Variant report

Variant	nsv830397
Chromosome Location	chr5:91213921-91396644
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	chr5:91225091-91225393	HepG2	liver:	n/a	n/a
2	BATF	chr5:91227634-91227833	GM12878	blood:	n/a	chr5:91227743-91227754
3	BHLHE40	chr5:91375827-91375830	GM12878	blood:	n/a	n/a
4	CBX3	chr5:91315122-91315650	HCT-116	colon:	n/a	n/a
5	CBX3	chr5:91313395-91314027	HCT-116	colon:	n/a	n/a
6	CEBPB	chr5:91252099-91252272	HepG2	liver:	n/a	chr5:91252162-91252175 chr5:91252162-91252173 chr5:91252164-91252175
7	CEBPB	chr5:91327553-91327814	A549	lung:	n/a	n/a
8	CEBPB	chr5:91313622-91314038	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr5:91281741-91282081	HepG2	liver:	n/a	chr5:91281924-91281935 chr5:91281925-91281936
10	CEBPB	chr5:91221103-91221469	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:91297589-91297834	HepG2	liver:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
12	CEBPB	chr5:91280927-91281141	HepG2	liver:	n/a	chr5:91281056-91281067
13	CEBPB	chr5:91375704-91376012	HepG2	liver:	n/a	chr5:91375852-91375863 chr5:91375852-91375865 chr5:91375853-91375864
14	CEBPB	chr5:91224169-91224446	HepG2	liver:	n/a	chr5:91224253-91224264
15	CEBPB	chr5:91375748-91376042	A549	lung:	n/a	chr5:91375852-91375863 chr5:91375852-91375865 chr5:91375853-91375864
16	CEBPB	chr5:91298908-91299168	HepG2	liver:	n/a	chr5:91299044-91299056
17	CEBPB	chr5:91297518-91297861	Hela-S3	cervix:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
18	CEBPB	chr5:91244707-91244803	HepG2	liver:	n/a	chr5:91244717-91244728 chr5:91244716-91244729 chr5:91244716-91244727 chr5:91244716-91244727
19	CEBPB	chr5:91261230-91261315	HepG2	liver:	n/a	n/a
20	CEBPB	chr5:91250007-91250340	MCF-7	breast:	n/a	chr5:91250037-91250050
21	CEBPB	chr5:91315118-91315514	Hela-S3	cervix:	n/a	chr5:91315210-91315221 chr5:91315210-91315223
22	CEBPB	chr5:91261232-91261348	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr5:91250031-91250152	H1-hESC	embryonic stem cell:	n/a	chr5:91250037-91250050
24	CEBPB	chr5:91366107-91366340	A549	lung:	n/a	chr5:91366257-91366268 chr5:91366316-91366327
25	CEBPB	chr5:91366092-91366382	HepG2	liver:	n/a	chr5:91366257-91366268 chr5:91366316-91366327
26	CEBPB	chr5:91274856-91275061	A549	lung:	n/a	chr5:91274933-91274946
27	CEBPB	chr5:91249914-91250302	Hela-S3	cervix:	n/a	chr5:91250037-91250050
28	CEBPB	chr5:91297576-91297842	A549	lung:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
29	CEBPB	chr5:91296321-91296513	HepG2	liver:	n/a	chr5:91296386-91296397
30	CEBPB	chr5:91224209-91224484	A549	lung:	n/a	chr5:91224253-91224264
31	CEBPB	chr5:91297546-91297863	IMR90	lung:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
32	CEBPB	chr5:91298859-91299124	IMR90	lung:	n/a	chr5:91299044-91299056
33	CTCF	chr5:91378200-91378350	BE2_C	brain:	n/a	n/a
34	CTCF	chr5:91215231-91215286	Fibrobl	skin:	n/a	n/a
35	CTCF	chr5:91225160-91225310	AG10803	skin:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
36	CTCF	chr5:91225020-91225170	HAc	cerebellar:	n/a	n/a
37	CTCF	chr5:91225139-91225314	GM10248	blood:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
38	CTCF	chr5:91225180-91225330	SAEC	small airway:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
39	CTCF	chr5:91225220-91225370	HFF	foreskin:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
40	CTCF	chr5:91225140-91225290	HRPEpiC	eye:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
41	CTCF	chr5:91225140-91225290	NHEK	skin:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
42	CTCF	chr5:91225180-91225330	HBMEC	blood vessel:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
43	CTCF	chr5:91225140-91225290	HCPEpiC	choroid plexus:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
44	CTCF	chr5:91359213-91359274	GM10266	blood:	n/a	n/a
45	CTCF	chr5:91225140-91225290	HEEpiC	esophagus:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
46	CTCF	chr5:91225160-91225310	HCFaa	heart:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
47	CTCF	chr5:91225160-91225310	HRE	kidney:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
48	CTCF	chr5:91225141-91225315	Spleen_OC	spleen:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
49	CTCF	chr5:91225140-91225290	AG04449	skin:	n/a	chr5:91225230-91225248 chr5:91225232-91225253
50	CTCF	chr5:91225060-91225210	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:91298666-91298716	HMEC	breast:	n/a
2	chr5:91303031-91303081	BE2_C	brain:	n/a
3	chr5:91303031-91303081	HEK293	kidney:	embryo
4	chr5:91303031-91303081	SKMC	muscle:	n/a
5	chr5:91298666-91298716	HEEpiC	esophagus:	n/a
6	chr5:91303031-91303081	HL-60	blood:	n/a
7	chr5:91303031-91303081	HUVEC	blood vessel:	n/a
8	chr5:91303031-91303081	Hepatocyte	liver:	n/a
9	chr5:91303031-91303081	NT2-D1	testis:	n/a
10	chr5:91303031-91303081	AG09309	skin:	n/a
11	chr5:91303031-91303081	RPTEC	kidney:	n/a
12	chr5:91298666-91298716	Hela-S3	cervix:	n/a
13	chr5:91303031-91303081	GM06990	blood:	n/a
14	chr5:91303031-91303081	AG09319	gingival:	n/a
15	chr5:91303031-91303081	GM12878	blood:	n/a
16	chr5:91298666-91298716	GM12891	blood:	n/a
17	chr5:91298666-91298716	HUVEC	blood vessel:	n/a
18	chr5:91303031-91303081	U87	brain:	n/a
19	chr5:91303031-91303081	A549	lung:	n/a
20	chr5:91303031-91303081	K562	blood:	n/a
21	chr5:91298666-91298716	GM12878	blood:	n/a
22	chr5:91298666-91298716	ovcar-3	ovarian:	n/a
23	chr5:91298666-91298716	LNCaP	prostate:	n/a
24	chr5:91298666-91298716	SAEC	small airway:	n/a
25	chr5:91303031-91303081	HRPEpiC	eye:	n/a
26	chr5:91303031-91303081	GM12891	blood:	n/a
27	chr5:91298666-91298716	HL-60	blood:	n/a
28	chr5:91303031-91303081	IMR90	lung:	fetal
29	chr5:91298666-91298716	HRCEpiC	kidney:	n/a
30	chr5:91303031-91303081	AG10803	skin:	n/a
31	chr5:91298666-91298716	RPTEC	kidney:	n/a
32	chr5:91303031-91303081	AG04449	skin:	fetal
33	chr5:91303031-91303081	HRE	kidney:	n/a
34	chr5:91303031-91303081	GM12892	blood:	n/a
35	chr5:91298666-91298716	HCT-116	colon:	n/a
36	chr5:91303031-91303081	PrEC	prostate:	n/a
37	chr5:91303031-91303081	HRCEpiC	kidney:	n/a
38	chr5:91298666-91298716	SKMC	muscle:	n/a
39	chr5:91303031-91303081	T-47D	breast:	n/a
40	chr5:91303031-91303081	ECC-1	luminal epithelium:	n/a
41	chr5:91303031-91303081	NH-A	brain:	n/a
42	chr5:91298666-91298716	ProgFib	skin:	n/a
43	chr5:91298666-91298716	T-47D	breast:	n/a
44	chr5:91298666-91298716	K562	blood:	n/a
45	chr5:91303031-91303081	HCT-116	colon:	n/a
46	chr5:91298666-91298716	Hepatocyte	liver:	n/a
47	chr5:91303031-91303081	Hela-S3	cervix:	n/a
48	chr5:91298666-91298716	HRPEpiC	eye:	n/a
49	chr5:91303031-91303081	HCM	heart:	n/a
50	chr5:91303031-91303081	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:13765598..13766099-chr5:91346247..91346777,2	MCF-7	breast:
2	chr5:91315876..91316579-chr6:144774937..144775884,2	MCF-7	breast:
3	chr5:91309512..91311831-chr5:91321119..91323779,2	K562	blood:
4	chr5:90141991..90142609-chr5:91326921..91327421,2	MCF-7	breast:
5	chr5:91233124..91235467-chr5:91239612..91241761,2	MCF-7	breast:
6	chr5:91224612..91225895-chr5:91517942..91518899,6	MCF-7	breast:
7	chr5:91233124..91235467-chr5:91239612..91241761,2	MCF-7	breast:
8	chr11:118661976..118663890-chr5:91336617..91338563,2	MCF-7	breast:
9	chr5:91264205..91265908-chr5:91266164..91267839,2	MCF-7	breast:
10	chr5:91309512..91311831-chr5:91321119..91323779,2	K562	blood:
11	chr5:91264205..91265908-chr5:91266164..91267839,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR98-5	chr5:91378414-91378637	XLOC_004470

Variant related genes	Relation type
ENSG00000250049	TF binding region
ENSG00000250049	CpG island
ENSG00000164199	chromatin interactions
ENSG00000101247	chromatin interactions

Extended variants
information (count: 2655 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2655 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188705302	chr5:91213935-91213936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs568558588	chr5:91213938-91213939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537196912	chr5:91213947-91213948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557436073	chr5:91213952-91213953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553642310	chr5:91214006-91214007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112452446	chr5:91214054-91214055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141775340	chr5:91214058-91214059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572043356	chr5:91214060-91214061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556478178	chr5:91214084-91214085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545484746	chr5:91214109-91214110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192543238	chr5:91214116-91214117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560793539	chr5:91214174-91214175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182764171	chr5:91214190-91214191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374003083	chr5:91214235-91214236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543110909	chr5:91214241-91214242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145471962	chr5:91214243-91214244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531984272	chr5:91214309-91214310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199827968	chr5:91214312-91214313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560076157	chr5:91214394-91214395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528837012	chr5:91214415-91214416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548799215	chr5:91214420-91214421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568627809	chr5:91214424-91214425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537665421	chr5:91214461-91214462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550766989	chr5:91214472-91214473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570950296	chr5:91214512-91214513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7724963	chr5:91214519-91214520	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs186667291	chr5:91214522-91214523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6452975	chr5:91214527-91214528	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs534558400	chr5:91214538-91214539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75037601	chr5:91214558-91214559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111853492	chr5:91214562-91214563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544619015	chr5:91214575-91214576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191563451	chr5:91214614-91214615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141790211	chr5:91214615-91214616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561621283	chr5:91214626-91214627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543624963	chr5:91214673-91214674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369831449	chr5:91214698-91214699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563215945	chr5:91214735-91214736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6866907	chr5:91214839-91214840	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs184828022	chr5:91214863-91214864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199859478	chr5:91214894-91214895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373325371	chr5:91214904-91214905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559440116	chr5:91214921-91214922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190577813	chr5:91214957-91214958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs193093487	chr5:91214966-91214967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547180756	chr5:91214994-91214995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548864449	chr5:91215003-91215004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185006676	chr5:91215035-91215036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530988198	chr5:91215079-91215080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551186623	chr5:91215095-91215096	Weak transcription	n/a	n/a	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	18451855	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91211000-91237600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:91215200-91215400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:91215600-91218000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:91217200-91217600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr5:91220200-91221000	Enhancers	Liver	Liver
6	chr5:91220800-91221600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr5:91221600-91224000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr5:91224000-91225600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr5:91224200-91225200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr5:91224200-91225200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr5:91224200-91225200	Enhancers	Muscle Satellite Cultured Cells	--
12	chr5:91224400-91225000	Enhancers	NH-A	brain
13	chr5:91224400-91225000	Enhancers	NHDF-Ad	bronchial
14	chr5:91224400-91225200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr5:91224400-91225200	Enhancers	Osteobl	bone
16	chr5:91224600-91224800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:91224600-91225800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr5:91225000-91226200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr5:91225200-91227400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:91225400-91225600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr5:91225400-91226000	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr5:91227400-91228000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr5:91228000-91232600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:91232400-91234800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:91232600-91235400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr5:91234200-91234600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr5:91234200-91234800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr5:91234200-91234800	Enhancers	Osteobl	bone
29	chr5:91234200-91235000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:91234200-91235000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr5:91234200-91235000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr5:91234400-91234800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr5:91234400-91235000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr5:91234400-91235000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr5:91234400-91235800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr5:91234600-91235600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr5:91234800-91235000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr5:91234800-91236000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr5:91234800-91236000	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr5:91235000-91237200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr5:91235000-91237600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr5:91235600-91236200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr5:91236000-91236200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr5:91236000-91236200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:91236000-91236400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr5:91236200-91237000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:91236200-91237400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr5:91236400-91237400	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr5:91237000-91237800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:91237200-91237800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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