Variant report

Variant	nsv432816
Chromosome Location	chr5:151691807-151875807
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	chr5:151867383-151867411	K562	blood:	n/a	n/a
2	ATF2	chr5:151817422-151817834	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:151860289-151860679	GM12878	blood:	n/a	n/a
4	ATF2	chr5:151860311-151860628	GM12878	blood:	n/a	n/a
5	ATF2	chr5:151836282-151836747	GM12878	blood:	n/a	n/a
6	BATF	chr5:151841937-151842242	GM12878	blood:	n/a	n/a
7	BATF	chr5:151836357-151836618	GM12878	blood:	n/a	n/a
8	BATF	chr5:151860286-151860606	GM12878	blood:	n/a	n/a
9	BATF	chr5:151860290-151860648	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:151860405-151860588	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:151860293-151860693	GM12878	blood:	n/a	n/a
12	CEBPB	chr5:151870955-151871156	IMR90	lung:	n/a	n/a
13	CEBPB	chr5:151692312-151692554	A549	lung:	n/a	chr5:151692462-151692473
14	CEBPB	chr5:151692351-151692580	K562	blood:	n/a	chr5:151692462-151692473
15	CEBPB	chr5:151710738-151710958	HepG2	liver:	n/a	chr5:151710812-151710823 chr5:151710836-151710847 chr5:151710812-151710825 chr5:151710813-151710824
16	CEBPB	chr5:151710559-151710979	MCF-7	breast:	n/a	chr5:151710812-151710823 chr5:151710836-151710847 chr5:151710812-151710825 chr5:151710813-151710824
17	CEBPB	chr5:151790205-151790488	MCF-7	breast:	n/a	chr5:151790304-151790315
18	CEBPB	chr5:151874107-151874130	A549	lung:	n/a	n/a
19	CEBPB	chr5:151790214-151790414	A549	lung:	n/a	chr5:151790304-151790315
20	CEBPB	chr5:151784381-151784411	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:151692299-151692632	HepG2	liver:	n/a	chr5:151692462-151692473
22	CEBPB	chr5:151871004-151871049	HepG2	liver:	n/a	n/a
23	CEBPB	chr5:151739257-151739339	HepG2	liver:	n/a	chr5:151739294-151739305
24	CEBPB	chr5:151851029-151851346	HepG2	liver:	n/a	chr5:151851034-151851047 chr5:151851209-151851222 chr5:151851210-151851221
25	CEBPB	chr5:151836895-151836919	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr5:151790171-151790461	HepG2	liver:	n/a	chr5:151790304-151790315
27	CEBPB	chr5:151692383-151692585	H1-hESC	embryonic stem cell:	n/a	chr5:151692462-151692473
28	CEBPB	chr5:151710621-151711067	MCF-7	breast:	n/a	chr5:151710812-151710823 chr5:151710836-151710847 chr5:151710812-151710825 chr5:151710813-151710824
29	CEBPB	chr5:151836740-151836934	A549	lung:	n/a	n/a
30	CEBPB	chr5:151692330-151692632	IMR90	lung:	n/a	chr5:151692462-151692473
31	CEBPB	chr5:151710669-151711025	A549	lung:	n/a	chr5:151710812-151710823 chr5:151710836-151710847 chr5:151710812-151710825 chr5:151710813-151710824
32	CEBPB	chr5:151710810-151710915	IMR90	lung:	n/a	chr5:151710812-151710823 chr5:151710836-151710847 chr5:151710812-151710825 chr5:151710813-151710824
33	CEBPB	chr5:151710662-151710991	A549	lung:	n/a	chr5:151710812-151710823 chr5:151710836-151710847 chr5:151710812-151710825 chr5:151710813-151710824
34	CEBPB	chr5:151766402-151766556	HepG2	liver:	n/a	chr5:151766469-151766480
35	CHD2	chr5:151777297-151777397	GM12878	blood:	n/a	n/a
36	CREB1	chr5:151865966-151866431	GM12878	blood:	n/a	n/a
37	CREB1	chr5:151836348-151837007	GM12878	blood:	n/a	n/a
38	CREB1	chr5:151860387-151860744	GM12878	blood:	n/a	n/a
39	CTCF	chr5:151729285-151729568	GM12878	blood:	n/a	chr5:151729403-151729424 chr5:151729408-151729426 chr5:151729409-151729425 chr5:151729414-151729423
40	CTCF	chr5:151729145-151729708	MCF-7	breast:	n/a	chr5:151729403-151729424 chr5:151729408-151729426 chr5:151729409-151729425 chr5:151729414-151729423
41	CTCF	chr5:151841751-151842039	A549	lung:	n/a	n/a
42	CTCF	chr5:151729312-151729546	SK-N-SH_RA	brain:	n/a	chr5:151729403-151729424 chr5:151729408-151729426 chr5:151729409-151729425 chr5:151729414-151729423
43	CTCF	chr5:151729120-151729207	GM12891	blood:	n/a	n/a
44	CTCF	chr5:151729216-151729629	GM12878	blood:	n/a	chr5:151729403-151729424 chr5:151729408-151729426 chr5:151729409-151729425 chr5:151729414-151729423
45	CTCF	chr5:151729360-151729510	HMF	breast:	n/a	chr5:151729403-151729424 chr5:151729408-151729426 chr5:151729409-151729425 chr5:151729414-151729423
46	CTCF	chr5:151729360-151729510	GM12864	blood:	n/a	chr5:151729403-151729424 chr5:151729408-151729426 chr5:151729409-151729425 chr5:151729414-151729423
47	CTCF	chr5:151841860-151842010	AG10803	skin:	n/a	n/a
48	CTCF	chr5:151842140-151842290	GM12872	blood:	n/a	n/a
49	CTCF	chr5:151729298-151729565	NHEK	skin:	n/a	chr5:151729403-151729424 chr5:151729408-151729426 chr5:151729409-151729425 chr5:151729414-151729423
50	CTCF	chr5:151804157-151804199	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:151785301-151785351	HEK293	kidney:	embryo
2	chr5:151785301-151785351	HEK293	kidney:	embryo
3	chr5:151784251-151784301	T-47D	breast:	n/a
4	chr5:151771606-151771656	GM12878	blood:	n/a
5	chr5:151784441-151784491	PrEC	prostate:	n/a
6	chr5:151785301-151785351	HCM	heart:	n/a
7	chr5:151785326-151785376	AG09319	gingival:	n/a
8	chr5:151785046-151785096	SK-N-SH_RA	brain:	n/a
9	chr5:151771606-151771656	HepG2	liver:	n/a
10	chr5:151784251-151784301	Jurkat	blood:	n/a
11	chr5:151784251-151784301	NH-A	brain:	n/a
12	chr5:151771606-151771656	RPTEC	kidney:	n/a
13	chr5:151774043-151774093	SK-N-SH_RA	brain:	n/a
14	chr5:151785326-151785376	SAEC	small airway:	n/a
15	chr5:151774043-151774093	ECC-1	luminal epithelium:	n/a
16	chr5:151785301-151785351	HPAEpiC	pulmonary alveolar:	n/a
17	chr5:151784326-151784376	SKMC	muscle:	n/a
18	chr5:151784251-151784301	Hepatocyte	liver:	n/a
19	chr5:151785046-151785096	IMR90	lung:	fetal
20	chr5:151784441-151784491	AG10803	skin:	n/a
21	chr5:151784326-151784376	AoSMC	blood vessel:	n/a
22	chr5:151785301-151785351	HepG2	liver:	n/a
23	chr5:151784441-151784491	HRCEpiC	kidney:	n/a
24	chr5:151774043-151774093	IMR90	lung:	fetal
25	chr5:151784326-151784376	AG09319	gingival:	n/a
26	chr5:151785046-151785096	HEK293	kidney:	embryo
27	chr5:151784326-151784376	HL-60	blood:	n/a
28	chr5:151785046-151785096	HCF	heart:	n/a
29	chr5:151785301-151785351	HUVEC	blood vessel:	n/a
30	chr5:151771606-151771656	SKMC	muscle:	n/a
31	chr5:151774043-151774093	U87	brain:	n/a
32	chr5:151774043-151774093	PFSK-1	brain:	n/a
33	chr5:151785046-151785096	GM12892	blood:	n/a
34	chr5:151785301-151785351	GM12891	blood:	n/a
35	chr5:151785301-151785351	HAEpiC	amniotic membrane:	n/a
36	chr5:151771606-151771656	SAEC	small airway:	n/a
37	chr5:151771606-151771656	U87	brain:	n/a
38	chr5:151771606-151771656	SK-N-MC	brain:	n/a
39	chr5:151771606-151771656	HUVEC	blood vessel:	n/a
40	chr5:151774043-151774093	MCF-7	breast:	n/a
41	chr5:151784441-151784491	SAEC	small airway:	n/a
42	chr5:151784326-151784376	GM06990	blood:	n/a
43	chr5:151774043-151774093	HRCEpiC	kidney:	n/a
44	chr5:151784441-151784491	A549	lung:	n/a
45	chr5:151785326-151785376	NB4	blood:	n/a
46	chr5:151784326-151784376	BJ	skin:	n/a
47	chr5:151785301-151785351	HRCEpiC	kidney:	n/a
48	chr5:151785046-151785096	AG09319	gingival:	n/a
49	chr5:151784441-151784491	HEK293	kidney:	embryo
50	chr5:151784441-151784491	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:151712934..151714874-chr5:151715943..151718623,2	MCF-7	breast:
2	chr5:151779839..151782578-chr5:151794544..151796062,2	K562	blood:
3	chr5:151811992..151815220-chr5:151816698..151819608,3	K562	blood:
4	chr5:151732642..151735217-chr5:151736155..151738969,2	K562	blood:
5	chr5:151732642..151735217-chr5:151736155..151738969,2	K562	blood:
6	chr5:151677422..151680418-chr5:151713174..151715118,2	MCF-7	breast:
7	chr5:151712934..151714874-chr5:151715943..151718623,2	MCF-7	breast:
8	chr5:75032759..75033454-chr5:151772671..151773601,2	HCT-116	colon:
9	chr5:151522014..151522696-chr5:151729134..151730175,3	MCF-7	breast:
10	chr5:151758708..151759606-chr5:151884751..151885744,6	MCF-7	breast:
11	chr5:151758495..151759365-chr5:151885022..151886235,3	MCF-7	breast:
12	chr5:151784366..151785986-chr5:151789259..151790973,2	K562	blood:
13	chr5:151204608..151205517-chr5:151728966..151729819,3	MCF-7	breast:
14	chr5:151800546..151802374-chr5:151805983..151807538,2	MCF-7	breast:
15	chr5:151812372..151815220-chr5:151816698..151819117,2	K562	blood:
16	chr5:151779839..151782578-chr5:151794544..151796062,2	K562	blood:
17	chr5:151779366..151781044-chr5:151783263..151784808,2	MCF-7	breast:
18	chr5:151728938..151729896-chr5:151885133..151885910,3	MCF-7	breast:
19	chr5:151800546..151802374-chr5:151805983..151807538,2	MCF-7	breast:
20	chr5:151779366..151781044-chr5:151783263..151784808,2	MCF-7	breast:
21	chr5:151650666..151651425-chr5:151728944..151730018,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMUR2-3	chr5:151875279-151875578	NONHSAT104653

Variant related genes	Relation type
NMUR2	TF binding region
ENSG00000242080	TF binding region
NMUR2	CpG island
ENSG00000242080	CpG island
ENSG00000132911	chromatin interactions

Extended variants
information (count: 4424 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4424 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549241013	chr5:151691825-151691826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs577598457	chr5:151691833-151691834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116109914	chr5:151691854-151691855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563638907	chr5:151691855-151691856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73279045	chr5:151691856-151691857	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs542414408	chr5:151691884-151691885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560706184	chr5:151691925-151691926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529361725	chr5:151691937-151691938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145273628	chr5:151691963-151691964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559571393	chr5:151691965-151691966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533397633	chr5:151691986-151691987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76540439	chr5:151691994-151691995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs151013236	chr5:151692021-151692022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537701237	chr5:151692026-151692027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549615226	chr5:151692051-151692052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73796880	chr5:151692054-151692055	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs183220128	chr5:151692062-151692063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553069475	chr5:151692064-151692065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73796881	chr5:151692066-151692067	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs73796882	chr5:151692081-151692082	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs4958527	chr5:151692097-151692098	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs575182770	chr5:151692103-151692104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140441837	chr5:151692124-151692125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560768849	chr5:151692128-151692129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116804638	chr5:151692162-151692163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540038058	chr5:151692164-151692165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540832584	chr5:151692175-151692176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559845125	chr5:151692206-151692207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150415192	chr5:151692253-151692254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73796884	chr5:151692261-151692262	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs372434771	chr5:151692282-151692283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187934378	chr5:151692330-151692331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577851703	chr5:151692337-151692338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545003131	chr5:151692348-151692349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542599291	chr5:151692351-151692352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551762507	chr5:151692374-151692375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138201150	chr5:151692393-151692394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563163747	chr5:151692401-151692402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73796885	chr5:151692403-151692404	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549727272	chr5:151692421-151692422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535196450	chr5:151692488-151692489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567947015	chr5:151692490-151692491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs73796886	chr5:151692546-151692547	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs141316162	chr5:151692573-151692574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571319117	chr5:151692575-151692576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540303091	chr5:151692592-151692593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538312989	chr5:151692647-151692648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549132471	chr5:151692721-151692722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs72806368	chr5:151692742-151692743	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs574864373	chr5:151692747-151692748	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	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
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Hyperekplexia	16941485	CNVD
Myelofibrosis	22110671	CNVD
Crohn''s disease	20877625	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
Crohn''s disease	20106866	CNVD
Breast cancer	20409316	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151690400-151692800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:151691400-151692800	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr5:151691800-151692400	Enhancers	Fetal Lung	lung
4	chr5:151692000-151692200	Enhancers	Gastric	stomach
5	chr5:151692000-151692200	Enhancers	Stomach Mucosa	stomach
6	chr5:151693000-151693200	Enhancers	Gastric	stomach
7	chr5:151694000-151694400	Enhancers	HSMM	muscle
8	chr5:151694400-151694600	Enhancers	Gastric	stomach
9	chr5:151708400-151708600	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr5:151709200-151715200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr5:151709400-151709600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:151709400-151709800	Enhancers	Gastric	stomach
13	chr5:151709400-151712800	Enhancers	Adipose Nuclei	Adipose
14	chr5:151709600-151709800	Enhancers	Right Ventricle	heart
15	chr5:151709800-151711800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr5:151710000-151711600	Enhancers	Stomach Mucosa	stomach
17	chr5:151710200-151712800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:151710400-151710600	Enhancers	Right Ventricle	heart
19	chr5:151711600-151711800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr5:151711600-151711800	Enhancers	Gastric	stomach
21	chr5:151711600-151712200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr5:151711800-151712000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:151712600-151712800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr5:151714600-151715200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr5:151714600-151716000	Enhancers	Brain Cingulate Gyrus	brain
26	chr5:151714600-151716000	Enhancers	Brain Hippocampus Middle	brain
27	chr5:151714800-151716600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr5:151715400-151715800	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr5:151715400-151716000	Enhancers	Brain Anterior Caudate	brain
30	chr5:151715600-151716000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr5:151725400-151725600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr5:151725400-151725600	Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr5:151725400-151725800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
34	chr5:151725600-151725800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr5:151725600-151725800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr5:151725600-151725800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr5:151725800-151726000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr5:151725800-151726000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr5:151725800-151726200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
40	chr5:151727600-151727800	Enhancers	Fetal Lung	lung
41	chr5:151728000-151729000	Weak transcription	Fetal Lung	lung
42	chr5:151728800-151731200	Enhancers	Stomach Mucosa	stomach
43	chr5:151729000-151730200	Enhancers	Fetal Stomach	stomach
44	chr5:151729000-151730400	Enhancers	Fetal Lung	lung
45	chr5:151729600-151730000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr5:151729600-151730000	Enhancers	HepG2	liver
47	chr5:151729600-151730200	Enhancers	Fetal Heart	heart
48	chr5:151729600-151730200	Enhancers	Fetal Intestine Large	intestine
49	chr5:151729600-151730400	Enhancers	Left Ventricle	heart
50	chr5:151729600-151730400	Enhancers	Pancreas	Pancrea

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