Variant report

Variant	nsv546689
Chromosome Location	chr1:84531117-84670816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1647)
CpG islands
(count:854)
Chromatin interactive
region (count:97)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1647 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:84588503-84588838	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:84539139-84539400	K562	blood:	n/a	n/a
3	ARID3A	chr1:84568896-84569476	K562	blood:	n/a	n/a
4	ARID3A	chr1:84544449-84544500	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:84543380-84543588	HepG2	liver:	n/a	n/a
6	ATF1	chr1:84568983-84569442	K562	blood:	n/a	n/a
7	ATF1	chr1:84625274-84625597	K562	blood:	n/a	n/a
8	ATF2	chr1:84618224-84618863	GM12878	blood:	n/a	n/a
9	ATF2	chr1:84569015-84569438	GM12878	blood:	n/a	n/a
10	ATF3	chr1:84569103-84569374	K562	blood:	n/a	n/a
11	ATF3	chr1:84621649-84622441	HCT-116	colon:	n/a	n/a
12	ATF3	chr1:84639743-84640360	A549	lung:	n/a	n/a
13	ATF3	chr1:84543471-84543757	K562	blood:	n/a	chr1:84543641-84543650 chr1:84543645-84543654 chr1:84543690-84543699 chr1:84543605-84543614 chr1:84543554-84543574
14	ATF3	chr1:84543513-84543717	H1-hESC	embryonic stem cell:	n/a	chr1:84543641-84543650 chr1:84543645-84543654 chr1:84543690-84543699 chr1:84543605-84543614 chr1:84543554-84543574
15	ATF3	chr1:84568989-84569425	K562	blood:	n/a	n/a
16	BACH1	chr1:84543125-84543656	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:84568830-84569522	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr1:84544537-84544708	K562	blood:	n/a	n/a
19	BACH1	chr1:84568927-84569534	K562	blood:	n/a	n/a
20	BATF	chr1:84622058-84622350	GM12878	blood:	n/a	chr1:84622196-84622207
21	BATF	chr1:84573215-84573613	GM12878	blood:	n/a	chr1:84573424-84573435
22	BATF	chr1:84569141-84569355	GM12878	blood:	n/a	n/a
23	BATF	chr1:84618271-84618830	GM12878	blood:	n/a	n/a
24	BATF	chr1:84573219-84573600	GM12878	blood:	n/a	chr1:84573424-84573435
25	BATF	chr1:84632577-84632840	GM12878	blood:	n/a	chr1:84632738-84632749
26	BATF	chr1:84618291-84618802	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:84618235-84618750	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:84618300-84618565	GM12878	blood:	n/a	n/a
29	BCL3	chr1:84543469-84543767	GM12878	blood:	n/a	chr1:84543694-84543707 chr1:84543570-84543579 chr1:84543635-84543644
30	BCL3	chr1:84543200-84543635	A549	lung:	n/a	chr1:84543570-84543579
31	BCLAF1	chr1:84543128-84543608	GM12878	blood:	n/a	chr1:84543570-84543579
32	BCLAF1	chr1:84618223-84618787	GM12878	blood:	n/a	n/a
33	BHLHE40	chr1:84543041-84543667	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:84569016-84569438	K562	blood:	n/a	n/a
35	BHLHE40	chr1:84543976-84544360	K562	blood:	n/a	n/a
36	BHLHE40	chr1:84622132-84622332	A549	lung:	n/a	n/a
37	BHLHE40	chr1:84543122-84543669	K562	blood:	n/a	n/a
38	BRCA1	chr1:84543387-84543473	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr1:84542671-84544001	Hela-S3	cervix:	n/a	chr1:84543052-84543059
40	BRCA1	chr1:84568769-84569351	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr1:84639583-84640587	HCT-116	colon:	n/a	n/a
42	CBX3	chr1:84568973-84569422	K562	blood:	n/a	n/a
43	CBX3	chr1:84639712-84640465	HCT-116	colon:	n/a	n/a
44	CBX3	chr1:84573647-84573938	K562	blood:	n/a	n/a
45	CBX3	chr1:84568901-84569481	K562	blood:	n/a	n/a
46	CBX3	chr1:84621201-84622949	HCT-116	colon:	n/a	chr1:84621269-84621280
47	CBX3	chr1:84609716-84610267	HCT-116	colon:	n/a	n/a
48	CBX3	chr1:84534959-84535365	HCT-116	colon:	n/a	n/a
49	CBX3	chr1:84556118-84556668	HCT-116	colon:	n/a	n/a
50	CBX3	chr1:84561005-84561353	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:84543156-84543206	Hepatocyte	liver:	n/a
2	chr1:84544220-84544270	HMEC	breast:	n/a
3	chr1:84543369-84543419	HEEpiC	esophagus:	n/a
4	chr1:84544220-84544270	BE2_C	brain:	n/a
5	chr1:84543156-84543206	HRCEpiC	kidney:	n/a
6	chr1:84543369-84543419	HIPEpiC	eye:	n/a
7	chr1:84543951-84544001	SK-N-MC	brain:	n/a
8	chr1:84544097-84544147	LNCaP	prostate:	n/a
9	chr1:84543558-84543608	T-47D	breast:	n/a
10	chr1:84543539-84543589	Hela-S3	cervix:	n/a
11	chr1:84543539-84543589	MCF-7	breast:	n/a
12	chr1:84543551-84543601	NHBE	bronchial:	n/a
13	chr1:84543374-84543424	SAEC	small airway:	n/a
14	chr1:84543539-84543589	GM12892	blood:	n/a
15	chr1:84541035-84541085	HNPCEpiC	eye:	n/a
16	chr1:84544220-84544270	SKMC	muscle:	n/a
17	chr1:84543539-84543589	BE2_C	brain:	n/a
18	chr1:84544097-84544147	SK-N-SH_RA	brain:	n/a
19	chr1:84543369-84543419	K562	blood:	n/a
20	chr1:84609007-84609057	AG10803	skin:	n/a
21	chr1:84544220-84544270	GM12878	blood:	n/a
22	chr1:84543551-84543601	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:84543369-84543419	SK-N-SH_RA	brain:	n/a
24	chr1:84544284-84544334	PANC-1	pancreas:	n/a
25	chr1:84543369-84543419	AoSMC	blood vessel:	n/a
26	chr1:84541035-84541085	NT2-D1	testis:	n/a
27	chr1:84547955-84548005	BE2_C	brain:	n/a
28	chr1:84543951-84544001	HepG2	liver:	n/a
29	chr1:84543156-84543206	HCT-116	colon:	n/a
30	chr1:84543551-84543601	NH-A	brain:	n/a
31	chr1:84543156-84543206	NHDF-neo	bronchial:	n/a
32	chr1:84547955-84548005	PANC-1	pancreas:	n/a
33	chr1:84541035-84541085	Hela-S3	cervix:	n/a
34	chr1:84547955-84548005	Jurkat	blood:	n/a
35	chr1:84544284-84544334	HRCEpiC	kidney:	n/a
36	chr1:84543374-84543424	U87	brain:	n/a
37	chr1:84547955-84548005	AG04449	skin:	fetal
38	chr1:84543374-84543424	SKMC	muscle:	n/a
39	chr1:84543951-84544001	H1-hESC	embryonic stem cell:	embryo
40	chr1:84543369-84543419	HRPEpiC	eye:	n/a
41	chr1:84543374-84543424	PrEC	prostate:	n/a
42	chr1:84544097-84544147	K562	blood:	n/a
43	chr1:84609007-84609057	BJ	skin:	n/a
44	chr1:84547955-84548005	HCM	heart:	n/a
45	chr1:84543156-84543206	A549	lung:	n/a
46	chr1:84543374-84543424	HEK293	kidney:	embryo
47	chr1:84609007-84609057	AG09319	gingival:	n/a
48	chr1:84543156-84543206	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:84541035-84541085	PFSK-1	brain:	n/a
50	chr1:84609007-84609057	CMK	blood:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:84547756..84549761-chr1:84565111..84567613,2	K562	blood:
2	chr1:84549009..84550573-chr1:84552589..84554754,2	K562	blood:
3	chr1:84594754..84597545-chr1:84597865..84602064,4	K562	blood:
4	chr1:84541371..84543109-chr1:84583953..84586517,2	K562	blood:
5	chr1:84413047..84415136-chr1:84540240..84542127,2	K562	blood:
6	chr1:84553847..84557736-chr1:84560723..84565476,4	K562	blood:
7	chr1:84397136..84397730-chr1:84588264..84588912,2	MCF-7	breast:
8	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
9	chr1:84550235..84552065-chr1:84552906..84555426,2	MCF-7	breast:
10	chr1:84577775..84580533-chr1:84581972..84584955,2	K562	blood:
11	chr1:84543365..84543953-chr2:136633448..136634387,2	Hela-S3	cervix:
12	chr1:84596861..84598405-chr1:84603464..84605048,2	K562	blood:
13	chr1:84556236..84558984-chr1:84559547..84561523,2	MCF-7	breast:
14	chr1:84541598..84548799-chr1:84549003..84554628,15	K562	blood:
15	chr1:84541438..84545739-chr1:84555567..84558104,4	K562	blood:
16	chr1:84377090..84379247-chr1:84542414..84544902,2	K562	blood:
17	chr1:84553847..84557736-chr1:84560723..84565476,4	K562	blood:
18	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
19	chr1:84545204..84547427-chr1:84607809..84609728,2	K562	blood:
20	chr1:84371561..84374304-chr1:84536819..84538453,2	K562	blood:
21	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
22	chr1:84642752..84644786-chr1:84646959..84648659,2	K562	blood:
23	chr1:84551652..84556823-chr1:84558383..84561144,5	K562	blood:
24	chr1:84463824..84465552-chr1:84584447..84586130,2	MCF-7	breast:
25	chr1:84543836..84545852-chr1:84545884..84547709,2	K562	blood:
26	chr1:84662036..84663948-chr1:84669561..84672181,4	K562	blood:
27	chr1:84606626..84607485-chr1:85006757..85007586,2	MCF-7	breast:
28	chr1:84536131..84538617-chr1:84567747..84570815,3	K562	blood:
29	chr1:84563814..84566575-chr1:84567797..84569864,2	K562	blood:
30	chr1:84530745..84533538-chr1:84541261..84543799,3	K562	blood:
31	chr1:84587966..84589963-chr1:84603179..84604852,2	K562	blood:
32	chr1:84554743..84559247-chr1:84561300..84565476,7	K562	blood:
33	chr1:84539639..84541968-chr1:84547734..84550751,3	K562	blood:
34	chr1:84547756..84549761-chr1:84565111..84567613,2	K562	blood:
35	chr1:84528524..84531344-chr1:84538975..84541375,2	MCF-7	breast:
36	chr1:84594754..84597545-chr1:84597865..84602064,4	K562	blood:
37	chr1:84550027..84551748-chr1:84557212..84559116,2	MCF-7	breast:
38	chr1:84541371..84543109-chr1:84583953..84586517,2	K562	blood:
39	chr1:84543517..84544097-chr5:34915086..34915845,2	Hela-S3	cervix:
40	chr1:84542977..84543701-chr9:140135375..140136244,2	Hela-S3	cervix:
41	chr1:84536131..84538617-chr1:84567747..84570815,3	K562	blood:
42	chr1:84587966..84589963-chr1:84603179..84604852,2	K562	blood:
43	chr1:84545204..84547427-chr1:84607809..84609728,2	K562	blood:
44	chr1:84540590..84543508-chr1:84558962..84560991,2	K562	blood:
45	chr1:84542019..84545394-chr1:84564150..84567617,5	K562	blood:
46	chr1:84541330..84545077-chr1:84567686..84570781,4	K562	blood:
47	chr1:84411907..84414547-chr1:84539636..84541740,2	K562	blood:
48	chr1:84528524..84531344-chr1:84538975..84541375,2	MCF-7	breast:
49	chr1:84543429..84544009-chr3:122233490..122234112,2	Hela-S3	cervix:
50	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004190
2	lnc-TTLL7-3	chr1:84542062-84543325	XLOC_000889
3	lnc-SAMD13-1	chr1:84644860-84644921	NONHSAT004188
4	lnc-TTLL7-3	chr1:84542014-84543655	NONHSAT004184
5	lnc-TTLL7-3	chr1:84542014-84543614	ENSG00000271576.1
6	lnc-SAMD13-1	chr1:84644861-84644903	NONHSAT004191
7	lnc-SAMD13-1	chr1:84640717-84640739	NONHSAT004191
8	lnc-SAMD13-1	chr1:84644860-84644903	NONHSAT004190
9	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004188
10	lnc-SAMD13-1	chr1:84630580-84630696	NONHSAT004190
11	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004190
12	lnc-SAMD13-1	chr1:84630387-84630696	NONHSAT004188
13	lnc-TTLL7-3	chr1:84543564-84543595	XLOC_000889
14	lnc-SAMD13-1	chr1:84639013-84639035	NONHSAT004191
15	lnc-SAMD13-1	chr1:84630581-84630696	NONHSAT004191
16	lnc-SAMD13-1	chr1:84641482-84641490	NONHSAT004190
17	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004188

No data

Variant related genes	Relation type
ENSG00000271576	TF binding region
ENSG00000213540	TF binding region
PRKACB	TF binding region
ENSG00000271576	CpG island
ENSG00000213540	CpG island
PRKACB	CpG island
ENSG00000162616	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000113456	chromatin interactions
ENSG00000271576	chromatin interactions
ENSG00000026025	chromatin interactions
ENSG00000213540	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000142875	chromatin interactions
ENSG00000137941	chromatin interactions
ENSG00000174021	chromatin interactions
ENSG00000113460	chromatin interactions
ENSG00000076003	chromatin interactions
ENSG00000117155	chromatin interactions
ENSG00000114030	chromatin interactions
ENSG00000273338	chromatin interactions
ENSG00000122432	chromatin interactions
ARHGAP12	miRNA target sites
GCFC1	miRNA target sites
FBXO28	miRNA target sites
GCNT2	miRNA target sites
GCH1	miRNA target sites

Extended variants
information (count: 4623 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:4623 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3861699	chr1:84531117-84531118	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574804141	chr1:84531141-84531142	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534413454	chr1:84531203-84531204	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs554025621	chr1:84531266-84531267	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs544264798	chr1:84531282-84531283	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs143377905	chr1:84531287-84531288	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs184131555	chr1:84531296-84531297	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576082964	chr1:84531446-84531447	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs5775774	chr1:84531447-84531448	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs112307904	chr1:84531448-84531449	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs541430020	chr1:84531456-84531457	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs188147135	chr1:84531586-84531587	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs527358145	chr1:84531599-84531600	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547574354	chr1:84531669-84531670	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs114712145	chr1:84531670-84531671	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs533099539	chr1:84531697-84531698	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs180948350	chr1:84531728-84531729	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549650776	chr1:84531730-84531731	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs568939260	chr1:84531772-84531773	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs187141038	chr1:84531801-84531802	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs116236145	chr1:84531831-84531832	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs151329160	chr1:84531870-84531871	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs534030234	chr1:84531900-84531901	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs529096991	chr1:84531934-84531935	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs190504960	chr1:84531970-84531971	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs372353320	chr1:84532043-84532044	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs617568	chr1:84532056-84532057	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs72938456	chr1:84532077-84532078	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs552504412	chr1:84532105-84532106	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs576778508	chr1:84532134-84532135	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs182219437	chr1:84532143-84532144	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs555018452	chr1:84532270-84532271	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs559550241	chr1:84532297-84532298	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs528266559	chr1:84532319-84532320	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs548414510	chr1:84532325-84532326	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs562024877	chr1:84532391-84532392	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs572154044	chr1:84532422-84532423	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs368102319	chr1:84532430-84532431	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs375314904	chr1:84532443-84532444	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs532939432	chr1:84532518-84532519	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs140527394	chr1:84532624-84532625	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs563251607	chr1:84532669-84532670	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs549211181	chr1:84532738-84532739	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs548609270	chr1:84532742-84532743	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186788577	chr1:84532744-84532745	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs527818921	chr1:84532749-84532750	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs190787049	chr1:84532753-84532754	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs570928339	chr1:84532758-84532759	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs75493233	chr1:84532770-84532771	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs112343138	chr1:84532794-84532795	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2911 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84528400-84532600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:84531400-84532000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:84531400-84532200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:84532600-84533600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:84532800-84533600	Enhancers	Brain Hippocampus Middle	brain
6	chr1:84533000-84533400	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr1:84533200-84533600	Enhancers	Brain Substantia Nigra	brain
8	chr1:84533400-84534600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr1:84533600-84534400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:84534200-84535000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:84534400-84534600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:84536600-84537600	Enhancers	K562	blood
13	chr1:84536600-84542400	Weak transcription	Fetal Lung	lung
14	chr1:84537600-84541000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr1:84537600-84541000	Weak transcription	K562	blood
16	chr1:84538000-84538200	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr1:84538000-84541200	Weak transcription	Liver	Liver
18	chr1:84538000-84542000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:84538400-84542400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr1:84538400-84542800	Weak transcription	HSMM	muscle
21	chr1:84538600-84542000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr1:84538600-84542400	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr1:84538600-84542400	Weak transcription	Osteobl	bone
24	chr1:84538800-84542200	Weak transcription	Fetal Brain Male	brain
25	chr1:84539200-84542000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:84539200-84542400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:84540200-84542400	Weak transcription	Colon Smooth Muscle	Colon
28	chr1:84540800-84541000	Enhancers	A549	lung
29	chr1:84541000-84541200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr1:84541000-84541200	Weak transcription	Brain Substantia Nigra	brain
31	chr1:84541000-84541400	Enhancers	Brain Anterior Caudate	brain
32	chr1:84541000-84542000	Weak transcription	A549	lung
33	chr1:84541000-84542000	Enhancers	K562	blood
34	chr1:84541000-84542400	Enhancers	HepG2	liver
35	chr1:84541200-84541400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:84541200-84541400	Enhancers	Liver	Liver
37	chr1:84541200-84541400	Enhancers	Brain Substantia Nigra	brain
38	chr1:84541200-84541600	Enhancers	GM12878-XiMat	blood
39	chr1:84541200-84541800	Enhancers	Brain Cingulate Gyrus	brain
40	chr1:84541200-84542400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:84541200-84542400	Enhancers	Brain Hippocampus Middle	brain
42	chr1:84541200-84542400	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr1:84541200-84542400	Enhancers	Dnd41	blood
44	chr1:84541400-84542000	Weak transcription	Liver	Liver
45	chr1:84541400-84542400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:84541400-84542400	Weak transcription	Brain Anterior Caudate	brain
47	chr1:84541400-84542600	Weak transcription	Brain Substantia Nigra	brain
48	chr1:84541600-84542000	Weak transcription	GM12878-XiMat	blood
49	chr1:84541800-84542200	Weak transcription	Brain Cingulate Gyrus	brain
50	chr1:84542000-84542200	Enhancers	Hela-S3	cervix

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