Variant report

Variant	nsv541883
Chromosome Location	chr13:96508530-97020734
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3031)
CpG islands
(count:2814)
Chromatin interactive
region (count:93)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3031 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:96673132-96673488	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:96705446-96705959	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:96632838-96633002	K562	blood:	n/a	n/a
4	ARID3A	chr13:96517464-96517648	K562	blood:	n/a	n/a
5	ARID3A	chr13:96624887-96625205	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:96548454-96548878	K562	blood:	n/a	n/a
7	ARID3A	chr13:96710321-96710493	K562	blood:	n/a	n/a
8	ATF1	chr13:96608880-96609099	K562	blood:	n/a	n/a
9	ATF1	chr13:96704862-96705264	K562	blood:	n/a	n/a
10	ATF2	chr13:96705443-96705765	GM12878	blood:	n/a	n/a
11	ATF2	chr13:96704816-96705230	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr13:96704875-96705211	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr13:96704708-96705377	GM12878	blood:	n/a	n/a
14	ATF2	chr13:96704761-96705830	GM12878	blood:	n/a	n/a
15	ATF3	chr13:96608777-96609107	K562	blood:	n/a	n/a
16	ATF3	chr13:96705437-96705791	A549	lung:	n/a	n/a
17	BACH1	chr13:96761604-96761614	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr13:96705515-96705712	K562	blood:	n/a	n/a
19	BACH1	chr13:96602381-96602390	K562	blood:	n/a	n/a
20	BACH1	chr13:96761376-96761557	K562	blood:	n/a	n/a
21	BACH1	chr13:96705010-96706104	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr13:96891281-96891533	GM12878	blood:	n/a	chr13:96891397-96891408 chr13:96891398-96891408
23	BCL11A	chr13:96891297-96891565	GM12878	blood:	n/a	chr13:96891400-96891409
24	BCL11A	chr13:96606653-96606944	H1-hESC	embryonic stem cell:	n/a	n/a
25	BHLHE40	chr13:96705452-96705826	K562	blood:	n/a	n/a
26	BHLHE40	chr13:96808141-96808327	HepG2	liver:	n/a	n/a
27	BHLHE40	chr13:96673960-96673961	GM12878	blood:	n/a	n/a
28	BHLHE40	chr13:96704992-96706021	GM12878	blood:	n/a	n/a
29	BHLHE40	chr13:96705078-96705207	K562	blood:	n/a	n/a
30	BHLHE40	chr13:96632919-96632932	K562	blood:	n/a	n/a
31	BRCA1	chr13:96705801-96705964	HepG2	liver:	n/a	n/a
32	BRCA1	chr13:96704813-96705240	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr13:96705537-96706241	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr13:96961633-96961819	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr13:96705530-96705786	GM12878	blood:	n/a	n/a
36	BRCA1	chr13:96516087-96516280	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr13:96942285-96942294	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr13:96705964-96706299	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr13:96608842-96609006	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr13:96760331-96760577	K562	blood:	n/a	n/a
41	CBX3	chr13:96705479-96705930	K562	blood:	n/a	n/a
42	CBX3	chr13:96710079-96710563	HCT-116	colon:	n/a	n/a
43	CBX3	chr13:96760389-96760640	K562	blood:	n/a	n/a
44	CBX3	chr13:96612468-96612822	K562	blood:	n/a	n/a
45	CBX3	chr13:96698869-96699225	K562	blood:	n/a	n/a
46	CCNT2	chr13:96589983-96590394	K562	blood:	n/a	n/a
47	CCNT2	chr13:96525602-96525816	K562	blood:	n/a	n/a
48	CCNT2	chr13:96608827-96609027	K562	blood:	n/a	n/a
49	CCNT2	chr13:96704993-96706008	K562	blood:	n/a	n/a
50	CEBPB	chr13:96885624-96885671	K562	blood:	n/a	n/a

(count:2814 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96743754-96743804	GM12878	blood:	n/a
2	chr13:96744161-96744211	AG04449	skin:	fetal
3	chr13:96654416-96654466	SK-N-MC	brain:	n/a
4	chr13:96743110-96743160	PrEC	prostate:	n/a
5	chr13:96583885-96583935	HepG2	liver:	n/a
6	chr13:96705594-96705644	HIPEpiC	eye:	n/a
7	chr13:96583885-96583935	NT2-D1	testis:	n/a
8	chr13:96744161-96744211	H1-hESC	embryonic stem cell:	embryo
9	chr13:96743754-96743804	GM12878	blood:	n/a
10	chr13:96744161-96744211	AG04449	skin:	fetal
11	chr13:96654416-96654466	SK-N-MC	brain:	n/a
12	chr13:96743110-96743160	PrEC	prostate:	n/a
13	chr13:96583885-96583935	HepG2	liver:	n/a
14	chr13:96705594-96705644	HIPEpiC	eye:	n/a
15	chr13:96583885-96583935	NT2-D1	testis:	n/a
16	chr13:96744161-96744211	H1-hESC	embryonic stem cell:	embryo
17	chr13:96743583-96743633	HL-60	blood:	n/a
18	chr13:96743110-96743160	GM12891	blood:	n/a
19	chr13:96738685-96738735	SK-N-SH	brain:	n/a
20	chr13:96743170-96743220	SKMC	muscle:	n/a
21	chr13:96743170-96743220	HPAEpiC	pulmonary alveolar:	n/a
22	chr13:96742413-96742463	BE2_C	brain:	n/a
23	chr13:96705847-96705897	Hepatocyte	liver:	n/a
24	chr13:96742056-96742106	IMR90	lung:	fetal
25	chr13:96707199-96707249	NB4	blood:	n/a
26	chr13:96743895-96743945	AG09309	skin:	n/a
27	chr13:96705853-96705903	GM06990	blood:	n/a
28	chr13:96583885-96583935	HEK293	kidney:	embryo
29	chr13:96583751-96583801	HRPEpiC	eye:	n/a
30	chr13:96744289-96744339	CMK	blood:	n/a
31	chr13:96738685-96738735	LNCaP	prostate:	n/a
32	chr13:96705929-96705979	AoSMC	blood vessel:	n/a
33	chr13:96706104-96706154	H1-hESC	embryonic stem cell:	embryo
34	chr13:96744289-96744339	AG04449	skin:	fetal
35	chr13:96705712-96705762	NHDF-neo	bronchial:	n/a
36	chr13:96984133-96984183	HUVEC	blood vessel:	n/a
37	chr13:96744289-96744339	GM12892	blood:	n/a
38	chr13:96705853-96705903	PFSK-1	brain:	n/a
39	chr13:96706045-96706095	AoSMC	blood vessel:	n/a
40	chr13:96706773-96706823	NT2-D1	testis:	n/a
41	chr13:96743895-96743945	AG04450	lung:	fetal
42	chr13:96744289-96744339	Caco-2	colon:	n/a
43	chr13:96705847-96705897	MCF10A-Er-Src	breast:	n/a
44	chr13:96705929-96705979	BJ	skin:	n/a
45	chr13:96742413-96742463	HRCEpiC	kidney:	n/a
46	chr13:96706104-96706154	ovcar-3	ovarian:	n/a
47	chr13:96742056-96742106	HCPEpiC	choroid plexus:	n/a
48	chr13:96708764-96708814	HNPCEpiC	eye:	n/a
49	chr13:96654416-96654466	AG04450	lung:	fetal
50	chr13:96742905-96742955	NH-A	brain:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:96632367..96634450-chr13:96637310..96639783,2	K562	blood:
2	chr13:96632367..96634450-chr13:96637310..96639783,2	K562	blood:
3	chr13:96704511..96706638-chr13:96708531..96711999,4	MCF-7	breast:
4	chr13:96793442..96793947-chr13:96881310..96882180,2	MCF-7	breast:
5	chr13:96506532..96508738-chr13:96509011..96511057,2	K562	blood:
6	chr13:96704560..96706140-chr13:96731564..96733725,2	MCF-7	breast:
7	chr13:96812563..96814558-chr13:96818191..96820152,2	MCF-7	breast:
8	chr13:96951281..96952208-chr13:97448274..97448845,2	MCF-7	breast:
9	chr13:96705422..96706004-chr16:74337665..74338558,2	NB4	blood:
10	chr13:96705761..96707656-chr13:96724280..96725801,2	MCF-7	breast:
11	chr13:96732215..96734781-chr13:96740954..96743608,2	MCF-7	breast:
12	chr13:96933248..96934803-chr13:96938522..96940997,2	MCF-7	breast:
13	chr13:96837155..96838668-chr13:96842443..96845430,2	MCF-7	breast:
14	chr13:96586030..96588095-chr13:96594403..96597240,2	MCF-7	breast:
15	chr13:96946178..96948064-chr13:96950276..96952772,2	K562	blood:
16	chr13:96705303..96706107-chr17:73775369..73775878,2	Hela-S3	cervix:
17	chr13:96806648..96808895-chr13:96812833..96815729,2	K562	blood:
18	chr13:96705350..96706193-chr15:72520336..72521147,2	Hela-S3	cervix:
19	chr13:96806648..96808895-chr13:96812833..96815729,2	K562	blood:
20	chr13:96705368..96706022-chr3:169482389..169482964,2	Hela-S3	cervix:
21	chr13:96645821..96648157-chr13:96652865..96656450,3	K562	blood:
22	chr13:96681222..96683044-chr13:96705277..96706981,2	MCF-7	breast:
23	chr13:96623472..96625702-chr13:96633366..96635270,2	K562	blood:
24	chr13:96822546..96824465-chr13:96826052..96828818,3	K562	blood:
25	chr13:96746204..96748627-chr13:96759326..96761567,2	K562	blood:
26	chr13:96506532..96508738-chr13:96509011..96511057,2	K562	blood:
27	chr13:96838474..96840209-chr13:96843029..96845173,2	K562	blood:
28	chr13:96520254..96522290-chr13:96547977..96549685,2	MCF-7	breast:
29	chr13:96711531..96713496-chr13:96738453..96740111,2	MCF-7	breast:
30	chr13:96642387..96644158-chr13:96654027..96655529,2	K562	blood:
31	chr13:96821572..96824428-chr13:96824997..96828818,3	K562	blood:
32	chr13:96632367..96634292-chr13:96635472..96638810,3	K562	blood:
33	chr13:96666484..96668467-chr13:96672707..96674381,2	K562	blood:
34	chr13:96534402..96536224-chr13:96544660..96547266,2	K562	blood:
35	chr13:96951968..96953789-chr17:79366532..79368897,2	MCF-7	breast:
36	chr13:96638885..96641405-chr13:96646337..96648047,2	K562	blood:
37	chr13:96746204..96748627-chr13:96759326..96761567,2	K562	blood:
38	chr13:96632367..96634292-chr13:96635472..96638810,3	K562	blood:
39	chr13:96705694..96707387-chr13:96740919..96743720,3	MCF-7	breast:
40	chr13:96704049..96706835-chr13:96874982..96877650,2	MCF-7	breast:
41	chr13:96676638..96679476-chr13:96757318..96759037,2	MCF-7	breast:
42	chr13:96793442..96793947-chr13:96881310..96882180,2	MCF-7	breast:
43	chr13:96757574..96759639-chr13:96771275..96774077,2	MCF-7	breast:
44	chr13:96812563..96814558-chr13:96818191..96820152,2	MCF-7	breast:
45	chr13:96711531..96713496-chr13:96738453..96740111,2	MCF-7	breast:
46	chr13:96654618..96657100-chr13:96704216..96707114,2	MCF-7	breast:
47	chr13:96933248..96934803-chr13:96938522..96940997,2	MCF-7	breast:
48	chr13:96676019..96678407-chr13:96704479..96707236,2	K562	blood:
49	chr13:96646657..96649376-chr13:96653623..96656450,2	K562	blood:
50	chr13:96646657..96649376-chr13:96653623..96656450,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGGT2-1	chr13:96737151-96737367	XLOC_010699
2	lnc-DNAJC3-2	chr13:96805879-96806509	expReg_chr13_3550_+
3	lnc-UGGT2-1	chr13:96737150-96737367	NONHSAT034782
4	lnc-DZIP1-9	chr13:96629582-96629877	NONHSAT034781
5	lnc-HS6ST3-1	chr13:96675417-96675649	expReg_chr13_3428_+
6	lnc-DZIP1-9	chr13:96622724-96623119	NONHSAT034781
7	lnc-UGGT2-2	chr13:96806821-96807071	uc_356_-
8	lnc-DNAJC3-3	chr13:96821799-96822099	NONHSAT034784
9	lnc-DZIP1-3	chr13:96568212-96568330	ENSG00000237822.1
10	lnc-DZIP1-3	chr13:96567601-96567944	ENSG00000237822.1
11	lnc-DNAJC3-4	chr13:96991437-96991547	l_903_chr13:96989763-96999042_testes
12	lnc-DNAJC3-4	chr13:96998816-96999042	l_903_chr13:96989763-96999042_testes
13	lnc-DNAJC3-4	chr13:96989764-96989936	l_903_chr13:96989763-96999042_testes
14	lnc-UGGT2-1	chr13:96739248-96739285	NONHSAT034782
15	lnc-UGGT2-1	chr13:96739249-96739285	XLOC_010699

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
ENSG00000103035	chromatin interactions
ENSG00000102595	chromatin interactions
ENSG00000116984	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000215908	chromatin interactions
ENSG00000270141	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000242614	chromatin interactions
ENSG00000185352	chromatin interactions
ATP13A3	miRNA target sites
ATP2A2	miRNA target sites
FSTL1	miRNA target sites
ZNF280C	miRNA target sites

Extended variants
information (count: 15947 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:15947 , 50 per page) page: 1 2 3 4 5 6 7 ... 319

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367639805	chr13:96508558-96508559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs35123499	chr13:96508566-96508567	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs199990074	chr13:96508579-96508580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs202165826	chr13:96508580-96508581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370373684	chr13:96508607-96508608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530319617	chr13:96508610-96508611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571805945	chr13:96508622-96508623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371730845	chr13:96508634-96508635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552221089	chr13:96508660-96508661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184695113	chr13:96508665-96508666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557245601	chr13:96508674-96508675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567370976	chr13:96508688-96508689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374989722	chr13:96508696-96508697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371277364	chr13:96508742-96508743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553085346	chr13:96508783-96508784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138884485	chr13:96508802-96508803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545013227	chr13:96508812-96508813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188715197	chr13:96508813-96508814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541120628	chr13:96508864-96508865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181411616	chr13:96508909-96508910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183772098	chr13:96508994-96508995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188403338	chr13:96509004-96509005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560956571	chr13:96509014-96509015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557381113	chr13:96509049-96509050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564705556	chr13:96509064-96509065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142006599	chr13:96509069-96509070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542760060	chr13:96509086-96509087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574243170	chr13:96509123-96509124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559410774	chr13:96509129-96509130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528475949	chr13:96509395-96509396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551313818	chr13:96509402-96509403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571931656	chr13:96509436-96509437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531077834	chr13:96509544-96509545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374487203	chr13:96509567-96509568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182332516	chr13:96509630-96509631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536838241	chr13:96509641-96509642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187277715	chr13:96509706-96509707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59685940	chr13:96509845-96509846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538643103	chr13:96509846-96509847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558230906	chr13:96509854-96509855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575159184	chr13:96509903-96509904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368851557	chr13:96510001-96510002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191711818	chr13:96510010-96510011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs578202337	chr13:96510101-96510102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs574586063	chr13:96510202-96510203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142034627	chr13:96510203-96510204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559422777	chr13:96510249-96510250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200464341	chr13:96510253-96510254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs71113957	chr13:96510254-96510255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572975458	chr13:96510258-96510259	Weak transcription Enhancers	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:3506 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96478000-96568400	Weak transcription	Placenta	Placenta
2	chr13:96487000-96510000	Weak transcription	HUVEC	blood vessel
3	chr13:96495000-96590800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr13:96498400-96549800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr13:96499400-96515400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr13:96502000-96522400	Weak transcription	Colon Smooth Muscle	Colon
7	chr13:96502400-96535400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr13:96502600-96552600	Weak transcription	Brain Germinal Matrix	brain
9	chr13:96502800-96514800	Weak transcription	Gastric	stomach
10	chr13:96502800-96562600	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr13:96503000-96508600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr13:96503000-96510600	Weak transcription	NHLF	lung
13	chr13:96503000-96517400	Weak transcription	K562	blood
14	chr13:96503000-96522600	Weak transcription	Aorta	Aorta
15	chr13:96503000-96522600	Weak transcription	Pancreas	Pancrea
16	chr13:96503000-96523600	Weak transcription	Esophagus	oesophagus
17	chr13:96503000-96526800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr13:96503000-96527200	Weak transcription	Fetal Kidney	kidney
19	chr13:96503000-96567400	Weak transcription	NHEK	skin
20	chr13:96503200-96510200	Weak transcription	Hela-S3	cervix
21	chr13:96503200-96510400	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr13:96503200-96522600	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr13:96503200-96522800	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr13:96503200-96527800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr13:96503200-96535200	Weak transcription	HepG2	liver
26	chr13:96503200-96542000	Weak transcription	Brain Substantia Nigra	brain
27	chr13:96503200-96542000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr13:96503200-96542200	Weak transcription	Brain Hippocampus Middle	brain
29	chr13:96503200-96558000	Weak transcription	NHDF-Ad	bronchial
30	chr13:96503200-96558200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr13:96503200-96558800	Weak transcription	Primary hematopoietic stem cells	blood
32	chr13:96503400-96520400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr13:96503400-96521800	Weak transcription	HSMMtube	muscle
34	chr13:96503400-96522600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr13:96503400-96528600	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr13:96503400-96542000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr13:96503400-96555400	Weak transcription	Fetal Heart	heart
38	chr13:96503400-96580800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr13:96503600-96510400	Weak transcription	Psoas Muscle	Psoas
40	chr13:96503600-96510400	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr13:96503600-96510600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr13:96503600-96510600	Weak transcription	Stomach Mucosa	stomach
43	chr13:96503600-96510800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr13:96503600-96528600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr13:96503600-96528600	Weak transcription	Duodenum Mucosa	Duodenum
46	chr13:96503600-96559000	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr13:96503600-96562800	Weak transcription	Fetal Brain Female	brain
48	chr13:96503800-96509000	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr13:96503800-96510600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr13:96503800-96510800	Weak transcription	Osteobl	bone

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