Variant report

Variant	nsv882669
Chromosome Location	chr5:105619741-105936330
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	ATF1	chr5:105859633-105859780	K562	blood:	n/a	n/a
2	BACH1	chr5:105679829-105679900	K562	blood:	n/a	n/a
3	BACH1	chr5:105735164-105735374	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:105656980-105657327	H1-hESC	embryonic stem cell:	n/a	chr5:105657149-105657163
5	BATF	chr5:105889076-105889285	GM12878	blood:	n/a	n/a
6	BATF	chr5:105871246-105871400	GM12878	blood:	n/a	n/a
7	BATF	chr5:105889044-105889346	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:105871234-105871399	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:105889001-105889386	GM12878	blood:	n/a	n/a
10	BCL3	chr5:105735041-105735392	A549	lung:	n/a	chr5:105735250-105735259
11	BCL3	chr5:105735051-105735584	A549	lung:	n/a	chr5:105735250-105735259
12	BHLHE40	chr5:105889035-105889258	HepG2	liver:	n/a	n/a
13	BHLHE40	chr5:105887552-105887806	GM12878	blood:	n/a	n/a
14	BRCA1	chr5:105871319-105871346	GM12878	blood:	n/a	n/a
15	CBX3	chr5:105705555-105705987	HCT-116	colon:	n/a	n/a
16	CBX3	chr5:105733268-105733945	HCT-116	colon:	n/a	n/a
17	CBX3	chr5:105790354-105791158	HCT-116	colon:	n/a	n/a
18	CCNT2	chr5:105664275-105664538	K562	blood:	n/a	n/a
19	CEBPB	chr5:105739618-105740208	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:105814096-105814440	Hela-S3	cervix:	n/a	chr5:105814270-105814281
21	CEBPB	chr5:105799818-105800083	H1-hESC	embryonic stem cell:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
22	CEBPB	chr5:105744771-105744988	HepG2	liver:	n/a	chr5:105744829-105744840 chr5:105744827-105744838
23	CEBPB	chr5:105755825-105756145	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:105813435-105813964	MCF-7	breast:	n/a	chr5:105813644-105813656
25	CEBPB	chr5:105744757-105744935	A549	lung:	n/a	chr5:105744829-105744840 chr5:105744827-105744838
26	CEBPB	chr5:105859114-105859462	IMR90	lung:	n/a	chr5:105859114-105859125 chr5:105859284-105859295
27	CEBPB	chr5:105755852-105756151	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr5:105624755-105625063	IMR90	lung:	n/a	n/a
29	CEBPB	chr5:105814124-105814357	A549	lung:	n/a	chr5:105814270-105814281
30	CEBPB	chr5:105642809-105643093	HepG2	liver:	n/a	chr5:105642947-105642958
31	CEBPB	chr5:105718081-105718347	HepG2	liver:	n/a	chr5:105718203-105718214 chr5:105718205-105718214 chr5:105718160-105718173
32	CEBPB	chr5:105650149-105650481	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:105642777-105643105	A549	lung:	n/a	chr5:105642947-105642958
34	CEBPB	chr5:105683996-105684271	HepG2	liver:	n/a	chr5:105684127-105684138
35	CEBPB	chr5:105893027-105893313	A549	lung:	n/a	chr5:105893187-105893198 chr5:105893189-105893200 chr5:105893187-105893200
36	CEBPB	chr5:105751136-105751473	A549	lung:	n/a	n/a
37	CEBPB	chr5:105755861-105756158	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:105770388-105770650	IMR90	lung:	n/a	chr5:105770535-105770548 chr5:105770535-105770548 chr5:105770534-105770551 chr5:105770536-105770547
39	CEBPB	chr5:105893061-105893350	IMR90	lung:	n/a	chr5:105893187-105893198 chr5:105893189-105893200 chr5:105893187-105893200
40	CEBPB	chr5:105670301-105670553	HepG2	liver:	n/a	chr5:105670470-105670481
41	CEBPB	chr5:105935606-105935875	A549	lung:	n/a	chr5:105935743-105935756 chr5:105935745-105935754
42	CEBPB	chr5:105755845-105756150	K562	blood:	n/a	n/a
43	CEBPB	chr5:105891864-105892159	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:105624716-105625099	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr5:105755813-105756182	IMR90	lung:	n/a	n/a
46	CEBPB	chr5:105702772-105702972	A549	lung:	n/a	chr5:105702877-105702888
47	CEBPB	chr5:105826569-105826777	HepG2	liver:	n/a	chr5:105826713-105826724
48	CEBPB	chr5:105902109-105902237	A549	lung:	n/a	n/a
49	CEBPB	chr5:105857479-105858427	A549	lung:	n/a	chr5:105858325-105858337
50	CEBPB	chr5:105891868-105892016	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:105791135-105791185	ECC-1	luminal epithelium:	n/a
2	chr5:105753028-105753078	PFSK-1	brain:	n/a
3	chr5:105753028-105753078	HNPCEpiC	eye:	n/a
4	chr5:105753028-105753078	AG10803	skin:	n/a
5	chr5:105753028-105753078	ovcar-3	ovarian:	n/a
6	chr5:105791135-105791185	U87	brain:	n/a
7	chr5:105753028-105753078	AG04449	skin:	fetal
8	chr5:105791135-105791185	SAEC	small airway:	n/a
9	chr5:105791135-105791185	T-47D	breast:	n/a
10	chr5:105791135-105791185	A549	lung:	n/a
11	chr5:105753028-105753078	K562	blood:	n/a
12	chr5:105791135-105791185	Caco-2	colon:	n/a
13	chr5:105791135-105791185	SK-N-MC	brain:	n/a
14	chr5:105753028-105753078	HUVEC	blood vessel:	n/a
15	chr5:105753028-105753078	HEK293	kidney:	embryo
16	chr5:105753028-105753078	HCPEpiC	choroid plexus:	n/a
17	chr5:105791135-105791185	SKMC	muscle:	n/a
18	chr5:105791135-105791185	NHBE	bronchial:	n/a
19	chr5:105791135-105791185	Hela-S3	cervix:	n/a
20	chr5:105753028-105753078	A549	lung:	n/a
21	chr5:105753028-105753078	HAEpiC	amniotic membrane:	n/a
22	chr5:105753028-105753078	NH-A	brain:	n/a
23	chr5:105791135-105791185	BE2_C	brain:	n/a
24	chr5:105753028-105753078	LNCaP	prostate:	n/a
25	chr5:105753028-105753078	HEEpiC	esophagus:	n/a
26	chr5:105791135-105791185	NT2-D1	testis:	n/a
27	chr5:105753028-105753078	SK-N-SH	brain:	n/a
28	chr5:105791135-105791185	GM12878	blood:	n/a
29	chr5:105753028-105753078	SK-N-MC	brain:	n/a
30	chr5:105753028-105753078	HL-60	blood:	n/a
31	chr5:105791135-105791185	HMEC	breast:	n/a
32	chr5:105753028-105753078	HPAEpiC	pulmonary alveolar:	n/a
33	chr5:105791135-105791185	HEEpiC	esophagus:	n/a
34	chr5:105791135-105791185	BJ	skin:	n/a
35	chr5:105791135-105791185	PFSK-1	brain:	n/a
36	chr5:105753028-105753078	GM12891	blood:	n/a
37	chr5:105753028-105753078	HRPEpiC	eye:	n/a
38	chr5:105791135-105791185	HL-60	blood:	n/a
39	chr5:105791135-105791185	IMR90	lung:	fetal
40	chr5:105791135-105791185	GM19239	blood:	n/a
41	chr5:105791135-105791185	HEK293	kidney:	embryo
42	chr5:105753028-105753078	GM06990	blood:	n/a
43	chr5:105791135-105791185	Hepatocyte	liver:	n/a
44	chr5:105753028-105753078	HRE	kidney:	n/a
45	chr5:105753028-105753078	GM19239	blood:	n/a
46	chr5:105791135-105791185	AG09319	gingival:	n/a
47	chr5:105753028-105753078	SAEC	small airway:	n/a
48	chr5:105791135-105791185	HepG2	liver:	n/a
49	chr5:105753028-105753078	GM12878	blood:	n/a
50	chr5:105753028-105753078	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:105678713..105680256-chr5:105733390..105735536,2	K562	blood:
2	chr5:105577079..105577725-chr5:105702519..105703290,2	MCF-7	breast:
3	chr5:105620861..105623100-chr5:106539185..106542118,2	MCF-7	breast:
4	chr5:105807775..105809773-chr5:105811667..105814083,2	MCF-7	breast:
5	chr5:105690890..105692893-chr5:105701188..105703588,2	MCF-7	breast:
6	chr5:105907774..105910252-chr5:105911884..105914582,2	K562	blood:
7	chr5:105907051..105910252-chr5:105911452..105914582,3	K562	blood:
8	chr5:105683065..105685836-chr5:105691749..105694214,2	MCF-7	breast:
9	chr5:105907051..105910252-chr5:105911452..105914582,3	K562	blood:
10	chr5:105790013..105791980-chr5:105793268..105795138,2	MCF-7	breast:
11	chr5:105790013..105791980-chr5:105793268..105795138,2	MCF-7	breast:
12	chr5:105907774..105910252-chr5:105911884..105914582,2	K562	blood:
13	chr5:105624522..105627380-chr5:105627786..105629917,2	MCF-7	breast:
14	chr5:105616059..105617713-chr5:105623412..105625878,2	MCF-7	breast:
15	chr5:105624522..105627380-chr5:105627786..105629917,2	MCF-7	breast:
16	chr5:105678713..105680256-chr5:105733390..105735536,2	K562	blood:
17	chr5:105683065..105685836-chr5:105691749..105694214,2	MCF-7	breast:
18	chr5:105775699..105778002-chr5:105784029..105786359,2	MCF-7	breast:
19	chr5:105695067..105695819-chr7:152358250..152358853,2	MCF-7	breast:
20	chr5:105690890..105692893-chr5:105701188..105703588,2	MCF-7	breast:
21	chr5:105807775..105809773-chr5:105811667..105814083,2	MCF-7	breast:
22	chr5:52211080..52211594-chr5:105856085..105856865,2	MCF-7	breast:
23	chr5:105775699..105778002-chr5:105784029..105786359,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000250145	TF binding region
ENSG00000251204	TF binding region
ENSG00000252337	TF binding region
ENSG00000250145	CpG island
ENSG00000251204	CpG island
ENSG00000252337	CpG island

Extended variants
information (count: 4096 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4096 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542146658	chr5:105620202-105620203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs116688231	chr5:105620204-105620205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181567503	chr5:105620212-105620213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114549337	chr5:105620246-105620247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78241416	chr5:105620313-105620314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532501669	chr5:105620326-105620327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575916880	chr5:105620341-105620342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147036424	chr5:105620356-105620357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531846808	chr5:105620367-105620368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75748669	chr5:105620374-105620375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112832349	chr5:105620379-105620380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147679081	chr5:105624404-105624405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371732795	chr5:105624421-105624422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186723246	chr5:105624539-105624540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551919099	chr5:105624546-105624547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192083133	chr5:105624563-105624564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537627375	chr5:105624636-105624637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557315309	chr5:105624642-105624643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs10037741	chr5:105624643-105624644	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs547408883	chr5:105624647-105624648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533711983	chr5:105624756-105624757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546977941	chr5:105624827-105624828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78540705	chr5:105624830-105624831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552893632	chr5:105624857-105624858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77258882	chr5:105624933-105624934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182025226	chr5:105624941-105624942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558207567	chr5:105624966-105624967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565716092	chr5:105624967-105624968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186115686	chr5:105625126-105625127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544384826	chr5:105625145-105625146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560972486	chr5:105625173-105625174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7732235	chr5:105625193-105625194	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs540163591	chr5:105625263-105625264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559747049	chr5:105625316-105625317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528515196	chr5:105625382-105625383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551835173	chr5:105625389-105625390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190966041	chr5:105625475-105625476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531076949	chr5:105625484-105625485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376637627	chr5:105625485-105625486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551109946	chr5:105625486-105625487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567773874	chr5:105625503-105625504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536916943	chr5:105625519-105625520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116042852	chr5:105625531-105625532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566854091	chr5:105625541-105625542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538230629	chr5:105625554-105625555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576094500	chr5:105625563-105625564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558170717	chr5:105625568-105625569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574991774	chr5:105625646-105625647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537547033	chr5:105625647-105625648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567835768	chr5:105625650-105625651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
Retinoblastoma	22278416	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
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:105620200-105620400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:105624400-105625600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:105624600-105625400	Enhancers	Hela-S3	cervix
4	chr5:105624800-105625400	Enhancers	Osteobl	bone
5	chr5:105625000-105625600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr5:105625400-105625800	Weak transcription	Osteobl	bone
7	chr5:105625400-105626400	Weak transcription	Hela-S3	cervix
8	chr5:105625600-105626000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:105625600-105626000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr5:105625800-105626600	Enhancers	Osteobl	bone
11	chr5:105626000-105627400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr5:105626000-105629400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:105626200-105626600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr5:105626400-105626600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:105626400-105626800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr5:105626400-105626800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr5:105626400-105626800	Enhancers	Hela-S3	cervix
18	chr5:105626600-105628000	Weak transcription	Osteobl	bone
19	chr5:105626600-105629600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:105626800-105628000	Weak transcription	Hela-S3	cervix
21	chr5:105626800-105628600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:105627400-105627800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr5:105627800-105629600	Enhancers	Muscle Satellite Cultured Cells	--
24	chr5:105628000-105629400	Enhancers	Osteobl	bone
25	chr5:105628400-105628600	Enhancers	Hela-S3	cervix
26	chr5:105628600-105631600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr5:105629600-105631400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr5:105630000-105630400	Enhancers	H9 Cell Line	embryonic stem cell
29	chr5:105630000-105630400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr5:105630000-105630600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr5:105630000-105630600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr5:105630000-105630800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr5:105630200-105630600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr5:105639000-105639600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr5:105639200-105639600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:105639600-105639800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr5:105639600-105640200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr5:105639800-105640000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr5:105639800-105640000	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr5:105639800-105640000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr5:105640000-105640200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr5:105640000-105640200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr5:105640000-105640200	Enhancers	Osteobl	bone
44	chr5:105640000-105641200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr5:105640000-105641400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr5:105640200-105641200	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:105641200-105643200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr5:105641200-105643800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr5:105641400-105643400	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr5:105641600-105642000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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