Variant report

Variant	nsv592084
Chromosome Location	chr3:155751484-155830578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:531)
CpG islands
(count:366)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:155768722-155769099	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:155768670-155769123	K562	blood:	n/a	n/a
3	BATF	chr3:155761753-155761990	GM12878	blood:	n/a	n/a
4	BCL11A	chr3:155761735-155761903	GM12878	blood:	n/a	n/a
5	BRCA1	chr3:155761783-155761903	H1-hESC	embryonic stem cell:	n/a	n/a
6	CBX3	chr3:155824871-155825161	HCT-116	colon:	n/a	n/a
7	CBX3	chr3:155769358-155769543	K562	blood:	n/a	n/a
8	CEBPB	chr3:155777478-155777759	A549	lung:	n/a	n/a
9	CEBPB	chr3:155824938-155825032	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr3:155821208-155821512	IMR90	lung:	n/a	chr3:155821376-155821387
11	CEBPB	chr3:155777477-155777744	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:155821214-155821541	HepG2	liver:	n/a	chr3:155821376-155821387
13	CEBPB	chr3:155812242-155812524	HepG2	liver:	n/a	n/a
14	CEBPB	chr3:155821266-155821466	A549	lung:	n/a	chr3:155821376-155821387
15	CEBPB	chr3:155761802-155761973	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:155789289-155789401	K562	blood:	n/a	n/a
17	CEBPB	chr3:155811847-155812008	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr3:155777504-155777754	IMR90	lung:	n/a	n/a
19	CHD2	chr3:155816563-155816671	GM12878	blood:	n/a	n/a
20	CTCF	chr3:155761715-155761960	GM13976	blood:	n/a	chr3:155761841-155761857 chr3:155761840-155761858 chr3:155761843-155761856
21	CTCF	chr3:155824840-155824990	GM06990	blood:	n/a	n/a
22	CTCF	chr3:155800060-155800210	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr3:155761780-155761930	AG04449	skin:	n/a	chr3:155761841-155761857 chr3:155761840-155761858 chr3:155761843-155761856
24	CTCF	chr3:155774620-155774770	NHEK	skin:	n/a	n/a
25	CTCF	chr3:155761700-155761850	WI-38	lung:	n/a	n/a
26	CTCF	chr3:155761700-155761850	HFF-Myc	foreskin:	n/a	n/a
27	CTCF	chr3:155824900-155825050	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr3:155761680-155761830	RPTEC	kidney:	n/a	n/a
29	CTCF	chr3:155761760-155761910	WERI-Rb-1	eye:	n/a	chr3:155761841-155761857 chr3:155761840-155761858 chr3:155761843-155761856
30	CTCF	chr3:155761680-155761830	HCT-116	colon:	n/a	n/a
31	CTCF	chr3:155800120-155800270	HRE	kidney:	n/a	n/a
32	CTCF	chr3:155824940-155825090	GM12873	blood:	n/a	n/a
33	CTCF	chr3:155799940-155800090	SAEC	small airway:	n/a	n/a
34	CTCF	chr3:155824920-155825070	AG04450	lung:	n/a	n/a
35	CTCF	chr3:155761920-155762070	NHLF	lung:	n/a	n/a
36	CTCF	chr3:155761700-155761850	HCT-116	colon:	n/a	n/a
37	CTCF	chr3:155824820-155824970	HVMF	connective:	n/a	n/a
38	CTCF	chr3:155761739-155761960	ProgFib	skin:	n/a	chr3:155761841-155761857 chr3:155761840-155761858 chr3:155761843-155761856
39	CTCF	chr3:155761727-155761979	GM19238	blood:	n/a	chr3:155761841-155761857 chr3:155761840-155761858 chr3:155761843-155761856
40	CTCF	chr3:155761515-155762140	A549	lung:	n/a	chr3:155761841-155761857 chr3:155761840-155761858 chr3:155761843-155761856
41	CTCF	chr3:155767060-155767210	GM06990	blood:	n/a	n/a
42	CTCF	chr3:155824860-155825010	SAEC	small airway:	n/a	n/a
43	CTCF	chr3:155761680-155761830	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr3:155761680-155761830	BJ	skin:	n/a	n/a
45	CTCF	chr3:155761760-155761910	GM12872	blood:	n/a	chr3:155761841-155761857 chr3:155761840-155761858 chr3:155761843-155761856
46	CTCF	chr3:155761740-155761890	GM12878	blood:	n/a	chr3:155761841-155761857 chr3:155761840-155761858 chr3:155761843-155761856
47	CTCF	chr3:155824820-155824970	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr3:155761742-155761991	Fibrobl	skin:	n/a	chr3:155761841-155761857 chr3:155761840-155761858 chr3:155761843-155761856
49	CTCF	chr3:155800080-155800230	HCFaa	heart:	n/a	n/a
50	CTCF	chr3:155761680-155761830	HFF-Myc	foreskin:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:155760176-155760226	U87	brain:	n/a
2	chr3:155817887-155817937	NHDF-neo	bronchial:	n/a
3	chr3:155759425-155759475	BE2_C	brain:	n/a
4	chr3:155817341-155817391	U87	brain:	n/a
5	chr3:155817887-155817937	MCF-7	breast:	n/a
6	chr3:155817341-155817391	HCF	heart:	n/a
7	chr3:155817341-155817391	Hepatocyte	liver:	n/a
8	chr3:155760037-155760087	A549	lung:	n/a
9	chr3:155817341-155817391	K562	blood:	n/a
10	chr3:155760037-155760087	NHBE	bronchial:	n/a
11	chr3:155817341-155817391	BJ	skin:	n/a
12	chr3:155817341-155817391	NT2-D1	testis:	n/a
13	chr3:155759425-155759475	PrEC	prostate:	n/a
14	chr3:155760037-155760087	PFSK-1	brain:	n/a
15	chr3:155760037-155760087	HRE	kidney:	n/a
16	chr3:155812108-155812158	GM19239	blood:	n/a
17	chr3:155759425-155759475	ovcar-3	ovarian:	n/a
18	chr3:155759425-155759475	HAEpiC	amniotic membrane:	n/a
19	chr3:155817887-155817937	Jurkat	blood:	n/a
20	chr3:155817887-155817937	HNPCEpiC	eye:	n/a
21	chr3:155759425-155759475	Caco-2	colon:	n/a
22	chr3:155759425-155759475	GM06990	blood:	n/a
23	chr3:155817887-155817937	HMEC	breast:	n/a
24	chr3:155760037-155760087	GM12892	blood:	n/a
25	chr3:155760037-155760087	H1-hESC	embryonic stem cell:	embryo
26	chr3:155812108-155812158	SK-N-SH	brain:	n/a
27	chr3:155817341-155817391	A549	lung:	n/a
28	chr3:155817341-155817391	GM19239	blood:	n/a
29	chr3:155812108-155812158	ProgFib	skin:	n/a
30	chr3:155817887-155817937	U87	brain:	n/a
31	chr3:155760037-155760087	HAEpiC	amniotic membrane:	n/a
32	chr3:155817341-155817391	LNCaP	prostate:	n/a
33	chr3:155760037-155760087	HUVEC	blood vessel:	n/a
34	chr3:155817341-155817391	GM12892	blood:	n/a
35	chr3:155817341-155817391	RPTEC	kidney:	n/a
36	chr3:155760037-155760087	HepG2	liver:	n/a
37	chr3:155817887-155817937	AG04449	skin:	fetal
38	chr3:155817341-155817391	HEK293	kidney:	embryo
39	chr3:155812108-155812158	ovcar-3	ovarian:	n/a
40	chr3:155817887-155817937	A549	lung:	n/a
41	chr3:155759425-155759475	SK-N-SH_RA	brain:	n/a
42	chr3:155817887-155817937	BJ	skin:	n/a
43	chr3:155817341-155817391	ovcar-3	ovarian:	n/a
44	chr3:155812108-155812158	GM06990	blood:	n/a
45	chr3:155817887-155817937	T-47D	breast:	n/a
46	chr3:155812108-155812158	HNPCEpiC	eye:	n/a
47	chr3:155817341-155817391	AG04450	lung:	fetal
48	chr3:155817887-155817937	GM12891	blood:	n/a
49	chr3:155760176-155760226	BE2_C	brain:	n/a
50	chr3:155760037-155760087	BJ	skin:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:155766964..155770494-chr3:155772877..155775974,3	K562	blood:
2	chr3:155766964..155770494-chr3:155772877..155775974,3	K562	blood:
3	chr3:155804123..155806644-chr3:155808208..155811120,2	MCF-7	breast:
4	chr3:155795732..155798670-chr3:155800435..155803039,2	K562	blood:
5	chr3:155804123..155806644-chr3:155808208..155811120,2	MCF-7	breast:
6	chr3:155693529..155695336-chr3:155776745..155779647,2	K562	blood:
7	chr3:155802547..155805092-chr3:155805319..155806843,2	K562	blood:
8	chr3:155803528..155806801-chr3:155807011..155810632,3	MCF-7	breast:
9	chr3:155802547..155805092-chr3:155805319..155806843,2	K562	blood:
10	chr3:155811121..155812697-chr4:74123629..74125315,2	MCF-7	breast:
11	chr3:155795732..155798670-chr3:155800435..155803039,2	K562	blood:
12	chr3:155803528..155806801-chr3:155807011..155810632,3	MCF-7	breast:
13	chr2:139513660..139514160-chr3:155809718..155810241,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNAB1-1	chr3:155755490-155755534	NONHSAT092851

No data

Variant related genes	Relation type
ALG1L15P	TF binding region
VN2R1P	TF binding region
KCNAB1	TF binding region
ALG1L15P	CpG island
VN2R1P	CpG island
KCNAB1	CpG island
ENSG00000250220	chromatin interactions
ENSG00000132466	chromatin interactions

Extended variants
information (count: 2127 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2127 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6781558	chr3:155751484-155751485	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150883558	chr3:155751577-155751578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180965509	chr3:155751585-155751586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115889536	chr3:155751606-155751607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538021994	chr3:155751619-155751620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556840043	chr3:155751659-155751660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs578148040	chr3:155751667-155751668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139339811	chr3:155751685-155751686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150070115	chr3:155751724-155751725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368387427	chr3:155751737-155751738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187069081	chr3:155751827-155751828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200463141	chr3:155751863-155751864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543118892	chr3:155751873-155751874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561896031	chr3:155751891-155751892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561306573	chr3:155751920-155751921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190804794	chr3:155751936-155751937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146628838	chr3:155751972-155751973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550473451	chr3:155751976-155751977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562811990	chr3:155751996-155751997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533070354	chr3:155752016-155752017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551010931	chr3:155752064-155752065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566112758	chr3:155752076-155752077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533674767	chr3:155752094-155752095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140047109	chr3:155752134-155752135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567221931	chr3:155752139-155752140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538437688	chr3:155752150-155752151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142293012	chr3:155752162-155752163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs13074135	chr3:155752166-155752167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201693251	chr3:155752170-155752171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75566613	chr3:155752182-155752183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs62284910	chr3:155752213-155752214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs111565866	chr3:155752232-155752233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539336571	chr3:155752255-155752256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554236192	chr3:155752258-155752259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572453598	chr3:155752265-155752266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543006906	chr3:155752266-155752267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561453198	chr3:155752273-155752274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113252355	chr3:155752298-155752299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544437731	chr3:155752317-155752318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544840010	chr3:155752321-155752322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374641359	chr3:155752339-155752340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544890086	chr3:155752343-155752344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559981754	chr3:155752349-155752350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565259718	chr3:155752373-155752374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532562893	chr3:155752420-155752421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527314027	chr3:155752421-155752422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148961327	chr3:155752471-155752472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562563005	chr3:155752532-155752533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567362696	chr3:155752543-155752544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9880809	chr3:155752562-155752563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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	22032731	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
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Cancer	17440070	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155750800-155751600	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr3:155751000-155751600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr3:155751000-155751600	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr3:155751000-155751600	Enhancers	Brain Hippocampus Middle	brain
5	chr3:155751000-155751600	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr3:155751000-155751600	Enhancers	Brain Substantia Nigra	brain
7	chr3:155751200-155751600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr3:155751200-155751600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:155751400-155754400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr3:155751600-155754200	Weak transcription	Brain Hippocampus Middle	brain
11	chr3:155751600-155754200	Weak transcription	Brain Substantia Nigra	brain
12	chr3:155751600-155754400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr3:155751600-155754400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr3:155754200-155755200	Enhancers	Brain Substantia Nigra	brain
15	chr3:155754200-155758200	Enhancers	Brain Hippocampus Middle	brain
16	chr3:155754400-155754800	Enhancers	Brain Angular Gyrus	brain
17	chr3:155754400-155754800	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr3:155754400-155755000	Enhancers	Brain Anterior Caudate	brain
19	chr3:155754400-155755400	Enhancers	Brain Cingulate Gyrus	brain
20	chr3:155754400-155755600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr3:155754400-155755600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr3:155754400-155755600	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr3:155754600-155755600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:155754800-155758000	Weak transcription	Brain Angular Gyrus	brain
25	chr3:155754800-155758000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr3:155755000-155755600	Active TSS	Brain Anterior Caudate	brain
27	chr3:155755200-155756800	Weak transcription	Brain Substantia Nigra	brain
28	chr3:155755600-155756800	Weak transcription	Brain Anterior Caudate	brain
29	chr3:155756800-155757000	Enhancers	Brain Anterior Caudate	brain
30	chr3:155756800-155757200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr3:155756800-155757200	Enhancers	Brain Substantia Nigra	brain
32	chr3:155756800-155757200	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr3:155757000-155757200	Enhancers	Osteobl	bone
34	chr3:155757000-155758800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr3:155758000-155758200	Enhancers	Brain Angular Gyrus	brain
36	chr3:155758000-155758200	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr3:155758000-155764800	Weak transcription	Right Atrium	heart
38	chr3:155759800-155761000	Enhancers	HepG2	liver
39	chr3:155761800-155762200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr3:155761800-155762200	Enhancers	Placenta	Placenta
41	chr3:155762000-155762200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr3:155762000-155762400	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr3:155762200-155763400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr3:155762400-155762600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr3:155762400-155763600	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr3:155762600-155769400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr3:155763400-155763800	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr3:155763400-155763800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr3:155763800-155764000	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr3:155768600-155769200	Enhancers	A549	lung

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