Variant report

Variant	nsv882378
Chromosome Location	chr5:91477046-91601492
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	BACH1	chr5:91499487-91499515	K562	blood:	n/a	n/a
2	CEBPB	chr5:91563083-91563247	H1-hESC	embryonic stem cell:	n/a	chr5:91563188-91563197 chr5:91563188-91563197 chr5:91563186-91563199 chr5:91563186-91563197 chr5:91563188-91563197 chr5:91563188-91563197 chr5:91563186-91563199
3	CEBPB	chr5:91481243-91481718	HepG2	liver:	n/a	chr5:91481506-91481517
4	CEBPB	chr5:91515445-91515605	HepG2	liver:	n/a	chr5:91515531-91515542
5	CEBPB	chr5:91527192-91527342	H1-hESC	embryonic stem cell:	n/a	chr5:91527284-91527293 chr5:91527284-91527293
6	CEBPB	chr5:91542428-91542496	HepG2	liver:	n/a	n/a
7	CEBPB	chr5:91501985-91502306	IMR90	lung:	n/a	chr5:91502183-91502194 chr5:91502184-91502195 chr5:91502120-91502133 chr5:91502183-91502196
8	CEBPB	chr5:91501973-91502288	A549	lung:	n/a	chr5:91502183-91502194 chr5:91502184-91502195 chr5:91502120-91502133 chr5:91502183-91502196
9	CEBPB	chr5:91501995-91502323	HepG2	liver:	n/a	chr5:91502183-91502194 chr5:91502184-91502195 chr5:91502120-91502133 chr5:91502183-91502196
10	CEBPB	chr5:91527192-91527443	A549	lung:	n/a	chr5:91527284-91527293 chr5:91527284-91527293
11	CEBPB	chr5:91515461-91515628	A549	lung:	n/a	chr5:91515531-91515542
12	CEBPB	chr5:91502105-91502252	H1-hESC	embryonic stem cell:	n/a	chr5:91502183-91502194 chr5:91502184-91502195 chr5:91502120-91502133 chr5:91502183-91502196
13	CEBPB	chr5:91502019-91502252	Hela-S3	cervix:	n/a	chr5:91502183-91502194 chr5:91502184-91502195 chr5:91502120-91502133 chr5:91502183-91502196
14	CEBPB	chr5:91509554-91509607	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:91563075-91563337	HepG2	liver:	n/a	chr5:91563188-91563197 chr5:91563188-91563197 chr5:91563186-91563199 chr5:91563186-91563197 chr5:91563188-91563197 chr5:91563188-91563197 chr5:91563186-91563199
16	CEBPB	chr5:91481417-91481681	Hela-S3	cervix:	n/a	chr5:91481506-91481517
17	CEBPB	chr5:91498994-91499178	HepG2	liver:	n/a	n/a
18	CTCF	chr5:91508198-91508264	Medullo	brain:	n/a	n/a
19	CTCF	chr5:91518360-91518510	GM12873	blood:	n/a	n/a
20	CTCF	chr5:91518423-91518545	A549	lung:	n/a	n/a
21	CTCF	chr5:91518385-91518583	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:91518382-91518498	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr5:91518362-91518591	MCF-7	breast:	n/a	n/a
24	CTCF	chr5:91518411-91518536	HepG2	liver:	n/a	n/a
25	CTCF	chr5:91582135-91582162	LNCaP	prostate:	n/a	n/a
26	CTCF	chr5:91524360-91524510	HepG2	liver:	n/a	n/a
27	CTCF	chr5:91518380-91518530	AG04449	skin:	n/a	n/a
28	CTCF	chr5:91538127-91538203	A549	lung:	n/a	n/a
29	CTCF	chr5:91538080-91538230	MCF-7	breast:	n/a	n/a
30	CTCF	chr5:91518400-91518550	BJ	skin:	n/a	n/a
31	CTCF	chr5:91524360-91524510	HCT-116	colon:	n/a	n/a
32	CTCF	chr5:91518434-91518610	K562	blood:	n/a	n/a
33	CTCF	chr5:91518380-91518530	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr5:91518340-91518490	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr5:91518410-91518566	LNCaP	prostate:	n/a	n/a
36	CTCF	chr5:91518389-91518552	ProgFib	skin:	n/a	n/a
37	CTCF	chr5:91518400-91518550	AG09309	skin:	n/a	n/a
38	CTCF	chr5:91518400-91518550	Caco-2	colon:	n/a	n/a
39	CTCF	chr5:91518311-91518667	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr5:91507715-91507745	GM20000	blood:	n/a	n/a
41	CTCF	chr5:91518320-91518470	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr5:91509969-91510079	LNCaP	prostate:	n/a	n/a
43	CTCF	chr5:91518400-91518550	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:91518480-91518630	HepG2	liver:	n/a	n/a
45	CTCF	chr5:91518380-91518530	HCT-116	colon:	n/a	n/a
46	CTCF	chr5:91509801-91509843	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr5:91518360-91518531	HepG2	liver:	n/a	n/a
48	CTCF	chr5:91518320-91518470	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr5:91518400-91518550	GM12872	blood:	n/a	n/a
50	CTCF	chr5:91518280-91518430	HFF	foreskin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:91598517-91598567	A549	lung:	n/a
2	chr5:91598517-91598567	A549	lung:	n/a
3	chr5:91598546-91598596	MCF-7	breast:	n/a
4	chr5:91598517-91598567	HRE	kidney:	n/a
5	chr5:91495209-91495259	SK-N-SH	brain:	n/a
6	chr5:91598546-91598596	ECC-1	luminal epithelium:	n/a
7	chr5:91598517-91598567	HRPEpiC	eye:	n/a
8	chr5:91598546-91598596	MCF10A-Er-Src	breast:	n/a
9	chr5:91598517-91598567	U87	brain:	n/a
10	chr5:91598517-91598567	Caco-2	colon:	n/a
11	chr5:91598517-91598567	K562	blood:	n/a
12	chr5:91598517-91598567	PFSK-1	brain:	n/a
13	chr5:91598517-91598567	HCT-116	colon:	n/a
14	chr5:91495209-91495259	NB4	blood:	n/a
15	chr5:91598546-91598596	HCT-116	colon:	n/a
16	chr5:91598517-91598567	BJ	skin:	n/a
17	chr5:91495209-91495259	GM06990	blood:	n/a
18	chr5:91598546-91598596	SK-N-SH	brain:	n/a
19	chr5:91598546-91598596	AG10803	skin:	n/a
20	chr5:91598546-91598596	HPAEpiC	pulmonary alveolar:	n/a
21	chr5:91598517-91598567	HEK293	kidney:	embryo
22	chr5:91495209-91495259	PANC-1	pancreas:	n/a
23	chr5:91598546-91598596	RPTEC	kidney:	n/a
24	chr5:91598546-91598596	H1-hESC	embryonic stem cell:	embryo
25	chr5:91598546-91598596	HNPCEpiC	eye:	n/a
26	chr5:91598517-91598567	LNCaP	prostate:	n/a
27	chr5:91495209-91495259	HRE	kidney:	n/a
28	chr5:91598517-91598567	NH-A	brain:	n/a
29	chr5:91598546-91598596	PrEC	prostate:	n/a
30	chr5:91598546-91598596	U87	brain:	n/a
31	chr5:91598546-91598596	HAEpiC	amniotic membrane:	n/a
32	chr5:91495209-91495259	MCF-7	breast:	n/a
33	chr5:91495209-91495259	AG09319	gingival:	n/a
34	chr5:91598546-91598596	BJ	skin:	n/a
35	chr5:91598546-91598596	HL-60	blood:	n/a
36	chr5:91598517-91598567	AG09319	gingival:	n/a
37	chr5:91598546-91598596	HMEC	breast:	n/a
38	chr5:91598517-91598567	NHDF-neo	bronchial:	n/a
39	chr5:91598546-91598596	AG09319	gingival:	n/a
40	chr5:91598546-91598596	GM12891	blood:	n/a
41	chr5:91495209-91495259	ovcar-3	ovarian:	n/a
42	chr5:91598546-91598596	GM12878	blood:	n/a
43	chr5:91598517-91598567	HRCEpiC	kidney:	n/a
44	chr5:91598546-91598596	AoSMC	blood vessel:	n/a
45	chr5:91598546-91598596	GM19239	blood:	n/a
46	chr5:91598546-91598596	T-47D	breast:	n/a
47	chr5:91598517-91598567	NB4	blood:	n/a
48	chr5:91495209-91495259	HCPEpiC	choroid plexus:	n/a
49	chr5:91598517-91598567	PrEC	prostate:	n/a
50	chr5:91598517-91598567	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:91404571..91406524-chr5:91570041..91571594,2	MCF-7	breast:
2	chr5:90937319..90938246-chr5:91517993..91518879,4	MCF-7	breast:
3	chr5:91538345..91540049-chr5:91542932..91545443,2	K562	blood:
4	chr5:91538345..91540049-chr5:91542932..91545443,2	K562	blood:
5	chr5:91224612..91225895-chr5:91517942..91518899,6	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR98-15	chr5:91531110-91531201	ucscGeneNc_uc003kkb_1
2	lnc-GPR98-5	chr5:91500422-91500501	XLOC_004470
3	lnc-GPR98-5	chr5:91495354-91495445	XLOC_004470
4	lnc-GPR98-5	chr5:91500422-91500501	XLOC_004470
5	lnc-GPR98-15	chr5:91536178-91536257	ucscGeneNc_uc003kkb_1
6	lnc-GPR98-5	chr5:91601297-91601452	XLOC_004470

Variant related genes	Relation type
ENSG00000250049	TF binding region
ENSG00000250049	CpG island
PPP1R15B	miRNA target sites
C5orf41	miRNA target sites
RIMS3	miRNA target sites

Extended variants
information (count: 775 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531851083	chr5:91494479-91494480	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs551934563	chr5:91494502-91494503	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs141216956	chr5:91494506-91494507	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs146187072	chr5:91494509-91494510	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs571796124	chr5:91494537-91494538	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs548662507	chr5:91494570-91494571	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs527807186	chr5:91494573-91494574	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs10474392	chr5:91494593-91494594	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs193137484	chr5:91494597-91494598	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs564881714	chr5:91494610-91494611	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs536604109	chr5:91494614-91494615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs555423458	chr5:91494640-91494641	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs185258104	chr5:91494656-91494657	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs13186387	chr5:91494660-91494661	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs188570083	chr5:91494677-91494678	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs369071155	chr5:91494712-91494713	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs557508864	chr5:91494730-91494731	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs370480411	chr5:91494745-91494746	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs112103467	chr5:91494756-91494757	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs377025314	chr5:91494768-91494769	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs371454153	chr5:91494802-91494803	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs553403501	chr5:91494825-91494826	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs573602035	chr5:91494837-91494838	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs542597147	chr5:91494846-91494847	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs373822753	chr5:91494848-91494849	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs13187090	chr5:91494852-91494853	Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs545348114	chr5:91494863-91494864	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs565491609	chr5:91494865-91494866	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs550542929	chr5:91494933-91494934	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs567550025	chr5:91494955-91494956	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs547917615	chr5:91494970-91494971	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs567762694	chr5:91494972-91494973	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs370479218	chr5:91494973-91494974	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs530081775	chr5:91494974-91494975	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs550135749	chr5:91494976-91494977	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs569085510	chr5:91494991-91494992	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs111316991	chr5:91494994-91494995	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs184009069	chr5:91495009-91495010	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs571119114	chr5:91495017-91495018	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs536577371	chr5:91495023-91495024	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs188743554	chr5:91495024-91495025	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs553491162	chr5:91495027-91495028	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs373921021	chr5:91495030-91495031	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs180761783	chr5:91495032-91495033	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs183895616	chr5:91495040-91495041	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs566490650	chr5:91495042-91495043	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs190571263	chr5:91495049-91495050	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs565530147	chr5:91495054-91495055	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs375373247	chr5:91495055-91495056	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs527937743	chr5:91495057-91495058	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	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
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91494800-91495200	Active TSS	H9 Cell Line	embryonic stem cell
2	chr5:91494800-91495400	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr5:91494800-91495400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:91494800-91495400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:91494800-91495600	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr5:91494800-91496000	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr5:91495000-91495400	Active TSS	H1 Cell Line	embryonic stem cell
8	chr5:91495000-91495400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr5:91495000-91495600	Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr5:91495200-91495800	Active TSS	HepG2	liver
11	chr5:91495400-91495600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr5:91495600-91495800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr5:91496000-91496400	Enhancers	HepG2	liver
14	chr5:91509600-91509800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr5:91513200-91513400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
16	chr5:91513400-91516800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr5:91519800-91520800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
18	chr5:91520000-91520600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:91533200-91533800	Enhancers	Spleen	Spleen
20	chr5:91533400-91533800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr5:91533400-91533800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr5:91533400-91534000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr5:91535600-91536000	Enhancers	Fetal Intestine Small	intestine
24	chr5:91544400-91545200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr5:91545200-91546200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr5:91553200-91553600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr5:91558400-91558600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr5:91558600-91559600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr5:91558600-91560200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr5:91558600-91560200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr5:91559200-91560400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr5:91559400-91560400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr5:91559400-91560400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr5:91559600-91560000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr5:91559800-91560200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr5:91559800-91560200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr5:91563600-91563800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr5:91564000-91564600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr5:91567400-91567600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:91567600-91571800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr5:91571800-91572000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr5:91601200-91604000	Weak transcription	A549	lung

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