Variant report

Variant	nsv520020
Chromosome Location	chr19:36721368-36822594
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:886)
CpG islands
(count:2138)
Chromatin interactive
region (count:17)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:886 , 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	ATF1	chr19:36757608-36757618	K562	blood:	n/a	n/a
2	BACH1	chr19:36736052-36736534	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr19:36822319-36822665	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr19:36728581-36729227	K562	blood:	n/a	n/a
5	BCL3	chr19:36729902-36731362	A549	lung:	n/a	n/a
6	BCL3	chr19:36736776-36737392	GM12878	blood:	n/a	n/a
7	BCL3	chr19:36736809-36737328	GM12878	blood:	n/a	n/a
8	BCL3	chr19:36731641-36732205	A549	lung:	n/a	n/a
9	BHLHE40	chr19:36757499-36757673	K562	blood:	n/a	n/a
10	BHLHE40	chr19:36822480-36822814	GM12878	blood:	n/a	n/a
11	BHLHE40	chr19:36822590-36822698	K562	blood:	n/a	n/a
12	BRCA1	chr19:36736302-36736619	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr19:36762836-36763037	HepG2	liver:	n/a	n/a
14	CBX3	chr19:36727143-36728326	K562	blood:	n/a	n/a
15	CBX3	chr19:36727309-36727522	K562	blood:	n/a	n/a
16	CBX3	chr19:36762724-36763179	K562	blood:	n/a	n/a
17	CBX3	chr19:36782055-36782327	K562	blood:	n/a	n/a
18	CBX3	chr19:36785308-36785504	K562	blood:	n/a	n/a
19	CBX3	chr19:36789665-36790026	K562	blood:	n/a	n/a
20	CBX3	chr19:36787829-36788041	K562	blood:	n/a	n/a
21	CBX3	chr19:36768844-36769134	K562	blood:	n/a	n/a
22	CBX3	chr19:36795732-36796004	K562	blood:	n/a	n/a
23	CBX3	chr19:36796036-36796224	K562	blood:	n/a	n/a
24	CCNT2	chr19:36757335-36757662	K562	blood:	n/a	n/a
25	CEBPB	chr19:36737188-36737309	A549	lung:	n/a	n/a
26	CEBPB	chr19:36737103-36737306	IMR90	lung:	n/a	n/a
27	CEBPB	chr19:36822504-36822774	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr19:36757408-36757715	K562	blood:	n/a	n/a
29	CHD1	chr19:36821511-36822557	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr19:36762837-36763034	HepG2	liver:	n/a	n/a
31	CHD2	chr19:36735997-36736651	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr19:36727668-36728226	K562	blood:	n/a	n/a
33	CHD2	chr19:36822351-36823045	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr19:36822518-36822932	GM12878	blood:	n/a	n/a
35	CREB1	chr19:36822377-36823060	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr19:36822370-36822951	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr19:36822580-36822730	HAc	cerebellar:	n/a	n/a
38	CTCF	chr19:36806159-36806371	LNCaP	prostate:	n/a	n/a
39	CTCF	chr19:36822260-36822410	NHEK	skin:	n/a	n/a
40	CTCF	chr19:36806168-36806277	MCF-7	breast:	n/a	n/a
41	CTCF	chr19:36820740-36820758	LNCaP	prostate:	n/a	n/a
42	CTCF	chr19:36782028-36782324	K562	blood:	n/a	n/a
43	CTCF	chr19:36736040-36736190	AG04450	lung:	n/a	n/a
44	CTCF	chr19:36736080-36736230	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr19:36806213-36806359	Fibrobl	skin:	n/a	n/a
46	CTCF	chr19:36806748-36806813	GM13976	blood:	n/a	n/a
47	CTCF	chr19:36736140-36736290	HEK293	kidney:	n/a	n/a
48	CTCF	chr19:36822440-36822590	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr19:36736060-36736210	BE2_C	brain:	n/a	n/a
50	CTCF	chr19:36735020-36735170	Hela-S3	cervix:	n/a	n/a

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36739015-36739065	HMEC	breast:	n/a
2	chr19:36736272-36736322	GM12891	blood:	n/a
3	chr19:36736872-36736922	AG04450	lung:	fetal
4	chr19:36739015-36739065	HMEC	breast:	n/a
5	chr19:36736272-36736322	GM12891	blood:	n/a
6	chr19:36736872-36736922	AG04450	lung:	fetal
7	chr19:36736272-36736322	NT2-D1	testis:	n/a
8	chr19:36822549-36822599	PFSK-1	brain:	n/a
9	chr19:36739015-36739065	PANC-1	pancreas:	n/a
10	chr19:36736272-36736322	U87	brain:	n/a
11	chr19:36759220-36759270	AG09309	skin:	n/a
12	chr19:36746473-36746523	SK-N-SH	brain:	n/a
13	chr19:36818607-36818657	HCT-116	colon:	n/a
14	chr19:36729234-36729284	HNPCEpiC	eye:	n/a
15	chr19:36799625-36799675	HIPEpiC	eye:	n/a
16	chr19:36726985-36727035	NT2-D1	testis:	n/a
17	chr19:36749224-36749274	K562	blood:	n/a
18	chr19:36801408-36801458	U87	brain:	n/a
19	chr19:36801408-36801458	HNPCEpiC	eye:	n/a
20	chr19:36739015-36739065	SK-N-SH	brain:	n/a
21	chr19:36736477-36736527	MCF-7	breast:	n/a
22	chr19:36822442-36822492	BE2_C	brain:	n/a
23	chr19:36739015-36739065	SKMC	muscle:	n/a
24	chr19:36802391-36802441	K562	blood:	n/a
25	chr19:36749224-36749274	HEEpiC	esophagus:	n/a
26	chr19:36822564-36822614	ProgFib	skin:	n/a
27	chr19:36801484-36801534	H1-hESC	embryonic stem cell:	embryo
28	chr19:36739015-36739065	AoSMC	blood vessel:	n/a
29	chr19:36732345-36732395	U87	brain:	n/a
30	chr19:36801503-36801553	NHDF-neo	bronchial:	n/a
31	chr19:36727978-36728028	GM12892	blood:	n/a
32	chr19:36726982-36727032	AG04449	skin:	fetal
33	chr19:36746737-36746787	BJ	skin:	n/a
34	chr19:36764158-36764208	PrEC	prostate:	n/a
35	chr19:36727978-36728028	HEK293	kidney:	embryo
36	chr19:36822311-36822361	HRE	kidney:	n/a
37	chr19:36764158-36764208	HIPEpiC	eye:	n/a
38	chr19:36744465-36744515	HEEpiC	esophagus:	n/a
39	chr19:36801484-36801534	HAEpiC	amniotic membrane:	n/a
40	chr19:36801484-36801534	HCM	heart:	n/a
41	chr19:36739015-36739065	HCPEpiC	choroid plexus:	n/a
42	chr19:36822564-36822614	AG04450	lung:	fetal
43	chr19:36794212-36794262	NT2-D1	testis:	n/a
44	chr19:36818607-36818657	Caco-2	colon:	n/a
45	chr19:36801408-36801458	HPAEpiC	pulmonary alveolar:	n/a
46	chr19:36794212-36794262	GM12878	blood:	n/a
47	chr19:36758736-36758786	HUVEC	blood vessel:	n/a
48	chr19:36746473-36746523	PrEC	prostate:	n/a
49	chr19:36739015-36739065	HAEpiC	amniotic membrane:	n/a
50	chr19:36801408-36801458	GM12878	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:36729380..36732375-chr19:36732759..36734481,3	MCF-7	breast:
2	chr19:36709335..36711888-chr19:36719668..36721435,2	K562	blood:
3	chr19:36705785..36707917-chr19:36719166..36721745,2	K562	blood:
4	chr19:36713025..36717797-chr19:36719610..36723880,4	K562	blood:
5	chr19:36721445..36724084-chr19:36726404..36728465,2	K562	blood:
6	chr19:36729000..36731636-chr19:36732341..36735804,4	K562	blood:
7	chr19:36727989..36729931-chr19:37016866..37019433,2	MCF-7	breast:
8	chr19:36705688..36707627-chr19:36722412..36724988,2	K562	blood:
9	chr19:36728377..36730727-chr19:36868352..36870714,2	MCF-7	breast:
10	chr19:36721445..36724084-chr19:36726404..36728465,2	K562	blood:
11	chr19:36740128..36741923-chr19:36743583..36745191,2	K562	blood:
12	chr19:36705904..36707565-chr19:36739272..36742019,2	K562	blood:
13	chr19:36729552..36731662-chr19:36736640..36739209,2	K562	blood:
14	chr19:36729000..36731636-chr19:36732341..36735804,4	K562	blood:
15	chr19:36730136..36732594-chr19:36734296..36737243,2	K562	blood:
16	chr19:36740128..36741923-chr19:36743583..36745191,2	K562	blood:
17	chr19:36729380..36732375-chr19:36732759..36734481,3	MCF-7	breast:

(count:45 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF146-1	chr19:36802083-36802290	XLOC_013054
2	lnc-ZFP14-1	chr19:36806262-36806430	ENSG00000232677
3	lnc-ZFP14-1	chr19:36812202-36812259	NONHSAT065992
4	lnc-ZFP14-1	chr19:36813032-36813112	ENSG00000232677
5	lnc-ZFP14-1	chr19:36811507-36811662	ENSG00000232677
6	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677.2
7	lnc-ZFP14-1	chr19:36813032-36813286	ENSG00000232677
8	lnc-ZNF146-1	chr19:36801260-36803564	ENSG00000267053.2
9	lnc-ZFP14-1	chr19:36806859-36807236	NONHSAT065983
10	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
11	lnc-ZFP14-1	chr19:36806859-36806972	NONHSAT065986
12	lnc-ZNF146-1	chr19:36802446-36802694	ENSG00000267053.2
13	lnc-ZNF146-1	chr19:36803424-36803570	NONHSAT065980
14	lnc-ZFP14-1	chr19:36822349-36822602	ENSG00000232677
15	lnc-ZFP14-1	chr19:36803969-36806639	ENSG00000232677.2
16	lnc-ZNF146-1	chr19:36802245-36802694	XLOC_013054
17	lnc-ZFP14-1	chr19:36811026-36811662	NONHSAT065992
18	lnc-ZFP14-1	chr19:36813032-36813130	ENSG00000232677.2
19	lnc-ZFP14-1	chr19:36803622-36804224	NONHSAT065983
20	lnc-ZNF146-1	chr19:36803424-36803568	XLOC_013054
21	lnc-ZNF146-1	chr19:36811922-36812260	XLOC_013054
22	lnc-ZNF146-1	chr19:36802245-36802694	NONHSAT065980
23	lnc-ZNF146-1	chr19:36803424-36803537	XLOC_013054
24	lnc-ZFP14-1	chr19:36806859-36806972	ENSG00000232677
25	lnc-ZFP14-1	chr19:36807080-36807229	NONHSAT065986
26	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
27	lnc-ZFP14-1	chr19:36813032-36813127	ENSG00000232677
28	lnc-ZFP14-1	chr19:36804644-36804814	ENSG00000232677
29	lnc-ZFP14-1	chr19:36806478-36806972	ENSG00000232677.2
30	lnc-ZNF146-1	chr19:36811922-36812194	XLOC_013054
31	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
32	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
33	lnc-ZFP14-1	chr19:36812895-36812933	NONHSAT065992
34	lnc-ZNF146-1	chr19:36803410-36803537	XLOC_013054
35	lnc-ZNF146-1	chr19:36803424-36803570	ENSG00000267053.2
36	lnc-ZNF146-1	chr19:36801260-36803563	ENSG00000267053.2
37	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
38	lnc-ZNF146-1	chr19:36802525-36802694	XLOC_013054
39	lnc-ZFP14-1	chr19:36806859-36806972	ENSG00000232677
40	lnc-ZNF146-1	chr19:36803424-36803537	XLOC_013054
41	lnc-ZNF146-1	chr19:36811922-36812079	XLOC_013054
42	lnc-ZNF146-1	chr19:36802423-36802694	XLOC_013054
43	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
44	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677.2
45	lnc-ZFP14-1	chr19:36803973-36804224	NONHSAT065986

No data

Variant related genes	Relation type
LINC00665	TF binding region
ZNF565	TF binding region
ENSG00000222730	TF binding region
ENSG00000267053	TF binding region
LINC00665	CpG island
ZNF565	CpG island
ENSG00000222730	CpG island
ENSG00000267053	CpG island
ENSG00000266973	chromatin interactions
ENSG00000142065	chromatin interactions
ENSG00000254004	chromatin interactions
ENSG00000167635	chromatin interactions
ENSG00000196357	chromatin interactions
ENSG00000228629	chromatin interactions
SLC35F3	miRNA target sites
SLC35F5	miRNA target sites
SLC35D2	miRNA target sites

Extended variants
information (count: 3030 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3030 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549475834	chr19:36721368-36721369	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs565013637	chr19:36721374-36721375	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs75793223	chr19:36721378-36721379	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573178159	chr19:36721382-36721383	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs554210909	chr19:36721408-36721409	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs59295196	chr19:36721457-36721458	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs559895185	chr19:36721463-36721464	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs10414754	chr19:36721467-36721468	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs78096559	chr19:36721473-36721474	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs78989652	chr19:36721480-36721481	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs537916795	chr19:36721500-36721501	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs117478882	chr19:36721506-36721507	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs10416509	chr19:36721510-36721511	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs191462347	chr19:36721529-36721530	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs184254575	chr19:36721554-36721555	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs553990271	chr19:36721577-36721578	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs572358414	chr19:36721605-36721606	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs536289124	chr19:36721654-36721655	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs554541785	chr19:36721676-36721677	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs576162159	chr19:36721694-36721695	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs112189944	chr19:36721698-36721699	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs375312395	chr19:36721699-36721700	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs117194308	chr19:36721714-36721715	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs188019291	chr19:36721778-36721779	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs2918375	chr19:36721781-36721782	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs192844353	chr19:36721796-36721797	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs370303475	chr19:36721802-36721803	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs145431235	chr19:36721850-36721851	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs373972571	chr19:36721857-36721858	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs368119509	chr19:36721860-36721861	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs2918376	chr19:36721890-36721891	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs185258602	chr19:36721900-36721901	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs531451808	chr19:36721963-36721964	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs61413061	chr19:36721990-36721991	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs190349414	chr19:36721997-36721998	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs61326559	chr19:36721999-36722000	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs547266611	chr19:36722005-36722006	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs566013167	chr19:36722057-36722058	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs541242396	chr19:36722097-36722098	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs75186918	chr19:36722103-36722104	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs547454595	chr19:36722116-36722117	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs554558073	chr19:36722146-36722147	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs569685482	chr19:36722167-36722168	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs181549835	chr19:36722178-36722179	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs376815656	chr19:36722204-36722205	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs577253896	chr19:36722232-36722233	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs56345729	chr19:36722258-36722259	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs541654494	chr19:36722264-36722265	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs55665245	chr19:36722268-36722269	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs55680501	chr19:36722330-36722331	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1691 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36707000-36726800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:36707400-36730200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:36707600-36731800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr19:36708200-36730800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr19:36709000-36723000	Strong transcription	HUES48 Cell Line	embryonic stem cell
6	chr19:36709000-36723800	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chr19:36709000-36724000	Strong transcription	H1 Cell Line	embryonic stem cell
8	chr19:36709400-36723800	Strong transcription	Fetal Muscle Trunk	muscle
9	chr19:36710000-36725000	ZNF genes & repeats	GM12878-XiMat	blood
10	chr19:36710000-36732200	ZNF genes & repeats	A549	lung
11	chr19:36710000-36732200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
12	chr19:36710800-36721800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
13	chr19:36710800-36723200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr19:36711000-36723200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
15	chr19:36711000-36723400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr19:36711000-36724000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr19:36711200-36728400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
18	chr19:36711800-36725000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr19:36711800-36726600	Strong transcription	Fetal Muscle Leg	muscle
20	chr19:36713000-36730200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
21	chr19:36713400-36726600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr19:36714000-36731000	Strong transcription	Dnd41	blood
23	chr19:36714400-36731400	ZNF genes & repeats	Liver	Liver
24	chr19:36715200-36723600	Strong transcription	Placenta	Placenta
25	chr19:36715200-36731200	Strong transcription	Fetal Brain Female	brain
26	chr19:36715200-36731600	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
27	chr19:36715400-36724200	Strong transcription	Hela-S3	cervix
28	chr19:36715800-36726800	ZNF genes & repeats	Fetal Intestine Small	intestine
29	chr19:36716000-36724400	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr19:36716200-36722000	Strong transcription	HepG2	liver
31	chr19:36716200-36723600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr19:36716200-36728600	ZNF genes & repeats	Fetal Intestine Large	intestine
33	chr19:36716400-36721400	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr19:36716400-36721400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr19:36716400-36723400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
36	chr19:36716400-36723600	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr19:36716400-36726600	Weak transcription	Fetal Heart	heart
38	chr19:36716400-36730000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr19:36716400-36730200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr19:36716600-36722200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr19:36716600-36724600	Strong transcription	Fetal Lung	lung
42	chr19:36716600-36725600	Strong transcription	Primary B cells from peripheral blood	blood
43	chr19:36716600-36727200	Strong transcription	Adipose Nuclei	Adipose
44	chr19:36716600-36728200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr19:36716600-36728200	ZNF genes & repeats	Lung	lung
46	chr19:36716600-36731400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
47	chr19:36716800-36722800	Strong transcription	H9 Cell Line	embryonic stem cell
48	chr19:36716800-36725400	Strong transcription	Pancreas	Pancrea
49	chr19:36716800-36728000	Strong transcription	Placenta Amnion	Placenta Amnion
50	chr19:36716800-36730000	Strong transcription	Brain Germinal Matrix	brain

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