Variant report

Variant	nsv831085
Chromosome Location	chr7:103140672-103342388
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1517)
CpG islands
(count:244)
Chromatin interactive
region (count:163)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1517 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:103213857-103214344	K562	blood:	n/a	n/a
2	ARID3A	chr7:103319899-103320230	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:103297830-103298390	K562	blood:	n/a	n/a
4	ARID3A	chr7:103331784-103332058	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:103301632-103301797	K562	blood:	n/a	n/a
6	ARID3A	chr7:103292475-103292581	K562	blood:	n/a	n/a
7	ARID3A	chr7:103213944-103214228	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:103254691-103255182	K562	blood:	n/a	n/a
9	ARID3A	chr7:103300589-103301706	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:103303101-103303301	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:103272498-103272859	K562	blood:	n/a	n/a
12	ARID3A	chr7:103298538-103298740	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:103300792-103301326	K562	blood:	n/a	n/a
14	ARID3A	chr7:103305068-103305251	K562	blood:	n/a	n/a
15	ARID3A	chr7:103254955-103255128	HepG2	liver:	n/a	n/a
16	ATF1	chr7:103181075-103181326	K562	blood:	n/a	n/a
17	ATF1	chr7:103254370-103255262	K562	blood:	n/a	n/a
18	ATF1	chr7:103297848-103298247	K562	blood:	n/a	n/a
19	ATF1	chr7:103270803-103271170	K562	blood:	n/a	n/a
20	ATF1	chr7:103272544-103272989	K562	blood:	n/a	n/a
21	ATF1	chr7:103301009-103301317	K562	blood:	n/a	n/a
22	ATF1	chr7:103229030-103229053	K562	blood:	n/a	n/a
23	ATF3	chr7:103254679-103254888	K562	blood:	n/a	n/a
24	ATF3	chr7:103270774-103271095	K562	blood:	n/a	n/a
25	ATF3	chr7:103300900-103301322	K562	blood:	n/a	n/a
26	ATF3	chr7:103297853-103298436	K562	blood:	n/a	n/a
27	BACH1	chr7:103272623-103272854	K562	blood:	n/a	n/a
28	BACH1	chr7:103169886-103170043	K562	blood:	n/a	n/a
29	BATF	chr7:103188327-103188616	GM12878	blood:	n/a	n/a
30	BATF	chr7:103188378-103188618	GM12878	blood:	n/a	n/a
31	BCLAF1	chr7:103297809-103298425	K562	blood:	n/a	n/a
32	BHLHE40	chr7:103164790-103165165	K562	blood:	n/a	n/a
33	BHLHE40	chr7:103177290-103177312	K562	blood:	n/a	n/a
34	BHLHE40	chr7:103298673-103298683	K562	blood:	n/a	n/a
35	BHLHE40	chr7:103297004-103297036	K562	blood:	n/a	n/a
36	BHLHE40	chr7:103300942-103301872	K562	blood:	n/a	n/a
37	BHLHE40	chr7:103215055-103215244	K562	blood:	n/a	chr7:103215193-103215202 chr7:103215194-103215203 chr7:103215187-103215208 chr7:103215191-103215204 chr7:103215192-103215201 chr7:103215193-103215202
38	BHLHE40	chr7:103300881-103301800	HepG2	liver:	n/a	n/a
39	BHLHE40	chr7:103300976-103301276	HepG2	liver:	n/a	n/a
40	BHLHE40	chr7:103254146-103254993	K562	blood:	n/a	n/a
41	BHLHE40	chr7:103298944-103299312	K562	blood:	n/a	n/a
42	BHLHE40	chr7:103297785-103298424	K562	blood:	n/a	n/a
43	BHLHE40	chr7:103213977-103214317	GM12878	blood:	n/a	n/a
44	BRCA1	chr7:103213969-103214313	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr7:103301680-103301812	GM12878	blood:	n/a	n/a
46	CBX3	chr7:103287263-103287578	K562	blood:	n/a	n/a
47	CBX3	chr7:103297810-103298390	K562	blood:	n/a	n/a
48	CBX3	chr7:103284757-103285106	K562	blood:	n/a	n/a
49	CBX3	chr7:103288018-103288455	K562	blood:	n/a	n/a
50	CBX3	chr7:103284768-103285082	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:103301932-103301982	HL-60	blood:	n/a
2	chr7:103260062-103260112	CMK	blood:	n/a
3	chr7:103210555-103210605	NHBE	bronchial:	n/a
4	chr7:103260062-103260112	PFSK-1	brain:	n/a
5	chr7:103279088-103279138	HCPEpiC	choroid plexus:	n/a
6	chr7:103210555-103210605	AG04450	lung:	fetal
7	chr7:103279088-103279138	Jurkat	blood:	n/a
8	chr7:103210555-103210605	A549	lung:	n/a
9	chr7:103210555-103210605	HCF	heart:	n/a
10	chr7:103301932-103301982	HRE	kidney:	n/a
11	chr7:103301932-103301982	GM12892	blood:	n/a
12	chr7:103210555-103210605	HEK293	kidney:	embryo
13	chr7:103279088-103279138	SK-N-MC	brain:	n/a
14	chr7:103279088-103279138	SAEC	small airway:	n/a
15	chr7:103301932-103301982	GM06990	blood:	n/a
16	chr7:103260062-103260112	AG10803	skin:	n/a
17	chr7:103301932-103301982	HCF	heart:	n/a
18	chr7:103260062-103260112	MCF10A-Er-Src	breast:	n/a
19	chr7:103301932-103301982	NB4	blood:	n/a
20	chr7:103301932-103301982	ovcar-3	ovarian:	n/a
21	chr7:103279088-103279138	HRE	kidney:	n/a
22	chr7:103301932-103301982	HMEC	breast:	n/a
23	chr7:103260062-103260112	RPTEC	kidney:	n/a
24	chr7:103279088-103279138	MCF-7	breast:	n/a
25	chr7:103260062-103260112	AG09309	skin:	n/a
26	chr7:103210555-103210605	HRCEpiC	kidney:	n/a
27	chr7:103301932-103301982	H1-hESC	embryonic stem cell:	embryo
28	chr7:103301932-103301982	GM19239	blood:	n/a
29	chr7:103279088-103279138	GM12878	blood:	n/a
30	chr7:103279088-103279138	RPTEC	kidney:	n/a
31	chr7:103279088-103279138	AoSMC	blood vessel:	n/a
32	chr7:103301932-103301982	HCPEpiC	choroid plexus:	n/a
33	chr7:103301932-103301982	GM12891	blood:	n/a
34	chr7:103301932-103301982	SKMC	muscle:	n/a
35	chr7:103279088-103279138	PrEC	prostate:	n/a
36	chr7:103260062-103260112	H1-hESC	embryonic stem cell:	embryo
37	chr7:103260062-103260112	HAEpiC	amniotic membrane:	n/a
38	chr7:103279088-103279138	HUVEC	blood vessel:	n/a
39	chr7:103210555-103210605	U87	brain:	n/a
40	chr7:103260062-103260112	HCF	heart:	n/a
41	chr7:103260062-103260112	HUVEC	blood vessel:	n/a
42	chr7:103301932-103301982	HCM	heart:	n/a
43	chr7:103260062-103260112	GM12892	blood:	n/a
44	chr7:103279088-103279138	Caco-2	colon:	n/a
45	chr7:103279088-103279138	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:103210555-103210605	HCPEpiC	choroid plexus:	n/a
47	chr7:103210555-103210605	ECC-1	luminal epithelium:	n/a
48	chr7:103301932-103301982	HCT-116	colon:	n/a
49	chr7:103210555-103210605	GM06990	blood:	n/a
50	chr7:103301932-103301982	NHDF-neo	bronchial:	n/a

(count:163 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:103250881..103252737-chr7:103255714..103258571,2	K562	blood:
2	chr7:103253081..103256166-chr7:103404446..103406601,3	K562	blood:
3	chr7:103218935..103220580-chr7:103231967..103234763,2	K562	blood:
4	chr7:103133039..103134783-chr7:103140614..103142460,2	K562	blood:
5	chr7:103239547..103241356-chr7:103252874..103254925,2	K562	blood:
6	chr7:103305325..103307446-chr7:103308405..103311533,3	K562	blood:
7	chr7:103169385..103171495-chr7:103172563..103174585,2	K562	blood:
8	chr7:103331145..103334618-chr7:103343062..103346104,3	K562	blood:
9	chr7:103199365..103201003-chr7:103418048..103420205,2	K562	blood:
10	chr7:103274516..103276734-chr7:103323210..103324865,2	K562	blood:
11	chr7:103297764..103300699-chr7:103309943..103311774,3	K562	blood:
12	chr7:103294590..103296926-chr7:103297378..103300214,2	MCF-7	breast:
13	chr7:103244860..103246643-chr7:103247635..103250475,2	K562	blood:
14	chr7:103204866..103206437-chr7:103295560..103298235,2	K562	blood:
15	chr7:103282215..103284239-chr7:103291796..103293845,2	K562	blood:
16	chr7:103220150..103223008-chr7:103223285..103225999,2	K562	blood:
17	chr7:103287552..103290222-chr7:103293075..103295780,3	K562	blood:
18	chr7:103184302..103189500-chr7:103191909..103194832,5	K562	blood:
19	chr7:103253816..103255808-chr7:103257490..103259015,2	K562	blood:
20	chr7:103274516..103276734-chr7:103323210..103324865,2	K562	blood:
21	chr7:103213854..103214659-chr7:103393202..103393902,2	MCF-7	breast:
22	chr7:103166728..103167430-chr7:103797013..103797864,2	MCF-7	breast:
23	chr7:103192696..103194335-chr7:103197390..103199163,2	K562	blood:
24	chr7:103253287..103254849-chr7:103287404..103290090,2	K562	blood:
25	chr7:103237346..103240101-chr7:103240935..103244727,4	K562	blood:
26	chr7:103262129..103264756-chr7:103265630..103268934,3	K562	blood:
27	chr7:103229859..103231946-chr7:103786886..103788520,2	K562	blood:
28	chr7:103302444..103304759-chr7:103358804..103361595,2	K562	blood:
29	chr7:103299107..103301619-chr7:103313448..103316125,2	K562	blood:
30	chr7:103296674..103299385-chr7:103636597..103638114,2	K562	blood:
31	chr7:103172799..103178070-chr7:103178210..103181701,6	K562	blood:
32	chr7:103294590..103296926-chr7:103297378..103300214,2	MCF-7	breast:
33	chr7:103224194..103227224-chr7:103230117..103233349,3	K562	blood:
34	chr7:103313587..103316408-chr7:103317847..103320002,2	K562	blood:
35	chr7:103253816..103255808-chr7:103257490..103259015,2	K562	blood:
36	chr7:103153712..103155227-chr7:103156826..103158839,2	K562	blood:
37	chr7:103155726..103158237-chr7:103158510..103161401,2	MCF-7	breast:
38	chr7:103190662..103192734-chr7:103192820..103195209,2	K562	blood:
39	chr7:103214074..103215207-chr7:103796999..103797844,3	MCF-7	breast:
40	chr7:103164895..103165412-chr7:104559006..104559639,2	K562	blood:
41	chr7:103178267..103180295-chr7:103189000..103191734,2	K562	blood:
42	chr7:103139301..103141097-chr7:103143967..103145942,2	MCF-7	breast:
43	chr7:103215772..103217971-chr7:103405659..103407400,2	K562	blood:
44	chr7:103232129..103235431-chr7:103236152..103239545,4	K562	blood:
45	chr7:103334750..103336512-chr7:103338855..103341152,3	K562	blood:
46	chr7:103215795..103218619-chr7:103769174..103771262,2	K562	blood:
47	chr7:103262757..103265718-chr7:103587401..103589902,2	K562	blood:
48	chr7:103253053..103254863-chr7:103298954..103300587,2	K562	blood:
49	chr7:103164482..103165037-chr7:103393511..103394116,2	K562	blood:
50	chr7:103313587..103316408-chr7:103317847..103320002,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSMC2-1	chr7:103153216-103154454	ENSG00000234715
2	lnc-PSMC2-1	chr7:103144851-103144971	ENSG00000234715

No data

Variant related genes	Relation type
RELN	TF binding region
RELN	CpG island
ENSG00000189056	chromatin interactions
ENSG00000154945	chromatin interactions
CDK19	miRNA target sites
TRIM59	miRNA target sites

Extended variants
information (count: 8180 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:8180 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529488301	chr7:103140761-103140762	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74532616	chr7:103140794-103140795	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534482373	chr7:103140811-103140812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149534236	chr7:103140842-103140843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369494025	chr7:103140846-103140847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541344973	chr7:103140866-103140867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559068623	chr7:103140872-103140873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs367683962	chr7:103140950-103140951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183747921	chr7:103140978-103140979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541560717	chr7:103141019-103141020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372300446	chr7:103141043-103141044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563351490	chr7:103141083-103141084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376638963	chr7:103141089-103141090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186206325	chr7:103141121-103141122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147789346	chr7:103141126-103141127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375684028	chr7:103141141-103141142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13232021	chr7:103141147-103141148	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs113113916	chr7:103141152-103141153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373180515	chr7:103141166-103141167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79222798	chr7:103141167-103141168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374916288	chr7:103141185-103141186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565935986	chr7:103141206-103141207	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369307806	chr7:103141219-103141220	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113775740	chr7:103141221-103141222	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377429197	chr7:103141225-103141226	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371264058	chr7:103141233-103141234	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190273964	chr7:103141234-103141235	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373868525	chr7:103141253-103141254	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201982015	chr7:103141255-103141256	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147624295	chr7:103141317-103141318	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2229862	chr7:103141351-103141352	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs144309551	chr7:103141353-103141354	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374053764	chr7:103141366-103141367	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147760518	chr7:103141367-103141368	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373564931	chr7:103141372-103141373	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs13235135	chr7:103141437-103141438	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs558761209	chr7:103141458-103141459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373648444	chr7:103141495-103141496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144789858	chr7:103141525-103141526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534605616	chr7:103141540-103141541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76545984	chr7:103141543-103141544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574650940	chr7:103141560-103141561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373714654	chr7:103141575-103141576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541771809	chr7:103141587-103141588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550912776	chr7:103141619-103141620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556554812	chr7:103141660-103141661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562889001	chr7:103141666-103141667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs17152161	chr7:103141703-103141704	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs565122746	chr7:103141742-103141743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138717147	chr7:103141747-103141748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	21147910	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:560 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103122800-103141000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:103130800-103155000	Weak transcription	Brain Substantia Nigra	brain
3	chr7:103130800-103163600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr7:103131200-103145000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:103137400-103164400	Weak transcription	Brain Anterior Caudate	brain
6	chr7:103138000-103144200	Strong transcription	HepG2	liver
7	chr7:103138800-103142800	Weak transcription	K562	blood
8	chr7:103139800-103140800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:103140800-103141200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:103141200-103141400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:103141400-103143000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:103142800-103143600	Strong transcription	K562	blood
13	chr7:103143000-103143600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:103143600-103144800	Weak transcription	K562	blood
15	chr7:103143600-103153200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr7:103144200-103153000	Weak transcription	HepG2	liver
17	chr7:103144800-103145000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:103144800-103145000	Enhancers	K562	blood
19	chr7:103145000-103145200	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr7:103145000-103145400	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr7:103145000-103145400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:103145000-103145600	Flanking Active TSS	K562	blood
23	chr7:103145000-103145800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr7:103145200-103145400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr7:103145200-103145400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:103145200-103145600	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr7:103145200-103145800	Enhancers	Stomach Mucosa	stomach
28	chr7:103145600-103145800	Enhancers	K562	blood
29	chr7:103153000-103153600	Strong transcription	HepG2	liver
30	chr7:103153200-103153600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:103153600-103155600	Weak transcription	HepG2	liver
32	chr7:103155000-103156400	Strong transcription	Brain Substantia Nigra	brain
33	chr7:103155600-103161000	Strong transcription	HepG2	liver
34	chr7:103156000-103162400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr7:103156400-103163800	Weak transcription	Brain Substantia Nigra	brain
36	chr7:103158000-103198600	Weak transcription	Liver	Liver
37	chr7:103158200-103158600	Enhancers	K562	blood
38	chr7:103161000-103168000	Weak transcription	HepG2	liver
39	chr7:103161400-103163400	Weak transcription	Brain Cingulate Gyrus	brain
40	chr7:103162200-103162600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr7:103162400-103162800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr7:103162400-103162800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:103162400-103162800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr7:103162400-103163000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:103162400-103163000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr7:103162400-103163000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr7:103162400-103163200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:103162400-103163200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:103162600-103163200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr7:103162800-103168000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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