45794787	GM12878	blood:	n/a	n/a
20	BRCA1	chr5:45624018-45624277	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr5:45551191-45551382	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr5:45564807-45564864	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr5:45412229-45412265	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr5:45696466-45696687	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr5:45277804-45278448	HCT-116	colon:	n/a	n/a
26	CBX3	chr5:45385629-45386224	HCT-116	colon:	n/a	n/a
27	CBX3	chr5:45279148-45279663	HCT-116	colon:	n/a	n/a
28	CBX3	chr5:45385462-45386770	HCT-116	colon:	n/a	n/a
29	CEBPB	chr5:45609832-45610172	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:45454133-45454270	HepG2	liver:	n/a	chr5:45454221-45454232
31	CEBPB	chr5:45787427-45787684	IMR90	lung:	n/a	chr5:45787597-45787608
32	CEBPB	chr5:45529506-45529762	HepG2	liver:	n/a	chr5:45529613-45529626 chr5:45529613-45529624 chr5:45529614-45529625 chr5:45529615-45529624
33	CEBPB	chr5:45529565-45529645	A549	lung:	n/a	chr5:45529613-45529626 chr5:45529613-45529624 chr5:45529614-45529625 chr5:45529615-45529624
34	CEBPB	chr5:45376452-45376910	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:45787466-45787674	HepG2	liver:	n/a	chr5:45787597-45787608
36	CEBPB	chr5:45588337-45588611	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:45775648-45775852	HepG2	liver:	n/a	chr5:45775697-45775708 chr5:45775698-45775709 chr5:45775697-45775710 chr5:45775697-45775710 chr5:45775697-45775710
38	CEBPB	chr5:45684241-45684601	IMR90	lung:	n/a	chr5:45684417-45684428 chr5:45684416-45684429 chr5:45684418-45684427 chr5:45684416-45684427 chr5:45684418-45684427 chr5:45684416-45684429 chr5:45684418-45684427 chr5:45684418-45684427
39	CEBPB	chr5:45279219-45279745	HCT-116	colon:	n/a	n/a
40	CEBPB	chr5:45740075-45740364	A549	lung:	n/a	chr5:45740245-45740256
41	CEBPB	chr5:45787482-45787676	A549	lung:	n/a	chr5:45787597-45787608
42	CEBPB	chr5:45509316-45509326	A549	lung:	n/a	n/a
43	CEBPB	chr5:45684266-45684560	HepG2	liver:	n/a	chr5:45684417-45684428 chr5:45684416-45684429 chr5:45684418-45684427 chr5:45684416-45684427 chr5:45684418-45684427 chr5:45684416-45684429 chr5:45684418-45684427 chr5:45684418-45684427
44	CEBPB	chr5:45382708-45383117	Hela-S3	cervix:	n/a	chr5:45382913-45382922 chr5:45382896-45382907 chr5:45382913-45382922
45	CEBPB	chr5:45509164-45509380	HepG2	liver:	n/a	n/a
46	CEBPB	chr5:45382746-45383041	IMR90	lung:	n/a	chr5:45382913-45382922 chr5:45382896-45382907 chr5:45382913-45382922
47	CEBPB	chr5:45382769-45383034	HepG2	liver:	n/a	chr5:45382913-45382922 chr5:45382896-45382907 chr5:45382913-45382922
48	CEBPB	chr5:45684295-45684568	A549	lung:	n/a	chr5:45684417-45684428 chr5:45684416-45684429 chr5:45684418-45684427 chr5:45684416-45684427 chr5:45684418-45684427 chr5:45684416-45684429 chr5:45684418-45684427 chr5:45684418-45684427
49	CEBPB	chr5:45654134-45654270	A549	lung:	n/a	chr5:45654198-45654211 chr5:45654198-45654211 chr5:45654198-45654209 chr5:45654198-45654211
50	CEBPB	chr5:45822073-45822347	HepG2	liver:	n/a	chr5:45822202-45822215 chr5:45822242-45822253 chr5:45822202-45822213

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:45696928-45696978	AG09309	skin:	n/a
2	chr5:45696928-45696978	AG09309	skin:	n/a
3	chr5:45696592-45696642	NH-A	brain:	n/a
4	chr5:45693264-45693314	HRPEpiC	eye:	n/a
5	chr5:45696928-45696978	BE2_C	brain:	n/a
6	chr5:45569042-45569092	RPTEC	kidney:	n/a
7	chr5:45288543-45288593	HEEpiC	esophagus:	n/a
8	chr5:45696491-45696541	HCT-116	colon:	n/a
9	chr5:45694523-45694573	AG09309	skin:	n/a
10	chr5:45696455-45696505	NT2-D1	testis:	n/a
11	chr5:45695467-45695517	SK-N-SH	brain:	n/a
12	chr5:45695922-45695972	ovcar-3	ovarian:	n/a
13	chr5:45696928-45696978	RPTEC	kidney:	n/a
14	chr5:45695839-45695889	AG10803	skin:	n/a
15	chr5:45696491-45696541	AG09319	gingival:	n/a
16	chr5:45678610-45678660	AG10803	skin:	n/a
17	chr5:45693264-45693314	HL-60	blood:	n/a
18	chr5:45649048-45649098	HCPEpiC	choroid plexus:	n/a
19	chr5:45700402-45700452	HRPEpiC	eye:	n/a
20	chr5:45696491-45696541	PANC-1	pancreas:	n/a
21	chr5:45695922-45695972	Hela-S3	cervix:	n/a
22	chr5:45696491-45696541	AG09309	skin:	n/a
23	chr5:45693264-45693314	PANC-1	pancreas:	n/a
24	chr5:45553518-45553568	HCF	heart:	n/a
25	chr5:45499395-45499445	SK-N-MC	brain:	n/a
26	chr5:45696592-45696642	GM19239	blood:	n/a
27	chr5:45678610-45678660	AG04449	skin:	fetal
28	chr5:45695839-45695889	GM12878	blood:	n/a
29	chr5:45696491-45696541	ProgFib	skin:	n/a
30	chr5:45553518-45553568	HepG2	liver:	n/a
31	chr5:45695467-45695517	U87	brain:	n/a
32	chr5:45696491-45696541	MCF10A-Er-Src	breast:	n/a
33	chr5:45724903-45724953	GM12892	blood:	n/a
34	chr5:45678610-45678660	PANC-1	pancreas:	n/a
35	chr5:45649048-45649098	HCM	heart:	n/a
36	chr5:45649048-45649098	SK-N-SH_RA	brain:	n/a
37	chr5:45499395-45499445	SKMC	muscle:	n/a
38	chr5:45724903-45724953	LNCaP	prostate:	n/a
39	chr5:45696206-45696256	HCT-116	colon:	n/a
40	chr5:45695241-45695291	H1-hESC	embryonic stem cell:	embryo
41	chr5:45569042-45569092	HNPCEpiC	eye:	n/a
42	chr5:45695922-45695972	GM12891	blood:	n/a
43	chr5:45693264-45693314	GM12878	blood:	n/a
44	chr5:45695839-45695889	HUVEC	blood vessel:	n/a
45	chr5:45695922-45695972	H1-hESC	embryonic stem cell:	embryo
46	chr5:45696592-45696642	HRE	kidney:	n/a
47	chr5:45695922-45695972	HCT-116	colon:	n/a
48	chr5:45696455-45696505	Hepatocyte	liver:	n/a
49	chr5:45695643-45695693	AG04449	skin:	fetal
50	chr5:45695643-45695693	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:45038409..45039119-chr5:45520902..45521831,4	MCF-7	breast:
2	chr5:45389967..45392520-chr5:45393920..45396887,2	K562	blood:
3	chr11:62608627..62609151-chr5:45773998..45774657,2	MCF-7	breast:
4	chr5:44952200..44952811-chr5:45521283..45521849,2	MCF-7	breast:
5	chr5:45700474..45703420-chr5:45719507..45722171,2	MCF-7	breast:
6	chr15:66571588..66572090-chr5:45541388..45542303,2	MCF-7	breast:
7	chr5:44952363..44953098-chr5:45773975..45774930,2	MCF-7	breast:
8	chr5:45688826..45690382-chr5:45691879..45693420,2	K562	blood:
9	chr5:45423533..45425292-chr5:45434104..45435924,2	MCF-7	breast:
10	chr5:45635537..45637341-chr5:45642108..45644494,2	K562	blood:
11	chr5:45435601..45437646-chr5:45441992..45444757,2	K562	blood:
12	chr5:45423533..45425292-chr5:45434104..45435924,2	MCF-7	breast:
13	chr5:45435601..45437646-chr5:45441992..45444757,2	K562	blood:
14	chr5:45038244..45038751-chr5:45773997..45774955,2	MCF-7	breast:
15	chr5:45292372..45295265-chr5:45301198..45304020,2	MCF-7	breast:
16	chr17:56742322..56745282-chr5:45859385..45861280,2	MCF-7	breast:
17	chr5:45292372..45295265-chr5:45301198..45304020,2	MCF-7	breast:
18	chr1:205318512..205319277-chr5:45469628..45470349,2	MCF-7	breast:
19	chr5:45468898..45471467-chr5:45477657..45479826,2	MCF-7	breast:
20	chr5:45232284..45234490-chr5:45416046..45418115,2	MCF-7	breast:
21	chr5:45688826..45690382-chr5:45691879..45693420,2	K562	blood:
22	chr5:45468898..45471467-chr5:45477657..45479826,2	MCF-7	breast:
23	chr5:45389967..45392520-chr5:45393920..45396887,2	K562	blood:
24	chr5:45487505..45488239-chr6:10695353..10695968,2	MCF-7	breast:
25	chr5:44952326..44952886-chr5:45639183..45639775,2	MCF-7	breast:
26	chr5:45635537..45637341-chr5:45642108..45644494,2	K562	blood:
27	chr5:45700474..45703420-chr5:45719507..45722171,2	MCF-7	breast:
28	chr3:104438340..104439030-chr5:45401914..45402431,2	MCF-7	breast:
29	chr13:55537336..55537947-chr5:45562607..45563107,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPS30-13	chr5:45574692-45576714	NONHSAT101361
2	lnc-MRPS30-14	chr5:45749057-45749335	NONHSAT101363
3	lnc-MRPS30-12	chr5:45558021-45560088	NONHSAT101360
4	lnc-MRPS30-14	chr5:45752904-45753159	NONHSAT101363
5	lnc-FGF10-4	chr5:45267793-45268115	ENSG00000251117.1
6	lnc-FGF10-4	chr5:45266826-45266920	ENSG00000251117.1
7	lnc-MRPS30-14	chr5:45753168-45753300	NONHSAT101363

Variant related genes	Relation type
HCN1	TF binding region
ENSG00000250422	TF binding region
ENSG00000250017	TF binding region
HCN1	CpG island
ENSG00000250422	CpG island
ENSG00000250017	CpG island
ENSG00000199426	chromatin interactions

Extended variants
information (count: 7762 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:7762 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541319118	chr5:45264672-45264673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189535581	chr5:45264696-45264697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533125424	chr5:45264712-45264713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371156989	chr5:45264742-45264743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536837263	chr5:45264776-45264777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376924860	chr5:45264790-45264791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543906068	chr5:45264886-45264887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563594846	chr5:45264894-45264895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537015867	chr5:45264897-45264898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531554925	chr5:45264917-45264918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548432081	chr5:45264924-45264925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370006472	chr5:45264949-45264950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568245376	chr5:45264975-45264976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372476051	chr5:45264988-45264989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182616113	chr5:45265018-45265019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186890407	chr5:45265019-45265020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539030850	chr5:45265032-45265033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6870996	chr5:45265035-45265036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34751562	chr5:45265044-45265045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569681557	chr5:45265081-45265082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535520403	chr5:45265096-45265097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548988987	chr5:45265120-45265121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572304716	chr5:45265163-45265164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567903745	chr5:45265191-45265192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541327117	chr5:45265223-45265224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35954404	chr5:45265238-45265239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375617218	chr5:45265245-45265246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577981705	chr5:45265290-45265291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34632955	chr5:45265291-45265292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs68104098	chr5:45265292-45265293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76090506	chr5:45265306-45265307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62367519	chr5:45265308-45265309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78727872	chr5:45265325-45265326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563677454	chr5:45265341-45265342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182816519	chr5:45265353-45265354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553669951	chr5:45265400-45265401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543135009	chr5:45265443-45265444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188930031	chr5:45265472-45265473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527442580	chr5:45265474-45265475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6451792	chr5:45265510-45265511	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs564197737	chr5:45265546-45265547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373830495	chr5:45265554-45265555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113689530	chr5:45265569-45265570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549547361	chr5:45265585-45265586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112616378	chr5:45265622-45265623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139237113	chr5:45265633-45265634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539270794	chr5:45265637-45265638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142447191	chr5:45265676-45265677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113369731	chr5:45265751-45265752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13180087	chr5:45265768-45265769	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	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
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hirschsprung''s Disease	21712996	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:45263400-45271200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr5:45270200-45272200	Enhancers	Fetal Heart	heart
3	chr5:45271200-45271600	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr5:45271200-45271800	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr5:45271600-45272000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr5:45272000-45277400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr5:45272200-45273200	Weak transcription	Fetal Heart	heart
8	chr5:45273400-45273600	Enhancers	Fetal Heart	heart
9	chr5:45273400-45273600	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr5:45273400-45273600	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr5:45273600-45274800	Enhancers	Liver	Liver
12	chr5:45274000-45275000	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr5:45274800-45275000	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr5:45275000-45276000	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr5:45276000-45276400	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr5:45277000-45278000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr5:45277400-45280400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr5:45277800-45278200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr5:45277800-45278200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:45277800-45279800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:45277800-45279800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr5:45278000-45279000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr5:45278000-45279800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr5:45278200-45278400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr5:45278200-45278400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr5:45278200-45279600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr5:45278400-45280400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr5:45278400-45280600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr5:45279000-45279600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr5:45279000-45279600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr5:45279800-45280400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr5:45280000-45280600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:45280200-45280400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr5:45280400-45280800	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr5:45280400-45281400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
36	chr5:45280400-45281400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
37	chr5:45280600-45280800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
38	chr5:45280600-45280800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
39	chr5:45281400-45287800	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr5:45284200-45285200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr5:45284600-45284800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr5:45284600-45285000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr5:45284600-45285200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:45284600-45285400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr5:45284800-45288000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:45285000-45288600	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:45285200-45288400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:45285200-45288400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:45285400-45287800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr5:45287800-45289000	Enhancers	H1 Cell Line	embryonic stem cell

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