Variant report

Variant	esv1846303
Chromosome Location	chr16:33961093-34020957
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2583)
CpG islands
(count:977)
Chromatin interactive
region (count:90)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2583 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:33983236-33983294	K562	blood:	n/a	n/a
2	ARID3A	chr16:33962896-33964273	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:33964513-33966330	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:33964706-33966039	K562	blood:	n/a	n/a
5	ARID3A	chr16:33960210-33961488	K562	blood:	n/a	n/a
6	ARID3A	chr16:33962893-33964420	K562	blood:	n/a	n/a
7	ARID3A	chr16:33960368-33961487	HepG2	liver:	n/a	n/a
8	ATF1	chr16:33962891-33964418	K562	blood:	n/a	n/a
9	ATF1	chr16:33974192-33974712	K562	blood:	n/a	n/a
10	ATF1	chr16:33973569-33973930	K562	blood:	n/a	n/a
11	ATF1	chr16:33968378-33968581	K562	blood:	n/a	n/a
12	ATF1	chr16:33984608-33984623	K562	blood:	n/a	n/a
13	ATF1	chr16:33975025-33975862	K562	blood:	n/a	n/a
14	ATF1	chr16:33967674-33967696	K562	blood:	n/a	n/a
15	ATF1	chr16:33972180-33973058	K562	blood:	n/a	n/a
16	ATF1	chr16:33970969-33971315	K562	blood:	n/a	n/a
17	ATF1	chr16:33960215-33961326	K562	blood:	n/a	n/a
18	ATF2	chr16:33962889-33964272	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr16:33962927-33964315	GM12878	blood:	n/a	n/a
20	ATF2	chr16:33962931-33964214	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr16:33962966-33964217	GM12878	blood:	n/a	n/a
22	ATF3	chr16:33962852-33964220	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr16:33962912-33964331	A549	lung:	n/a	n/a
24	ATF3	chr16:33965422-33965909	HepG2	liver:	n/a	chr16:33965641-33965661
25	ATF3	chr16:33961000-33961464	HepG2	liver:	n/a	n/a
26	ATF3	chr16:33963662-33964122	GM12878	blood:	n/a	n/a
27	ATF3	chr16:33973555-33973880	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF3	chr16:33962954-33964219	K562	blood:	n/a	n/a
29	ATF3	chr16:33965408-33965721	K562	blood:	n/a	chr16:33965641-33965661
30	ATF3	chr16:33965359-33965751	A549	lung:	n/a	chr16:33965641-33965661
31	ATF3	chr16:33962927-33964197	HepG2	liver:	n/a	n/a
32	ATF3	chr16:33963037-33963475	K562	blood:	n/a	n/a
33	ATF3	chr16:33964689-33965129	HepG2	liver:	n/a	chr16:33964780-33964788
34	ATF3	chr16:33963055-33963400	GM12878	blood:	n/a	n/a
35	ATF3	chr16:33974571-33975483	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF3	chr16:33964812-33965018	GM12878	blood:	n/a	n/a
37	ATF3	chr16:33962812-33964301	A549	lung:	n/a	n/a
38	ATF3	chr16:33960968-33961544	A549	lung:	n/a	n/a
39	ATF3	chr16:33964755-33965215	A549	lung:	n/a	chr16:33964780-33964788
40	ATF3	chr16:33962971-33964222	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr16:33960108-33961493	K562	blood:	n/a	n/a
42	BACH1	chr16:33974185-33974892	K562	blood:	n/a	n/a
43	BACH1	chr16:33962884-33966516	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr16:33962894-33966086	K562	blood:	n/a	n/a
45	BATF	chr16:33973966-33976036	GM12878	blood:	n/a	n/a
46	BATF	chr16:34002032-34002307	GM12878	blood:	n/a	n/a
47	BATF	chr16:34016087-34016380	GM12878	blood:	n/a	n/a
48	BATF	chr16:33962476-33964260	GM12878	blood:	n/a	n/a
49	BATF	chr16:33962426-33964358	GM12878	blood:	n/a	n/a
50	BATF	chr16:34014972-34015325	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33961872-33961922	HEK293	kidney:	embryo
2	chr16:33961872-33961922	HEK293	kidney:	embryo
3	chr16:33966494-33966544	HRPEpiC	eye:	n/a
4	chr16:33962359-33962409	AG04450	lung:	fetal
5	chr16:33968626-33968676	HCM	heart:	n/a
6	chr16:33965879-33965929	HPAEpiC	pulmonary alveolar:	n/a
7	chr16:33962359-33962409	CMK	blood:	n/a
8	chr16:33966494-33966544	HCF	heart:	n/a
9	chr16:33961872-33961922	IMR90	lung:	fetal
10	chr16:33965435-33965485	HUVEC	blood vessel:	n/a
11	chr16:33965879-33965929	A549	lung:	n/a
12	chr16:33962675-33962725	NB4	blood:	n/a
13	chr16:33965255-33965305	ECC-1	luminal epithelium:	n/a
14	chr16:33965255-33965305	HMEC	breast:	n/a
15	chr16:33961515-33961565	H1-hESC	embryonic stem cell:	embryo
16	chr16:33961517-33961567	NHDF-neo	bronchial:	n/a
17	chr16:33966494-33966544	AG09319	gingival:	n/a
18	chr16:33962359-33962409	AG09319	gingival:	n/a
19	chr16:33963473-33963523	PFSK-1	brain:	n/a
20	chr16:33964200-33964250	HPAEpiC	pulmonary alveolar:	n/a
21	chr16:33963216-33963266	AG09319	gingival:	n/a
22	chr16:33968626-33968676	HIPEpiC	eye:	n/a
23	chr16:33961517-33961567	HL-60	blood:	n/a
24	chr16:33964783-33964833	SK-N-SH_RA	brain:	n/a
25	chr16:33961517-33961567	Hela-S3	cervix:	n/a
26	chr16:33964200-33964250	AG09319	gingival:	n/a
27	chr16:33962675-33962725	GM06990	blood:	n/a
28	chr16:33965879-33965929	HNPCEpiC	eye:	n/a
29	chr16:33965322-33965372	ovcar-3	ovarian:	n/a
30	chr16:33961515-33961565	GM12892	blood:	n/a
31	chr16:33965322-33965372	HPAEpiC	pulmonary alveolar:	n/a
32	chr16:33965322-33965372	HNPCEpiC	eye:	n/a
33	chr16:33965322-33965372	IMR90	lung:	fetal
34	chr16:33965322-33965372	NHDF-neo	bronchial:	n/a
35	chr16:33965573-33965623	PFSK-1	brain:	n/a
36	chr16:33965435-33965485	HRPEpiC	eye:	n/a
37	chr16:33962675-33962725	AG09309	skin:	n/a
38	chr16:33965322-33965372	HIPEpiC	eye:	n/a
39	chr16:33961872-33961922	SK-N-SH	brain:	n/a
40	chr16:33964783-33964833	HCPEpiC	choroid plexus:	n/a
41	chr16:33965255-33965305	K562	blood:	n/a
42	chr16:33965879-33965929	BE2_C	brain:	n/a
43	chr16:33961517-33961567	BJ	skin:	n/a
44	chr16:33963473-33963523	AG09309	skin:	n/a
45	chr16:33964200-33964250	HRPEpiC	eye:	n/a
46	chr16:33964200-33964250	ProgFib	skin:	n/a
47	chr16:33962675-33962725	SKMC	muscle:	n/a
48	chr16:33965879-33965929	NHBE	bronchial:	n/a
49	chr16:33965573-33965623	GM12892	blood:	n/a
50	chr16:33966494-33966544	HRCEpiC	kidney:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:20702881..20704418-chr16:33963254..33964855,3	MCF-7	breast:
2	chr12:20703904..20704960-chr16:33963177..33964348,6	MCF-7	breast:
3	chr16:33962594..33963953-chr21:9825062..9826789,10	MCF-7	breast:
4	chr16:33962741..33963365-chr21:9827377..9827961,3	MCF-7	breast:
5	chr16:33965082..33965611-chr5:74062938..74063440,2	K562	blood:
6	chr16:33963139..33963772-chr2:133012277..133013465,4	MCF-7	breast:
7	chr16:33964377..33964927-chr21:9825880..9826590,2	K562	blood:
8	chr16:33960798..33961786-chr2:133014647..133015193,3	MCF-7	breast:
9	chr16:33962584..33963994-chr21:9826768..9828002,25	MCF-7	breast:
10	chr16:33960878..33961871-chr20:26188853..26189656,7	MCF-7	breast:
11	chr16:33960797..33961973-chr2:133014348..133015268,4	MCF-7	breast:
12	chr16:33962585..33964163-chr21:9825930..9828023,31	MCF-7	breast:
13	chr16:33961286..33962956-chr20:26188880..26190564,2	MCF-7	breast:
14	chr16:33964535..33965625-chr21:9825570..9826552,3	MCF-7	breast:
15	chr12:20702878..20705929-chr16:33961732..33966726,6	K562	blood:
16	chr16:33963368..33965221-chr5:71145359..71146901,3	K562	blood:
17	chr16:33959788..33961476-chr20:26187808..26190098,5	MCF-7	breast:
18	chr12:127649393..127652006-chr16:33961856..33963373,2	K562	blood:
19	chr16:33958834..33966480-chr2:133009904..133018933,30	MCF-7	breast:
20	chr16:33965457..33966053-chr18:74799776..74800776,2	MCF-7	breast:
21	chr16:33962565..33963882-chr21:9826382..9828000,18	K562	blood:
22	chr16:33960813..33961898-chr21:9825677..9826870,3	MCF-7	breast:
23	chr16:33962856..33963882-chr20:26188364..26189806,5	K562	blood:
24	chr16:33962584..33963354-chr2:133014717..133015279,2	MCF-7	breast:
25	chr11:85193511..85195081-chr16:33965594..33967907,2	MCF-7	breast:
26	chr16:33961284..33961954-chr21:9824986..9825946,2	MCF-7	breast:
27	chr12:127650506..127652112-chr16:33963460..33966451,2	K562	blood:
28	chr11:85193566..85195120-chr16:33965483..33967840,2	MCF-7	breast:
29	chr16:33963452..33965034-chr17:76921426..76922946,2	K562	blood:
30	chr16:33959794..33966526-chr21:9824121..9828982,56	K562	blood:
31	chr16:33961812..33963365-chr7:80963081..80964594,2	MCF-7	breast:
32	chr16:33963239..33964145-chr21:9825276..9826165,3	K562	blood:
33	chr16:33962887..33963658-chr7:80962606..80963603,2	MCF-7	breast:
34	chr16:33966063..33966904-chr17:33478173..33478769,2	K562	blood:
35	chr16:33963159..33963977-chr21:9825413..9825941,2	MCF-7	breast:
36	chr16:33963085..33964229-chr2:133012332..133013517,6	HCT-116	colon:
37	chr16:33962584..33964169-chr21:9826366..9828015,22	MCF-7	breast:
38	chr16:33961305..33961892-chr20:26188839..26189533,2	MCF-7	breast:
39	chr16:33960780..33961953-chr20:26188513..26190294,8	MCF-7	breast:
40	chr16:33962666..33964534-chr17:31149759..31151378,2	K562	blood:
41	chr11:85194541..85195128-chr16:33965453..33966369,3	MCF-7	breast:
42	chr11:85195106..85195725-chr16:33963665..33964258,2	MCF-7	breast:
43	chr16:33962970..33963747-chr21:9827034..9827981,2	MCF-7	breast:
44	chr12:20703919..20704937-chr16:33963436..33964235,5	MCF-7	breast:
45	chr16:33966317..33966922-chr17:33478190..33478708,2	MCF-7	breast:
46	chr16:33961272..33961954-chr21:9825039..9826711,7	MCF-7	breast:
47	chr16:33962974..33964644-chr2:133011974..133013442,13	MCF-7	breast:
48	chr12:20703883..20704912-chr16:33962873..33964246,7	MCF-7	breast:
49	chr11:45847777..45848777-chr16:33963130..33963930,2	MCF-7	breast:
50	chr16:33964441..33965474-chr21:9825911..9827244,4	MCF-7	breast:

No data

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

Extended variants
information (count: 9252 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:9252 , 50 per page) page: 1 2 3 4 5 6 7 ... 186

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11863617	chr16:33961093-33961094	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs76554412	chr16:33961095-33961096	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs79672649	chr16:33961102-33961103	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs11861275	chr16:33961123-33961124	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs80040038	chr16:33961138-33961139	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs62028806	chr16:33961159-33961160	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs572032696	chr16:33961167-33961168	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs74349926	chr16:33961169-33961170	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs113238987	chr16:33961189-33961190	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs190658771	chr16:33961192-33961193	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs144627200	chr16:33961200-33961201	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs72806338	chr16:33961201-33961202	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs112992603	chr16:33961212-33961213	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs112567409	chr16:33961214-33961215	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs554739358	chr16:33961219-33961220	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs543727456	chr16:33961228-33961229	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs78683214	chr16:33961238-33961239	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs561704724	chr16:33961244-33961245	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs62028807	chr16:33961246-33961247	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs529099713	chr16:33961247-33961248	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs62028808	chr16:33961248-33961249	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs75317413	chr16:33961249-33961250	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs80127282	chr16:33961250-33961251	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs62028809	chr16:33961254-33961255	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs62028810	chr16:33961265-33961266	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs541916204	chr16:33961271-33961272	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs560213588	chr16:33961283-33961284	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs78597029	chr16:33961295-33961296	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs76215403	chr16:33961302-33961303	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs79975380	chr16:33961314-33961315	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs75989665	chr16:33961317-33961318	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs76610547	chr16:33961318-33961319	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs371701506	chr16:33961323-33961324	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs75001436	chr16:33961324-33961325	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs79375500	chr16:33961327-33961328	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs527825963	chr16:33961329-33961330	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs62028811	chr16:33961334-33961335	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs552140991	chr16:33961338-33961339	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs564171934	chr16:33961359-33961360	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs531891328	chr16:33961368-33961369	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs72797450	chr16:33961370-33961371	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs77172352	chr16:33961379-33961380	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs76955817	chr16:33961382-33961383	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs76705741	chr16:33961386-33961387	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs199599611	chr16:33961395-33961396	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs113037697	chr16:33961400-33961401	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs200479697	chr16:33961402-33961403	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs112037328	chr16:33961411-33961412	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs113700972	chr16:33961418-33961419	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs74375516	chr16:33961444-33961445	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

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
Breast cancer	21364760	CNVD
Renal cell carcinoma	18194544	CNVD

Chromatin state (count:670 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33932400-33961800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
2	chr16:33932800-33966600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
3	chr16:33933000-33961600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr16:33947400-33961600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr16:33947600-33961600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
6	chr16:33947600-33966400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
7	chr16:33948400-33961600	ZNF genes & repeats	Hela-S3	cervix
8	chr16:33948600-33961800	ZNF genes & repeats	Primary T cells from cord blood	blood
9	chr16:33949200-33966200	ZNF genes & repeats	Fetal Stomach	stomach
10	chr16:33950000-33966000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
11	chr16:33950000-33966200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr16:33950200-33966200	ZNF genes & repeats	Fetal Intestine Large	intestine
13	chr16:33952400-33961800	ZNF genes & repeats	Dnd41	blood
14	chr16:33952600-33961800	ZNF genes & repeats	Fetal Brain Male	brain
15	chr16:33952800-33961600	ZNF genes & repeats	Primary B cells from cord blood	blood
16	chr16:33954800-33966200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
17	chr16:33955200-33966400	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
18	chr16:33957800-33966400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
19	chr16:33958000-33961400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr16:33958000-33962000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr16:33958000-33979600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
22	chr16:33958400-33961600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
23	chr16:33958600-33961400	ZNF genes & repeats	Placenta Amnion	Placenta Amnion
24	chr16:33959600-33961800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
25	chr16:33959600-33963000	ZNF genes & repeats	Colonic Mucosa	Colon
26	chr16:33959600-33966600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
27	chr16:33959600-33976400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
28	chr16:33959600-33979600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
29	chr16:33959800-33979800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
30	chr16:33960200-33961600	ZNF genes & repeats	NH-A	brain
31	chr16:33960200-33963000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
32	chr16:33960200-33965000	ZNF genes & repeats	HepG2	liver
33	chr16:33960400-33961400	ZNF genes & repeats	NHDF-Ad	bronchial
34	chr16:33960400-33961600	ZNF genes & repeats	NHEK	skin
35	chr16:33960400-33962000	ZNF genes & repeats	GM12878-XiMat	blood
36	chr16:33960800-33961400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
37	chr16:33960800-33961400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
38	chr16:33960800-33961400	ZNF genes & repeats	Colon Smooth Muscle	Colon
39	chr16:33960800-33961400	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
40	chr16:33960800-33961600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
41	chr16:33960800-33961600	ZNF genes & repeats	NHLF	lung
42	chr16:33960800-33961800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
43	chr16:33960800-33961800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
44	chr16:33960800-33963000	Weak transcription	Fetal Kidney	kidney
45	chr16:33961000-33961200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr16:33961000-33961200	Bivalent Enhancer	Aorta	Aorta
47	chr16:33961000-33961200	Active TSS	Fetal Heart	heart
48	chr16:33961000-33961200	Bivalent Enhancer	Right Ventricle	heart
49	chr16:33961000-33961200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
50	chr16:33961000-33961400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell

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