Variant report

Variant	esv1809802
Chromosome Location	chr2:133009421-133041986
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6748)
CpG islands
(count:3483)
Chromatin interactive
region (count:257)
LncRNA
region (count:8)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:6748 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:133011761-133013355	K562	blood:	n/a	n/a
2	ARID3A	chr2:133037976-133039294	K562	blood:	n/a	n/a
3	ARID3A	chr2:133010732-133010763	K562	blood:	n/a	n/a
4	ARID3A	chr2:133035680-133036126	K562	blood:	n/a	n/a
5	ARID3A	chr2:133032280-133033731	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:133032461-133033743	K562	blood:	n/a	n/a
7	ARID3A	chr2:133015019-133015747	K562	blood:	n/a	n/a
8	ARID3A	chr2:133041164-133041233	K562	blood:	n/a	n/a
9	ARID3A	chr2:133024999-133028006	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:133024878-133031935	K562	blood:	n/a	n/a
11	ARID3A	chr2:133021777-133024659	K562	blood:	n/a	n/a
12	ATF1	chr2:133018613-133021289	K562	blood:	n/a	n/a
13	ATF1	chr2:133011772-133013346	K562	blood:	n/a	n/a
14	ATF1	chr2:133009295-133009427	K562	blood:	n/a	n/a
15	ATF1	chr2:133032469-133033732	K562	blood:	n/a	n/a
16	ATF1	chr2:133016237-133017446	K562	blood:	n/a	n/a
17	ATF1	chr2:133021765-133024691	K562	blood:	n/a	n/a
18	ATF1	chr2:133024991-133031933	K562	blood:	n/a	n/a
19	ATF2	chr2:133012312-133013340	GM12878	blood:	n/a	n/a
20	ATF2	chr2:133012462-133013089	GM12878	blood:	n/a	n/a
21	ATF2	chr2:133011836-133012126	GM12878	blood:	n/a	n/a
22	ATF2	chr2:133011823-133013332	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr2:133011825-133013352	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr2:133028916-133031075	GM12878	blood:	n/a	n/a
25	ATF2	chr2:133011789-133012265	GM12878	blood:	n/a	n/a
26	ATF3	chr2:133023013-133023655	HepG2	liver:	n/a	n/a
27	ATF3	chr2:133015084-133015367	K562	blood:	n/a	n/a
28	ATF3	chr2:133015023-133015421	HepG2	liver:	n/a	n/a
29	ATF3	chr2:133012465-133012990	GM12878	blood:	n/a	n/a
30	ATF3	chr2:133011744-133013434	A549	lung:	n/a	n/a
31	ATF3	chr2:133035538-133036154	A549	lung:	n/a	n/a
32	ATF3	chr2:133014997-133015569	A549	lung:	n/a	n/a
33	ATF3	chr2:133032577-133032719	K562	blood:	n/a	n/a
34	ATF3	chr2:133026082-133027274	HepG2	liver:	n/a	n/a
35	ATF3	chr2:133022578-133022840	K562	blood:	n/a	n/a
36	ATF3	chr2:133011829-133012122	HepG2	liver:	n/a	n/a
37	ATF3	chr2:133015086-133015491	A549	lung:	n/a	n/a
38	ATF3	chr2:133018709-133019159	HepG2	liver:	n/a	n/a
39	ATF3	chr2:133029515-133030022	K562	blood:	n/a	n/a
40	ATF3	chr2:133032559-133032768	HepG2	liver:	n/a	n/a
41	ATF3	chr2:133012465-133013223	K562	blood:	n/a	n/a
42	ATF3	chr2:133020043-133020233	K562	blood:	n/a	n/a
43	ATF3	chr2:133025728-133025957	K562	blood:	n/a	n/a
44	ATF3	chr2:133032785-133033604	HepG2	liver:	n/a	n/a
45	ATF3	chr2:133025667-133026458	K562	blood:	n/a	n/a
46	ATF3	chr2:133016628-133016997	K562	blood:	n/a	n/a
47	ATF3	chr2:133030081-133030808	K562	blood:	n/a	n/a
48	ATF3	chr2:133026094-133026523	K562	blood:	n/a	n/a
49	ATF3	chr2:133038024-133038380	A549	lung:	n/a	n/a
50	ATF3	chr2:133012403-133013259	HepG2	liver:	n/a	n/a

(count:3483 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133038912-133038962	SK-N-SH	brain:	n/a
2	chr2:133016799-133016849	A549	lung:	n/a
3	chr2:133012853-133012903	HMEC	breast:	n/a
4	chr2:133014805-133014855	ovcar-3	ovarian:	n/a
5	chr2:133038098-133038148	HepG2	liver:	n/a
6	chr2:133015670-133015720	BJ	skin:	n/a
7	chr2:133038912-133038962	SK-N-SH	brain:	n/a
8	chr2:133016799-133016849	A549	lung:	n/a
9	chr2:133012853-133012903	HMEC	breast:	n/a
10	chr2:133014805-133014855	ovcar-3	ovarian:	n/a
11	chr2:133038098-133038148	HepG2	liver:	n/a
12	chr2:133015670-133015720	BJ	skin:	n/a
13	chr2:133014765-133014815	H1-hESC	embryonic stem cell:	embryo
14	chr2:133011643-133011693	HNPCEpiC	eye:	n/a
15	chr2:133025835-133025885	Hela-S3	cervix:	n/a
16	chr2:133037153-133037203	HCF	heart:	n/a
17	chr2:133025917-133025967	Caco-2	colon:	n/a
18	chr2:133013028-133013078	GM06990	blood:	n/a
19	chr2:133011643-133011693	NT2-D1	testis:	n/a
20	chr2:133038836-133038886	NHDF-neo	bronchial:	n/a
21	chr2:133039152-133039202	LNCaP	prostate:	n/a
22	chr2:133037636-133037686	ECC-1	luminal epithelium:	n/a
23	chr2:133038261-133038311	A549	lung:	n/a
24	chr2:133012853-133012903	HRE	kidney:	n/a
25	chr2:133014663-133014713	GM12892	blood:	n/a
26	chr2:133012853-133012903	HNPCEpiC	eye:	n/a
27	chr2:133023100-133023150	K562	blood:	n/a
28	chr2:133030701-133030751	BE2_C	brain:	n/a
29	chr2:133014698-133014748	AG04450	lung:	fetal
30	chr2:133036548-133036598	A549	lung:	n/a
31	chr2:133038927-133038977	BE2_C	brain:	n/a
32	chr2:133039779-133039829	CMK	blood:	n/a
33	chr2:133015670-133015720	AG09319	gingival:	n/a
34	chr2:133018841-133018891	MCF10A-Er-Src	breast:	n/a
35	chr2:133014805-133014855	LNCaP	prostate:	n/a
36	chr2:133016453-133016503	GM12892	blood:	n/a
37	chr2:133015268-133015318	GM06990	blood:	n/a
38	chr2:133012853-133012903	RPTEC	kidney:	n/a
39	chr2:133033270-133033320	RPTEC	kidney:	n/a
40	chr2:133015665-133015715	HEEpiC	esophagus:	n/a
41	chr2:133037636-133037686	HAEpiC	amniotic membrane:	n/a
42	chr2:133014784-133014834	AG04450	lung:	fetal
43	chr2:133013792-133013842	HCPEpiC	choroid plexus:	n/a
44	chr2:133039152-133039202	HRE	kidney:	n/a
45	chr2:133036695-133036745	GM12892	blood:	n/a
46	chr2:133039143-133039193	HAEpiC	amniotic membrane:	n/a
47	chr2:133036935-133036985	BJ	skin:	n/a
48	chr2:133036873-133036923	Hela-S3	cervix:	n/a
49	chr2:133013048-133013098	ovcar-3	ovarian:	n/a
50	chr2:133030691-133030741	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:34416748..34417268-chr2:133025884..133026405,2	MCF-7	breast:
2	chr17:45213139..45213977-chr2:133022711..133023395,2	MCF-7	breast:
3	chr2:133012082..133013943-chr21:9825567..9828064,27	MCF-7	breast:
4	chr2:133012270..133013258-chr7:80963109..80963626,3	MCF-7	breast:
5	chr2:133012152..133012832-chr4:183777693..183778673,2	MCF-7	breast:
6	chr16:33957999..33960795-chr2:133021474..133023187,2	K562	blood:
7	chr11:45847793..45848776-chr2:133011952..133012946,3	K562	blood:
8	chr12:127650410..127651159-chr2:133035504..133036500,2	MCF-7	breast:
9	chr2:133033299..133034050-chrX:136520044..136520933,2	MCF-7	breast:
10	chr2:133010417..133016800-chr21:9824146..9829019,50	K562	blood:
11	chr2:133038209..133039052-chr5:71146751..71147399,3	MCF-7	breast:
12	chr16:14579410..14580924-chr2:133031239..133034174,2	K562	blood:
13	chr2:120288604..120289171-chr2:133037653..133038211,2	MCF-7	breast:
14	chr1:108113044..108113591-chr2:133038209..133039151,2	MCF-7	breast:
15	chr2:133034721..133036011-chr6:119558119..119559094,3	MCF-7	breast:
16	chr17:31149756..31151304-chr2:133036010..133037634,2	MCF-7	breast:
17	chr12:20703898..20704919-chr2:133012092..133013365,7	MCF-7	breast:
18	chr17:45214288..45216196-chr2:133019606..133021862,2	MCF-7	breast:
19	chr2:133032278..133034990-chr21:9826150..9828910,2	MCF-7	breast:
20	chr16:33952703..33953232-chr2:133029675..133030305,3	MCF-7	breast:
21	chr16:14580920..14581474-chr2:133032885..133033534,3	MCF-7	breast:
22	chr1:91851357..91852890-chr2:133010879..133013835,2	K562	blood:
23	chr12:20703892..20704983-chr2:133011971..133012956,17	MCF-7	breast:
24	chr16:33955898..33957631-chr2:133025048..133026808,38	MCF-7	breast:
25	chr1:205242237..205242803-chr2:133028691..133029317,2	MCF-7	breast:
26	chr16:33954432..33957320-chr2:133023311..133028999,7	MCF-7	breast:
27	chr2:133032297..133036217-chrX:136519059..136522057,4	MCF-7	breast:
28	chr2:133034324..133035211-chr8:40458783..40459782,2	MCF-7	breast:
29	chr2:133010417..133015279-chr21:9824040..9829010,45	K562	blood:
30	chr12:38535401..38535902-chr2:133016817..133017415,2	MCF-7	breast:
31	chr12:20703909..20705005-chr2:133012056..133013289,12	MCF-7	breast:
32	chr2:133011277..133016757-chr20:26187363..26191986,20	K562	blood:
33	chr17:45219278..45221259-chr2:133018860..133021838,2	MCF-7	breast:
34	chr19:24184114..24184636-chr2:133038429..133039143,2	MCF-7	breast:
35	chr16:33963085..33964229-chr2:133012332..133013517,6	HCT-116	colon:
36	chr16:33960797..33961973-chr2:133014348..133015268,4	MCF-7	breast:
37	chr2:133037674..133038178-chr21:9826291..9827058,2	MCF-7	breast:
38	chr2:133011920..133013710-chr21:9825482..9828043,33	MCF-7	breast:
39	chr2:133026098..133026689-chr2:133106836..133107370,2	MCF-7	breast:
40	chr12:133713986..133716965-chr2:133016799..133018923,2	MCF-7	breast:
41	chr2:133038140..133038648-chr5:71146774..71147415,2	MCF-7	breast:
42	chr2:133012621..133013397-chr20:26188383..26189327,2	MCF-7	breast:
43	chr2:133033298..133034623-chrX:136519950..136520939,4	MCF-7	breast:
44	chr2:133033275..133034052-chrX:136520019..136520544,2	HCT-116	colon:
45	chr16:33963139..33963772-chr2:133012277..133013465,4	MCF-7	breast:
46	chr17:31149455..31151173-chr2:133037551..133039052,2	K562	blood:
47	chr2:133035372..133036357-chr6:119558115..119558640,6	MCF-7	breast:
48	chr2:133014691..133015233-chr21:9825130..9825665,3	MCF-7	breast:
49	chr2:133015237..133015768-chr20:26189161..26190454,3	K562	blood:
50	chr1:91852393..91852995-chr2:133036535..133037053,3	MCF-7	breast:

(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-GPR39-9	chr2:133019901-133020615	NONHSAT074520
4	lnc-GPR39-10	chr2:133013340-133013485	NONHSAT074516
5	lnc-GPR39-7	chr2:133037726-133037732	NONHSAT074524
6	lnc-GPR39-7	chr2:133038981-133039086	NONHSAT074524
7	lnc-ANKRD30BL-3	chr2:133015102-133015542	NONHSAT074513
8	lnc-GPR39-10	chr2:133013066-133013266	NONHSAT074516

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

Extended variants
information (count: 5876 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5876 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142717186	chr2:133009423-133009424	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs113111985	chr2:133009436-133009437	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs74543669	chr2:133009439-133009440	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs546018927	chr2:133009451-133009452	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs74582346	chr2:133009453-133009454	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs16849050	chr2:133009460-133009461	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs564692320	chr2:133009461-133009462	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs76325504	chr2:133009478-133009479	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs199770604	chr2:133009485-133009486	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs80057156	chr2:133009487-133009488	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs112971076	chr2:133009489-133009490	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs528624050	chr2:133009494-133009495	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs75196205	chr2:133009499-133009500	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs16849048	chr2:133009505-133009506	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs147558830	chr2:133009513-133009514	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs80241515	chr2:133009518-133009519	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs16849046	chr2:133009519-133009520	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs201978751	chr2:133009535-133009536	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs145177178	chr2:133009540-133009541	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs113772091	chr2:133009550-133009551	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs10173268	chr2:133009569-133009570	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs548526407	chr2:133009578-133009579	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs371644806	chr2:133009585-133009586	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs181713707	chr2:133009593-133009594	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs79165572	chr2:133009598-133009599	ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs537328182	chr2:133009631-133009632	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs200955942	chr2:133009633-133009634	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs16849044	chr2:133009634-133009635	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs201687371	chr2:133009646-133009647	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs76829726	chr2:133009671-133009672	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs76606727	chr2:133009675-133009676	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs369587631	chr2:133009691-133009692	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs143410027	chr2:133009697-133009698	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs78380124	chr2:133009699-133009700	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs552444184	chr2:133009700-133009701	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs570626297	chr2:133009705-133009706	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs76492634	chr2:133009710-133009711	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs112708269	chr2:133009716-133009717	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs373206283	chr2:133009720-133009721	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs376708062	chr2:133009722-133009723	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs62164983	chr2:133009759-133009760	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs75555666	chr2:133009768-133009769	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs74378356	chr2:133009769-133009770	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs75678520	chr2:133009776-133009777	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs201219984	chr2:133009777-133009778	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs552994042	chr2:133009791-133009792	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs76727598	chr2:133009792-133009793	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs112624703	chr2:133009795-133009796	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs74981233	chr2:133009798-133009799	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs373411621	chr2:133009801-133009802	ZNF genes & repeats Weak transcription	Chromatin interactive region	5 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:2117 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:132994800-133009800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:132996000-133009800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr2:133002200-133009600	ZNF genes & repeats	Liver	Liver
4	chr2:133002200-133009800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
5	chr2:133003200-133011000	ZNF genes & repeats	Adipose Nuclei	Adipose
6	chr2:133004400-133012000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:133007400-133009800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr2:133008400-133013200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
9	chr2:133008400-133017400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
10	chr2:133009400-133009600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
11	chr2:133009400-133009800	ZNF genes & repeats	Fetal Brain Male	brain
12	chr2:133009600-133012000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:133009600-133012000	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr2:133009800-133011800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr2:133009800-133017400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr2:133009800-133017600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr2:133010000-133012000	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
18	chr2:133010200-133010800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:133010400-133017400	ZNF genes & repeats	Colonic Mucosa	Colon
20	chr2:133010400-133017400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
21	chr2:133010400-133017600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
22	chr2:133010600-133011400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr2:133010600-133012600	ZNF genes & repeats	Fetal Stomach	stomach
24	chr2:133010600-133017400	ZNF genes & repeats	Dnd41	blood
25	chr2:133010800-133012000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr2:133011000-133011800	Weak transcription	Adipose Nuclei	Adipose
27	chr2:133011000-133017600	ZNF genes & repeats	Fetal Intestine Large	intestine
28	chr2:133011400-133017400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
29	chr2:133011600-133017400	ZNF genes & repeats	Fetal Thymus	thymus
30	chr2:133011800-133012000	ZNF genes & repeats	Adipose Nuclei	Adipose
31	chr2:133011800-133012200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:133011800-133012600	ZNF genes & repeats	Fetal Muscle Leg	muscle
33	chr2:133011800-133013200	Flanking Bivalent TSS/Enh	Gastric	stomach
34	chr2:133011800-133013200	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
35	chr2:133011800-133013400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:133011800-133013400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr2:133011800-133013400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
38	chr2:133011800-133013400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
39	chr2:133011800-133013400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
40	chr2:133011800-133013400	ZNF genes & repeats	Primary T cells from cord blood	blood
41	chr2:133011800-133013400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
42	chr2:133011800-133013400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
43	chr2:133011800-133013400	ZNF genes & repeats	Ovary	ovary
44	chr2:133011800-133013400	ZNF genes & repeats	Rectal Smooth Muscle	rectum
45	chr2:133011800-133013400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
46	chr2:133011800-133013400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
47	chr2:133011800-133013800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:133011800-133013800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:133011800-133014400	ZNF genes & repeats	Brain Germinal Matrix	brain
50	chr2:133011800-133016000	ZNF genes & repeats	Fetal Brain Male	brain

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