Variant report

Variant	nsv821722
Chromosome Location	chr2:133010192-133039368
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6644)
CpG islands
(count:3361)
Chromatin interactive
region (count:257)
LncRNA
region (count:8)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:6644 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:133015019-133015747	K562	blood:	n/a	n/a
2	ARID3A	chr2:133021777-133024659	K562	blood:	n/a	n/a
3	ARID3A	chr2:133024999-133028006	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:133032461-133033743	K562	blood:	n/a	n/a
5	ARID3A	chr2:133024878-133031935	K562	blood:	n/a	n/a
6	ARID3A	chr2:133035680-133036126	K562	blood:	n/a	n/a
7	ARID3A	chr2:133010732-133010763	K562	blood:	n/a	n/a
8	ARID3A	chr2:133011761-133013355	K562	blood:	n/a	n/a
9	ARID3A	chr2:133032280-133033731	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:133037976-133039294	K562	blood:	n/a	n/a
11	ATF1	chr2:133011772-133013346	K562	blood:	n/a	n/a
12	ATF1	chr2:133021765-133024691	K562	blood:	n/a	n/a
13	ATF1	chr2:133016237-133017446	K562	blood:	n/a	n/a
14	ATF1	chr2:133032469-133033732	K562	blood:	n/a	n/a
15	ATF1	chr2:133018613-133021289	K562	blood:	n/a	n/a
16	ATF1	chr2:133024991-133031933	K562	blood:	n/a	n/a
17	ATF2	chr2:133011836-133012126	GM12878	blood:	n/a	n/a
18	ATF2	chr2:133011823-133013332	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr2:133011825-133013352	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr2:133012312-133013340	GM12878	blood:	n/a	n/a
21	ATF2	chr2:133028916-133031075	GM12878	blood:	n/a	n/a
22	ATF2	chr2:133012462-133013089	GM12878	blood:	n/a	n/a
23	ATF2	chr2:133011789-133012265	GM12878	blood:	n/a	n/a
24	ATF3	chr2:133029476-133030077	HepG2	liver:	n/a	n/a
25	ATF3	chr2:133021822-133031930	K562	blood:	n/a	n/a
26	ATF3	chr2:133025667-133026458	K562	blood:	n/a	n/a
27	ATF3	chr2:133012403-133013259	HepG2	liver:	n/a	n/a
28	ATF3	chr2:133016311-133016564	HepG2	liver:	n/a	n/a
29	ATF3	chr2:133012465-133013223	K562	blood:	n/a	n/a
30	ATF3	chr2:133034363-133034795	K562	blood:	n/a	n/a
31	ATF3	chr2:133011744-133013434	A549	lung:	n/a	n/a
32	ATF3	chr2:133032577-133032719	K562	blood:	n/a	n/a
33	ATF3	chr2:133018709-133019159	HepG2	liver:	n/a	n/a
34	ATF3	chr2:133016618-133017347	HepG2	liver:	n/a	n/a
35	ATF3	chr2:133025728-133025957	K562	blood:	n/a	n/a
36	ATF3	chr2:133031489-133031880	HepG2	liver:	n/a	n/a
37	ATF3	chr2:133034301-133034812	HepG2	liver:	n/a	n/a
38	ATF3	chr2:133028832-133029372	HepG2	liver:	n/a	n/a
39	ATF3	chr2:133023013-133023655	HepG2	liver:	n/a	n/a
40	ATF3	chr2:133023055-133023668	K562	blood:	n/a	n/a
41	ATF3	chr2:133022327-133022859	HepG2	liver:	n/a	n/a
42	ATF3	chr2:133017036-133017375	K562	blood:	n/a	n/a
43	ATF3	chr2:133032785-133033604	HepG2	liver:	n/a	n/a
44	ATF3	chr2:133025549-133026035	HepG2	liver:	n/a	n/a
45	ATF3	chr2:133015023-133015421	HepG2	liver:	n/a	n/a
46	ATF3	chr2:133012465-133012990	GM12878	blood:	n/a	n/a
47	ATF3	chr2:133028279-133028662	HepG2	liver:	n/a	n/a
48	ATF3	chr2:133015927-133017546	K562	blood:	n/a	n/a
49	ATF3	chr2:133011829-133012122	HepG2	liver:	n/a	n/a
50	ATF3	chr2:133030353-133031098	HepG2	liver:	n/a	n/a

(count:3361 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133038098-133038148	K562	blood:	n/a
2	chr2:133036873-133036923	HMEC	breast:	n/a
3	chr2:133038912-133038962	HUVEC	blood vessel:	n/a
4	chr2:133037546-133037596	ECC-1	luminal epithelium:	n/a
5	chr2:133012853-133012903	SK-N-MC	brain:	n/a
6	chr2:133039143-133039193	HIPEpiC	eye:	n/a
7	chr2:133038098-133038148	K562	blood:	n/a
8	chr2:133036873-133036923	HMEC	breast:	n/a
9	chr2:133038912-133038962	HUVEC	blood vessel:	n/a
10	chr2:133037546-133037596	ECC-1	luminal epithelium:	n/a
11	chr2:133012853-133012903	SK-N-MC	brain:	n/a
12	chr2:133039143-133039193	HIPEpiC	eye:	n/a
13	chr2:133022980-133023030	HUVEC	blood vessel:	n/a
14	chr2:133023100-133023150	NHBE	bronchial:	n/a
15	chr2:133014663-133014713	SK-N-SH	brain:	n/a
16	chr2:133038912-133038962	ovcar-3	ovarian:	n/a
17	chr2:133013792-133013842	NT2-D1	testis:	n/a
18	chr2:133012353-133012403	SKMC	muscle:	n/a
19	chr2:133037153-133037203	GM06990	blood:	n/a
20	chr2:133013489-133013539	HCPEpiC	choroid plexus:	n/a
21	chr2:133038912-133038962	AG04449	skin:	fetal
22	chr2:133036194-133036244	SK-N-SH_RA	brain:	n/a
23	chr2:133039152-133039202	SKMC	muscle:	n/a
24	chr2:133013489-133013539	RPTEC	kidney:	n/a
25	chr2:133036548-133036598	SK-N-SH_RA	brain:	n/a
26	chr2:133015665-133015715	NHBE	bronchial:	n/a
27	chr2:133036073-133036123	AG04450	lung:	fetal
28	chr2:133033270-133033320	AG04450	lung:	fetal
29	chr2:133011849-133011899	HRPEpiC	eye:	n/a
30	chr2:133037153-133037203	NHBE	bronchial:	n/a
31	chr2:133039152-133039202	ovcar-3	ovarian:	n/a
32	chr2:133014698-133014748	SK-N-MC	brain:	n/a
33	chr2:133014805-133014855	SKMC	muscle:	n/a
34	chr2:133033270-133033320	HepG2	liver:	n/a
35	chr2:133012853-133012903	HRCEpiC	kidney:	n/a
36	chr2:133037057-133037107	Hepatocyte	liver:	n/a
37	chr2:133022807-133022857	SK-N-SH_RA	brain:	n/a
38	chr2:133036019-133036069	BE2_C	brain:	n/a
39	chr2:133015670-133015720	LNCaP	prostate:	n/a
40	chr2:133014765-133014815	GM19239	blood:	n/a
41	chr2:133015670-133015720	A549	lung:	n/a
42	chr2:133014640-133014690	HCM	heart:	n/a
43	chr2:133013489-133013539	GM06990	blood:	n/a
44	chr2:133013028-133013078	AG04449	skin:	fetal
45	chr2:133030691-133030741	Caco-2	colon:	n/a
46	chr2:133016799-133016849	AG09319	gingival:	n/a
47	chr2:133014765-133014815	NHBE	bronchial:	n/a
48	chr2:133015639-133015689	T-47D	breast:	n/a
49	chr2:133038912-133038962	SAEC	small airway:	n/a
50	chr2:133036194-133036244	Hepatocyte	liver:	n/a

(count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr1:91851302..91853083-chr2:133035035..133039055,6	K562	blood:
2	chr17:45213142..45213821-chr2:133022688..133023208,2	MCF-7	breast:
3	chr16:33951108..33953775-chr2:133025255..133028257,3	MCF-7	breast:
4	chr2:133035583..133038926-chr2:230044088..230047023,3	K562	blood:
5	chr2:133024300..133026801-chr2:133029084..133032122,3	K562	blood:
6	chr16:33956590..33957780-chr2:133025048..133026320,9	MCF-7	breast:
7	chr2:133034324..133035211-chr8:40458783..40459782,2	MCF-7	breast:
8	chr16:33951695..33952511-chr2:133030758..133031458,2	MCF-7	breast:
9	chr17:45213971..45214683-chr2:133020743..133021713,3	MCF-7	breast:
10	chr11:45847777..45848777-chr2:133012311..133012945,4	MCF-7	breast:
11	chr16:33952703..33953232-chr2:133029675..133030305,3	MCF-7	breast:
12	chr2:133033413..133033973-chrX:136519940..136520483,3	MCF-7	breast:
13	chr12:38450015..38451840-chr2:133028967..133030976,3	MCF-7	breast:
14	chr2:133021735..133023570-chr2:133028674..133030666,2	K562	blood:
15	chr2:133014702..133015258-chr21:9825106..9825674,2	MCF-7	breast:
16	chr16:14580901..14581477-chr2:133032758..133033798,4	MCF-7	breast:
17	chr2:133027500..133031769-chr21:9825905..9828905,4	MCF-7	breast:
18	chr12:20702909..20705960-chr2:133011295..133014432,7	K562	blood:
19	chr16:33956695..33957643-chr2:133025283..133025850,2	MCF-7	breast:
20	chr16:33956479..33957946-chr2:133025178..133026405,11	MCF-7	breast:
21	chr2:133011920..133013710-chr21:9825482..9828043,33	MCF-7	breast:
22	chr16:33955996..33957194-chr2:133025297..133026709,5	MCF-7	breast:
23	chr16:33953770..33959520-chr2:133023575..133028433,10	K562	blood:
24	chr2:133014633..133016102-chr20:26188637..26190095,17	MCF-7	breast:
25	chr19:7635601..7636121-chr2:133015921..133016809,2	MCF-7	breast:
26	chr2:133011277..133016757-chr20:26187363..26191986,20	K562	blood:
27	chr16:33962831..33965453-chr2:133011419..133013464,21	MCF-7	breast:
28	chr12:38444829..38445449-chr2:133022690..133023552,2	MCF-7	breast:
29	chr2:133026098..133026689-chr2:133106836..133107370,2	MCF-7	breast:
30	chr2:133022864..133024457-chr20:26188888..26191437,2	MCF-7	breast:
31	chr2:133012862..133013586-chr21:9827253..9827981,2	MCF-7	breast:
32	chr2:133012736..133013451-chr7:80963085..80963599,2	MCF-7	breast:
33	chr16:33959224..33959998-chr2:133022949..133023703,3	MCF-7	breast:
34	chr16:33955610..33959101-chr2:133023879..133027782,14	K562	blood:
35	chr16:14580920..14581474-chr2:133032885..133033534,3	MCF-7	breast:
36	chr2:133035511..133036512-chr6:119558095..119559109,4	MCF-7	breast:
37	chr2:133014691..133015233-chr21:9825130..9825665,3	MCF-7	breast:
38	chr16:33963085..33964229-chr2:133012332..133013517,6	HCT-116	colon:
39	chr2:133011384..133014243-chr4:70295163..70298145,2	K562	blood:
40	chr16:33961297..33961852-chr2:133012609..133013167,2	MCF-7	breast:
41	chr1:91852784..91853360-chr2:133037036..133037536,2	MCF-7	breast:
42	chr2:133012039..133013664-chr21:9825450..9827984,21	MCF-7	breast:
43	chr2:133033539..133035957-chr6:119557078..119558606,2	K562	blood:
44	chr11:85193628..85196531-chr2:133032953..133034631,2	K562	blood:
45	chr19:24183267..24184972-chr2:133036687..133040151,3	K562	blood:
46	chr2:133015211..133015762-chr20:26189170..26190019,2	MCF-7	breast:
47	chr1:156185068..156187965-chr2:133025307..133027312,2	K562	blood:
48	chr17:31149781..31150380-chr2:133035854..133036526,6	MCF-7	breast:
49	chr16:33958834..33966480-chr2:133009904..133018933,30	MCF-7	breast:
50	chr17:31149448..31151294-chr2:133036023..133039051,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR39-7	chr2:133038656-133038732	NONHSAT074524
2	lnc-GPR39-7	chr2:133036673-133036713	NONHSAT074524
3	lnc-ANKRD30BL-3	chr2:133015102-133015542	NONHSAT074513
4	lnc-GPR39-7	chr2:133038981-133039086	NONHSAT074524
5	lnc-GPR39-10	chr2:133013340-133013485	NONHSAT074516
6	lnc-GPR39-10	chr2:133013066-133013266	NONHSAT074516
7	lnc-GPR39-7	chr2:133037726-133037732	NONHSAT074524
8	lnc-GPR39-9	chr2:133019901-133020615	NONHSAT074520

miRNA name	Chromosome Location	mirBase accession
hsa-miR-663b	chr2:133014543-133014564	MIMAT0005867

No data

Variant related genes	Relation type
ANKRD30BL	TF binding region
CDC27P1	TF binding region
MIR663B	TF binding region
RNA5-8SP5	TF binding region
ANKRD30BL	CpG island
CDC27P1	CpG island
MIR663B	CpG island
RNA5-8SP5	CpG island
ENSG00000200434	chromatin interactions
ENSG00000168056	chromatin interactions
ENSG00000140538	chromatin interactions
ENSG00000256663	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000256642	chromatin interactions
ENSG00000104497	chromatin interactions
ENSG00000004897	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000227195	chromatin interactions
ENSG00000239776	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000207986	chromatin interactions
ENSG00000161888	chromatin interactions
ENSG00000198133	chromatin interactions
ENSG00000107968	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000256616	chromatin interactions
ENSG00000226958	chromatin interactions
HRASLS5	Mature miRNA region

Extended variants
information (count: 5481 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5481 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75328019	chr2:133010192-133010193	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs75500415	chr2:133010199-133010200	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs79900427	chr2:133010200-133010201	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs568179661	chr2:133010225-133010226	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs34344452	chr2:133010226-133010227	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs75675375	chr2:133010231-133010232	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs77206083	chr2:133010234-133010235	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs77964005	chr2:133010240-133010241	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs74776002	chr2:133010242-133010243	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs112970998	chr2:133010246-133010247	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs80183166	chr2:133010253-133010254	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs201259121	chr2:133010255-133010256	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs556585264	chr2:133010274-133010275	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs574846049	chr2:133010285-133010286	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs78198482	chr2:133010287-133010288	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs79044118	chr2:133010296-133010297	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs79585564	chr2:133010297-133010298	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs72866797	chr2:133010304-133010305	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs72866798	chr2:133010311-133010312	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs190303870	chr2:133010312-133010313	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs35362333	chr2:133010319-133010320	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs74647033	chr2:133010326-133010327	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs79119866	chr2:133010329-133010330	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs73957359	chr2:133010333-133010334	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs77382622	chr2:133010335-133010336	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs75512559	chr2:133010338-133010339	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs76317881	chr2:133010358-133010359	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs573379887	chr2:133010359-133010360	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs74765152	chr2:133010377-133010378	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs75395416	chr2:133010378-133010379	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs16849038	chr2:133010400-133010401	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs199833914	chr2:133010413-133010414	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs35100872	chr2:133010422-133010423	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs540851509	chr2:133010424-133010425	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs79621824	chr2:133010431-133010432	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs34585481	chr2:133010435-133010436	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs72866799	chr2:133010445-133010446	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs562126676	chr2:133010450-133010451	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs574226156	chr2:133010452-133010453	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs77639175	chr2:133010453-133010454	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs78764384	chr2:133010456-133010457	ZNF genes & repeats Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs79636259	chr2:133010457-133010458	ZNF genes & repeats Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs544718093	chr2:133010471-133010472	ZNF genes & repeats Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs113386070	chr2:133010480-133010481	ZNF genes & repeats Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs562876334	chr2:133010486-133010487	ZNF genes & repeats Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs75936687	chr2:133010487-133010488	ZNF genes & repeats Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs76199855	chr2:133010488-133010489	ZNF genes & repeats Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs113852789	chr2:133010523-133010524	ZNF genes & repeats Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs533327977	chr2:133010524-133010525	ZNF genes & repeats Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs545796637	chr2:133010525-133010526	ZNF genes & repeats Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2105 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133003200-133011000	ZNF genes & repeats	Adipose Nuclei	Adipose
2	chr2:133004400-133012000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:133008400-133013200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
4	chr2:133008400-133017400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
5	chr2:133009600-133012000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr2:133009600-133012000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr2:133009800-133011800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr2:133009800-133017400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:133009800-133017600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:133010000-133012000	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
11	chr2:133010200-133010800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr2:133010400-133017400	ZNF genes & repeats	Colonic Mucosa	Colon
13	chr2:133010400-133017400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
14	chr2:133010400-133017600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
15	chr2:133010600-133011400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr2:133010600-133012600	ZNF genes & repeats	Fetal Stomach	stomach
17	chr2:133010600-133017400	ZNF genes & repeats	Dnd41	blood
18	chr2:133010800-133012000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:133011000-133011800	Weak transcription	Adipose Nuclei	Adipose
20	chr2:133011000-133017600	ZNF genes & repeats	Fetal Intestine Large	intestine
21	chr2:133011400-133017400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
22	chr2:133011600-133017400	ZNF genes & repeats	Fetal Thymus	thymus
23	chr2:133011800-133012000	ZNF genes & repeats	Adipose Nuclei	Adipose
24	chr2:133011800-133012200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr2:133011800-133012600	ZNF genes & repeats	Fetal Muscle Leg	muscle
26	chr2:133011800-133013200	Flanking Bivalent TSS/Enh	Gastric	stomach
27	chr2:133011800-133013200	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
28	chr2:133011800-133013400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:133011800-133013400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr2:133011800-133013400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
31	chr2:133011800-133013400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
32	chr2:133011800-133013400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
33	chr2:133011800-133013400	ZNF genes & repeats	Primary T cells from cord blood	blood
34	chr2:133011800-133013400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
35	chr2:133011800-133013400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
36	chr2:133011800-133013400	ZNF genes & repeats	Ovary	ovary
37	chr2:133011800-133013400	ZNF genes & repeats	Rectal Smooth Muscle	rectum
38	chr2:133011800-133013400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
39	chr2:133011800-133013400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
40	chr2:133011800-133013800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr2:133011800-133013800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr2:133011800-133014400	ZNF genes & repeats	Brain Germinal Matrix	brain
43	chr2:133011800-133016000	ZNF genes & repeats	Fetal Brain Male	brain
44	chr2:133011800-133016600	ZNF genes & repeats	Pancreas	Pancrea
45	chr2:133011800-133017400	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
46	chr2:133011800-133017400	ZNF genes & repeats	Esophagus	oesophagus
47	chr2:133011800-133017400	ZNF genes & repeats	Fetal Brain Female	brain
48	chr2:133011800-133017400	ZNF genes & repeats	Small Intestine	intestine
49	chr2:133011800-133017400	ZNF genes & repeats	Thymus	Thymus
50	chr2:133011800-133017400	ZNF genes & repeats	Spleen	Spleen

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