Variant report

Variant	nsv882502
Chromosome Location	chr5:101291960-101392473
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	chr5:101338849-101338931	K562	blood:	n/a	n/a
2	ATF3	chr5:101384616-101385017	HCT-116	colon:	n/a	n/a
3	BHLHE40	chr5:101313640-101313757	GM12878	blood:	n/a	n/a
4	CEBPB	chr5:101368294-101368640	HepG2	liver:	n/a	chr5:101368460-101368473 chr5:101368460-101368471 chr5:101368460-101368473 chr5:101368462-101368473
5	CEBPB	chr5:101342030-101342234	A549	lung:	n/a	chr5:101342206-101342219
6	CEBPB	chr5:101384625-101384967	IMR90	lung:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
7	CEBPB	chr5:101385196-101385613	HCT-116	colon:	n/a	n/a
8	CEBPB	chr5:101307371-101307487	A549	lung:	n/a	chr5:101307466-101307477
9	CEBPB	chr5:101343099-101343242	A549	lung:	n/a	n/a
10	CEBPB	chr5:101384705-101384969	MCF-7	breast:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
11	CEBPB	chr5:101368316-101368637	A549	lung:	n/a	chr5:101368460-101368473 chr5:101368460-101368471 chr5:101368460-101368473 chr5:101368462-101368473
12	CEBPB	chr5:101384640-101384936	A549	lung:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
13	CEBPB	chr5:101385222-101385558	MCF-7	breast:	n/a	n/a
14	CEBPB	chr5:101384546-101385005	HCT-116	colon:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
15	CEBPB	chr5:101385370-101385528	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr5:101384613-101384975	HepG2	liver:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
17	CEBPB	chr5:101368296-101368559	MCF-7	breast:	n/a	chr5:101368460-101368473 chr5:101368460-101368471 chr5:101368460-101368473 chr5:101368462-101368473
18	CEBPB	chr5:101384643-101384986	ECC-1	luminal epithelium:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
19	CEBPB	chr5:101385277-101385561	HepG2	liver:	n/a	n/a
20	CEBPB	chr5:101368319-101368603	Hela-S3	cervix:	n/a	chr5:101368460-101368473 chr5:101368460-101368471 chr5:101368460-101368473 chr5:101368462-101368473
21	CEBPB	chr5:101384652-101384939	K562	blood:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
22	CEBPB	chr5:101373464-101373634	HepG2	liver:	n/a	chr5:101373550-101373561
23	CEBPB	chr5:101307299-101307533	HepG2	liver:	n/a	chr5:101307466-101307477
24	CEBPB	chr5:101384635-101384970	H1-hESC	embryonic stem cell:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
25	CEBPB	chr5:101384642-101384977	Hela-S3	cervix:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
26	CEBPB	chr5:101336311-101336608	HepG2	liver:	n/a	chr5:101336472-101336483
27	CEBPB	chr5:101368447-101368563	H1-hESC	embryonic stem cell:	n/a	chr5:101368460-101368473 chr5:101368460-101368471 chr5:101368460-101368473 chr5:101368462-101368473
28	CEBPB	chr5:101373342-101373696	Hela-S3	cervix:	n/a	chr5:101373550-101373561
29	CEBPB	chr5:101368313-101368639	IMR90	lung:	n/a	chr5:101368460-101368473 chr5:101368460-101368471 chr5:101368460-101368473 chr5:101368462-101368473
30	CEBPB	chr5:101310922-101310941	A549	lung:	n/a	n/a
31	CEBPB	chr5:101384615-101384959	ECC-1	luminal epithelium:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
32	CEBPB	chr5:101336317-101336589	A549	lung:	n/a	chr5:101336472-101336483
33	CEBPB	chr5:101323591-101323733	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr5:101384563-101385024	HCT-116	colon:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
35	CEBPB	chr5:101331266-101331761	MCF-7	breast:	n/a	n/a
36	CTCF	chr5:101313575-101313724	Kidney_OC	kidney:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
37	CTCF	chr5:101313489-101313748	HepG2	liver:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
38	CTCF	chr5:101313560-101313710	HCPEpiC	choroid plexus:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
39	CTCF	chr5:101313580-101313730	NHDF-neo	bronchial:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
40	CTCF	chr5:101313538-101313765	GM13977	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
41	CTCF	chr5:101313560-101313710	AG10803	skin:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
42	CTCF	chr5:101313552-101313752	Lung_OC	lung:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
43	CTCF	chr5:101313560-101313710	GM12878	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
44	CTCF	chr5:101313532-101313736	MCF-7	breast:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
45	CTCF	chr5:101313560-101313710	HUVEC	blood vessel:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
46	CTCF	chr5:101313560-101313710	HMF	breast:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
47	CTCF	chr5:101313560-101313710	AG04449	skin:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
48	CTCF	chr5:101313520-101313670	HVMF	connective:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
49	CTCF	chr5:101313620-101313770	GM12875	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
50	CTCF	chr5:101313620-101313770	NHEK	skin:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:101297137-101297187	Hela-S3	cervix:	n/a
2	chr5:101297174-101297224	HUVEC	blood vessel:	n/a
3	chr5:101297137-101297187	HMEC	breast:	n/a
4	chr5:101297174-101297224	HL-60	blood:	n/a
5	chr5:101297174-101297224	Hepatocyte	liver:	n/a
6	chr5:101297174-101297224	GM06990	blood:	n/a
7	chr5:101297174-101297224	HCF	heart:	n/a
8	chr5:101297174-101297224	HNPCEpiC	eye:	n/a
9	chr5:101297174-101297224	IMR90	lung:	fetal
10	chr5:101297137-101297187	A549	lung:	n/a
11	chr5:101297174-101297224	ProgFib	skin:	n/a
12	chr5:101297174-101297224	ovcar-3	ovarian:	n/a
13	chr5:101297137-101297187	SK-N-SH_RA	brain:	n/a
14	chr5:101297137-101297187	PANC-1	pancreas:	n/a
15	chr5:101297174-101297224	Jurkat	blood:	n/a
16	chr5:101297137-101297187	U87	brain:	n/a
17	chr5:101297137-101297187	Jurkat	blood:	n/a
18	chr5:101297137-101297187	K562	blood:	n/a
19	chr5:101297137-101297187	NT2-D1	testis:	n/a
20	chr5:101297137-101297187	HRCEpiC	kidney:	n/a
21	chr5:101297137-101297187	MCF-7	breast:	n/a
22	chr5:101297137-101297187	HCM	heart:	n/a
23	chr5:101297137-101297187	GM19239	blood:	n/a
24	chr5:101297137-101297187	T-47D	breast:	n/a
25	chr5:101297137-101297187	ECC-1	luminal epithelium:	n/a
26	chr5:101297174-101297224	SKMC	muscle:	n/a
27	chr5:101297137-101297187	HAEpiC	amniotic membrane:	n/a
28	chr5:101297174-101297224	K562	blood:	n/a
29	chr5:101297137-101297187	LNCaP	prostate:	n/a
30	chr5:101297174-101297224	MCF10A-Er-Src	breast:	n/a
31	chr5:101297137-101297187	MCF10A-Er-Src	breast:	n/a
32	chr5:101297174-101297224	AG10803	skin:	n/a
33	chr5:101297137-101297187	HRPEpiC	eye:	n/a
34	chr5:101297174-101297224	HCPEpiC	choroid plexus:	n/a
35	chr5:101297137-101297187	SK-N-MC	brain:	n/a
36	chr5:101297137-101297187	HIPEpiC	eye:	n/a
37	chr5:101297137-101297187	Caco-2	colon:	n/a
38	chr5:101297137-101297187	HL-60	blood:	n/a
39	chr5:101297174-101297224	Hela-S3	cervix:	n/a
40	chr5:101297137-101297187	NB4	blood:	n/a
41	chr5:101297137-101297187	SAEC	small airway:	n/a
42	chr5:101297174-101297224	NH-A	brain:	n/a
43	chr5:101297174-101297224	ECC-1	luminal epithelium:	n/a
44	chr5:101297174-101297224	LNCaP	prostate:	n/a
45	chr5:101297137-101297187	HEK293	kidney:	embryo
46	chr5:101297174-101297224	BJ	skin:	n/a
47	chr5:101297174-101297224	NHBE	bronchial:	n/a
48	chr5:101297137-101297187	RPTEC	kidney:	n/a
49	chr5:101297174-101297224	HRE	kidney:	n/a
50	chr5:101297174-101297224	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:101312840..101313801-chr5:101426237..101427126,3	MCF-7	breast:
2	chr5:101341869..101344693-chr5:101345059..101347272,2	MCF-7	breast:
3	chr5:101326987..101328842-chr5:101335717..101338180,2	MCF-7	breast:
4	chr5:101361879..101363839-chr5:101365059..101366576,2	MCF-7	breast:
5	chr17:27716905..27717691-chr5:101351042..101351795,2	MCF-7	breast:
6	chr5:101326987..101328842-chr5:101335717..101338180,2	MCF-7	breast:
7	chr5:101341869..101344693-chr5:101345059..101347272,2	MCF-7	breast:
8	chr5:101361879..101363839-chr5:101365059..101366576,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAM-8	chr5:101312000-101312502	NONHSAT103019

Variant related genes	Relation type
ENSG00000249495	TF binding region
ENSG00000249495	CpG island
ENSG00000160551	chromatin interactions
ENSG00000263719	chromatin interactions

Extended variants
information (count: 1262 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1262 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6870397	chr5:101291960-101291961	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576575427	chr5:101291972-101291973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537540312	chr5:101291983-101291984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185131539	chr5:101291985-101291986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555954491	chr5:101292022-101292023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs6874565	chr5:101292035-101292036	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs542828551	chr5:101292037-101292038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544927008	chr5:101292059-101292060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543855584	chr5:101292117-101292118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145586743	chr5:101292120-101292121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573562689	chr5:101292143-101292144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148875573	chr5:101292144-101292145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565277011	chr5:101292273-101292274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532507426	chr5:101292312-101292313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374980926	chr5:101292313-101292314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551056495	chr5:101292345-101292346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189939635	chr5:101292349-101292350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529285022	chr5:101300800-101300801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6886984	chr5:101300824-101300825	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs368870282	chr5:101300891-101300892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566091747	chr5:101300914-101300915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539916267	chr5:101300917-101300918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184376924	chr5:101300972-101300973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562529150	chr5:101301010-101301011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551535434	chr5:101301011-101301012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569851369	chr5:101301012-101301013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371298527	chr5:101301056-101301057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537207411	chr5:101301084-101301085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189989161	chr5:101301102-101301103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35435657	chr5:101301130-101301131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34937259	chr5:101301142-101301143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192851554	chr5:101301170-101301171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144543429	chr5:101301191-101301192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10688189	chr5:101301192-101301193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs67106500	chr5:101301193-101301194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10655237	chr5:101301194-101301195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184831484	chr5:101301221-101301222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116281864	chr5:101301240-101301241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552924313	chr5:101301267-101301268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149871651	chr5:101301293-101301294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545092095	chr5:101301301-101301302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563209753	chr5:101301317-101301318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115147193	chr5:101301359-101301360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563511721	chr5:101301395-101301396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs899045	chr5:101301416-101301417	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs76372458	chr5:101301419-101301420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78305184	chr5:101301429-101301430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540899531	chr5:101301442-101301443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144950405	chr5:101301470-101301471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550805256	chr5:101301484-101301485	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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	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
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
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	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
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:101289800-101292000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr5:101291200-101292400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr5:101291400-101292200	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr5:101291400-101292200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr5:101291800-101292200	Enhancers	Fetal Stomach	stomach
6	chr5:101292000-101292400	Enhancers	Primary hematopoietic stem cells	blood
7	chr5:101300800-101303000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr5:101302000-101302800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:101302200-101302600	Enhancers	Brain Germinal Matrix	brain
10	chr5:101302200-101302800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:101302400-101302800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr5:101303000-101305400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr5:101305000-101306000	Enhancers	HepG2	liver
14	chr5:101305400-101305600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr5:101305600-101306000	Enhancers	Liver	Liver
16	chr5:101305600-101306000	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr5:101305600-101306000	Enhancers	Fetal Lung	lung
18	chr5:101306400-101306800	Enhancers	Fetal Stomach	stomach
19	chr5:101313000-101313600	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr5:101313200-101313600	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr5:101313200-101313600	Enhancers	Brain Germinal Matrix	brain
22	chr5:101313200-101314000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:101315400-101316000	Enhancers	Stomach Mucosa	stomach
24	chr5:101316000-101317000	Weak transcription	Stomach Mucosa	stomach
25	chr5:101317000-101317200	Enhancers	Stomach Mucosa	stomach
26	chr5:101325600-101325800	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr5:101325800-101329000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr5:101329000-101331000	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr5:101329800-101332800	Enhancers	Fetal Intestine Small	intestine
30	chr5:101330000-101331000	Enhancers	Fetal Intestine Large	intestine
31	chr5:101330800-101331000	Enhancers	Psoas Muscle	Psoas
32	chr5:101330800-101331200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:101330800-101331400	Enhancers	H9 Cell Line	embryonic stem cell
34	chr5:101330800-101331600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr5:101330800-101333200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr5:101331000-101331200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
37	chr5:101331000-101332600	Weak transcription	Psoas Muscle	Psoas
38	chr5:101331200-101331600	Active TSS	Rectal Mucosa Donor 31	rectum
39	chr5:101331200-101331800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr5:101331400-101332200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:101331400-101332600	Enhancers	Placenta Amnion	Placenta Amnion
42	chr5:101331600-101331800	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr5:101332600-101332800	Active TSS	Psoas Muscle	Psoas
44	chr5:101343400-101344800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr5:101343600-101344600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:101354000-101354800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr5:101354000-101355000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr5:101354200-101354400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr5:101354200-101354800	Enhancers	H1 Cell Line	embryonic stem cell
50	chr5:101354200-101354800	Enhancers	HUES48 Cell Line	embryonic stem cell

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