Variant report

Variant	esv2755872
Chromosome Location	chr8:25499467-25598598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:327)
CpG islands
(count:367)
Chromatin interactive
region (count:20)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:25530675-25530727	K562	blood:	n/a	n/a
2	ATF2	chr8:25532945-25533257	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr8:25532946-25533235	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr8:25532942-25533168	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr8:25530564-25530834	K562	blood:	n/a	n/a
6	CBX3	chr8:25530449-25530840	K562	blood:	n/a	n/a
7	CEBPB	chr8:25542333-25542409	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr8:25542285-25542413	A549	lung:	n/a	n/a
9	CEBPB	chr8:25542327-25542429	IMR90	lung:	n/a	n/a
10	CEBPB	chr8:25542201-25542502	HepG2	liver:	n/a	n/a
11	CHD2	chr8:25532974-25533337	H1-hESC	embryonic stem cell:	n/a	chr8:25533019-25533029
12	CTCF	chr8:25503663-25503733	LNCaP	prostate:	n/a	n/a
13	CTCF	chr8:25503655-25503797	MCF-7	breast:	n/a	n/a
14	CTCF	chr8:25503640-25503790	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr8:25542432-25542467	Lung_OC	lung:	n/a	n/a
16	CTCF	chr8:25543080-25543230	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr8:25503640-25503790	BE2_C	brain:	n/a	n/a
18	CTCF	chr8:25503673-25503800	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:25543100-25543250	BE2_C	brain:	n/a	n/a
20	CTCF	chr8:25503651-25503796	GM19240	blood:	n/a	n/a
21	CTCF	chr8:25503635-25503808	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr8:25503670-25503788	GM19238	blood:	n/a	n/a
23	CTCF	chr8:25515159-25515200	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr8:25503640-25503790	NB4	blood:	n/a	n/a
25	CTCF	chr8:25597240-25597390	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr8:25503600-25503750	MCF-7	breast:	n/a	n/a
27	CTCF	chr8:25503679-25503797	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:25503735-25503750	LNCaP	prostate:	n/a	n/a
29	CTCF	chr8:25503663-25503788	GM13977	blood:	n/a	n/a
30	CTCF	chr8:25503640-25503790	GM12873	blood:	n/a	n/a
31	CTCF	chr8:25545460-25545610	BE2_C	brain:	n/a	n/a
32	CTCF	chr8:25515146-25515204	GM10248	blood:	n/a	n/a
33	CTCF	chr8:25503480-25503630	HCM	heart:	n/a	n/a
34	CTCF	chr8:25503687-25503753	GM12878	blood:	n/a	n/a
35	CTCF	chr8:25503560-25503710	GM12874	blood:	n/a	n/a
36	CTCF	chr8:25503580-25503730	GM12873	blood:	n/a	n/a
37	CTCF	chr8:25503580-25503730	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr8:25503555-25503839	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr8:25503681-25503799	GM19239	blood:	n/a	n/a
40	CTCF	chr8:25503500-25503650	NHEK	skin:	n/a	n/a
41	CTCF	chr8:25503651-25503789	Gliobla	brain:	n/a	n/a
42	CTCF	chr8:25539626-25539684	LNCaP	prostate:	n/a	n/a
43	CTCF	chr8:25503658-25503778	GM12892	blood:	n/a	n/a
44	CTCF	chr8:25503683-25503783	ProgFib	skin:	n/a	n/a
45	CTCF	chr8:25503660-25503801	Fibrobl	skin:	n/a	n/a
46	CTCF	chr8:25503681-25503766	MCF-7	breast:	n/a	n/a
47	CTCF	chr8:25531063-25531125	GM20000	blood:	n/a	n/a
48	CTCF	chr8:25503640-25503790	GM12875	blood:	n/a	n/a
49	CTCF	chr8:25549640-25549790	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr8:25503616-25503798	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:25593585-25593635	HRCEpiC	kidney:	n/a
2	chr8:25593585-25593635	HRCEpiC	kidney:	n/a
3	chr8:25543202-25543252	AG09319	gingival:	n/a
4	chr8:25546737-25546787	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:25538546-25538596	Caco-2	colon:	n/a
6	chr8:25501771-25501821	U87	brain:	n/a
7	chr8:25501771-25501821	HRCEpiC	kidney:	n/a
8	chr8:25543184-25543234	MCF-7	breast:	n/a
9	chr8:25593585-25593635	AG04450	lung:	fetal
10	chr8:25538546-25538596	RPTEC	kidney:	n/a
11	chr8:25593585-25593635	HEEpiC	esophagus:	n/a
12	chr8:25543202-25543252	Hela-S3	cervix:	n/a
13	chr8:25538546-25538596	SAEC	small airway:	n/a
14	chr8:25501771-25501821	HRPEpiC	eye:	n/a
15	chr8:25593585-25593635	HRPEpiC	eye:	n/a
16	chr8:25546737-25546787	LNCaP	prostate:	n/a
17	chr8:25543184-25543234	T-47D	breast:	n/a
18	chr8:25501771-25501821	NHDF-neo	bronchial:	n/a
19	chr8:25501771-25501821	NT2-D1	testis:	n/a
20	chr8:25543202-25543252	NHDF-neo	bronchial:	n/a
21	chr8:25538546-25538596	A549	lung:	n/a
22	chr8:25501771-25501821	SKMC	muscle:	n/a
23	chr8:25543184-25543234	ProgFib	skin:	n/a
24	chr8:25543202-25543252	A549	lung:	n/a
25	chr8:25543202-25543252	Jurkat	blood:	n/a
26	chr8:25593585-25593635	MCF10A-Er-Src	breast:	n/a
27	chr8:25538546-25538596	HCT-116	colon:	n/a
28	chr8:25538546-25538596	GM12892	blood:	n/a
29	chr8:25543202-25543252	LNCaP	prostate:	n/a
30	chr8:25593585-25593635	HMEC	breast:	n/a
31	chr8:25543202-25543252	AG04450	lung:	fetal
32	chr8:25543202-25543252	AG09309	skin:	n/a
33	chr8:25546737-25546787	GM12891	blood:	n/a
34	chr8:25546737-25546787	K562	blood:	n/a
35	chr8:25593585-25593635	AG04449	skin:	fetal
36	chr8:25501771-25501821	HAEpiC	amniotic membrane:	n/a
37	chr8:25593585-25593635	SK-N-SH	brain:	n/a
38	chr8:25543202-25543252	RPTEC	kidney:	n/a
39	chr8:25593585-25593635	SKMC	muscle:	n/a
40	chr8:25543184-25543234	U87	brain:	n/a
41	chr8:25538546-25538596	HAEpiC	amniotic membrane:	n/a
42	chr8:25501771-25501821	ProgFib	skin:	n/a
43	chr8:25543202-25543252	HCPEpiC	choroid plexus:	n/a
44	chr8:25543184-25543234	HAEpiC	amniotic membrane:	n/a
45	chr8:25501771-25501821	SK-N-SH_RA	brain:	n/a
46	chr8:25538546-25538596	HCPEpiC	choroid plexus:	n/a
47	chr8:25543202-25543252	SK-N-MC	brain:	n/a
48	chr8:25538546-25538596	NH-A	brain:	n/a
49	chr8:25543184-25543234	NHDF-neo	bronchial:	n/a
50	chr8:25501771-25501821	AoSMC	blood vessel:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:25530880..25534453-chr8:25535358..25538817,3	K562	blood:
2	chr8:25530880..25534453-chr8:25535358..25538817,3	K562	blood:
3	chr8:25438833..25440348-chr8:25528267..25531117,2	K562	blood:
4	chr8:25509449..25512241-chr8:25544932..25546879,2	K562	blood:
5	chr1:244624166..244626522-chr8:25561893..25564687,2	MCF-7	breast:
6	chr8:25521644..25523787-chr8:25523861..25526254,3	K562	blood:
7	chr8:25522229..25524978-chr8:25528807..25530481,2	K562	blood:
8	chr8:25570406..25573230-chr8:25575445..25578017,2	K562	blood:
9	chr8:25519646..25521463-chr8:25528350..25530494,2	K562	blood:
10	chr8:25519646..25521463-chr8:25528350..25530494,2	K562	blood:
11	chr8:25509449..25512241-chr8:25544932..25546879,2	K562	blood:
12	chr8:25522229..25524889-chr8:25527309..25530307,2	K562	blood:
13	chr8:25518164..25520145-chr8:25522608..25524182,2	MCF-7	breast:
14	chr8:25518164..25520145-chr8:25522608..25524182,2	MCF-7	breast:
15	chr8:25570406..25573230-chr8:25575445..25578017,2	K562	blood:
16	chr8:25536297..25539174-chr8:25541358..25543304,2	K562	blood:
17	chr8:25521644..25523787-chr8:25523861..25526254,3	K562	blood:
18	chr8:25536297..25539174-chr8:25541358..25543304,2	K562	blood:
19	chr8:25522229..25524889-chr8:25527309..25530307,2	K562	blood:
20	chr8:25522229..25524978-chr8:25528807..25530481,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDCA2-1	chr8:25528812-25529202	NONHSAT125632
2	lnc-CDCA2-1	chr8:25544025-25545018	NONHSAT125632
3	lnc-CDCA2-10	chr8:25584729-25585119	l_3566_chr8:25584060-25601195_testes
4	lnc-CDCA2-1	chr8:25543314-25543428	ENSG00000253100
5	lnc-CDCA2-1	chr8:25544025-25545040	ENSG00000253100
6	lnc-CDCA2-10	chr8:25584061-25584117	l_3566_chr8:25584060-25601195_testes
7	lnc-CDCA2-1	chr8:25528155-25528200	NONHSAT125632

No data

Variant related genes	Relation type
ENSG00000253100	TF binding region
ENSG00000253100	CpG island
ENSG00000179397	chromatin interactions

Extended variants
information (count: 2233 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:2233 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17054083	chr8:25499467-25499468	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376910924	chr8:25499508-25499509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573589177	chr8:25499513-25499514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372613429	chr8:25499524-25499525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535246389	chr8:25499661-25499662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114170349	chr8:25499701-25499702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190031689	chr8:25499705-25499706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371615733	chr8:25499735-25499736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146288302	chr8:25499753-25499754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375885750	chr8:25499764-25499765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541174759	chr8:25499774-25499775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368872881	chr8:25499822-25499823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552817304	chr8:25499853-25499854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181285012	chr8:25499901-25499902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2433072	chr8:25499909-25499910	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs545523749	chr8:25499914-25499915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563249292	chr8:25499925-25499926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557452792	chr8:25499947-25499948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373444570	chr8:25499967-25499968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184280460	chr8:25500012-25500013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562364878	chr8:25500040-25500041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575750359	chr8:25500060-25500061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139039462	chr8:25500087-25500088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141621196	chr8:25500119-25500120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566056911	chr8:25500134-25500135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147066686	chr8:25500139-25500140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551409680	chr8:25500140-25500141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189225612	chr8:25500146-25500147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528387781	chr8:25500204-25500205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530483785	chr8:25500232-25500233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537008446	chr8:25500236-25500237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111292262	chr8:25500240-25500241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4428678	chr8:25500252-25500253	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs4617162	chr8:25500274-25500275	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs181786090	chr8:25500301-25500302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577839061	chr8:25500329-25500330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138236821	chr8:25500342-25500343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538683919	chr8:25500348-25500349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149608731	chr8:25500365-25500366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186368743	chr8:25500397-25500398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542597918	chr8:25500462-25500463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562265951	chr8:25500469-25500470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188867988	chr8:25500506-25500507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574241109	chr8:25500609-25500610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181684424	chr8:25500700-25500701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529159599	chr8:25500711-25500712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74541990	chr8:25500762-25500763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76251414	chr8:25500790-25500791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556816892	chr8:25500801-25500802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2467726	chr8:25500860-25500861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	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
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	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
Colorectal cancer	16272173	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
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Breast cancer	20409316	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Gastric adenocarcinoma	19115996	CNVD
Breast cancer	21806811	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	19363497	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD

Chromatin state (count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:25489000-25501400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:25490200-25501600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr8:25494800-25501800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:25500600-25501200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr8:25501400-25501600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr8:25501400-25503600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr8:25501400-25503600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr8:25501600-25502200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr8:25501600-25503600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr8:25501600-25503600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr8:25501600-25503600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr8:25501600-25503600	Enhancers	Fetal Kidney	kidney
13	chr8:25501600-25504000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr8:25501800-25502600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:25501800-25503200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:25501800-25503400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr8:25501800-25503600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr8:25502000-25502200	Enhancers	NHDF-Ad	bronchial
19	chr8:25502000-25503400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:25502200-25502400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:25502200-25503400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr8:25502200-25503600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr8:25502600-25503200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:25502800-25503600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:25502800-25503600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:25503000-25503200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr8:25503000-25503600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr8:25503200-25503400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:25503200-25503600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr8:25503200-25503600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
31	chr8:25503600-25503800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr8:25511200-25511600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr8:25511600-25511800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:25517800-25518400	Enhancers	Lung	lung
35	chr8:25518000-25518400	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr8:25518000-25518400	Active TSS	H9 Cell Line	embryonic stem cell
37	chr8:25518000-25518400	Active TSS	A549	lung
38	chr8:25518200-25518600	Active TSS	K562	blood
39	chr8:25518200-25518800	Enhancers	NHEK	skin
40	chr8:25518400-25518600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr8:25523000-25523400	Active TSS	Gastric	stomach
42	chr8:25527800-25528200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr8:25527800-25528400	Enhancers	Placenta	Placenta
44	chr8:25528000-25528600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:25528200-25528400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
46	chr8:25528200-25528400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
47	chr8:25528200-25528400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr8:25528200-25528600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr8:25528400-25528600	Enhancers	Brain Germinal Matrix	brain
50	chr8:25528600-25528800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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