Variant report

Variant	nsv539714
Chromosome Location	chr8:108224295-108466437
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1406)
CpG islands
(count:916)
Chromatin interactive
region (count:120)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:108307010-108307086	K562	blood:	n/a	n/a
2	ARID3A	chr8:108299697-108300171	K562	blood:	n/a	n/a
3	ARID3A	chr8:108317027-108317777	K562	blood:	n/a	n/a
4	ARID3A	chr8:108346555-108347811	K562	blood:	n/a	n/a
5	ARID3A	chr8:108335073-108335222	K562	blood:	n/a	n/a
6	ARID3A	chr8:108348924-108349468	K562	blood:	n/a	n/a
7	ARID3A	chr8:108333818-108334046	K562	blood:	n/a	n/a
8	ARID3A	chr8:108337533-108337702	K562	blood:	n/a	n/a
9	ARID3A	chr8:108327268-108328057	K562	blood:	n/a	n/a
10	ARID3A	chr8:108322085-108323462	K562	blood:	n/a	chr8:108322161-108322177
11	ARID3A	chr8:108356444-108357357	K562	blood:	n/a	n/a
12	ATF1	chr8:108385249-108385486	K562	blood:	n/a	n/a
13	ATF1	chr8:108300549-108300640	K562	blood:	n/a	n/a
14	ATF1	chr8:108327332-108327831	K562	blood:	n/a	n/a
15	ATF1	chr8:108299729-108300273	K562	blood:	n/a	n/a
16	ATF1	chr8:108448644-108449009	K562	blood:	n/a	n/a
17	ATF1	chr8:108438458-108438647	K562	blood:	n/a	n/a
18	ATF1	chr8:108319459-108319785	K562	blood:	n/a	n/a
19	ATF1	chr8:108428678-108428855	K562	blood:	n/a	n/a
20	ATF1	chr8:108460992-108461378	K562	blood:	n/a	n/a
21	ATF1	chr8:108335129-108335332	K562	blood:	n/a	n/a
22	ATF1	chr8:108227519-108227917	K562	blood:	n/a	n/a
23	ATF1	chr8:108459631-108459979	K562	blood:	n/a	n/a
24	ATF1	chr8:108322486-108323333	K562	blood:	n/a	n/a
25	ATF1	chr8:108294452-108294537	K562	blood:	n/a	n/a
26	ATF1	chr8:108317326-108317759	K562	blood:	n/a	n/a
27	ATF1	chr8:108318725-108318911	K562	blood:	n/a	n/a
28	ATF1	chr8:108403978-108404116	K562	blood:	n/a	n/a
29	ATF1	chr8:108417162-108417185	K562	blood:	n/a	n/a
30	ATF1	chr8:108336368-108336835	K562	blood:	n/a	n/a
31	ATF1	chr8:108376243-108376331	K562	blood:	n/a	n/a
32	ATF1	chr8:108427026-108427455	K562	blood:	n/a	n/a
33	ATF1	chr8:108356405-108356784	K562	blood:	n/a	n/a
34	ATF1	chr8:108395511-108395693	K562	blood:	n/a	n/a
35	ATF1	chr8:108343912-108344454	K562	blood:	n/a	n/a
36	ATF2	chr8:108456935-108457376	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF3	chr8:108322410-108322926	K562	blood:	n/a	n/a
38	BACH1	chr8:108299333-108299369	K562	blood:	n/a	n/a
39	BACH1	chr8:108457047-108457419	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr8:108452759-108452762	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr8:108361212-108361266	K562	blood:	n/a	n/a
42	BATF	chr8:108365875-108366174	GM12878	blood:	n/a	chr8:108366037-108366048 chr8:108366038-108366048 chr8:108366034-108366044
43	BCLAF1	chr8:108322500-108323004	K562	blood:	n/a	n/a
44	BCLAF1	chr8:108322422-108323013	K562	blood:	n/a	n/a
45	BHLHE40	chr8:108227598-108227877	K562	blood:	n/a	n/a
46	BHLHE40	chr8:108343892-108344235	K562	blood:	n/a	n/a
47	BHLHE40	chr8:108365936-108366101	GM12878	blood:	n/a	n/a
48	BHLHE40	chr8:108344695-108344719	K562	blood:	n/a	n/a
49	BHLHE40	chr8:108322524-108323281	K562	blood:	n/a	n/a
50	BHLHE40	chr8:108347613-108347807	K562	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:108239870-108239920	K562	blood:	n/a
2	chr8:108239870-108239920	K562	blood:	n/a
3	chr8:108344200-108344250	PrEC	prostate:	n/a
4	chr8:108457411-108457461	SK-N-SH_RA	brain:	n/a
5	chr8:108441547-108441597	Hela-S3	cervix:	n/a
6	chr8:108401517-108401567	RPTEC	kidney:	n/a
7	chr8:108314948-108314998	SKMC	muscle:	n/a
8	chr8:108359437-108359487	BJ	skin:	n/a
9	chr8:108263868-108263918	ECC-1	luminal epithelium:	n/a
10	chr8:108432158-108432208	K562	blood:	n/a
11	chr8:108238734-108238784	AG10803	skin:	n/a
12	chr8:108238734-108238784	MCF-7	breast:	n/a
13	chr8:108441547-108441597	MCF-7	breast:	n/a
14	chr8:108351562-108351612	HAEpiC	amniotic membrane:	n/a
15	chr8:108298379-108298429	H1-hESC	embryonic stem cell:	embryo
16	chr8:108457411-108457461	PANC-1	pancreas:	n/a
17	chr8:108263868-108263918	AG04450	lung:	fetal
18	chr8:108351562-108351612	HCF	heart:	n/a
19	chr8:108344200-108344250	MCF-7	breast:	n/a
20	chr8:108298379-108298429	CMK	blood:	n/a
21	chr8:108314948-108314998	HEEpiC	esophagus:	n/a
22	chr8:108344200-108344250	GM12891	blood:	n/a
23	chr8:108401517-108401567	ovcar-3	ovarian:	n/a
24	chr8:108457411-108457461	MCF-7	breast:	n/a
25	chr8:108432158-108432208	BJ	skin:	n/a
26	chr8:108263868-108263918	HEEpiC	esophagus:	n/a
27	chr8:108238734-108238784	AoSMC	blood vessel:	n/a
28	chr8:108253163-108253213	LNCaP	prostate:	n/a
29	chr8:108351562-108351612	HMEC	breast:	n/a
30	chr8:108344200-108344250	K562	blood:	n/a
31	chr8:108393034-108393084	SKMC	muscle:	n/a
32	chr8:108359437-108359487	SK-N-MC	brain:	n/a
33	chr8:108441547-108441597	Jurkat	blood:	n/a
34	chr8:108314948-108314998	HAEpiC	amniotic membrane:	n/a
35	chr8:108253163-108253213	MCF-7	breast:	n/a
36	chr8:108239870-108239920	HUVEC	blood vessel:	n/a
37	chr8:108457411-108457461	HIPEpiC	eye:	n/a
38	chr8:108344200-108344250	RPTEC	kidney:	n/a
39	chr8:108298379-108298429	A549	lung:	n/a
40	chr8:108432158-108432208	HEEpiC	esophagus:	n/a
41	chr8:108441547-108441597	SKMC	muscle:	n/a
42	chr8:108401517-108401567	A549	lung:	n/a
43	chr8:108263868-108263918	RPTEC	kidney:	n/a
44	chr8:108239870-108239920	HEEpiC	esophagus:	n/a
45	chr8:108401517-108401567	HepG2	liver:	n/a
46	chr8:108314948-108314998	GM12878	blood:	n/a
47	chr8:108238734-108238784	PFSK-1	brain:	n/a
48	chr8:108441547-108441597	HEEpiC	esophagus:	n/a
49	chr8:108393034-108393084	HRPEpiC	eye:	n/a
50	chr8:108457411-108457461	IMR90	lung:	fetal

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:108277151..108279545-chr8:108305828..108308489,2	K562	blood:
2	chr8:108296299..108298566-chr8:108418407..108420457,2	K562	blood:
3	chr8:108305763..108307455-chr8:108312597..108314682,2	K562	blood:
4	chr8:108311610..108313878-chr8:108319645..108322310,2	MCF-7	breast:
5	chr8:108323328..108325135-chr8:108339439..108342402,2	MCF-7	breast:
6	chr8:108242225..108244174-chr8:108244733..108247005,2	K562	blood:
7	chr8:108419893..108422484-chr8:108427371..108429959,2	MCF-7	breast:
8	chr8:108310092..108312826-chr8:108342773..108344986,2	K562	blood:
9	chr8:108306316..108309008-chr8:108341130..108342850,2	K562	blood:
10	chr8:108323328..108325135-chr8:108339439..108342402,2	MCF-7	breast:
11	chr8:108398155..108399861-chr8:108402340..108405261,2	MCF-7	breast:
12	chr8:108327353..108329181-chr8:108342640..108344430,2	K562	blood:
13	chr8:108324753..108329300-chr8:108347441..108349729,6	K562	blood:
14	chr8:108353442..108355542-chr8:108360326..108364497,3	K562	blood:
15	chr8:108364652..108367113-chr8:108367728..108369614,2	K562	blood:
16	chr8:108242225..108244174-chr8:108244733..108247005,2	K562	blood:
17	chr8:108368066..108369728-chr8:108370980..108373315,2	K562	blood:
18	chr8:108327353..108329181-chr8:108342640..108344430,2	K562	blood:
19	chr8:108278229..108280437-chr8:108281922..108284571,2	K562	blood:
20	chr8:108230563..108232066-chr8:108238210..108240412,2	K562	blood:
21	chr8:108349228..108351182-chr8:108352238..108354935,4	K562	blood:
22	chr8:108325638..108328700-chr8:108330925..108333725,3	K562	blood:
23	chr8:108312705..108315142-chr8:108317270..108319695,2	MCF-7	breast:
24	chr8:108275649..108277512-chr8:108280010..108282429,2	K562	blood:
25	chr8:108349228..108350761-chr8:108352462..108354445,2	K562	blood:
26	chr8:108304210..108306382-chr8:108346732..108349257,2	K562	blood:
27	chr8:108323023..108324851-chr8:108334237..108336849,2	K562	blood:
28	chr8:108439594..108441286-chr8:108441699..108444192,2	K562	blood:
29	chr8:108220971..108223007-chr8:108226339..108229011,2	K562	blood:
30	chr8:108300911..108303354-chr8:108304518..108307945,3	K562	blood:
31	chr8:108453384..108454985-chr8:108455120..108456621,2	K562	blood:
32	chr8:108236936..108239830-chr8:108242541..108244471,2	K562	blood:
33	chr8:108320101..108322841-chr8:108505986..108508292,3	K562	blood:
34	chr8:108312705..108315142-chr8:108317270..108319695,2	MCF-7	breast:
35	chr8:108332354..108335105-chr8:108336203..108338362,2	K562	blood:
36	chr8:108282161..108284434-chr8:108289622..108291631,3	K562	blood:
37	chr8:108457328..108458028-chr8:108544558..108545071,2	MCF-7	breast:
38	chr8:108359440..108363202-chr8:108363264..108367284,4	K562	blood:
39	chr8:108419893..108422484-chr8:108427371..108429959,2	MCF-7	breast:
40	chr16:27438763..27439721-chr8:108270035..108270959,2	MCF-7	breast:
41	chr8:108230563..108232066-chr8:108238210..108240412,2	K562	blood:
42	chr8:108369396..108371453-chr8:108377363..108379660,2	K562	blood:
43	chr8:108320818..108322841-chr8:108505986..108508104,2	K562	blood:
44	chr8:108438018..108441094-chr8:108441728..108444192,3	K562	blood:
45	chr8:108296299..108298566-chr8:108418407..108420457,2	K562	blood:
46	chr8:108315162..108317666-chr8:108340503..108343303,2	K562	blood:
47	chr8:108349228..108351182-chr8:108352238..108354935,4	K562	blood:
48	chr8:108265967..108267545-chr8:108271069..108273603,2	K562	blood:
49	chr8:108297619..108300531-chr8:108300720..108302749,2	K562	blood:
50	chr8:108304086..108305949-chr8:108321318..108324299,2	K562	blood:

No data

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

Extended variants
information (count: 8832 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:8832 , 50 per page) page: 1 2 3 4 5 6 7 ... 177

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567268486	chr8:108224384-108224385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs192612625	chr8:108224484-108224485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73700035	chr8:108224485-108224486	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs17358910	chr8:108224488-108224489	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs546129298	chr8:108224541-108224542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556497963	chr8:108224568-108224569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200910631	chr8:108224584-108224585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558025664	chr8:108224603-108224604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576280724	chr8:108224609-108224610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543617664	chr8:108224681-108224682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs16875856	chr8:108224687-108224688	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs140416296	chr8:108224689-108224690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142681423	chr8:108224703-108224704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4305876	chr8:108224765-108224766	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs113513008	chr8:108224863-108224864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533349656	chr8:108224913-108224914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551755209	chr8:108224958-108224959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7006210	chr8:108224973-108224974	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs374482947	chr8:108225020-108225021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11396235	chr8:108225021-108225022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185540552	chr8:108225086-108225087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549221734	chr8:108225100-108225101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73700036	chr8:108225155-108225156	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs73700038	chr8:108225193-108225194	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs140144949	chr8:108225201-108225202	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576588393	chr8:108225216-108225217	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114817096	chr8:108225257-108225258	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545665302	chr8:108225258-108225259	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538249113	chr8:108225316-108225317	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556497604	chr8:108225317-108225318	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78787381	chr8:108225340-108225341	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34599548	chr8:108225386-108225387	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537317083	chr8:108225395-108225396	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565402440	chr8:108225405-108225406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555708801	chr8:108225415-108225416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574159757	chr8:108225537-108225538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527997976	chr8:108225554-108225555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546939672	chr8:108225598-108225599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559802929	chr8:108225627-108225628	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73700039	chr8:108225650-108225651	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs112922631	chr8:108225654-108225655	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115524836	chr8:108225668-108225669	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs151128955	chr8:108225729-108225730	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376530423	chr8:108225749-108225750	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190391821	chr8:108225751-108225752	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114555114	chr8:108225762-108225763	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181747164	chr8:108225828-108225829	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs139857630	chr8:108225845-108225846	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs149833908	chr8:108225946-108225947	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs75499579	chr8:108225963-108225964	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2317 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:108223000-108224800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:108223200-108225200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:108223800-108225000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:108224000-108224400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:108224000-108224400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:108224000-108224400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr8:108224000-108224800	Enhancers	Adipose Nuclei	Adipose
8	chr8:108224000-108225600	Weak transcription	Aorta	Aorta
9	chr8:108224800-108225000	Enhancers	Fetal Lung	lung
10	chr8:108224800-108225600	Weak transcription	Adipose Nuclei	Adipose
11	chr8:108225000-108225800	Weak transcription	Fetal Lung	lung
12	chr8:108225200-108225400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:108225400-108225600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:108225600-108226000	ZNF genes & repeats	Aorta	Aorta
15	chr8:108225600-108226200	ZNF genes & repeats	Adipose Nuclei	Adipose
16	chr8:108225600-108226400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:108225800-108226200	ZNF genes & repeats	Fetal Lung	lung
18	chr8:108226000-108227600	Weak transcription	Aorta	Aorta
19	chr8:108226200-108227200	Weak transcription	Fetal Lung	lung
20	chr8:108226200-108227600	Weak transcription	Adipose Nuclei	Adipose
21	chr8:108226400-108227400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:108226800-108228800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr8:108227000-108228000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr8:108227200-108228000	Enhancers	Fetal Lung	lung
25	chr8:108227200-108228000	Enhancers	K562	blood
26	chr8:108227200-108228600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:108227400-108227800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:108227400-108228000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr8:108227400-108228000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr8:108227400-108228400	Enhancers	NHDF-Ad	bronchial
31	chr8:108227600-108227800	Enhancers	Aorta	Aorta
32	chr8:108227600-108228000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr8:108227600-108228000	Enhancers	Adipose Nuclei	Adipose
34	chr8:108227600-108228000	Enhancers	Osteobl	bone
35	chr8:108227600-108228400	Enhancers	Fetal Kidney	kidney
36	chr8:108227800-108228000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:108227800-108228000	Enhancers	NHLF	lung
38	chr8:108227800-108228200	Enhancers	A549	lung
39	chr8:108227800-108276200	Weak transcription	Aorta	Aorta
40	chr8:108228000-108228800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:108228000-108233200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr8:108228000-108235200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr8:108228200-108230000	Weak transcription	A549	lung
44	chr8:108228400-108233200	Weak transcription	NHDF-Ad	bronchial
45	chr8:108228600-108233800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr8:108228800-108234000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr8:108230000-108230400	Enhancers	A549	lung
48	chr8:108230200-108234000	Weak transcription	NHLF	lung
49	chr8:108230400-108235200	Weak transcription	A549	lung
50	chr8:108231600-108232200	Enhancers	Monocytes-CD14+_RO01746	blood

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