Variant report

Variant	nsv1021139
Chromosome Location	chr5:115036724-115131280
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	chr5:115044384-115044841	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:115074466-115074872	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:115106286-115106387	HepG2	liver:	n/a	n/a
4	ATF1	chr5:115117221-115117224	K562	blood:	n/a	n/a
5	BHLHE40	chr5:115106248-115106424	K562	blood:	n/a	n/a
6	BHLHE40	chr5:115044554-115044948	HepG2	liver:	n/a	n/a
7	CBX3	chr5:115084602-115085146	HCT-116	colon:	n/a	n/a
8	CBX3	chr5:115080299-115080557	K562	blood:	n/a	n/a
9	CBX3	chr5:115080231-115080576	HCT-116	colon:	n/a	n/a
10	CEBPB	chr5:115044258-115044929	HepG2	liver:	n/a	chr5:115044532-115044540
11	CEBPB	chr5:115124158-115124512	A549	lung:	n/a	chr5:115124329-115124342 chr5:115124331-115124340 chr5:115124331-115124340 chr5:115124331-115124340
12	CEBPB	chr5:115071751-115072118	IMR90	lung:	n/a	chr5:115071936-115071945 chr5:115071936-115071945 chr5:115071936-115071945 chr5:115071934-115071947 chr5:115071936-115071945 chr5:115071934-115071945 chr5:115071936-115071947
13	CEBPB	chr5:115044666-115044877	HepG2	liver:	n/a	n/a
14	CEBPB	chr5:115124151-115124492	IMR90	lung:	n/a	chr5:115124329-115124342 chr5:115124331-115124340 chr5:115124331-115124340 chr5:115124331-115124340
15	CEBPB	chr5:115124161-115124505	K562	blood:	n/a	chr5:115124329-115124342 chr5:115124331-115124340 chr5:115124331-115124340 chr5:115124331-115124340
16	CEBPB	chr5:115071513-115072071	H1-hESC	embryonic stem cell:	n/a	chr5:115071936-115071945 chr5:115071936-115071945 chr5:115071936-115071945 chr5:115071934-115071947 chr5:115071936-115071945 chr5:115071934-115071945 chr5:115071699-115071712 chr5:115071936-115071947
17	CEBPB	chr5:115039261-115039549	K562	blood:	n/a	n/a
18	CEBPB	chr5:115044206-115044967	HepG2	liver:	n/a	chr5:115044532-115044540
19	CEBPB	chr5:115071784-115072108	K562	blood:	n/a	chr5:115071936-115071945 chr5:115071936-115071945 chr5:115071936-115071945 chr5:115071934-115071947 chr5:115071936-115071945 chr5:115071934-115071945 chr5:115071936-115071947
20	CEBPB	chr5:115076716-115076915	IMR90	lung:	n/a	chr5:115076866-115076877
21	CEBPB	chr5:115071755-115072105	HepG2	liver:	n/a	chr5:115071936-115071945 chr5:115071936-115071945 chr5:115071936-115071945 chr5:115071934-115071947 chr5:115071936-115071945 chr5:115071934-115071945 chr5:115071936-115071947
22	CEBPB	chr5:115044220-115044439	IMR90	lung:	n/a	n/a
23	CEBPB	chr5:115070812-115071095	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:115124224-115124478	Hela-S3	cervix:	n/a	chr5:115124329-115124342 chr5:115124331-115124340 chr5:115124331-115124340 chr5:115124331-115124340
25	CEBPB	chr5:115044633-115044866	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:115076756-115077007	A549	lung:	n/a	chr5:115076866-115076877
27	CEBPB	chr5:115124153-115124510	HepG2	liver:	n/a	chr5:115124329-115124342 chr5:115124331-115124340 chr5:115124331-115124340 chr5:115124331-115124340
28	CEBPB	chr5:115074865-115074915	HepG2	liver:	n/a	n/a
29	CEBPB	chr5:115039290-115039547	K562	blood:	n/a	n/a
30	CEBPB	chr5:115068240-115068409	HepG2	liver:	n/a	chr5:115068305-115068318 chr5:115068307-115068318 chr5:115068305-115068316
31	CEBPB	chr5:115076720-115076939	HepG2	liver:	n/a	chr5:115076866-115076877
32	CEBPB	chr5:115124169-115124470	H1-hESC	embryonic stem cell:	n/a	chr5:115124329-115124342 chr5:115124331-115124340 chr5:115124331-115124340 chr5:115124331-115124340
33	CEBPB	chr5:115071749-115072083	A549	lung:	n/a	chr5:115071936-115071945 chr5:115071936-115071945 chr5:115071936-115071945 chr5:115071934-115071947 chr5:115071936-115071945 chr5:115071934-115071945 chr5:115071936-115071947
34	CEBPD	chr5:115044652-115044826	HepG2	liver:	n/a	n/a
35	CEBPD	chr5:115044656-115044892	HepG2	liver:	n/a	n/a
36	CHD1	chr5:115072788-115072867	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr5:115106373-115106407	HepG2	liver:	n/a	n/a
38	CTCF	chr5:115106340-115106490	HVMF	connective:	n/a	n/a
39	CTCF	chr5:115103226-115103408	GM12878	blood:	n/a	n/a
40	CTCF	chr5:115106240-115106390	GM12874	blood:	n/a	n/a
41	CTCF	chr5:115106280-115106430	GM06990	blood:	n/a	n/a
42	CTCF	chr5:115106264-115106478	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:115106260-115106410	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:115106300-115106450	GM12864	blood:	n/a	n/a
45	CTCF	chr5:115106280-115106430	GM12864	blood:	n/a	n/a
46	CTCF	chr5:115106182-115106543	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr5:115106340-115106490	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr5:115106300-115106450	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr5:115087793-115087858	GM10248	blood:	n/a	n/a
50	CTCF	chr5:115106300-115106450	Caco-2	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115087169-115087219	HEK293	kidney:	embryo
2	chr5:115087169-115087219	GM19239	blood:	n/a
3	chr5:115087169-115087219	HRE	kidney:	n/a
4	chr5:115087169-115087219	BJ	skin:	n/a
5	chr5:115087169-115087219	HRPEpiC	eye:	n/a
6	chr5:115087169-115087219	PANC-1	pancreas:	n/a
7	chr5:115087169-115087219	HUVEC	blood vessel:	n/a
8	chr5:115087169-115087219	GM12892	blood:	n/a
9	chr5:115087169-115087219	PFSK-1	brain:	n/a
10	chr5:115087169-115087219	AG04450	lung:	fetal
11	chr5:115087169-115087219	SK-N-SH_RA	brain:	n/a
12	chr5:115087169-115087219	HRCEpiC	kidney:	n/a
13	chr5:115087169-115087219	AG04449	skin:	fetal
14	chr5:115087169-115087219	AG10803	skin:	n/a
15	chr5:115087169-115087219	CMK	blood:	n/a
16	chr5:115087169-115087219	HAEpiC	amniotic membrane:	n/a
17	chr5:115087169-115087219	BE2_C	brain:	n/a
18	chr5:115087169-115087219	HCF	heart:	n/a
19	chr5:115087169-115087219	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:115087169-115087219	NB4	blood:	n/a
21	chr5:115087169-115087219	GM06990	blood:	n/a
22	chr5:115087169-115087219	HCT-116	colon:	n/a
23	chr5:115087169-115087219	AG09309	skin:	n/a
24	chr5:115087169-115087219	U87	brain:	n/a
25	chr5:115087169-115087219	RPTEC	kidney:	n/a
26	chr5:115087169-115087219	HMEC	breast:	n/a
27	chr5:115087169-115087219	Hela-S3	cervix:	n/a
28	chr5:115087169-115087219	AoSMC	blood vessel:	n/a
29	chr5:115087169-115087219	PrEC	prostate:	n/a
30	chr5:115087169-115087219	Caco-2	colon:	n/a
31	chr5:115087169-115087219	T-47D	breast:	n/a
32	chr5:115087169-115087219	H1-hESC	embryonic stem cell:	embryo
33	chr5:115087169-115087219	NHBE	bronchial:	n/a
34	chr5:115087169-115087219	Jurkat	blood:	n/a
35	chr5:115087169-115087219	SAEC	small airway:	n/a
36	chr5:115087169-115087219	ProgFib	skin:	n/a
37	chr5:115087169-115087219	GM12878	blood:	n/a
38	chr5:115087169-115087219	MCF10A-Er-Src	breast:	n/a
39	chr5:115087169-115087219	GM12891	blood:	n/a
40	chr5:115087169-115087219	SK-N-MC	brain:	n/a
41	chr5:115087169-115087219	HCPEpiC	choroid plexus:	n/a
42	chr5:115087169-115087219	MCF-7	breast:	n/a
43	chr5:115087169-115087219	NH-A	brain:	n/a
44	chr5:115087169-115087219	A549	lung:	n/a
45	chr5:115087169-115087219	NT2-D1	testis:	n/a
46	chr5:115087169-115087219	HNPCEpiC	eye:	n/a
47	chr5:115087169-115087219	IMR90	lung:	fetal
48	chr5:115087169-115087219	HEEpiC	esophagus:	n/a
49	chr5:115087169-115087219	Hepatocyte	liver:	n/a
50	chr5:115087169-115087219	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:115062310..115063859-chr5:115064887..115067469,2	MCF-7	breast:
2	chr5:115083059..115085192-chr5:115085470..115087199,2	MCF-7	breast:
3	chr5:115083087..115085435-chr5:115086975..115089402,2	K562	blood:
4	chr5:115109021..115111170-chr5:115113297..115115929,2	MCF-7	breast:
5	chr5:115122571..115125137-chr5:115132852..115135417,2	K562	blood:
6	chr5:115039339..115041396-chr5:115050888..115053179,2	K562	blood:
7	chr5:115130205..115131867-chr5:115132318..115134731,2	K562	blood:
8	chr5:115117741..115119948-chr5:115190584..115192982,2	K562	blood:
9	chr5:115069007..115070824-chr5:115175846..115177904,2	K562	blood:
10	chr5:115089796..115091437-chr5:115120054..115122203,2	MCF-7	breast:
11	chr5:115113442..115116376-chr5:115135444..115138235,2	MCF-7	breast:
12	chr5:115083087..115085435-chr5:115086975..115089402,2	K562	blood:
13	chr5:115039339..115041396-chr5:115050888..115053179,2	K562	blood:
14	chr15:86588289..86588860-chr5:115112842..115113676,2	MCF-7	breast:
15	chr5:114970470..114971000-chr5:115106287..115106794,2	MCF-7	breast:
16	chr5:115024245..115026026-chr5:115036571..115038503,2	K562	blood:
17	chr5:115083059..115085192-chr5:115085470..115087199,2	MCF-7	breast:
18	chr5:115062310..115063859-chr5:115064887..115067469,2	MCF-7	breast:
19	chr5:114960202..114961794-chr5:115068533..115071255,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP3S1-2	chr5:115074779-115074811	XLOC_004515
2	lnc-AP3S1-2	chr5:115090392-115093563	NONHSAT103321
3	lnc-CDO1-2	chr5:115102647-115102714	l_2998_chr5:115102646-115120121_liver
4	lnc-AP3S1-7	chr5:115106283-115106686	NONHSAT103323
5	lnc-AP3S1-2	chr5:115091341-115091983	ENSG00000248709
6	lnc-AP3S1-3	chr5:115040462-115040554	NONHSAT103317
7	lnc-AP3S1-2	chr5:115090955-115092222	XLOC_004515
8	lnc-CDO1-2	chr5:115118858-115120121	l_2998_chr5:115102646-115120121_liver
9	lnc-AP3S1-3	chr5:115044263-115044690	XLOC_004514
10	lnc-AP3S1-2	chr5:115074710-115074811	NONHSAT103319
11	lnc-AP3S1-3	chr5:115040462-115040554	FPKM1_group_26169_transcript_1
12	lnc-AP3S1-3	chr5:115040463-115040554	XLOC_004514
13	lnc-AP3S1-2	chr5:115090955-115092939	NONHSAT103319
14	lnc-AP3S1-2	chr5:115091088-115092939	NONHSAT103320
15	lnc-AP3S1-2	chr5:115074710-115074811	NONHSAT103320
16	lnc-AP3S1-3	chr5:115044262-115044690	NONHSAT103317
17	lnc-AP3S1-3	chr5:115040500-115040928	FPKM1_group_26169_transcript_1
18	lnc-AP3S1-2	chr5:115074730-115074811	NONHSAT103321
19	lnc-AP3S1-2	chr5:115094177-115095533	NONHSAT103321
20	lnc-AP3S1-2	chr5:115074782-115074811	XLOC_004515
21	lnc-AP3S1-2	chr5:115091088-115092222	XLOC_004515
22	lnc-AP3S1-2	chr5:115093739-115093903	NONHSAT103321

Variant related genes	Relation type
RNU2-49P	TF binding region
ENSG00000251118	TF binding region
ENSG00000248709	TF binding region
RNU2-49P	CpG island
ENSG00000251118	CpG island
ENSG00000248709	CpG island
ENSG00000248709	chromatin interactions
ENSG00000145782	chromatin interactions
ENSG00000134970	chromatin interactions
ENSG00000222598	chromatin interactions
ENSG00000251201	chromatin interactions
ENSG00000177879	chromatin interactions
MCL1	miRNA target sites

Extended variants
information (count: 3911 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3911 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs466506	chr5:115036724-115036725	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs455226	chr5:115036743-115036744	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574146620	chr5:115036744-115036745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536399187	chr5:115036749-115036750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556448315	chr5:115036763-115036764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576294457	chr5:115036768-115036769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543825999	chr5:115036769-115036770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562986939	chr5:115036837-115036838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577708698	chr5:115036883-115036884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539951430	chr5:115036906-115036907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560146097	chr5:115036955-115036956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562682240	chr5:115036973-115036974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529087901	chr5:115036979-115036980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71612049	chr5:115036983-115036984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549166786	chr5:115036988-115036989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144803195	chr5:115037030-115037031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562795147	chr5:115037045-115037046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147939479	chr5:115037076-115037077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141768283	chr5:115037094-115037095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187070481	chr5:115037123-115037124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534347267	chr5:115037124-115037125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547574950	chr5:115037138-115037139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574547914	chr5:115037148-115037149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567710821	chr5:115037156-115037157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536463234	chr5:115037219-115037220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556309703	chr5:115037220-115037221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576355767	chr5:115037253-115037254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373382759	chr5:115037307-115037308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150316071	chr5:115037310-115037311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527791002	chr5:115037316-115037317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs461393	chr5:115037347-115037348	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs531415155	chr5:115037367-115037368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs459386	chr5:115037388-115037389	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs144948497	chr5:115037412-115037413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191091093	chr5:115037419-115037420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149022145	chr5:115037445-115037446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562659090	chr5:115037478-115037479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200972839	chr5:115037525-115037526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531675466	chr5:115037550-115037551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs458555	chr5:115037555-115037556	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs143048426	chr5:115037569-115037570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182063461	chr5:115037597-115037598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138756245	chr5:115037667-115037668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533938808	chr5:115037671-115037672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140432173	chr5:115037684-115037685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114874228	chr5:115037714-115037715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75784650	chr5:115037719-115037720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187019583	chr5:115037720-115037721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569914039	chr5:115037722-115037723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191864264	chr5:115037726-115037727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115035600-115036800	Enhancers	Liver	Liver
2	chr5:115036800-115041800	Weak transcription	Liver	Liver
3	chr5:115041800-115043200	Enhancers	Liver	Liver
4	chr5:115043200-115044000	Flanking Active TSS	Liver	Liver
5	chr5:115044000-115045200	Enhancers	Liver	Liver
6	chr5:115044400-115046000	Enhancers	HepG2	liver
7	chr5:115044600-115046200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr5:115044600-115046200	Enhancers	Aorta	Aorta
9	chr5:115044800-115046000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr5:115045000-115045600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr5:115045000-115045600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:115045000-115045600	Enhancers	Adipose Nuclei	Adipose
13	chr5:115045200-115045400	Flanking Active TSS	Liver	Liver
14	chr5:115045200-115045800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr5:115045200-115045800	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr5:115045400-115045800	Enhancers	Liver	Liver
17	chr5:115045800-115046200	Flanking Active TSS	Liver	Liver
18	chr5:115046200-115047200	Weak transcription	Aorta	Aorta
19	chr5:115047200-115047800	ZNF genes & repeats	Aorta	Aorta
20	chr5:115047800-115053200	Weak transcription	Aorta	Aorta
21	chr5:115053200-115054000	Enhancers	Aorta	Aorta
22	chr5:115053800-115055600	Enhancers	Fetal Lung	lung
23	chr5:115054000-115056800	Weak transcription	Aorta	Aorta
24	chr5:115054400-115055000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:115054400-115055400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr5:115054600-115055000	Enhancers	Adipose Nuclei	Adipose
27	chr5:115054800-115055000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr5:115055000-115055400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:115055000-115058200	Weak transcription	Adipose Nuclei	Adipose
30	chr5:115055400-115057000	Enhancers	Liver	Liver
31	chr5:115055400-115057200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:115055600-115058800	Weak transcription	Fetal Lung	lung
33	chr5:115056800-115057200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr5:115056800-115059400	Enhancers	Aorta	Aorta
35	chr5:115057000-115058800	Weak transcription	Liver	Liver
36	chr5:115057200-115058000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr5:115057200-115058800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:115058000-115059400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr5:115058000-115060000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr5:115058200-115059200	Enhancers	Adipose Nuclei	Adipose
41	chr5:115058200-115059400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr5:115058200-115059400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr5:115058600-115058800	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr5:115058600-115059200	Enhancers	Fetal Kidney	kidney
45	chr5:115058800-115059200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr5:115058800-115059200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr5:115058800-115059200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:115058800-115059400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:115058800-115059400	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr5:115058800-115059400	Enhancers	Fetal Lung	lung

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