Variant report

Variant	nsv891312
Chromosome Location	chr8:112111911-112238390
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:513)
CpG islands
(count:62)
Chromatin interactive
region (count:37)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:112132480-112132510	K562	blood:	n/a	n/a
2	ATF1	chr8:112198523-112198679	K562	blood:	n/a	n/a
3	ATF2	chr8:112162891-112163440	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:112162917-112163564	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:112212038-112212250	H1-hESC	embryonic stem cell:	n/a	chr8:112212195-112212209
6	BATF	chr8:112113181-112113447	GM12878	blood:	n/a	n/a
7	BCL11A	chr8:112162999-112163239	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr8:112162971-112163355	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr8:112113324-112113447	K562	blood:	n/a	n/a
10	BRCA1	chr8:112152605-112152831	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr8:112112808-112113129	K562	blood:	n/a	n/a
12	CEBPB	chr8:112152567-112153096	MCF-7	breast:	n/a	n/a
13	CEBPB	chr8:112199716-112199940	A549	lung:	n/a	n/a
14	CEBPB	chr8:112181017-112181272	HepG2	liver:	n/a	chr8:112181166-112181177
15	CEBPB	chr8:112152585-112152901	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:112149466-112149680	HepG2	liver:	n/a	chr8:112149616-112149627
17	CEBPB	chr8:112199683-112200014	HepG2	liver:	n/a	n/a
18	CREB1	chr8:112162994-112163540	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr8:112163049-112163325	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:112192053-112192105	MCF-7	breast:	n/a	n/a
21	CTCF	chr8:112112860-112113010	HMEC	breast:	n/a	n/a
22	CTCF	chr8:112152422-112152968	MCF-7	breast:	n/a	n/a
23	CTCF	chr8:112113156-112113271	GM20000	blood:	n/a	n/a
24	CTCF	chr8:112188876-112188920	GM10248	blood:	n/a	n/a
25	CTCF	chr8:112112817-112113120	MCF-7	breast:	n/a	n/a
26	CTCF	chr8:112152640-112152790	BE2_C	brain:	n/a	n/a
27	CTCF	chr8:112152611-112152788	GM13977	blood:	n/a	n/a
28	CTCF	chr8:112152473-112152873	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr8:112112900-112113050	NHEK	skin:	n/a	n/a
30	CTCF	chr8:112152620-112152770	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr8:112112580-112112730	SAEC	small airway:	n/a	n/a
32	CTCF	chr8:112112860-112113010	GM12872	blood:	n/a	n/a
33	CTCF	chr8:112112840-112112990	HCM	heart:	n/a	n/a
34	CTCF	chr8:112112840-112112990	HRE	kidney:	n/a	n/a
35	CTCF	chr8:112112789-112113076	A549	lung:	n/a	n/a
36	CTCF	chr8:112112881-112113050	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr8:112112819-112113155	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:112112908-112113012	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr8:112112900-112113050	K562	blood:	n/a	n/a
40	CTCF	chr8:112112838-112113097	Gliobla	brain:	n/a	n/a
41	CTCF	chr8:112152660-112152810	GM12864	blood:	n/a	n/a
42	CTCF	chr8:112112910-112113026	GM20000	blood:	n/a	n/a
43	CTCF	chr8:112167310-112167539	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr8:112112840-112112990	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr8:112112820-112112970	HepG2	liver:	n/a	n/a
46	CTCF	chr8:112152459-112152888	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr8:112167367-112167528	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:112112854-112113100	K562	blood:	n/a	n/a
49	CTCF	chr8:112112873-112113048	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr8:112152621-112152772	MCF-7	breast:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112163550-112163600	HAEpiC	amniotic membrane:	n/a
2	chr8:112163550-112163600	HAEpiC	amniotic membrane:	n/a
3	chr8:112163550-112163600	ProgFib	skin:	n/a
4	chr8:112163550-112163600	PFSK-1	brain:	n/a
5	chr8:112163550-112163600	SK-N-MC	brain:	n/a
6	chr8:112163550-112163600	AG04449	skin:	fetal
7	chr8:112163550-112163600	GM19239	blood:	n/a
8	chr8:112163550-112163600	NT2-D1	testis:	n/a
9	chr8:112163550-112163600	NHDF-neo	bronchial:	n/a
10	chr8:112163550-112163600	H1-hESC	embryonic stem cell:	embryo
11	chr8:112163550-112163600	AG09319	gingival:	n/a
12	chr8:112163550-112163600	SKMC	muscle:	n/a
13	chr8:112163550-112163600	HL-60	blood:	n/a
14	chr8:112163550-112163600	SK-N-SH	brain:	n/a
15	chr8:112163550-112163600	AG09309	skin:	n/a
16	chr8:112163550-112163600	T-47D	breast:	n/a
17	chr8:112163550-112163600	HCPEpiC	choroid plexus:	n/a
18	chr8:112163550-112163600	HNPCEpiC	eye:	n/a
19	chr8:112163550-112163600	MCF10A-Er-Src	breast:	n/a
20	chr8:112163550-112163600	NB4	blood:	n/a
21	chr8:112163550-112163600	SAEC	small airway:	n/a
22	chr8:112163550-112163600	NHBE	bronchial:	n/a
23	chr8:112163550-112163600	NH-A	brain:	n/a
24	chr8:112163550-112163600	SK-N-SH_RA	brain:	n/a
25	chr8:112163550-112163600	LNCaP	prostate:	n/a
26	chr8:112163550-112163600	CMK	blood:	n/a
27	chr8:112163550-112163600	Hela-S3	cervix:	n/a
28	chr8:112163550-112163600	HUVEC	blood vessel:	n/a
29	chr8:112163550-112163600	PANC-1	pancreas:	n/a
30	chr8:112163550-112163600	GM12878	blood:	n/a
31	chr8:112163550-112163600	HCM	heart:	n/a
32	chr8:112163550-112163600	BJ	skin:	n/a
33	chr8:112163550-112163600	HMEC	breast:	n/a
34	chr8:112163550-112163600	ovcar-3	ovarian:	n/a
35	chr8:112163550-112163600	HEEpiC	esophagus:	n/a
36	chr8:112163550-112163600	HCT-116	colon:	n/a
37	chr8:112163550-112163600	HIPEpiC	eye:	n/a
38	chr8:112163550-112163600	MCF-7	breast:	n/a
39	chr8:112163550-112163600	GM06990	blood:	n/a
40	chr8:112163550-112163600	IMR90	lung:	fetal
41	chr8:112163550-112163600	U87	brain:	n/a
42	chr8:112163550-112163600	GM12891	blood:	n/a
43	chr8:112163550-112163600	Jurkat	blood:	n/a
44	chr8:112163550-112163600	RPTEC	kidney:	n/a
45	chr8:112163550-112163600	AG04450	lung:	fetal
46	chr8:112163550-112163600	Caco-2	colon:	n/a
47	chr8:112163550-112163600	GM12892	blood:	n/a
48	chr8:112163550-112163600	HRE	kidney:	n/a
49	chr8:112163550-112163600	Hepatocyte	liver:	n/a
50	chr8:112163550-112163600	A549	lung:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:112154689..112157253-chr8:112157958..112160941,2	MCF-7	breast:
2	chr8:112127583..112130124-chr8:112133579..112135146,2	MCF-7	breast:
3	chr1:120421655..120422591-chr8:112129482..112130279,2	MCF-7	breast:
4	chr8:112188112..112190074-chr8:112196600..112198573,2	MCF-7	breast:
5	chr8:112151809..112153959-chr8:112263594..112266459,2	MCF-7	breast:
6	chr8:112121761..112124184-chr8:112126207..112129085,2	K562	blood:
7	chr8:112126432..112126980-chr8:112164515..112165028,2	MCF-7	breast:
8	chr8:112115345..112116966-chr8:112124670..112126786,2	MCF-7	breast:
9	chr8:112142087..112143993-chr8:112151164..112153566,2	MCF-7	breast:
10	chr8:112112298..112113981-chr8:112264995..112266040,10	MCF-7	breast:
11	chr8:112139232..112142043-chr8:112142133..112144046,2	MCF-7	breast:
12	chr8:112164287..112166378-chr8:112180703..112183075,2	MCF-7	breast:
13	chr8:112152245..112153161-chr8:112248220..112248923,2	MCF-7	breast:
14	chr8:112133641..112134299-chr9:13359583..13360482,2	MCF-7	breast:
15	chr8:112164287..112166378-chr8:112180703..112183075,2	MCF-7	breast:
16	chr8:112152279..112153092-chr8:121617588..121618297,2	MCF-7	breast:
17	chr8:112123114..112125207-chr8:112128541..112131451,2	K562	blood:
18	chr8:112166075..112166697-chr8:112248498..112249074,2	MCF-7	breast:
19	chr8:112121761..112124184-chr8:112126207..112129085,2	K562	blood:
20	chr8:112123114..112125207-chr8:112128541..112131451,2	K562	blood:
21	chr8:112152211..112153851-chr8:112248272..112249455,10	MCF-7	breast:
22	chr8:112115345..112116966-chr8:112124670..112126786,2	MCF-7	breast:
23	chr8:111877803..111878676-chr8:112126153..112126932,3	MCF-7	breast:
24	chr8:112210861..112213766-chr8:112215369..112218286,2	K562	blood:
25	chr8:112127583..112130124-chr8:112133579..112135146,2	MCF-7	breast:
26	chr8:112139232..112142043-chr8:112142133..112144046,2	MCF-7	breast:
27	chr8:112126432..112126980-chr8:112164515..112165028,2	MCF-7	breast:
28	chr8:112152351..112153276-chr8:112265083..112266006,7	MCF-7	breast:
29	chr8:112188112..112190074-chr8:112196600..112198573,2	MCF-7	breast:
30	chr8:112112573..112113471-chr8:121617637..121618420,2	MCF-7	breast:
31	chr8:112112155..112113418-chr8:112247960..112249178,7	MCF-7	breast:
32	chr8:112142087..112143993-chr8:112151164..112153566,2	MCF-7	breast:
33	chr8:112210861..112213766-chr8:112215369..112218286,2	K562	blood:
34	chr8:112113576..112114171-chr8:112248201..112249138,2	MCF-7	breast:
35	chr8:112154689..112157253-chr8:112157958..112160941,2	MCF-7	breast:
36	chr8:111877803..111878653-chr8:112126153..112126716,2	MCF-7	breast:
37	chr8:112152279..112153172-chr8:112264812..112266234,7	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSMD3-3	chr8:112128764-112128829	ENSG00000253103
2	lnc-CSMD3-2	chr8:112191422-112191587	ENSG00000253489
3	lnc-RP11-422N16.3.1-8	chr8:112237814-112238443	NONHSAT128324
4	lnc-CSMD3-2	chr8:112192077-112192101	ENSG00000253489
5	lnc-CSMD3-3	chr8:112195521-112195964	ENSG00000253103
6	lnc-RP11-422N16.3.1-7	chr8:112174769-112174905	l_3668_chr8:112174768-112194925_testes
7	lnc-CSMD3-3	chr8:112125661-112125749	ENSG00000253103
8	lnc-RP11-422N16.3.1-7	chr8:112194839-112194925	l_3668_chr8:112174768-112194925_testes

No data

Variant related genes	Relation type
ENSG00000253489	TF binding region
EEF1A1P37	TF binding region
ENSG00000253489	CpG island
EEF1A1P37	CpG island
ENSG00000253103	chromatin interactions

Extended variants
information (count: 1561 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1561 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144378531	chr8:112112192-112112193	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs10102552	chr8:112112222-112112223	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs545908917	chr8:112112251-112112252	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563694841	chr8:112112278-112112279	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs561754254	chr8:112112286-112112287	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368686519	chr8:112112312-112112313	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565085896	chr8:112112315-112112316	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs531734584	chr8:112112327-112112328	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs147018570	chr8:112112332-112112333	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527780011	chr8:112112429-112112430	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs530362178	chr8:112112451-112112452	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs548801398	chr8:112112457-112112458	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs570189177	chr8:112112544-112112545	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs138082073	chr8:112112565-112112566	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs573263738	chr8:112112569-112112570	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs571091651	chr8:112112627-112112628	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs532919753	chr8:112112647-112112648	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542562784	chr8:112112716-112112717	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs547960328	chr8:112112722-112112723	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575986605	chr8:112112763-112112764	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs149522232	chr8:112112796-112112797	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs28447600	chr8:112112804-112112805	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs549123388	chr8:112112822-112112823	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565845856	chr8:112112837-112112838	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs28547967	chr8:112112875-112112876	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs558012695	chr8:112112933-112112934	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375095587	chr8:112113014-112113015	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs577909251	chr8:112113037-112113038	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs189619122	chr8:112113049-112113050	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539813237	chr8:112113056-112113057	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs182693657	chr8:112113088-112113089	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576248668	chr8:112113128-112113129	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576030081	chr8:112113134-112113135	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs369664708	chr8:112113149-112113150	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs201532715	chr8:112113151-112113152	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187936872	chr8:112113160-112113161	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs561858955	chr8:112113164-112113165	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs80051107	chr8:112113185-112113186	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs143988204	chr8:112113238-112113239	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs564798107	chr8:112113264-112113265	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs148640394	chr8:112113295-112113296	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs193163039	chr8:112113320-112113321	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs141185524	chr8:112113359-112113360	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs10106508	chr8:112113384-112113385	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs58186156	chr8:112113581-112113582	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs200682647	chr8:112113587-112113588	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556856110	chr8:112113594-112113595	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs192406786	chr8:112113628-112113629	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs146189146	chr8:112113640-112113641	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs10106880	chr8:112113689-112113690	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	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
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
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	21163964	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112126000-112126800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:112126400-112126800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr8:112132600-112133000	Enhancers	Fetal Heart	heart
4	chr8:112133400-112134400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:112135800-112136600	Enhancers	Brain Hippocampus Middle	brain
6	chr8:112148400-112148800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
7	chr8:112148800-112149000	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr8:112152400-112153000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr8:112152400-112153000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr8:112152400-112153600	Enhancers	HMEC	breast
11	chr8:112152800-112153200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr8:112152800-112153200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr8:112152800-112153800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:112152800-112161800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:112153000-112159200	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr8:112153800-112155600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr8:112155600-112155800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:112155800-112156000	Enhancers	HMEC	breast
19	chr8:112159200-112161200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
20	chr8:112159800-112160800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
21	chr8:112160800-112161600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr8:112161200-112161400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr8:112161200-112164400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr8:112161200-112165200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr8:112161400-112162800	Enhancers	H1 Cell Line	embryonic stem cell
26	chr8:112161400-112163400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr8:112161400-112165200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr8:112161600-112162400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr8:112161800-112162600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr8:112162000-112164600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr8:112162400-112163000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr8:112162400-112165200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr8:112162600-112164000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:112162800-112164000	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr8:112163000-112163400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr8:112163200-112163400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:112163400-112163800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
38	chr8:112163400-112164200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr8:112163400-112164800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr8:112163800-112164800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr8:112164000-112164400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:112164000-112164800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr8:112164200-112164400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr8:112164200-112164800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr8:112164200-112165000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:112164400-112164800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr8:112164400-112164800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr8:112164400-112165200	Genic enhancers	H9 Cell Line	embryonic stem cell
49	chr8:112164800-112165200	Enhancers	HMEC	breast
50	chr8:112164800-112166000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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