Variant report

Variant	esv1822457
Chromosome Location	chr16:33939146-33965281
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4962)
CpG islands
(count:1953)
Chromatin interactive
region (count:141)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4962 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:33962896-33964273	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:33960210-33961488	K562	blood:	n/a	n/a
3	ARID3A	chr16:33954207-33954728	K562	blood:	n/a	n/a
4	ARID3A	chr16:33947476-33947858	K562	blood:	n/a	n/a
5	ARID3A	chr16:33941019-33941023	K562	blood:	n/a	n/a
6	ARID3A	chr16:33952173-33953799	K562	blood:	n/a	n/a
7	ARID3A	chr16:33955044-33957934	K562	blood:	n/a	n/a
8	ARID3A	chr16:33960368-33961487	HepG2	liver:	n/a	n/a
9	ARID3A	chr16:33943175-33943309	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:33964706-33966039	K562	blood:	n/a	n/a
11	ARID3A	chr16:33958278-33959783	HepG2	liver:	n/a	n/a
12	ARID3A	chr16:33964513-33966330	HepG2	liver:	n/a	n/a
13	ARID3A	chr16:33945691-33946332	K562	blood:	n/a	n/a
14	ARID3A	chr16:33958282-33959785	K562	blood:	n/a	n/a
15	ARID3A	chr16:33962893-33964420	K562	blood:	n/a	n/a
16	ATF1	chr16:33960215-33961326	K562	blood:	n/a	n/a
17	ATF1	chr16:33958276-33959793	K562	blood:	n/a	n/a
18	ATF1	chr16:33942494-33942869	K562	blood:	n/a	n/a
19	ATF1	chr16:33955043-33956019	K562	blood:	n/a	n/a
20	ATF1	chr16:33956301-33958052	K562	blood:	n/a	n/a
21	ATF1	chr16:33945681-33946253	K562	blood:	n/a	n/a
22	ATF1	chr16:33950018-33951511	K562	blood:	n/a	n/a
23	ATF1	chr16:33947663-33948001	K562	blood:	n/a	n/a
24	ATF1	chr16:33954192-33954783	K562	blood:	n/a	n/a
25	ATF1	chr16:33962891-33964418	K562	blood:	n/a	n/a
26	ATF1	chr16:33940512-33940714	K562	blood:	n/a	n/a
27	ATF1	chr16:33941402-33941555	K562	blood:	n/a	n/a
28	ATF1	chr16:33952165-33953795	K562	blood:	n/a	n/a
29	ATF2	chr16:33962927-33964315	GM12878	blood:	n/a	n/a
30	ATF2	chr16:33962966-33964217	GM12878	blood:	n/a	n/a
31	ATF2	chr16:33962931-33964214	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr16:33952910-33953517	GM12878	blood:	n/a	n/a
33	ATF2	chr16:33962889-33964272	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF3	chr16:33962954-33964219	K562	blood:	n/a	n/a
35	ATF3	chr16:33962912-33964331	A549	lung:	n/a	n/a
36	ATF3	chr16:33964812-33965018	GM12878	blood:	n/a	n/a
37	ATF3	chr16:33964689-33965129	HepG2	liver:	n/a	chr16:33964780-33964788
38	ATF3	chr16:33958303-33958826	HepG2	liver:	n/a	n/a
39	ATF3	chr16:33962927-33964197	HepG2	liver:	n/a	n/a
40	ATF3	chr16:33963037-33963475	K562	blood:	n/a	n/a
41	ATF3	chr16:33955591-33955932	K562	blood:	n/a	n/a
42	ATF3	chr16:33952968-33953866	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF3	chr16:33952996-33953485	HepG2	liver:	n/a	n/a
44	ATF3	chr16:33956419-33956754	K562	blood:	n/a	n/a
45	ATF3	chr16:33958389-33958603	K562	blood:	n/a	n/a
46	ATF3	chr16:33957033-33957912	HepG2	liver:	n/a	chr16:33957162-33957172 chr16:33957159-33957172 chr16:33957158-33957173 chr16:33957161-33957169 chr16:33957159-33957170 chr16:33957162-33957172 chr16:33957162-33957170 chr16:33957162-33957169 chr16:33957159-33957172
47	ATF3	chr16:33959008-33959389	K562	blood:	n/a	n/a
48	ATF3	chr16:33962812-33964301	A549	lung:	n/a	n/a
49	ATF3	chr16:33962852-33964220	H1-hESC	embryonic stem cell:	n/a	n/a
50	ATF3	chr16:33955548-33956006	HepG2	liver:	n/a	n/a

(count:1953 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33965255-33965305	Hela-S3	cervix:	n/a
2	chr16:33965255-33965305	Hela-S3	cervix:	n/a
3	chr16:33948849-33948899	HAEpiC	amniotic membrane:	n/a
4	chr16:33959595-33959645	GM06990	blood:	n/a
5	chr16:33952528-33952578	BJ	skin:	n/a
6	chr16:33949459-33949509	GM12878	blood:	n/a
7	chr16:33952528-33952578	CMK	blood:	n/a
8	chr16:33956457-33956507	HMEC	breast:	n/a
9	chr16:33959785-33959835	HCM	heart:	n/a
10	chr16:33961872-33961922	HRE	kidney:	n/a
11	chr16:33948885-33948935	RPTEC	kidney:	n/a
12	chr16:33956603-33956653	HMEC	breast:	n/a
13	chr16:33939550-33939600	NHDF-neo	bronchial:	n/a
14	chr16:33942675-33942725	HCM	heart:	n/a
15	chr16:33952673-33952723	AG04449	skin:	fetal
16	chr16:33956603-33956653	HEK293	kidney:	embryo
17	chr16:33961515-33961565	ovcar-3	ovarian:	n/a
18	chr16:33964200-33964250	GM12891	blood:	n/a
19	chr16:33961872-33961922	NB4	blood:	n/a
20	chr16:33961515-33961565	SK-N-SH_RA	brain:	n/a
21	chr16:33957271-33957321	SK-N-SH_RA	brain:	n/a
22	chr16:33961517-33961567	AG04450	lung:	fetal
23	chr16:33952528-33952578	NT2-D1	testis:	n/a
24	chr16:33961872-33961922	HEK293	kidney:	embryo
25	chr16:33939152-33939202	SKMC	muscle:	n/a
26	chr16:33961517-33961567	HEK293	kidney:	embryo
27	chr16:33949584-33949634	HEK293	kidney:	embryo
28	chr16:33961515-33961565	HEEpiC	esophagus:	n/a
29	chr16:33959595-33959645	K562	blood:	n/a
30	chr16:33959785-33959835	CMK	blood:	n/a
31	chr16:33961515-33961565	HRE	kidney:	n/a
32	chr16:33963473-33963523	SAEC	small airway:	n/a
33	chr16:33948806-33948856	H1-hESC	embryonic stem cell:	embryo
34	chr16:33948806-33948856	HNPCEpiC	eye:	n/a
35	chr16:33956603-33956653	MCF10A-Er-Src	breast:	n/a
36	chr16:33945328-33945378	HIPEpiC	eye:	n/a
37	chr16:33962675-33962725	AG09319	gingival:	n/a
38	chr16:33964783-33964833	HIPEpiC	eye:	n/a
39	chr16:33959595-33959645	BE2_C	brain:	n/a
40	chr16:33943412-33943462	Caco-2	colon:	n/a
41	chr16:33949584-33949634	HNPCEpiC	eye:	n/a
42	chr16:33945328-33945378	ECC-1	luminal epithelium:	n/a
43	chr16:33952673-33952723	U87	brain:	n/a
44	chr16:33964783-33964833	T-47D	breast:	n/a
45	chr16:33964783-33964833	HMEC	breast:	n/a
46	chr16:33948806-33948856	BE2_C	brain:	n/a
47	chr16:33956717-33956767	HCPEpiC	choroid plexus:	n/a
48	chr16:33956717-33956767	HEK293	kidney:	embryo
49	chr16:33942523-33942573	NHDF-neo	bronchial:	n/a
50	chr16:33957271-33957321	A549	lung:	n/a

(count:141 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr16:33959013..33960783-chr17:21284023..21285523,2	MCF-7	breast:
2	chr16:33955196..33957971-chr18:33676982..33678678,2	MCF-7	breast:
3	chr16:33963452..33965034-chr17:76921426..76922946,2	K562	blood:
4	chr16:33960804..33961476-chr21:9826473..9827159,2	MCF-7	breast:
5	chr16:14580478..14581474-chr16:33949673..33950197,2	MCF-7	breast:
6	chr16:33957128..33958102-chr4:80274126..80274833,2	MCF-7	breast:
7	chr16:33952012..33953185-chr2:133030483..133031473,5	MCF-7	breast:
8	chr16:33956695..33957643-chr2:133025283..133025850,2	MCF-7	breast:
9	chr16:33962594..33963953-chr21:9825062..9826789,10	MCF-7	breast:
10	chr16:33965082..33965611-chr5:74062938..74063440,2	K562	blood:
11	chr11:45847777..45848777-chr16:33963130..33963930,2	MCF-7	breast:
12	chr16:33962856..33963882-chr20:26188364..26189806,5	K562	blood:
13	chr16:33964537..33965670-chr20:26188912..26190067,3	K562	blood:
14	chr16:33939878..33940836-chr8:52730956..52731844,2	MCF-7	breast:
15	chr16:33959789..33967924-chr21:9824121..9829063,70	K562	blood:
16	chr12:20703919..20704937-chr16:33963436..33964235,5	MCF-7	breast:
17	chr16:33963139..33963772-chr2:133012277..133013465,4	MCF-7	breast:
18	chr16:33960778..33961976-chr20:26188545..26190262,6	K562	blood:
19	chr16:33962970..33963730-chr22:30819310..30819829,2	MCF-7	breast:
20	chr16:33957999..33960795-chr2:133021474..133023187,2	K562	blood:
21	chr16:33955610..33959101-chr2:133023879..133027782,14	K562	blood:
22	chr16:33951907..33953719-chr2:133029106..133032192,3	MCF-7	breast:
23	chr16:33963085..33964229-chr2:133012332..133013517,6	HCT-116	colon:
24	chr16:33957408..33958237-chr2:133027029..133027823,2	MCF-7	breast:
25	chr16:33961812..33963365-chr7:80963081..80964594,2	MCF-7	breast:
26	chr16:33965176..33965978-chr2:133010227..133011402,4	MCF-7	breast:
27	chr16:33961286..33962956-chr20:26188880..26190564,2	MCF-7	breast:
28	chr16:33953770..33959520-chr2:133023575..133028433,10	K562	blood:
29	chr16:33618869..33619686-chr16:33955996..33956882,3	MCF-7	breast:
30	chr16:33955968..33957203-chr2:133025182..133026996,13	MCF-7	breast:
31	chr16:33955361..33957320-chr21:9825635..9828856,3	MCF-7	breast:
32	chr16:33955647..33957340-chr2:133030573..133032108,2	K562	blood:
33	chr16:33962563..33964255-chr21:9826866..9828063,39	MCF-7	breast:
34	chr16:33958782..33959817-chr2:133022675..133023764,8	MCF-7	breast:
35	chr16:33962584..33963994-chr21:9826768..9828002,25	MCF-7	breast:
36	chr12:127649393..127652006-chr16:33961856..33963373,2	K562	blood:
37	chr16:33960800..33961892-chr20:26188687..26190008,21	MCF-7	breast:
38	chr12:34416477..34418281-chr16:33956682..33958772,3	MCF-7	breast:
39	chr16:33962741..33963365-chr21:9827377..9827961,3	MCF-7	breast:
40	chr16:33955725..33957601-chr2:133029342..133031796,2	MCF-7	breast:
41	chr16:33952098..33953697-chr21:9825775..9827386,2	K562	blood:
42	chr16:33962970..33965065-chr2:133011472..133013456,38	MCF-7	breast:
43	chr12:20703904..20704960-chr16:33963177..33964348,6	MCF-7	breast:
44	chr12:20702878..20705929-chr16:33961732..33966726,6	K562	blood:
45	chr16:33961661..33967162-chr2:133010338..133015206,18	K562	blood:
46	chr16:33948697..33951102-chr16:33957145..33959288,2	K562	blood:
47	chr16:33959973..33964975-chr2:133010437..133015799,15	MCF-7	breast:
48	chr16:33959793..33967555-chr20:26187372..26191632,15	K562	blood:
49	chr16:33950585..33951554-chr2:133031749..133032658,2	MCF-7	breast:
50	chr12:127649114..127650896-chr16:33956470..33958618,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2144E22.5.1-21	chr16:33946090-33946338	NONHSAT142132
2	lnc-CTD-2144E22.5.1-22	chr16:33945490-33945742	NONHSAT142130

No data

Variant related genes	Relation type
PCMTD1P2	TF binding region
LINC00273	TF binding region
ENSG00000260207	TF binding region
ENSG00000261440	TF binding region
ENSG00000265616	TF binding region
RNA5-8SP2	TF binding region
ENSG00000207986	TF binding region
ENSG00000259987	TF binding region
PCMTD1P2	CpG island
LINC00273	CpG island
ENSG00000260207	CpG island
ENSG00000261440	CpG island
ENSG00000265616	CpG island
RNA5-8SP2	CpG island
ENSG00000207986	CpG island
ENSG00000259987	CpG island
ENSG00000239776	chromatin interactions
ENSG00000221288	chromatin interactions
ENSG00000164346	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000202174	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000223514	chromatin interactions
ENSG00000035862	chromatin interactions
ENSG00000163046	chromatin interactions
ENSG00000164347	chromatin interactions
ENSG00000256663	chromatin interactions
ENSG00000227195	chromatin interactions
ENSG00000124575	chromatin interactions

Extended variants
information (count: 4831 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:4831 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77627169	chr16:33939152-33939153	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs546626620	chr16:33939153-33939154	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs74015477	chr16:33939156-33939157	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs77054443	chr16:33939163-33939164	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs74015478	chr16:33939167-33939168	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs74626517	chr16:33939172-33939173	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs72806304	chr16:33939178-33939179	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs143163526	chr16:33939198-33939199	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs112623706	chr16:33939199-33939200	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs74616543	chr16:33939202-33939203	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs571412762	chr16:33939214-33939215	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs77237979	chr16:33939220-33939221	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs192780727	chr16:33939221-33939222	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs551440534	chr16:33939222-33939223	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs374609313	chr16:33939238-33939239	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs78066968	chr16:33939245-33939246	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs75416009	chr16:33939247-33939248	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs79168016	chr16:33939248-33939249	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs74470951	chr16:33939260-33939261	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs72806306	chr16:33939273-33939274	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs111714275	chr16:33939274-33939275	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs112389106	chr16:33939275-33939276	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs79641120	chr16:33939276-33939277	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs78685608	chr16:33939292-33939293	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs569838304	chr16:33939297-33939298	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs76863593	chr16:33939299-33939300	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs111253012	chr16:33939321-33939322	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs113913390	chr16:33939325-33939326	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs75347612	chr16:33939326-33939327	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs143207501	chr16:33939332-33939333	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs375910576	chr16:33939348-33939349	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs79203616	chr16:33939350-33939351	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs200766904	chr16:33939353-33939354	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs370017175	chr16:33939354-33939355	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs147762435	chr16:33939355-33939356	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs79425542	chr16:33939373-33939374	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs76486269	chr16:33939379-33939380	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs112743875	chr16:33939389-33939390	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs148198955	chr16:33939405-33939406	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs79117630	chr16:33939409-33939410	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs75512394	chr16:33939413-33939414	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs79597798	chr16:33939429-33939430	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs79771015	chr16:33939430-33939431	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs386790392	chr16:33939432-33939433	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs74015481	chr16:33939433-33939434	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs567816320	chr16:33939440-33939441	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs141453352	chr16:33939441-33939442	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs113529366	chr16:33939443-33939444	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs67484207	chr16:33939444-33939445	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs77655504	chr16:33939451-33939452	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Ductal carcinoma	22052326	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD

Chromatin state (count:1136 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33932000-33941200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr16:33932200-33957000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr16:33932200-33957200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
4	chr16:33932400-33951600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr16:33932400-33957000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr16:33932400-33957000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
7	chr16:33932400-33961800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
8	chr16:33932800-33966600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
9	chr16:33933000-33941000	ZNF genes & repeats	Fetal Brain Male	brain
10	chr16:33933000-33961600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr16:33933200-33940800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
12	chr16:33933800-33941200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
13	chr16:33934200-33939600	ZNF genes & repeats	Liver	Liver
14	chr16:33934200-33939800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
15	chr16:33934200-33939800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr16:33934400-33939400	ZNF genes & repeats	Thymus	Thymus
17	chr16:33934800-33939600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr16:33935000-33939600	ZNF genes & repeats	Right Ventricle	heart
19	chr16:33935000-33939800	ZNF genes & repeats	Esophagus	oesophagus
20	chr16:33935000-33939800	ZNF genes & repeats	HepG2	liver
21	chr16:33935000-33940000	ZNF genes & repeats	Fetal Muscle Trunk	muscle
22	chr16:33935200-33939400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
23	chr16:33935200-33939600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr16:33935200-33939600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
25	chr16:33935200-33939600	ZNF genes & repeats	Adipose Nuclei	Adipose
26	chr16:33935200-33939800	ZNF genes & repeats	Gastric	stomach
27	chr16:33935200-33939800	ZNF genes & repeats	Lung	lung
28	chr16:33935200-33939800	ZNF genes & repeats	Spleen	Spleen
29	chr16:33935200-33939800	ZNF genes & repeats	NHEK	skin
30	chr16:33935400-33939400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr16:33935400-33939400	ZNF genes & repeats	Rectal Smooth Muscle	rectum
32	chr16:33935400-33939400	ZNF genes & repeats	Hela-S3	cervix
33	chr16:33935400-33939600	ZNF genes & repeats	Pancreas	Pancrea
34	chr16:33935400-33939600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
35	chr16:33935400-33939800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr16:33935400-33940000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr16:33935600-33939600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
38	chr16:33935600-33940000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr16:33936200-33939200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr16:33936600-33939200	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
41	chr16:33936600-33939400	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
42	chr16:33936600-33939600	ZNF genes & repeats	Colonic Mucosa	Colon
43	chr16:33937000-33939200	ZNF genes & repeats	Brain Anterior Caudate	brain
44	chr16:33937400-33940000	Weak transcription	Fetal Heart	heart
45	chr16:33937800-33939600	ZNF genes & repeats	Brain Hippocampus Middle	brain
46	chr16:33938200-33939400	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
47	chr16:33938200-33939800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr16:33938200-33941400	ZNF genes & repeats	Primary T cells from cord blood	blood
49	chr16:33938400-33939200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
50	chr16:33938400-33939600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell

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