Variant report

Variant	nsv3949
Chromosome Location	chr3:111998512-112044060
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:648)
CpG islands
(count:671)
Chromatin interactive
region (count:11)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:112012201-112012527	K562	blood:	n/a	n/a
2	ATF2	chr3:112021890-112022672	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr3:112021897-112022624	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:112021360-112021516	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:112022005-112022406	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr3:112012086-112012623	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:112012260-112012698	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:112012974-112013152	GM12878	blood:	n/a	n/a
9	BRCA1	chr3:112012541-112012773	GM12878	blood:	n/a	n/a
10	BRCA1	chr3:112012234-112012555	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr3:112039657-112039920	IMR90	lung:	n/a	n/a
12	CEBPB	chr3:112027527-112027551	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:112012177-112012553	MCF-7	breast:	n/a	n/a
14	CEBPB	chr3:112039630-112039848	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr3:112008258-112008479	IMR90	lung:	n/a	chr3:112008372-112008383
16	CEBPB	chr3:112021901-112022660	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr3:112039588-112039910	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:112039605-112039915	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:112012149-112012528	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:112012176-112012495	K562	blood:	n/a	n/a
21	CEBPB	chr3:112012186-112012525	A549	lung:	n/a	n/a
22	CEBPB	chr3:112008238-112008495	HepG2	liver:	n/a	chr3:112008372-112008383
23	CEBPB	chr3:112012155-112012523	A549	lung:	n/a	n/a
24	CEBPB	chr3:112039605-112039911	A549	lung:	n/a	n/a
25	CEBPB	chr3:112021013-112021159	K562	blood:	n/a	n/a
26	CEBPB	chr3:112008324-112008428	A549	lung:	n/a	chr3:112008372-112008383
27	CEBPB	chr3:112012145-112012604	MCF-7	breast:	n/a	n/a
28	CEBPB	chr3:112012131-112012641	A549	lung:	n/a	n/a
29	CEBPB	chr3:112012158-112012514	IMR90	lung:	n/a	n/a
30	CEBPB	chr3:112012184-112012760	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr3:112027052-112027708	IMR90	lung:	n/a	n/a
32	CHD1	chr3:112021904-112022583	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr3:112021818-112022916	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr3:112012587-112012703	GM12878	blood:	n/a	n/a
35	CTBP2	chr3:112021346-112022312	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr3:112012549-112012593	GM20000	blood:	n/a	n/a
37	CTCF	chr3:112012320-112012470	K562	blood:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
38	CTCF	chr3:112012300-112012450	HEEpiC	esophagus:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
39	CTCF	chr3:112023600-112023750	GM12864	blood:	n/a	n/a
40	CTCF	chr3:112012280-112012430	HUVEC	blood vessel:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
41	CTCF	chr3:112012091-112012929	HCT-116	colon:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
42	CTCF	chr3:112022880-112023030	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr3:112023540-112023690	RPTEC	kidney:	n/a	n/a
44	CTCF	chr3:112012300-112012450	MCF-7	breast:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
45	CTCF	chr3:112023540-112023690	AG04449	skin:	n/a	n/a
46	CTCF	chr3:112012780-112012930	HCT-116	colon:	n/a	n/a
47	CTCF	chr3:112023560-112023710	RPTEC	kidney:	n/a	n/a
48	CTCF	chr3:112022040-112022190	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr3:112023520-112023670	A549	lung:	n/a	n/a
50	CTCF	chr3:112023520-112023670	GM12873	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:112013646-112013696	ovcar-3	ovarian:	n/a
2	chr3:112013231-112013281	HL-60	blood:	n/a
3	chr3:112021096-112021146	AG09309	skin:	n/a
4	chr3:112023284-112023334	BE2_C	brain:	n/a
5	chr3:112013231-112013281	HMEC	breast:	n/a
6	chr3:112023284-112023334	Hepatocyte	liver:	n/a
7	chr3:112013130-112013180	A549	lung:	n/a
8	chr3:112013646-112013696	AG04450	lung:	fetal
9	chr3:112013130-112013180	PANC-1	pancreas:	n/a
10	chr3:112013231-112013281	NHBE	bronchial:	n/a
11	chr3:112022442-112022492	HRPEpiC	eye:	n/a
12	chr3:112013231-112013281	SKMC	muscle:	n/a
13	chr3:112012867-112012917	HMEC	breast:	n/a
14	chr3:112013357-112013407	NHBE	bronchial:	n/a
15	chr3:112021096-112021146	HRPEpiC	eye:	n/a
16	chr3:112012867-112012917	HIPEpiC	eye:	n/a
17	chr3:112021096-112021146	AoSMC	blood vessel:	n/a
18	chr3:112012867-112012917	Caco-2	colon:	n/a
19	chr3:112013231-112013281	HAEpiC	amniotic membrane:	n/a
20	chr3:112021096-112021146	HIPEpiC	eye:	n/a
21	chr3:112021179-112021229	GM12878	blood:	n/a
22	chr3:112021179-112021229	AG09319	gingival:	n/a
23	chr3:112013079-112013129	HCF	heart:	n/a
24	chr3:112013646-112013696	AG09309	skin:	n/a
25	chr3:112013646-112013696	NT2-D1	testis:	n/a
26	chr3:112013063-112013113	NT2-D1	testis:	n/a
27	chr3:112013646-112013696	Hepatocyte	liver:	n/a
28	chr3:112013646-112013696	LNCaP	prostate:	n/a
29	chr3:112022442-112022492	T-47D	breast:	n/a
30	chr3:112013063-112013113	HMEC	breast:	n/a
31	chr3:112021096-112021146	GM19239	blood:	n/a
32	chr3:112012867-112012917	LNCaP	prostate:	n/a
33	chr3:112013079-112013129	HEEpiC	esophagus:	n/a
34	chr3:112013357-112013407	H1-hESC	embryonic stem cell:	embryo
35	chr3:112021179-112021229	SKMC	muscle:	n/a
36	chr3:112022442-112022492	AG04449	skin:	fetal
37	chr3:112012867-112012917	HPAEpiC	pulmonary alveolar:	n/a
38	chr3:112013231-112013281	GM06990	blood:	n/a
39	chr3:112013063-112013113	ovcar-3	ovarian:	n/a
40	chr3:112012867-112012917	A549	lung:	n/a
41	chr3:112021096-112021146	NHDF-neo	bronchial:	n/a
42	chr3:112013079-112013129	NB4	blood:	n/a
43	chr3:112021096-112021146	SKMC	muscle:	n/a
44	chr3:112013646-112013696	AoSMC	blood vessel:	n/a
45	chr3:112013079-112013129	IMR90	lung:	fetal
46	chr3:112013063-112013113	GM12878	blood:	n/a
47	chr3:112021096-112021146	LNCaP	prostate:	n/a
48	chr3:112021179-112021229	IMR90	lung:	fetal
49	chr3:112013231-112013281	T-47D	breast:	n/a
50	chr3:112023284-112023334	HEEpiC	esophagus:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:111994958..111997172-chr3:111998544..112001325,2	K562	blood:
2	chr3:112030207..112032434-chr3:112262315..112264380,2	K562	blood:
3	chr3:112011328..112014210-chr3:112359098..112361496,2	MCF-7	breast:
4	chr3:111998157..111999865-chr3:112007204..112009141,2	MCF-7	breast:
5	chr3:112003335..112004963-chr3:112013883..112016627,2	MCF-7	breast:
6	chr3:111993821..111999199-chr3:111999738..112003552,5	K562	blood:
7	chr3:111998157..111999865-chr3:112007204..112009141,2	MCF-7	breast:
8	chr3:112003335..112004963-chr3:112013883..112016627,2	MCF-7	breast:
9	chr3:111991351..111994279-chr3:111999124..112001304,2	K562	blood:
10	chr3:111993821..111999199-chr3:111999738..112003552,5	K562	blood:
11	chr3:112012262..112013019-chr3:112156556..112157096,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GCET2-2	chr3:112005551-112005725	NONHSAT091162
2	lnc-CD200-1	chr3:112021322-112021561	NONHSAT091164
3	lnc-CD200-1	chr3:112025968-112026045	ENSG00000239482.2
4	lnc-GCET2-2	chr3:112012940-112013063	NONHSAT091162
5	lnc-CD200-1	chr3:112021325-112021561	ENSG00000239482
6	lnc-GCET2-2	chr3:111999530-111999630	NONHSAT091162

No data

Variant related genes	Relation type
SLC9C1	TF binding region
ENSG00000239482	TF binding region
SLC9C1	CpG island
ENSG00000239482	CpG island
ENSG00000091986	chromatin interactions
GDF11	miRNA target sites

Extended variants
information (count: 1661 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1661 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181780971	chr3:111998521-111998522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186901605	chr3:111998538-111998539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544211284	chr3:111998541-111998542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370118428	chr3:111998597-111998598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533021983	chr3:111998625-111998626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190095594	chr3:111998642-111998643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560309014	chr3:111998683-111998684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138191523	chr3:111998701-111998702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548980686	chr3:111998807-111998808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112351651	chr3:111998883-111998884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4234415	chr3:111998908-111998909	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs9843431	chr3:111998937-111998938	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs570983239	chr3:111999029-111999030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539649209	chr3:111999101-111999102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182681544	chr3:111999132-111999133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566640152	chr3:111999184-111999185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535587950	chr3:111999229-111999230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4585166	chr3:111999230-111999231	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs185513697	chr3:111999262-111999263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144018478	chr3:111999274-111999275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377506719	chr3:111999276-111999277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370696262	chr3:111999277-111999278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs375503318	chr3:111999278-111999279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376594565	chr3:111999279-111999280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542239313	chr3:111999291-111999292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544488626	chr3:111999364-111999365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557224599	chr3:111999369-111999370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575522476	chr3:111999389-111999390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557768689	chr3:111999392-111999393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141249964	chr3:111999439-111999440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112771429	chr3:111999460-111999461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201270154	chr3:111999500-111999501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200711528	chr3:111999540-111999541	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs528974870	chr3:111999598-111999599	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs542790411	chr3:111999640-111999641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374881198	chr3:111999670-111999671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562493564	chr3:111999678-111999679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs182268755	chr3:111999731-111999732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201197182	chr3:111999732-111999733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs202204934	chr3:111999733-111999734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200279331	chr3:111999734-111999735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201059239	chr3:111999735-111999736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs199851723	chr3:111999736-111999737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs59138652	chr3:111999739-111999740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75323480	chr3:111999740-111999741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188914415	chr3:111999747-111999748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373593779	chr3:111999808-111999809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533314977	chr3:111999883-111999884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368582515	chr3:111999886-111999887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372087611	chr3:111999912-111999913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1066 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111972200-111999000	Weak transcription	Left Ventricle	heart
2	chr3:111998600-111999400	Enhancers	Fetal Intestine Large	intestine
3	chr3:111999400-112000000	Weak transcription	Fetal Intestine Large	intestine
4	chr3:111999600-112000000	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr3:112000000-112000200	Enhancers	Fetal Intestine Large	intestine
6	chr3:112001800-112002400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr3:112002400-112004200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr3:112002800-112003000	Flanking Active TSS	GM12878-XiMat	blood
9	chr3:112003000-112003400	Enhancers	GM12878-XiMat	blood
10	chr3:112003200-112003600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:112003200-112003600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr3:112003600-112004800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:112004200-112004800	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr3:112004800-112005800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr3:112005800-112006600	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr3:112006000-112006200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr3:112006400-112006600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr3:112006600-112007200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr3:112006600-112012400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr3:112007400-112010000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:112008200-112008800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr3:112008400-112008600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr3:112008400-112008600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr3:112008600-112012200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr3:112008600-112012400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr3:112009800-112010000	ZNF genes & repeats	Fetal Brain Male	brain
27	chr3:112009800-112012400	Weak transcription	Lung	lung
28	chr3:112010000-112011600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr3:112010000-112012400	Weak transcription	Fetal Brain Male	brain
30	chr3:112010600-112010800	Enhancers	GM12878-XiMat	blood
31	chr3:112010800-112012000	Weak transcription	GM12878-XiMat	blood
32	chr3:112010800-112012200	Weak transcription	Primary B cells from cord blood	blood
33	chr3:112011600-112011800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:112011800-112012200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr3:112012000-112012200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:112012000-112012200	Enhancers	Adipose Nuclei	Adipose
37	chr3:112012000-112012200	Enhancers	Duodenum Mucosa	Duodenum
38	chr3:112012000-112012200	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr3:112012000-112012200	Enhancers	GM12878-XiMat	blood
40	chr3:112012200-112012400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr3:112012200-112012400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:112012200-112012400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr3:112012200-112012400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr3:112012200-112012400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr3:112012200-112012400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr3:112012200-112012400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr3:112012200-112012400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr3:112012200-112012400	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr3:112012200-112012400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr3:112012200-112012400	Enhancers	Primary monocytes fromperipheralblood	blood

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