Variant report

Variant	nsv528954
Chromosome Location	chr3:142164017-142219542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:759)
CpG islands
(count:550)
Chromatin interactive
region (count:29)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:142164561-142164907	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:142208918-142209055	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:142164559-142164562	K562	blood:	n/a	n/a
4	ARID3A	chr3:142166751-142167232	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:142166757-142167391	K562	blood:	n/a	n/a
6	ATF1	chr3:142166651-142167117	K562	blood:	n/a	n/a
7	ATF2	chr3:142166292-142167285	GM12878	blood:	n/a	n/a
8	ATF2	chr3:142166627-142167059	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr3:142164617-142165188	GM12878	blood:	n/a	n/a
10	ATF2	chr3:142166586-142167263	GM12878	blood:	n/a	n/a
11	ATF2	chr3:142166613-142167076	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr3:142166680-142167092	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr3:142166666-142167015	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr3:142166739-142166998	HepG2	liver:	n/a	n/a
15	ATF3	chr3:142166731-142166953	GM12878	blood:	n/a	n/a
16	ATF3	chr3:142166710-142167023	K562	blood:	n/a	n/a
17	ATF3	chr3:142166732-142167135	K562	blood:	n/a	n/a
18	BACH1	chr3:142166917-142167234	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr3:142164703-142164947	GM12878	blood:	n/a	n/a
20	BATF	chr3:142164672-142165015	GM12878	blood:	n/a	n/a
21	BCL3	chr3:142166604-142167439	A549	lung:	n/a	chr3:142166983-142166996 chr3:142166980-142166993
22	BCL3	chr3:142166436-142167267	A549	lung:	n/a	chr3:142166983-142166996 chr3:142166980-142166993
23	BCL3	chr3:142166661-142167156	GM12878	blood:	n/a	chr3:142166983-142166996 chr3:142166980-142166993
24	BCLAF1	chr3:142166005-142167259	GM12878	blood:	n/a	chr3:142166983-142166996 chr3:142166980-142166993
25	BCLAF1	chr3:142166597-142167179	K562	blood:	n/a	chr3:142166983-142166996 chr3:142166980-142166993
26	BCLAF1	chr3:142166610-142167248	GM12878	blood:	n/a	chr3:142166983-142166996 chr3:142166980-142166993
27	BHLHE40	chr3:142166557-142167213	K562	blood:	n/a	n/a
28	BHLHE40	chr3:142166500-142167212	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:142166168-142166292	K562	blood:	n/a	n/a
30	BRCA1	chr3:142166786-142167211	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr3:142166846-142167162	HepG2	liver:	n/a	n/a
32	BRCA1	chr3:142166838-142167056	GM12878	blood:	n/a	n/a
33	BRCA1	chr3:142166712-142167511	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr3:142166379-142166460	GM12878	blood:	n/a	n/a
35	CBX3	chr3:142199985-142200480	K562	blood:	n/a	n/a
36	CBX3	chr3:142200070-142200401	K562	blood:	n/a	n/a
37	CBX3	chr3:142166657-142167246	K562	blood:	n/a	n/a
38	CCNT2	chr3:142166405-142167154	K562	blood:	n/a	chr3:142166951-142166960
39	CEBPB	chr3:142166737-142167382	K562	blood:	n/a	n/a
40	CEBPB	chr3:142166712-142167221	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr3:142189681-142190047	HepG2	liver:	n/a	chr3:142189856-142189867
42	CEBPB	chr3:142186622-142186940	IMR90	lung:	n/a	chr3:142186780-142186791
43	CEBPB	chr3:142187407-142187651	A549	lung:	n/a	chr3:142187506-142187519 chr3:142187507-142187518
44	CEBPB	chr3:142186763-142186841	H1-hESC	embryonic stem cell:	n/a	chr3:142186780-142186791
45	CEBPB	chr3:142187432-142187639	K562	blood:	n/a	chr3:142187506-142187519 chr3:142187507-142187518
46	CEBPB	chr3:142189757-142189981	K562	blood:	n/a	chr3:142189856-142189867
47	CEBPB	chr3:142166503-142167338	A549	lung:	n/a	n/a
48	CEBPB	chr3:142189671-142190127	A549	lung:	n/a	chr3:142189856-142189867
49	CEBPB	chr3:142189676-142190055	IMR90	lung:	n/a	chr3:142189856-142189867
50	CEBPB	chr3:142189691-142190053	H1-hESC	embryonic stem cell:	n/a	chr3:142189856-142189867

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:142169703-142169753	CMK	blood:	n/a
2	chr3:142169703-142169753	CMK	blood:	n/a
3	chr3:142164840-142164890	HCM	heart:	n/a
4	chr3:142165032-142165082	Caco-2	colon:	n/a
5	chr3:142164840-142164890	Caco-2	colon:	n/a
6	chr3:142167140-142167190	HL-60	blood:	n/a
7	chr3:142166793-142166843	HL-60	blood:	n/a
8	chr3:142164840-142164890	BE2_C	brain:	n/a
9	chr3:142167140-142167190	IMR90	lung:	fetal
10	chr3:142166793-142166843	T-47D	breast:	n/a
11	chr3:142165032-142165082	BE2_C	brain:	n/a
12	chr3:142169703-142169753	A549	lung:	n/a
13	chr3:142164840-142164890	CMK	blood:	n/a
14	chr3:142167140-142167190	HRPEpiC	eye:	n/a
15	chr3:142167057-142167107	CMK	blood:	n/a
16	chr3:142166789-142166839	SKMC	muscle:	n/a
17	chr3:142167057-142167107	SK-N-SH_RA	brain:	n/a
18	chr3:142164840-142164890	ProgFib	skin:	n/a
19	chr3:142166789-142166839	NHDF-neo	bronchial:	n/a
20	chr3:142164840-142164890	AG10803	skin:	n/a
21	chr3:142166793-142166843	K562	blood:	n/a
22	chr3:142166793-142166843	HMEC	breast:	n/a
23	chr3:142166531-142166581	SAEC	small airway:	n/a
24	chr3:142169703-142169753	NT2-D1	testis:	n/a
25	chr3:142166793-142166843	GM12891	blood:	n/a
26	chr3:142164840-142164890	HRCEpiC	kidney:	n/a
27	chr3:142167057-142167107	ovcar-3	ovarian:	n/a
28	chr3:142167140-142167190	HCPEpiC	choroid plexus:	n/a
29	chr3:142169703-142169753	BJ	skin:	n/a
30	chr3:142164840-142164890	HIPEpiC	eye:	n/a
31	chr3:142166789-142166839	SAEC	small airway:	n/a
32	chr3:142167057-142167107	Hepatocyte	liver:	n/a
33	chr3:142164840-142164890	HEK293	kidney:	embryo
34	chr3:142166789-142166839	GM12878	blood:	n/a
35	chr3:142167057-142167107	NHDF-neo	bronchial:	n/a
36	chr3:142167140-142167190	HAEpiC	amniotic membrane:	n/a
37	chr3:142166789-142166839	SK-N-MC	brain:	n/a
38	chr3:142166531-142166581	HepG2	liver:	n/a
39	chr3:142167140-142167190	AG09319	gingival:	n/a
40	chr3:142167140-142167190	GM06990	blood:	n/a
41	chr3:142169703-142169753	HIPEpiC	eye:	n/a
42	chr3:142166789-142166839	BJ	skin:	n/a
43	chr3:142166793-142166843	A549	lung:	n/a
44	chr3:142166203-142166253	AG09309	skin:	n/a
45	chr3:142165032-142165082	HRPEpiC	eye:	n/a
46	chr3:142167140-142167190	HRCEpiC	kidney:	n/a
47	chr3:142167140-142167190	NB4	blood:	n/a
48	chr3:142167140-142167190	AG04449	skin:	fetal
49	chr3:142169703-142169753	HNPCEpiC	eye:	n/a
50	chr3:142167057-142167107	Caco-2	colon:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:142165266..142167494-chr3:142176108..142178776,2	K562	blood:
2	chr3:142219298..142222317-chr3:142296108..142299028,3	MCF-7	breast:
3	chr3:142164012..142167326-chr3:142183262..142187265,3	K562	blood:
4	chr3:142165537..142167981-chr3:142173026..142174613,2	K562	blood:
5	chr3:142217843..142219879-chr3:142296547..142298953,2	MCF-7	breast:
6	chr3:142166755..142169411-chr3:142174583..142176894,2	K562	blood:
7	chr3:142166774..142168881-chr3:142175818..142179023,4	MCF-7	breast:
8	chr3:142165266..142167494-chr3:142176108..142178776,2	K562	blood:
9	chr3:142167068..142168704-chr3:142178358..142179911,2	K562	blood:
10	chr3:142146723..142149402-chr3:142165233..142167666,2	K562	blood:
11	chr3:142186201..142188360-chr3:142189453..142190962,2	K562	blood:
12	chr3:142164997..142168564-chr3:142170242..142173896,7	MCF-7	breast:
13	chr3:142167068..142168704-chr3:142178358..142179911,2	K562	blood:
14	chr3:142173107..142175736-chr3:142179768..142182228,2	K562	blood:
15	chr3:142166774..142168881-chr3:142175818..142179023,4	MCF-7	breast:
16	chr3:142210650..142212164-chr3:142212182..142213935,2	K562	blood:
17	chr3:142164765..142166960-chr3:142189962..142191863,2	K562	blood:
18	chr3:142164147..142165687-chr3:142176096..142178245,2	K562	blood:
19	chr3:142205435..142207089-chr3:142209696..142212453,2	K562	blood:
20	chr1:32479224..32479963-chr3:142166959..142167563,2	MCF-7	breast:
21	chr3:142210650..142212164-chr3:142212182..142213935,2	K562	blood:
22	chr3:142173107..142175736-chr3:142179768..142182228,2	K562	blood:
23	chr3:142165499..142167998-chr3:142184965..142186898,2	MCF-7	breast:
24	chr3:142205435..142207089-chr3:142209696..142212453,2	K562	blood:
25	chr3:142176585..142179002-chr3:142191298..142192825,2	K562	blood:
26	chr3:142164997..142168564-chr3:142170242..142173896,7	MCF-7	breast:
27	chr3:142166755..142169411-chr3:142174583..142176894,2	K562	blood:
28	chr3:142165889..142168366-chr3:142183445..142185488,2	MCF-7	breast:
29	chr3:142164765..142166960-chr3:142189962..142191863,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XRN1-1	chr3:142190912-142191179	ENSG00000244327.1
2	lnc-PLS1-5	chr3:142168990-142169199	expReg_chr3_9540_+
3	lnc-PLS1-4	chr3:142169997-142170968	expReg_chr3_9541_+
4	lnc-XRN1-1	chr3:142184157-142184653	ENSG00000244327.1
5	lnc-PLS1-3	chr3:142171318-142171592	expReg_chr3_9542_+

No data

Variant related genes	Relation type
XRN1	TF binding region
ENSG00000244327	TF binding region
ATR	TF binding region
ENSG00000242479	TF binding region
XRN1	CpG island
ENSG00000244327	CpG island
ATR	CpG island
ENSG00000242479	CpG island
ENSG00000121774	chromatin interactions
ENSG00000244327	chromatin interactions
ENSG00000114127	chromatin interactions
ENSG00000175054	chromatin interactions
ENSG00000242479	chromatin interactions

Extended variants
information (count: 2038 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:2038 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11719737	chr3:142164017-142164018	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74773739	chr3:142164064-142164065	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs143747595	chr3:142164097-142164098	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs551341675	chr3:142164098-142164099	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs370338853	chr3:142164105-142164106	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs200085141	chr3:142164148-142164149	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs181426378	chr3:142164163-142164164	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs112042804	chr3:142164169-142164170	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs186183554	chr3:142164217-142164218	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs191861183	chr3:142164219-142164220	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs181582819	chr3:142164247-142164248	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs536717257	chr3:142164256-142164257	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs186563041	chr3:142164390-142164391	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113865853	chr3:142164507-142164508	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs562061356	chr3:142164527-142164528	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs574228023	chr3:142164531-142164532	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs190971698	chr3:142164532-142164533	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs559752893	chr3:142164618-142164619	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs148143767	chr3:142164693-142164694	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs141074643	chr3:142164715-142164716	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs150271181	chr3:142164731-142164732	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs12635931	chr3:142164735-142164736	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs531499511	chr3:142164753-142164754	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs549405569	chr3:142164818-142164819	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs534804808	chr3:142164841-142164842	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs567726868	chr3:142164842-142164843	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs552921536	chr3:142164849-142164850	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs547194547	chr3:142164856-142164857	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs565732305	chr3:142164887-142164888	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs137905032	chr3:142164893-142164894	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs558310966	chr3:142164895-142164896	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs377757024	chr3:142164900-142164901	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs576856655	chr3:142164913-142164914	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs75509148	chr3:142165033-142165034	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs112926683	chr3:142165073-142165074	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs577855090	chr3:142165096-142165097	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs375351989	chr3:142165097-142165098	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs147162088	chr3:142165101-142165102	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs564851828	chr3:142165106-142165107	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs182390475	chr3:142165142-142165143	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs138751445	chr3:142165171-142165172	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs531362458	chr3:142165194-142165195	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs549667243	chr3:142165234-142165235	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs79308860	chr3:142165246-142165247	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs142761065	chr3:142165290-142165291	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs144526668	chr3:142165318-142165319	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs565664125	chr3:142165365-142165366	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs538575083	chr3:142165378-142165379	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs187951013	chr3:142165432-142165433	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs551730474	chr3:142165547-142165548	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 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
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
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
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
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1889 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142138600-142164600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:142142200-142165400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr3:142146600-142164200	Weak transcription	Stomach Mucosa	stomach
4	chr3:142149800-142165000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:142150000-142164400	Weak transcription	Aorta	Aorta
6	chr3:142150000-142164600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr3:142150200-142164400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr3:142150200-142164400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr3:142150200-142164600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr3:142150200-142164600	Weak transcription	HSMMtube	muscle
11	chr3:142150400-142164400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr3:142150400-142164400	Weak transcription	HSMM	muscle
13	chr3:142150400-142164600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:142150400-142164600	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr3:142150400-142164600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr3:142150600-142165400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr3:142151600-142164400	Weak transcription	Osteobl	bone
18	chr3:142151600-142164600	Weak transcription	NH-A	brain
19	chr3:142151800-142164600	Weak transcription	Fetal Lung	lung
20	chr3:142152000-142164200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:142152200-142164400	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr3:142152200-142164400	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr3:142152200-142164400	Weak transcription	Stomach Smooth Muscle	stomach
24	chr3:142154000-142164400	Weak transcription	HUVEC	blood vessel
25	chr3:142154600-142166000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr3:142156200-142164600	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr3:142158800-142164600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr3:142158800-142164600	Weak transcription	Right Atrium	heart
29	chr3:142159000-142164400	Weak transcription	NHEK	skin
30	chr3:142159000-142164600	Weak transcription	Esophagus	oesophagus
31	chr3:142159400-142164400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr3:142159400-142164600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr3:142159800-142164200	Weak transcription	K562	blood
34	chr3:142159800-142164400	Weak transcription	Primary hematopoietic stem cells	blood
35	chr3:142159800-142164600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr3:142159800-142164600	Weak transcription	Gastric	stomach
37	chr3:142160000-142164600	Weak transcription	Left Ventricle	heart
38	chr3:142160000-142166000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr3:142160600-142164400	Weak transcription	Psoas Muscle	Psoas
40	chr3:142160800-142165400	Weak transcription	Fetal Muscle Leg	muscle
41	chr3:142161200-142164400	Weak transcription	HMEC	breast
42	chr3:142161600-142164200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr3:142162000-142164200	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr3:142162000-142164400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr3:142162000-142164400	Enhancers	Liver	Liver
46	chr3:142162000-142164600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr3:142162200-142164200	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr3:142162200-142164400	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr3:142162400-142164400	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr3:142162400-142164800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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