Variant report

Variant	nsv458569
Chromosome Location	chr19:37331614-37412887
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:881)
CpG islands
(count:2079)
Chromatin interactive
region (count:31)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:881 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:37340907-37341297	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:37407439-37407639	HepG2	liver:	n/a	n/a
3	ATF2	chr19:37341530-37341899	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr19:37407123-37407453	H1-hESC	embryonic stem cell:	n/a	chr19:37407148-37407156
5	BACH1	chr19:37406796-37407749	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr19:37340771-37342363	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr19:37340499-37340785	GM12878	blood:	n/a	n/a
8	BCL11A	chr19:37338953-37339190	GM12878	blood:	n/a	n/a
9	BCLAF1	chr19:37406973-37407538	GM12878	blood:	n/a	chr19:37407255-37407264 chr19:37407385-37407398 chr19:37407195-37407204
10	BCLAF1	chr19:37340487-37340876	GM12878	blood:	n/a	n/a
11	BCLAF1	chr19:37340807-37342313	GM12878	blood:	n/a	n/a
12	BHLHE40	chr19:37340497-37342133	GM12878	blood:	n/a	n/a
13	BHLHE40	chr19:37407226-37407625	GM12878	blood:	n/a	chr19:37407387-37407403 chr19:37407364-37407380
14	BRCA1	chr19:37341252-37341986	GM12878	blood:	n/a	chr19:37341729-37341738
15	BRCA1	chr19:37340977-37342008	HepG2	liver:	n/a	chr19:37341729-37341738
16	BRCA1	chr19:37342206-37342225	GM12878	blood:	n/a	n/a
17	BRCA1	chr19:37340791-37342011	H1-hESC	embryonic stem cell:	n/a	chr19:37341729-37341738
18	BRCA1	chr19:37406852-37407051	HepG2	liver:	n/a	n/a
19	BRCA1	chr19:37406863-37407378	GM12878	blood:	n/a	n/a
20	BRCA1	chr19:37406771-37407709	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr19:37406786-37407541	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr19:37406812-37407114	HepG2	liver:	n/a	n/a
23	CEBPB	chr19:37406694-37407173	MCF-7	breast:	n/a	n/a
24	CEBPB	chr19:37358231-37358415	HepG2	liver:	n/a	chr19:37358324-37358335
25	CEBPB	chr19:37358188-37358458	IMR90	lung:	n/a	chr19:37358324-37358335
26	CEBPB	chr19:37358259-37358429	A549	lung:	n/a	chr19:37358324-37358335
27	CEBPB	chr19:37407545-37407755	HepG2	liver:	n/a	n/a
28	CEBPB	chr19:37406755-37407818	IMR90	lung:	n/a	n/a
29	CEBPB	chr19:37411948-37412009	A549	lung:	n/a	n/a
30	CEBPB	chr19:37341593-37341917	HepG2	liver:	n/a	n/a
31	CHD1	chr19:37341929-37341969	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr19:37341738-37342494	GM12878	blood:	n/a	n/a
33	CHD1	chr19:37340451-37341380	GM12878	blood:	n/a	n/a
34	CHD1	chr19:37340654-37340757	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr19:37406776-37407462	GM12878	blood:	n/a	n/a
36	CHD2	chr19:37406737-37407607	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr19:37406795-37407449	HepG2	liver:	n/a	n/a
38	CHD2	chr19:37341010-37341974	K562	blood:	n/a	n/a
39	CHD2	chr19:37340553-37342488	GM12878	blood:	n/a	n/a
40	CHD2	chr19:37340985-37342202	HepG2	liver:	n/a	n/a
41	CHD2	chr19:37340792-37342343	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr19:37406901-37406994	K562	blood:	n/a	n/a
43	CREB1	chr19:37406726-37407667	GM12878	blood:	n/a	n/a
44	CREB1	chr19:37406700-37407638	HepG2	liver:	n/a	n/a
45	CREB1	chr19:37406681-37407438	A549	lung:	n/a	n/a
46	CREB1	chr19:37406719-37407603	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr19:37406746-37407660	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr19:37406750-37407546	HepG2	liver:	n/a	n/a
49	CTBP2	chr19:37406863-37407581	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr19:37407280-37407430	HEK293	kidney:	n/a	chr19:37407361-37407377 chr19:37407391-37407401 chr19:37407360-37407378

(count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:37407214-37407264	H1-hESC	embryonic stem cell:	embryo
2	chr19:37407041-37407091	HCPEpiC	choroid plexus:	n/a
3	chr19:37407123-37407173	T-47D	breast:	n/a
4	chr19:37406932-37406982	SK-N-SH_RA	brain:	n/a
5	chr19:37341169-37341219	HepG2	liver:	n/a
6	chr19:37407214-37407264	H1-hESC	embryonic stem cell:	embryo
7	chr19:37407041-37407091	HCPEpiC	choroid plexus:	n/a
8	chr19:37407123-37407173	T-47D	breast:	n/a
9	chr19:37406932-37406982	SK-N-SH_RA	brain:	n/a
10	chr19:37341169-37341219	HepG2	liver:	n/a
11	chr19:37341166-37341216	HCT-116	colon:	n/a
12	chr19:37341166-37341216	RPTEC	kidney:	n/a
13	chr19:37337985-37338035	HepG2	liver:	n/a
14	chr19:37407152-37407202	HRE	kidney:	n/a
15	chr19:37341103-37341153	HRE	kidney:	n/a
16	chr19:37407889-37407939	MCF-7	breast:	n/a
17	chr19:37341052-37341102	HPAEpiC	pulmonary alveolar:	n/a
18	chr19:37407374-37407424	HCPEpiC	choroid plexus:	n/a
19	chr19:37406949-37406999	PFSK-1	brain:	n/a
20	chr19:37340694-37340744	RPTEC	kidney:	n/a
21	chr19:37407462-37407512	SKMC	muscle:	n/a
22	chr19:37341261-37341311	HRE	kidney:	n/a
23	chr19:37340694-37340744	HNPCEpiC	eye:	n/a
24	chr19:37407060-37407110	MCF10A-Er-Src	breast:	n/a
25	chr19:37407486-37407536	K562	blood:	n/a
26	chr19:37340694-37340744	NB4	blood:	n/a
27	chr19:37341219-37341269	BJ	skin:	n/a
28	chr19:37341373-37341423	BJ	skin:	n/a
29	chr19:37403956-37404006	U87	brain:	n/a
30	chr19:37341870-37341920	U87	brain:	n/a
31	chr19:37403956-37404006	NB4	blood:	n/a
32	chr19:37407374-37407424	GM12878	blood:	n/a
33	chr19:37407123-37407173	AG09309	skin:	n/a
34	chr19:37382272-37382322	AG04449	skin:	fetal
35	chr19:37407041-37407091	A549	lung:	n/a
36	chr19:37341373-37341423	LNCaP	prostate:	n/a
37	chr19:37407257-37407307	NHDF-neo	bronchial:	n/a
38	chr19:37342585-37342635	HUVEC	blood vessel:	n/a
39	chr19:37341103-37341153	AoSMC	blood vessel:	n/a
40	chr19:37368471-37368521	MCF10A-Er-Src	breast:	n/a
41	chr19:37407284-37407334	HEK293	kidney:	embryo
42	chr19:37341103-37341153	PFSK-1	brain:	n/a
43	chr19:37341734-37341784	AG09319	gingival:	n/a
44	chr19:37403956-37404006	GM06990	blood:	n/a
45	chr19:37341103-37341153	BE2_C	brain:	n/a
46	chr19:37409826-37409876	HAEpiC	amniotic membrane:	n/a
47	chr19:37341261-37341311	HAEpiC	amniotic membrane:	n/a
48	chr19:37341261-37341311	HIPEpiC	eye:	n/a
49	chr19:37341219-37341269	HepG2	liver:	n/a
50	chr19:37407462-37407512	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:37339729..37341977-chr19:37344945..37346837,2	K562	blood:
2	chr19:37338913..37342435-chr19:37343992..37346462,3	K562	blood:
3	chr19:37327752..37331008-chr19:37336124..37344037,12	MCF-7	breast:
4	chr19:37341751..37343883-chr19:37348520..37351258,2	K562	blood:
5	chr19:37287538..37289947-chr19:37340425..37342708,2	MCF-7	breast:
6	chr19:37327731..37330688-chr19:37341355..37343335,2	K562	blood:
7	chr19:37342451..37344780-chr19:37351760..37354112,2	K562	blood:
8	chr19:36629161..36631921-chr19:37341375..37343285,2	MCF-7	breast:
9	chr19:37341751..37345172-chr19:37348520..37351258,3	K562	blood:
10	chr19:37368925..37371871-chr19:37383138..37385642,2	MCF-7	breast:
11	chr19:37329288..37331381-chr19:37334889..37337614,2	K562	blood:
12	chr19:37341026..37342586-chr19:37347410..37350051,2	MCF-7	breast:
13	chr19:37331659..37333471-chr19:37334083..37336419,2	MCF-7	breast:
14	chr19:37405380..37408333-chr19:37412047..37415045,3	MCF-7	breast:
15	chr19:37340586..37343118-chr19:37344104..37346997,2	MCF-7	breast:
16	chr19:37335646..37338151-chr19:37339338..37341642,2	K562	blood:
17	chr19:37327831..37331190-chr19:37339964..37343241,7	MCF-7	breast:
18	chr19:37328893..37331026-chr19:37332754..37334779,3	K562	blood:
19	chr19:37341026..37342586-chr19:37347410..37350051,2	MCF-7	breast:
20	chr19:37329308..37331359-chr19:37364409..37366170,2	K562	blood:
21	chr19:37331659..37333471-chr19:37334083..37336419,2	MCF-7	breast:
22	chr19:37341751..37345172-chr19:37348520..37351258,3	K562	blood:
23	chr19:37368925..37371871-chr19:37383138..37385642,2	MCF-7	breast:
24	chr19:37328153..37331214-chr19:37339535..37342855,6	K562	blood:
25	chr19:37402448..37404618-chr19:37405463..37407897,2	MCF-7	breast:
26	chr19:37328191..37330014-chr19:37367737..37370320,2	MCF-7	breast:
27	chr19:37341916..37344029-chr19:37407089..37408811,2	MCF-7	breast:
28	chr19:37341751..37343883-chr19:37348520..37351258,2	K562	blood:
29	chr19:37332133..37336118-chr19:37338996..37342341,4	MCF-7	breast:
30	chr19:37411760..37413673-chr19:37428843..37431824,2	MCF-7	breast:
31	chr19:37341916..37344029-chr19:37407089..37408811,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF345-4	chr19:37389067-37389188	l_1678_chr19:37389066-37399110_whiteBloodCell
2	lnc-ZNF345-2	chr19:37383720-37383936	NONHSAT066056
3	lnc-ZNF790-1	chr19:37341779-37342087	ENSG00000254435.1
4	lnc-ZNF790-1	chr19:37342310-37342418	ENSG00000254435.1
5	lnc-ZNF345-2	chr19:37383720-37384120	NONHSAT066053
6	lnc-ZNF345-2	chr19:37342732-37342806	NONHSAT066054
7	lnc-ZNF345-2	chr19:37383720-37383887	NONHSAT066054
8	lnc-ZNF345-2	chr19:37342732-37342806	NONHSAT066053
9	lnc-ZNF345-2	chr19:37345352-37345496	NONHSAT066057
10	lnc-ZNF345-2	chr19:37383720-37383936	NONHSAT066055
11	lnc-ZNF345-2	chr19:37341788-37341870	NONHSAT066053
12	lnc-ZNF345-2	chr19:37342732-37342806	NONHSAT066055
13	lnc-ZNF345-2	chr19:37342647-37342806	NONHSAT066056
14	lnc-ZNF345-2	chr19:37341832-37341870	NONHSAT066054
15	lnc-ZNF345-4	chr19:37399035-37399110	l_1678_chr19:37389066-37399110_whiteBloodCell
16	lnc-ZNF345-2	chr19:37383720-37383932	NONHSAT066057
17	lnc-ZNF345-2	chr19:37403629-37403931	NONHSAT066054
18	lnc-ZNF345-4	chr19:37389239-37389247	l_1678_chr19:37389066-37399110_whiteBloodCell
19	lnc-ZNF345-2	chr19:37342557-37342625	NONHSAT066055
20	lnc-ZNF345-2	chr19:37342754-37342806	NONHSAT066057

No data

Variant related genes	Relation type
ZNF790	TF binding region
ZNF829	TF binding region
ZNF568	TF binding region
ENSG00000206669	TF binding region
RPL31P61	TF binding region
ZNF345	TF binding region
ZNF790	CpG island
ZNF829	CpG island
ZNF568	CpG island
ENSG00000206669	CpG island
RPL31P61	CpG island
ZNF345	CpG island
ENSG00000251247	chromatin interactions
ENSG00000126247	chromatin interactions
ENSG00000267254	chromatin interactions
ENSG00000206669	chromatin interactions
ENSG00000185869	chromatin interactions
ENSG00000198453	chromatin interactions
ENSG00000197863	chromatin interactions

Extended variants
information (count: 2710 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2710 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1144539	chr19:37331614-37331615	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs1227560	chr19:37331639-37331640	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs545934603	chr19:37331683-37331684	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557433089	chr19:37331776-37331777	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530987418	chr19:37331811-37331812	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557728829	chr19:37331858-37331859	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572907863	chr19:37331904-37331905	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540533006	chr19:37331915-37331916	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562423841	chr19:37331943-37331944	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529441317	chr19:37332112-37332113	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544773310	chr19:37332221-37332222	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs376952592	chr19:37332249-37332250	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs563111370	chr19:37332282-37332283	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs530614298	chr19:37332322-37332323	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs190508022	chr19:37332385-37332386	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs570416520	chr19:37332414-37332415	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs528098679	chr19:37332429-37332430	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs113968228	chr19:37332448-37332449	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs546544446	chr19:37332487-37332488	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs145043990	chr19:37332526-37332527	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs535418077	chr19:37332528-37332529	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs556727367	chr19:37332558-37332559	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568757599	chr19:37332559-37332560	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs539499454	chr19:37332587-37332588	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs369700621	chr19:37332604-37332605	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs376146438	chr19:37332633-37332634	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs557837225	chr19:37332654-37332655	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs572865095	chr19:37332750-37332751	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs181385254	chr19:37332751-37332752	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs370781210	chr19:37332766-37332767	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201434175	chr19:37332787-37332788	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs574261863	chr19:37332798-37332799	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs563812054	chr19:37332852-37332853	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs544621212	chr19:37333022-37333023	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs563071782	chr19:37333060-37333061	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs578220854	chr19:37333073-37333074	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs186419276	chr19:37333088-37333089	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs567624401	chr19:37333097-37333098	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs561926207	chr19:37333131-37333132	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs11883279	chr19:37333138-37333139	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs190869874	chr19:37333168-37333169	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs547257804	chr19:37333222-37333223	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs11883155	chr19:37333223-37333224	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs1227561	chr19:37333332-37333333	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs182671024	chr19:37333359-37333360	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs529183831	chr19:37333383-37333384	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs78297558	chr19:37333385-37333386	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs11883207	chr19:37333430-37333431	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs539261562	chr19:37333434-37333435	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs531022010	chr19:37333567-37333568	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3343 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:37329800-37333800	Weak transcription	Ovary	ovary
2	chr19:37329800-37334000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr19:37329800-37334000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr19:37329800-37334000	Weak transcription	Thymus	Thymus
5	chr19:37329800-37337000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr19:37329800-37339000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr19:37329800-37339600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr19:37329800-37339600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr19:37330000-37333600	Weak transcription	Primary T cells from cord blood	blood
10	chr19:37330000-37333800	Weak transcription	NH-A	brain
11	chr19:37330000-37334000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr19:37330000-37334000	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr19:37330000-37334000	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr19:37330000-37334000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr19:37330000-37334000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr19:37330000-37334000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr19:37330000-37334000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr19:37330000-37334000	Weak transcription	Brain Substantia Nigra	brain
19	chr19:37330000-37334000	Weak transcription	Fetal Muscle Trunk	muscle
20	chr19:37330000-37334000	Weak transcription	Fetal Muscle Leg	muscle
21	chr19:37330000-37334000	Weak transcription	Left Ventricle	heart
22	chr19:37330000-37334000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr19:37330000-37334200	Weak transcription	Fetal Stomach	stomach
24	chr19:37330000-37334200	Weak transcription	Pancreas	Pancrea
25	chr19:37330000-37334400	Weak transcription	Esophagus	oesophagus
26	chr19:37330000-37335000	Weak transcription	Fetal Thymus	thymus
27	chr19:37330000-37335200	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr19:37330000-37336400	Weak transcription	Primary B cells from peripheral blood	blood
29	chr19:37330000-37339600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr19:37330000-37340000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr19:37330000-37340000	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr19:37330000-37340000	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr19:37330000-37340000	Weak transcription	Fetal Brain Male	brain
34	chr19:37330000-37340000	Weak transcription	Right Ventricle	heart
35	chr19:37330000-37340400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr19:37330000-37340400	Weak transcription	Colonic Mucosa	Colon
37	chr19:37330000-37340400	Weak transcription	Placenta	Placenta
38	chr19:37330000-37340400	Weak transcription	Stomach Mucosa	stomach
39	chr19:37330000-37340600	Weak transcription	Gastric	stomach
40	chr19:37330000-37340600	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr19:37330000-37340600	Weak transcription	Spleen	Spleen
42	chr19:37330000-37340600	Weak transcription	HSMM	muscle
43	chr19:37330200-37332000	Weak transcription	NHLF	lung
44	chr19:37330200-37332800	Weak transcription	Duodenum Mucosa	Duodenum
45	chr19:37330200-37332800	Weak transcription	Fetal Intestine Large	intestine
46	chr19:37330200-37334000	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr19:37330200-37334000	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr19:37330200-37334000	Weak transcription	HUVEC	blood vessel
49	chr19:37330200-37334200	Weak transcription	Brain Germinal Matrix	brain
50	chr19:37330200-37334200	Weak transcription	Fetal Brain Female	brain

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