Variant report

Variant	nsv1016586
Chromosome Location	chr5:116317968-116377074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:148)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:148 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr5:116361519-116361714	K562	blood:	n/a	n/a
2	CEBPB	chr5:116355458-116355994	HepG2	liver:	n/a	n/a
3	CEBPB	chr5:116355462-116355747	A549	lung:	n/a	n/a
4	CEBPB	chr5:116355475-116355742	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr5:116355490-116355602	MCF-7	breast:	n/a	n/a
6	CTCF	chr5:116325880-116326030	GM12865	blood:	n/a	n/a
7	CTCF	chr5:116349320-116349470	HEK293	kidney:	n/a	n/a
8	CTCF	chr5:116355340-116355490	GM12872	blood:	n/a	n/a
9	CTCF	chr5:116355460-116355724	GM12878	blood:	n/a	n/a
10	CTCF	chr5:116322664-116322715	HepG2	liver:	n/a	n/a
11	CTCF	chr5:116325960-116326110	HAc	cerebellar:	n/a	n/a
12	CTCF	chr5:116355515-116355591	MCF-7	breast:	n/a	n/a
13	CTCF	chr5:116325980-116326130	BE2_C	brain:	n/a	n/a
14	CTCF	chr5:116325880-116326030	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr5:116325940-116326090	BE2_C	brain:	n/a	n/a
16	CTCF	chr5:116349454-116349456	MCF-7	breast:	n/a	n/a
17	CTCF	chr5:116355440-116355590	MCF-7	breast:	n/a	n/a
18	CTCF	chr5:116355499-116355594	LNCaP	prostate:	n/a	n/a
19	CTCF	chr5:116325920-116326070	GM12870	blood:	n/a	n/a
20	CTCF	chr5:116355420-116355570	MCF-7	breast:	n/a	n/a
21	E2F4	chr5:116351968-116352394	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr5:116353954-116354273	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr5:116355522-116355775	MCF10A-Er-Src	breast:	n/a	n/a
24	EBF1	chr5:116325660-116325870	GM12878	blood:	n/a	n/a
25	EP300	chr5:116328423-116328599	GM12878	blood:	n/a	n/a
26	EP300	chr5:116355594-116355668	Hela-S3	cervix:	n/a	n/a
27	EP300	chr5:116328485-116328502	GM12878	blood:	n/a	n/a
28	ESR1	chr5:116361526-116361864	T-47D	breast:	n/a	n/a
29	ESR1	chr5:116361558-116361843	T-47D	breast:	n/a	n/a
30	ESR1	chr5:116361568-116361815	T-47D	breast:	n/a	n/a
31	FAM48A	chr5:116318711-116318843	GM12878	blood:	n/a	n/a
32	FOS	chr5:116353991-116354273	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr5:116356414-116356623	MCF10A-Er-Src	breast:	n/a	chr5:116356525-116356533
34	FOS	chr5:116355444-116355790	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr5:116355397-116355790	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr5:116355421-116355806	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr5:116353934-116354365	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr5:116353947-116354397	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr5:116353905-116354347	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr5:116356414-116356655	MCF10A-Er-Src	breast:	n/a	chr5:116356525-116356533
41	FOS	chr5:116368715-116368802	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr5:116355447-116355685	MCF10A-Er-Src	breast:	n/a	n/a
43	GATA3	chr5:116326657-116327105	MCF-7	breast:	n/a	n/a
44	GATA3	chr5:116326223-116326395	SH-SY5Y	brain:	n/a	chr5:116326375-116326387 chr5:116326377-116326385 chr5:116326375-116326388
45	GATA3	chr5:116326683-116327058	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr5:116356800-116357005	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr5:116361524-116361826	T-47D	breast:	n/a	n/a
48	IRF3	chr5:116363912-116363931	GM12878	blood:	n/a	n/a
49	JUN	chr5:116366214-116366310	H1-hESC	embryonic stem cell:	n/a	n/a
50	JUND	chr5:116366691-116366971	HepG2	liver:	n/a	chr5:116366838-116366847

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:116355027-116355077	HCT-116	colon:	n/a
2	chr5:116355027-116355077	HRE	kidney:	n/a
3	chr5:116355027-116355077	U87	brain:	n/a
4	chr5:116355027-116355077	SK-N-SH	brain:	n/a
5	chr5:116356275-116356325	AG09319	gingival:	n/a
6	chr5:116355027-116355077	AG10803	skin:	n/a
7	chr5:116356275-116356325	AoSMC	blood vessel:	n/a
8	chr5:116356275-116356325	Jurkat	blood:	n/a
9	chr5:116356275-116356325	H1-hESC	embryonic stem cell:	embryo
10	chr5:116356275-116356325	SK-N-MC	brain:	n/a
11	chr5:116355027-116355077	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:116356275-116356325	PANC-1	pancreas:	n/a
13	chr5:116355027-116355077	HCM	heart:	n/a
14	chr5:116355027-116355077	NB4	blood:	n/a
15	chr5:116355027-116355077	RPTEC	kidney:	n/a
16	chr5:116356275-116356325	ProgFib	skin:	n/a
17	chr5:116355027-116355077	PrEC	prostate:	n/a
18	chr5:116355027-116355077	A549	lung:	n/a
19	chr5:116355027-116355077	SKMC	muscle:	n/a
20	chr5:116356275-116356325	LNCaP	prostate:	n/a
21	chr5:116356275-116356325	PrEC	prostate:	n/a
22	chr5:116355027-116355077	SK-N-SH_RA	brain:	n/a
23	chr5:116355027-116355077	AG04450	lung:	fetal
24	chr5:116355027-116355077	SK-N-MC	brain:	n/a
25	chr5:116356275-116356325	HRE	kidney:	n/a
26	chr5:116355027-116355077	HRPEpiC	eye:	n/a
27	chr5:116356275-116356325	HCPEpiC	choroid plexus:	n/a
28	chr5:116355027-116355077	NT2-D1	testis:	n/a
29	chr5:116356275-116356325	AG04450	lung:	fetal
30	chr5:116356275-116356325	HNPCEpiC	eye:	n/a
31	chr5:116356275-116356325	SK-N-SH_RA	brain:	n/a
32	chr5:116355027-116355077	SAEC	small airway:	n/a
33	chr5:116356275-116356325	NH-A	brain:	n/a
34	chr5:116355027-116355077	MCF-7	breast:	n/a
35	chr5:116356275-116356325	HRPEpiC	eye:	n/a
36	chr5:116356275-116356325	CMK	blood:	n/a
37	chr5:116356275-116356325	GM19239	blood:	n/a
38	chr5:116355027-116355077	BE2_C	brain:	n/a
39	chr5:116355027-116355077	HEK293	kidney:	embryo
40	chr5:116356275-116356325	HepG2	liver:	n/a
41	chr5:116356275-116356325	ECC-1	luminal epithelium:	n/a
42	chr5:116355027-116355077	GM06990	blood:	n/a
43	chr5:116356275-116356325	HCM	heart:	n/a
44	chr5:116356275-116356325	NHBE	bronchial:	n/a
45	chr5:116356275-116356325	GM12892	blood:	n/a
46	chr5:116355027-116355077	HEEpiC	esophagus:	n/a
47	chr5:116355027-116355077	CMK	blood:	n/a
48	chr5:116356275-116356325	ovcar-3	ovarian:	n/a
49	chr5:116356275-116356325	HCT-116	colon:	n/a
50	chr5:116356275-116356325	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:116370263..116371870-chr5:116372681..116375033,2	K562	blood:
2	chr20:49334975..49335937-chr5:116357755..116358651,2	MCF-7	breast:
3	chr5:116370263..116371870-chr5:116372681..116375033,2	K562	blood:
4	chr4:181060859..181061364-chr5:116353318..116353952,2	MCF-7	breast:
5	chr5:116360894..116363806-chr5:116375344..116377265,2	MCF-7	breast:
6	chr5:116360894..116363806-chr5:116375344..116377265,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD10-4	chr5:116374077-116374265	XLOC_004521
2	lnc-COMMD10-4	chr5:116366896-116367126	XLOC_004521

No data

Variant related genes	Relation type
ENSG00000250650	TF binding region
ENSG00000250949	TF binding region
ENSG00000250650	CpG island
ENSG00000250949	CpG island
RBFOX2	miRNA target sites

Extended variants
information (count: 2304 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2304 , 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	rs564883791	chr5:116319628-116319629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142858921	chr5:116319644-116319645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs80345064	chr5:116319698-116319699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541588059	chr5:116319720-116319721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561346333	chr5:116319734-116319735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187333137	chr5:116319764-116319765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542859953	chr5:116319799-116319800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4920944	chr5:116319808-116319809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs531643157	chr5:116319809-116319810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12655103	chr5:116319819-116319820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191851806	chr5:116319831-116319832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113267200	chr5:116319853-116319854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112213340	chr5:116319860-116319861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547122393	chr5:116319862-116319863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78928377	chr5:116320059-116320060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142337119	chr5:116320084-116320085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141990165	chr5:116320107-116320108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72237125	chr5:116320113-116320114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs60373007	chr5:116320114-116320115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374419545	chr5:116320115-116320116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533619114	chr5:116320145-116320146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34143318	chr5:116320150-116320151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557437028	chr5:116320175-116320176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146906253	chr5:116320226-116320227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182945861	chr5:116320251-116320252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10040194	chr5:116320258-116320259	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs572435779	chr5:116320269-116320270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10040196	chr5:116320280-116320281	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs147943471	chr5:116320315-116320316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535713157	chr5:116320362-116320363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575009786	chr5:116320420-116320421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76776267	chr5:116320431-116320432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372408896	chr5:116320500-116320501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562743055	chr5:116320535-116320536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34466902	chr5:116320537-116320538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576153059	chr5:116320544-116320545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116480565	chr5:116320585-116320586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545314149	chr5:116320614-116320615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557582787	chr5:116320642-116320643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141772510	chr5:116320649-116320650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113101918	chr5:116320650-116320651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575855099	chr5:116320661-116320662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547008944	chr5:116320670-116320671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548956579	chr5:116320675-116320676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560498572	chr5:116320708-116320709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546142884	chr5:116320715-116320716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529748002	chr5:116320727-116320728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138261224	chr5:116320765-116320766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570279129	chr5:116320780-116320781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564302584	chr5:116320829-116320830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116319600-116319800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:116319800-116322000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr5:116321600-116321800	ZNF genes & repeats	Brain Cingulate Gyrus	brain
4	chr5:116321800-116324800	Weak transcription	Brain Cingulate Gyrus	brain
5	chr5:116323200-116323400	Enhancers	Fetal Muscle Leg	muscle
6	chr5:116323400-116324600	Weak transcription	Fetal Muscle Leg	muscle
7	chr5:116324600-116326200	Enhancers	Fetal Muscle Leg	muscle
8	chr5:116324600-116328200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr5:116324800-116325400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr5:116324800-116325400	Enhancers	Brain Cingulate Gyrus	brain
11	chr5:116324800-116326200	Enhancers	Brain Substantia Nigra	brain
12	chr5:116324800-116328200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:116325000-116325400	Enhancers	Brain Hippocampus Middle	brain
14	chr5:116325000-116326600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr5:116325200-116326000	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr5:116325200-116326200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr5:116326200-116327000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:116327000-116328200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:116327800-116328400	Enhancers	HSMMtube	muscle
20	chr5:116328200-116328600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:116328200-116335200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:116333200-116333400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr5:116333400-116334000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr5:116333800-116334000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr5:116335200-116336000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:116336000-116341000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr5:116337200-116337400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
28	chr5:116338600-116339400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
29	chr5:116339400-116339800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr5:116340600-116341600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr5:116341000-116341600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:116346200-116349200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:116347400-116347800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
34	chr5:116347800-116349000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr5:116348400-116349400	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr5:116349000-116349400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr5:116349000-116349600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr5:116349000-116349600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr5:116349000-116349600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr5:116349200-116349600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr5:116349200-116349600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr5:116349200-116349600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:116349200-116349600	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr5:116349200-116349600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr5:116349200-116349600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr5:116349200-116349600	Enhancers	Esophagus	oesophagus
47	chr5:116349200-116349800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr5:116349400-116349600	Enhancers	H9 Cell Line	embryonic stem cell
49	chr5:116349400-116352800	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr5:116349600-116351000	Weak transcription	H9 Cell Line	embryonic stem cell

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