Variant report

Variant	nsv599487
Chromosome Location	chr5:116732456-116772093
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	CEBPB	chr5:116764460-116764736	HepG2	liver:	n/a	chr5:116764597-116764608
2	CEBPB	chr5:116739875-116740143	Hela-S3	cervix:	n/a	n/a
3	CTCF	chr5:116743691-116743731	Kidney_OC	kidney:	n/a	n/a
4	CTCF	chr5:116747996-116748051	Spleen_OC	spleen:	n/a	n/a
5	CTCF	chr5:116766960-116767110	SAEC	small airway:	n/a	n/a
6	EP300	chr5:116753704-116754080	MCF-7	breast:	n/a	n/a
7	EP300	chr5:116753098-116753488	MCF-7	breast:	n/a	chr5:116753240-116753248
8	FOS	chr5:116750693-116750960	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr5:116769356-116769481	MCF10A-Er-Src	breast:	n/a	n/a
10	FOXA1	chr5:116739742-116739952	T-47D	breast:	n/a	n/a
11	FOXM1	chr5:116752885-116753585	MCF-7	breast:	n/a	n/a
12	GATA2	chr5:116732019-116732541	SH-SY5Y	brain:	n/a	n/a
13	GATA2	chr5:116750613-116750993	HUVEC	blood vessel:	n/a	n/a
14	GATA3	chr5:116752957-116754076	MCF-7	breast:	n/a	n/a
15	GATA3	chr5:116752973-116753809	MCF-7	breast:	n/a	n/a
16	GATA3	chr5:116752939-116754092	MCF-7	breast:	n/a	n/a
17	GATA3	chr5:116751266-116751607	SH-SY5Y	brain:	n/a	n/a
18	GATA3	chr5:116748482-116748952	MCF-7	breast:	n/a	chr5:116748757-116748770
19	GATA3	chr5:116752692-116754339	MCF-7	breast:	n/a	n/a
20	GATA3	chr5:116748535-116748905	MCF-7	breast:	n/a	chr5:116748757-116748770
21	JUN	chr5:116764428-116764453	HepG2	liver:	n/a	n/a
22	MAFF	chr5:116769986-116770274	HepG2	liver:	n/a	n/a
23	MAFF	chr5:116760297-116760597	HepG2	liver:	n/a	chr5:116760448-116760462 chr5:116760449-116760467
24	MAFK	chr5:116770010-116770275	HepG2	liver:	n/a	chr5:116770057-116770067
25	MAFK	chr5:116740448-116740645	HepG2	liver:	n/a	n/a
26	MAFK	chr5:116760275-116760636	HepG2	liver:	n/a	chr5:116760448-116760462 chr5:116760453-116760467 chr5:116760450-116760465 chr5:116760454-116760465 chr5:116760449-116760459 chr5:116760445-116760465 chr5:116760447-116760463 chr5:116760455-116760466 chr5:116760455-116760466 chr5:116760450-116760466
27	MAFK	chr5:116748907-116749107	IMR90	lung:	n/a	chr5:116748986-116749002 chr5:116748986-116749001
28	MAFK	chr5:116760295-116760626	HepG2	liver:	n/a	chr5:116760448-116760462 chr5:116760453-116760467 chr5:116760450-116760465 chr5:116760454-116760465 chr5:116760449-116760459 chr5:116760445-116760465 chr5:116760447-116760463 chr5:116760455-116760466 chr5:116760455-116760466 chr5:116760450-116760466
29	MAFK	chr5:116760314-116760591	IMR90	lung:	n/a	chr5:116760448-116760462 chr5:116760453-116760467 chr5:116760450-116760465 chr5:116760454-116760465 chr5:116760449-116760459 chr5:116760445-116760465 chr5:116760447-116760463 chr5:116760455-116760466 chr5:116760455-116760466 chr5:116760450-116760466
30	MAFK	chr5:116770012-116770256	IMR90	lung:	n/a	chr5:116770057-116770067
31	MAFK	chr5:116760316-116760576	H1-hESC	embryonic stem cell:	n/a	chr5:116760448-116760462 chr5:116760453-116760467 chr5:116760450-116760465 chr5:116760454-116760465 chr5:116760449-116760459 chr5:116760445-116760465 chr5:116760447-116760463 chr5:116760455-116760466 chr5:116760455-116760466 chr5:116760450-116760466
32	MAFK	chr5:116748869-116749153	HepG2	liver:	n/a	chr5:116748986-116749002 chr5:116748986-116749001
33	MAFK	chr5:116770016-116770268	HepG2	liver:	n/a	chr5:116770057-116770067
34	MAFK	chr5:116748900-116749100	HepG2	liver:	n/a	chr5:116748986-116749002 chr5:116748986-116749001
35	MAZ	chr5:116737980-116738008	HepG2	liver:	n/a	n/a
36	NFYB	chr5:116742941-116743364	K562	blood:	n/a	n/a
37	NFYB	chr5:116761456-116761562	GM12878	blood:	n/a	n/a
38	NFYB	chr5:116742971-116743315	GM12878	blood:	n/a	n/a
39	NR2F2	chr5:116753017-116753542	MCF-7	breast:	n/a	chr5:116753503-116753518
40	POLR2A	chr5:116738719-116738904	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr5:116767259-116767298	A549	lung:	n/a	n/a
42	POLR2A	chr5:116766037-116766176	GM12878	blood:	n/a	n/a
43	POLR2A	chr5:116759970-116760085	A549	lung:	n/a	n/a
44	POLR2A	chr5:116767220-116767256	A549	lung:	n/a	n/a
45	POLR2A	chr5:116739766-116739824	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr5:116741093-116741272	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr5:116751459-116751565	GM12878	blood:	n/a	n/a
48	POLR2A	chr5:116734192-116734196	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr5:116752171-116752267	GM12878	blood:	n/a	n/a
50	POLR2A	chr5:116770321-116770343	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:116751135-116751185	BE2_C	brain:	n/a
2	chr5:116751135-116751185	ProgFib	skin:	n/a
3	chr5:116751135-116751185	HRPEpiC	eye:	n/a
4	chr5:116751135-116751185	NT2-D1	testis:	n/a
5	chr5:116751135-116751185	HEK293	kidney:	embryo
6	chr5:116751135-116751185	Jurkat	blood:	n/a
7	chr5:116751135-116751185	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:116751135-116751185	SAEC	small airway:	n/a
9	chr5:116751135-116751185	MCF10A-Er-Src	breast:	n/a
10	chr5:116751135-116751185	HCPEpiC	choroid plexus:	n/a
11	chr5:116751135-116751185	HCT-116	colon:	n/a
12	chr5:116751135-116751185	MCF-7	breast:	n/a
13	chr5:116751135-116751185	Caco-2	colon:	n/a
14	chr5:116751135-116751185	Hepatocyte	liver:	n/a
15	chr5:116751135-116751185	NB4	blood:	n/a
16	chr5:116751135-116751185	HMEC	breast:	n/a
17	chr5:116751135-116751185	U87	brain:	n/a
18	chr5:116751135-116751185	HL-60	blood:	n/a
19	chr5:116751135-116751185	Hela-S3	cervix:	n/a
20	chr5:116751135-116751185	IMR90	lung:	fetal
21	chr5:116751135-116751185	ECC-1	luminal epithelium:	n/a
22	chr5:116751135-116751185	HRCEpiC	kidney:	n/a
23	chr5:116751135-116751185	GM06990	blood:	n/a
24	chr5:116751135-116751185	SK-N-SH	brain:	n/a
25	chr5:116751135-116751185	HCM	heart:	n/a
26	chr5:116751135-116751185	HRE	kidney:	n/a
27	chr5:116751135-116751185	AG10803	skin:	n/a
28	chr5:116751135-116751185	SK-N-MC	brain:	n/a
29	chr5:116751135-116751185	PFSK-1	brain:	n/a
30	chr5:116751135-116751185	T-47D	breast:	n/a
31	chr5:116751135-116751185	HepG2	liver:	n/a
32	chr5:116751135-116751185	GM12892	blood:	n/a
33	chr5:116751135-116751185	NHDF-neo	bronchial:	n/a
34	chr5:116751135-116751185	CMK	blood:	n/a
35	chr5:116751135-116751185	BJ	skin:	n/a
36	chr5:116751135-116751185	GM19239	blood:	n/a
37	chr5:116751135-116751185	LNCaP	prostate:	n/a
38	chr5:116751135-116751185	K562	blood:	n/a
39	chr5:116751135-116751185	AG04449	skin:	fetal
40	chr5:116751135-116751185	AoSMC	blood vessel:	n/a
41	chr5:116751135-116751185	AG09319	gingival:	n/a
42	chr5:116751135-116751185	PANC-1	pancreas:	n/a
43	chr5:116751135-116751185	PrEC	prostate:	n/a
44	chr5:116751135-116751185	GM12878	blood:	n/a
45	chr5:116751135-116751185	H1-hESC	embryonic stem cell:	embryo
46	chr5:116751135-116751185	AG09309	skin:	n/a
47	chr5:116751135-116751185	NHBE	bronchial:	n/a
48	chr5:116751135-116751185	HIPEpiC	eye:	n/a
49	chr5:116751135-116751185	RPTEC	kidney:	n/a
50	chr5:116751135-116751185	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:116749500..116751869-chr5:116751888..116755550,3	MCF-7	breast:
2	chr5:116769502..116772047-chr5:116790908..116792461,2	MCF-7	breast:
3	chr5:116752873..116753980-chr5:117345444..117346250,3	MCF-7	breast:
4	chr5:116744135..116746719-chr5:116750453..116752242,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD10-5	chr5:116751208-116751435	NONHSAT103387
2	lnc-COMMD10-5	chr5:116751205-116751435	ENSG00000248663
3	lnc-COMMD10-5	chr5:116751084-116751435	NONHSAT147358

Variant related genes	Relation type
LINC00992	TF binding region
LINC00992	CpG island
ENSG00000248663	chromatin interactions

Extended variants
information (count: 1008 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146441117	chr5:116732825-116732826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs369386719	chr5:116732826-116732827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184443453	chr5:116732848-116732849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568266201	chr5:116732875-116732876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545335480	chr5:116732957-116732958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140814717	chr5:116732978-116732979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2560600	chr5:116732988-116732989	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs570886772	chr5:116732994-116732995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533034581	chr5:116733077-116733078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539807730	chr5:116733128-116733129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187784016	chr5:116733147-116733148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143010929	chr5:116733154-116733155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534868778	chr5:116733179-116733180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533362593	chr5:116733200-116733201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148188515	chr5:116733202-116733203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551295136	chr5:116733230-116733231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574650759	chr5:116733257-116733258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543664141	chr5:116733267-116733268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191832037	chr5:116733273-116733274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560409930	chr5:116733370-116733371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183953608	chr5:116733405-116733406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371195605	chr5:116733433-116733434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188360210	chr5:116733446-116733447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377730529	chr5:116733448-116733449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541746366	chr5:116733449-116733450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542075888	chr5:116733462-116733463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192132499	chr5:116733479-116733480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530978602	chr5:116733511-116733512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561950836	chr5:116733524-116733525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374197141	chr5:116733526-116733527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79431583	chr5:116733538-116733539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570917835	chr5:116733545-116733546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs17141696	chr5:116733625-116733626	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs13183369	chr5:116733635-116733636	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs185138124	chr5:116733638-116733639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141381516	chr5:116733679-116733680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567209226	chr5:116733704-116733705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568392992	chr5:116733710-116733711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537227814	chr5:116733739-116733740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556915056	chr5:116733794-116733795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190470216	chr5:116733796-116733797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545530991	chr5:116733876-116733877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs553040718	chr5:116733877-116733878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs199593451	chr5:116733926-116733927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572468575	chr5:116733928-116733929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541443504	chr5:116733963-116733964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562031095	chr5:116733982-116733983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551193879	chr5:116733997-116733998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544401152	chr5:116734034-116734035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564478247	chr5:116734060-116734061	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116732800-116734400	Enhancers	Fetal Lung	lung
2	chr5:116733200-116734600	Enhancers	Fetal Stomach	stomach
3	chr5:116733800-116734200	Enhancers	Fetal Brain Female	brain
4	chr5:116733800-116734800	Enhancers	Brain Germinal Matrix	brain
5	chr5:116739200-116740000	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr5:116739800-116740400	Active TSS	Placenta	Placenta
7	chr5:116740000-116741000	Active TSS	Hela-S3	cervix
8	chr5:116740000-116741200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr5:116741000-116741800	Enhancers	Colon Smooth Muscle	Colon
10	chr5:116741200-116741800	Enhancers	Rectal Mucosa Donor 29	rectum
11	chr5:116741200-116742000	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr5:116747000-116748200	Enhancers	HUVEC	blood vessel
13	chr5:116747200-116747600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr5:116747200-116747600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr5:116747200-116747600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr5:116747200-116747800	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr5:116747200-116748000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr5:116747400-116747800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr5:116747400-116747800	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr5:116748000-116748800	Enhancers	Fetal Lung	lung
21	chr5:116748800-116752600	Weak transcription	Fetal Lung	lung
22	chr5:116750600-116753200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr5:116752600-116752800	Enhancers	Fetal Lung	lung
24	chr5:116752800-116753200	Weak transcription	Fetal Lung	lung
25	chr5:116753200-116753600	Enhancers	Fetal Lung	lung
26	chr5:116756400-116756800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr5:116760400-116761800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr5:116760400-116761800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr5:116760800-116761400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr5:116760800-116761600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr5:116761000-116761400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr5:116761000-116761400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:116766600-116766800	Enhancers	Stomach Smooth Muscle	stomach
34	chr5:116766600-116767400	Enhancers	Colon Smooth Muscle	Colon
35	chr5:116766600-116767400	Enhancers	Rectal Smooth Muscle	rectum
36	chr5:116766800-116767400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr5:116766800-116769600	Weak transcription	Stomach Smooth Muscle	stomach
38	chr5:116767400-116769000	Weak transcription	Colon Smooth Muscle	Colon
39	chr5:116767400-116769400	Weak transcription	Rectal Smooth Muscle	rectum
40	chr5:116767800-116768000	Enhancers	Fetal Stomach	stomach
41	chr5:116768000-116769000	Weak transcription	Fetal Stomach	stomach
42	chr5:116769000-116770400	Enhancers	Fetal Stomach	stomach
43	chr5:116769000-116772200	Enhancers	Colon Smooth Muscle	Colon
44	chr5:116769400-116769800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr5:116769400-116770200	Enhancers	H9 Cell Line	embryonic stem cell
46	chr5:116769400-116770400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr5:116769400-116770600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr5:116769400-116770600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:116769400-116770800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:116769400-116770800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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