Variant report

Variant	nsv877340
Chromosome Location	chr3:111936961-112013546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:413)
CpG islands
(count:368)
Chromatin interactive
region (count:14)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr3:111966499-111967264	GM12878	blood:	n/a	n/a
3	BATF	chr3:111950575-111950855	GM12878	blood:	n/a	n/a
4	BATF	chr3:111966726-111967170	GM12878	blood:	n/a	n/a
5	BATF	chr3:111950548-111950867	GM12878	blood:	n/a	n/a
6	BATF	chr3:111966761-111967135	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:111966778-111967019	GM12878	blood:	n/a	n/a
8	BCLAF1	chr3:111966566-111967245	GM12878	blood:	n/a	chr3:111966681-111966690
9	BCLAF1	chr3:112012086-112012623	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:112012974-112013152	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:112012260-112012698	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:111950471-111950910	GM12878	blood:	n/a	n/a
13	BRCA1	chr3:112012541-112012773	GM12878	blood:	n/a	n/a
14	BRCA1	chr3:112012234-112012555	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:112008238-112008495	HepG2	liver:	n/a	chr3:112008372-112008383
16	CEBPB	chr3:112012131-112012641	A549	lung:	n/a	n/a
17	CEBPB	chr3:111991955-111992251	A549	lung:	n/a	n/a
18	CEBPB	chr3:111996209-111996253	A549	lung:	n/a	n/a
19	CEBPB	chr3:112008324-112008428	A549	lung:	n/a	chr3:112008372-112008383
20	CEBPB	chr3:112012149-112012528	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:112012177-112012553	MCF-7	breast:	n/a	n/a
22	CEBPB	chr3:111992352-111992683	H1-hESC	embryonic stem cell:	n/a	chr3:111992522-111992535 chr3:111992524-111992533 chr3:111992522-111992533
23	CEBPB	chr3:112012155-112012523	A549	lung:	n/a	n/a
24	CEBPB	chr3:112012184-112012760	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr3:112012186-112012525	A549	lung:	n/a	n/a
26	CEBPB	chr3:111949674-111949973	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr3:111988164-111988366	HepG2	liver:	n/a	chr3:111988288-111988299
28	CEBPB	chr3:111991981-111992262	HepG2	liver:	n/a	n/a
29	CEBPB	chr3:111992529-111992555	A549	lung:	n/a	n/a
30	CEBPB	chr3:111980719-111980802	IMR90	lung:	n/a	chr3:111980778-111980789
31	CEBPB	chr3:112012145-112012604	MCF-7	breast:	n/a	n/a
32	CEBPB	chr3:112008258-112008479	IMR90	lung:	n/a	chr3:112008372-112008383
33	CEBPB	chr3:111980644-111980950	HepG2	liver:	n/a	chr3:111980778-111980789
34	CEBPB	chr3:112012158-112012514	IMR90	lung:	n/a	n/a
35	CEBPB	chr3:112012176-112012495	K562	blood:	n/a	n/a
36	CEBPB	chr3:111992505-111992598	HepG2	liver:	n/a	chr3:111992522-111992535 chr3:111992524-111992533 chr3:111992522-111992533
37	CEBPB	chr3:111947629-111947892	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr3:111939290-111939316	HepG2	liver:	n/a	n/a
39	CHD2	chr3:112012587-112012703	GM12878	blood:	n/a	n/a
40	CTCF	chr3:112012300-112012450	NHLF	lung:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
41	CTCF	chr3:112012233-112012489	GM13977	blood:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
42	CTCF	chr3:112002968-112003024	GM13976	blood:	n/a	n/a
43	CTCF	chr3:112012320-112012470	WERI-Rb-1	eye:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
44	CTCF	chr3:112012114-112012614	A549	lung:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
45	CTCF	chr3:112012300-112012450	HCFaa	heart:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
46	CTCF	chr3:112012297-112012413	NHEK	skin:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
47	CTCF	chr3:112012360-112012510	HRE	kidney:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
48	CTCF	chr3:112012205-112012478	K562	blood:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
49	CTCF	chr3:112012228-112012511	HepG2	liver:	n/a	chr3:112012360-112012378 chr3:112012362-112012383
50	CTCF	chr3:112012243-112012468	HepG2	liver:	n/a	chr3:112012360-112012378 chr3:112012362-112012383

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:112013130-112013180	H1-hESC	embryonic stem cell:	embryo
2	chr3:112013079-112013129	HCF	heart:	n/a
3	chr3:112013130-112013180	H1-hESC	embryonic stem cell:	embryo
4	chr3:112013079-112013129	HCF	heart:	n/a
5	chr3:112013357-112013407	Caco-2	colon:	n/a
6	chr3:112013079-112013129	RPTEC	kidney:	n/a
7	chr3:112013063-112013113	RPTEC	kidney:	n/a
8	chr3:112013231-112013281	HCM	heart:	n/a
9	chr3:112013231-112013281	SK-N-SH_RA	brain:	n/a
10	chr3:112013231-112013281	MCF10A-Er-Src	breast:	n/a
11	chr3:112013231-112013281	HMEC	breast:	n/a
12	chr3:112013079-112013129	PrEC	prostate:	n/a
13	chr3:112013063-112013113	Hela-S3	cervix:	n/a
14	chr3:112013357-112013407	SAEC	small airway:	n/a
15	chr3:112013231-112013281	U87	brain:	n/a
16	chr3:112013130-112013180	PANC-1	pancreas:	n/a
17	chr3:112013231-112013281	GM19239	blood:	n/a
18	chr3:112013063-112013113	NH-A	brain:	n/a
19	chr3:112012867-112012917	HCT-116	colon:	n/a
20	chr3:112013357-112013407	GM12892	blood:	n/a
21	chr3:112013231-112013281	NB4	blood:	n/a
22	chr3:112013357-112013407	HCF	heart:	n/a
23	chr3:112013231-112013281	T-47D	breast:	n/a
24	chr3:112012867-112012917	ovcar-3	ovarian:	n/a
25	chr3:112013357-112013407	SKMC	muscle:	n/a
26	chr3:112013079-112013129	HPAEpiC	pulmonary alveolar:	n/a
27	chr3:112013130-112013180	HL-60	blood:	n/a
28	chr3:112012867-112012917	HCPEpiC	choroid plexus:	n/a
29	chr3:112013357-112013407	HMEC	breast:	n/a
30	chr3:112013231-112013281	HRPEpiC	eye:	n/a
31	chr3:112013130-112013180	NHBE	bronchial:	n/a
32	chr3:112013357-112013407	HEK293	kidney:	embryo
33	chr3:112012867-112012917	HL-60	blood:	n/a
34	chr3:112013231-112013281	H1-hESC	embryonic stem cell:	embryo
35	chr3:112012867-112012917	GM12878	blood:	n/a
36	chr3:112012867-112012917	SK-N-SH	brain:	n/a
37	chr3:112012867-112012917	GM19239	blood:	n/a
38	chr3:112013063-112013113	HNPCEpiC	eye:	n/a
39	chr3:112012867-112012917	A549	lung:	n/a
40	chr3:112013079-112013129	GM12892	blood:	n/a
41	chr3:112013079-112013129	CMK	blood:	n/a
42	chr3:112013063-112013113	NHBE	bronchial:	n/a
43	chr3:112013130-112013180	AG10803	skin:	n/a
44	chr3:112012867-112012917	PrEC	prostate:	n/a
45	chr3:112013130-112013180	Caco-2	colon:	n/a
46	chr3:112013357-112013407	HEEpiC	esophagus:	n/a
47	chr3:112013357-112013407	ovcar-3	ovarian:	n/a
48	chr3:112013130-112013180	GM19239	blood:	n/a
49	chr3:112013231-112013281	HIPEpiC	eye:	n/a
50	chr3:112013231-112013281	Hepatocyte	liver:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:111991351..111994279-chr3:111999124..112001304,2	K562	blood:
2	chr3:111993821..111999199-chr3:111999738..112003552,5	K562	blood:
3	chr3:111998157..111999865-chr3:112007204..112009141,2	MCF-7	breast:
4	chr3:112011328..112014210-chr3:112359098..112361496,2	MCF-7	breast:
5	chr3:112012262..112013019-chr3:112156556..112157096,2	MCF-7	breast:
6	chr3:111991351..111994279-chr3:111999124..112001304,2	K562	blood:
7	chr3:111987883..111989746-chr3:111993499..111996170,2	K562	blood:
8	chr3:111994958..111997172-chr3:111998544..112001325,2	K562	blood:
9	chr3:111998157..111999865-chr3:112007204..112009141,2	MCF-7	breast:
10	chr3:111966492..111967258-chr6:9984662..9985547,2	MCF-7	breast:
11	chr3:111993821..111999199-chr3:111999738..112003552,5	K562	blood:
12	chr3:111994958..111997172-chr3:111998544..112001325,2	K562	blood:
13	chr3:112003335..112004963-chr3:112013883..112016627,2	MCF-7	breast:
14	chr3:111987883..111989746-chr3:111993499..111996170,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GCET2-2	chr3:111997615-111997781	NONHSAT091162
2	lnc-GCET2-2	chr3:112012940-112013063	NONHSAT091162
3	lnc-GCET2-2	chr3:111999530-111999630	NONHSAT091162
4	lnc-GCET2-2	chr3:112005551-112005725	NONHSAT091162

No data

Variant related genes	Relation type
SLC9C1	TF binding region
SLC9C1	CpG island
ENSG00000091986	chromatin interactions

Extended variants
information (count: 2307 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2307 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61498352	chr3:111937022-111937023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532171555	chr3:111937023-111937024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs75880863	chr3:111937038-111937039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs62276847	chr3:111937040-111937041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13064242	chr3:111937105-111937106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs566135645	chr3:111937145-111937146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs367692542	chr3:111937218-111937219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200872127	chr3:111937282-111937283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71134804	chr3:111937285-111937286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13064151	chr3:111937286-111937287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200323649	chr3:111937293-111937294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs13086800	chr3:111937294-111937295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74968858	chr3:111937295-111937296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74339757	chr3:111937297-111937298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77714269	chr3:111937299-111937300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201833938	chr3:111937300-111937301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs398062690	chr3:111937301-111937302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543633594	chr3:111937320-111937321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138396002	chr3:111937321-111937322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576996887	chr3:111937324-111937325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545928011	chr3:111937355-111937356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368095045	chr3:111937398-111937399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78819805	chr3:111937399-111937400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541666765	chr3:111937408-111937409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561411489	chr3:111937421-111937422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530469953	chr3:111937497-111937498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79310601	chr3:111937514-111937515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569952259	chr3:111937532-111937533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4638935	chr3:111937534-111937535	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs73853364	chr3:111937550-111937551	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs372299747	chr3:111937587-111937588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566019169	chr3:111937596-111937597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs36084390	chr3:111937598-111937599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534718023	chr3:111937626-111937627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548605204	chr3:111937658-111937659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4383485	chr3:111937659-111937660	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs2131233	chr3:111937667-111937668	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs185861798	chr3:111937669-111937670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576746667	chr3:111937680-111937681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560961800	chr3:111937683-111937684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149253109	chr3:111937699-111937700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62276848	chr3:111937708-111937709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs552800571	chr3:111937760-111937761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79795266	chr3:111937783-111937784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572931248	chr3:111937791-111937792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541456425	chr3:111937800-111937801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189101464	chr3:111937869-111937870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574778847	chr3:111937885-111937886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543723086	chr3:111937933-111937934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563514866	chr3:111937946-111937947	Weak transcription	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:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111937000-111942800	Weak transcription	Left Ventricle	heart
2	chr3:111939200-111939600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr3:111942400-111952400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:111942800-111943000	ZNF genes & repeats	Gastric	stomach
5	chr3:111942800-111943000	ZNF genes & repeats	Pancreas	Pancrea
6	chr3:111942800-111943200	ZNF genes & repeats	Left Ventricle	heart
7	chr3:111943200-111945200	Weak transcription	Left Ventricle	heart
8	chr3:111945200-111945600	ZNF genes & repeats	Left Ventricle	heart
9	chr3:111945600-111950600	Weak transcription	Left Ventricle	heart
10	chr3:111946800-111948200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:111949000-111949200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr3:111950400-111950600	Active TSS	GM12878-XiMat	blood
13	chr3:111950600-111950800	Flanking Active TSS	GM12878-XiMat	blood
14	chr3:111950800-111951400	Enhancers	GM12878-XiMat	blood
15	chr3:111951000-111951600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:111955600-111955800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr3:111959200-111959600	ZNF genes & repeats	Left Ventricle	heart
18	chr3:111965000-111966200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr3:111965000-111966400	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr3:111965000-111967000	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr3:111965400-111965600	Enhancers	GM12878-XiMat	blood
22	chr3:111965400-111966000	Enhancers	Primary B cells from cord blood	blood
23	chr3:111965400-111966000	Enhancers	Primary hematopoietic stem cells	blood
24	chr3:111965400-111966000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:111965400-111967000	Enhancers	Primary B cells from peripheral blood	blood
26	chr3:111965600-111965800	Flanking Active TSS	GM12878-XiMat	blood
27	chr3:111965600-111966600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr3:111965600-111966600	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr3:111965800-111966000	Enhancers	GM12878-XiMat	blood
30	chr3:111966000-111967600	Flanking Active TSS	GM12878-XiMat	blood
31	chr3:111970800-111973200	ZNF genes & repeats	GM12878-XiMat	blood
32	chr3:111971600-111972400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr3:111972000-111972200	ZNF genes & repeats	Left Ventricle	heart
34	chr3:111972000-111972600	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr3:111972200-111999000	Weak transcription	Left Ventricle	heart
36	chr3:111980400-111980800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr3:111980400-111981200	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr3:111980400-111981200	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr3:111980600-111981000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr3:111980600-111981000	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr3:111980600-111981200	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr3:111990400-111991200	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr3:111990600-111991000	Enhancers	Primary B cells from peripheral blood	blood
44	chr3:111990600-111991000	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr3:111992000-111992600	Enhancers	H9 Cell Line	embryonic stem cell
46	chr3:111992200-111992600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:111992200-111992800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr3:111992200-111992800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr3:111992200-111993000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr3:111997000-111997400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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