Variant report

Variant	nsv877532
Chromosome Location	chr3:136526939-136662603
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2222)
CpG islands
(count:2688)
Chromatin interactive
region (count:114)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2222 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:136580608-136581236	K562	blood:	n/a	n/a
2	ARID3A	chr3:136586175-136586445	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:136580940-136581709	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:136618377-136619044	K562	blood:	n/a	n/a
5	ARID3A	chr3:136559106-136559425	K562	blood:	n/a	n/a
6	ARID3A	chr3:136554996-136555038	K562	blood:	n/a	n/a
7	ARID3A	chr3:136649588-136649739	K562	blood:	n/a	n/a
8	ARID3A	chr3:136557683-136558219	K562	blood:	n/a	n/a
9	ARID3A	chr3:136537128-136537410	HepG2	liver:	n/a	n/a
10	ATF1	chr3:136601470-136601780	K562	blood:	n/a	n/a
11	ATF1	chr3:136537075-136537410	K562	blood:	n/a	n/a
12	ATF1	chr3:136635180-136635380	K562	blood:	n/a	n/a
13	ATF1	chr3:136618450-136618980	K562	blood:	n/a	n/a
14	ATF1	chr3:136580797-136581332	K562	blood:	n/a	n/a
15	ATF1	chr3:136559082-136559397	K562	blood:	n/a	n/a
16	ATF2	chr3:136580227-136582000	GM12878	blood:	n/a	n/a
17	ATF3	chr3:136557787-136558073	K562	blood:	n/a	n/a
18	BACH1	chr3:136538511-136539234	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr3:136557790-136558314	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr3:136580786-136581788	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr3:136539539-136539549	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr3:136557525-136558265	K562	blood:	n/a	n/a
23	BACH1	chr3:136537164-136538218	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr3:136638684-136638851	GM12878	blood:	n/a	n/a
25	BATF	chr3:136644286-136644529	GM12878	blood:	n/a	n/a
26	BATF	chr3:136616380-136616562	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:136638722-136638924	GM12878	blood:	n/a	chr3:136638764-136638771
28	BCL3	chr3:136580579-136581295	A549	lung:	n/a	chr3:136581083-136581096 chr3:136581087-136581096 chr3:136581090-136581099 chr3:136581084-136581093 chr3:136581079-136581092
29	BCLAF1	chr3:136580520-136581427	GM12878	blood:	n/a	chr3:136581348-136581357 chr3:136581083-136581096 chr3:136581087-136581096 chr3:136581090-136581099 chr3:136581084-136581093 chr3:136581079-136581092
30	BCLAF1	chr3:136581463-136581950	GM12878	blood:	n/a	n/a
31	BCLAF1	chr3:136580389-136581423	GM12878	blood:	n/a	chr3:136581348-136581357 chr3:136581083-136581096 chr3:136581087-136581096 chr3:136581090-136581099 chr3:136581084-136581093 chr3:136581079-136581092
32	BCLAF1	chr3:136651385-136651753	GM12878	blood:	n/a	n/a
33	BHLHE40	chr3:136537075-136537399	K562	blood:	n/a	n/a
34	BHLHE40	chr3:136580509-136581913	K562	blood:	n/a	chr3:136581480-136581496
35	BHLHE40	chr3:136559068-136559308	K562	blood:	n/a	n/a
36	BHLHE40	chr3:136537681-136537988	K562	blood:	n/a	n/a
37	BHLHE40	chr3:136580453-136581815	GM12878	blood:	n/a	chr3:136581480-136581496
38	BHLHE40	chr3:136580853-136582133	HepG2	liver:	n/a	chr3:136581480-136581496
39	BHLHE40	chr3:136618455-136618770	K562	blood:	n/a	n/a
40	BHLHE40	chr3:136537544-136538055	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:136538307-136538540	HepG2	liver:	n/a	n/a
42	BRCA1	chr3:136580657-136581278	GM12878	blood:	n/a	n/a
43	BRCA1	chr3:136581143-136581651	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr3:136580537-136582484	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr3:136537107-136537991	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr3:136602624-136602654	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr3:136580980-136581671	HepG2	liver:	n/a	n/a
48	BRCA1	chr3:136581578-136581673	GM12878	blood:	n/a	n/a
49	BRCA1	chr3:136538363-136538731	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr3:136580320-136581375	K562	blood:	n/a	n/a

(count:2688 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:136539113-136539163	HNPCEpiC	eye:	n/a
2	chr3:136581777-136581827	GM06990	blood:	n/a
3	chr3:136618442-136618492	BJ	skin:	n/a
4	chr3:136612288-136612338	HRPEpiC	eye:	n/a
5	chr3:136539113-136539163	HNPCEpiC	eye:	n/a
6	chr3:136581777-136581827	GM06990	blood:	n/a
7	chr3:136618442-136618492	BJ	skin:	n/a
8	chr3:136612288-136612338	HRPEpiC	eye:	n/a
9	chr3:136581720-136581770	BJ	skin:	n/a
10	chr3:136538369-136538419	HCT-116	colon:	n/a
11	chr3:136537817-136537867	Hepatocyte	liver:	n/a
12	chr3:136538801-136538851	PANC-1	pancreas:	n/a
13	chr3:136538990-136539040	MCF-7	breast:	n/a
14	chr3:136537856-136537906	AG10803	skin:	n/a
15	chr3:136537863-136537913	GM19239	blood:	n/a
16	chr3:136538934-136538984	HNPCEpiC	eye:	n/a
17	chr3:136539113-136539163	A549	lung:	n/a
18	chr3:136580967-136581017	HEK293	kidney:	embryo
19	chr3:136581189-136581239	K562	blood:	n/a
20	chr3:136580959-136581009	NHBE	bronchial:	n/a
21	chr3:136556829-136556879	GM12891	blood:	n/a
22	chr3:136601982-136602032	HNPCEpiC	eye:	n/a
23	chr3:136608208-136608258	HL-60	blood:	n/a
24	chr3:136581033-136581083	RPTEC	kidney:	n/a
25	chr3:136556829-136556879	U87	brain:	n/a
26	chr3:136537169-136537219	HMEC	breast:	n/a
27	chr3:136538601-136538651	MCF10A-Er-Src	breast:	n/a
28	chr3:136608958-136609008	U87	brain:	n/a
29	chr3:136539113-136539163	NHBE	bronchial:	n/a
30	chr3:136533970-136534020	NT2-D1	testis:	n/a
31	chr3:136538801-136538851	NH-A	brain:	n/a
32	chr3:136580769-136580819	U87	brain:	n/a
33	chr3:136581189-136581239	RPTEC	kidney:	n/a
34	chr3:136618442-136618492	ProgFib	skin:	n/a
35	chr3:136537267-136537317	GM12878	blood:	n/a
36	chr3:136537817-136537867	PFSK-1	brain:	n/a
37	chr3:136538801-136538851	HCPEpiC	choroid plexus:	n/a
38	chr3:136533970-136534020	SK-N-MC	brain:	n/a
39	chr3:136537694-136537744	MCF-7	breast:	n/a
40	chr3:136537817-136537867	PrEC	prostate:	n/a
41	chr3:136539113-136539163	HCF	heart:	n/a
42	chr3:136538801-136538851	AG09309	skin:	n/a
43	chr3:136538369-136538419	BJ	skin:	n/a
44	chr3:136537817-136537867	HUVEC	blood vessel:	n/a
45	chr3:136537863-136537913	HNPCEpiC	eye:	n/a
46	chr3:136581033-136581083	IMR90	lung:	fetal
47	chr3:136556829-136556879	Hela-S3	cervix:	n/a
48	chr3:136581777-136581827	NHDF-neo	bronchial:	n/a
49	chr3:136573684-136573734	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:136579741-136579791	NB4	blood:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:136471389..136473293-chr3:136580852..136582413,2	MCF-7	breast:
2	chr3:136633616..136635722-chr3:136639383..136641177,2	MCF-7	breast:
3	chr3:136658510..136660043-chr3:136661343..136664014,2	MCF-7	breast:
4	chr3:136604140..136607087-chr3:136614887..136617471,2	K562	blood:
5	chr3:136660015..136662071-chr3:136665348..136667006,2	MCF-7	breast:
6	chr3:136554139..136557282-chr3:136559965..136563273,3	MCF-7	breast:
7	chr3:136598088..136600803-chr3:136614859..136618063,3	MCF-7	breast:
8	chr3:136540164..136541710-chr3:136544564..136546317,2	K562	blood:
9	chr3:136583214..136585739-chr3:136588131..136591435,3	K562	blood:
10	chr3:136578448..136581953-chr3:136588575..136593594,6	MCF-7	breast:
11	chr11:118965747..118966339-chr3:136580483..136581270,2	Hela-S3	cervix:
12	chr19:33182612..33183467-chr3:136537028..136537847,2	Hela-S3	cervix:
13	chr3:136540164..136541710-chr3:136544564..136546317,2	K562	blood:
14	chr3:49449318..49450076-chr3:136537776..136538465,2	Hela-S3	cervix:
15	chr3:136535239..136537634-chr3:136579848..136582645,2	MCF-7	breast:
16	chr3:136580474..136583340-chr3:136584375..136587999,4	K562	blood:
17	chr3:136657952..136660440-chr3:136666983..136671053,4	MCF-7	breast:
18	chr3:136598088..136600803-chr3:136614859..136618063,3	MCF-7	breast:
19	chr3:136652282..136654491-chr3:136657095..136659566,2	K562	blood:
20	chr3:136578882..136581930-chr3:136596540..136599331,4	MCF-7	breast:
21	chr3:136583214..136585739-chr3:136588131..136591435,3	K562	blood:
22	chr3:136580801..136581574-chr9:35161852..35162499,2	Hela-S3	cervix:
23	chr3:136578871..136581174-chr3:136618112..136620330,2	K562	blood:
24	chr3:136579717..136582234-chr3:136620305..136621833,2	MCF-7	breast:
25	chr12:66563320..66563841-chr3:136557779..136558286,2	MCF-7	breast:
26	chr11:62608645..62609483-chr3:136581135..136581937,2	Hela-S3	cervix:
27	chr3:136565388..136567977-chr3:136579840..136581431,2	MCF-7	breast:
28	chr3:136471469..136473912-chr3:136531466..136533756,2	MCF-7	breast:
29	chr3:136469358..136473351-chr3:136579831..136582888,9	MCF-7	breast:
30	chr1:51983714..51984668-chr3:136580705..136581230,2	Hela-S3	cervix:
31	chr3:136548915..136551546-chr3:136552798..136555438,3	K562	blood:
32	chr3:136537560..136539935-chr3:136579290..136582081,4	K562	blood:
33	chr3:136557267..136559403-chr3:136563410..136566256,3	K562	blood:
34	chr3:136604140..136607087-chr3:136614887..136617471,2	K562	blood:
35	chr3:136573273..136574958-chr3:136579585..136582154,2	K562	blood:
36	chr3:136581094..136582950-chr3:136617390..136620227,2	MCF-7	breast:
37	chr3:136621285..136624241-chr3:136629189..136631419,2	K562	blood:
38	chr3:136649399..136652137-chr3:136652248..136655510,3	MCF-7	breast:
39	chr3:136660169..136663903-chr3:136675087..136677294,3	K562	blood:
40	chr3:136583020..136585823-chr3:136647471..136649175,2	MCF-7	breast:
41	chr3:136636446..136639325-chr3:136639955..136642368,3	K562	blood:
42	chr3:136537560..136539935-chr3:136579290..136582081,4	K562	blood:
43	chr3:136466613..136474326-chr3:136579481..136583133,10	K562	blood:
44	chr3:136621285..136624241-chr3:136629189..136631419,2	K562	blood:
45	chr3:136578871..136581174-chr3:136618112..136620330,2	K562	blood:
46	chr3:136658510..136660043-chr3:136661343..136664014,2	MCF-7	breast:
47	chr3:136471409..136475684-chr3:136558625..136561500,4	MCF-7	breast:
48	chr3:136556513..136558493-chr3:136581161..136583381,2	K562	blood:
49	chr3:136579482..136582272-chr3:136609445..136613552,4	MCF-7	breast:
50	chr2:101924375..101925199-chr3:136580770..136581475,2	Hela-S3	cervix:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STAG1-1	chr3:136580589-136580905	NR_110175
2	lnc-STAG1-1	chr3:136565370-136565428	NR_110176
3	lnc-STAG1-1	chr3:136560818-136561411	NR_110176
4	lnc-STAG1-1	chr3:136560568-136561411	ENSG00000239213.1
5	lnc-STAG1-1	chr3:136580457-136580905	NR_110176
6	lnc-STAG1-1	chr3:136561033-136561411	ENSG00000239213.1
7	lnc-STAG1-1	chr3:136560818-136561411	NR_110177
8	lnc-STAG1-1	chr3:136565370-136565428	ENSG00000239213.1
9	lnc-STAG1-1	chr3:136580589-136580879	ENSG00000239213.1
10	lnc-STAG1-1	chr3:136580589-136580891	ENSG00000239213.1
11	lnc-STAG1-5	chr3:136527393-136527924	NONHSAT092286
12	lnc-TMEM22-2	chr3:136561194-136562164	NONHSAT092287
13	lnc-STAG1-1	chr3:136580472-136580901	NONHSAT092292
14	lnc-STAG1-1	chr3:136576895-136577445	NONHSAT092291
15	lnc-STAG1-1	chr3:136565370-136565428	ENSG00000239213.1
16	lnc-STAG1-5	chr3:136528289-136528465	NONHSAT092286
17	lnc-STAG1-1	chr3:136580589-136580905	NR_110177
18	lnc-STAG1-6	chr3:136556180-136557863	ENSG00000273486.1
19	lnc-STAG1-1	chr3:136565370-136565428	NR_110175
20	lnc-STAG1-1	chr3:136577360-136577445	ENSG00000239213.1
21	lnc-TMEM22-2	chr3:136537489-136539354	NONHSAT092287
22	lnc-STAG1-1	chr3:136560818-136561411	NR_110175
23	lnc-STAG1-1	chr3:136565370-136565428	ENSG00000239213.1
24	lnc-STAG1-1	chr3:136580589-136580854	NONHSAT092291
25	lnc-STAG1-1	chr3:136565370-136565428	NR_110177
26	lnc-STAG1-1	chr3:136561299-136561411	ENSG00000239213.1
27	lnc-STAG1-1	chr3:136577360-136577445	NR_110175
28	lnc-STAG1-1	chr3:136580457-136580896	ENSG00000239213.1

No data

Variant related genes	Relation type
ENSG00000239213	TF binding region
SLC35G2	TF binding region
IL20RB	TF binding region
ENSG00000273486	TF binding region
ENSG00000214283	TF binding region
NCK1	TF binding region
ENSG00000242968	TF binding region
ENSG00000239213	CpG island
SLC35G2	CpG island
IL20RB	CpG island
ENSG00000273486	CpG island
ENSG00000214283	CpG island
NCK1	CpG island
ENSG00000242968	CpG island
ENSG00000261758	chromatin interactions
ENSG00000239213	chromatin interactions
ENSG00000213965	chromatin interactions
ENSG00000214283	chromatin interactions
ENSG00000072682	chromatin interactions
ENSG00000174579	chromatin interactions
ENSG00000067560	chromatin interactions
ENSG00000118007	chromatin interactions
ENSG00000158092	chromatin interactions
ENSG00000174564	chromatin interactions
ENSG00000145022	chromatin interactions
ENSG00000267475	chromatin interactions
ENSG00000160219	chromatin interactions
ENSG00000162889	chromatin interactions
ENSG00000227070	chromatin interactions
ENSG00000198722	chromatin interactions
ENSG00000188486	chromatin interactions
ENSG00000125835	chromatin interactions
ENSG00000228474	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000168917	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000163162	chromatin interactions
ENSG00000273486	chromatin interactions
ENSG00000155957	chromatin interactions

Extended variants
information (count: 4895 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:4895 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17300138	chr3:136526939-136526940	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530815194	chr3:136526963-136526964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113843773	chr3:136526975-136526976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189814404	chr3:136526988-136526989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78881079	chr3:136527415-136527416	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs552706793	chr3:136527466-136527467	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs192185346	chr3:136527467-136527468	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs530360414	chr3:136527496-136527497	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs116391144	chr3:136527508-136527509	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs75790861	chr3:136527513-136527514	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs545784184	chr3:136527546-136527547	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs532880791	chr3:136527565-136527566	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs80238731	chr3:136527577-136527578	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs62410360	chr3:136527580-136527581	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs115154226	chr3:136527608-136527609	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs367744956	chr3:136527640-136527641	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs565575054	chr3:136527649-136527650	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs555137912	chr3:136527760-136527761	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs187244629	chr3:136527784-136527785	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs568157275	chr3:136527807-136527808	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs536803182	chr3:136527809-136527810	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs72981371	chr3:136527847-136527848	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs536763777	chr3:136528339-136528340	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs2343680	chr3:136528342-136528343	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs371963638	chr3:136528386-136528387	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs539342161	chr3:136528397-136528398	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs182487495	chr3:136528415-136528416	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs559515499	chr3:136528426-136528427	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs144775760	chr3:136528895-136528896	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs539220387	chr3:136528916-136528917	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs1300058	chr3:136529240-136529241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201040582	chr3:136529241-136529242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546050206	chr3:136529246-136529247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1296306	chr3:136529257-136529258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1280706	chr3:136529269-136529270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1280705	chr3:136529276-136529277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533285028	chr3:136529347-136529348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573442914	chr3:136529359-136529360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141585249	chr3:136529404-136529405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77525836	chr3:136529475-136529476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150750402	chr3:136529517-136529518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530461573	chr3:136529616-136529617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540976960	chr3:136529682-136529683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543811850	chr3:136529683-136529684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563793137	chr3:136529690-136529691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138997717	chr3:136529719-136529720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546446473	chr3:136529732-136529733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566696213	chr3:136529759-136529760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150782622	chr3:136529769-136529770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368634133	chr3:136529850-136529851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18511947	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4389 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:136521800-136527000	Weak transcription	Hela-S3	cervix
2	chr3:136529200-136530000	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:136530000-136531000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
4	chr3:136530600-136531000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr3:136531000-136535400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr3:136531000-136535800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr3:136535400-136536800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr3:136535400-136537200	Enhancers	Fetal Lung	lung
9	chr3:136535600-136536000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr3:136535600-136537200	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr3:136535800-136536000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr3:136535800-136536000	Enhancers	Fetal Kidney	kidney
13	chr3:136535800-136536800	Enhancers	HepG2	liver
14	chr3:136535800-136537000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr3:136535800-136537200	Enhancers	Brain Anterior Caudate	brain
16	chr3:136535800-136537200	Enhancers	Brain Germinal Matrix	brain
17	chr3:136536000-136536200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr3:136536000-136536200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr3:136536000-136536400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:136536000-136536400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr3:136536000-136537000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:136536000-136537000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
23	chr3:136536000-136537200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr3:136536000-136537200	Enhancers	A549	lung
25	chr3:136536000-136537400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr3:136536200-136536600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr3:136536200-136537000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr3:136536200-136537200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr3:136536200-136537200	Enhancers	Brain Hippocampus Middle	brain
30	chr3:136536400-136536600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr3:136536400-136537000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr3:136536400-136537000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr3:136536400-136537000	Enhancers	Dnd41	blood
34	chr3:136536400-136537400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr3:136536600-136536800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr3:136536600-136536800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:136536600-136536800	Enhancers	Stomach Smooth Muscle	stomach
38	chr3:136536600-136537000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
39	chr3:136536600-136537000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
40	chr3:136536600-136537000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr3:136536600-136537000	Enhancers	Hela-S3	cervix
42	chr3:136536600-136537200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr3:136536600-136537200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr3:136536600-136537200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr3:136536600-136537200	Enhancers	Adipose Nuclei	Adipose
46	chr3:136536600-136537200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr3:136536600-136537200	Enhancers	HUVEC	blood vessel
48	chr3:136536600-136537200	Enhancers	NHLF	lung
49	chr3:136536600-136537200	Enhancers	Osteobl	bone
50	chr3:136536600-136537400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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