Variant report

Variant	esv1000212
Chromosome Location	chr19:36494643-36508508
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:902)
CpG islands
(count:1467)
Chromatin interactive
region (count:36)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:902 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:36499236-36499496	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:36505052-36505146	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:36505033-36505527	K562	blood:	n/a	n/a
4	ATF1	chr19:36505030-36505495	K562	blood:	n/a	n/a
5	ATF2	chr19:36505250-36505722	GM12878	blood:	n/a	n/a
6	ATF2	chr19:36504904-36505613	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr19:36505240-36505848	A549	lung:	n/a	n/a
8	BACH1	chr19:36500174-36500457	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr19:36505245-36505630	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr19:36504255-36505909	A549	lung:	n/a	chr19:36505533-36505542 chr19:36505395-36505408
11	BCL3	chr19:36504850-36505744	A549	lung:	n/a	chr19:36505533-36505542 chr19:36505395-36505408
12	BCL3	chr19:36500068-36501114	A549	lung:	n/a	chr19:36500627-36500640
13	BCL3	chr19:36499205-36500045	A549	lung:	n/a	chr19:36499717-36499726
14	BHLHE40	chr19:36505087-36505615	K562	blood:	n/a	chr19:36505392-36505408
15	BHLHE40	chr19:36504930-36505661	GM12878	blood:	n/a	chr19:36505392-36505408
16	BRCA1	chr19:36504783-36505563	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr19:36505349-36505767	GM12878	blood:	n/a	n/a
18	CBX3	chr19:36505023-36505687	K562	blood:	n/a	n/a
19	CBX3	chr19:36504155-36504584	K562	blood:	n/a	n/a
20	CCNT2	chr19:36505138-36505497	K562	blood:	n/a	n/a
21	CEBPB	chr19:36505022-36505199	K562	blood:	n/a	n/a
22	CEBPB	chr19:36494960-36495036	HepG2	liver:	n/a	n/a
23	CEBPB	chr19:36500390-36500398	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr19:36503056-36503213	HepG2	liver:	n/a	n/a
25	CEBPB	chr19:36494911-36495119	A549	lung:	n/a	n/a
26	CEBPB	chr19:36504979-36505306	Hela-S3	cervix:	n/a	n/a
27	CEBPZ	chr19:36505036-36505456	HepG2	liver:	n/a	n/a
28	CHD1	chr19:36505319-36505648	GM12878	blood:	n/a	n/a
29	CHD2	chr19:36504889-36505602	K562	blood:	n/a	n/a
30	CHD2	chr19:36499699-36499896	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr19:36504933-36505562	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr19:36504963-36505679	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr19:36504788-36505662	GM12878	blood:	n/a	n/a
34	CHD2	chr19:36504982-36505432	HepG2	liver:	n/a	n/a
35	CREB1	chr19:36504876-36505786	HepG2	liver:	n/a	n/a
36	CREB1	chr19:36504551-36505638	A549	lung:	n/a	n/a
37	CREB1	chr19:36504867-36505700	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr19:36504822-36505768	GM12878	blood:	n/a	n/a
39	CREB1	chr19:36504967-36505685	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr19:36504903-36505604	ECC-1	luminal epithelium:	n/a	n/a
41	CREB1	chr19:36504924-36505611	A549	lung:	n/a	n/a
42	CREB1	chr19:36500196-36500521	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr19:36504879-36505600	K562	blood:	n/a	n/a
44	CREB1	chr19:36500065-36500619	A549	lung:	n/a	n/a
45	CREB1	chr19:36504886-36505720	HepG2	liver:	n/a	n/a
46	CTBP2	chr19:36499510-36500463	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr19:36505360-36505510	AG10803	skin:	n/a	n/a
48	CTCF	chr19:36500350-36500420	GM19238	blood:	n/a	n/a
49	CTCF	chr19:36505420-36505570	MCF-7	breast:	n/a	n/a
50	CTCF	chr19:36505395-36505553	GM19240	blood:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36507075-36507125	HEK293	kidney:	embryo
2	chr19:36499721-36499771	T-47D	breast:	n/a
3	chr19:36504952-36505002	HIPEpiC	eye:	n/a
4	chr19:36507075-36507125	HEK293	kidney:	embryo
5	chr19:36499721-36499771	T-47D	breast:	n/a
6	chr19:36504952-36505002	HIPEpiC	eye:	n/a
7	chr19:36505394-36505444	AG04450	lung:	fetal
8	chr19:36505164-36505214	U87	brain:	n/a
9	chr19:36505305-36505355	PrEC	prostate:	n/a
10	chr19:36500444-36500494	RPTEC	kidney:	n/a
11	chr19:36504494-36504544	HRPEpiC	eye:	n/a
12	chr19:36504952-36505002	LNCaP	prostate:	n/a
13	chr19:36505899-36505949	ovcar-3	ovarian:	n/a
14	chr19:36504952-36505002	HUVEC	blood vessel:	n/a
15	chr19:36504952-36505002	HRE	kidney:	n/a
16	chr19:36505305-36505355	SK-N-MC	brain:	n/a
17	chr19:36505654-36505704	SKMC	muscle:	n/a
18	chr19:36507004-36507054	SAEC	small airway:	n/a
19	chr19:36506269-36506319	HRCEpiC	kidney:	n/a
20	chr19:36500529-36500579	HCM	heart:	n/a
21	chr19:36504494-36504544	GM12878	blood:	n/a
22	chr19:36505322-36505372	MCF-7	breast:	n/a
23	chr19:36505654-36505704	Jurkat	blood:	n/a
24	chr19:36505654-36505704	HEK293	kidney:	embryo
25	chr19:36505305-36505355	HCM	heart:	n/a
26	chr19:36505899-36505949	MCF-7	breast:	n/a
27	chr19:36500529-36500579	CMK	blood:	n/a
28	chr19:36507075-36507125	PFSK-1	brain:	n/a
29	chr19:36499666-36499716	HPAEpiC	pulmonary alveolar:	n/a
30	chr19:36500444-36500494	AG09309	skin:	n/a
31	chr19:36500444-36500494	HNPCEpiC	eye:	n/a
32	chr19:36505305-36505355	A549	lung:	n/a
33	chr19:36505139-36505189	GM12891	blood:	n/a
34	chr19:36499666-36499716	Hela-S3	cervix:	n/a
35	chr19:36505899-36505949	NB4	blood:	n/a
36	chr19:36499666-36499716	AG09319	gingival:	n/a
37	chr19:36505899-36505949	HPAEpiC	pulmonary alveolar:	n/a
38	chr19:36506269-36506319	NH-A	brain:	n/a
39	chr19:36507004-36507054	HIPEpiC	eye:	n/a
40	chr19:36505164-36505214	Caco-2	colon:	n/a
41	chr19:36499721-36499771	Hepatocyte	liver:	n/a
42	chr19:36499326-36499376	AG04450	lung:	fetal
43	chr19:36504952-36505002	HL-60	blood:	n/a
44	chr19:36505899-36505949	NT2-D1	testis:	n/a
45	chr19:36500494-36500544	HEK293	kidney:	embryo
46	chr19:36504952-36505002	SAEC	small airway:	n/a
47	chr19:36504494-36504544	HPAEpiC	pulmonary alveolar:	n/a
48	chr19:36505322-36505372	RPTEC	kidney:	n/a
49	chr19:36505654-36505704	Hepatocyte	liver:	n/a
50	chr19:36505164-36505214	AG10803	skin:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:36508348..36511238-chr19:36524542..36526846,2	K562	blood:
2	chr19:36484302..36487799-chr19:36505417..36507868,3	K562	blood:
3	chr19:36506976..36509848-chr19:36525241..36526846,2	K562	blood:
4	chr19:36485859..36488292-chr19:36497907..36499980,2	K562	blood:
5	chr19:36489874..36492558-chr19:36494414..36497214,4	K562	blood:
6	chr19:36388094..36390635-chr19:36498099..36499853,2	K562	blood:
7	chr19:36485859..36488292-chr19:36497907..36499980,3	K562	blood:
8	chr19:36484693..36488797-chr19:36489372..36495554,13	MCF-7	breast:
9	chr19:36497746..36499339-chr19:36508373..36509944,2	MCF-7	breast:
10	chr19:36505412..36512625-chr19:36513263..36519988,12	K562	blood:
11	chr19:36496294..36501686-chr19:36543356..36547257,9	MCF-7	breast:
12	chr19:36497884..36507784-chr19:36542079..36547610,17	MCF-7	breast:
13	chr19:36502180..36504188-chr19:36532444..36535158,2	MCF-7	breast:
14	chr19:36485744..36488936-chr19:36494222..36497401,4	K562	blood:
15	chr19:36499093..36500043-chr20:47894726..47895550,2	HCT-116	colon:
16	chr19:36503789..36506155-chr19:36544255..36546130,2	K562	blood:
17	chr19:36358531..36360792-chr19:36503749..36506105,2	MCF-7	breast:
18	chr19:36464329..36466760-chr19:36500199..36501728,2	K562	blood:
19	chr17:56708054..56710965-chr19:36499452..36500976,2	MCF-7	breast:
20	chr19:36502189..36508386-chr19:36540645..36546835,9	MCF-7	breast:
21	chr19:36507173..36509172-chr19:36603738..36605911,2	MCF-7	breast:
22	chr1:148241081..148242033-chr19:36504905..36505426,2	Hela-S3	cervix:
23	chr19:36456558..36458643-chr19:36500647..36502286,2	K562	blood:
24	chr19:36505439..36507215-chr19:36510451..36512262,2	MCF-7	breast:
25	chr19:36494473..36501836-chr19:36501930..36505739,14	K562	blood:
26	chr17:39684092..39684606-chr19:36499761..36500329,2	HCT-116	colon:
27	chr19:36502464..36504075-chr19:36504262..36506420,2	K562	blood:
28	chr19:36484477..36488406-chr19:36502641..36506978,6	K562	blood:
29	chr19:36487282..36490058-chr19:36500834..36502670,2	K562	blood:
30	chr12:57082188..57083012-chr19:36500019..36500573,2	HCT-116	colon:
31	chr19:36480405..36483326-chr19:36494595..36496601,2	K562	blood:
32	chr19:36497746..36499339-chr19:36508373..36509944,2	MCF-7	breast:
33	chr19:36494473..36501836-chr19:36501930..36505739,14	K562	blood:
34	chr19:36498267..36501775-chr19:36606279..36609989,4	MCF-7	breast:
35	chr19:36208921..36210608-chr19:36499552..36501350,2	MCF-7	breast:
36	chr19:36504655..36506922-chr19:36544255..36547222,4	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C19orf46-1	chr19:36499119-36499512	NONHSAT065945
2	lnc-C19orf46-1	chr19:36496235-36496339	NONHSAT065945
3	lnc-ALKBH6-2	chr19:36498460-36498684	uc_451_-
4	lnc-SDHAF1-1	chr19:36498460-36498684	uc_451_+

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CLIP3	hsa-miR-335-5p	chr19:36506656-36506678

Variant related genes	Relation type
ALKBH6	TF binding region
SYNE4	TF binding region
ENSG00000248101	TF binding region
ENSG00000267698	TF binding region
ALKBH6	CpG island
SYNE4	CpG island
ENSG00000248101	CpG island
ENSG00000267698	CpG island
ENSG00000209042	chromatin interactions
ENSG00000105270	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000167604	chromatin interactions
ENSG00000075702	chromatin interactions
ENSG00000177410	chromatin interactions
ENSG00000171345	chromatin interactions
ENSG00000239382	chromatin interactions
ENSG00000161277	chromatin interactions
ENSG00000105258	chromatin interactions
ENSG00000105254	chromatin interactions
ENSG00000207501	chromatin interactions
ENSG00000267698	chromatin interactions
ENSG00000205138	chromatin interactions
ENSG00000181392	chromatin interactions
ENSG00000105290	chromatin interactions
ENSG00000161270	chromatin interactions
ENSG00000272333	chromatin interactions

Extended variants
information (count: 562 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:562 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554794711	chr19:36494644-36494645	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs368933746	chr19:36494655-36494656	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs150431129	chr19:36494666-36494667	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs373888049	chr19:36494681-36494682	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs558845225	chr19:36494708-36494709	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs375701144	chr19:36494712-36494713	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs540997708	chr19:36494747-36494748	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs559322399	chr19:36494764-36494765	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs374060690	chr19:36494765-36494766	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs138029196	chr19:36494844-36494845	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs548425900	chr19:36494867-36494868	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs190050006	chr19:36494872-36494873	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs531172533	chr19:36494917-36494918	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs552513051	chr19:36494918-36494919	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs564773572	chr19:36494998-36494999	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs528799979	chr19:36495007-36495008	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs547378305	chr19:36495010-36495011	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs565718527	chr19:36495031-36495032	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs77328940	chr19:36495079-36495080	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs149521826	chr19:36495107-36495108	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs144116928	chr19:36495124-36495125	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs535795229	chr19:36495171-36495172	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs138967177	chr19:36495184-36495185	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs373201690	chr19:36495214-36495215	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs369780172	chr19:36495220-36495221	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs534611188	chr19:36495283-36495284	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs183605612	chr19:36495304-36495305	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs565540387	chr19:36495353-36495354	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs539688178	chr19:36495390-36495391	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs563835716	chr19:36495420-36495421	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs142912893	chr19:36495433-36495434	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs73607766	chr19:36495502-36495503	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs576437305	chr19:36495507-36495508	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs377195980	chr19:36495523-36495524	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs188649664	chr19:36495533-36495534	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs546332350	chr19:36495550-36495551	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs371741417	chr19:36495572-36495573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs193100857	chr19:36495582-36495583	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs528786033	chr19:36495592-36495593	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs540973613	chr19:36495619-36495620	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs537242234	chr19:36495654-36495655	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs559368943	chr19:36495707-36495708	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs372274893	chr19:36495768-36495769	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs200230086	chr19:36495771-36495772	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs568210744	chr19:36495772-36495773	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs59700541	chr19:36495794-36495795	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs529749961	chr19:36495814-36495815	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs113888225	chr19:36495856-36495857	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs569702602	chr19:36495872-36495873	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs555643088	chr19:36495873-36495874	Weak transcription Strong transcription	Chromatin interactive region	3 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
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	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
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1341 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36487200-36499000	Weak transcription	Fetal Kidney	kidney
2	chr19:36487200-36499200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:36487200-36504200	Weak transcription	HSMMtube	muscle
4	chr19:36487600-36499000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr19:36487600-36499000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr19:36487600-36499200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr19:36487600-36499800	Weak transcription	HUVEC	blood vessel
8	chr19:36487600-36500000	Weak transcription	HSMM	muscle
9	chr19:36487800-36498800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr19:36487800-36498800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr19:36487800-36499000	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr19:36487800-36499200	Weak transcription	HMEC	breast
13	chr19:36487800-36499600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr19:36487800-36499600	Weak transcription	NHEK	skin
15	chr19:36488000-36495400	Weak transcription	K562	blood
16	chr19:36488000-36499000	Weak transcription	Rectal Smooth Muscle	rectum
17	chr19:36488000-36499600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr19:36488000-36504000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr19:36488400-36496200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr19:36488400-36499400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr19:36488400-36499600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr19:36488400-36504200	Weak transcription	Primary B cells from cord blood	blood
23	chr19:36488600-36498200	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr19:36488600-36499600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr19:36488600-36503800	Weak transcription	GM12878-XiMat	blood
26	chr19:36488800-36499000	Weak transcription	Stomach Mucosa	stomach
27	chr19:36488800-36499600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr19:36488800-36504000	Weak transcription	Hela-S3	cervix
29	chr19:36489000-36500000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr19:36489600-36498400	Weak transcription	Esophagus	oesophagus
31	chr19:36489600-36499600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr19:36490200-36499000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr19:36490200-36499400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr19:36490400-36499000	Weak transcription	Brain Germinal Matrix	brain
35	chr19:36490400-36499200	Weak transcription	Fetal Brain Female	brain
36	chr19:36490400-36499600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr19:36490400-36499600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr19:36490400-36499600	Weak transcription	Right Ventricle	heart
39	chr19:36490400-36499800	Weak transcription	NHDF-Ad	bronchial
40	chr19:36490600-36495000	Weak transcription	HepG2	liver
41	chr19:36490600-36499800	Weak transcription	Right Atrium	heart
42	chr19:36490800-36497600	Weak transcription	Psoas Muscle	Psoas
43	chr19:36490800-36499600	Weak transcription	Brain Cingulate Gyrus	brain
44	chr19:36490800-36499800	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr19:36490800-36500000	Weak transcription	Ovary	ovary
46	chr19:36491000-36499600	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr19:36491000-36499800	Weak transcription	Colon Smooth Muscle	Colon
48	chr19:36491000-36500400	Weak transcription	NHLF	lung
49	chr19:36491200-36497600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr19:36491200-36499400	Weak transcription	Brain Hippocampus Middle	brain

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