Variant report

Variant	nsv933522
Chromosome Location	chr3:135968919-135981180
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:135969896-135970500	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:135974327-135974914	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:135969875-135970236	K562	blood:	n/a	n/a
4	ARID3A	chr3:135968840-135969614	HepG2	liver:	n/a	n/a
5	ATF2	chr3:135968769-135969758	GM12878	blood:	n/a	n/a
6	ATF2	chr3:135968916-135969955	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr3:135969099-135969587	GM12878	blood:	n/a	n/a
8	ATF3	chr3:135969091-135969326	K562	blood:	n/a	n/a
9	BACH1	chr3:135969046-135969547	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr3:135969731-135970321	GM12878	blood:	n/a	chr3:135970232-135970241
11	BCLAF1	chr3:135968732-135969383	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:135968891-135970408	K562	blood:	n/a	chr3:135969109-135969125
13	BHLHE40	chr3:135974568-135974795	HepG2	liver:	n/a	n/a
14	BHLHE40	chr3:135968908-135970335	GM12878	blood:	n/a	chr3:135969109-135969125
15	BHLHE40	chr3:135969035-135970296	HepG2	liver:	n/a	chr3:135969109-135969125
16	BRCA1	chr3:135969027-135969471	HepG2	liver:	n/a	n/a
17	BRCA1	chr3:135968861-135969794	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr3:135968981-135969557	K562	blood:	n/a	n/a
19	CBX3	chr3:135969694-135970536	K562	blood:	n/a	n/a
20	CBX3	chr3:135969000-135969321	K562	blood:	n/a	n/a
21	CBX3	chr3:135969740-135970225	K562	blood:	n/a	n/a
22	CCNT2	chr3:135968969-135969561	K562	blood:	n/a	n/a
23	CCNT2	chr3:135969903-135970290	K562	blood:	n/a	n/a
24	CEBPB	chr3:135970392-135970768	Hela-S3	cervix:	n/a	chr3:135970665-135970676 chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
25	CEBPB	chr3:135970370-135970714	HepG2	liver:	n/a	chr3:135970665-135970676 chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
26	CEBPB	chr3:135968439-135969426	K562	blood:	n/a	chr3:135968595-135968606
27	CEBPB	chr3:135968446-135969485	HepG2	liver:	n/a	chr3:135968595-135968606
28	CEBPB	chr3:135970397-135970755	HepG2	liver:	n/a	chr3:135970665-135970676 chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
29	CEBPB	chr3:135970385-135970726	K562	blood:	n/a	chr3:135970665-135970676 chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
30	CEBPB	chr3:135968445-135969893	Hela-S3	cervix:	n/a	chr3:135968595-135968606
31	CEBPB	chr3:135970331-135970764	K562	blood:	n/a	chr3:135970665-135970676 chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
32	CEBPB	chr3:135968834-135969618	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr3:135970422-135970669	A549	lung:	n/a	chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
34	CEBPB	chr3:135970384-135970762	HepG2	liver:	n/a	chr3:135970665-135970676 chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
35	CEBPB	chr3:135974492-135974848	HepG2	liver:	n/a	n/a
36	CEBPB	chr3:135970509-135970657	H1-hESC	embryonic stem cell:	n/a	chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
37	CEBPB	chr3:135969081-135969247	HepG2	liver:	n/a	n/a
38	CEBPB	chr3:135970331-135970724	MCF-7	breast:	n/a	chr3:135970665-135970676 chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
39	CEBPB	chr3:135970449-135970657	HepG2	liver:	n/a	chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
40	CEBPD	chr3:135968982-135969487	HepG2	liver:	n/a	n/a
41	CEBPD	chr3:135969823-135970332	K562	blood:	n/a	n/a
42	CEBPD	chr3:135969887-135970300	K562	blood:	n/a	n/a
43	CHD1	chr3:135969731-135969946	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr3:135968875-135969418	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr3:135968802-135969885	GM12878	blood:	n/a	n/a
46	CHD2	chr3:135968895-135970290	GM12878	blood:	n/a	n/a
47	CHD2	chr3:135968913-135970006	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr3:135968870-135969727	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr3:135969187-135970003	HepG2	liver:	n/a	n/a
50	CHD2	chr3:135968966-135970301	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:135969981-135970031	HCPEpiC	choroid plexus:	n/a
2	chr3:135969981-135970031	HCPEpiC	choroid plexus:	n/a
3	chr3:135969981-135970031	PrEC	prostate:	n/a
4	chr3:135969043-135969093	HRPEpiC	eye:	n/a
5	chr3:135969733-135969783	AG09309	skin:	n/a
6	chr3:135969387-135969437	H1-hESC	embryonic stem cell:	embryo
7	chr3:135969556-135969606	H1-hESC	embryonic stem cell:	embryo
8	chr3:135969136-135969186	PFSK-1	brain:	n/a
9	chr3:135972373-135972423	HNPCEpiC	eye:	n/a
10	chr3:135969063-135969113	MCF-7	breast:	n/a
11	chr3:135969063-135969113	HL-60	blood:	n/a
12	chr3:135969063-135969113	HRE	kidney:	n/a
13	chr3:135969043-135969093	HUVEC	blood vessel:	n/a
14	chr3:135969429-135969479	HIPEpiC	eye:	n/a
15	chr3:135969733-135969783	GM06990	blood:	n/a
16	chr3:135969958-135970008	Caco-2	colon:	n/a
17	chr3:135969981-135970031	GM06990	blood:	n/a
18	chr3:135969958-135970008	CMK	blood:	n/a
19	chr3:135969981-135970031	HEK293	kidney:	embryo
20	chr3:135969136-135969186	HCM	heart:	n/a
21	chr3:135969981-135970031	SK-N-SH	brain:	n/a
22	chr3:135969556-135969606	HRE	kidney:	n/a
23	chr3:135969916-135969966	U87	brain:	n/a
24	chr3:135968952-135969002	AG04449	skin:	fetal
25	chr3:135969041-135969091	RPTEC	kidney:	n/a
26	chr3:135969116-135969166	GM12878	blood:	n/a
27	chr3:135969116-135969166	Caco-2	colon:	n/a
28	chr3:135969043-135969093	ECC-1	luminal epithelium:	n/a
29	chr3:135969958-135970008	HL-60	blood:	n/a
30	chr3:135969116-135969166	A549	lung:	n/a
31	chr3:135969981-135970031	MCF10A-Er-Src	breast:	n/a
32	chr3:135969958-135970008	GM06990	blood:	n/a
33	chr3:135969043-135969093	GM12878	blood:	n/a
34	chr3:135969063-135969113	PFSK-1	brain:	n/a
35	chr3:135969043-135969093	Hepatocyte	liver:	n/a
36	chr3:135969981-135970031	HRCEpiC	kidney:	n/a
37	chr3:135969958-135970008	AoSMC	blood vessel:	n/a
38	chr3:135969043-135969093	HEK293	kidney:	embryo
39	chr3:135969981-135970031	HMEC	breast:	n/a
40	chr3:135969116-135969166	CMK	blood:	n/a
41	chr3:135969116-135969166	Hepatocyte	liver:	n/a
42	chr3:135969053-135969103	GM19239	blood:	n/a
43	chr3:135969136-135969186	BJ	skin:	n/a
44	chr3:135969041-135969091	GM19239	blood:	n/a
45	chr3:135968952-135969002	GM12891	blood:	n/a
46	chr3:135972373-135972423	MCF-7	breast:	n/a
47	chr3:135969958-135970008	HRPEpiC	eye:	n/a
48	chr3:135969556-135969606	HCF	heart:	n/a
49	chr3:135972373-135972423	BE2_C	brain:	n/a
50	chr3:135969916-135969966	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:135968756..135970580-chr3:136469634..136471998,2	K562	blood:
2	chr11:10830178..10831145-chr3:135969170..135969695,2	Hela-S3	cervix:
3	chr3:135912324..135920790-chr3:135965276..135971841,24	K562	blood:
4	chr3:135914832..135915585-chr3:135969132..135969693,2	MCF-7	breast:
5	chr3:135968947..135969500-chr6:27100458..27101422,2	HCT-116	colon:
6	chr3:135914289..135916961-chr3:135976114..135978100,2	MCF-7	breast:
7	chr3:135968568..135972532-chr3:135974380..135977728,5	K562	blood:
8	chr3:135968568..135972532-chr3:135974380..135977728,5	K562	blood:
9	chr3:135913308..135916970-chr3:135973705..135976198,3	K562	blood:
10	chr3:135968107..135969967-chr3:136470513..136472370,2	MCF-7	breast:
11	chr3:135967759..135970710-chr3:135979580..135983206,3	K562	blood:
12	chr3:135820564..135822131-chr3:135979717..135981662,2	MCF-7	breast:
13	chr3:135913275..135917052-chr3:135966241..135970685,15	MCF-7	breast:
14	chr3:135912206..135917353-chr3:135967047..135972220,20	MCF-7	breast:
15	chr3:135974598..135977486-chr3:135979875..135981480,2	MCF-7	breast:
16	chr3:135967505..135970256-chr3:136469769..136472442,3	K562	blood:
17	chr3:135914645..135915534-chr3:135968907..135969695,2	Hela-S3	cervix:
18	chr3:135967759..135969790-chr3:135979580..135981663,2	K562	blood:
19	chr3:135967895..135971293-chr3:135973278..135977937,5	MCF-7	breast:
20	chr3:135914058..135916023-chr3:135977800..135980119,2	MCF-7	breast:
21	chr3:135967895..135971293-chr3:135973278..135977937,5	MCF-7	breast:
22	chr3:135912523..135919453-chr3:135966949..135972062,29	K562	blood:
23	chr3:135969104..135971090-chr3:136470031..136473091,3	MCF-7	breast:

Variant related genes	Relation type
PCCB	TF binding region
PCCB	CpG island
ENSG00000118007	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000073711	chromatin interactions
ENSG00000114054	chromatin interactions
ENSG00000174579	chromatin interactions
ENSG00000261758	chromatin interactions
ENSG00000246308	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000110321	chromatin interactions

Extended variants
information (count: 538 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545764604	chr3:135968942-135968943	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs79940405	chr3:135968955-135968956	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs369593612	chr3:135968984-135968985	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs149770129	chr3:135969019-135969020	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs114666363	chr3:135969063-135969064	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs561296185	chr3:135969065-135969066	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs16843806	chr3:135969078-135969079	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs550327268	chr3:135969081-135969082	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs570033857	chr3:135969090-135969091	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs532365071	chr3:135969094-135969095	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs551301286	chr3:135969097-135969098	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs571188323	chr3:135969129-135969130	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs189166481	chr3:135969153-135969154	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs546682085	chr3:135969160-135969161	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs553950866	chr3:135969167-135969168	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs567310996	chr3:135969168-135969169	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs145734157	chr3:135969181-135969182	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs372649775	chr3:135969184-135969185	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs377349557	chr3:135969200-135969201	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs369284492	chr3:135969212-135969213	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs398123462	chr3:135969219-135969220	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs398123464	chr3:135969220-135969221	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs373685372	chr3:135969225-135969226	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs377681768	chr3:135969233-135969234	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs200185747	chr3:135969266-135969267	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs559320564	chr3:135969286-135969287	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs35838767	chr3:135969293-135969294	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs141137691	chr3:135969299-135969300	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs182412270	chr3:135969333-135969334	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs375014273	chr3:135969348-135969349	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs145075817	chr3:135969355-135969356	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs199935380	chr3:135969356-135969357	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs376983709	chr3:135969359-135969360	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs561539546	chr3:135969380-135969381	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs371406048	chr3:135969386-135969387	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs200636968	chr3:135969387-135969388	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs147954363	chr3:135969392-135969393	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs140636870	chr3:135969397-135969398	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs398123460	chr3:135969401-135969402	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs398123461	chr3:135969403-135969404	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs34167145	chr3:135969415-135969416	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs139744249	chr3:135969455-135969456	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs543941015	chr3:135969461-135969462	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs570284303	chr3:135969465-135969466	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs532403026	chr3:135969505-135969506	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs147606121	chr3:135969537-135969538	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs565705171	chr3:135969538-135969539	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs527592486	chr3:135969542-135969543	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs547330460	chr3:135969547-135969548	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs190302995	chr3:135969556-135969557	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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

Chromatin state (count:846 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135967600-135969000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr3:135968000-135969000	Flanking Active TSS	HepG2	liver
3	chr3:135968600-135969000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:135968600-135969000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
5	chr3:135968600-135969000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr3:135968600-135969000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr3:135968600-135969000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:135968600-135969000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
9	chr3:135968600-135969000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:135968600-135969000	Flanking Active TSS	Liver	Liver
11	chr3:135968600-135969000	Flanking Active TSS	Brain Substantia Nigra	brain
12	chr3:135968600-135969000	Flanking Active TSS	GM12878-XiMat	blood
13	chr3:135968600-135969000	Flanking Active TSS	Hela-S3	cervix
14	chr3:135968600-135969000	Flanking Active TSS	NHEK	skin
15	chr3:135968600-135969000	Flanking Active TSS	Osteobl	bone
16	chr3:135968600-135969200	Flanking Active TSS	Fetal Muscle Trunk	muscle
17	chr3:135968600-135969200	Flanking Active TSS	Dnd41	blood
18	chr3:135968600-135969400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr3:135968600-135969600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr3:135968600-135969600	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr3:135968600-135969600	Active TSS	Brain Germinal Matrix	brain
22	chr3:135968600-135969600	Active TSS	Rectal Mucosa Donor 29	rectum
23	chr3:135968600-135969800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr3:135968600-135969800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr3:135968600-135969800	Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr3:135968600-135969800	Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr3:135968600-135969800	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr3:135968600-135969800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr3:135968600-135969800	Active TSS	Breast Myoepithelial Primary Cells	Breast
30	chr3:135968600-135969800	Active TSS	Primary T helper naive cells from peripheral blood	blood
31	chr3:135968600-135969800	Active TSS	Brain Anterior Caudate	brain
32	chr3:135968600-135969800	Active TSS	Fetal Brain Female	brain
33	chr3:135968600-135969800	Active TSS	Fetal Intestine Large	intestine
34	chr3:135968600-135969800	Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr3:135968600-135969800	Enhancers	Spleen	Spleen
36	chr3:135968600-135970000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr3:135968600-135970200	Active TSS	Fetal Lung	lung
38	chr3:135968600-135970200	Active TSS	Rectal Smooth Muscle	rectum
39	chr3:135968600-135970400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
40	chr3:135968600-135970400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
41	chr3:135968800-135969000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
42	chr3:135968800-135969000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr3:135968800-135969000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr3:135968800-135969000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr3:135968800-135969000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr3:135968800-135969000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr3:135968800-135969000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
48	chr3:135968800-135969000	Flanking Active TSS	Primary B cells from cord blood	blood
49	chr3:135968800-135969000	Flanking Active TSS	Primary B cells from peripheral blood	blood
50	chr3:135968800-135969000	Flanking Active TSS	Primary hematopoietic stem cells	blood

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