Variant report

Variant	nsv877531
Chromosome Location	chr3:136517016-136662954
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2310)
CpG islands
(count:2689)
Chromatin interactive
region (count:117)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2310 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:136537128-136537410	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:136649588-136649739	K562	blood:	n/a	n/a
3	ARID3A	chr3:136557683-136558219	K562	blood:	n/a	n/a
4	ARID3A	chr3:136559106-136559425	K562	blood:	n/a	n/a
5	ARID3A	chr3:136580940-136581709	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:136586175-136586445	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:136554996-136555038	K562	blood:	n/a	n/a
8	ARID3A	chr3:136618377-136619044	K562	blood:	n/a	n/a
9	ARID3A	chr3:136580608-136581236	K562	blood:	n/a	n/a
10	ATF1	chr3:136618450-136618980	K562	blood:	n/a	n/a
11	ATF1	chr3:136580797-136581332	K562	blood:	n/a	n/a
12	ATF1	chr3:136601470-136601780	K562	blood:	n/a	n/a
13	ATF1	chr3:136559082-136559397	K562	blood:	n/a	n/a
14	ATF1	chr3:136635180-136635380	K562	blood:	n/a	n/a
15	ATF1	chr3:136537075-136537410	K562	blood:	n/a	n/a
16	ATF2	chr3:136521138-136521806	GM12878	blood:	n/a	n/a
17	ATF2	chr3:136580227-136582000	GM12878	blood:	n/a	n/a
18	ATF2	chr3:136524458-136525098	GM12878	blood:	n/a	n/a
19	ATF2	chr3:136521175-136521760	GM12878	blood:	n/a	n/a
20	ATF3	chr3:136557787-136558073	K562	blood:	n/a	n/a
21	BACH1	chr3:136557525-136558265	K562	blood:	n/a	n/a
22	BACH1	chr3:136557790-136558314	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr3:136580786-136581788	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr3:136538511-136539234	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr3:136537164-136538218	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr3:136539539-136539549	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr3:136524585-136524979	GM12878	blood:	n/a	n/a
28	BATF	chr3:136644286-136644529	GM12878	blood:	n/a	n/a
29	BATF	chr3:136616380-136616562	GM12878	blood:	n/a	n/a
30	BATF	chr3:136521227-136521566	GM12878	blood:	n/a	chr3:136521382-136521393
31	BATF	chr3:136521167-136521585	GM12878	blood:	n/a	chr3:136521382-136521393
32	BATF	chr3:136638684-136638851	GM12878	blood:	n/a	n/a
33	BATF	chr3:136524597-136524992	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:136638722-136638924	GM12878	blood:	n/a	chr3:136638764-136638771
35	BCL3	chr3:136580579-136581295	A549	lung:	n/a	chr3:136581083-136581096 chr3:136581087-136581096 chr3:136581090-136581099 chr3:136581084-136581093 chr3:136581079-136581092
36	BCLAF1	chr3:136651385-136651753	GM12878	blood:	n/a	n/a
37	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
38	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
39	BCLAF1	chr3:136581463-136581950	GM12878	blood:	n/a	n/a
40	BCLAF1	chr3:136521240-136521781	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:136559068-136559308	K562	blood:	n/a	n/a
42	BHLHE40	chr3:136538307-136538540	HepG2	liver:	n/a	n/a
43	BHLHE40	chr3:136580453-136581815	GM12878	blood:	n/a	chr3:136581480-136581496
44	BHLHE40	chr3:136580509-136581913	K562	blood:	n/a	chr3:136581480-136581496
45	BHLHE40	chr3:136618455-136618770	K562	blood:	n/a	n/a
46	BHLHE40	chr3:136537544-136538055	GM12878	blood:	n/a	n/a
47	BHLHE40	chr3:136537681-136537988	K562	blood:	n/a	n/a
48	BHLHE40	chr3:136521329-136521750	GM12878	blood:	n/a	n/a
49	BHLHE40	chr3:136524760-136524906	GM12878	blood:	n/a	n/a
50	BHLHE40	chr3:136580853-136582133	HepG2	liver:	n/a	chr3:136581480-136581496

(count:2689 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:136538089-136538139	ProgFib	skin:	n/a
2	chr3:136612288-136612338	SK-N-SH	brain:	n/a
3	chr3:136538934-136538984	A549	lung:	n/a
4	chr3:136537786-136537836	GM06990	blood:	n/a
5	chr3:136533970-136534020	HEK293	kidney:	embryo
6	chr3:136538089-136538139	ProgFib	skin:	n/a
7	chr3:136612288-136612338	SK-N-SH	brain:	n/a
8	chr3:136538934-136538984	A549	lung:	n/a
9	chr3:136537786-136537836	GM06990	blood:	n/a
10	chr3:136533970-136534020	HEK293	kidney:	embryo
11	chr3:136579741-136579791	HCT-116	colon:	n/a
12	chr3:136537790-136537840	SK-N-SH	brain:	n/a
13	chr3:136573684-136573734	HEK293	kidney:	embryo
14	chr3:136537817-136537867	RPTEC	kidney:	n/a
15	chr3:136578209-136578259	HepG2	liver:	n/a
16	chr3:136660121-136660171	GM12891	blood:	n/a
17	chr3:136533970-136534020	SKMC	muscle:	n/a
18	chr3:136537863-136537913	AG09319	gingival:	n/a
19	chr3:136537817-136537867	Jurkat	blood:	n/a
20	chr3:136537786-136537836	HEEpiC	esophagus:	n/a
21	chr3:136581720-136581770	BJ	skin:	n/a
22	chr3:136601982-136602032	NT2-D1	testis:	n/a
23	chr3:136581031-136581081	HepG2	liver:	n/a
24	chr3:136537817-136537867	K562	blood:	n/a
25	chr3:136579741-136579791	NHBE	bronchial:	n/a
26	chr3:136608958-136609008	PANC-1	pancreas:	n/a
27	chr3:136580769-136580819	SK-N-MC	brain:	n/a
28	chr3:136649333-136649383	GM06990	blood:	n/a
29	chr3:136537817-136537867	HEK293	kidney:	embryo
30	chr3:136537694-136537744	HEK293	kidney:	embryo
31	chr3:136538934-136538984	GM19239	blood:	n/a
32	chr3:136537786-136537836	HEK293	kidney:	embryo
33	chr3:136649333-136649383	HL-60	blood:	n/a
34	chr3:136581033-136581083	HPAEpiC	pulmonary alveolar:	n/a
35	chr3:136556829-136556879	HRPEpiC	eye:	n/a
36	chr3:136580967-136581017	HNPCEpiC	eye:	n/a
37	chr3:136612288-136612338	A549	lung:	n/a
38	chr3:136537709-136537759	HCM	heart:	n/a
39	chr3:136539328-136539378	PFSK-1	brain:	n/a
40	chr3:136608958-136609008	NH-A	brain:	n/a
41	chr3:136609157-136609207	PFSK-1	brain:	n/a
42	chr3:136537817-136537867	SKMC	muscle:	n/a
43	chr3:136581031-136581081	ECC-1	luminal epithelium:	n/a
44	chr3:136612288-136612338	AoSMC	blood vessel:	n/a
45	chr3:136573684-136573734	PrEC	prostate:	n/a
46	chr3:136539328-136539378	HRCEpiC	kidney:	n/a
47	chr3:136609080-136609130	HIPEpiC	eye:	n/a
48	chr3:136581720-136581770	NHBE	bronchial:	n/a
49	chr3:136580959-136581009	BJ	skin:	n/a
50	chr3:136539328-136539378	U87	brain:	n/a

(count:117 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:136578448..136581953-chr3:136588575..136593594,6	MCF-7	breast:
2	chr3:136660317..136661826-chr3:136665286..136667612,2	K562	blood:
3	chr3:136637702..136640627-chr3:136641838..136645550,3	MCF-7	breast:
4	chr3:136658510..136660043-chr3:136661343..136664014,2	MCF-7	breast:
5	chr3:136468701..136475672-chr3:136535815..136540749,9	K562	blood:
6	chr3:136581094..136582950-chr3:136617390..136620227,2	MCF-7	breast:
7	chr3:136591585..136593473-chr3:136601721..136603894,2	MCF-7	breast:
8	chr3:136536665..136539935-chr3:136579370..136582081,3	K562	blood:
9	chr3:136554235..136556505-chr3:136559214..136561778,2	K562	blood:
10	chr3:49449318..49450076-chr3:136537776..136538465,2	Hela-S3	cervix:
11	chr3:136573273..136574958-chr3:136579585..136582154,2	K562	blood:
12	chr20:2450893..2451640-chr3:136580454..136581436,2	Hela-S3	cervix:
13	chr3:136598088..136600803-chr3:136614859..136618063,3	MCF-7	breast:
14	chr3:136540164..136541710-chr3:136544564..136546317,2	K562	blood:
15	chr11:62608645..62609483-chr3:136581135..136581937,2	Hela-S3	cervix:
16	chr3:136537175..136537835-chrX:153978897..153979889,2	NB4	blood:
17	chr3:136636446..136639325-chr3:136639955..136642368,3	K562	blood:
18	chr3:136471409..136475684-chr3:136558625..136561500,4	MCF-7	breast:
19	chr3:136470323..136472944-chr3:136524724..136526254,2	K562	blood:
20	chr3:136565388..136567977-chr3:136579840..136581431,2	MCF-7	breast:
21	chr3:136471389..136473293-chr3:136580852..136582413,2	MCF-7	breast:
22	chr3:136471469..136473912-chr3:136531466..136533756,2	MCF-7	breast:
23	chr3:136573010..136575502-chr3:136579664..136581454,2	MCF-7	breast:
24	chr3:136581094..136582950-chr3:136617390..136620227,2	MCF-7	breast:
25	chr3:136537560..136539935-chr3:136579290..136582081,4	K562	blood:
26	chr3:136583020..136585823-chr3:136647471..136649175,2	MCF-7	breast:
27	chr1:93347932..93348855-chr3:136601084..136601683,2	NB4	blood:
28	chr3:136579717..136582234-chr3:136620305..136621833,2	MCF-7	breast:
29	chr3:136535239..136537634-chr3:136579848..136582645,2	MCF-7	breast:
30	chr3:136581625..136583340-chr3:136586499..136589172,2	K562	blood:
31	chr3:136598088..136600803-chr3:136614859..136618063,3	MCF-7	breast:
32	chr3:136580996..136583825-chr3:136586940..136590069,3	MCF-7	breast:
33	chr3:135915450..135917077-chr3:136578286..136581089,2	MCF-7	breast:
34	chr3:136568394..136571514-chr3:136574804..136577535,3	K562	blood:
35	chr3:136655622..136657688-chr3:136659902..136662004,2	MCF-7	breast:
36	chr3:136559234..136561266-chr3:136568039..136570871,2	K562	blood:
37	chr3:136636446..136639325-chr3:136639955..136642368,3	K562	blood:
38	chr3:136580843..136582615-chr3:136582882..136586674,6	MCF-7	breast:
39	chr3:136580801..136581574-chr9:35161852..35162499,2	Hela-S3	cervix:
40	chr3:136658510..136660043-chr3:136661343..136664014,2	MCF-7	breast:
41	chr3:136649399..136652137-chr3:136652248..136655510,3	MCF-7	breast:
42	chr3:136469311..136474326-chr3:136579207..136583133,7	K562	blood:
43	chr3:136578882..136581930-chr3:136596540..136599331,4	MCF-7	breast:
44	chr3:136521855..136523669-chr3:136580388..136582521,2	MCF-7	breast:
45	chr3:136597721..136599414-chr3:136607033..136609685,2	MCF-7	breast:
46	chr3:136633616..136635722-chr3:136639383..136641177,2	MCF-7	breast:
47	chr3:136660317..136661930-chr3:136664435..136666786,2	K562	blood:
48	chr3:136570595..136572217-chr3:136572560..136574490,2	MCF-7	breast:
49	chr3:136470203..136472947-chr3:136592469..136594327,2	K562	blood:
50	chr3:136621285..136624241-chr3:136629189..136631419,2	K562	blood:

(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	ENSG00000239213.1
3	lnc-STAG1-1	chr3:136565370-136565428	NR_110177
4	lnc-STAG1-1	chr3:136565370-136565428	ENSG00000239213.1
5	lnc-STAG1-1	chr3:136580589-136580879	ENSG00000239213.1
6	lnc-STAG1-1	chr3:136565370-136565428	NR_110175
7	lnc-STAG1-6	chr3:136556180-136557863	ENSG00000273486.1
8	lnc-STAG1-1	chr3:136576895-136577445	NONHSAT092291
9	lnc-STAG1-1	chr3:136580457-136580896	ENSG00000239213.1
10	lnc-TMEM22-2	chr3:136537489-136539354	NONHSAT092287
11	lnc-TMEM22-2	chr3:136561194-136562164	NONHSAT092287
12	lnc-STAG1-1	chr3:136580457-136580905	NR_110176
13	lnc-STAG1-1	chr3:136560818-136561411	NR_110175
14	lnc-STAG1-1	chr3:136580589-136580854	NONHSAT092291
15	lnc-STAG1-1	chr3:136565370-136565428	NR_110176
16	lnc-STAG1-1	chr3:136577360-136577445	NR_110175
17	lnc-STAG1-1	chr3:136561299-136561411	ENSG00000239213.1
18	lnc-STAG1-1	chr3:136580589-136580905	NR_110177
19	lnc-STAG1-1	chr3:136560818-136561411	NR_110176
20	lnc-STAG1-1	chr3:136561033-136561411	ENSG00000239213.1
21	lnc-STAG1-1	chr3:136580472-136580901	NONHSAT092292
22	lnc-STAG1-5	chr3:136528289-136528465	NONHSAT092286
23	lnc-STAG1-1	chr3:136565370-136565428	ENSG00000239213.1
24	lnc-STAG1-5	chr3:136527393-136527924	NONHSAT092286
25	lnc-STAG1-1	chr3:136560568-136561411	ENSG00000239213.1
26	lnc-STAG1-1	chr3:136560818-136561411	NR_110177
27	lnc-STAG1-1	chr3:136580589-136580891	ENSG00000239213.1
28	lnc-STAG1-1	chr3:136577360-136577445	ENSG00000239213.1

No data

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

Extended variants
information (count: 5226 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:5226 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7621932	chr3:136517016-136517017	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7633629	chr3:136517028-136517029	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs375759040	chr3:136517075-136517076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs9858560	chr3:136517154-136517155	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs189782701	chr3:136517158-136517159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140476606	chr3:136517185-136517186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77693707	chr3:136517257-136517258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145257586	chr3:136517292-136517293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373197440	chr3:136517302-136517303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145825610	chr3:136517317-136517318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373549520	chr3:136517363-136517364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541178140	chr3:136517366-136517367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561086560	chr3:136517439-136517440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529911064	chr3:136517489-136517490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183486891	chr3:136517647-136517648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569134566	chr3:136517648-136517649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563333258	chr3:136517665-136517666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4600775	chr3:136517683-136517684	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs187970350	chr3:136517743-136517744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571361145	chr3:136517805-136517806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534050525	chr3:136517824-136517825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553914402	chr3:136517833-136517834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192397887	chr3:136517877-136517878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536525948	chr3:136517967-136517968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113048795	chr3:136517980-136517981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs57881857	chr3:136517999-136518000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs185316424	chr3:136518005-136518006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369973635	chr3:136518007-136518008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544978320	chr3:136518023-136518024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373114663	chr3:136518078-136518079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558587854	chr3:136518113-136518114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147062910	chr3:136518127-136518128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541141523	chr3:136518152-136518153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560909359	chr3:136518162-136518163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529926614	chr3:136518164-136518165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543348038	chr3:136518208-136518209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188193614	chr3:136518248-136518249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565505833	chr3:136518250-136518251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375619130	chr3:136518285-136518286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551334457	chr3:136518366-136518367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527961996	chr3:136518397-136518398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs193007214	chr3:136518402-136518403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369400106	chr3:136518462-136518463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552515493	chr3:136518509-136518510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548107320	chr3:136518514-136518515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138266211	chr3:136518538-136518539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527766707	chr3:136518551-136518552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143846826	chr3:136518553-136518554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567757435	chr3:136518568-136518569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536894812	chr3:136518575-136518576	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:4516 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:136506400-136521000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr3:136506600-136521000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:136506600-136521200	Weak transcription	Hela-S3	cervix
4	chr3:136513000-136520400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:136513800-136517200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:136513800-136521400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr3:136513800-136521600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr3:136514400-136520800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr3:136514600-136520200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr3:136515200-136517400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr3:136517200-136517600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr3:136517400-136517600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr3:136517600-136520800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr3:136520000-136520200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr3:136520200-136521200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr3:136520200-136522000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr3:136520200-136523200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr3:136520200-136525400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr3:136520400-136520800	Enhancers	NH-A	brain
20	chr3:136520400-136521200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr3:136520400-136521400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:136520400-136522000	Enhancers	Adipose Nuclei	Adipose
23	chr3:136520400-136522600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:136520600-136521000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr3:136520600-136521000	Enhancers	K562	blood
26	chr3:136520600-136521400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr3:136520600-136521600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr3:136520600-136521800	Enhancers	Aorta	Aorta
29	chr3:136520600-136521800	Enhancers	Pancreas	Pancrea
30	chr3:136520600-136521800	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr3:136520600-136522200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr3:136520600-136522400	Enhancers	Brain Hippocampus Middle	brain
33	chr3:136520800-136521000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr3:136520800-136521000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr3:136520800-136521200	Weak transcription	NH-A	brain
36	chr3:136520800-136521400	Enhancers	Brain Anterior Caudate	brain
37	chr3:136520800-136521400	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr3:136520800-136521600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:136520800-136521600	Enhancers	Fetal Brain Female	brain
40	chr3:136520800-136521800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr3:136520800-136521800	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr3:136520800-136522000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr3:136520800-136522000	Enhancers	Brain Cingulate Gyrus	brain
44	chr3:136520800-136522000	Enhancers	HSMMtube	muscle
45	chr3:136520800-136522000	Enhancers	Osteobl	bone
46	chr3:136520800-136522200	Enhancers	Brain Angular Gyrus	brain
47	chr3:136520800-136522200	Enhancers	Fetal Muscle Leg	muscle
48	chr3:136520800-136522200	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr3:136520800-136522800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr3:136521000-136521200	Enhancers	Pancreatic Islets	Pancreatic Islet

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