Variant report

Variant	nsv4183
Chromosome Location	chr3:196034067-196079109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1491)
CpG islands
(count:1710)
Chromatin interactive
region (count:116)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1491 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:196065223-196065568	K562	blood:	n/a	n/a
2	ARID3A	chr3:196044868-196045005	HepG2	liver:	n/a	chr3:196044911-196044926
3	ARID3A	chr3:196074051-196074658	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:196045131-196045281	K562	blood:	n/a	n/a
5	ARID3A	chr3:196066607-196067672	K562	blood:	n/a	n/a
6	ATF1	chr3:196045048-196045429	K562	blood:	n/a	n/a
7	ATF1	chr3:196066740-196066989	K562	blood:	n/a	n/a
8	ATF1	chr3:196064298-196064679	K562	blood:	n/a	n/a
9	ATF2	chr3:196045027-196045420	GM12878	blood:	n/a	n/a
10	ATF3	chr3:196044913-196045235	A549	lung:	n/a	n/a
11	ATF3	chr3:196065271-196065725	K562	blood:	n/a	n/a
12	ATF3	chr3:196045004-196045333	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr3:196065258-196065615	K562	blood:	n/a	n/a
14	ATF3	chr3:196045000-196045380	K562	blood:	n/a	n/a
15	ATF3	chr3:196045007-196045237	GM12878	blood:	n/a	n/a
16	ATF3	chr3:196066697-196066945	K562	blood:	n/a	n/a
17	ATF3	chr3:196066623-196067055	K562	blood:	n/a	n/a
18	ATF3	chr3:196044982-196045321	HepG2	liver:	n/a	n/a
19	ATF3	chr3:196064125-196064652	K562	blood:	n/a	n/a
20	BACH1	chr3:196067324-196067631	K562	blood:	n/a	n/a
21	BACH1	chr3:196064626-196065196	K562	blood:	n/a	n/a
22	BACH1	chr3:196044422-196044653	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr3:196045139-196045376	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr3:196066604-196067061	K562	blood:	n/a	n/a
25	BACH1	chr3:196052444-196052596	K562	blood:	n/a	n/a
26	BACH1	chr3:196066659-196066986	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr3:196043609-196044354	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:196043957-196044390	GM12878	blood:	n/a	n/a
29	BCL3	chr3:196044726-196045192	A549	lung:	n/a	chr3:196044851-196044860
30	BCL3	chr3:196071710-196072170	GM12878	blood:	n/a	n/a
31	BCL3	chr3:196044293-196045431	A549	lung:	n/a	chr3:196044851-196044860 chr3:196044658-196044667
32	BCLAF1	chr3:196044834-196045494	GM12878	blood:	n/a	chr3:196044851-196044860
33	BCLAF1	chr3:196066716-196067272	K562	blood:	n/a	n/a
34	BHLHE40	chr3:196044374-196044680	K562	blood:	n/a	n/a
35	BHLHE40	chr3:196074164-196074525	HepG2	liver:	n/a	n/a
36	BHLHE40	chr3:196074220-196074547	HepG2	liver:	n/a	n/a
37	BHLHE40	chr3:196074104-196074694	HepG2	liver:	n/a	n/a
38	BHLHE40	chr3:196044896-196045345	HepG2	liver:	n/a	chr3:196045077-196045093
39	BHLHE40	chr3:196066468-196067076	K562	blood:	n/a	n/a
40	BHLHE40	chr3:196065282-196065567	HepG2	liver:	n/a	n/a
41	BHLHE40	chr3:196067388-196067554	K562	blood:	n/a	n/a
42	BHLHE40	chr3:196063493-196063804	K562	blood:	n/a	n/a
43	BHLHE40	chr3:196044955-196045363	K562	blood:	n/a	chr3:196045077-196045093
44	BHLHE40	chr3:196074282-196074482	A549	lung:	n/a	n/a
45	BHLHE40	chr3:196050619-196050946	HepG2	liver:	n/a	n/a
46	BHLHE40	chr3:196050608-196050937	K562	blood:	n/a	n/a
47	BHLHE40	chr3:196044478-196045374	GM12878	blood:	n/a	chr3:196045077-196045093 chr3:196044716-196044732
48	BHLHE40	chr3:196075572-196075865	HepG2	liver:	n/a	n/a
49	BHLHE40	chr3:196064059-196065735	K562	blood:	n/a	n/a
50	BRCA1	chr3:196065333-196065678	Hela-S3	cervix:	n/a	n/a

(count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:196044948-196044998	PrEC	prostate:	n/a
2	chr3:196065106-196065156	ovcar-3	ovarian:	n/a
3	chr3:196044948-196044998	PrEC	prostate:	n/a
4	chr3:196065106-196065156	ovcar-3	ovarian:	n/a
5	chr3:196065306-196065356	AG09309	skin:	n/a
6	chr3:196045338-196045388	HIPEpiC	eye:	n/a
7	chr3:196065569-196065619	AoSMC	blood vessel:	n/a
8	chr3:196046080-196046130	A549	lung:	n/a
9	chr3:196046080-196046130	HRE	kidney:	n/a
10	chr3:196065688-196065738	LNCaP	prostate:	n/a
11	chr3:196065306-196065356	SK-N-SH	brain:	n/a
12	chr3:196065569-196065619	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:196046093-196046143	HL-60	blood:	n/a
14	chr3:196045224-196045274	HPAEpiC	pulmonary alveolar:	n/a
15	chr3:196065289-196065339	LNCaP	prostate:	n/a
16	chr3:196044948-196044998	SK-N-SH_RA	brain:	n/a
17	chr3:196045342-196045392	BJ	skin:	n/a
18	chr3:196065189-196065239	SK-N-SH_RA	brain:	n/a
19	chr3:196065569-196065619	Hepatocyte	liver:	n/a
20	chr3:196044632-196044682	AoSMC	blood vessel:	n/a
21	chr3:196045283-196045333	PFSK-1	brain:	n/a
22	chr3:196050645-196050695	NT2-D1	testis:	n/a
23	chr3:196045222-196045272	A549	lung:	n/a
24	chr3:196042855-196042905	SK-N-SH_RA	brain:	n/a
25	chr3:196045342-196045392	SK-N-MC	brain:	n/a
26	chr3:196065306-196065356	SKMC	muscle:	n/a
27	chr3:196065106-196065156	U87	brain:	n/a
28	chr3:196065320-196065370	SAEC	small airway:	n/a
29	chr3:196065506-196065556	HEEpiC	esophagus:	n/a
30	chr3:196065320-196065370	AG10803	skin:	n/a
31	chr3:196045224-196045274	NB4	blood:	n/a
32	chr3:196045342-196045392	Hepatocyte	liver:	n/a
33	chr3:196065357-196065407	PANC-1	pancreas:	n/a
34	chr3:196046093-196046143	HIPEpiC	eye:	n/a
35	chr3:196065328-196065378	CMK	blood:	n/a
36	chr3:196046080-196046130	LNCaP	prostate:	n/a
37	chr3:196065320-196065370	NB4	blood:	n/a
38	chr3:196065569-196065619	MCF10A-Er-Src	breast:	n/a
39	chr3:196042855-196042905	ECC-1	luminal epithelium:	n/a
40	chr3:196065328-196065378	Hela-S3	cervix:	n/a
41	chr3:196045435-196045485	HCM	heart:	n/a
42	chr3:196065289-196065339	Hela-S3	cervix:	n/a
43	chr3:196045342-196045392	HIPEpiC	eye:	n/a
44	chr3:196065318-196065368	Hepatocyte	liver:	n/a
45	chr3:196050645-196050695	HEEpiC	esophagus:	n/a
46	chr3:196065569-196065619	SKMC	muscle:	n/a
47	chr3:196065106-196065156	AG04450	lung:	fetal
48	chr3:196065106-196065156	HAEpiC	amniotic membrane:	n/a
49	chr3:196065189-196065239	NB4	blood:	n/a
50	chr3:196042855-196042905	HCM	heart:	n/a

(count:116 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr19:2234775..2236762-chr3:196074276..196076794,2	MCF-7	breast:
2	chr3:196038505..196041350-chr3:196041984..196044639,3	K562	blood:
3	chr3:196045621..196048927-chr3:196067958..196070489,3	MCF-7	breast:
4	chr3:196043597..196046330-chr3:196059490..196061514,2	K562	blood:
5	chr3:196045968..196048750-chr3:196049262..196052287,4	K562	blood:
6	chr3:196043597..196046565-chr3:196058227..196060990,3	K562	blood:
7	chr3:196048792..196050575-chr3:196065911..196067478,2	MCF-7	breast:
8	chr3:196065700..196067576-chr3:196094863..196096889,2	K562	blood:
9	chr3:196048971..196051262-chr3:196068046..196070208,4	MCF-7	breast:
10	chr3:196043128..196045052-chr3:196273376..196275560,2	MCF-7	breast:
11	chr3:196054872..196057138-chr3:196227517..196230475,2	K562	blood:
12	chr3:196057685..196059203-chr3:196062080..196064140,2	MCF-7	breast:
13	chr3:196062616..196065996-chr3:196228027..196230994,3	K562	blood:
14	chr19:47614926..47617518-chr3:196050016..196052373,2	MCF-7	breast:
15	chr3:196035189..196038386-chr3:196041731..196043557,3	K562	blood:
16	chr3:196069432..196071670-chr3:196228598..196230533,2	MCF-7	breast:
17	chr3:196012377..196016502-chr3:196041586..196047553,11	K562	blood:
18	chr3:196071912..196074086-chr3:196075769..196077797,2	MCF-7	breast:
19	chr3:196043015..196047197-chr3:196061951..196068288,11	K562	blood:
20	chr3:196043658..196046454-chr3:196052736..196055681,2	MCF-7	breast:
21	chr3:196047776..196049836-chr3:196051866..196054572,2	MCF-7	breast:
22	chr3:196075208..196077147-chr3:196092835..196095668,2	MCF-7	breast:
23	chr3:196014008..196016212-chr3:196034020..196035688,2	MCF-7	breast:
24	chr3:196070078..196071619-chr3:196082742..196085208,2	MCF-7	breast:
25	chr3:196068585..196071026-chr3:196125432..196127097,2	MCF-7	breast:
26	chr3:196050651..196052787-chr3:196063529..196066112,3	K562	blood:
27	chr3:196033596..196035352-chr3:196043609..196046306,2	K562	blood:
28	chr3:196062380..196065036-chr3:196160453..196162910,2	MCF-7	breast:
29	chr3:196062778..196068235-chr3:196157235..196160927,9	K562	blood:
30	chr3:196044828..196047817-chr3:196050115..196053393,5	K562	blood:
31	chr3:196068688..196070476-chr3:196293348..196295714,2	MCF-7	breast:
32	chr3:196039550..196042176-chr3:196054293..196056157,2	K562	blood:
33	chr3:196035189..196038386-chr3:196041731..196043557,3	K562	blood:
34	chr3:196064683..196067033-chr3:196229952..196232006,2	K562	blood:
35	chr3:196022549..196024808-chr3:196044443..196046676,2	K562	blood:
36	chr3:196057685..196059203-chr3:196062080..196064140,2	MCF-7	breast:
37	chr3:196013567..196017227-chr3:196043342..196045325,4	MCF-7	breast:
38	chr3:196043015..196046706-chr3:196061951..196066451,7	K562	blood:
39	chr3:196044330..196045109-chr5:44808668..44809542,2	Hela-S3	cervix:
40	chr3:196078088..196079673-chr3:196083665..196086587,2	MCF-7	breast:
41	chr3:196043015..196046706-chr3:196061951..196066451,7	K562	blood:
42	chr3:196012352..196016755-chr3:196062622..196069148,9	K562	blood:
43	chr3:196044828..196047817-chr3:196050115..196053393,5	K562	blood:
44	chr3:196043730..196046568-chr3:196064807..196067685,4	MCF-7	breast:
45	chr3:195976340..195978485-chr3:196049925..196051821,2	K562	blood:
46	chr3:196050279..196052047-chr3:196065186..196067594,2	MCF-7	breast:
47	chr3:196043015..196047197-chr3:196061951..196068288,11	K562	blood:
48	chr3:196070139..196072879-chr3:196076090..196077663,2	K562	blood:
49	chr3:195995012..195996670-chr3:196038187..196039923,2	MCF-7	breast:
50	chr3:196074463..196076751-chr3:196080961..196082599,3	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC069257.9.1-3	chr3:196050628-196051059	ENSG00000235897.1
2	lnc-AC069257.9.1-3	chr3:196045245-196045308	NONHSAT094327
3	lnc-AC069257.9.1-3	chr3:196050628-196050852	NONHSAT094327
4	lnc-AC069257.9.1-3	chr3:196045277-196045308	ENSG00000235897.1
5	lnc-AC069257.9.1-3	chr3:196045221-196045308	ENSG00000235897.1
6	lnc-AC069257.9.1-3	chr3:196050701-196052441	ENSG00000235897.1
7	lnc-AC069257.9.1-3	chr3:196045201-196045308	ENSG00000235897.1
8	lnc-AC069257.9.1-3	chr3:196050331-196050544	ENSG00000235897.1
9	lnc-AC069257.9.1-3	chr3:196052471-196052758	NONHSAT094327
10	lnc-AC069257.9.1-3	chr3:196051153-196051737	NONHSAT094327

No data

Variant related genes	Relation type
TCTEX1D2	TF binding region
ENSG00000273331	TF binding region
RNU6-910P	TF binding region
ENSG00000272741	TF binding region
TM4SF19-AS1	TF binding region
TM4SF19	TF binding region
TCTEX1D2	CpG island
ENSG00000273331	CpG island
RNU6-910P	CpG island
ENSG00000272741	CpG island
TM4SF19-AS1	CpG island
TM4SF19	CpG island
ENSG00000072274	chromatin interactions
ENSG00000142230	chromatin interactions
ENSG00000174013	chromatin interactions
ENSG00000130749	chromatin interactions
ENSG00000104897	chromatin interactions
ENSG00000148154	chromatin interactions
ENSG00000112996	chromatin interactions
ENSG00000273331	chromatin interactions
ENSG00000259248	chromatin interactions
ENSG00000225822	chromatin interactions
ENSG00000272741	chromatin interactions
ENSG00000212146	chromatin interactions
ENSG00000185798	chromatin interactions
ENSG00000094631	chromatin interactions
ENSG00000163960	chromatin interactions
ENSG00000163961	chromatin interactions
ENSG00000235897	chromatin interactions
ENSG00000161217	chromatin interactions
ENSG00000251141	chromatin interactions
ENSG00000213123	chromatin interactions
ENSG00000104886	chromatin interactions
ENSG00000243339	chromatin interactions
ENSG00000228028	chromatin interactions
ENSG00000145107	chromatin interactions

Extended variants
information (count: 1890 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1890 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114389373	chr3:196034083-196034084	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs192285746	chr3:196034111-196034112	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs527909467	chr3:196034134-196034135	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs67127834	chr3:196034138-196034139	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs182741421	chr3:196034141-196034142	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs536833004	chr3:196034177-196034178	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs141109644	chr3:196034184-196034185	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs549764821	chr3:196034208-196034209	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs569013814	chr3:196034249-196034250	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs529990559	chr3:196034250-196034251	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs548232552	chr3:196034290-196034291	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs566635729	chr3:196034296-196034297	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs534014299	chr3:196034321-196034322	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs146968129	chr3:196034372-196034373	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs374328194	chr3:196034384-196034385	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs138012899	chr3:196034393-196034394	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs537801237	chr3:196034404-196034405	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs73212160	chr3:196034405-196034406	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs62409175	chr3:196034462-196034463	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs74289369	chr3:196034525-196034526	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs554200128	chr3:196034574-196034575	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs369898399	chr3:196034609-196034610	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs112107280	chr3:196034610-196034611	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs546006559	chr3:196034672-196034673	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs138875005	chr3:196034779-196034780	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs186742482	chr3:196034844-196034845	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs543596433	chr3:196034845-196034846	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs562113083	chr3:196034860-196034861	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs377338827	chr3:196034869-196034870	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs149437980	chr3:196034884-196034885	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs566669438	chr3:196034907-196034908	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs191873608	chr3:196034913-196034914	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs113458475	chr3:196034953-196034954	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs201886079	chr3:196034954-196034955	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs552409515	chr3:196035036-196035037	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs570699969	chr3:196035047-196035048	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs537935438	chr3:196035114-196035115	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs556012722	chr3:196035147-196035148	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs550061662	chr3:196035149-196035150	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs182753346	chr3:196035176-196035177	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs535119924	chr3:196035201-196035202	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs62409176	chr3:196035229-196035230	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs370629938	chr3:196035280-196035281	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs572406272	chr3:196035300-196035301	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs57164208	chr3:196035301-196035302	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs144830365	chr3:196035344-196035345	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs187048025	chr3:196035489-196035490	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs538832119	chr3:196035548-196035549	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs547612339	chr3:196035550-196035551	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs562077318	chr3:196035684-196035685	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	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
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1077 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:196015200-196038800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:196015200-196044400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr3:196015400-196043800	Weak transcription	Brain Substantia Nigra	brain
4	chr3:196015400-196043800	Weak transcription	Fetal Kidney	kidney
5	chr3:196015400-196043800	Weak transcription	Fetal Lung	lung
6	chr3:196015400-196044400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr3:196015400-196044400	Weak transcription	Colon Smooth Muscle	Colon
8	chr3:196015400-196044400	Weak transcription	Lung	lung
9	chr3:196015600-196034200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr3:196015600-196034400	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr3:196015600-196034800	Weak transcription	HSMMtube	muscle
12	chr3:196015600-196036200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:196015600-196041400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr3:196015600-196043600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr3:196015600-196043600	Weak transcription	Fetal Brain Male	brain
16	chr3:196015600-196043800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr3:196015600-196043800	Weak transcription	Brain Angular Gyrus	brain
18	chr3:196015600-196044200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr3:196015600-196044200	Weak transcription	Adipose Nuclei	Adipose
20	chr3:196015600-196044400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr3:196015800-196038800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr3:196015800-196042800	Weak transcription	HMEC	breast
23	chr3:196015800-196043000	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr3:196015800-196043400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr3:196015800-196043600	Weak transcription	A549	lung
26	chr3:196015800-196043800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr3:196015800-196043800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr3:196015800-196043800	Weak transcription	Stomach Smooth Muscle	stomach
29	chr3:196015800-196043800	Weak transcription	HSMM	muscle
30	chr3:196015800-196044200	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr3:196015800-196044400	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr3:196016000-196043600	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr3:196016000-196043600	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr3:196018600-196044200	Weak transcription	Fetal Intestine Large	intestine
35	chr3:196023200-196044400	Weak transcription	Left Ventricle	heart
36	chr3:196023400-196044400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:196024800-196043600	Weak transcription	GM12878-XiMat	blood
38	chr3:196025200-196044400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr3:196025600-196043800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr3:196026400-196044200	Weak transcription	Placenta	Placenta
41	chr3:196027000-196037200	Weak transcription	Ovary	ovary
42	chr3:196027200-196036600	Weak transcription	Fetal Heart	heart
43	chr3:196027400-196043800	Weak transcription	Thymus	Thymus
44	chr3:196027600-196041600	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr3:196027800-196044200	Weak transcription	Fetal Intestine Small	intestine
46	chr3:196028200-196043800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr3:196029000-196044200	Weak transcription	Brain Anterior Caudate	brain
48	chr3:196029400-196041000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr3:196029400-196043600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:196029600-196041000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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