Variant report

Variant	nsv878095
Chromosome Location	chr3:190586181-190657163
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	chr3:190602248-190602331	K562	blood:	n/a	n/a
2	BDP1	chr3:190595766-190596006	K562	blood:	n/a	n/a
3	BHLHE40	chr3:190599409-190599484	GM12878	blood:	n/a	n/a
4	CBX3	chr3:190595798-190596041	K562	blood:	n/a	n/a
5	CBX3	chr3:190595747-190596087	K562	blood:	n/a	n/a
6	CCNT2	chr3:190626181-190626314	K562	blood:	n/a	n/a
7	CEBPB	chr3:190651236-190651559	IMR90	lung:	n/a	chr3:190651389-190651400
8	CEBPB	chr3:190612784-190612984	HepG2	liver:	n/a	chr3:190612900-190612911
9	CEBPB	chr3:190651225-190651566	HepG2	liver:	n/a	chr3:190651389-190651400
10	CEBPB	chr3:190651233-190651540	A549	lung:	n/a	chr3:190651389-190651400
11	CEBPB	chr3:190618965-190619043	HepG2	liver:	n/a	chr3:190618972-190618983 chr3:190618973-190618982 chr3:190618971-190618984
12	CEBPB	chr3:190607200-190607388	HepG2	liver:	n/a	chr3:190607311-190607322
13	CTCF	chr3:190602540-190602690	GM12865	blood:	n/a	n/a
14	CTCF	chr3:190595783-190596124	K562	blood:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595812-190595825 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
15	CTCF	chr3:190595863-190596027	GM12892	blood:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
16	CTCF	chr3:190595940-190596090	K562	blood:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
17	CTCF	chr3:190595903-190596049	Lung_OC	lung:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
18	CTCF	chr3:190602064-190602297	MCF-7	breast:	n/a	chr3:190602194-190602210
19	CTCF	chr3:190602120-190602270	BJ	skin:	n/a	chr3:190602194-190602210
20	CTCF	chr3:190602000-190602150	A549	lung:	n/a	n/a
21	CTCF	chr3:190602012-190602326	T-47D	breast:	n/a	chr3:190602194-190602210
22	CTCF	chr3:190595758-190596296	SK-N-SH	brain:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595812-190595825 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
23	CTCF	chr3:190595821-190596079	HepG2	liver:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
24	CTCF	chr3:190595900-190596050	HepG2	liver:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
25	CTCF	chr3:190602040-190602190	NHEK	skin:	n/a	n/a
26	CTCF	chr3:190595908-190596039	HepG2	liver:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
27	CTCF	chr3:190602060-190602210	GM12872	blood:	n/a	chr3:190602194-190602210
28	CTCF	chr3:190602120-190602270	HPAF	blood vessel:	n/a	chr3:190602194-190602210
29	CTCF	chr3:190595780-190595930	HRPEpiC	eye:	n/a	chr3:190595812-190595825
30	CTCF	chr3:190595900-190596050	GM12868	blood:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
31	CTCF	chr3:190595860-190596010	HL-60	blood:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
32	CTCF	chr3:190595900-190596035	Spleen_OC	spleen:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
33	CTCF	chr3:190595900-190596050	AG04449	skin:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
34	CTCF	chr3:190595839-190596058	H1-hESC	embryonic stem cell:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
35	CTCF	chr3:190602089-190602290	K562	blood:	n/a	chr3:190602194-190602210
36	CTCF	chr3:190602100-190602250	GM12801	blood:	n/a	chr3:190602194-190602210
37	CTCF	chr3:190602140-190602290	NHLF	lung:	n/a	chr3:190602194-190602210
38	CTCF	chr3:190602120-190602270	HBMEC	blood vessel:	n/a	chr3:190602194-190602210
39	CTCF	chr3:190595840-190595990	HEEpiC	esophagus:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
40	CTCF	chr3:190595860-190596010	AG09309	skin:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
41	CTCF	chr3:190595880-190596030	SAEC	small airway:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
42	CTCF	chr3:190595881-190596064	HUVEC	blood vessel:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
43	CTCF	chr3:190602078-190602276	SK-N-SH_RA	brain:	n/a	chr3:190602194-190602210
44	CTCF	chr3:190595960-190596110	WI-38	lung:	n/a	chr3:190595961-190595970
45	CTCF	chr3:190595846-190596055	GM13977	blood:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
46	CTCF	chr3:190595880-190596030	GM06990	blood:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
47	CTCF	chr3:190595900-190596050	GM12871	blood:	n/a	chr3:190595961-190595970 chr3:190595958-190595968 chr3:190595955-190595973 chr3:190595957-190595970 chr3:190595950-190595971 chr3:190595956-190595972
48	CTCF	chr3:190602015-190602339	GM12878	blood:	n/a	chr3:190602194-190602210
49	CTCF	chr3:190602103-190602261	NHEK	skin:	n/a	chr3:190602194-190602210
50	CTCF	chr3:190604740-190604890	GM06990	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:190594718-190594768	H1-hESC	embryonic stem cell:	embryo
2	chr3:190594718-190594768	HCPEpiC	choroid plexus:	n/a
3	chr3:190594718-190594768	HRCEpiC	kidney:	n/a
4	chr3:190594718-190594768	HepG2	liver:	n/a
5	chr3:190594456-190594506	HUVEC	blood vessel:	n/a
6	chr3:190594718-190594768	A549	lung:	n/a
7	chr3:190595776-190595826	PFSK-1	brain:	n/a
8	chr3:190595776-190595826	LNCaP	prostate:	n/a
9	chr3:190594718-190594768	HUVEC	blood vessel:	n/a
10	chr3:190594456-190594506	HCF	heart:	n/a
11	chr3:190594718-190594768	AG09309	skin:	n/a
12	chr3:190595776-190595826	AG09319	gingival:	n/a
13	chr3:190595776-190595826	ovcar-3	ovarian:	n/a
14	chr3:190595776-190595826	GM12891	blood:	n/a
15	chr3:190594718-190594768	PANC-1	pancreas:	n/a
16	chr3:190595776-190595826	H1-hESC	embryonic stem cell:	embryo
17	chr3:190594718-190594768	NHBE	bronchial:	n/a
18	chr3:190594456-190594506	HRPEpiC	eye:	n/a
19	chr3:190594456-190594506	GM06990	blood:	n/a
20	chr3:190594718-190594768	NB4	blood:	n/a
21	chr3:190595776-190595826	Jurkat	blood:	n/a
22	chr3:190594456-190594506	RPTEC	kidney:	n/a
23	chr3:190594718-190594768	HNPCEpiC	eye:	n/a
24	chr3:190595776-190595826	HRE	kidney:	n/a
25	chr3:190595776-190595826	GM06990	blood:	n/a
26	chr3:190594456-190594506	HAEpiC	amniotic membrane:	n/a
27	chr3:190594718-190594768	GM12891	blood:	n/a
28	chr3:190594718-190594768	ProgFib	skin:	n/a
29	chr3:190594718-190594768	PFSK-1	brain:	n/a
30	chr3:190594456-190594506	PFSK-1	brain:	n/a
31	chr3:190594718-190594768	IMR90	lung:	fetal
32	chr3:190594718-190594768	BE2_C	brain:	n/a
33	chr3:190595776-190595826	NHDF-neo	bronchial:	n/a
34	chr3:190594456-190594506	SK-N-SH	brain:	n/a
35	chr3:190595776-190595826	HepG2	liver:	n/a
36	chr3:190595776-190595826	BJ	skin:	n/a
37	chr3:190594718-190594768	HPAEpiC	pulmonary alveolar:	n/a
38	chr3:190594456-190594506	HCT-116	colon:	n/a
39	chr3:190594718-190594768	T-47D	breast:	n/a
40	chr3:190594718-190594768	SAEC	small airway:	n/a
41	chr3:190594456-190594506	HL-60	blood:	n/a
42	chr3:190594456-190594506	ovcar-3	ovarian:	n/a
43	chr3:190594456-190594506	HCPEpiC	choroid plexus:	n/a
44	chr3:190594456-190594506	MCF-7	breast:	n/a
45	chr3:190594718-190594768	CMK	blood:	n/a
46	chr3:190595776-190595826	HCM	heart:	n/a
47	chr3:190594456-190594506	HRCEpiC	kidney:	n/a
48	chr3:190594718-190594768	NHDF-neo	bronchial:	n/a
49	chr3:190595776-190595826	SK-N-SH	brain:	n/a
50	chr3:190594718-190594768	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:190601679..190602537-chr3:190768672..190769490,5	MCF-7	breast:
2	chr3:190418930..190419478-chr3:190601767..190602267,2	MCF-7	breast:
3	chr12:87572443..87573395-chr3:190629682..190630453,2	MCF-7	breast:
4	chr3:190645157..190647983-chr3:190753958..190756596,2	K562	blood:
5	chr3:190601751..190602362-chr3:192162433..192162941,2	K562	blood:

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

Extended variants
information (count: 412 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566858790	chr3:190586207-190586208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs9837390	chr3:190586223-190586224	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs538645163	chr3:190586240-190586241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs9874876	chr3:190586244-190586245	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs9837551	chr3:190586274-190586275	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs191603406	chr3:190586279-190586280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181035301	chr3:190586309-190586310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs16865973	chr3:190586321-190586322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543556919	chr3:190586400-190586401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145139524	chr3:190591821-190591822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538211315	chr3:190591838-190591839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558522396	chr3:190591852-190591853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148351022	chr3:190591871-190591872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534399444	chr3:190591899-190591900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10937448	chr3:190591911-190591912	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs74780432	chr3:190591915-190591916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs80178098	chr3:190591926-190591927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150539691	chr3:190592013-190592014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs9868955	chr3:190592125-190592126	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs199996778	chr3:190592137-190592138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565271167	chr3:190592191-190592192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560666138	chr3:190592203-190592204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183655035	chr3:190592308-190592309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547887079	chr3:190592379-190592380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561386955	chr3:190592396-190592397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546653784	chr3:190602036-190602037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566961159	chr3:190602053-190602054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9818981	chr3:190602087-190602088	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs371108862	chr3:190602117-190602118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549548194	chr3:190602123-190602124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569388320	chr3:190602141-190602142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs74588302	chr3:190602152-190602153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558511586	chr3:190602193-190602194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577678829	chr3:190602259-190602260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9290957	chr3:190602301-190602302	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs553539176	chr3:190602346-190602347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573676191	chr3:190602347-190602348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542398686	chr3:190602367-190602368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185157800	chr3:190602376-190602377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188028889	chr3:190602391-190602392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146013675	chr3:190602403-190602404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564849629	chr3:190602410-190602411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139913570	chr3:190602453-190602454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192826354	chr3:190602493-190602494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560327803	chr3:190602511-190602512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191882089	chr3:190604618-190604619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183377065	chr3:190604709-190604710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs187296382	chr3:190604711-190604712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs192137623	chr3:190604720-190604721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375990541	chr3:190604742-190604743	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Lung cancer	19547694	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Optic atrophy	21457585	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	16397240	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:190586200-190586400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:190591800-190592400	Enhancers	Fetal Heart	heart
3	chr3:190602000-190602600	Enhancers	Liver	Liver
4	chr3:190602200-190602400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr3:190604600-190605200	Enhancers	NHEK	skin
6	chr3:190610200-190610800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr3:190610600-190610800	Bivalent Enhancer	Esophagus	oesophagus
8	chr3:190610600-190611000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:190611000-190611200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:190627600-190627800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr3:190627800-190628400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr3:190628400-190629400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr3:190628600-190629200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr3:190628800-190629400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr3:190628800-190629600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr3:190629000-190629600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr3:190629000-190630000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr3:190629000-190630600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:190629200-190629600	Enhancers	H1 Cell Line	embryonic stem cell
20	chr3:190629200-190629600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr3:190629400-190629600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr3:190630400-190630800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr3:190630400-190631200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr3:190633000-190633200	Enhancers	Muscle Satellite Cultured Cells	--
25	chr3:190634400-190635400	Enhancers	Ovary	ovary
26	chr3:190644000-190644600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr3:190644400-190644800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr3:190645800-190646000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:190652000-190652800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr3:190652200-190652800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr3:190652200-190653000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr3:190652200-190653000	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr3:190652600-190653000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr3:190652600-190653000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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