Variant report

Variant	nsv882615
Chromosome Location	chr5:104626717-104767470
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	ARID3A	chr5:104729126-104729280	K562	blood:	n/a	n/a
2	ARID3A	chr5:104726542-104727019	K562	blood:	n/a	n/a
3	ARID3A	chr5:104728602-104728921	K562	blood:	n/a	n/a
4	ATF1	chr5:104733331-104733371	K562	blood:	n/a	n/a
5	ATF1	chr5:104728486-104728895	K562	blood:	n/a	n/a
6	BACH1	chr5:104738330-104738373	K562	blood:	n/a	n/a
7	BHLHE40	chr5:104728493-104728748	K562	blood:	n/a	n/a
8	CBX3	chr5:104728363-104729015	K562	blood:	n/a	n/a
9	CBX3	chr5:104755081-104755354	K562	blood:	n/a	n/a
10	CBX3	chr5:104699005-104699210	K562	blood:	n/a	n/a
11	CBX3	chr5:104686453-104686733	K562	blood:	n/a	n/a
12	CBX3	chr5:104728451-104728993	K562	blood:	n/a	n/a
13	CBX3	chr5:104755037-104755389	K562	blood:	n/a	n/a
14	CCNT2	chr5:104727769-104728552	K562	blood:	n/a	n/a
15	CEBPB	chr5:104720977-104721172	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr5:104709884-104709984	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr5:104665950-104666211	Hela-S3	cervix:	n/a	chr5:104666084-104666093 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666082-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666083-104666094
18	CEBPB	chr5:104626968-104627293	HepG2	liver:	n/a	chr5:104627123-104627134
19	CEBPB	chr5:104665908-104666270	HepG2	liver:	n/a	chr5:104666084-104666093 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666082-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666083-104666094
20	CEBPB	chr5:104709840-104710114	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:104665902-104666250	IMR90	lung:	n/a	chr5:104666084-104666093 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666082-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666083-104666094
22	CEBPB	chr5:104647437-104647690	K562	blood:	n/a	chr5:104647455-104647466 chr5:104647453-104647466 chr5:104647453-104647466
23	CEBPB	chr5:104720876-104721252	K562	blood:	n/a	n/a
24	CEBPB	chr5:104665990-104666190	H1-hESC	embryonic stem cell:	n/a	chr5:104666084-104666093 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666082-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666083-104666094
25	CEBPB	chr5:104709810-104710130	A549	lung:	n/a	n/a
26	CEBPB	chr5:104709824-104710103	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:104665939-104666271	K562	blood:	n/a	chr5:104666084-104666093 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666082-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666083-104666094
28	CEBPB	chr5:104660073-104660304	HepG2	liver:	n/a	chr5:104660167-104660178 chr5:104660226-104660237 chr5:104660267-104660279 chr5:104660224-104660237
29	CEBPB	chr5:104665178-104665382	HepG2	liver:	n/a	chr5:104665268-104665280 chr5:104665263-104665274
30	CHD2	chr5:104728384-104728863	K562	blood:	n/a	n/a
31	CHD2	chr5:104727637-104727834	K562	blood:	n/a	n/a
32	CTCF	chr5:104640720-104640870	HRE	kidney:	n/a	n/a
33	CTCF	chr5:104674521-104674610	GM10266	blood:	n/a	n/a
34	CTCF	chr5:104640700-104640850	K562	blood:	n/a	n/a
35	CTCF	chr5:104727920-104728070	HepG2	liver:	n/a	n/a
36	CTCF	chr5:104640740-104640890	GM12865	blood:	n/a	n/a
37	CTCF	chr5:104640620-104640770	HMF	breast:	n/a	n/a
38	CTCF	chr5:104640680-104640830	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr5:104640760-104640910	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr5:104640640-104640790	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr5:104640700-104640850	HepG2	liver:	n/a	n/a
42	CTCF	chr5:104640620-104640770	HPF	lung:	n/a	n/a
43	CTCF	chr5:104640660-104640810	HCT-116	colon:	n/a	n/a
44	CTCF	chr5:104640620-104640770	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:104640680-104640830	GM12878	blood:	n/a	n/a
46	CTCF	chr5:104640700-104640850	HEK293	kidney:	n/a	n/a
47	CTCF	chr5:104640640-104640790	HMEC	breast:	n/a	n/a
48	CTCF	chr5:104640640-104640790	AG04450	lung:	n/a	n/a
49	CTCF	chr5:104640680-104640830	HCFaa	heart:	n/a	n/a
50	CTCF	chr5:104646160-104646310	AoAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104728220-104728270	LNCaP	prostate:	n/a
2	chr5:104728427-104728477	PANC-1	pancreas:	n/a
3	chr5:104728220-104728270	ovcar-3	ovarian:	n/a
4	chr5:104728427-104728477	T-47D	breast:	n/a
5	chr5:104728220-104728270	H1-hESC	embryonic stem cell:	embryo
6	chr5:104728427-104728477	BE2_C	brain:	n/a
7	chr5:104728427-104728477	PrEC	prostate:	n/a
8	chr5:104728220-104728270	GM12891	blood:	n/a
9	chr5:104728220-104728270	PFSK-1	brain:	n/a
10	chr5:104728220-104728270	HCPEpiC	choroid plexus:	n/a
11	chr5:104728427-104728477	HRPEpiC	eye:	n/a
12	chr5:104728427-104728477	NT2-D1	testis:	n/a
13	chr5:104728220-104728270	HUVEC	blood vessel:	n/a
14	chr5:104728220-104728270	NB4	blood:	n/a
15	chr5:104728427-104728477	SK-N-MC	brain:	n/a
16	chr5:104728427-104728477	GM19239	blood:	n/a
17	chr5:104728427-104728477	Caco-2	colon:	n/a
18	chr5:104728220-104728270	U87	brain:	n/a
19	chr5:104728427-104728477	HCT-116	colon:	n/a
20	chr5:104728427-104728477	ovcar-3	ovarian:	n/a
21	chr5:104728220-104728270	Hepatocyte	liver:	n/a
22	chr5:104728427-104728477	GM12892	blood:	n/a
23	chr5:104728220-104728270	IMR90	lung:	fetal
24	chr5:104728427-104728477	MCF-7	breast:	n/a
25	chr5:104728220-104728270	Caco-2	colon:	n/a
26	chr5:104728220-104728270	GM12892	blood:	n/a
27	chr5:104728220-104728270	SK-N-SH	brain:	n/a
28	chr5:104728220-104728270	GM12878	blood:	n/a
29	chr5:104728220-104728270	ProgFib	skin:	n/a
30	chr5:104728220-104728270	HIPEpiC	eye:	n/a
31	chr5:104728220-104728270	BJ	skin:	n/a
32	chr5:104728220-104728270	HRCEpiC	kidney:	n/a
33	chr5:104728427-104728477	GM12878	blood:	n/a
34	chr5:104728220-104728270	GM19239	blood:	n/a
35	chr5:104728220-104728270	PANC-1	pancreas:	n/a
36	chr5:104728220-104728270	HMEC	breast:	n/a
37	chr5:104728220-104728270	K562	blood:	n/a
38	chr5:104728220-104728270	AG04449	skin:	fetal
39	chr5:104728220-104728270	HRPEpiC	eye:	n/a
40	chr5:104728427-104728477	AoSMC	blood vessel:	n/a
41	chr5:104728427-104728477	AG04450	lung:	fetal
42	chr5:104728427-104728477	GM06990	blood:	n/a
43	chr5:104728427-104728477	Jurkat	blood:	n/a
44	chr5:104728427-104728477	HMEC	breast:	n/a
45	chr5:104728220-104728270	NT2-D1	testis:	n/a
46	chr5:104728220-104728270	AG09309	skin:	n/a
47	chr5:104728220-104728270	SKMC	muscle:	n/a
48	chr5:104728220-104728270	HEK293	kidney:	embryo
49	chr5:104728427-104728477	SK-N-SH	brain:	n/a
50	chr5:104728220-104728270	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:104712112..104715391-chr5:104727182..104729595,3	K562	blood:
2	chr5:104645770..104648035-chr5:104661663..104663662,2	MCF-7	breast:
3	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
4	chr5:104682524..104684533-chr5:104692732..104695457,2	MCF-7	breast:
5	chr5:104682524..104684533-chr5:104692732..104695457,2	MCF-7	breast:
6	chr5:104716167..104718489-chr5:104728063..104729895,2	K562	blood:
7	chr5:104679097..104680828-chr5:104708980..104711591,2	K562	blood:
8	chr5:104733236..104736068-chr5:104886596..104888346,2	MCF-7	breast:
9	chr5:104711472..104715081-chr5:104725603..104729958,5	K562	blood:
10	chr5:104710520..104712024-chr5:104741469..104744150,2	K562	blood:
11	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
12	chr5:104679097..104680828-chr5:104708980..104711591,2	K562	blood:
13	chr5:104727742..104729434-chr5:104763198..104765492,2	K562	blood:
14	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
15	chr5:104660610..104663385-chr5:104663843..104665843,2	K562	blood:
16	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
17	chr5:103843512..103846064-chr5:104654970..104657716,2	K562	blood:
18	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
19	chr5:104649160..104650852-chr5:104651591..104654211,3	K562	blood:
20	chr5:104686842..104688917-chr5:104691899..104693400,2	K562	blood:
21	chr5:104686842..104688917-chr5:104691899..104693400,2	K562	blood:
22	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
23	chr5:104682989..104685447-chr5:104726579..104728705,2	K562	blood:
24	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
25	chr5:104726359..104728666-chr5:105131284..105132821,2	K562	blood:
26	chr5:104649160..104650852-chr5:104651591..104654211,3	K562	blood:
27	chr5:104726534..104729492-chr5:107716153..107718681,2	K562	blood:
28	chr5:104660610..104663385-chr5:104663843..104665843,2	K562	blood:
29	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
30	chr5:104710520..104712024-chr5:104741469..104744150,2	K562	blood:
31	chr5:104645770..104648035-chr5:104661663..104663662,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104728462-104728989	NONHSAT103097
2	lnc-NUDT12-6	chr5:104728462-104728671	ENSG00000251574

Variant related genes	Relation type
ENSG00000251574	TF binding region
ENSG00000251574	CpG island
ENSG00000251574	chromatin interactions
ENSG00000145743	chromatin interactions

Extended variants
information (count: 1480 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1480 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183986027	chr5:104626859-104626860	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs573681448	chr5:104626947-104626948	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs112933022	chr5:104626960-104626961	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs9327935	chr5:104626973-104626974	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs559100099	chr5:104626980-104626981	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs533505033	chr5:104627025-104627026	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs573438462	chr5:104627127-104627128	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs376106687	chr5:104627130-104627131	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs369310854	chr5:104627162-104627163	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs10069587	chr5:104627182-104627183	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs139228276	chr5:104627246-104627247	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs116090635	chr5:104627278-104627279	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs549283597	chr5:104627288-104627289	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs569183722	chr5:104627291-104627292	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs530154208	chr5:104627343-104627344	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs538055734	chr5:104627346-104627347	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs377514697	chr5:104627367-104627368	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs114289065	chr5:104627375-104627376	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs528020819	chr5:104627397-104627398	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs370606191	chr5:104627402-104627403	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs547761912	chr5:104627504-104627505	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs551689277	chr5:104627530-104627531	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs571602073	chr5:104627555-104627556	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs143243154	chr5:104627621-104627622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374350542	chr5:104627631-104627632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566507030	chr5:104627638-104627639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557214273	chr5:104627647-104627648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10074955	chr5:104627654-104627655	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs535969875	chr5:104627672-104627673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543368030	chr5:104627675-104627676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553079824	chr5:104627681-104627682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572741137	chr5:104627700-104627701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187254461	chr5:104627775-104627776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565219576	chr5:104627810-104627811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575557968	chr5:104627833-104627834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147483051	chr5:104627868-104627869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148545171	chr5:104627908-104627909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142755841	chr5:104627928-104627929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552772226	chr5:104627990-104627991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7728401	chr5:104627992-104627993	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs560673787	chr5:104628057-104628058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77169327	chr5:104628100-104628101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6867329	chr5:104628129-104628130	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs7732879	chr5:104628200-104628201	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs559479022	chr5:104628206-104628207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367705854	chr5:104628237-104628238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550708804	chr5:104628254-104628255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7733023	chr5:104628294-104628295	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs192023836	chr5:104628361-104628362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552778262	chr5:104628366-104628367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104626800-104627600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:104627600-104628400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:104628400-104629200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:104629200-104629600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:104629600-104630000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:104630000-104630200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:104630200-104630600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:104630600-104631000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:104631000-104631200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:104631200-104636400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:104636400-104636800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:104649600-104649800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:104655200-104655800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:104686200-104686400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:104686400-104689000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr5:104715600-104716800	Enhancers	Fetal Brain Male	brain
17	chr5:104722000-104722200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr5:104722200-104722600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr5:104722200-104722800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr5:104722200-104723200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr5:104722400-104723400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr5:104722400-104723600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr5:104722600-104723000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr5:104724800-104725800	Enhancers	K562	blood
25	chr5:104725800-104726400	Weak transcription	K562	blood
26	chr5:104726400-104729200	Active TSS	K562	blood
27	chr5:104727400-104727600	Enhancers	Placenta	Placenta
28	chr5:104727600-104727800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:104727600-104728000	Flanking Active TSS	Placenta	Placenta
30	chr5:104727600-104729000	Active TSS	HepG2	liver
31	chr5:104727800-104728000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr5:104727800-104728600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr5:104728000-104728400	Active TSS	Placenta	Placenta
34	chr5:104728400-104728800	ZNF genes & repeats	Placenta	Placenta
35	chr5:104742400-104743400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr5:104742400-104743600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr5:104742400-104743600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr5:104742600-104743400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr5:104742800-104743200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr5:104742800-104743400	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr5:104748600-104749200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr5:104748800-104749200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr5:104749200-104749600	Bivalent Enhancer	Placenta	Placenta
44	chr5:104749200-104749800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr5:104757800-104758600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr5:104763400-104764400	Enhancers	Fetal Intestine Large	intestine
47	chr5:104766000-104767600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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