Variant report

Variant	nsv532133
Chromosome Location	chr5:36834932-36906436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1792)
CpG islands
(count:793)
Chromatin interactive
region (count:123)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1792 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:36877448-36877506	K562	blood:	n/a	n/a
2	ARID3A	chr5:36862561-36862602	K562	blood:	n/a	n/a
3	ARID3A	chr5:36876734-36876922	K562	blood:	n/a	chr5:36876821-36876829
4	ARID3A	chr5:36875117-36876260	K562	blood:	n/a	n/a
5	ARID3A	chr5:36870521-36870915	K562	blood:	n/a	n/a
6	ARID3A	chr5:36875963-36876262	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:36878258-36879060	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:36874538-36874821	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:36880541-36881243	K562	blood:	n/a	n/a
10	ARID3A	chr5:36881558-36882796	K562	blood:	n/a	n/a
11	ARID3A	chr5:36876653-36877035	HepG2	liver:	n/a	chr5:36876821-36876829
12	ARID3A	chr5:36870528-36870945	HepG2	liver:	n/a	n/a
13	ARID3A	chr5:36878225-36879394	K562	blood:	n/a	n/a
14	ARID3A	chr5:36873646-36874913	K562	blood:	n/a	n/a
15	ARID3A	chr5:36873187-36873243	K562	blood:	n/a	n/a
16	ATF1	chr5:36897552-36897595	K562	blood:	n/a	n/a
17	ATF1	chr5:36840705-36840908	K562	blood:	n/a	n/a
18	ATF1	chr5:36870575-36870891	K562	blood:	n/a	n/a
19	ATF1	chr5:36876694-36876994	K562	blood:	n/a	n/a
20	ATF2	chr5:36877473-36877865	GM12878	blood:	n/a	n/a
21	ATF2	chr5:36875717-36876321	GM12878	blood:	n/a	n/a
22	ATF2	chr5:36876526-36877013	GM12878	blood:	n/a	n/a
23	ATF3	chr5:36880793-36881181	K562	blood:	n/a	n/a
24	ATF3	chr5:36876567-36876889	K562	blood:	n/a	n/a
25	BACH1	chr5:36875421-36875622	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr5:36887049-36887187	K562	blood:	n/a	n/a
27	BACH1	chr5:36875864-36876905	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr5:36877670-36877747	K562	blood:	n/a	n/a
29	BATF	chr5:36870485-36870767	GM12878	blood:	n/a	n/a
30	BATF	chr5:36870519-36870816	GM12878	blood:	n/a	n/a
31	BATF	chr5:36876625-36876916	GM12878	blood:	n/a	n/a
32	BCL3	chr5:36876030-36876468	A549	lung:	n/a	n/a
33	BCL3	chr5:36876558-36877081	A549	lung:	n/a	chr5:36877022-36877035 chr5:36876857-36876866
34	BCL3	chr5:36876631-36876914	GM12878	blood:	n/a	chr5:36876857-36876866
35	BCLAF1	chr5:36877288-36878128	GM12878	blood:	n/a	chr5:36877500-36877513
36	BCLAF1	chr5:36870475-36870863	GM12878	blood:	n/a	n/a
37	BCLAF1	chr5:36875865-36877235	GM12878	blood:	n/a	chr5:36877022-36877035 chr5:36876857-36876866
38	BCLAF1	chr5:36876485-36877585	K562	blood:	n/a	chr5:36877500-36877513 chr5:36877022-36877035 chr5:36876857-36876866
39	BCLAF1	chr5:36876597-36877103	K562	blood:	n/a	chr5:36877022-36877035 chr5:36876857-36876866
40	BCLAF1	chr5:36875847-36877061	GM12878	blood:	n/a	chr5:36877022-36877035 chr5:36876857-36876866
41	BHLHE40	chr5:36887755-36887957	GM12878	blood:	n/a	n/a
42	BHLHE40	chr5:36876613-36877355	HepG2	liver:	n/a	n/a
43	BHLHE40	chr5:36876610-36878052	GM12878	blood:	n/a	n/a
44	BHLHE40	chr5:36875938-36877752	K562	blood:	n/a	n/a
45	BHLHE40	chr5:36882261-36882800	GM12878	blood:	n/a	n/a
46	BHLHE40	chr5:36873526-36873582	K562	blood:	n/a	n/a
47	BHLHE40	chr5:36854626-36854934	HepG2	liver:	n/a	n/a
48	BHLHE40	chr5:36878854-36879075	K562	blood:	n/a	n/a
49	BHLHE40	chr5:36875674-36876308	GM12878	blood:	n/a	n/a
50	BRCA1	chr5:36873964-36874028	Hela-S3	cervix:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:36876954-36877004	Caco-2	colon:	n/a
2	chr5:36876667-36876717	NB4	blood:	n/a
3	chr5:36875537-36875587	SK-N-MC	brain:	n/a
4	chr5:36875537-36875587	GM12892	blood:	n/a
5	chr5:36877216-36877266	BJ	skin:	n/a
6	chr5:36877216-36877266	HNPCEpiC	eye:	n/a
7	chr5:36876111-36876161	MCF-7	breast:	n/a
8	chr5:36882196-36882246	H1-hESC	embryonic stem cell:	embryo
9	chr5:36876537-36876587	CMK	blood:	n/a
10	chr5:36876680-36876730	SAEC	small airway:	n/a
11	chr5:36875537-36875587	HCM	heart:	n/a
12	chr5:36877626-36877676	AoSMC	blood vessel:	n/a
13	chr5:36875434-36875484	SAEC	small airway:	n/a
14	chr5:36876954-36877004	HRE	kidney:	n/a
15	chr5:36876680-36876730	ovcar-3	ovarian:	n/a
16	chr5:36876680-36876730	HEEpiC	esophagus:	n/a
17	chr5:36876114-36876164	ProgFib	skin:	n/a
18	chr5:36876833-36876883	HAEpiC	amniotic membrane:	n/a
19	chr5:36876537-36876587	BE2_C	brain:	n/a
20	chr5:36876114-36876164	HPAEpiC	pulmonary alveolar:	n/a
21	chr5:36876680-36876730	HepG2	liver:	n/a
22	chr5:36876111-36876161	ProgFib	skin:	n/a
23	chr5:36876667-36876717	ProgFib	skin:	n/a
24	chr5:36877216-36877266	GM12892	blood:	n/a
25	chr5:36876537-36876587	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:36876537-36876587	SK-N-SH	brain:	n/a
27	chr5:36877216-36877266	H1-hESC	embryonic stem cell:	embryo
28	chr5:36876954-36877004	GM12878	blood:	n/a
29	chr5:36876114-36876164	T-47D	breast:	n/a
30	chr5:36876833-36876883	SKMC	muscle:	n/a
31	chr5:36882196-36882246	NH-A	brain:	n/a
32	chr5:36877626-36877676	ProgFib	skin:	n/a
33	chr5:36875537-36875587	AG04450	lung:	fetal
34	chr5:36877216-36877266	T-47D	breast:	n/a
35	chr5:36876114-36876164	SKMC	muscle:	n/a
36	chr5:36876680-36876730	SK-N-MC	brain:	n/a
37	chr5:36876111-36876161	CMK	blood:	n/a
38	chr5:36877626-36877676	HCT-116	colon:	n/a
39	chr5:36876833-36876883	HepG2	liver:	n/a
40	chr5:36876680-36876730	GM12892	blood:	n/a
41	chr5:36876537-36876587	H1-hESC	embryonic stem cell:	embryo
42	chr5:36876114-36876164	AG10803	skin:	n/a
43	chr5:36875434-36875484	HCF	heart:	n/a
44	chr5:36875537-36875587	GM12891	blood:	n/a
45	chr5:36877379-36877429	GM12878	blood:	n/a
46	chr5:36876667-36876717	IMR90	lung:	fetal
47	chr5:36876111-36876161	AG09309	skin:	n/a
48	chr5:36876667-36876717	K562	blood:	n/a
49	chr5:36876667-36876717	HRPEpiC	eye:	n/a
50	chr5:36875434-36875484	GM06990	blood:	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:36728405..36730840-chr5:36886021..36888598,2	MCF-7	breast:
2	chr5:36739352..36740196-chr5:36875690..36876608,3	MCF-7	breast:
3	chr5:36862319..36866798-chr5:36867132..36872368,6	K562	blood:
4	chr5:36777088..36777847-chr5:36869730..36870372,2	MCF-7	breast:
5	chr5:36852700..36856054-chr5:36857270..36861770,4	K562	blood:
6	chr5:36876233..36877782-chr5:36895355..36898025,2	MCF-7	breast:
7	chr5:36857086..36859417-chr5:36866349..36868294,2	K562	blood:
8	chr5:36894674..36897624-chr5:36903658..36906079,2	K562	blood:
9	chr5:36876319..36879960-chr5:36897656..36900567,3	K562	blood:
10	chr5:36876650..36877236-chr7:99933531..99934342,2	Hela-S3	cervix:
11	chr5:36835501..36837986-chr5:36868760..36872023,3	MCF-7	breast:
12	chr5:36842024..36844943-chr5:36873859..36876803,3	K562	blood:
13	chr5:36852700..36856054-chr5:36857270..36861770,4	K562	blood:
14	chr5:36744753..36745265-chr5:36870351..36870936,2	MCF-7	breast:
15	chr5:36876342..36877209-chrX:153626319..153627100,2	Hela-S3	cervix:
16	chr5:36891948..36893628-chr5:36897697..36899677,2	K562	blood:
17	chr5:36727925..36729564-chr5:36870241..36872217,2	K562	blood:
18	chr5:36887613..36889354-chr5:36924858..36926395,2	MCF-7	breast:
19	chr5:36891948..36893628-chr5:36897697..36899677,2	K562	blood:
20	chr5:36876363..36877049-chr7:39989868..39990637,2	Hela-S3	cervix:
21	chr5:36722181..36727364-chr5:36874838..36878996,5	MCF-7	breast:
22	chr5:36888811..36890696-chr5:36892108..36894974,2	K562	blood:
23	chr5:36870958..36873840-chr5:36982182..36984989,2	MCF-7	breast:
24	chr15:51057662..51059502-chr5:36875365..36877060,2	MCF-7	breast:
25	chr5:36777373..36779388-chr5:36874708..36876280,2	MCF-7	breast:
26	chr5:36856261..36858596-chr5:36864059..36865980,2	K562	blood:
27	chr17:79008801..79009359-chr5:36876376..36876943,2	Hela-S3	cervix:
28	chr11:62554095..62554682-chr5:36876746..36877433,2	Hela-S3	cervix:
29	chr5:36876413..36877387-chr6:32939757..32940537,2	Hela-S3	cervix:
30	chr16:77224141..77224935-chr5:36877159..36878081,2	Hela-S3	cervix:
31	chr1:145437800..145438586-chr5:36878077..36878735,2	Hela-S3	cervix:
32	chr5:36854199..36856066-chr5:36857945..36859943,2	K562	blood:
33	chr5:36739516..36740130-chr5:36870542..36871202,2	MCF-7	breast:
34	chr5:36874005..36875680-chr5:36879007..36880824,2	MCF-7	breast:
35	chr5:36875375..36878248-chr5:37375352..37377665,2	K562	blood:
36	chr5:36876398..36879013-chr5:36886021..36888865,3	MCF-7	breast:
37	chr5:36877079..36878828-chr5:36943978..36945931,2	MCF-7	breast:
38	chr5:36856339..36858783-chr5:36874945..36877432,2	K562	blood:
39	chr10:102820738..102821464-chr5:36876624..36877148,2	Hela-S3	cervix:
40	chr12:122907836..122908689-chr5:36876906..36877771,2	Hela-S3	cervix:
41	chr17:57915027..57916783-chr5:36875321..36877865,2	MCF-7	breast:
42	chr5:36881365..36883410-chr5:36892096..36895669,3	K562	blood:
43	chr5:36240939..36242558-chr5:36874591..36876688,2	K562	blood:
44	chr18:12947867..12948535-chr5:36876330..36876850,2	Hela-S3	cervix:
45	chr3:128444867..128445573-chr5:36876639..36877272,2	Hela-S3	cervix:
46	chr5:36856261..36858596-chr5:36864059..36865980,2	K562	blood:
47	chr5:36877699..36879526-chr5:36890759..36893139,2	MCF-7	breast:
48	chr17:41277189..41278053-chr5:36876513..36877425,3	NB4	blood:
49	chr5:36858168..36860650-chr5:36872272..36874447,2	K562	blood:
50	chr5:36854199..36856066-chr5:36857945..36859943,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf42-2	chr5:36864527-36866128	ENSG00000248044
2	lnc-NIPBL-1	chr5:36871457-36871997	XLOC_004339
3	lnc-C5orf42-2	chr5:36867686-36876860	NONHSAT101045
4	lnc-C5orf42-2	chr5:36871463-36876796	NONHSAT147328
5	lnc-C5orf42-2	chr5:36875773-36876759	ENSG00000248044
6	lnc-NIPBL-1	chr5:36874735-36876605	XLOC_004339
7	lnc-C5orf42-6	chr5:36861838-36862319	ENSG00000272103.1

No data

Variant related genes	Relation type
KRT18P31	TF binding region
ENSG00000272103	TF binding region
NIPBL	TF binding region
KRT18P31	CpG island
ENSG00000272103	CpG island
NIPBL	CpG island
ENSG00000255112	chromatin interactions
ENSG00000272752	chromatin interactions
ENSG00000249850	chromatin interactions
ENSG00000224418	chromatin interactions
ENSG00000167930	chromatin interactions
ENSG00000117385	chromatin interactions
ENSG00000152620	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000138600	chromatin interactions
ENSG00000103111	chromatin interactions
ENSG00000269176	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000012048	chromatin interactions
ENSG00000075785	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000250155	chromatin interactions
ENSG00000051825	chromatin interactions
ENSG00000242294	chromatin interactions
ENSG00000147403	chromatin interactions
ENSG00000250455	chromatin interactions
ENSG00000272103	chromatin interactions
ENSG00000175866	chromatin interactions
ENSG00000198496	chromatin interactions
ENSG00000273162	chromatin interactions
ENSG00000102572	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000155592	chromatin interactions
ENSG00000141582	chromatin interactions
ENSG00000085415	chromatin interactions
ENSG00000117289	chromatin interactions
ENSG00000171848	chromatin interactions
ENSG00000121716	chromatin interactions
ENSG00000166398	chromatin interactions
ENSG00000164190	chromatin interactions
ENSG00000164008	chromatin interactions
PTPRK	miRNA target sites
TMEM87A	miRNA target sites

Extended variants
information (count: 2060 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:2060 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116400220	chr5:36835407-36835408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs16903365	chr5:36835408-36835409	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs530739072	chr5:36835489-36835490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184927935	chr5:36835493-36835494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs72732600	chr5:36835509-36835510	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs370348762	chr5:36835528-36835529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150463799	chr5:36835552-36835553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147690113	chr5:36835553-36835554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549585297	chr5:36835563-36835564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374694928	chr5:36835589-36835590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34911537	chr5:36835677-36835678	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs571692890	chr5:36835722-36835723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539210519	chr5:36835760-36835761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142399020	chr5:36835861-36835862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569455545	chr5:36835894-36835895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs13181860	chr5:36835928-36835929	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs555312299	chr5:36835929-36835930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115073390	chr5:36835943-36835944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189689852	chr5:36835982-36835983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571265494	chr5:36836023-36836024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553022688	chr5:36836129-36836130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577699560	chr5:36836185-36836186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545164211	chr5:36836431-36836432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563308091	chr5:36836498-36836499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575409898	chr5:36836527-36836528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371943564	chr5:36836601-36836602	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs375754390	chr5:36836613-36836614	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs182354448	chr5:36836677-36836678	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs73093817	chr5:36836808-36836809	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs528459975	chr5:36836868-36836869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370597798	chr5:36836954-36836955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187682332	chr5:36836955-36836956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565360777	chr5:36836985-36836986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115104790	chr5:36836996-36836997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551070897	chr5:36837126-36837127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542443749	chr5:36837153-36837154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs35460988	chr5:36837155-36837156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79055870	chr5:36837276-36837277	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs76666345	chr5:36837283-36837284	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs569312429	chr5:36837297-36837298	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs536842356	chr5:36837308-36837309	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs548894803	chr5:36837311-36837312	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs567210683	chr5:36837341-36837342	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs143007192	chr5:36837351-36837352	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs538260128	chr5:36837407-36837408	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs552722853	chr5:36837428-36837429	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs571240336	chr5:36837439-36837440	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs143596424	chr5:36837518-36837519	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs557026716	chr5:36837527-36837528	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs368169107	chr5:36837552-36837553	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36835400-36837800	Enhancers	Ovary	ovary
2	chr5:36836400-36836600	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr5:36836400-36838000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr5:36836400-36844000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr5:36836600-36836800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr5:36836600-36838000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:36836800-36837200	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr5:36837000-36838000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:36837200-36838000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr5:36837400-36837600	Enhancers	Stomach Smooth Muscle	stomach
11	chr5:36837600-36837800	Enhancers	Primary hematopoietic stem cells	blood
12	chr5:36837600-36838000	Enhancers	Colon Smooth Muscle	Colon
13	chr5:36837800-36839000	Weak transcription	Ovary	ovary
14	chr5:36837800-36839000	Weak transcription	Stomach Smooth Muscle	stomach
15	chr5:36837800-36841600	Weak transcription	Primary hematopoietic stem cells	blood
16	chr5:36838000-36839200	Weak transcription	Colon Smooth Muscle	Colon
17	chr5:36838000-36839200	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr5:36838000-36840200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr5:36838000-36840200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:36838000-36840400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr5:36839000-36839200	Enhancers	Ovary	ovary
22	chr5:36839000-36839800	Enhancers	Stomach Smooth Muscle	stomach
23	chr5:36839200-36839800	Enhancers	Colon Smooth Muscle	Colon
24	chr5:36839200-36840800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr5:36840200-36840800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr5:36840200-36840800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:36840400-36842000	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr5:36840800-36841800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr5:36840800-36842000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr5:36840800-36842000	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr5:36841600-36842800	Enhancers	Primary hematopoietic stem cells	blood
32	chr5:36841600-36844600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr5:36841800-36842000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr5:36842000-36842200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr5:36842000-36842200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr5:36842000-36842400	Enhancers	Primary B cells from cord blood	blood
37	chr5:36842000-36842400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr5:36842000-36842600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr5:36842000-36842600	Enhancers	Primary B cells from peripheral blood	blood
40	chr5:36842000-36842800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
41	chr5:36842200-36842400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr5:36842200-36842400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr5:36842200-36842600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr5:36842200-36842600	Bivalent Enhancer	Dnd41	blood
45	chr5:36842200-36842800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:36842200-36842800	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr5:36842200-36842800	Enhancers	Primary T cells from cord blood	blood
48	chr5:36842400-36842600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
49	chr5:36842400-36843200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr5:36842600-36843000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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