Variant report

Variant	nsv1007641
Chromosome Location	chr4:120884220-121555889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3290)
CpG islands
(count:1588)
Chromatin interactive
region (count:132)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3290 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:121297907-121297919	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:121054162-121054389	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:120987541-120988819	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:120992355-120992705	K562	blood:	n/a	n/a
5	ARID3A	chr4:120971059-120971246	K562	blood:	n/a	n/a
6	ARID3A	chr4:120964875-120964999	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:120992391-120992688	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:120977380-120977726	K562	blood:	n/a	n/a
9	ATF1	chr4:120987815-120988827	K562	blood:	n/a	n/a
10	ATF2	chr4:121252954-121253319	GM12878	blood:	n/a	n/a
11	ATF2	chr4:121387504-121388036	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr4:120925034-120925381	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:120987566-120988000	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr4:121006482-121007083	GM12878	blood:	n/a	n/a
15	ATF2	chr4:121248398-121248789	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr4:120926115-120927036	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr4:121482693-121483215	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr4:120987363-120988630	GM12878	blood:	n/a	n/a
19	ATF2	chr4:120987755-120988596	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr4:121252922-121253430	GM12878	blood:	n/a	n/a
21	ATF2	chr4:120924730-120925731	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr4:121387529-121388007	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr4:120987572-120988624	GM12878	blood:	n/a	n/a
24	ATF3	chr4:120988077-120988606	GM12878	blood:	n/a	n/a
25	ATF3	chr4:121478440-121478964	HCT-116	colon:	n/a	n/a
26	ATF3	chr4:120988181-120988451	K562	blood:	n/a	n/a
27	ATF3	chr4:120988218-120988408	GM12878	blood:	n/a	n/a
28	BACH1	chr4:120994896-120994937	K562	blood:	n/a	n/a
29	BACH1	chr4:121158096-121158364	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr4:120987522-120988157	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr4:120985588-120985694	K562	blood:	n/a	n/a
32	BATF	chr4:121252898-121253394	GM12878	blood:	n/a	n/a
33	BATF	chr4:120929305-120929507	GM12878	blood:	n/a	n/a
34	BCL3	chr4:120930925-120931351	GM12878	blood:	n/a	n/a
35	BCL3	chr4:120987645-120988474	A549	lung:	n/a	n/a
36	BCL3	chr4:120930881-120931214	GM12878	blood:	n/a	n/a
37	BCL3	chr4:121344997-121345240	GM12878	blood:	n/a	n/a
38	BCLAF1	chr4:120987387-120988636	GM12878	blood:	n/a	n/a
39	BCLAF1	chr4:120987338-120988933	GM12878	blood:	n/a	n/a
40	BCLAF1	chr4:120970911-120971326	GM12878	blood:	n/a	n/a
41	BHLHE40	chr4:120987343-120988811	GM12878	blood:	n/a	chr4:120987705-120987721
42	BHLHE40	chr4:120987397-120989312	K562	blood:	n/a	chr4:120987705-120987721
43	BHLHE40	chr4:121036016-121036176	GM12878	blood:	n/a	n/a
44	BHLHE40	chr4:120975224-120975427	GM12878	blood:	n/a	n/a
45	BHLHE40	chr4:120971053-120971327	K562	blood:	n/a	n/a
46	BHLHE40	chr4:120901457-120901478	GM12878	blood:	n/a	n/a
47	BRCA1	chr4:120987783-120988674	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr4:121055133-121055194	GM12878	blood:	n/a	n/a
49	BRCA1	chr4:120925181-120925772	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr4:121252523-121252606	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120971108-120971158	BJ	skin:	n/a
2	chr4:121079963-121080013	AG04449	skin:	fetal
3	chr4:120971108-120971158	BJ	skin:	n/a
4	chr4:121079963-121080013	AG04449	skin:	fetal
5	chr4:121471496-121471546	Hela-S3	cervix:	n/a
6	chr4:121387400-121387450	NB4	blood:	n/a
7	chr4:120984505-120984555	GM12878	blood:	n/a
8	chr4:120898808-120898858	ProgFib	skin:	n/a
9	chr4:120988131-120988181	MCF10A-Er-Src	breast:	n/a
10	chr4:120988131-120988181	SK-N-SH_RA	brain:	n/a
11	chr4:121185048-121185098	SK-N-SH_RA	brain:	n/a
12	chr4:120987944-120987994	K562	blood:	n/a
13	chr4:120987944-120987994	HUVEC	blood vessel:	n/a
14	chr4:120987712-120987762	U87	brain:	n/a
15	chr4:120988587-120988637	HCT-116	colon:	n/a
16	chr4:121471886-121471936	PFSK-1	brain:	n/a
17	chr4:120984505-120984555	HEEpiC	esophagus:	n/a
18	chr4:121471496-121471546	ProgFib	skin:	n/a
19	chr4:120974344-120974394	HMEC	breast:	n/a
20	chr4:121387400-121387450	AG09319	gingival:	n/a
21	chr4:121185048-121185098	LNCaP	prostate:	n/a
22	chr4:120987944-120987994	NH-A	brain:	n/a
23	chr4:120984505-120984555	NHDF-neo	bronchial:	n/a
24	chr4:120987409-120987459	H1-hESC	embryonic stem cell:	embryo
25	chr4:120988131-120988181	SK-N-SH	brain:	n/a
26	chr4:120930379-120930429	Hepatocyte	liver:	n/a
27	chr4:120988417-120988467	A549	lung:	n/a
28	chr4:120988415-120988465	AG04450	lung:	fetal
29	chr4:120987944-120987994	HEEpiC	esophagus:	n/a
30	chr4:121471886-121471936	SKMC	muscle:	n/a
31	chr4:120984505-120984555	HNPCEpiC	eye:	n/a
32	chr4:120988155-120988205	GM12878	blood:	n/a
33	chr4:120987944-120987994	Hepatocyte	liver:	n/a
34	chr4:120988155-120988205	SK-N-MC	brain:	n/a
35	chr4:121471496-121471546	AG10803	skin:	n/a
36	chr4:120988018-120988068	AG10803	skin:	n/a
37	chr4:121471886-121471936	U87	brain:	n/a
38	chr4:120987944-120987994	SK-N-SH_RA	brain:	n/a
39	chr4:121185048-121185098	Jurkat	blood:	n/a
40	chr4:121471288-121471338	BE2_C	brain:	n/a
41	chr4:120984505-120984555	CMK	blood:	n/a
42	chr4:120988207-120988257	RPTEC	kidney:	n/a
43	chr4:120988155-120988205	CMK	blood:	n/a
44	chr4:120988417-120988467	HCF	heart:	n/a
45	chr4:120988587-120988637	GM12878	blood:	n/a
46	chr4:120988155-120988205	IMR90	lung:	fetal
47	chr4:120898808-120898858	NH-A	brain:	n/a
48	chr4:121185048-121185098	GM19239	blood:	n/a
49	chr4:120988018-120988068	HEK293	kidney:	embryo
50	chr4:120988337-120988387	GM12891	blood:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:120973200..120974897-chr4:120987662..120990383,3	K562	blood:
2	chr4:120899347..120901114-chr4:120901609..120903898,2	MCF-7	breast:
3	chr4:120131923..120135922-chr4:120985229..120990455,5	K562	blood:
4	chr4:120964367..120966016-chr4:120972622..120975603,2	K562	blood:
5	chr4:120230931..120233394-chr4:120986011..120987625,2	K562	blood:
6	chr4:120966303..120968314-chr4:120969694..120972264,2	K562	blood:
7	chr4:120550452..120551201-chr4:120970722..120971578,2	K562	blood:
8	chr4:121022913..121025564-chr4:121032231..121034639,2	K562	blood:
9	chr4:120975064..120977095-chr4:120978627..120980325,3	K562	blood:
10	chr4:121010217..121012586-chr4:121015718..121017417,2	MCF-7	breast:
11	chr4:120892542..120895411-chr4:120896318..120898714,2	MCF-7	breast:
12	chr4:120883690..120886191-chr4:120886858..120889545,2	K562	blood:
13	chr4:121185242..121187871-chr4:121188856..121190633,2	K562	blood:
14	chr4:120979559..120981440-chr4:120988106..120989709,2	MCF-7	breast:
15	chr15:77712383..77713035-chr4:120987269..120987962,2	Hela-S3	cervix:
16	chr4:120955421..120958256-chr4:120958733..120960538,2	K562	blood:
17	chr4:121526673..121529460-chr4:121534400..121537130,2	MCF-7	breast:
18	chr4:121078843..121079513-chr4:121208025..121208601,2	MCF-7	breast:
19	chr4:120958158..120959809-chr4:120965003..120967800,2	K562	blood:
20	chr4:120986684..120988546-chr4:121016523..121018736,2	K562	blood:
21	chr4:121189633..121192348-chr4:121208319..121209845,2	K562	blood:
22	chr4:121257279..121258865-chr4:121260585..121262446,2	K562	blood:
23	chr4:120955421..120958256-chr4:120958733..120960538,2	K562	blood:
24	chr4:120898790..120900807-chr4:120905834..120908765,2	K562	blood:
25	chr4:121303352..121305526-chr4:121306861..121309621,3	K562	blood:
26	chr4:121167566..121169623-chr4:121176920..121179543,2	MCF-7	breast:
27	chr4:120958158..120959809-chr4:120965003..120967800,2	K562	blood:
28	chr2:162678536..162680855-chr4:121354549..121356105,2	MCF-7	breast:
29	chr4:120899347..120901114-chr4:120901609..120903898,2	MCF-7	breast:
30	chr4:120987081..120989411-chr4:129732197..129734433,2	K562	blood:
31	chr4:121228431..121230743-chr4:121233140..121235922,2	K562	blood:
32	chr14:34419791..34420629-chr4:120987839..120988645,2	Hela-S3	cervix:
33	chr4:121309932..121311519-chr4:121313046..121315204,2	K562	blood:
34	chr4:121130697..121133786-chr4:121135139..121137341,3	K562	blood:
35	chr4:121015466..121017265-chr4:121020496..121022464,2	K562	blood:
36	chr4:120990955..120993835-chr4:120994776..120997866,3	K562	blood:
37	chr4:120987142..120989287-chr4:121074919..121077571,2	K562	blood:
38	chr4:121396849..121398573-chr4:121700140..121702182,2	K562	blood:
39	chr4:120692868..120695733-chr4:120948622..120950761,2	K562	blood:
40	chr4:120931283..120933611-chr4:120937604..120939144,2	MCF-7	breast:
41	chr4:120549969..120550595-chr4:120970742..120971442,3	MCF-7	breast:
42	chr4:120931283..120933611-chr4:120937604..120939144,2	MCF-7	breast:
43	chr4:121063487..121066067-chr4:121068181..121070663,2	K562	blood:
44	chr4:120973859..120975620-chr4:120985435..120987169,2	K562	blood:
45	chr4:120548059..120548579-chr4:120971160..120971673,2	K562	blood:
46	chr4:121077048..121077919-chr4:122017135..122018169,3	MCF-7	breast:
47	chr1:89990056..89990615-chr4:120987741..120988260,2	HCT-116	colon:
48	chr4:121526673..121529460-chr4:121534400..121537130,2	MCF-7	breast:
49	chr1:222885721..222886410-chr4:120987809..120988640,2	HCT-116	colon:
50	chr4:120988596..120990170-chr4:121080844..121082631,2	K562	blood:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC110373.1-6	chr4:121249688-121249741	ENSG00000250938.1
2	lnc-AC110373.1-6	chr4:121256793-121256886	ENSG00000250938.1
3	lnc-MAD2L1-3	chr4:120941240-120941365	ucscGeneNc_uc003idk_1
4	lnc-AC110373.1-6	chr4:120988113-120988156	ENSG00000250938.1
5	lnc-AC110373.1-6	chr4:121004440-121006734	ENSG00000250938.1
6	lnc-AC110373.1-6	chr4:121337705-121337921	ENSG00000250938.1
7	lnc-AC110373.1-6	chr4:120988015-120991623	NONHSAT098115
8	lnc-AC110373.1-6	chr4:121249688-121249741	ENSG00000250938.1
9	lnc-AC110373.1-6	chr4:121314655-121314709	ENSG00000250938.1
10	lnc-AC110373.1-6	chr4:121004440-121004486	ENSG00000250938.1
11	lnc-AC110373.1-6	chr4:121071698-121071776	ENSG00000250938.1
12	lnc-AC110373.1-12	chr4:121103326-121103369	NONHSAT098121
13	lnc-AC110373.1-6	chr4:120988125-120988156	ENSG00000250938.1
14	lnc-AC110373.1-12	chr4:121102663-121102842	NONHSAT098121
15	lnc-AC110373.1-6	chr4:120988666-120988756	ENSG00000250938.1
16	lnc-AC110373.1-6	chr4:121314655-121314877	ENSG00000250938.1
17	lnc-AC110373.1-5	chr4:120884943-120885376	ENSG00000250392.1
18	lnc-AC110373.1-5	chr4:120884943-120885053	NONHSAT098110
19	lnc-AC110373.1-5	chr4:120885151-120885352	NONHSAT098110
20	lnc-MAD2L1-3	chr4:120943327-120943495	ucscGeneNc_uc003idk_1
21	lnc-MAD2L1-3	chr4:120945055-120945118	ucscGeneNc_uc003idk_1
22	lnc-AC110373.1-6	chr4:121071698-121071776	ENSG00000250938.1
23	lnc-AC110373.1-6	chr4:121256793-121256886	ENSG00000250938.1
24	lnc-AC110373.1-11	chr4:120923406-120924078	NONHSAT098112
25	lnc-AC110373.1-6	chr4:121004440-121004486	ENSG00000250938.1
26	lnc-MAD2L1-1	chr4:120956188-120956353	ENSG00000253825
27	lnc-AC110373.1-6	chr4:121004440-121004486	ENSG00000250938.1
28	lnc-AC110373.1-5	chr4:120884943-120885385	NONHSAT098107
29	lnc-MAD2L1-3	chr4:120941955-120941997	ucscGeneNc_uc003idk_1
30	lnc-MAD2L1-2	chr4:121012201-121013437	NONHSAT098120
31	lnc-MAD2L1-3	chr4:120939709-120939839	ucscGeneNc_uc003idk_1
32	lnc-AC110373.1-13	chr4:121263212-121263784	NONHSAT098123
33	lnc-MAD2L1-1	chr4:120961463-120961770	ENSG00000253825
34	lnc-AC110373.1-6	chr4:120988113-120988156	ENSG00000250938.1
35	lnc-AC110373.1-5	chr4:120884943-120885448	ENSG00000250392.2
36	lnc-AC110373.1-13	chr4:121263211-121263802	NONHSAT098122
37	lnc-AC110373.1-6	chr4:121086645-121087047	ENSG00000250938.1

No data

Variant related genes	Relation type
LTV1P1	TF binding region
ENSG00000253825	TF binding region
ENSG00000250938	TF binding region
ENSG00000225665	TF binding region
MAD2L1	TF binding region
ENSG00000249409	TF binding region
LTV1P1	CpG island
ENSG00000253825	CpG island
ENSG00000250938	CpG island
ENSG00000225665	CpG island
MAD2L1	CpG island
ENSG00000249409	CpG island
ENSG00000120910	chromatin interactions
ENSG00000164109	chromatin interactions
ENSG00000250938	chromatin interactions
ENSG00000178636	chromatin interactions
ENSG00000173517	chromatin interactions
ENSG00000140382	chromatin interactions
ENSG00000186063	chromatin interactions
ENSG00000164096	chromatin interactions
ENSG00000141510	chromatin interactions
ENSG00000162819	chromatin interactions
ENSG00000138735	chromatin interactions
ENSG00000141499	chromatin interactions
ENSG00000077684	chromatin interactions
ENSG00000269893	chromatin interactions
ENSG00000163444	chromatin interactions
ENSG00000197147	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000145390	chromatin interactions
ENSG00000129521	chromatin interactions
GALNT1	miRNA target sites

Extended variants
information (count: 15077 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:15077 , 50 per page) page: 1 2 3 4 5 6 7 ... 302

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370403065	chr4:120884251-120884252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551855989	chr4:120884358-120884359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145818412	chr4:120884370-120884371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554414799	chr4:120884377-120884378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534624701	chr4:120884479-120884480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112043076	chr4:120884485-120884486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192195531	chr4:120884513-120884514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537386686	chr4:120884539-120884540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34408925	chr4:120884573-120884574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557587494	chr4:120884597-120884598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577518119	chr4:120884654-120884655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574406293	chr4:120884664-120884665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539901518	chr4:120884682-120884683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184972099	chr4:120884701-120884702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1558763	chr4:120884728-120884729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs1974704	chr4:120884849-120884850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371799989	chr4:120884906-120884907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542184584	chr4:120884936-120884937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561972754	chr4:120884937-120884938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574666088	chr4:120884952-120884953	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs189707699	chr4:120884965-120884966	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs563093378	chr4:120884998-120884999	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs562920942	chr4:120885002-120885003	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs532181143	chr4:120885095-120885096	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs545456664	chr4:120885099-120885100	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs181161080	chr4:120885117-120885118	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs144159045	chr4:120885136-120885137	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs184500782	chr4:120885174-120885175	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs62321762	chr4:120885211-120885212	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs188748709	chr4:120885240-120885241	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs531189419	chr4:120885249-120885250	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs551305964	chr4:120885250-120885251	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs17008198	chr4:120885257-120885258	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs17008199	chr4:120885264-120885265	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs140382793	chr4:120885266-120885267	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs113986436	chr4:120885284-120885285	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs79701105	chr4:120885302-120885303	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs146614481	chr4:120885311-120885312	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs187034524	chr4:120885330-120885331	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs535615433	chr4:120885356-120885357	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs548823687	chr4:120885371-120885372	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs555728781	chr4:120885389-120885390	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs74486654	chr4:120885439-120885440	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs149186793	chr4:120885458-120885459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116576217	chr4:120885462-120885463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143413242	chr4:120885622-120885623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545580286	chr4:120885647-120885648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559327545	chr4:120885700-120885701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148375750	chr4:120885736-120885737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73842779	chr4:120885753-120885754	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Myelodysplastic syndrome	18508791	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2109 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120883400-120903400	Weak transcription	Left Ventricle	heart
2	chr4:120891600-120893600	Enhancers	Fetal Kidney	kidney
3	chr4:120892600-120893600	Enhancers	Rectal Smooth Muscle	rectum
4	chr4:120892800-120893800	Enhancers	Colon Smooth Muscle	Colon
5	chr4:120893600-120897000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr4:120893600-120898200	Weak transcription	Fetal Kidney	kidney
7	chr4:120893800-120897600	Weak transcription	Colon Smooth Muscle	Colon
8	chr4:120897000-120900600	Enhancers	Rectal Smooth Muscle	rectum
9	chr4:120897600-120898800	Enhancers	H9 Cell Line	embryonic stem cell
10	chr4:120897600-120902000	Enhancers	Colon Smooth Muscle	Colon
11	chr4:120897800-120898600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr4:120898000-120898200	Enhancers	Stomach Smooth Muscle	stomach
13	chr4:120898000-120898800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr4:120898000-120898800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr4:120898200-120898600	Flanking Active TSS	Stomach Smooth Muscle	stomach
16	chr4:120898200-120898800	Enhancers	Fetal Kidney	kidney
17	chr4:120898200-120899000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr4:120898200-120899000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr4:120898200-120899400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr4:120898400-120898800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr4:120898400-120898800	Enhancers	Fetal Stomach	stomach
22	chr4:120898400-120899000	Enhancers	Fetal Muscle Leg	muscle
23	chr4:120898400-120899000	Enhancers	Right Atrium	heart
24	chr4:120898600-120899200	Enhancers	Stomach Smooth Muscle	stomach
25	chr4:120898600-120905800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr4:120898800-120901600	Weak transcription	Fetal Kidney	kidney
27	chr4:120900600-120901600	Weak transcription	Rectal Smooth Muscle	rectum
28	chr4:120901400-120901800	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr4:120901600-120901800	Enhancers	Fetal Lung	lung
30	chr4:120901600-120902600	Enhancers	Fetal Kidney	kidney
31	chr4:120901600-120902800	Enhancers	Rectal Smooth Muscle	rectum
32	chr4:120901800-120902400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:120901800-120902600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:120901800-120902600	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr4:120902600-120903800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr4:120902800-120905800	Weak transcription	Rectal Smooth Muscle	rectum
37	chr4:120903800-120904400	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr4:120903800-120906200	Enhancers	Fetal Lung	lung
39	chr4:120904400-120904800	Enhancers	Aorta	Aorta
40	chr4:120904800-120905600	Weak transcription	Aorta	Aorta
41	chr4:120905600-120906000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:120905600-120906000	Enhancers	Aorta	Aorta
43	chr4:120905600-120906200	Enhancers	Fetal Stomach	stomach
44	chr4:120905600-120906400	Enhancers	H9 Cell Line	embryonic stem cell
45	chr4:120905600-120906400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr4:120905800-120906200	Enhancers	Fetal Muscle Leg	muscle
47	chr4:120905800-120906200	Enhancers	Rectal Smooth Muscle	rectum
48	chr4:120905800-120906400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr4:120905800-120906400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr4:120905800-120906400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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