Variant report

Variant	nsv1033096
Chromosome Location	chr7:32965040-33039206
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1706)
CpG islands
(count:1588)
Chromatin interactive
region (count:96)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1706 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:32982676-32983138	K562	blood:	n/a	n/a
2	ARID3A	chr7:32997052-32997221	K562	blood:	n/a	n/a
3	ARID3A	chr7:32981602-32981742	K562	blood:	n/a	n/a
4	ARID3A	chr7:32982763-32983006	HepG2	liver:	n/a	n/a
5	ATF3	chr7:33018936-33019182	K562	blood:	n/a	n/a
6	BACH1	chr7:32996706-32997563	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:32982834-32982986	K562	blood:	n/a	n/a
8	BACH1	chr7:32982686-32983091	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr7:33004344-33004651	GM12878	blood:	n/a	n/a
10	BATF	chr7:33013068-33013309	GM12878	blood:	n/a	n/a
11	BATF	chr7:33013146-33013310	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:32980864-32981158	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr7:33004460-33004702	GM12878	blood:	n/a	n/a
14	BCL3	chr7:32996626-32998170	A549	lung:	n/a	chr7:32997495-32997504 chr7:32996820-32996829 chr7:32997559-32997568 chr7:32997799-32997808
15	BCL3	chr7:32977454-32977703	GM12878	blood:	n/a	n/a
16	BCLAF1	chr7:32981886-32982450	GM12878	blood:	n/a	chr7:32982211-32982224
17	BCLAF1	chr7:32982522-32983033	GM12878	blood:	n/a	chr7:32982839-32982852
18	BHLHE40	chr7:32997429-32997779	HepG2	liver:	n/a	chr7:32997584-32997597 chr7:32997586-32997595 chr7:32997587-32997596 chr7:32997586-32997595
19	BHLHE40	chr7:32982559-32983096	HepG2	liver:	n/a	chr7:32982826-32982842 chr7:32982833-32982849 chr7:32982839-32982855
20	BHLHE40	chr7:32996795-32997953	HepG2	liver:	n/a	chr7:32996925-32996941 chr7:32997584-32997597 chr7:32997586-32997595 chr7:32997587-32997596 chr7:32997586-32997595
21	BHLHE40	chr7:32982658-32982892	GM12878	blood:	n/a	chr7:32982826-32982842 chr7:32982833-32982849 chr7:32982839-32982855
22	BHLHE40	chr7:32997325-32997701	HepG2	liver:	n/a	chr7:32997584-32997597 chr7:32997586-32997595 chr7:32997587-32997596 chr7:32997586-32997595
23	BHLHE40	chr7:32996696-32997897	K562	blood:	n/a	chr7:32996925-32996941 chr7:32997584-32997597 chr7:32997586-32997595 chr7:32997587-32997596 chr7:32997586-32997595
24	BHLHE40	chr7:32977507-32977585	K562	blood:	n/a	n/a
25	BHLHE40	chr7:33027956-33028178	HepG2	liver:	n/a	n/a
26	BHLHE40	chr7:32981666-32982984	K562	blood:	n/a	chr7:32982826-32982842 chr7:32982833-32982849 chr7:32982839-32982855 chr7:32982456-32982472
27	BRCA1	chr7:32982600-32982752	HepG2	liver:	n/a	n/a
28	BRCA1	chr7:32982691-32983015	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr7:32981556-32982203	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr7:32996754-32997156	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr7:32997702-32997902	HepG2	liver:	n/a	n/a
32	CBX3	chr7:32997129-32997857	K562	blood:	n/a	n/a
33	CBX3	chr7:32983166-32983603	K562	blood:	n/a	n/a
34	CBX3	chr7:32981493-32983706	K562	blood:	n/a	n/a
35	CBX3	chr7:32987803-32988155	K562	blood:	n/a	n/a
36	CBX3	chr7:32987541-32988294	K562	blood:	n/a	n/a
37	CBX3	chr7:33037995-33038493	K562	blood:	n/a	n/a
38	CBX3	chr7:32996708-32997090	K562	blood:	n/a	n/a
39	CCNT2	chr7:32996720-32998028	K562	blood:	n/a	chr7:32997642-32997651
40	CCNT2	chr7:32981587-32983020	K562	blood:	n/a	n/a
41	CEBPB	chr7:32997272-32998016	MCF-7	breast:	n/a	chr7:32997730-32997741 chr7:32997732-32997741 chr7:32997730-32997743
42	CEBPB	chr7:33032846-33033019	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr7:32997534-32997926	A549	lung:	n/a	chr7:32997730-32997741 chr7:32997732-32997741 chr7:32997730-32997743
44	CEBPB	chr7:33018898-33019225	IMR90	lung:	n/a	chr7:33019062-33019075
45	CEBPB	chr7:32997487-32997910	H1-hESC	embryonic stem cell:	n/a	chr7:32997730-32997741 chr7:32997732-32997741 chr7:32997730-32997743
46	CEBPB	chr7:32987966-32988135	HepG2	liver:	n/a	chr7:32988063-32988074
47	CEBPB	chr7:32984252-32984452	A549	lung:	n/a	n/a
48	CEBPB	chr7:32982848-32983107	A549	lung:	n/a	n/a
49	CEBPB	chr7:33006795-33007049	IMR90	lung:	n/a	chr7:33006947-33006958 chr7:33006917-33006928
50	CEBPB	chr7:32982593-32983140	Hela-S3	cervix:	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	chr7:32983012-32983062	T-47D	breast:	n/a
2	chr7:32984998-32985048	HRE	kidney:	n/a
3	chr7:32983012-32983062	T-47D	breast:	n/a
4	chr7:32984998-32985048	HRE	kidney:	n/a
5	chr7:32994013-32994063	AG04449	skin:	fetal
6	chr7:32983012-32983062	HRPEpiC	eye:	n/a
7	chr7:32994013-32994063	HEEpiC	esophagus:	n/a
8	chr7:32996873-32996923	SK-N-MC	brain:	n/a
9	chr7:32997190-32997240	Jurkat	blood:	n/a
10	chr7:32996829-32996879	AG04450	lung:	fetal
11	chr7:32982957-32983007	Jurkat	blood:	n/a
12	chr7:32981826-32981876	HIPEpiC	eye:	n/a
13	chr7:32983364-32983414	HIPEpiC	eye:	n/a
14	chr7:32979849-32979899	ECC-1	luminal epithelium:	n/a
15	chr7:32997659-32997709	HEK293	kidney:	embryo
16	chr7:32995514-32995564	NHBE	bronchial:	n/a
17	chr7:33001327-33001377	Hela-S3	cervix:	n/a
18	chr7:32982519-32982569	HL-60	blood:	n/a
19	chr7:32997190-32997240	ProgFib	skin:	n/a
20	chr7:32996733-32996783	MCF-7	breast:	n/a
21	chr7:32996733-32996783	PrEC	prostate:	n/a
22	chr7:32996869-32996919	AG04449	skin:	fetal
23	chr7:32997111-32997161	HCT-116	colon:	n/a
24	chr7:32995514-32995564	HMEC	breast:	n/a
25	chr7:32996145-32996195	K562	blood:	n/a
26	chr7:32997590-32997640	PrEC	prostate:	n/a
27	chr7:32996733-32996783	HRPEpiC	eye:	n/a
28	chr7:32984998-32985048	HEEpiC	esophagus:	n/a
29	chr7:32994013-32994063	GM19239	blood:	n/a
30	chr7:32996829-32996879	GM12878	blood:	n/a
31	chr7:32996873-32996923	GM19239	blood:	n/a
32	chr7:32997094-32997144	T-47D	breast:	n/a
33	chr7:32996816-32996866	LNCaP	prostate:	n/a
34	chr7:32996816-32996866	K562	blood:	n/a
35	chr7:32996873-32996923	AG10803	skin:	n/a
36	chr7:32977142-32977192	ECC-1	luminal epithelium:	n/a
37	chr7:32996873-32996923	AoSMC	blood vessel:	n/a
38	chr7:32996869-32996919	SK-N-SH_RA	brain:	n/a
39	chr7:32996829-32996879	ProgFib	skin:	n/a
40	chr7:32996881-32996931	Caco-2	colon:	n/a
41	chr7:33001327-33001377	GM19239	blood:	n/a
42	chr7:32996733-32996783	NHDF-neo	bronchial:	n/a
43	chr7:33001327-33001377	HRCEpiC	kidney:	n/a
44	chr7:33001327-33001377	PFSK-1	brain:	n/a
45	chr7:32983012-32983062	SK-N-SH	brain:	n/a
46	chr7:32982519-32982569	SAEC	small airway:	n/a
47	chr7:33001327-33001377	GM12878	blood:	n/a
48	chr7:32979849-32979899	HCPEpiC	choroid plexus:	n/a
49	chr7:32982580-32982630	BJ	skin:	n/a
50	chr7:32982957-32983007	HCT-116	colon:	n/a

(count:96 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:32928752..32933141-chr7:32994641..32998863,8	K562	blood:
2	chr7:32929776..32933176-chr7:32979221..32984586,9	K562	blood:
3	chr7:32804013..32805676-chr7:32980838..32982358,2	K562	blood:
4	chr7:32989735..32994052-chr7:32995992..32998490,3	MCF-7	breast:
5	chr7:32980440..32983723-chr7:32985138..32989681,5	K562	blood:
6	chr7:32981269..32984259-chr7:33078718..33080736,2	K562	blood:
7	chr7:32960196..32964264-chr7:32965375..32969659,5	K562	blood:
8	chr15:90808808..90809337-chr7:32982351..32982935,2	Hela-S3	cervix:
9	chr7:32996658..32997591-chrX:23685231..23685895,2	Hela-S3	cervix:
10	chr6:97371814..97372480-chr7:32997365..32997998,2	Hela-S3	cervix:
11	chr7:32961822..32963720-chr7:32970947..32973878,2	K562	blood:
12	chr7:32982709..32984575-chr7:32997023..32999117,2	K562	blood:
13	chr7:32997056..32997696-chrX:117479336..117480081,2	Hela-S3	cervix:
14	chr17:4870652..4871308-chr7:32982116..32983060,2	Hela-S3	cervix:
15	chr7:32975404..32979316-chr7:32980628..32983456,5	MCF-7	breast:
16	chr17:7387236..7388162-chr7:32982349..32982980,2	NB4	blood:
17	chr6:159270909..159271734-chr7:32997213..32997774,2	Hela-S3	cervix:
18	chr7:32996766..32998569-chr7:33027965..33030293,2	K562	blood:
19	chr7:32990080..32992155-chr7:32993767..32995305,2	K562	blood:
20	chr7:32968245..32972427-chr7:32974851..32978457,6	K562	blood:
21	chr7:32981289..32983857-chr7:33147743..33149971,3	K562	blood:
22	chr7:32988824..32991717-chr7:32995412..32996950,2	MCF-7	breast:
23	chr7:32929839..32934078-chr7:32995806..32999171,10	MCF-7	breast:
24	chr7:32981007..32984575-chr7:32996149..32999305,3	K562	blood:
25	chr1:153599062..153600033-chr7:32982293..32983190,2	Hela-S3	cervix:
26	chr7:32961739..32963720-chr7:32969599..32973878,3	K562	blood:
27	chr7:32968245..32970619-chr7:32975458..32976987,2	K562	blood:
28	chr7:32947347..32949492-chr7:32969645..32971678,2	K562	blood:
29	chr7:32979720..32982452-chr7:32995227..32996993,2	MCF-7	breast:
30	chr1:45986841..45987635-chr7:32997004..32997876,2	Hela-S3	cervix:
31	chr7:32982489..32988008-chr7:32995538..32999914,10	MCF-7	breast:
32	chr7:32964311..32966953-chr7:32967722..32970087,2	K562	blood:
33	chr7:32929776..32933604-chr7:32979221..32983668,8	K562	blood:
34	chr7:32981286..32984219-chr7:32986840..32989077,2	MCF-7	breast:
35	chr7:32996678..32998583-chr7:33000534..33003060,3	MCF-7	breast:
36	chr7:32964311..32967262-chr7:32967722..32972400,5	K562	blood:
37	chr20:2633017..2633602-chr7:32996418..32997034,2	HCT-116	colon:
38	chr10:134145019..134145665-chr7:32996612..32997131,2	Hela-S3	cervix:
39	chr7:32981117..32983868-chr7:33100044..33104533,5	K562	blood:
40	chr7:32997687..32999563-chr7:33147479..33150290,2	K562	blood:
41	chr1:205600552..205601275-chr7:32996850..32997837,2	Hela-S3	cervix:
42	chr7:32989735..32994052-chr7:32995992..32998490,3	MCF-7	breast:
43	chr7:32974679..32979043-chr7:32979887..32983417,5	K562	blood:
44	chr7:32981007..32984575-chr7:32996149..32999305,3	K562	blood:
45	chr7:32957542..32959142-chr7:32967842..32969959,2	MCF-7	breast:
46	chr7:32981193..32983815-chr7:32991462..32995166,3	MCF-7	breast:
47	chr7:32995362..32998530-chr7:33097317..33102837,7	MCF-7	breast:
48	chr11:64684613..64685147-chr7:32997032..32997702,2	Hela-S3	cervix:
49	chr7:32917579..32920206-chr7:32981301..32983745,3	K562	blood:
50	chr7:32930067..32932198-chr7:32982416..32984052,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KBTBD2-2	chr7:32969690-32969720	NONHSAT120007
2	lnc-KBTBD2-2	chr7:32981932-32982159	NONHSAT120007
3	lnc-KBTBD2-2	chr7:32982482-32982575	NONHSAT120004
4	lnc-KBTBD2-2	chr7:32969690-32969720	NONHSAT120004
5	lnc-KBTBD2-2	chr7:32982482-32982838	NONHSAT147543
6	lnc-KBTBD2-2	chr7:32973433-32973508	NONHSAT147543
7	lnc-KBTBD2-2	chr7:32969690-32969720	NONHSAT120006
8	lnc-KBTBD2-2	chr7:32982482-32982774	NONHSAT120006

No data

Variant related genes	Relation type
FKBP9	TF binding region
ENSG00000224573	TF binding region
RP9P	TF binding region
FKBP9	CpG island
ENSG00000224573	CpG island
RP9P	CpG island
ENSG00000205763	chromatin interactions
ENSG00000123131	chromatin interactions
ENSG00000158711	chromatin interactions
ENSG00000130489	chromatin interactions
ENSG00000131725	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000068971	chromatin interactions
ENSG00000101361	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000122642	chromatin interactions
ENSG00000221062	chromatin interactions
ENSG00000181222	chromatin interactions
ENSG00000115073	chromatin interactions
ENSG00000170852	chromatin interactions
ENSG00000256632	chromatin interactions
ENSG00000122643	chromatin interactions
ENSG00000091640	chromatin interactions
ENSG00000165689	chromatin interactions
ENSG00000167515	chromatin interactions
ENSG00000166133	chromatin interactions
ENSG00000224573	chromatin interactions
ENSG00000174282	chromatin interactions
ENSG00000171224	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000137449	chromatin interactions
ENSG00000222326	chromatin interactions
ENSG00000165752	chromatin interactions
ENSG00000189171	chromatin interactions
ENSG00000236756	chromatin interactions
ENSG00000131759	chromatin interactions
ENSG00000148814	chromatin interactions
ENSG00000110046	chromatin interactions
ENSG00000164610	chromatin interactions
ENSG00000163660	chromatin interactions
ENSG00000262429	chromatin interactions
ENSG00000182768	chromatin interactions
ENSG00000229054	chromatin interactions

Extended variants
information (count: 3003 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3003 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12701264	chr7:32965040-32965041	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189678843	chr7:32965066-32965067	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574122431	chr7:32965076-32965077	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs180971871	chr7:32965088-32965089	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553369706	chr7:32965103-32965104	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs578104875	chr7:32965110-32965111	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs541834617	chr7:32965155-32965156	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs563773255	chr7:32965165-32965166	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530936948	chr7:32965197-32965198	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575813804	chr7:32965205-32965206	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552722144	chr7:32965230-32965231	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564563209	chr7:32965231-32965232	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561154180	chr7:32965245-32965246	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371697735	chr7:32965312-32965313	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528256335	chr7:32965338-32965339	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369073844	chr7:32965339-32965340	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs386711929	chr7:32965494-32965495	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546899716	chr7:32965496-32965497	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11981889	chr7:32965505-32965506	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs532019126	chr7:32965568-32965569	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185383386	chr7:32965572-32965573	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568466931	chr7:32965632-32965633	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536367963	chr7:32965653-32965654	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139218122	chr7:32965772-32965773	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547962615	chr7:32965797-32965798	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191503748	chr7:32965837-32965838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11978359	chr7:32965844-32965845	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs147519656	chr7:32965897-32965898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs56722236	chr7:32965957-32965958	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs183295320	chr7:32965958-32965959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557415882	chr7:32965964-32965965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7784688	chr7:32966042-32966043	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs376518962	chr7:32966048-32966049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150507122	chr7:32966049-32966050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139464618	chr7:32966086-32966087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111594178	chr7:32966122-32966123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540042213	chr7:32966130-32966131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372863886	chr7:32966184-32966185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs199922332	chr7:32966262-32966263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71856797	chr7:32966263-32966264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs60154883	chr7:32966276-32966277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188696394	chr7:32966384-32966385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191796896	chr7:32966397-32966398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541884872	chr7:32966402-32966403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544071929	chr7:32966439-32966440	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555151739	chr7:32966650-32966651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562158444	chr7:32966655-32966656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183347716	chr7:32966680-32966681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs80124039	chr7:32966688-32966689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566435766	chr7:32966704-32966705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Williams-beuren syndrome	18553513	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	19115005	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:2132 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:32945200-32971200	Weak transcription	Fetal Heart	heart
2	chr7:32945600-32969000	Weak transcription	Colonic Mucosa	Colon
3	chr7:32947600-32981200	Weak transcription	Stomach Mucosa	stomach
4	chr7:32953600-32973600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr7:32954200-32965200	Strong transcription	HSMM	muscle
6	chr7:32955000-32976000	Weak transcription	Right Ventricle	heart
7	chr7:32955000-32981000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:32956400-32966400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:32956400-32966400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr7:32956400-32967600	Weak transcription	Brain Hippocampus Middle	brain
11	chr7:32956600-32981000	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr7:32956600-32981000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr7:32956800-32967600	Weak transcription	Aorta	Aorta
14	chr7:32956800-32967600	Weak transcription	Brain Angular Gyrus	brain
15	chr7:32956800-32967600	Weak transcription	Gastric	stomach
16	chr7:32956800-32967600	Weak transcription	Lung	lung
17	chr7:32956800-32967600	Weak transcription	Pancreas	Pancrea
18	chr7:32956800-32967600	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr7:32956800-32967600	Weak transcription	Spleen	Spleen
20	chr7:32956800-32967800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr7:32956800-32969000	Weak transcription	Esophagus	oesophagus
22	chr7:32957800-32967600	Weak transcription	NHLF	lung
23	chr7:32958200-32967400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr7:32958400-32966200	Weak transcription	Colon Smooth Muscle	Colon
25	chr7:32958400-32976400	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr7:32958600-32966400	Weak transcription	Rectal Smooth Muscle	rectum
27	chr7:32958600-32966600	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr7:32958600-32967800	Weak transcription	Primary B cells from cord blood	blood
29	chr7:32958600-32976200	Weak transcription	Psoas Muscle	Psoas
30	chr7:32958800-32966600	Weak transcription	Fetal Lung	lung
31	chr7:32958800-32978600	Weak transcription	Primary hematopoietic stem cells	blood
32	chr7:32959200-32967800	Weak transcription	Fetal Brain Male	brain
33	chr7:32960000-32967400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr7:32960200-32967600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr7:32960200-32967600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr7:32960200-32967800	Weak transcription	Liver	Liver
37	chr7:32960400-32967800	Weak transcription	HSMMtube	muscle
38	chr7:32960400-32970800	Weak transcription	Hela-S3	cervix
39	chr7:32960400-32972800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr7:32960600-32972000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr7:32960800-32965600	Strong transcription	Muscle Satellite Cultured Cells	--
42	chr7:32961000-32966400	Weak transcription	Left Ventricle	heart
43	chr7:32961000-32966600	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr7:32961000-32968800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr7:32961400-32967600	Weak transcription	Brain Substantia Nigra	brain
46	chr7:32961600-32966600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr7:32961600-32971800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr7:32961600-32973600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr7:32961600-32974600	Strong transcription	Fetal Stomach	stomach
50	chr7:32961800-32966400	Weak transcription	Brain Inferior Temporal Lobe	brain

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