Variant report

Variant	nsv609905
Chromosome Location	chr8:5438130-5616990
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	BACH1	chr8:5607668-5608196	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr8:5532714-5533009	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr8:5447859-5447918	GM12878	blood:	n/a	n/a
4	BHLHE40	chr8:5472520-5472526	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:5606425-5606513	A549	lung:	n/a	n/a
6	CEBPB	chr8:5513789-5514104	HepG2	liver:	n/a	chr8:5513934-5513945
7	CEBPB	chr8:5572602-5572802	HepG2	liver:	n/a	chr8:5572684-5572695 chr8:5572683-5572694 chr8:5572683-5572696
8	CEBPB	chr8:5472168-5472184	H1-hESC	embryonic stem cell:	n/a	chr8:5472171-5472184
9	CEBPB	chr8:5472026-5472315	A549	lung:	n/a	chr8:5472171-5472184
10	CEBPB	chr8:5532924-5533107	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:5584989-5585024	HepG2	liver:	n/a	chr8:5584999-5585010
12	CEBPB	chr8:5532168-5532358	HepG2	liver:	n/a	chr8:5532275-5532288 chr8:5532276-5532287 chr8:5532275-5532286
13	CEBPB	chr8:5606430-5606630	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:5480182-5480464	HepG2	liver:	n/a	chr8:5480309-5480320
15	CHD2	chr8:5527476-5527834	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr8:5543700-5543850	NB4	blood:	n/a	n/a
17	CTCF	chr8:5543600-5543750	HEEpiC	esophagus:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
18	CTCF	chr8:5543600-5543750	HMF	breast:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
19	CTCF	chr8:5543340-5543490	NHEK	skin:	n/a	n/a
20	CTCF	chr8:5600919-5601010	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr8:5543500-5543650	HAc	cerebellar:	n/a	n/a
22	CTCF	chr8:5543520-5543670	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr8:5543363-5543413	Gliobla	brain:	n/a	n/a
24	CTCF	chr8:5543644-5543703	HUVEC	blood vessel:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
25	CTCF	chr8:5543639-5543719	HepG2	liver:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
26	CTCF	chr8:5543660-5543810	HL-60	blood:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
27	CTCF	chr8:5543620-5543770	Caco-2	colon:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
28	CTCF	chr8:5543652-5543717	MCF-7	breast:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
29	CTCF	chr8:5590310-5590375	Fibrobl	skin:	n/a	n/a
30	CTCF	chr8:5543580-5543730	AG04449	skin:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
31	CTCF	chr8:5543580-5543730	HCPEpiC	choroid plexus:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
32	CTCF	chr8:5543720-5543870	HFF	foreskin:	n/a	n/a
33	CTCF	chr8:5543680-5543830	A549	lung:	n/a	n/a
34	CTCF	chr8:5513840-5513990	BJ	skin:	n/a	n/a
35	CTCF	chr8:5543520-5543670	NB4	blood:	n/a	n/a
36	CTCF	chr8:5543560-5543710	NHEK	skin:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
37	CTCF	chr8:5543620-5543770	BJ	skin:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
38	CTCF	chr8:5543600-5543750	NHDF-neo	bronchial:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
39	CTCF	chr8:5543600-5543750	HMEC	breast:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
40	CTCF	chr8:5543620-5543770	BE2_C	brain:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
41	CTCF	chr8:5543620-5543770	HCPEpiC	choroid plexus:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
42	CTCF	chr8:5560300-5560450	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr8:5513960-5514110	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr8:5543584-5543778	Medullo	brain:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
45	CTCF	chr8:5543560-5543710	SK-N-SH_RA	brain:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
46	CTCF	chr8:5543660-5543810	WERI-Rb-1	eye:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
47	CTCF	chr8:5543540-5543690	BE2_C	brain:	n/a	n/a
48	CTCF	chr8:5543580-5543730	MCF-7	breast:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
49	CTCF	chr8:5543560-5543710	HEK293	kidney:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
50	CTCF	chr8:5543643-5543834	GM12878	blood:	n/a	chr8:5543674-5543692 chr8:5543676-5543697

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5526092-5526142	HNPCEpiC	eye:	n/a
2	chr8:5526092-5526142	HCM	heart:	n/a
3	chr8:5526092-5526142	SKMC	muscle:	n/a
4	chr8:5526092-5526142	T-47D	breast:	n/a
5	chr8:5526092-5526142	AG09309	skin:	n/a
6	chr8:5526092-5526142	Hepatocyte	liver:	n/a
7	chr8:5526092-5526142	PANC-1	pancreas:	n/a
8	chr8:5526092-5526142	BE2_C	brain:	n/a
9	chr8:5526092-5526142	IMR90	lung:	fetal
10	chr8:5526092-5526142	SK-N-MC	brain:	n/a
11	chr8:5526092-5526142	GM06990	blood:	n/a
12	chr8:5526092-5526142	SK-N-SH	brain:	n/a
13	chr8:5526092-5526142	GM19239	blood:	n/a
14	chr8:5526092-5526142	HCPEpiC	choroid plexus:	n/a
15	chr8:5526092-5526142	BJ	skin:	n/a
16	chr8:5526092-5526142	H1-hESC	embryonic stem cell:	embryo
17	chr8:5526092-5526142	NHBE	bronchial:	n/a
18	chr8:5526092-5526142	HRE	kidney:	n/a
19	chr8:5526092-5526142	MCF-7	breast:	n/a
20	chr8:5526092-5526142	AG09319	gingival:	n/a
21	chr8:5526092-5526142	MCF10A-Er-Src	breast:	n/a
22	chr8:5526092-5526142	GM12878	blood:	n/a
23	chr8:5526092-5526142	PFSK-1	brain:	n/a
24	chr8:5526092-5526142	HRCEpiC	kidney:	n/a
25	chr8:5526092-5526142	Hela-S3	cervix:	n/a
26	chr8:5526092-5526142	Jurkat	blood:	n/a
27	chr8:5526092-5526142	SK-N-SH_RA	brain:	n/a
28	chr8:5526092-5526142	CMK	blood:	n/a
29	chr8:5526092-5526142	HepG2	liver:	n/a
30	chr8:5526092-5526142	PrEC	prostate:	n/a
31	chr8:5526092-5526142	ECC-1	luminal epithelium:	n/a
32	chr8:5526092-5526142	ProgFib	skin:	n/a
33	chr8:5526092-5526142	HRPEpiC	eye:	n/a
34	chr8:5526092-5526142	HIPEpiC	eye:	n/a
35	chr8:5526092-5526142	Caco-2	colon:	n/a
36	chr8:5526092-5526142	LNCaP	prostate:	n/a
37	chr8:5526092-5526142	HMEC	breast:	n/a
38	chr8:5526092-5526142	HUVEC	blood vessel:	n/a
39	chr8:5526092-5526142	GM12891	blood:	n/a
40	chr8:5526092-5526142	HEK293	kidney:	embryo
41	chr8:5526092-5526142	NHDF-neo	bronchial:	n/a
42	chr8:5526092-5526142	A549	lung:	n/a
43	chr8:5526092-5526142	HEEpiC	esophagus:	n/a
44	chr8:5526092-5526142	SAEC	small airway:	n/a
45	chr8:5526092-5526142	HAEpiC	amniotic membrane:	n/a
46	chr8:5526092-5526142	U87	brain:	n/a
47	chr8:5526092-5526142	HCT-116	colon:	n/a
48	chr8:5526092-5526142	GM12892	blood:	n/a
49	chr8:5526092-5526142	RPTEC	kidney:	n/a
50	chr8:5526092-5526142	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:5539160..5541154-chr8:5572222..5575011,2	K562	blood:
2	chr8:5610821..5612324-chr8:5615595..5617703,2	K562	blood:
3	chr8:5535511..5537996-chr8:5538816..5540687,2	K562	blood:
4	chr4:47028381..47029208-chr8:5581216..5581723,2	MCF-7	breast:
5	chr8:5543604..5544126-chr8:5997197..5997756,2	MCF-7	breast:
6	chr8:5524220..5526546-chr8:5527520..5529311,2	K562	blood:
7	chr1:14651092..14651694-chr8:5507747..5508432,2	MCF-7	breast:
8	chr8:5610821..5612324-chr8:5615595..5617703,2	K562	blood:
9	chr8:5535511..5537996-chr8:5538816..5540687,2	K562	blood:
10	chr8:5539160..5541154-chr8:5572222..5575011,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSMD1-6	chr8:5517279-5517508	XLOC_006981
2	lnc-CSMD1-6	chr8:5527471-5527599	ENSG00000254007
3	lnc-CSMD1-6	chr8:5517201-5517508	ENSG00000254007
4	lnc-CSMD1-6	chr8:5522226-5522711	ENSG00000254007
5	lnc-CSMD1-6	chr8:5522226-5522285	XLOC_006981

Variant related genes	Relation type
ENSG00000254007	TF binding region
ENSG00000254007	CpG island
ENSG00000254007	chromatin interactions
STRADB	miRNA target sites
STRBP	miRNA target sites

Extended variants
information (count: 4636 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:4636 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78873003	chr8:5449809-5449810	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs547206103	chr8:5449822-5449823	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs565500230	chr8:5449854-5449855	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs188289371	chr8:5449860-5449861	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs551386111	chr8:5449875-5449876	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs569675982	chr8:5449885-5449886	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs117874707	chr8:5449894-5449895	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs370882926	chr8:5449897-5449898	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs567381725	chr8:5449907-5449908	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs534665139	chr8:5449940-5449941	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs543832000	chr8:5449964-5449965	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs117254115	chr8:5449971-5449972	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs540165382	chr8:5449975-5449976	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs558153047	chr8:5449976-5449977	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs113979094	chr8:5449977-5449978	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs543474616	chr8:5449979-5449980	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs561712648	chr8:5449982-5449983	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs573808161	chr8:5449996-5449997	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs541081740	chr8:5450001-5450002	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs559171038	chr8:5450026-5450027	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs532974962	chr8:5450027-5450028	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs551680194	chr8:5450040-5450041	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs563454254	chr8:5450041-5450042	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs530795809	chr8:5450052-5450053	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs146918231	chr8:5450081-5450082	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs548708582	chr8:5450084-5450085	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs530946977	chr8:5450087-5450088	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs567224637	chr8:5450090-5450091	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs116962869	chr8:5450099-5450100	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs200701753	chr8:5450109-5450110	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs181167822	chr8:5450111-5450112	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs566309682	chr8:5450113-5450114	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs551050430	chr8:5450114-5450115	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs147702250	chr8:5450115-5450116	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs116653852	chr8:5450127-5450128	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs13272972	chr8:5450176-5450177	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs558304582	chr8:5450179-5450180	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs576679993	chr8:5450184-5450185	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs185660882	chr8:5450189-5450190	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs555348022	chr8:5450193-5450194	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs575612331	chr8:5454804-5454805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75775808	chr8:5454824-5454825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560905824	chr8:5454842-5454843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538832802	chr8:5454853-5454854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563469446	chr8:5454859-5454860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572782293	chr8:5454873-5454874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532466135	chr8:5454896-5454897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539981962	chr8:5454911-5454912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs202112659	chr8:5454916-5454917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565013878	chr8:5454924-5454925	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:130)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Type 2 diabetes	21526130	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Obesity	21131291	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5449800-5450000	ZNF genes & repeats	Pancreas	Pancrea
2	chr8:5449800-5450200	Enhancers	Esophagus	oesophagus
3	chr8:5449800-5450200	ZNF genes & repeats	Gastric	stomach
4	chr8:5454800-5457200	Enhancers	Fetal Brain Male	brain
5	chr8:5457000-5458000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:5457600-5458000	Enhancers	Spleen	Spleen
7	chr8:5460800-5461200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:5461600-5462400	Enhancers	Brain Germinal Matrix	brain
9	chr8:5461600-5462600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:5462600-5468200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:5464600-5465000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:5467000-5467800	Enhancers	Brain Substantia Nigra	brain
13	chr8:5468200-5469600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr8:5468800-5469400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:5469000-5469400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr8:5469000-5469400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr8:5469000-5469400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr8:5469200-5469600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr8:5469400-5472400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:5470000-5470200	Enhancers	Pancreas	Pancrea
21	chr8:5471800-5472800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr8:5472400-5472800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:5472600-5476200	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr8:5472800-5476800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr8:5475000-5476400	Enhancers	Spleen	Spleen
26	chr8:5475200-5475600	Enhancers	Brain Anterior Caudate	brain
27	chr8:5475400-5475600	Enhancers	Brain Substantia Nigra	brain
28	chr8:5475400-5476200	Enhancers	Esophagus	oesophagus
29	chr8:5475400-5476400	Enhancers	Lung	lung
30	chr8:5476000-5476200	Enhancers	Stomach Smooth Muscle	stomach
31	chr8:5476800-5477600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr8:5485400-5486200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr8:5485400-5486200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr8:5499800-5500200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr8:5503000-5508000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:5511000-5511800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:5514000-5514600	Enhancers	Fetal Muscle Leg	muscle
38	chr8:5518400-5518600	Enhancers	H9 Cell Line	embryonic stem cell
39	chr8:5518600-5522200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr8:5518800-5519000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr8:5521200-5521400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr8:5522200-5522400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr8:5522400-5525800	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr8:5522800-5523000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr8:5523400-5525400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr8:5524600-5526000	Enhancers	Fetal Brain Male	brain
47	chr8:5525000-5526600	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr8:5525400-5528000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr8:5525400-5528200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:5525400-5528200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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