Variant report

Variant	nsv497805
Chromosome Location	chr8:107852509-108368371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2989)
CpG islands
(count:1220)
Chromatin interactive
region (count:178)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2989 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:108356444-108357357	K562	blood:	n/a	n/a
2	ARID3A	chr8:108327268-108328057	K562	blood:	n/a	n/a
3	ARID3A	chr8:108335073-108335222	K562	blood:	n/a	n/a
4	ARID3A	chr8:108307010-108307086	K562	blood:	n/a	n/a
5	ARID3A	chr8:108128388-108129306	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:108322085-108323462	K562	blood:	n/a	chr8:108322161-108322177
7	ARID3A	chr8:108333818-108334046	K562	blood:	n/a	n/a
8	ARID3A	chr8:108348924-108349468	K562	blood:	n/a	n/a
9	ARID3A	chr8:108346555-108347811	K562	blood:	n/a	n/a
10	ARID3A	chr8:108299697-108300171	K562	blood:	n/a	n/a
11	ARID3A	chr8:108337533-108337702	K562	blood:	n/a	n/a
12	ARID3A	chr8:108317027-108317777	K562	blood:	n/a	n/a
13	ATF1	chr8:108299729-108300273	K562	blood:	n/a	n/a
14	ATF1	chr8:108220761-108220901	K562	blood:	n/a	n/a
15	ATF1	chr8:108203175-108203176	K562	blood:	n/a	n/a
16	ATF1	chr8:107944698-107944731	K562	blood:	n/a	n/a
17	ATF1	chr8:108336368-108336835	K562	blood:	n/a	n/a
18	ATF1	chr8:108335129-108335332	K562	blood:	n/a	n/a
19	ATF1	chr8:108130183-108130443	K562	blood:	n/a	n/a
20	ATF1	chr8:108155224-108155260	K562	blood:	n/a	n/a
21	ATF1	chr8:108356405-108356784	K562	blood:	n/a	n/a
22	ATF1	chr8:107991251-107991436	K562	blood:	n/a	n/a
23	ATF1	chr8:108160223-108160605	K562	blood:	n/a	n/a
24	ATF1	chr8:108190858-108190862	K562	blood:	n/a	n/a
25	ATF1	chr8:108327332-108327831	K562	blood:	n/a	n/a
26	ATF1	chr8:108184522-108184787	K562	blood:	n/a	n/a
27	ATF1	chr8:108318725-108318911	K562	blood:	n/a	n/a
28	ATF1	chr8:108294452-108294537	K562	blood:	n/a	n/a
29	ATF1	chr8:108343912-108344454	K562	blood:	n/a	n/a
30	ATF1	chr8:107970799-107971055	K562	blood:	n/a	n/a
31	ATF1	chr8:108322486-108323333	K562	blood:	n/a	n/a
32	ATF1	chr8:108317326-108317759	K562	blood:	n/a	n/a
33	ATF1	chr8:108227519-108227917	K562	blood:	n/a	n/a
34	ATF1	chr8:108319459-108319785	K562	blood:	n/a	n/a
35	ATF1	chr8:108300549-108300640	K562	blood:	n/a	n/a
36	ATF1	chr8:108080937-108081234	K562	blood:	n/a	n/a
37	ATF2	chr8:107869938-107870367	GM12878	blood:	n/a	n/a
38	ATF3	chr8:107869846-107870396	A549	lung:	n/a	chr8:107870180-107870190 chr8:107870177-107870190 chr8:107870180-107870190 chr8:107870177-107870187 chr8:107870178-107870191 chr8:107870180-107870188 chr8:107870180-107870187 chr8:107870179-107870187 chr8:107870178-107870189 chr8:107870176-107870191 chr8:107870178-107870189
39	ATF3	chr8:108152827-108153465	A549	lung:	n/a	n/a
40	ATF3	chr8:108322410-108322926	K562	blood:	n/a	n/a
41	ATF3	chr8:107875898-107876687	A549	lung:	n/a	n/a
42	ATF3	chr8:107875874-107876817	A549	lung:	n/a	n/a
43	ATF3	chr8:108128397-108129326	A549	lung:	n/a	n/a
44	ATF3	chr8:107869820-107870425	A549	lung:	n/a	chr8:107870180-107870190 chr8:107870177-107870190 chr8:107870180-107870190 chr8:107870177-107870187 chr8:107870178-107870191 chr8:107870180-107870188 chr8:107870180-107870187 chr8:107870179-107870187 chr8:107870178-107870189 chr8:107870176-107870191 chr8:107870178-107870189
45	ATF3	chr8:108128510-108129327	A549	lung:	n/a	n/a
46	BACH1	chr8:108299333-108299369	K562	blood:	n/a	n/a
47	BACH1	chr8:108361212-108361266	K562	blood:	n/a	n/a
48	BACH1	chr8:108184808-108184812	K562	blood:	n/a	n/a
49	BACH1	chr8:108117123-108117620	K562	blood:	n/a	n/a
50	BACH1	chr8:107891138-107891321	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:107937633-107937683	U87	brain:	n/a
2	chr8:108163998-108164048	HepG2	liver:	n/a
3	chr8:108253163-108253213	HepG2	liver:	n/a
4	chr8:108263868-108263918	HepG2	liver:	n/a
5	chr8:107937633-107937683	RPTEC	kidney:	n/a
6	chr8:108208344-108208394	K562	blood:	n/a
7	chr8:108314948-108314998	Caco-2	colon:	n/a
8	chr8:108298379-108298429	GM06990	blood:	n/a
9	chr8:108253163-108253213	HRCEpiC	kidney:	n/a
10	chr8:108208344-108208394	HepG2	liver:	n/a
11	chr8:108314948-108314998	SK-N-SH_RA	brain:	n/a
12	chr8:107890251-107890301	H1-hESC	embryonic stem cell:	embryo
13	chr8:108238734-108238784	Hela-S3	cervix:	n/a
14	chr8:108344200-108344250	A549	lung:	n/a
15	chr8:107876626-107876676	HCF	heart:	n/a
16	chr8:107937633-107937683	SK-N-SH_RA	brain:	n/a
17	chr8:108298379-108298429	HRE	kidney:	n/a
18	chr8:108239870-108239920	LNCaP	prostate:	n/a
19	chr8:108238734-108238784	SAEC	small airway:	n/a
20	chr8:107994813-107994863	ProgFib	skin:	n/a
21	chr8:108263868-108263918	U87	brain:	n/a
22	chr8:107937633-107937683	ECC-1	luminal epithelium:	n/a
23	chr8:108359437-108359487	PANC-1	pancreas:	n/a
24	chr8:108253163-108253213	SK-N-SH	brain:	n/a
25	chr8:108163998-108164048	LNCaP	prostate:	n/a
26	chr8:108359437-108359487	HAEpiC	amniotic membrane:	n/a
27	chr8:108314948-108314998	NHBE	bronchial:	n/a
28	chr8:108263868-108263918	PANC-1	pancreas:	n/a
29	chr8:107937633-107937683	GM12878	blood:	n/a
30	chr8:108314948-108314998	HEEpiC	esophagus:	n/a
31	chr8:107937633-107937683	AG04449	skin:	fetal
32	chr8:108208344-108208394	HCF	heart:	n/a
33	chr8:107937633-107937683	MCF10A-Er-Src	breast:	n/a
34	chr8:108298379-108298429	ovcar-3	ovarian:	n/a
35	chr8:108344200-108344250	NHDF-neo	bronchial:	n/a
36	chr8:108208344-108208394	HNPCEpiC	eye:	n/a
37	chr8:108263868-108263918	PrEC	prostate:	n/a
38	chr8:108080760-108080810	GM12892	blood:	n/a
39	chr8:108239870-108239920	SK-N-MC	brain:	n/a
40	chr8:108344200-108344250	U87	brain:	n/a
41	chr8:107994813-107994863	NHDF-neo	bronchial:	n/a
42	chr8:108253163-108253213	SKMC	muscle:	n/a
43	chr8:108344200-108344250	HAEpiC	amniotic membrane:	n/a
44	chr8:108351562-108351612	GM12891	blood:	n/a
45	chr8:108298379-108298429	HNPCEpiC	eye:	n/a
46	chr8:108344200-108344250	HepG2	liver:	n/a
47	chr8:107870405-107870455	NT2-D1	testis:	n/a
48	chr8:108080760-108080810	K562	blood:	n/a
49	chr8:108359437-108359487	GM12878	blood:	n/a
50	chr8:108208344-108208394	GM12892	blood:	n/a

(count:178 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:108092379..108094443-chr8:108095250..108098096,2	K562	blood:
2	chr8:108320818..108322841-chr8:108505986..108508104,2	K562	blood:
3	chr8:108305763..108308421-chr8:108312233..108314682,3	K562	blood:
4	chr8:108310092..108312826-chr8:108342773..108344986,2	K562	blood:
5	chr8:108325638..108328700-chr8:108330925..108333725,3	K562	blood:
6	chr8:107857946..107858782-chr8:107868419..107869393,13	MCF-7	breast:
7	chr8:108323023..108324851-chr8:108334237..108336849,2	K562	blood:
8	chr8:108237961..108240814-chr8:108249385..108251392,2	K562	blood:
9	chr8:108230563..108232066-chr8:108238210..108240412,2	K562	blood:
10	chr8:107963274..107965164-chr8:107984156..107985885,2	K562	blood:
11	chr8:108349228..108351182-chr8:108352238..108354935,4	K562	blood:
12	chr8:108306316..108309008-chr8:108341130..108342850,2	K562	blood:
13	chr8:108111006..108113191-chr8:108114985..108117519,3	K562	blood:
14	chr8:108230563..108232066-chr8:108238210..108240412,2	K562	blood:
15	chr8:108046046..108048588-chr8:108049288..108050905,2	K562	blood:
16	chr8:108270297..108272923-chr8:108276260..108278146,2	K562	blood:
17	chr8:108311610..108313878-chr8:108319645..108322310,2	MCF-7	breast:
18	chr8:108325638..108328700-chr8:108330925..108333725,3	K562	blood:
19	chr8:107858296..107858832-chr8:107965934..107966511,2	MCF-7	breast:
20	chr8:108092379..108094443-chr8:108095250..108098096,2	K562	blood:
21	chr8:108349228..108350761-chr8:108352462..108354445,2	K562	blood:
22	chr8:107716793..107717867-chr8:107868568..107869413,5	MCF-7	breast:
23	chr8:107857830..107858766-chr8:107868427..107868948,2	MCF-7	breast:
24	chr8:107777209..107777910-chr8:107857636..107858793,3	MCF-7	breast:
25	chr8:107716434..107716966-chr8:107858248..107858913,2	MCF-7	breast:
26	chr8:108176802..108179290-chr8:108180812..108182744,2	K562	blood:
27	chr8:108290769..108291357-chr8:108544407..108545088,2	MCF-7	breast:
28	chr8:108304086..108305949-chr8:108321318..108324299,2	K562	blood:
29	chr8:108338212..108341049-chr8:108453971..108455686,2	K562	blood:
30	chr8:108242225..108244174-chr8:108244733..108247005,2	K562	blood:
31	chr8:108359440..108363202-chr8:108363264..108367284,4	K562	blood:
32	chr8:108320003..108323467-chr8:108344820..108346729,3	K562	blood:
33	chr8:108320769..108323724-chr8:108344479..108346213,2	K562	blood:
34	chr8:108154566..108158695-chr8:108159110..108161002,3	MCF-7	breast:
35	chr15:80292057..80292762-chr8:108158403..108159038,2	MCF-7	breast:
36	chr8:108267217..108269846-chr9:87536986..87539408,2	MCF-7	breast:
37	chr8:108295936..108300410-chr8:108304033..108310866,9	K562	blood:
38	chr8:108270297..108272923-chr8:108276260..108278146,2	K562	blood:
39	chr8:108346938..108349858-chr8:108355674..108360055,5	K562	blood:
40	chr20:52749860..52752197-chr8:108092484..108095332,2	MCF-7	breast:
41	chr8:108305763..108307455-chr8:108312597..108314682,2	K562	blood:
42	chr16:27438763..27439721-chr8:108270035..108270959,2	MCF-7	breast:
43	chr8:108304841..108306771-chr8:108325164..108328030,2	K562	blood:
44	chr8:108080620..108081304-chr8:108767705..108768455,2	K562	blood:
45	chr8:108353442..108355542-chr8:108360326..108364497,3	K562	blood:
46	chr8:108323328..108325135-chr8:108339439..108342402,2	MCF-7	breast:
47	chr8:108236936..108239830-chr8:108242541..108244471,2	K562	blood:
48	chr8:108305763..108307455-chr8:108312597..108314682,2	K562	blood:
49	chr8:108161198..108164148-chr8:108166546..108170354,3	K562	blood:
50	chr8:107948303..107950286-chr8:107953514..107955561,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT1-1	chr8:108184556-108184583	NONHSAT128258
2	lnc-ANGPT1-1	chr8:108178377-108178524	NONHSAT128258
3	lnc-ANGPT1-1	chr8:108178104-108178267	NONHSAT128258

No data

Variant related genes	Relation type
HMGB1P46	TF binding region
ENSG00000211995	TF binding region
ANGPT1	TF binding region
HMGB1P46	CpG island
ENSG00000211995	CpG island
ANGPT1	CpG island
ENSG00000183520	chromatin interactions
ENSG00000211995	chromatin interactions
ENSG00000104408	chromatin interactions
ENSG00000154188	chromatin interactions

Extended variants
information (count: 16718 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:16718 , 50 per page) page: 1 2 3 4 5 6 7 ... 335

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538428271	chr8:107852516-107852517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556724103	chr8:107852536-107852537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372696245	chr8:107852540-107852541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377005329	chr8:107852603-107852604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73702445	chr8:107852621-107852622	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs553840739	chr8:107852632-107852633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149127736	chr8:107852676-107852677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555110205	chr8:107852692-107852693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116005376	chr8:107852764-107852765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113594050	chr8:107852768-107852769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188710738	chr8:107852784-107852785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575866583	chr8:107852804-107852805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543189445	chr8:107852817-107852818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181226205	chr8:107852830-107852831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528945640	chr8:107852878-107852879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547375479	chr8:107852881-107852882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143239677	chr8:107852894-107852895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79043039	chr8:107852904-107852905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552940492	chr8:107852906-107852907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185429094	chr8:107852909-107852910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188229824	chr8:107852913-107852914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577053496	chr8:107852918-107852919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370842406	chr8:107852943-107852944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540997169	chr8:107852951-107852952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538465005	chr8:107852963-107852964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199740284	chr8:107852974-107852975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146835004	chr8:107852985-107852986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs67323194	chr8:107853016-107853017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs151009935	chr8:107853039-107853040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs57554448	chr8:107853066-107853067	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs180741314	chr8:107853080-107853081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2449840	chr8:107853092-107853093	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs111475738	chr8:107853112-107853113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112264605	chr8:107853128-107853129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539431879	chr8:107853138-107853139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557657116	chr8:107853174-107853175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575902323	chr8:107853175-107853176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543226125	chr8:107853220-107853221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146040255	chr8:107853240-107853241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573778552	chr8:107853268-107853269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187565238	chr8:107853277-107853278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559385432	chr8:107853307-107853308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191810670	chr8:107853320-107853321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544992953	chr8:107853323-107853324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564787177	chr8:107853328-107853329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138651582	chr8:107853352-107853353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141767512	chr8:107853387-107853388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200533851	chr8:107853388-107853389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568607484	chr8:107853396-107853397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529481062	chr8:107853420-107853421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2404 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107852000-107853600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr8:107852400-107865800	Weak transcription	NHDF-Ad	bronchial
3	chr8:107852600-107853000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr8:107863200-107863800	Enhancers	Primary T cells from cord blood	blood
5	chr8:107864200-107868400	Weak transcription	NHLF	lung
6	chr8:107865800-107866600	Enhancers	NHDF-Ad	bronchial
7	chr8:107866600-107868200	Weak transcription	NHDF-Ad	bronchial
8	chr8:107868200-107869800	Enhancers	NHDF-Ad	bronchial
9	chr8:107868400-107869600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr8:107868400-107869800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:107868400-107871200	Enhancers	NHLF	lung
12	chr8:107868600-107868800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr8:107868600-107869000	Enhancers	NHEK	skin
14	chr8:107868600-107869600	Enhancers	HSMMtube	muscle
15	chr8:107868600-107869800	Enhancers	A549	lung
16	chr8:107868600-107869800	Enhancers	NH-A	brain
17	chr8:107868600-107870200	Enhancers	HSMM	muscle
18	chr8:107868600-107870600	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr8:107868800-107869400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr8:107868800-107869800	Enhancers	Osteobl	bone
21	chr8:107868800-107870200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr8:107869000-107869400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr8:107869000-107869400	Weak transcription	NHEK	skin
24	chr8:107869000-107870200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr8:107869000-107871400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:107869400-107869800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr8:107869400-107869800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr8:107869400-107870000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr8:107869400-107870400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:107869400-107870600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr8:107869400-107870800	Enhancers	NHEK	skin
32	chr8:107869400-107871400	Enhancers	HMEC	breast
33	chr8:107869600-107870000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
34	chr8:107869600-107870000	Flanking Active TSS	HSMMtube	muscle
35	chr8:107869600-107870600	Enhancers	Aorta	Aorta
36	chr8:107869600-107870800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:107869600-107870800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:107869600-107870800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr8:107869600-107870800	Enhancers	Fetal Muscle Leg	muscle
40	chr8:107869800-107870000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr8:107869800-107870000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr8:107869800-107870000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr8:107869800-107870000	Flanking Active TSS	NHDF-Ad	bronchial
44	chr8:107869800-107870200	Enhancers	Fetal Kidney	kidney
45	chr8:107869800-107870400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:107869800-107870400	Enhancers	Adipose Nuclei	Adipose
47	chr8:107869800-107870600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr8:107869800-107870600	Enhancers	Colon Smooth Muscle	Colon
49	chr8:107869800-107870600	Flanking Active TSS	NH-A	brain
50	chr8:107869800-107870600	Flanking Active TSS	Osteobl	bone

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