Variant report

Variant	nsv817379
Chromosome Location	chr8:114338391-115011632
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2159)
CpG islands
(count:2690)
Chromatin interactive
region (count:46)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2159 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:114720963-114720970	K562	blood:	n/a	n/a
2	ATF1	chr8:114822095-114822305	K562	blood:	n/a	n/a
3	ATF1	chr8:114602201-114602508	K562	blood:	n/a	n/a
4	ATF2	chr8:114687413-114687961	GM12878	blood:	n/a	n/a
5	ATF2	chr8:114696927-114697818	GM12878	blood:	n/a	n/a
6	ATF2	chr8:114471062-114471408	GM12878	blood:	n/a	n/a
7	ATF2	chr8:114697164-114697813	GM12878	blood:	n/a	n/a
8	ATF2	chr8:114467086-114467688	GM12878	blood:	n/a	n/a
9	ATF2	chr8:114616410-114616887	GM12878	blood:	n/a	n/a
10	ATF2	chr8:114687470-114687947	GM12878	blood:	n/a	n/a
11	ATF2	chr8:114467167-114467695	GM12878	blood:	n/a	n/a
12	ATF2	chr8:114470955-114471450	GM12878	blood:	n/a	n/a
13	BACH1	chr8:114449187-114449193	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:114627036-114627067	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:114936321-114936398	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:114446826-114447369	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:114890099-114890104	K562	blood:	n/a	n/a
18	BACH1	chr8:114450116-114450235	K562	blood:	n/a	n/a
19	BACH1	chr8:114848077-114848163	K562	blood:	n/a	n/a
20	BACH1	chr8:114445876-114446024	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr8:114394599-114394673	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr8:114687598-114687903	GM12878	blood:	n/a	n/a
23	BATF	chr8:114467188-114467516	GM12878	blood:	n/a	chr8:114467347-114467358
24	BATF	chr8:114616476-114616789	GM12878	blood:	n/a	chr8:114616655-114616666
25	BATF	chr8:114471038-114471289	GM12878	blood:	n/a	n/a
26	BATF	chr8:114467187-114467469	GM12878	blood:	n/a	chr8:114467347-114467358
27	BATF	chr8:114558289-114558602	GM12878	blood:	n/a	chr8:114558418-114558429
28	BATF	chr8:114628233-114628445	GM12878	blood:	n/a	chr8:114628409-114628418
29	BATF	chr8:114697315-114697659	GM12878	blood:	n/a	n/a
30	BATF	chr8:114752604-114752779	GM12878	blood:	n/a	chr8:114752701-114752711 chr8:114752700-114752711 chr8:114752705-114752715
31	BATF	chr8:114557470-114557830	GM12878	blood:	n/a	n/a
32	BATF	chr8:114697001-114697705	GM12878	blood:	n/a	n/a
33	BATF	chr8:114616421-114616811	GM12878	blood:	n/a	chr8:114616655-114616666
34	BCL11A	chr8:114697247-114697780	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:114467236-114467485	GM12878	blood:	n/a	chr8:114467386-114467395
36	BCL11A	chr8:114628223-114628450	GM12878	blood:	n/a	n/a
37	BCL11A	chr8:114467146-114467583	GM12878	blood:	n/a	chr8:114467386-114467395
38	BCL11A	chr8:114697283-114697743	GM12878	blood:	n/a	n/a
39	BCL11A	chr8:114557482-114557775	GM12878	blood:	n/a	chr8:114557526-114557535
40	BCL11A	chr8:114558218-114558592	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:114664594-114664807	GM12878	blood:	n/a	chr8:114664679-114664688
42	BCL11A	chr8:114616465-114616808	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:114628249-114628426	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:114471051-114471373	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:114697011-114697230	GM12878	blood:	n/a	n/a
46	BCL11A	chr8:114557538-114557718	GM12878	blood:	n/a	n/a
47	BCL3	chr8:114616534-114616768	GM12878	blood:	n/a	n/a
48	BCLAF1	chr8:114697284-114697788	GM12878	blood:	n/a	n/a
49	BHLHE40	chr8:114449897-114450275	GM12878	blood:	n/a	n/a
50	BHLHE40	chr8:114449946-114450213	K562	blood:	n/a	n/a

(count:2690 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:114390877-114390927	Hela-S3	cervix:	n/a
2	chr8:114450579-114450629	MCF10A-Er-Src	breast:	n/a
3	chr8:114449011-114449061	AoSMC	blood vessel:	n/a
4	chr8:114447532-114447582	AoSMC	blood vessel:	n/a
5	chr8:114446439-114446489	SAEC	small airway:	n/a
6	chr8:114447871-114447921	HRPEpiC	eye:	n/a
7	chr8:114390877-114390927	Hela-S3	cervix:	n/a
8	chr8:114450579-114450629	MCF10A-Er-Src	breast:	n/a
9	chr8:114449011-114449061	AoSMC	blood vessel:	n/a
10	chr8:114447532-114447582	AoSMC	blood vessel:	n/a
11	chr8:114446439-114446489	SAEC	small airway:	n/a
12	chr8:114447871-114447921	HRPEpiC	eye:	n/a
13	chr8:114447346-114447396	BE2_C	brain:	n/a
14	chr8:114448721-114448771	Caco-2	colon:	n/a
15	chr8:114450347-114450397	HCT-116	colon:	n/a
16	chr8:114447532-114447582	SAEC	small airway:	n/a
17	chr8:114449272-114449322	HCT-116	colon:	n/a
18	chr8:114445084-114445134	HRPEpiC	eye:	n/a
19	chr8:114450347-114450397	GM12878	blood:	n/a
20	chr8:114444859-114444909	HEK293	kidney:	embryo
21	chr8:114446368-114446418	GM06990	blood:	n/a
22	chr8:114448721-114448771	MCF-7	breast:	n/a
23	chr8:114446282-114446332	HEEpiC	esophagus:	n/a
24	chr8:114450647-114450697	NHDF-neo	bronchial:	n/a
25	chr8:114450579-114450629	PANC-1	pancreas:	n/a
26	chr8:114896516-114896566	HEEpiC	esophagus:	n/a
27	chr8:114448665-114448715	GM12878	blood:	n/a
28	chr8:114449011-114449061	MCF10A-Er-Src	breast:	n/a
29	chr8:114447871-114447921	K562	blood:	n/a
30	chr8:114447871-114447921	HepG2	liver:	n/a
31	chr8:114444859-114444909	SK-N-MC	brain:	n/a
32	chr8:114449272-114449322	HRPEpiC	eye:	n/a
33	chr8:114389168-114389218	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:114446282-114446332	K562	blood:	n/a
35	chr8:114449226-114449276	AoSMC	blood vessel:	n/a
36	chr8:114450579-114450629	SKMC	muscle:	n/a
37	chr8:114447346-114447396	SKMC	muscle:	n/a
38	chr8:114449272-114449322	K562	blood:	n/a
39	chr8:114445084-114445134	Jurkat	blood:	n/a
40	chr8:114389479-114389529	PrEC	prostate:	n/a
41	chr8:114446439-114446489	HPAEpiC	pulmonary alveolar:	n/a
42	chr8:114389388-114389438	ovcar-3	ovarian:	n/a
43	chr8:114449418-114449468	AG04449	skin:	fetal
44	chr8:114447871-114447921	SAEC	small airway:	n/a
45	chr8:114445779-114445829	SAEC	small airway:	n/a
46	chr8:114444395-114444445	HNPCEpiC	eye:	n/a
47	chr8:114896516-114896566	SK-N-MC	brain:	n/a
48	chr8:114440908-114440958	GM12878	blood:	n/a
49	chr8:114445580-114445630	RPTEC	kidney:	n/a
50	chr8:114389479-114389529	HMEC	breast:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:114351216..114352805-chr8:114354250..114356486,2	MCF-7	breast:
2	chr8:114728056..114730786-chr8:114735490..114737141,2	MCF-7	breast:
3	chr8:114728056..114730786-chr8:114735490..114737141,2	MCF-7	breast:
4	chr8:114478442..114479179-chr8:115103168..115103714,3	MCF-7	breast:
5	chr8:114214112..114215316-chr8:114390224..114391492,6	MCF-7	breast:
6	chr8:114351216..114352805-chr8:114354250..114356486,2	MCF-7	breast:
7	chr7:150045798..150047502-chr8:114590956..114592459,2	MCF-7	breast:
8	chr8:114404848..114406539-chr8:114407896..114409695,2	K562	blood:
9	chr8:114189275..114190202-chr8:114449887..114450479,2	MCF-7	breast:
10	chr8:114441726..114443315-chr8:114445051..114447307,2	K562	blood:
11	chr20:52209488..52211712-chr8:114454464..114457142,2	MCF-7	breast:
12	chr8:114612946..114615304-chr8:114616262..114619018,2	K562	blood:
13	chr8:113774024..113774627-chr8:114390471..114391174,2	MCF-7	breast:
14	chr8:114666240..114668992-chr8:114678548..114680585,2	K562	blood:
15	chr8:114547467..114549500-chr8:114550748..114552358,2	MCF-7	breast:
16	chr8:114854128..114856443-chr8:114857146..114858735,2	MCF-7	breast:
17	chr8:114816422..114818283-chr8:114819579..114821682,2	K562	blood:
18	chr8:114674540..114677133-chr8:114678204..114681093,2	MCF-7	breast:
19	chr8:113476778..113477604-chr8:114449777..114450474,2	MCF-7	breast:
20	chr8:114541168..114543113-chr8:114544856..114546688,2	K562	blood:
21	chr8:114726767..114728382-chr8:114731029..114732643,2	K562	blood:
22	chr8:113774045..113774707-chr8:114449888..114450422,3	MCF-7	breast:
23	chr8:114726767..114728382-chr8:114731029..114732643,2	K562	blood:
24	chr8:114384438..114385053-chr8:114992865..114993457,2	MCF-7	breast:
25	chr8:113812991..113814473-chr8:114449636..114450437,5	MCF-7	breast:
26	chr8:114674540..114677133-chr8:114678204..114681093,2	MCF-7	breast:
27	chr6:55668603..55669259-chr8:114927462..114928176,2	MCF-7	breast:
28	chr8:112976625..112977471-chr8:114449676..114450374,2	MCF-7	breast:
29	chr8:114441726..114443315-chr8:114445051..114447307,2	K562	blood:
30	chr8:114435797..114438781-chr8:114443874..114445936,2	K562	blood:
31	chr8:114404848..114406539-chr8:114407896..114409695,2	K562	blood:
32	chr8:114384438..114385053-chr8:114992865..114993457,2	MCF-7	breast:
33	chr8:114541168..114543113-chr8:114544856..114546688,2	K562	blood:
34	chr8:114612946..114615304-chr8:114616262..114619018,2	K562	blood:
35	chr8:114547467..114549500-chr8:114550748..114552358,2	MCF-7	breast:
36	chr8:114823206..114825087-chr8:114825819..114828055,2	MCF-7	breast:
37	chr8:114966861..114968820-chr8:114970401..114973108,2	MCF-7	breast:
38	chr8:114966861..114968820-chr8:114970401..114973108,2	MCF-7	breast:
39	chr8:114666240..114668992-chr8:114678548..114680585,2	K562	blood:
40	chr8:114189402..114189999-chr8:114390956..114391473,2	MCF-7	breast:
41	chr8:114343342..114345070-chr8:114363394..114366144,2	MCF-7	breast:
42	chr8:114435797..114438781-chr8:114443874..114445936,2	K562	blood:
43	chr8:114816422..114818283-chr8:114819579..114821682,2	K562	blood:
44	chr8:114854128..114856443-chr8:114857146..114858735,2	MCF-7	breast:
45	chr8:114823206..114825087-chr8:114825819..114828055,2	MCF-7	breast:
46	chr8:114343342..114345070-chr8:114363394..114366144,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-67H2.1.1-4	chr8:114444770-114445524	NONHSAT128347
2	lnc-RP11-67H2.1.1-4	chr8:114444502-114444655	NONHSAT128347
3	lnc-TRPS1-4	chr8:114448906-114449019	NONHSAT128345

No data

Variant related genes	Relation type
CSMD3	TF binding region
ENSG00000227514	TF binding region
ENSG00000206719	TF binding region
ENSG00000253207	TF binding region
ENSG00000221610	TF binding region
CSMD3	CpG island
ENSG00000227514	CpG island
ENSG00000206719	CpG island
ENSG00000253207	CpG island
ENSG00000221610	CpG island
ENSG00000171940	chromatin interactions

Extended variants
information (count: 6436 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:6436 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187566997	chr8:114362202-114362203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs199595848	chr8:114362207-114362208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569032978	chr8:114362235-114362236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531075870	chr8:114362294-114362295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs58426306	chr8:114362376-114362377	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs544959170	chr8:114362413-114362414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551673440	chr8:114362414-114362415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148623952	chr8:114362449-114362450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376943933	chr8:114362472-114362473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115288306	chr8:114362475-114362476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141199010	chr8:114362490-114362491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538782367	chr8:114362503-114362504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190507543	chr8:114362531-114362532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557920049	chr8:114362538-114362539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575720761	chr8:114362550-114362551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538093961	chr8:114362568-114362569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35194520	chr8:114362593-114362594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6997630	chr8:114362600-114362601	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs571397636	chr8:114362632-114362633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182983840	chr8:114362648-114362649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574685749	chr8:114362677-114362678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186210663	chr8:114362773-114362774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190241494	chr8:114362777-114362778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183437810	chr8:114362805-114362806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573558856	chr8:114362832-114362833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545596195	chr8:114362864-114362865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371171440	chr8:114362936-114362937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540965412	chr8:114362943-114362944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562102720	chr8:114362944-114362945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562266580	chr8:114363031-114363032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553791490	chr8:114363064-114363065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187450778	chr8:114363066-114363067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150747308	chr8:114363077-114363078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192715187	chr8:114363123-114363124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368312645	chr8:114363162-114363163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139121485	chr8:114363179-114363180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75727049	chr8:114363201-114363202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76006469	chr8:114363202-114363203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547147896	chr8:114363226-114363227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4369017	chr8:114363286-114363287	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs183720121	chr8:114363303-114363304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552709516	chr8:114363322-114363323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145255852	chr8:114363334-114363335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11780684	chr8:114363337-114363338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1382469	chr8:114363347-114363348	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs187810593	chr8:114363422-114363423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4433179	chr8:114363434-114363435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs147209434	chr8:114363440-114363441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553896605	chr8:114363451-114363452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374321086	chr8:114363488-114363489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
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
Glioblastoma multiforme	21080181	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
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Schizophrenia	20967226	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:114362200-114363400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:114363400-114365200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:114365200-114366000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:114365400-114365800	Enhancers	Brain Germinal Matrix	brain
5	chr8:114386400-114387000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:114390400-114391000	Active TSS	Brain Angular Gyrus	brain
7	chr8:114390400-114391000	Active TSS	Brain Inferior Temporal Lobe	brain
8	chr8:114390400-114391000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
9	chr8:114390400-114391200	Active TSS	Brain Anterior Caudate	brain
10	chr8:114390400-114391200	Active TSS	Brain Substantia Nigra	brain
11	chr8:114390800-114391000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr8:114390800-114391000	Enhancers	Pancreas	Pancrea
13	chr8:114390800-114391000	Enhancers	Hela-S3	cervix
14	chr8:114391000-114391200	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr8:114391000-114391200	Enhancers	Fetal Lung	lung
16	chr8:114391200-114391400	Enhancers	Brain Anterior Caudate	brain
17	chr8:114391200-114392800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr8:114391400-114391800	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr8:114392000-114392200	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr8:114392000-114393000	Enhancers	Fetal Brain Female	brain
21	chr8:114392200-114392600	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr8:114392800-114393200	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr8:114393000-114393200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr8:114393200-114398800	Weak transcription	Fetal Lung	lung
25	chr8:114398800-114399000	Enhancers	Fetal Lung	lung
26	chr8:114399000-114399600	Weak transcription	Fetal Lung	lung
27	chr8:114399600-114399800	Enhancers	Fetal Lung	lung
28	chr8:114399800-114415000	Weak transcription	Fetal Lung	lung
29	chr8:114415000-114418400	Enhancers	Fetal Lung	lung
30	chr8:114424400-114424600	Enhancers	Fetal Lung	lung
31	chr8:114424600-114425600	Weak transcription	Fetal Lung	lung
32	chr8:114425600-114425800	Enhancers	Fetal Lung	lung
33	chr8:114430600-114430800	Enhancers	Brain Substantia Nigra	brain
34	chr8:114430800-114431000	Enhancers	Brain Anterior Caudate	brain
35	chr8:114430800-114433400	Weak transcription	Brain Substantia Nigra	brain
36	chr8:114431000-114431200	Enhancers	Brain Hippocampus Middle	brain
37	chr8:114431000-114434600	Weak transcription	Brain Anterior Caudate	brain
38	chr8:114433400-114433600	Enhancers	Brain Hippocampus Middle	brain
39	chr8:114433400-114433600	Enhancers	Brain Substantia Nigra	brain
40	chr8:114433400-114434000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:114433600-114434400	Weak transcription	Brain Substantia Nigra	brain
42	chr8:114433600-114435800	Weak transcription	Brain Hippocampus Middle	brain
43	chr8:114433800-114434000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr8:114434000-114434200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:114434000-114434800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:114434000-114434800	Enhancers	Hela-S3	cervix
47	chr8:114434200-114434400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr8:114434400-114434800	Enhancers	Brain Substantia Nigra	brain
49	chr8:114434400-114435000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:114434400-114435200	Enhancers	HUES6 Cell Line	embryonic stem cell

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