Variant report

Variant	nsv1041165
Chromosome Location	chr13:96522021-96966520
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2913)
CpG islands
(count:2688)
Chromatin interactive
region (count:90)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2913 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:96624887-96625205	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:96673132-96673488	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:96632838-96633002	K562	blood:	n/a	n/a
4	ARID3A	chr13:96705446-96705959	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:96710321-96710493	K562	blood:	n/a	n/a
6	ARID3A	chr13:96548454-96548878	K562	blood:	n/a	n/a
7	ATF1	chr13:96608880-96609099	K562	blood:	n/a	n/a
8	ATF1	chr13:96704862-96705264	K562	blood:	n/a	n/a
9	ATF2	chr13:96704761-96705830	GM12878	blood:	n/a	n/a
10	ATF2	chr13:96704875-96705211	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr13:96705443-96705765	GM12878	blood:	n/a	n/a
12	ATF2	chr13:96704708-96705377	GM12878	blood:	n/a	n/a
13	ATF2	chr13:96704816-96705230	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr13:96705437-96705791	A549	lung:	n/a	n/a
15	ATF3	chr13:96608777-96609107	K562	blood:	n/a	n/a
16	BACH1	chr13:96761604-96761614	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr13:96602381-96602390	K562	blood:	n/a	n/a
18	BACH1	chr13:96705515-96705712	K562	blood:	n/a	n/a
19	BACH1	chr13:96705010-96706104	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr13:96761376-96761557	K562	blood:	n/a	n/a
21	BATF	chr13:96891281-96891533	GM12878	blood:	n/a	chr13:96891397-96891408 chr13:96891398-96891408
22	BCL11A	chr13:96606653-96606944	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr13:96891297-96891565	GM12878	blood:	n/a	chr13:96891400-96891409
24	BHLHE40	chr13:96673960-96673961	GM12878	blood:	n/a	n/a
25	BHLHE40	chr13:96705078-96705207	K562	blood:	n/a	n/a
26	BHLHE40	chr13:96704992-96706021	GM12878	blood:	n/a	n/a
27	BHLHE40	chr13:96632919-96632932	K562	blood:	n/a	n/a
28	BHLHE40	chr13:96705452-96705826	K562	blood:	n/a	n/a
29	BHLHE40	chr13:96808141-96808327	HepG2	liver:	n/a	n/a
30	BRCA1	chr13:96942285-96942294	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr13:96705530-96705786	GM12878	blood:	n/a	n/a
32	BRCA1	chr13:96961633-96961819	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr13:96705801-96705964	HepG2	liver:	n/a	n/a
34	BRCA1	chr13:96608842-96609006	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr13:96704813-96705240	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr13:96705537-96706241	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr13:96705964-96706299	H1-hESC	embryonic stem cell:	n/a	n/a
38	CBX3	chr13:96698869-96699225	K562	blood:	n/a	n/a
39	CBX3	chr13:96612468-96612822	K562	blood:	n/a	n/a
40	CBX3	chr13:96710079-96710563	HCT-116	colon:	n/a	n/a
41	CBX3	chr13:96760331-96760577	K562	blood:	n/a	n/a
42	CBX3	chr13:96760389-96760640	K562	blood:	n/a	n/a
43	CBX3	chr13:96705479-96705930	K562	blood:	n/a	n/a
44	CCNT2	chr13:96704993-96706008	K562	blood:	n/a	n/a
45	CCNT2	chr13:96608827-96609027	K562	blood:	n/a	n/a
46	CCNT2	chr13:96525602-96525816	K562	blood:	n/a	n/a
47	CCNT2	chr13:96589983-96590394	K562	blood:	n/a	n/a
48	CEBPB	chr13:96626133-96626333	HepG2	liver:	n/a	chr13:96626229-96626240
49	CEBPB	chr13:96712903-96713202	HepG2	liver:	n/a	chr13:96713038-96713049
50	CEBPB	chr13:96796228-96796423	HepG2	liver:	n/a	n/a

(count:2688 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96705594-96705644	HPAEpiC	pulmonary alveolar:	n/a
2	chr13:96744289-96744339	MCF10A-Er-Src	breast:	n/a
3	chr13:96705712-96705762	NT2-D1	testis:	n/a
4	chr13:96743754-96743804	HUVEC	blood vessel:	n/a
5	chr13:96705594-96705644	HPAEpiC	pulmonary alveolar:	n/a
6	chr13:96744289-96744339	MCF10A-Er-Src	breast:	n/a
7	chr13:96705712-96705762	NT2-D1	testis:	n/a
8	chr13:96743754-96743804	HUVEC	blood vessel:	n/a
9	chr13:96743652-96743702	NT2-D1	testis:	n/a
10	chr13:96705594-96705644	HCF	heart:	n/a
11	chr13:96743087-96743137	GM12878	blood:	n/a
12	chr13:96707199-96707249	HCPEpiC	choroid plexus:	n/a
13	chr13:96742413-96742463	GM06990	blood:	n/a
14	chr13:96742905-96742955	NHDF-neo	bronchial:	n/a
15	chr13:96583970-96584020	SAEC	small airway:	n/a
16	chr13:96640017-96640067	HNPCEpiC	eye:	n/a
17	chr13:96705712-96705762	GM12892	blood:	n/a
18	chr13:96654416-96654466	NH-A	brain:	n/a
19	chr13:96744289-96744339	Jurkat	blood:	n/a
20	chr13:96949801-96949851	PANC-1	pancreas:	n/a
21	chr13:96705123-96705173	ECC-1	luminal epithelium:	n/a
22	chr13:96743652-96743702	AG09309	skin:	n/a
23	chr13:96743170-96743220	SK-N-SH_RA	brain:	n/a
24	chr13:96651633-96651683	NT2-D1	testis:	n/a
25	chr13:96742413-96742463	HIPEpiC	eye:	n/a
26	chr13:96742317-96742367	HRE	kidney:	n/a
27	chr13:96583970-96584020	SK-N-SH_RA	brain:	n/a
28	chr13:96743110-96743160	PFSK-1	brain:	n/a
29	chr13:96744289-96744339	ECC-1	luminal epithelium:	n/a
30	chr13:96705847-96705897	HPAEpiC	pulmonary alveolar:	n/a
31	chr13:96705712-96705762	H1-hESC	embryonic stem cell:	embryo
32	chr13:96583751-96583801	K562	blood:	n/a
33	chr13:96743754-96743804	AoSMC	blood vessel:	n/a
34	chr13:96742905-96742955	ovcar-3	ovarian:	n/a
35	chr13:96743110-96743160	ProgFib	skin:	n/a
36	chr13:96705853-96705903	SK-N-SH	brain:	n/a
37	chr13:96708764-96708814	SK-N-SH	brain:	n/a
38	chr13:96581176-96581226	AG09309	skin:	n/a
39	chr13:96705786-96705836	PrEC	prostate:	n/a
40	chr13:96742317-96742367	RPTEC	kidney:	n/a
41	chr13:96581176-96581226	SK-N-MC	brain:	n/a
42	chr13:96743583-96743633	HCM	heart:	n/a
43	chr13:96705847-96705897	Hela-S3	cervix:	n/a
44	chr13:96743895-96743945	LNCaP	prostate:	n/a
45	chr13:96743895-96743945	HCM	heart:	n/a
46	chr13:96744289-96744339	NH-A	brain:	n/a
47	chr13:96706104-96706154	HCT-116	colon:	n/a
48	chr13:96705712-96705762	HEK293	kidney:	embryo
49	chr13:96640017-96640067	HepG2	liver:	n/a
50	chr13:96706104-96706154	GM12878	blood:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:96666484..96668467-chr13:96672707..96674381,2	K562	blood:
2	chr13:96548785..96550762-chr13:96554235..96556207,2	K562	blood:
3	chr13:96575800..96578505-chr13:96580994..96583120,2	MCF-7	breast:
4	chr13:96691444..96693305-chr13:96704321..96706823,2	MCF-7	breast:
5	chr13:96586030..96588095-chr13:96594403..96597240,2	MCF-7	breast:
6	chr13:96705422..96706004-chr16:74337665..74338558,2	NB4	blood:
7	chr13:96741913..96744664-chr13:96755780..96757951,2	MCF-7	breast:
8	chr13:96654618..96657100-chr13:96704216..96707114,2	MCF-7	breast:
9	chr13:96548750..96552218-chr13:96554707..96557243,3	K562	blood:
10	chr13:96705350..96706193-chr15:72520336..72521147,2	Hela-S3	cervix:
11	chr13:96548785..96550762-chr13:96554235..96556207,2	K562	blood:
12	chr13:96812563..96814558-chr13:96818191..96820152,2	MCF-7	breast:
13	chr13:96676019..96678407-chr13:96704479..96707236,2	K562	blood:
14	chr13:96951281..96952208-chr13:97448274..97448845,2	MCF-7	breast:
15	chr13:96638885..96641405-chr13:96646337..96648047,2	K562	blood:
16	chr13:96704049..96706835-chr13:96874982..96877650,2	MCF-7	breast:
17	chr13:96676638..96679476-chr13:96757318..96759037,2	MCF-7	breast:
18	chr13:96946178..96948064-chr13:96950276..96952772,2	K562	blood:
19	chr13:96705761..96707656-chr13:96724280..96725801,2	MCF-7	breast:
20	chr13:96566533..96568077-chr9:100747317..100749032,2	MCF-7	breast:
21	chr13:96742136..96745093-chr13:96745710..96749821,3	MCF-7	breast:
22	chr13:96757574..96759639-chr13:96771275..96774077,2	MCF-7	breast:
23	chr13:96534402..96536224-chr13:96544660..96547266,2	K562	blood:
24	chr13:96645821..96648157-chr13:96652865..96656450,3	K562	blood:
25	chr13:96951968..96953789-chr17:79366532..79368897,2	MCF-7	breast:
26	chr13:96746204..96748627-chr13:96759326..96761567,2	K562	blood:
27	chr13:96645821..96648157-chr13:96652865..96656450,3	K562	blood:
28	chr13:96548750..96552218-chr13:96554707..96557243,3	K562	blood:
29	chr13:96704058..96705666-chr13:96708973..96710836,2	K562	blood:
30	chr13:96838474..96840209-chr13:96843029..96845173,2	K562	blood:
31	chr13:96806648..96808895-chr13:96812833..96815729,2	K562	blood:
32	chr13:96838474..96840209-chr13:96843029..96845173,2	K562	blood:
33	chr13:96575800..96578505-chr13:96580994..96583120,2	MCF-7	breast:
34	chr13:96757574..96759639-chr13:96771275..96774077,2	MCF-7	breast:
35	chr13:96705694..96707387-chr13:96740919..96743720,3	MCF-7	breast:
36	chr13:96725464..96726444-chr6:144512474..144513042,2	MCF-7	breast:
37	chr13:96646657..96649376-chr13:96653623..96656450,2	K562	blood:
38	chr13:96632367..96634450-chr13:96637310..96639783,2	K562	blood:
39	chr13:96704560..96706140-chr13:96731564..96733725,2	MCF-7	breast:
40	chr13:96623472..96625702-chr13:96633366..96635270,2	K562	blood:
41	chr13:96642387..96644158-chr13:96654027..96655529,2	K562	blood:
42	chr13:96666484..96668467-chr13:96672707..96674381,2	K562	blood:
43	chr13:96933248..96934803-chr13:96938522..96940997,2	MCF-7	breast:
44	chr13:96793442..96793947-chr13:96881310..96882180,2	MCF-7	breast:
45	chr13:96520254..96522290-chr13:96547977..96549685,2	MCF-7	breast:
46	chr13:96844015..96845659-chr13:96887223..96890032,2	MCF-7	breast:
47	chr13:96672084..96672616-chr13:97469396..97470262,2	MCF-7	breast:
48	chr13:96672513..96673053-chr13:97619391..97620229,2	K562	blood:
49	chr13:96705368..96706022-chr3:169482389..169482964,2	Hela-S3	cervix:
50	chr13:96676638..96679476-chr13:96757318..96759037,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGGT2-2	chr13:96806821-96807071	uc_356_-
2	lnc-DNAJC3-3	chr13:96821799-96822099	NONHSAT034784
3	lnc-UGGT2-1	chr13:96739248-96739285	NONHSAT034782
4	lnc-DNAJC3-2	chr13:96805879-96806509	expReg_chr13_3550_+
5	lnc-DZIP1-3	chr13:96567601-96567944	ENSG00000237822.1
6	lnc-DZIP1-3	chr13:96568212-96568330	ENSG00000237822.1
7	lnc-DZIP1-9	chr13:96629582-96629877	NONHSAT034781
8	lnc-UGGT2-1	chr13:96737151-96737367	XLOC_010699
9	lnc-DZIP1-9	chr13:96622724-96623119	NONHSAT034781
10	lnc-UGGT2-1	chr13:96739249-96739285	XLOC_010699
11	lnc-UGGT2-1	chr13:96737150-96737367	NONHSAT034782
12	lnc-HS6ST3-1	chr13:96675417-96675649	expReg_chr13_3428_+

No data

Variant related genes	Relation type
UGGT2	TF binding region
HS6ST3	TF binding region
RN7SL164P	TF binding region
UGGT2	CpG island
HS6ST3	CpG island
RN7SL164P	CpG island
ENSG00000102595	chromatin interactions
ENSG00000215908	chromatin interactions
ENSG00000185352	chromatin interactions
ENSG00000270141	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000242614	chromatin interactions
ENSG00000116984	chromatin interactions
ATP2A2	miRNA target sites
ATP13A3	miRNA target sites

Extended variants
information (count: 14675 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:14675 , 50 per page) page: 1 2 3 4 5 6 7 ... 294

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7336750	chr13:96522021-96522022	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559319408	chr13:96522172-96522173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142340607	chr13:96522186-96522187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs151258392	chr13:96522199-96522200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181596623	chr13:96522372-96522373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376618295	chr13:96522384-96522385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533163424	chr13:96522474-96522475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9561966	chr13:96522540-96522541	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs368004983	chr13:96522569-96522570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545120332	chr13:96522578-96522579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564748212	chr13:96522583-96522584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185872225	chr13:96522635-96522636	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551132096	chr13:96522669-96522670	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369628898	chr13:96522715-96522716	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200718737	chr13:96522726-96522727	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191171695	chr13:96522796-96522797	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564923985	chr13:96522805-96522806	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181824963	chr13:96522811-96522812	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6492824	chr13:96522827-96522828	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs535175774	chr13:96522834-96522835	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551198316	chr13:96522843-96522844	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141528567	chr13:96522848-96522849	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376908030	chr13:96522883-96522884	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147121353	chr13:96522934-96522935	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536251662	chr13:96522938-96522939	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573664277	chr13:96522939-96522940	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536589851	chr13:96522940-96522941	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553228791	chr13:96522944-96522945	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186513867	chr13:96523028-96523029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545145995	chr13:96523121-96523122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564437069	chr13:96523197-96523198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530625623	chr13:96523215-96523216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147750970	chr13:96523264-96523265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563385776	chr13:96523272-96523273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142604418	chr13:96523304-96523305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73558612	chr13:96523305-96523306	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs369139418	chr13:96523332-96523333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559957436	chr13:96523336-96523337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567305422	chr13:96523379-96523380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373290374	chr13:96523441-96523442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555170086	chr13:96523489-96523490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115705966	chr13:96523493-96523494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550714955	chr13:96523494-96523495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190466247	chr13:96523514-96523515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561048618	chr13:96523524-96523525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571849126	chr13:96523554-96523555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79325498	chr13:96523654-96523655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375874063	chr13:96523683-96523684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538958669	chr13:96523737-96523738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373795714	chr13:96523747-96523748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21785460	CNVD

Chromatin state (count:3344 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96478000-96568400	Weak transcription	Placenta	Placenta
2	chr13:96495000-96590800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr13:96498400-96549800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr13:96502000-96522400	Weak transcription	Colon Smooth Muscle	Colon
5	chr13:96502400-96535400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr13:96502600-96552600	Weak transcription	Brain Germinal Matrix	brain
7	chr13:96502800-96562600	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr13:96503000-96522600	Weak transcription	Aorta	Aorta
9	chr13:96503000-96522600	Weak transcription	Pancreas	Pancrea
10	chr13:96503000-96523600	Weak transcription	Esophagus	oesophagus
11	chr13:96503000-96526800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr13:96503000-96527200	Weak transcription	Fetal Kidney	kidney
13	chr13:96503000-96567400	Weak transcription	NHEK	skin
14	chr13:96503200-96522600	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr13:96503200-96522800	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr13:96503200-96527800	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr13:96503200-96535200	Weak transcription	HepG2	liver
18	chr13:96503200-96542000	Weak transcription	Brain Substantia Nigra	brain
19	chr13:96503200-96542000	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr13:96503200-96542200	Weak transcription	Brain Hippocampus Middle	brain
21	chr13:96503200-96558000	Weak transcription	NHDF-Ad	bronchial
22	chr13:96503200-96558200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr13:96503200-96558800	Weak transcription	Primary hematopoietic stem cells	blood
24	chr13:96503400-96522600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr13:96503400-96528600	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr13:96503400-96542000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr13:96503400-96555400	Weak transcription	Fetal Heart	heart
28	chr13:96503400-96580800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr13:96503600-96528600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr13:96503600-96528600	Weak transcription	Duodenum Mucosa	Duodenum
31	chr13:96503600-96559000	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr13:96503600-96562800	Weak transcription	Fetal Brain Female	brain
33	chr13:96503800-96522600	Weak transcription	Left Ventricle	heart
34	chr13:96503800-96522800	Weak transcription	Stomach Smooth Muscle	stomach
35	chr13:96503800-96526800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr13:96503800-96548200	Weak transcription	A549	lung
37	chr13:96504000-96528600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr13:96504000-96534000	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr13:96505200-96522400	Weak transcription	Fetal Muscle Trunk	muscle
40	chr13:96505400-96522400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr13:96506400-96522600	Weak transcription	Fetal Intestine Large	intestine
42	chr13:96506600-96522600	Weak transcription	Liver	Liver
43	chr13:96506600-96554800	Weak transcription	GM12878-XiMat	blood
44	chr13:96506800-96528400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr13:96506800-96528800	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr13:96506800-96536000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr13:96507000-96528600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr13:96510800-96522400	Weak transcription	Ovary	ovary
49	chr13:96510800-96556000	Weak transcription	Psoas Muscle	Psoas
50	chr13:96511000-96537400	Weak transcription	Sigmoid Colon	Sigmoid Colon

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