Variant report

Variant	nsv1018651
Chromosome Location	chr5:45003750-45437670
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1058)
CpG islands
(count:672)
Chromatin interactive
region (count:28)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1058 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	chr5:45096698-45096779	K562	blood:	n/a	n/a
3	ATF1	chr5:45168279-45168343	K562	blood:	n/a	n/a
4	ATF1	chr5:45138018-45138034	K562	blood:	n/a	n/a
5	ATF1	chr5:45174044-45174212	K562	blood:	n/a	n/a
6	ATF2	chr5:45205408-45206121	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:45205482-45205984	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:45194371-45194425	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr5:45017733-45018036	GM12878	blood:	n/a	chr5:45017901-45017912
10	BATF	chr5:45206930-45207199	GM12878	blood:	n/a	n/a
11	BATF	chr5:45206937-45207259	GM12878	blood:	n/a	n/a
12	BATF	chr5:45017504-45017655	GM12878	blood:	n/a	n/a
13	BATF	chr5:45206365-45206599	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:45205512-45205912	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr5:45205547-45205862	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr5:45206949-45207174	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:45017743-45018109	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:45038643-45038778	GM12878	blood:	n/a	n/a
19	BRCA1	chr5:45412229-45412265	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr5:45038492-45039027	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr5:45279148-45279663	HCT-116	colon:	n/a	n/a
22	CBX3	chr5:45385629-45386224	HCT-116	colon:	n/a	n/a
23	CBX3	chr5:45277804-45278448	HCT-116	colon:	n/a	n/a
24	CBX3	chr5:45152073-45152342	K562	blood:	n/a	n/a
25	CBX3	chr5:45385462-45386770	HCT-116	colon:	n/a	n/a
26	CEBPB	chr5:45187543-45187803	A549	lung:	n/a	chr5:45187663-45187674
27	CEBPB	chr5:45024506-45024752	A549	lung:	n/a	chr5:45024594-45024605
28	CEBPB	chr5:45009705-45009856	A549	lung:	n/a	n/a
29	CEBPB	chr5:45234640-45234841	A549	lung:	n/a	n/a
30	CEBPB	chr5:45382769-45383034	HepG2	liver:	n/a	chr5:45382913-45382922 chr5:45382896-45382907 chr5:45382913-45382922
31	CEBPB	chr5:45187482-45187821	Hela-S3	cervix:	n/a	chr5:45187663-45187674
32	CEBPB	chr5:45060873-45061152	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr5:45385237-45386284	HCT-116	colon:	n/a	n/a
34	CEBPB	chr5:45382746-45383041	IMR90	lung:	n/a	chr5:45382913-45382922 chr5:45382896-45382907 chr5:45382913-45382922
35	CEBPB	chr5:45417169-45418084	Hela-S3	cervix:	n/a	chr5:45417980-45417993
36	CEBPB	chr5:45338308-45338508	HepG2	liver:	n/a	chr5:45338439-45338452 chr5:45338440-45338451 chr5:45338439-45338452 chr5:45338439-45338450 chr5:45338439-45338450
37	CEBPB	chr5:45063322-45063617	HepG2	liver:	n/a	chr5:45063461-45063472
38	CEBPB	chr5:45382708-45383117	Hela-S3	cervix:	n/a	chr5:45382913-45382922 chr5:45382896-45382907 chr5:45382913-45382922
39	CEBPB	chr5:45180132-45180241	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr5:45199706-45200011	IMR90	lung:	n/a	chr5:45199846-45199859 chr5:45199847-45199858 chr5:45199856-45199869
41	CEBPB	chr5:45063400-45063803	A549	lung:	n/a	chr5:45063461-45063472
42	CEBPB	chr5:45187564-45187797	K562	blood:	n/a	chr5:45187663-45187674
43	CEBPB	chr5:45376452-45376910	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:45199694-45200007	Hela-S3	cervix:	n/a	chr5:45199846-45199859 chr5:45199847-45199858 chr5:45199856-45199869
45	CEBPB	chr5:45199682-45199996	HepG2	liver:	n/a	chr5:45199846-45199859 chr5:45199847-45199858 chr5:45199856-45199869
46	CEBPB	chr5:45024438-45024736	HepG2	liver:	n/a	chr5:45024594-45024605
47	CEBPB	chr5:45262779-45262913	HepG2	liver:	n/a	chr5:45262812-45262823
48	CEBPB	chr5:45214277-45214541	A549	lung:	n/a	chr5:45214406-45214417
49	CEBPB	chr5:45187527-45187841	HepG2	liver:	n/a	chr5:45187663-45187674
50	CEBPB	chr5:45405872-45406072	HepG2	liver:	n/a	chr5:45405921-45405934 chr5:45405921-45405934 chr5:45405921-45405932 chr5:45405923-45405934

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:45262268-45262318	GM12891	blood:	n/a
2	chr5:45262268-45262318	GM12891	blood:	n/a
3	chr5:45135681-45135731	NHDF-neo	bronchial:	n/a
4	chr5:45225802-45225852	ProgFib	skin:	n/a
5	chr5:45262443-45262493	CMK	blood:	n/a
6	chr5:45038752-45038802	Hepatocyte	liver:	n/a
7	chr5:45192536-45192586	HNPCEpiC	eye:	n/a
8	chr5:45038752-45038802	HL-60	blood:	n/a
9	chr5:45262329-45262379	LNCaP	prostate:	n/a
10	chr5:45262443-45262493	ovcar-3	ovarian:	n/a
11	chr5:45098028-45098078	HRCEpiC	kidney:	n/a
12	chr5:45262443-45262493	PrEC	prostate:	n/a
13	chr5:45225802-45225852	MCF-7	breast:	n/a
14	chr5:45038752-45038802	U87	brain:	n/a
15	chr5:45262268-45262318	SK-N-SH	brain:	n/a
16	chr5:45262268-45262318	MCF-7	breast:	n/a
17	chr5:45288543-45288593	U87	brain:	n/a
18	chr5:45288543-45288593	HepG2	liver:	n/a
19	chr5:45192536-45192586	SKMC	muscle:	n/a
20	chr5:45262329-45262379	PrEC	prostate:	n/a
21	chr5:45288543-45288593	HNPCEpiC	eye:	n/a
22	chr5:45262329-45262379	HepG2	liver:	n/a
23	chr5:45262443-45262493	GM06990	blood:	n/a
24	chr5:45135681-45135731	HNPCEpiC	eye:	n/a
25	chr5:45038752-45038802	GM12892	blood:	n/a
26	chr5:45288543-45288593	HIPEpiC	eye:	n/a
27	chr5:45135681-45135731	HRCEpiC	kidney:	n/a
28	chr5:45262268-45262318	HepG2	liver:	n/a
29	chr5:45192536-45192586	BE2_C	brain:	n/a
30	chr5:45038752-45038802	HNPCEpiC	eye:	n/a
31	chr5:45038752-45038802	AG10803	skin:	n/a
32	chr5:45225802-45225852	Caco-2	colon:	n/a
33	chr5:45262268-45262318	AG10803	skin:	n/a
34	chr5:45225802-45225852	GM12878	blood:	n/a
35	chr5:45260623-45260673	CMK	blood:	n/a
36	chr5:45038752-45038802	PFSK-1	brain:	n/a
37	chr5:45260623-45260673	HEEpiC	esophagus:	n/a
38	chr5:45288543-45288593	AG10803	skin:	n/a
39	chr5:45262329-45262379	Jurkat	blood:	n/a
40	chr5:45288543-45288593	HRPEpiC	eye:	n/a
41	chr5:45262268-45262318	PANC-1	pancreas:	n/a
42	chr5:45288543-45288593	GM12891	blood:	n/a
43	chr5:45262443-45262493	AG09309	skin:	n/a
44	chr5:45192536-45192586	MCF-7	breast:	n/a
45	chr5:45288543-45288593	A549	lung:	n/a
46	chr5:45192536-45192586	PANC-1	pancreas:	n/a
47	chr5:45262443-45262493	GM12891	blood:	n/a
48	chr5:45262329-45262379	NHDF-neo	bronchial:	n/a
49	chr5:45260623-45260673	SK-N-MC	brain:	n/a
50	chr5:45225802-45225852	AG09309	skin:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:45435601..45437646-chr5:45441992..45444757,2	K562	blood:
2	chr5:45037646..45040960-chr5:45042639..45045311,3	K562	blood:
3	chr5:45189744..45191464-chr5:45191625..45193258,2	MCF-7	breast:
4	chr5:45292372..45295265-chr5:45301198..45304020,2	MCF-7	breast:
5	chr5:45389967..45392520-chr5:45393920..45396887,2	K562	blood:
6	chr5:45037646..45040960-chr5:45042639..45045311,3	K562	blood:
7	chr5:45423533..45425292-chr5:45434104..45435924,2	MCF-7	breast:
8	chr5:45389967..45392520-chr5:45393920..45396887,2	K562	blood:
9	chr5:45126509..45127120-chr5:45135100..45135681,2	K562	blood:
10	chr20:20574263..20574997-chr5:45153290..45154223,2	MCF-7	breast:
11	chr5:45096908..45099179-chr5:45099441..45102408,2	MCF-7	breast:
12	chr5:45126509..45127120-chr5:45135100..45135681,2	K562	blood:
13	chr5:45189744..45191464-chr5:45191625..45193258,2	MCF-7	breast:
14	chr16:3076387..3078714-chr5:45193841..45195630,2	MCF-7	breast:
15	chr5:45232284..45234490-chr5:45416046..45418115,2	MCF-7	breast:
16	chr5:45228553..45229390-chr6:23065553..23066212,2	MCF-7	breast:
17	chr5:45096908..45099179-chr5:45099441..45102408,2	MCF-7	breast:
18	chr5:45259723..45261348-chr5:45262944..45264451,2	K562	blood:
19	chr5:44356260..44358499-chr5:45223439..45226183,2	K562	blood:
20	chr5:45232284..45234490-chr5:45416046..45418115,2	MCF-7	breast:
21	chr5:45056862..45058850-chr5:45061622..45064175,2	MCF-7	breast:
22	chr3:104438340..104439030-chr5:45401914..45402431,2	MCF-7	breast:
23	chr5:45038244..45038751-chr5:45773997..45774955,2	MCF-7	breast:
24	chr5:45423533..45425292-chr5:45434104..45435924,2	MCF-7	breast:
25	chr5:45292372..45295265-chr5:45301198..45304020,2	MCF-7	breast:
26	chr5:45259723..45261348-chr5:45262944..45264451,2	K562	blood:
27	chr5:45038409..45039119-chr5:45520902..45521831,4	MCF-7	breast:
28	chr5:45056862..45058850-chr5:45061622..45064175,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGF10-4	chr5:45267793-45268115	ENSG00000251117.1
2	lnc-FGF10-4	chr5:45266826-45266920	ENSG00000251117.1
3	lnc-MRPS30-4	chr5:45227480-45227662	XLOC_004375
4	lnc-MRPS30-3	chr5:45098008-45098749	XLOC_004374
5	lnc-MRPS30-11	chr5:45214560-45217161	NONHSAT101357
6	lnc-MRPS30-11	chr5:45212601-45212751	NONHSAT101357
7	lnc-MRPS30-3	chr5:45035301-45035378	XLOC_004374
8	lnc-MRPS30-4	chr5:45228193-45228451	XLOC_004375

No data

Variant related genes	Relation type
ENSG00000248148	TF binding region
ENSG00000248148	CpG island

Extended variants
information (count: 7071 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:7071 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543449479	chr5:45021414-45021415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370489775	chr5:45021451-45021452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111496654	chr5:45021513-45021514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534746602	chr5:45021514-45021515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183404953	chr5:45021516-45021517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542364174	chr5:45021543-45021544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187814846	chr5:45021553-45021554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528678630	chr5:45021581-45021582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192386709	chr5:45021587-45021588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551643422	chr5:45021626-45021627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182214430	chr5:45021629-45021630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78623137	chr5:45021634-45021635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187721868	chr5:45021665-45021666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111347238	chr5:45021750-45021751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552985363	chr5:45021777-45021778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550995166	chr5:45021778-45021779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs71610388	chr5:45021804-45021805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567554545	chr5:45021814-45021815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370157104	chr5:45021837-45021838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536722363	chr5:45021902-45021903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546793820	chr5:45021907-45021908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192787319	chr5:45021956-45021957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184881271	chr5:45021972-45021973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558078579	chr5:45021998-45021999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs578027315	chr5:45021999-45022000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190106554	chr5:45022003-45022004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556871018	chr5:45022014-45022015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142609091	chr5:45022054-45022055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542674719	chr5:45022092-45022093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192105366	chr5:45022142-45022143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184414568	chr5:45022240-45022241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372383103	chr5:45022241-45022242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373936709	chr5:45022242-45022243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545244713	chr5:45022252-45022253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554727655	chr5:45022253-45022254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565229598	chr5:45022263-45022264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531069952	chr5:45022270-45022271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112568684	chr5:45022311-45022312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75556319	chr5:45022340-45022341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530073307	chr5:45022370-45022371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189468527	chr5:45022376-45022377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148235268	chr5:45022443-45022444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141361358	chr5:45022462-45022463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376875903	chr5:45022467-45022468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548255132	chr5:45022470-45022471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200623554	chr5:45022480-45022481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371272116	chr5:45022524-45022525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551558762	chr5:45022526-45022527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545549638	chr5:45022553-45022554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571473154	chr5:45022559-45022560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Ovarian cancer	21720365	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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:464 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:45021400-45030200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:45024400-45024800	Enhancers	Liver	Liver
3	chr5:45030200-45030400	Strong transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:45030400-45036000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:45036000-45036200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:45036000-45036200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:45038400-45039000	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr5:45038400-45039200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr5:45038400-45039200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr5:45038800-45039200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr5:45038800-45039200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:45038800-45039200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr5:45038800-45039200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr5:45038800-45039200	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr5:45042400-45042800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr5:45054000-45054200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr5:45054000-45054600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr5:45054400-45055600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr5:45054600-45055800	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr5:45055200-45056000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr5:45055600-45055800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr5:45055600-45056000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr5:45055800-45056000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:45055800-45056200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr5:45056000-45057000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr5:45056000-45057000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr5:45056000-45057000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:45056000-45057200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr5:45056200-45057400	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr5:45057000-45057600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr5:45057000-45057600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr5:45057000-45059400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:45057200-45059200	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr5:45057200-45059400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr5:45057400-45057800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr5:45057400-45058600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr5:45057400-45059600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr5:45057400-45061800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr5:45057600-45058000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr5:45057600-45058200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr5:45057800-45060800	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr5:45058000-45059400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr5:45058200-45059400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr5:45058600-45060800	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr5:45059200-45060600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr5:45059400-45060600	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:45059400-45060600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr5:45059400-45060600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr5:45059400-45060600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr5:45059600-45060800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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