Variant report

Variant	nsv880325
Chromosome Location	chr5:8155254-8231744
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	CCNT2	chr5:8195851-8196050	K562	blood:	n/a	n/a
2	CEBPB	chr5:8176086-8176672	K562	blood:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
3	CEBPB	chr5:8176175-8176647	ECC-1	luminal epithelium:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
4	CEBPB	chr5:8176120-8176702	MCF-7	breast:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
5	CEBPB	chr5:8171355-8171673	HepG2	liver:	n/a	chr5:8171506-8171515 chr5:8171504-8171515 chr5:8171505-8171516
6	CEBPB	chr5:8176185-8176710	MCF-7	breast:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
7	CEBPB	chr5:8218514-8218589	A549	lung:	n/a	n/a
8	CEBPB	chr5:8176268-8176497	HepG2	liver:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
9	CEBPB	chr5:8176223-8176614	H1-hESC	embryonic stem cell:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
10	CEBPB	chr5:8176175-8176615	IMR90	lung:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
11	CEBPB	chr5:8176166-8176647	HepG2	liver:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
12	CEBPB	chr5:8176076-8176792	A549	lung:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
13	CEBPB	chr5:8216514-8216803	HepG2	liver:	n/a	chr5:8216679-8216690
14	CEBPB	chr5:8176228-8176611	HepG2	liver:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
15	CEBPB	chr5:8176221-8176582	K562	blood:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
16	CEBPB	chr5:8216559-8216802	IMR90	lung:	n/a	chr5:8216679-8216690
17	CEBPB	chr5:8176205-8176610	A549	lung:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
18	CEBPB	chr5:8177836-8178084	A549	lung:	n/a	chr5:8177973-8177986
19	CEBPB	chr5:8199705-8199921	IMR90	lung:	n/a	chr5:8199776-8199787
20	CEBPB	chr5:8199623-8199962	HepG2	liver:	n/a	chr5:8199776-8199787
21	CEBPB	chr5:8165153-8165357	HepG2	liver:	n/a	chr5:8165244-8165255
22	CEBPB	chr5:8176257-8176586	ECC-1	luminal epithelium:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
23	CEBPB	chr5:8176051-8176638	Hela-S3	cervix:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
24	CEBPB	chr5:8176289-8176531	K562	blood:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
25	CEBPB	chr5:8176222-8176613	HepG2	liver:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
26	CEBPB	chr5:8176180-8176653	A549	lung:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
27	CTCF	chr5:8184539-8184871	H1-hESC	embryonic stem cell:	n/a	chr5:8184770-8184779
28	CTCF	chr5:8184680-8184830	HEEpiC	esophagus:	n/a	chr5:8184770-8184779
29	CTCF	chr5:8184700-8184850	GM12869	blood:	n/a	chr5:8184770-8184779
30	CTCF	chr5:8184740-8184890	GM12873	blood:	n/a	chr5:8184770-8184779
31	CTCF	chr5:8184650-8184917	GM10266	blood:	n/a	chr5:8184770-8184779
32	CTCF	chr5:8184680-8184830	RPTEC	kidney:	n/a	chr5:8184770-8184779
33	CTCF	chr5:8184700-8184850	HCT-116	colon:	n/a	chr5:8184770-8184779
34	CTCF	chr5:8184623-8184855	HepG2	liver:	n/a	chr5:8184770-8184779
35	CTCF	chr5:8184649-8184914	ProgFib	skin:	n/a	chr5:8184770-8184779
36	CTCF	chr5:8184660-8184810	BE2_C	brain:	n/a	chr5:8184770-8184779
37	CTCF	chr5:8184680-8184830	HMF	breast:	n/a	chr5:8184770-8184779
38	CTCF	chr5:8184671-8184882	NHEK	skin:	n/a	chr5:8184770-8184779
39	CTCF	chr5:8184700-8184850	BJ	skin:	n/a	chr5:8184770-8184779
40	CTCF	chr5:8184680-8184830	GM12870	blood:	n/a	chr5:8184770-8184779
41	CTCF	chr5:8184680-8184830	GM06990	blood:	n/a	chr5:8184770-8184779
42	CTCF	chr5:8208657-8208675	Fibrobl	skin:	n/a	n/a
43	CTCF	chr5:8184320-8184470	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr5:8184720-8184870	HAc	cerebellar:	n/a	chr5:8184770-8184779
45	CTCF	chr5:8184720-8184870	AG09309	skin:	n/a	chr5:8184770-8184779
46	CTCF	chr5:8184740-8184890	GM12864	blood:	n/a	chr5:8184770-8184779
47	CTCF	chr5:8184740-8184890	HA-sp	spinal cord:	n/a	chr5:8184770-8184779
48	CTCF	chr5:8184700-8184850	AG04450	lung:	n/a	chr5:8184770-8184779
49	CTCF	chr5:8184570-8184877	HepG2	liver:	n/a	chr5:8184770-8184779
50	CTCF	chr5:8184700-8184850	HCPEpiC	choroid plexus:	n/a	chr5:8184770-8184779

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:8217287-8217337	ProgFib	skin:	n/a
2	chr5:8217322-8217372	BJ	skin:	n/a
3	chr5:8217322-8217372	Hela-S3	cervix:	n/a
4	chr5:8217322-8217372	HCT-116	colon:	n/a
5	chr5:8217322-8217372	HL-60	blood:	n/a
6	chr5:8217322-8217372	HUVEC	blood vessel:	n/a
7	chr5:8217236-8217286	HEEpiC	esophagus:	n/a
8	chr5:8217287-8217337	HUVEC	blood vessel:	n/a
9	chr5:8217236-8217286	HPAEpiC	pulmonary alveolar:	n/a
10	chr5:8217236-8217286	HepG2	liver:	n/a
11	chr5:8217236-8217286	HCF	heart:	n/a
12	chr5:8217322-8217372	GM12892	blood:	n/a
13	chr5:8217322-8217372	HRE	kidney:	n/a
14	chr5:8217322-8217372	HRCEpiC	kidney:	n/a
15	chr5:8217287-8217337	SK-N-SH	brain:	n/a
16	chr5:8217236-8217286	GM06990	blood:	n/a
17	chr5:8217236-8217286	CMK	blood:	n/a
18	chr5:8217287-8217337	SKMC	muscle:	n/a
19	chr5:8217322-8217372	SK-N-SH_RA	brain:	n/a
20	chr5:8217236-8217286	AG09319	gingival:	n/a
21	chr5:8217287-8217337	T-47D	breast:	n/a
22	chr5:8217322-8217372	SKMC	muscle:	n/a
23	chr5:8217236-8217286	SK-N-SH	brain:	n/a
24	chr5:8217322-8217372	BE2_C	brain:	n/a
25	chr5:8217287-8217337	HCPEpiC	choroid plexus:	n/a
26	chr5:8217322-8217372	AG04450	lung:	fetal
27	chr5:8217236-8217286	MCF10A-Er-Src	breast:	n/a
28	chr5:8217287-8217337	GM06990	blood:	n/a
29	chr5:8217322-8217372	SK-N-MC	brain:	n/a
30	chr5:8217322-8217372	NHBE	bronchial:	n/a
31	chr5:8217287-8217337	ovcar-3	ovarian:	n/a
32	chr5:8217236-8217286	SAEC	small airway:	n/a
33	chr5:8217287-8217337	HEK293	kidney:	embryo
34	chr5:8217236-8217286	HCPEpiC	choroid plexus:	n/a
35	chr5:8217287-8217337	BJ	skin:	n/a
36	chr5:8217287-8217337	SAEC	small airway:	n/a
37	chr5:8217287-8217337	BE2_C	brain:	n/a
38	chr5:8217236-8217286	HCT-116	colon:	n/a
39	chr5:8217287-8217337	AG09309	skin:	n/a
40	chr5:8217287-8217337	AG04449	skin:	fetal
41	chr5:8217236-8217286	Caco-2	colon:	n/a
42	chr5:8217287-8217337	HepG2	liver:	n/a
43	chr5:8217236-8217286	BE2_C	brain:	n/a
44	chr5:8217322-8217372	AG04449	skin:	fetal
45	chr5:8217236-8217286	HNPCEpiC	eye:	n/a
46	chr5:8217236-8217286	RPTEC	kidney:	n/a
47	chr5:8217287-8217337	SK-N-SH_RA	brain:	n/a
48	chr5:8217236-8217286	HRPEpiC	eye:	n/a
49	chr5:8217322-8217372	HRPEpiC	eye:	n/a
50	chr5:8217322-8217372	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:8181808..8184211-chr5:8185968..8188351,2	K562	blood:
2	chr5:8181808..8184211-chr5:8185968..8188351,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FASTKD3-4	chr5:8157654-8157901	NONHSAT100281

Variant related genes	Relation type
ENSG00000249486	TF binding region
ENSG00000249486	CpG island

Extended variants
information (count: 1428 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1428 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183705553	chr5:8157658-8157659	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs336151	chr5:8157714-8157715	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs187249706	chr5:8157835-8157836	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs192624562	chr5:8157879-8157880	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs1506128	chr5:8157886-8157887	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs543441389	chr5:8157971-8157972	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs183188662	chr5:8157993-8157994	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs532258165	chr5:8158020-8158021	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs114191473	chr5:8158049-8158050	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs568684238	chr5:8158122-8158123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186806247	chr5:8158137-8158138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559128216	chr5:8158140-8158141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148351846	chr5:8158141-8158142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528308127	chr5:8158179-8158180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs28552487	chr5:8158181-8158182	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs336150	chr5:8158239-8158240	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs530698587	chr5:8158253-8158254	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs550164330	chr5:8158270-8158271	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs370131667	chr5:8158273-8158274	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs569922742	chr5:8158309-8158310	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs71609178	chr5:8158316-8158317	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs75482507	chr5:8158319-8158320	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs59876090	chr5:8158328-8158329	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs58808476	chr5:8158339-8158340	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs13188805	chr5:8158343-8158344	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs539133042	chr5:8158378-8158379	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs559134688	chr5:8158421-8158422	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs566176979	chr5:8158428-8158429	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs192708202	chr5:8158435-8158436	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs199674698	chr5:8158474-8158475	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs555187675	chr5:8158475-8158476	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs140437507	chr5:8158487-8158488	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs144285689	chr5:8158502-8158503	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs147365275	chr5:8158538-8158539	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs576720657	chr5:8158610-8158611	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs545382038	chr5:8158618-8158619	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs533449359	chr5:8159751-8159752	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs182030423	chr5:8159760-8159761	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs371765478	chr5:8159776-8159777	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs376225215	chr5:8159819-8159820	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs535108389	chr5:8159820-8159821	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs186410949	chr5:8159826-8159827	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs189349553	chr5:8159872-8159873	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs567920815	chr5:8159882-8159883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537917184	chr5:8159887-8159888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557669856	chr5:8159898-8159899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577869799	chr5:8159914-8159915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540416708	chr5:8159916-8159917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6882310	chr5:8159967-8159968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs336202	chr5:8159976-8159977	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:107)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:8157600-8158400	Weak transcription	Spleen	Spleen
2	chr5:8158400-8158600	Enhancers	Spleen	Spleen
3	chr5:8159800-8160000	Enhancers	H9 Cell Line	embryonic stem cell
4	chr5:8166000-8166200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:8166200-8166400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr5:8166200-8166600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:8166200-8166800	ZNF genes & repeats	Pancreas	Pancrea
8	chr5:8166400-8166600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:8166800-8180800	Weak transcription	Pancreas	Pancrea
10	chr5:8172600-8173600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:8173600-8174800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:8175000-8175200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:8176000-8176400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr5:8176000-8176600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:8176200-8176400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr5:8176200-8176400	Enhancers	Gastric	stomach
17	chr5:8176200-8176800	Enhancers	Ovary	ovary
18	chr5:8176400-8180800	Weak transcription	Gastric	stomach
19	chr5:8176600-8188200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr5:8180200-8181600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr5:8180400-8181400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr5:8180600-8181400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr5:8180800-8181200	Enhancers	Gastric	stomach
24	chr5:8180800-8181400	Enhancers	H9 Cell Line	embryonic stem cell
25	chr5:8180800-8181400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr5:8180800-8181400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr5:8180800-8181400	Enhancers	Pancreas	Pancrea
28	chr5:8180800-8181600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr5:8181000-8181400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr5:8181000-8181400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr5:8181200-8181600	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr5:8181400-8189400	Weak transcription	Pancreas	Pancrea
33	chr5:8181600-8182600	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr5:8182600-8183200	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr5:8186400-8187000	Enhancers	Fetal Brain Male	brain
36	chr5:8188200-8188400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr5:8188400-8188800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr5:8188800-8190000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr5:8189000-8189600	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr5:8189000-8190000	Enhancers	Dnd41	blood
41	chr5:8189200-8190000	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr5:8189400-8190000	Enhancers	Pancreas	Pancrea
43	chr5:8192400-8193400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
44	chr5:8193000-8193400	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr5:8195800-8196400	Enhancers	Fetal Stomach	stomach
46	chr5:8206000-8207000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr5:8208000-8213200	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr5:8208400-8208800	Enhancers	Pancreas	Pancrea
49	chr5:8208600-8208800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr5:8208600-8208800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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