Variant report

Variant	nsv599268
Chromosome Location	chr5:104458953-105031008
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1425)
CpG islands
(count:183)
Chromatin interactive
region (count:110)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1425 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104574137-104574841	K562	blood:	n/a	n/a
2	ARID3A	chr5:104729126-104729280	K562	blood:	n/a	n/a
3	ARID3A	chr5:104565880-104566023	K562	blood:	n/a	n/a
4	ARID3A	chr5:104728602-104728921	K562	blood:	n/a	n/a
5	ARID3A	chr5:104726542-104727019	K562	blood:	n/a	n/a
6	ARID3A	chr5:104599139-104599705	K562	blood:	n/a	n/a
7	ATF1	chr5:104728486-104728895	K562	blood:	n/a	n/a
8	ATF1	chr5:104475478-104475496	K562	blood:	n/a	n/a
9	ATF1	chr5:104599299-104599581	K562	blood:	n/a	n/a
10	ATF1	chr5:104733331-104733371	K562	blood:	n/a	n/a
11	ATF1	chr5:104566225-104566645	K562	blood:	n/a	n/a
12	ATF3	chr5:104890433-104890632	K562	blood:	n/a	n/a
13	BACH1	chr5:104738330-104738373	K562	blood:	n/a	n/a
14	BACH1	chr5:104541248-104541265	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:104923724-104924138	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr5:104923763-104924073	K562	blood:	n/a	n/a
17	BACH1	chr5:104779909-104779930	K562	blood:	n/a	n/a
18	BCL11A	chr5:104502865-104503067	H1-hESC	embryonic stem cell:	n/a	n/a
19	BHLHE40	chr5:104928859-104929002	K562	blood:	n/a	n/a
20	BHLHE40	chr5:104728493-104728748	K562	blood:	n/a	n/a
21	BRCA1	chr5:105023264-105023360	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr5:104868861-104868905	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr5:104488401-104488414	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr5:104928778-104929345	K562	blood:	n/a	n/a
25	CBX3	chr5:104699005-104699210	K562	blood:	n/a	n/a
26	CBX3	chr5:104755037-104755389	K562	blood:	n/a	n/a
27	CBX3	chr5:104728363-104729015	K562	blood:	n/a	n/a
28	CBX3	chr5:104866542-104866887	K562	blood:	n/a	n/a
29	CBX3	chr5:104923689-104924055	K562	blood:	n/a	n/a
30	CBX3	chr5:104686453-104686733	K562	blood:	n/a	n/a
31	CBX3	chr5:104728451-104728993	K562	blood:	n/a	n/a
32	CBX3	chr5:104866626-104866912	K562	blood:	n/a	n/a
33	CBX3	chr5:104796463-104796676	K562	blood:	n/a	n/a
34	CBX3	chr5:104796414-104796740	K562	blood:	n/a	n/a
35	CBX3	chr5:104939067-104939376	K562	blood:	n/a	n/a
36	CBX3	chr5:104755081-104755354	K562	blood:	n/a	n/a
37	CCNT2	chr5:104566220-104566624	K562	blood:	n/a	n/a
38	CCNT2	chr5:104890165-104890637	K562	blood:	n/a	n/a
39	CCNT2	chr5:104599218-104599525	K562	blood:	n/a	n/a
40	CCNT2	chr5:104928811-104929257	K562	blood:	n/a	n/a
41	CCNT2	chr5:104727769-104728552	K562	blood:	n/a	n/a
42	CEBPB	chr5:104788546-104788789	A549	lung:	n/a	chr5:104788606-104788619 chr5:104788606-104788617 chr5:104788603-104788620
43	CEBPB	chr5:104475627-104475670	K562	blood:	n/a	n/a
44	CEBPB	chr5:104665178-104665382	HepG2	liver:	n/a	chr5:104665268-104665280 chr5:104665263-104665274
45	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
46	CEBPB	chr5:104475600-104475772	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:104952330-104952720	MCF-7	breast:	n/a	n/a
48	CEBPB	chr5:104613163-104613370	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:104923760-104923972	K562	blood:	n/a	n/a
50	CEBPB	chr5:104709824-104710103	IMR90	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104728220-104728270	HNPCEpiC	eye:	n/a
2	chr5:104854808-104854858	PrEC	prostate:	n/a
3	chr5:104854808-104854858	HCM	heart:	n/a
4	chr5:104728220-104728270	AG04449	skin:	fetal
5	chr5:104728220-104728270	HCPEpiC	choroid plexus:	n/a
6	chr5:104854808-104854858	PANC-1	pancreas:	n/a
7	chr5:104728220-104728270	HIPEpiC	eye:	n/a
8	chr5:104854808-104854858	GM12892	blood:	n/a
9	chr5:104728220-104728270	SK-N-MC	brain:	n/a
10	chr5:104728220-104728270	MCF-7	breast:	n/a
11	chr5:104728427-104728477	IMR90	lung:	fetal
12	chr5:104854808-104854858	ovcar-3	ovarian:	n/a
13	chr5:104854808-104854858	HNPCEpiC	eye:	n/a
14	chr5:104728220-104728270	IMR90	lung:	fetal
15	chr5:104728427-104728477	GM06990	blood:	n/a
16	chr5:104728220-104728270	GM12892	blood:	n/a
17	chr5:104728427-104728477	AG04449	skin:	fetal
18	chr5:104854808-104854858	HL-60	blood:	n/a
19	chr5:104728220-104728270	SKMC	muscle:	n/a
20	chr5:104854808-104854858	BJ	skin:	n/a
21	chr5:104728220-104728270	MCF10A-Er-Src	breast:	n/a
22	chr5:104854808-104854858	ECC-1	luminal epithelium:	n/a
23	chr5:104728220-104728270	PrEC	prostate:	n/a
24	chr5:104854808-104854858	SK-N-SH_RA	brain:	n/a
25	chr5:104854808-104854858	HMEC	breast:	n/a
26	chr5:104854808-104854858	K562	blood:	n/a
27	chr5:104728220-104728270	PANC-1	pancreas:	n/a
28	chr5:104728220-104728270	AoSMC	blood vessel:	n/a
29	chr5:104854808-104854858	AoSMC	blood vessel:	n/a
30	chr5:104728220-104728270	NHBE	bronchial:	n/a
31	chr5:104728427-104728477	BE2_C	brain:	n/a
32	chr5:104854808-104854858	GM12891	blood:	n/a
33	chr5:104728427-104728477	HAEpiC	amniotic membrane:	n/a
34	chr5:104728427-104728477	Caco-2	colon:	n/a
35	chr5:104728427-104728477	AG09309	skin:	n/a
36	chr5:104728427-104728477	Hepatocyte	liver:	n/a
37	chr5:104728427-104728477	CMK	blood:	n/a
38	chr5:104854808-104854858	Jurkat	blood:	n/a
39	chr5:104728427-104728477	AG09319	gingival:	n/a
40	chr5:104728427-104728477	PANC-1	pancreas:	n/a
41	chr5:104854808-104854858	Hepatocyte	liver:	n/a
42	chr5:104854808-104854858	PFSK-1	brain:	n/a
43	chr5:104728427-104728477	HNPCEpiC	eye:	n/a
44	chr5:104728220-104728270	Hela-S3	cervix:	n/a
45	chr5:104728220-104728270	NB4	blood:	n/a
46	chr5:104728427-104728477	U87	brain:	n/a
47	chr5:104854808-104854858	H1-hESC	embryonic stem cell:	embryo
48	chr5:104728427-104728477	Hela-S3	cervix:	n/a
49	chr5:104854808-104854858	ProgFib	skin:	n/a
50	chr5:104728427-104728477	HEK293	kidney:	embryo

(count:110 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:104726534..104729492-chr5:107716153..107718681,2	K562	blood:
2	chr4:114611671..114612572-chr5:104870661..104871343,2	MCF-7	breast:
3	chr5:104584886..104590168-chr5:104590478..104594256,4	K562	blood:
4	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
5	chr5:104604624..104606834-chr5:104613480..104615859,2	K562	blood:
6	chr5:104545106..104548123-chr5:104549429..104551527,3	K562	blood:
7	chr5:104369743..104372595-chr5:104912590..104914639,2	K562	blood:
8	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:
9	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
10	chr19:12903711..12905991-chr5:104578289..104580216,2	MCF-7	breast:
11	chr5:104710520..104712024-chr5:104741469..104744150,2	K562	blood:
12	chr5:104649160..104650852-chr5:104651591..104654211,3	K562	blood:
13	chr5:104645770..104648035-chr5:104661663..104663662,2	MCF-7	breast:
14	chr5:105020604..105022819-chr5:105026023..105028609,2	K562	blood:
15	chr5:104711472..104715081-chr5:104725603..104729958,5	K562	blood:
16	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
17	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
18	chr5:103982040..103982621-chr5:104952113..104952873,2	MCF-7	breast:
19	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
20	chr5:104928031..104930264-chr5:104952247..104955234,2	MCF-7	breast:
21	chr5:104952005..104953083-chr5:105576858..105577888,9	MCF-7	breast:
22	chr5:104682524..104684533-chr5:104692732..104695457,2	MCF-7	breast:
23	chr5:104927470..104929144-chr5:104929220..104932182,2	K562	blood:
24	chr5:104582906..104584797-chr5:104601356..104603170,2	K562	blood:
25	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
26	chr5:104995980..104998958-chr5:105000581..105003176,3	MCF-7	breast:
27	chr5:104995980..104998958-chr5:105000581..105003176,3	MCF-7	breast:
28	chr5:104660610..104663385-chr5:104663843..104665843,2	K562	blood:
29	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:
30	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
31	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
32	chr5:104712112..104715391-chr5:104727182..104729595,3	K562	blood:
33	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
34	chr5:104927470..104929144-chr5:104929220..104932182,2	K562	blood:
35	chr5:104943469..104946264-chr5:104959458..104962320,2	K562	blood:
36	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:
37	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
38	chr5:104928031..104930264-chr5:104952247..104955234,2	MCF-7	breast:
39	chr5:104576197..104577737-chr5:104582724..104585208,2	K562	blood:
40	chr5:104686842..104688917-chr5:104691899..104693400,2	K562	blood:
41	chr5:104926004..104928970-chr5:104930124..104932222,3	K562	blood:
42	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
43	chr5:104565194..104566957-chr5:104571048..104573999,2	K562	blood:
44	chr5:104810915..104813579-chr5:104817384..104819206,2	MCF-7	breast:
45	chr5:104768629..104770858-chr5:104785097..104787270,2	K562	blood:
46	chr5:104810915..104813579-chr5:104817384..104819206,2	MCF-7	breast:
47	chr5:104545961..104548123-chr5:104549429..104551527,2	K562	blood:
48	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
49	chr5:104567163..104569932-chr5:104572220..104574679,2	MCF-7	breast:
50	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-6	chr5:104728462-104728671	ENSG00000251574
2	lnc-NUDT12-7	chr5:104581998-104582065	ENSG00000253584
3	lnc-NUDT12-7	chr5:104582013-104582067	NONHSAT103097
4	lnc-NUDT12-7	chr5:104728462-104728989	NONHSAT103097

No data

Variant related genes	Relation type
ENSG00000253584	TF binding region
ENSG00000251574	TF binding region
ENSG00000253584	CpG island
ENSG00000251574	CpG island
ENSG00000132874	chromatin interactions
ENSG00000145743	chromatin interactions
ENSG00000251574	chromatin interactions

Extended variants
information (count: 6875 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:6875 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561996612	chr5:104459643-104459644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs112839934	chr5:104459773-104459774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183620590	chr5:104459777-104459778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374154702	chr5:104459809-104459810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570477323	chr5:104459829-104459830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113904205	chr5:104459918-104459919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144732693	chr5:104459924-104459925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs294151	chr5:104459950-104459951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115767407	chr5:104459972-104459973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181049994	chr5:104459985-104459986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575435940	chr5:104460005-104460006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs114035053	chr5:104460067-104460068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs555527134	chr5:104460090-104460091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs294150	chr5:104460100-104460101	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs185697539	chr5:104460107-104460108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557997351	chr5:104460114-104460115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577624259	chr5:104460135-104460136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554468110	chr5:104460137-104460138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189961562	chr5:104460141-104460142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543754136	chr5:104460153-104460154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140732388	chr5:104460154-104460155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143761806	chr5:104460159-104460160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs294149	chr5:104460160-104460161	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs530989260	chr5:104460176-104460177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561885931	chr5:104460180-104460181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527448376	chr5:104460193-104460194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552623379	chr5:104460198-104460199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35372162	chr5:104468251-104468252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35874247	chr5:104468276-104468277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113282533	chr5:104468286-104468287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567672099	chr5:104468303-104468304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75324829	chr5:104468333-104468334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547160967	chr5:104468399-104468400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113486277	chr5:104468401-104468402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566841620	chr5:104468406-104468407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115212270	chr5:104468435-104468436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557647621	chr5:104468519-104468520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192639438	chr5:104468548-104468549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536964089	chr5:104468577-104468578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561983592	chr5:104468583-104468584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74355166	chr5:104468627-104468628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184485364	chr5:104468632-104468633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs148408688	chr5:104468637-104468638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541049944	chr5:104468662-104468663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545058576	chr5:104468668-104468669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573978185	chr5:104468692-104468693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565351200	chr5:104468730-104468731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77453892	chr5:104468752-104468753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs75935338	chr5:104468762-104468763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549768611	chr5:104468794-104468795	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Myelofibrosis	22110671	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
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104459600-104460200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr5:104468200-104468800	Enhancers	Brain Germinal Matrix	brain
3	chr5:104469400-104470600	Enhancers	Liver	Liver
4	chr5:104472600-104473200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:104473200-104474200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:104474200-104474400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:104485600-104486600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:104486000-104486600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:104488800-104489000	Enhancers	Fetal Lung	lung
10	chr5:104489000-104490800	Weak transcription	Fetal Lung	lung
11	chr5:104490800-104491200	ZNF genes & repeats	Fetal Lung	lung
12	chr5:104492600-104492800	ZNF genes & repeats	Aorta	Aorta
13	chr5:104492800-104494200	Weak transcription	Aorta	Aorta
14	chr5:104494000-104495600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr5:104503600-104504400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr5:104503800-104504400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr5:104503800-104504600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr5:104503800-104504600	Enhancers	Hela-S3	cervix
19	chr5:104504400-104505400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr5:104505800-104506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr5:104512000-104512400	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr5:104541800-104542600	Enhancers	Brain Germinal Matrix	brain
23	chr5:104550000-104550400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr5:104550200-104550600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:104550200-104550600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr5:104550200-104550600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr5:104550200-104550800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr5:104550400-104550600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr5:104550600-104552600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:104550800-104554800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr5:104552600-104553600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:104553000-104553800	Enhancers	Brain Germinal Matrix	brain
33	chr5:104553200-104554200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr5:104553600-104555200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:104554200-104554600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr5:104554600-104555400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr5:104554800-104555200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr5:104555000-104556600	Enhancers	Primary hematopoietic stem cells	blood
39	chr5:104555200-104555400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:104555400-104555800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:104555800-104557400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:104556200-104556600	Active TSS	Primary T helper cells PMA-I stimulated	--
43	chr5:104565200-104565400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:104565400-104565800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:104565600-104566600	Enhancers	K562	blood
46	chr5:104565800-104566800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:104565800-104566800	Enhancers	Colon Smooth Muscle	Colon
48	chr5:104566000-104566400	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr5:104566200-104566800	Enhancers	Fetal Lung	lung
50	chr5:104566800-104567600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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