Variant report

Variant	nsv4706
Chromosome Location	chr5:7917701-7956246
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	chr5:7927953-7928244	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:7927926-7928261	K562	blood:	n/a	n/a
3	ATF3	chr5:7927466-7927598	K562	blood:	n/a	n/a
4	BHLHE40	chr5:7918663-7918695	GM12878	blood:	n/a	n/a
5	BRCA1	chr5:7927938-7928252	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:7917491-7917819	K562	blood:	n/a	chr5:7917640-7917651
7	CEBPB	chr5:7917466-7917815	HepG2	liver:	n/a	chr5:7917640-7917651
8	CEBPB	chr5:7917463-7917820	IMR90	lung:	n/a	chr5:7917640-7917651
9	CEBPB	chr5:7917486-7917794	Hela-S3	cervix:	n/a	chr5:7917640-7917651
10	CEBPB	chr5:7926162-7926865	IMR90	lung:	n/a	n/a
11	CEBPB	chr5:7931690-7931807	K562	blood:	n/a	n/a
12	CEBPB	chr5:7917518-7917789	A549	lung:	n/a	chr5:7917640-7917651
13	CHD2	chr5:7926508-7926509	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr5:7927932-7928178	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr5:7927781-7928364	MCF-7	breast:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
16	CTCF	chr5:7927900-7928202	GM19238	blood:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
17	CTCF	chr5:7927935-7928211	A549	lung:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
18	CTCF	chr5:7926440-7926590	BJ	skin:	n/a	chr5:7926459-7926472
19	CTCF	chr5:7926340-7926490	HCPEpiC	choroid plexus:	n/a	chr5:7926459-7926472
20	CTCF	chr5:7927980-7928130	Hela-S3	cervix:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
21	CTCF	chr5:7927855-7928318	IMR90	lung:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
22	CTCF	chr5:7927950-7928200	HepG2	liver:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
23	CTCF	chr5:7928000-7928150	GM12873	blood:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
24	CTCF	chr5:7927980-7928130	AG04450	lung:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
25	CTCF	chr5:7927980-7928130	HMF	breast:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
26	CTCF	chr5:7927736-7927813	ProgFib	skin:	n/a	n/a
27	CTCF	chr5:7927220-7927370	GM12874	blood:	n/a	n/a
28	CTCF	chr5:7927960-7928110	GM12870	blood:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
29	CTCF	chr5:7927460-7927610	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr5:7927440-7927590	GM12870	blood:	n/a	n/a
31	CTCF	chr5:7927980-7928130	GM12875	blood:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
32	CTCF	chr5:7926340-7926490	AG04449	skin:	n/a	chr5:7926459-7926472
33	CTCF	chr5:7927960-7928110	GM12874	blood:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
34	CTCF	chr5:7928020-7928170	AG09319	gingival:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
35	CTCF	chr5:7926380-7926530	AG09309	skin:	n/a	chr5:7926459-7926472
36	CTCF	chr5:7928000-7928150	MCF-7	breast:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
37	CTCF	chr5:7927908-7928212	Gliobla	brain:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
38	CTCF	chr5:7928000-7928150	HUVEC	blood vessel:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
39	CTCF	chr5:7927960-7928110	GM12865	blood:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
40	CTCF	chr5:7927980-7928130	AG04449	skin:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
41	CTCF	chr5:7928020-7928170	GM12873	blood:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
42	CTCF	chr5:7944160-7944310	GM06990	blood:	n/a	n/a
43	CTCF	chr5:7928000-7928150	GM12868	blood:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
44	CTCF	chr5:7927921-7928195	ProgFib	skin:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
45	CTCF	chr5:7927730-7927777	GM12892	blood:	n/a	n/a
46	CTCF	chr5:7927721-7927783	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:7927980-7928130	AG09319	gingival:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
48	CTCF	chr5:7927500-7927650	RPTEC	kidney:	n/a	n/a
49	CTCF	chr5:7928000-7928150	HRE	kidney:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074
50	CTCF	chr5:7927980-7928130	HCM	heart:	n/a	chr5:7928067-7928088 chr5:7928065-7928083 chr5:7928061-7928074

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:7926692-7926742	ProgFib	skin:	n/a
2	chr5:7926692-7926742	HCT-116	colon:	n/a
3	chr5:7926692-7926742	HIPEpiC	eye:	n/a
4	chr5:7926692-7926742	BE2_C	brain:	n/a
5	chr5:7926692-7926742	Hela-S3	cervix:	n/a
6	chr5:7926692-7926742	HPAEpiC	pulmonary alveolar:	n/a
7	chr5:7926692-7926742	ovcar-3	ovarian:	n/a
8	chr5:7926692-7926742	Caco-2	colon:	n/a
9	chr5:7926692-7926742	PrEC	prostate:	n/a
10	chr5:7926692-7926742	RPTEC	kidney:	n/a
11	chr5:7926692-7926742	GM12891	blood:	n/a
12	chr5:7926692-7926742	SK-N-SH	brain:	n/a
13	chr5:7926692-7926742	PFSK-1	brain:	n/a
14	chr5:7926692-7926742	HEK293	kidney:	embryo
15	chr5:7926692-7926742	A549	lung:	n/a
16	chr5:7926692-7926742	U87	brain:	n/a
17	chr5:7926692-7926742	K562	blood:	n/a
18	chr5:7926692-7926742	NT2-D1	testis:	n/a
19	chr5:7926692-7926742	HCPEpiC	choroid plexus:	n/a
20	chr5:7926692-7926742	HepG2	liver:	n/a
21	chr5:7926692-7926742	Hepatocyte	liver:	n/a
22	chr5:7926692-7926742	HMEC	breast:	n/a
23	chr5:7926692-7926742	GM12892	blood:	n/a
24	chr5:7926692-7926742	HCM	heart:	n/a
25	chr5:7926692-7926742	CMK	blood:	n/a
26	chr5:7926692-7926742	NHDF-neo	bronchial:	n/a
27	chr5:7926692-7926742	HRCEpiC	kidney:	n/a
28	chr5:7926692-7926742	NH-A	brain:	n/a
29	chr5:7926692-7926742	IMR90	lung:	fetal
30	chr5:7926692-7926742	HEEpiC	esophagus:	n/a
31	chr5:7926692-7926742	HNPCEpiC	eye:	n/a
32	chr5:7926692-7926742	AG10803	skin:	n/a
33	chr5:7926692-7926742	GM19239	blood:	n/a
34	chr5:7926692-7926742	AG04450	lung:	fetal
35	chr5:7926692-7926742	Jurkat	blood:	n/a
36	chr5:7926692-7926742	ECC-1	luminal epithelium:	n/a
37	chr5:7926692-7926742	H1-hESC	embryonic stem cell:	embryo
38	chr5:7926692-7926742	GM12878	blood:	n/a
39	chr5:7926692-7926742	HRE	kidney:	n/a
40	chr5:7926692-7926742	HUVEC	blood vessel:	n/a
41	chr5:7926692-7926742	NHBE	bronchial:	n/a
42	chr5:7926692-7926742	NB4	blood:	n/a
43	chr5:7926692-7926742	HL-60	blood:	n/a
44	chr5:7926692-7926742	SK-N-SH_RA	brain:	n/a
45	chr5:7926692-7926742	HAEpiC	amniotic membrane:	n/a
46	chr5:7926692-7926742	AoSMC	blood vessel:	n/a
47	chr5:7926692-7926742	SK-N-MC	brain:	n/a
48	chr5:7926692-7926742	MCF-7	breast:	n/a
49	chr5:7926692-7926742	AG04449	skin:	fetal
50	chr5:7926692-7926742	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:7927725..7928301-chr5:8047816..8048769,2	K562	blood:
2	chr5:7932719..7935095-chr5:7939432..7941071,2	K562	blood:
3	chr5:7921024..7923404-chr5:7924962..7926484,2	K562	blood:
4	chr5:7932719..7935095-chr5:7939432..7941071,2	K562	blood:
5	chr5:7913593..7916151-chr5:7918931..7921579,2	K562	blood:
6	chr5:7908992..7910576-chr5:7919203..7920908,2	K562	blood:
7	chr5:7951526..7954393-chr5:7958036..7960440,2	K562	blood:
8	chr5:7927628..7928513-chr5:8394887..8395661,2	MCF-7	breast:
9	chr5:7870008..7871996-chr5:7953650..7955606,2	K562	blood:
10	chr5:7868364..7870448-chr5:7925047..7928034,2	MCF-7	breast:
11	chr5:7921024..7923404-chr5:7924962..7926484,2	K562	blood:
12	chr5:7941523..7943649-chr5:9008284..9009858,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTRR-1	chr5:7924405-7924491	XLOC_004282
2	lnc-MTRR-1	chr5:7925067-7925110	XLOC_004282
3	lnc-MTRR-1	chr5:7925348-7925511	XLOC_004282

Variant related genes	Relation type
ENSG00000251168	TF binding region
ENSG00000251168	CpG island
ENSG00000124279	chromatin interactions
ENSG00000124275	chromatin interactions

Extended variants
information (count: 387 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530854375	chr5:7917737-7917738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76231165	chr5:7917739-7917740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145532675	chr5:7917741-7917742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147807567	chr5:7917767-7917768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141197386	chr5:7917781-7917782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567081157	chr5:7917813-7917814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187759577	chr5:7917836-7917837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192463357	chr5:7917839-7917840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540424280	chr5:7917882-7917883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs162273	chr5:7917934-7917935	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs28829123	chr5:7917953-7917954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148099112	chr5:7917989-7917990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374983505	chr5:7920044-7920045	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs557748709	chr5:7920077-7920078	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs562895254	chr5:7920214-7920215	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs186061911	chr5:7920247-7920248	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs545366538	chr5:7920248-7920249	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs191344144	chr5:7920255-7920256	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs573984136	chr5:7920587-7920588	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs369511260	chr5:7920651-7920652	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs70940767	chr5:7920682-7920683	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs398108567	chr5:7920691-7920692	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs80145706	chr5:7920692-7920693	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs190700940	chr5:7920700-7920701	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs182983424	chr5:7920716-7920717	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs77056991	chr5:7921478-7921479	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs188403610	chr5:7921553-7921554	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs543378117	chr5:7921596-7921597	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs558671768	chr5:7921842-7921843	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs572290456	chr5:7921849-7921850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs2613670	chr5:7921873-7921874	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs554886335	chr5:7921897-7921898	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs7356617	chr5:7921908-7921909	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs369964428	chr5:7921965-7921966	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs187008236	chr5:7922285-7922286	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs561746461	chr5:7922298-7922299	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs377363160	chr5:7922328-7922329	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs573170948	chr5:7924453-7924454	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs367703379	chr5:7924491-7924492	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs541827927	chr5:7924616-7924617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544085688	chr5:7924626-7924627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562125674	chr5:7924634-7924635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114518899	chr5:7924680-7924681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556276252	chr5:7924698-7924699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551095310	chr5:7924745-7924746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72716547	chr5:7924786-7924787	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs537546314	chr5:7925134-7925135	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs182139954	chr5:7925220-7925221	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs3816908	chr5:7925225-7925226	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs540230559	chr5:7925241-7925242	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Lung cancer	21911935	CNVD
Cri-du chat syndrome	21549014	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
early-passage human iPS cells	21368824	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:7917600-7918000	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr5:7924600-7924800	Enhancers	Fetal Muscle Trunk	muscle
3	chr5:7925400-7926000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:7925400-7927800	Enhancers	HSMM	muscle
5	chr5:7925400-7927800	Enhancers	NHLF	lung
6	chr5:7925400-7928000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr5:7925400-7928200	Enhancers	NHDF-Ad	bronchial
8	chr5:7925400-7928400	Enhancers	Osteobl	bone
9	chr5:7925600-7926000	Enhancers	Fetal Intestine Small	intestine
10	chr5:7925600-7927600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr5:7925600-7928000	Enhancers	NH-A	brain
12	chr5:7925800-7928000	Enhancers	Muscle Satellite Cultured Cells	--
13	chr5:7926000-7926400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr5:7926000-7926400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr5:7926000-7926400	Weak transcription	Fetal Intestine Small	intestine
16	chr5:7926200-7928000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr5:7926400-7926600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr5:7926400-7927000	Enhancers	Fetal Intestine Small	intestine
19	chr5:7926400-7928000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr5:7926400-7928400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:7926600-7926800	Enhancers	Fetal Intestine Large	intestine
22	chr5:7926600-7927000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr5:7926600-7927000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
24	chr5:7926600-7927800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr5:7926800-7927000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:7926800-7927000	Enhancers	HSMMtube	muscle
27	chr5:7926800-7927800	Weak transcription	Fetal Intestine Large	intestine
28	chr5:7927000-7927200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr5:7927000-7927800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:7927000-7928200	Weak transcription	Fetal Intestine Small	intestine
31	chr5:7927200-7928200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr5:7927600-7928000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:7927600-7928400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:7927800-7928000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr5:7927800-7928000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:7927800-7928000	Enhancers	Liver	Liver
37	chr5:7927800-7928200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr5:7927800-7928400	Enhancers	Fetal Muscle Trunk	muscle
39	chr5:7927800-7928400	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr5:7927800-7929200	Enhancers	Fetal Intestine Large	intestine
41	chr5:7928000-7928400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr5:7928200-7928400	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr5:7928200-7928400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:7928200-7928400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr5:7928200-7928400	Enhancers	Brain Angular Gyrus	brain
46	chr5:7928200-7928400	Enhancers	Brain Substantia Nigra	brain
47	chr5:7928200-7928400	Enhancers	Duodenum Mucosa	Duodenum
48	chr5:7928200-7928400	Enhancers	Fetal Intestine Small	intestine
49	chr5:7928200-7928600	Enhancers	Fetal Muscle Leg	muscle
50	chr5:7928400-7929000	Weak transcription	Fetal Intestine Small	intestine

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