Variant report

Variant	nsv137930
Chromosome Location	chr19:40019489-40027856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:577)
CpG islands
(count:976)
Chromatin interactive
region (count:31)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40023272-40023768	HepG2	liver:	n/a	n/a
2	ATF2	chr19:40023131-40023850	GM12878	blood:	n/a	n/a
3	ATF3	chr19:40023277-40023731	GM12878	blood:	n/a	n/a
4	ATF3	chr19:40023311-40023712	K562	blood:	n/a	n/a
5	ATF3	chr19:40022437-40023864	A549	lung:	n/a	n/a
6	ATF3	chr19:40023409-40023642	HepG2	liver:	n/a	n/a
7	ATF3	chr19:40022709-40023859	A549	lung:	n/a	n/a
8	ATF3	chr19:40023352-40023663	K562	blood:	n/a	n/a
9	ATF3	chr19:40023265-40023800	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr19:40022529-40022572	K562	blood:	n/a	n/a
11	BACH1	chr19:40023369-40023719	K562	blood:	n/a	n/a
12	BCL3	chr19:40022619-40023847	A549	lung:	n/a	n/a
13	BCL3	chr19:40023096-40023955	A549	lung:	n/a	n/a
14	BCLAF1	chr19:40023073-40023819	GM12878	blood:	n/a	n/a
15	BHLHE40	chr19:40022786-40023724	K562	blood:	n/a	n/a
16	BHLHE40	chr19:40023379-40023752	GM12878	blood:	n/a	n/a
17	BRCA1	chr19:40023317-40023733	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr19:40023362-40023699	HepG2	liver:	n/a	n/a
19	BRCA1	chr19:40023268-40023730	GM12878	blood:	n/a	n/a
20	CCNT2	chr19:40023112-40023650	K562	blood:	n/a	n/a
21	CEBPB	chr19:40022228-40022511	K562	blood:	n/a	chr19:40022343-40022354
22	CEBPB	chr19:40022198-40022466	HepG2	liver:	n/a	chr19:40022343-40022354
23	CEBPB	chr19:40022759-40023131	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr19:40022778-40023074	A549	lung:	n/a	n/a
25	CEBPB	chr19:40022848-40023115	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr19:40026584-40026796	K562	blood:	n/a	chr19:40026681-40026692
27	CEBPB	chr19:40023241-40023797	GM12878	blood:	n/a	n/a
28	CEBPB	chr19:40022764-40023190	K562	blood:	n/a	n/a
29	CEBPB	chr19:40026579-40026813	HepG2	liver:	n/a	chr19:40026681-40026692 chr19:40026797-40026810
30	CEBPB	chr19:40022205-40022492	A549	lung:	n/a	chr19:40022343-40022354
31	CEBPD	chr19:40023218-40023593	HepG2	liver:	n/a	n/a
32	CHD1	chr19:40022938-40023218	GM12878	blood:	n/a	n/a
33	CHD2	chr19:40022876-40023669	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr19:40023175-40023677	K562	blood:	n/a	n/a
35	CHD2	chr19:40022878-40023763	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr19:40023397-40023695	HepG2	liver:	n/a	n/a
37	CREB1	chr19:40023270-40023817	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr19:40023321-40023684	A549	lung:	n/a	n/a
39	CREB1	chr19:40022847-40023778	A549	lung:	n/a	n/a
40	CTCF	chr19:40023323-40023775	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr19:40023433-40023740	MCF-7	breast:	n/a	n/a
42	CTCF	chr19:40023500-40023650	BJ	skin:	n/a	n/a
43	CTCF	chr19:40023211-40023834	MCF-7	breast:	n/a	n/a
44	CTCF	chr19:40023102-40023912	HCT-116	colon:	n/a	n/a
45	CTCF	chr19:40023447-40023733	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr19:40023273-40023817	MCF-7	breast:	n/a	n/a
47	CTCF	chr19:40023460-40023610	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr19:40023470-40023722	HepG2	liver:	n/a	n/a
49	CTCF	chr19:40023540-40023690	WI-38	lung:	n/a	n/a
50	CTCF	chr19:40023460-40023610	GM06990	blood:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40023281-40023331	GM12891	blood:	n/a
2	chr19:40023568-40023618	AG10803	skin:	n/a
3	chr19:40023527-40023577	IMR90	lung:	fetal
4	chr19:40023334-40023384	NT2-D1	testis:	n/a
5	chr19:40023151-40023201	HepG2	liver:	n/a
6	chr19:40023334-40023384	A549	lung:	n/a
7	chr19:40023459-40023509	HCPEpiC	choroid plexus:	n/a
8	chr19:40023568-40023618	SK-N-SH	brain:	n/a
9	chr19:40027263-40027313	AG09309	skin:	n/a
10	chr19:40019862-40019912	HL-60	blood:	n/a
11	chr19:40019862-40019912	CMK	blood:	n/a
12	chr19:40019862-40019912	GM12878	blood:	n/a
13	chr19:40022828-40022878	HEK293	kidney:	embryo
14	chr19:40023281-40023331	NHDF-neo	bronchial:	n/a
15	chr19:40023151-40023201	Caco-2	colon:	n/a
16	chr19:40023459-40023509	MCF10A-Er-Src	breast:	n/a
17	chr19:40027263-40027313	Caco-2	colon:	n/a
18	chr19:40023503-40023553	GM12891	blood:	n/a
19	chr19:40019862-40019912	HRPEpiC	eye:	n/a
20	chr19:40023509-40023559	HCPEpiC	choroid plexus:	n/a
21	chr19:40023494-40023544	HAEpiC	amniotic membrane:	n/a
22	chr19:40022828-40022878	ovcar-3	ovarian:	n/a
23	chr19:40023568-40023618	MCF-7	breast:	n/a
24	chr19:40023527-40023577	AG10803	skin:	n/a
25	chr19:40023540-40023590	HRCEpiC	kidney:	n/a
26	chr19:40023334-40023384	HCT-116	colon:	n/a
27	chr19:40027263-40027313	PANC-1	pancreas:	n/a
28	chr19:40023568-40023618	ECC-1	luminal epithelium:	n/a
29	chr19:40023281-40023331	PFSK-1	brain:	n/a
30	chr19:40023509-40023559	GM06990	blood:	n/a
31	chr19:40023459-40023509	Caco-2	colon:	n/a
32	chr19:40023151-40023201	SK-N-MC	brain:	n/a
33	chr19:40023459-40023509	HPAEpiC	pulmonary alveolar:	n/a
34	chr19:40027263-40027313	ECC-1	luminal epithelium:	n/a
35	chr19:40023494-40023544	GM12878	blood:	n/a
36	chr19:40023334-40023384	GM12892	blood:	n/a
37	chr19:40023509-40023559	NB4	blood:	n/a
38	chr19:40023527-40023577	NT2-D1	testis:	n/a
39	chr19:40025600-40025650	SK-N-SH_RA	brain:	n/a
40	chr19:40022828-40022878	GM12891	blood:	n/a
41	chr19:40023527-40023577	K562	blood:	n/a
42	chr19:40019862-40019912	GM19239	blood:	n/a
43	chr19:40023527-40023577	GM12878	blood:	n/a
44	chr19:40019862-40019912	HepG2	liver:	n/a
45	chr19:40023509-40023559	Hela-S3	cervix:	n/a
46	chr19:40023568-40023618	HIPEpiC	eye:	n/a
47	chr19:40023715-40023765	MCF10A-Er-Src	breast:	n/a
48	chr19:40023568-40023618	AG09319	gingival:	n/a
49	chr19:40023540-40023590	ovcar-3	ovarian:	n/a
50	chr19:40023509-40023559	SAEC	small airway:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:39923941..39928347-chr19:40027705..40030840,3	MCF-7	breast:
2	chr19:40024943..40026873-chr19:40027805..40030767,4	MCF-7	breast:
3	chr19:39925397..39928122-chr19:40019873..40021401,2	K562	blood:
4	chr19:39902534..39904778-chr19:40022453..40024067,3	MCF-7	breast:
5	chr19:40021563..40023552-chr19:40334495..40337354,2	K562	blood:
6	chr19:39832237..39832969-chr19:40023143..40024117,2	K562	blood:
7	chr19:39898615..39904728-chr19:40019936..40025504,8	K562	blood:
8	chr19:39934545..39937545-chr19:40023023..40025430,4	MCF-7	breast:
9	chr19:39898615..39903463-chr19:40021264..40024360,6	K562	blood:
10	chr19:39969179..39972823-chr19:40019268..40024259,8	K562	blood:
11	chr19:39930777..39932408-chr19:40023425..40025081,2	K562	blood:
12	chr19:39988241..39989038-chr19:40023625..40024451,2	MCF-7	breast:
13	chr15:59224951..59225680-chr19:40022590..40023096,2	Hela-S3	cervix:
14	chr19:39881003..39882919-chr19:40020303..40023234,2	K562	blood:
15	chr19:39880509..39882503-chr19:40021734..40025038,3	K562	blood:
16	chr19:40017029..40019869-chr19:40021904..40023558,2	K562	blood:
17	chr19:40023014..40023615-chr5:65439737..65440573,2	Hela-S3	cervix:
18	chr19:40009365..40013772-chr19:40013811..40019532,6	K562	blood:
19	chr19:39969762..39972823-chr19:40020818..40024781,5	K562	blood:
20	chr19:39963222..39966724-chr19:40022598..40024872,4	K562	blood:
21	chr19:40009271..40012163-chr19:40025249..40026752,2	K562	blood:
22	chr19:39961748..39964722-chr19:40022955..40025016,3	K562	blood:
23	chr19:39925075..39926642-chr19:40022135..40025107,3	K562	blood:
24	chr19:39988746..39992361-chr19:40020493..40024366,5	MCF-7	breast:
25	chr19:39934791..39938517-chr19:40022234..40026334,4	K562	blood:
26	chr19:39935867..39937651-chr19:40022035..40024212,2	MCF-7	breast:
27	chr19:40016281..40019888-chr19:40020670..40023558,4	K562	blood:
28	chr19:40023614..40026391-chr19:40028689..40031990,5	MCF-7	breast:
29	chr19:39880299..39881893-chr19:40023517..40025617,2	K562	blood:
30	chr19:39923160..39926894-chr19:40022027..40025011,8	K562	blood:
31	chr19:40019907..40024445-chr19:40029285..40031709,4	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EID2-1	chr19:40021977-40022153	NONHSAT066310
2	lnc-SELV.1-4	chr19:40024567-40024592	l_1683_chr19:40024566-40034013_testes
3	lnc-SELV.1-2	chr19:40024974-40025062	ENSG00000269792.1
4	lnc-SELV.1-2	chr19:40023756-40023876	ENSG00000269792.1
5	lnc-SELV.1-1	chr19:40019263-40019553	XLOC_013072
6	lnc-SELV.1-3	chr19:40025103-40025661	NONHSAT066312
7	lnc-SELV.1-1	chr19:40018847-40020008	NONHSAT066308
8	lnc-SELV.1-2	chr19:40023052-40023488	ENSG00000269792.1
9	lnc-EID2-1	chr19:40023380-40023483	NONHSAT066310

No data

Variant related genes	Relation type
ENSG00000269792	TF binding region
TDGF1P7	TF binding region
EID2B	TF binding region
ENSG00000269792	CpG island
TDGF1P7	CpG island
EID2B	CpG island
ENSG00000153914	chromatin interactions
ENSG00000266559	chromatin interactions
ENSG00000090932	chromatin interactions
ENSG00000269246	chromatin interactions
ENSG00000105197	chromatin interactions
ENSG00000176401	chromatin interactions
ENSG00000090924	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000006712	chromatin interactions
ENSG00000105202	chromatin interactions
ENSG00000105193	chromatin interactions
ENSG00000196235	chromatin interactions
ENSG00000269584	chromatin interactions
ENSG00000176396	chromatin interactions
ENSG00000063322	chromatin interactions
ENSG00000269792	chromatin interactions

Extended variants
information (count: 342 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552186881	chr19:40019490-40019491	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs377577300	chr19:40019524-40019525	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs201412011	chr19:40019539-40019540	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs10423870	chr19:40019543-40019544	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs10423872	chr19:40019548-40019549	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs570452452	chr19:40019549-40019550	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs79565091	chr19:40019551-40019552	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs534414298	chr19:40019552-40019553	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs560712603	chr19:40019553-40019554	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs145601777	chr19:40019555-40019556	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs375905095	chr19:40019603-40019604	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs577203238	chr19:40019615-40019616	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs553071389	chr19:40019627-40019628	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs192904436	chr19:40019693-40019694	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs576938979	chr19:40019694-40019695	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs34271968	chr19:40019695-40019696	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs575177581	chr19:40019764-40019765	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs373609331	chr19:40019778-40019779	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs377068720	chr19:40019794-40019795	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
20	rs184869926	chr19:40019863-40019864	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs140764961	chr19:40019871-40019872	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs541076991	chr19:40019901-40019902	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs559750800	chr19:40019904-40019905	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs369767300	chr19:40019910-40019911	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs373660014	chr19:40019912-40019913	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs55760116	chr19:40019925-40019926	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
27	rs144715805	chr19:40019934-40019935	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs542407555	chr19:40019946-40019947	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
29	rs563906685	chr19:40019972-40019973	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
30	rs531206054	chr19:40019985-40019986	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
31	rs552877422	chr19:40019990-40019991	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
32	rs563915408	chr19:40020000-40020001	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
33	rs528046450	chr19:40020001-40020002	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
34	rs188140453	chr19:40020009-40020010	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs535210319	chr19:40020022-40020023	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs542853507	chr19:40020056-40020057	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs371364034	chr19:40020107-40020108	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs550341846	chr19:40020121-40020122	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs539402290	chr19:40020158-40020159	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs76784399	chr19:40020170-40020171	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs528395413	chr19:40020172-40020173	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs557993432	chr19:40020183-40020184	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs573059186	chr19:40020197-40020198	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs113947725	chr19:40020203-40020204	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs534987007	chr19:40020241-40020242	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs553107311	chr19:40020275-40020276	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs148925393	chr19:40020403-40020404	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs574969221	chr19:40020494-40020495	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs542370692	chr19:40020495-40020496	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs563866078	chr19:40020574-40020575	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD

Chromatin state (count:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40006600-40022800	Weak transcription	Lung	lung
2	chr19:40007000-40022400	Weak transcription	Right Ventricle	heart
3	chr19:40008000-40022200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr19:40009400-40021200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr19:40009800-40022200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr19:40009800-40022400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr19:40009800-40022600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr19:40009800-40022600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr19:40010000-40022200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr19:40010000-40022200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr19:40010000-40022600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr19:40010000-40022600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:40010200-40022400	Weak transcription	Fetal Muscle Leg	muscle
14	chr19:40011000-40022000	Weak transcription	Fetal Thymus	thymus
15	chr19:40011200-40021200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr19:40011200-40022200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr19:40011200-40022400	Weak transcription	Fetal Kidney	kidney
18	chr19:40011400-40020600	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr19:40011600-40022200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr19:40011800-40021200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr19:40012000-40022000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr19:40012000-40022200	Weak transcription	Brain Hippocampus Middle	brain
23	chr19:40012000-40022200	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr19:40012200-40022200	Weak transcription	Stomach Smooth Muscle	stomach
25	chr19:40012400-40022400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr19:40012600-40022400	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr19:40012600-40022400	Weak transcription	Primary B cells from peripheral blood	blood
28	chr19:40012600-40022600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr19:40013000-40021600	Weak transcription	Colon Smooth Muscle	Colon
30	chr19:40013000-40021600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr19:40013000-40022200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr19:40013200-40021800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr19:40013200-40022400	Weak transcription	Thymus	Thymus
34	chr19:40014200-40020400	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr19:40014200-40021600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr19:40014200-40022400	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr19:40015200-40021200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr19:40015400-40021600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr19:40015400-40021600	Weak transcription	Duodenum Mucosa	Duodenum
40	chr19:40015400-40021600	Weak transcription	HepG2	liver
41	chr19:40015400-40022400	Weak transcription	Adipose Nuclei	Adipose
42	chr19:40015600-40022600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr19:40016000-40021800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr19:40016200-40019600	Weak transcription	Fetal Stomach	stomach
45	chr19:40016200-40021600	Weak transcription	Fetal Lung	lung
46	chr19:40016800-40020000	Weak transcription	Fetal Brain Male	brain
47	chr19:40016800-40022400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr19:40017000-40020800	Weak transcription	Fetal Brain Female	brain
49	chr19:40017000-40021600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr19:40017000-40022200	Weak transcription	NH-A	brain

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