Variant report

Variant	rs577580162
Chromosome Location	chr16:34405733-34405734
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr16:34405613-34405792	NB4	blood:	n/a	chr16:34405685-34405696 chr16:34405684-34405697 chr16:34405688-34405695

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34405690-34405740	LNCaP	prostate:	n/a
2	chr16:34405690-34405740	HL-60	blood:	n/a
3	chr16:34405690-34405740	RPTEC	kidney:	n/a
4	chr16:34405690-34405740	HepG2	liver:	n/a
5	chr16:34405690-34405740	GM12878	blood:	n/a
6	chr16:34405690-34405740	HUVEC	blood vessel:	n/a
7	chr16:34405690-34405740	HCM	heart:	n/a
8	chr16:34405690-34405740	GM19239	blood:	n/a
9	chr16:34405690-34405740	SK-N-MC	brain:	n/a
10	chr16:34405690-34405740	SKMC	muscle:	n/a
11	chr16:34405690-34405740	Jurkat	blood:	n/a
12	chr16:34405690-34405740	HEEpiC	esophagus:	n/a
13	chr16:34405690-34405740	NHBE	bronchial:	n/a
14	chr16:34405690-34405740	Caco-2	colon:	n/a
15	chr16:34405690-34405740	HRPEpiC	eye:	n/a
16	chr16:34405690-34405740	AoSMC	blood vessel:	n/a
17	chr16:34405690-34405740	GM06990	blood:	n/a
18	chr16:34405690-34405740	AG10803	skin:	n/a
19	chr16:34405690-34405740	Hela-S3	cervix:	n/a
20	chr16:34405690-34405740	AG09309	skin:	n/a
21	chr16:34405690-34405740	MCF10A-Er-Src	breast:	n/a
22	chr16:34405690-34405740	CMK	blood:	n/a
23	chr16:34405690-34405740	HMEC	breast:	n/a
24	chr16:34405690-34405740	ECC-1	luminal epithelium:	n/a
25	chr16:34405690-34405740	HEK293	kidney:	embryo
26	chr16:34405690-34405740	AG04449	skin:	fetal
27	chr16:34405690-34405740	H1-hESC	embryonic stem cell:	embryo
28	chr16:34405690-34405740	NH-A	brain:	n/a
29	chr16:34405690-34405740	A549	lung:	n/a
30	chr16:34405690-34405740	HPAEpiC	pulmonary alveolar:	n/a
31	chr16:34405690-34405740	PANC-1	pancreas:	n/a
32	chr16:34405690-34405740	HCT-116	colon:	n/a
33	chr16:34405690-34405740	BJ	skin:	n/a
34	chr16:34405690-34405740	HCF	heart:	n/a
35	chr16:34405690-34405740	HIPEpiC	eye:	n/a
36	chr16:34405690-34405740	HCPEpiC	choroid plexus:	n/a
37	chr16:34405690-34405740	HRE	kidney:	n/a
38	chr16:34405690-34405740	HAEpiC	amniotic membrane:	n/a
39	chr16:34405690-34405740	GM12891	blood:	n/a
40	chr16:34405690-34405740	Hepatocyte	liver:	n/a
41	chr16:34405690-34405740	HRCEpiC	kidney:	n/a
42	chr16:34405690-34405740	MCF-7	breast:	n/a
43	chr16:34405690-34405740	SK-N-SH	brain:	n/a
44	chr16:34405690-34405740	T-47D	breast:	n/a
45	chr16:34405690-34405740	K562	blood:	n/a
46	chr16:34405690-34405740	NHDF-neo	bronchial:	n/a
47	chr16:34405690-34405740	ProgFib	skin:	n/a
48	chr16:34405690-34405740	BE2_C	brain:	n/a
49	chr16:34405690-34405740	PFSK-1	brain:	n/a
50	chr16:34405690-34405740	IMR90	lung:	fetal

No data

Variant related genes	Relation type
UBE2MP1	TF binding region
SLC25A1P4	TF binding region
UBE2MP1	CpG island
SLC25A1P4	CpG island

Extended variants
information (count: 28 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv32538	chr16:33935506-34459464	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
2	nsv431453	chr16:33940200-34760967	ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	74 gene(s)	inside rSNPs	diseases
3	nsv542904	chr16:33942289-34427860	ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
4	nsv906655	chr16:34176875-34597156	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
5	nsv1066136	chr16:34197339-34434323	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv1064842	chr16:34197339-34472275	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv1063819	chr16:34197339-34492332	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
8	nsv1056658	chr16:34197339-34682514	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
9	nsv917674	chr16:34201887-34682588	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
10	nsv1067686	chr16:34202088-35147508	ZNF genes & repeats Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
11	nsv532260	chr16:34202088-35147508	Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
12	nsv457484	chr16:34221454-34535583	ZNF genes & repeats Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
13	nsv572376	chr16:34221454-34535583	ZNF genes & repeats Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
14	nsv521817	chr16:34221454-35168832	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	81 gene(s)	inside rSNPs	diseases
15	nsv521994	chr16:34221454-35168832	Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	81 gene(s)	inside rSNPs	diseases
16	nsv906656	chr16:34243979-34535583	ZNF genes & repeats Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
17	nsv516385	chr16:34259805-34805859	ZNF genes & repeats Weak transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
18	esv2751557	chr16:34263599-34757071	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
19	nsv906657	chr16:34284743-34517789	ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
20	nsv431454	chr16:34321463-34790434	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
21	nsv428326	chr16:34357763-34769642	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
22	nsv431455	chr16:34359599-34796499	ZNF genes & repeats Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
23	esv2758422	chr16:34362213-34769642	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
24	nsv510685	chr16:34373795-34438368	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
25	nsv143	chr16:34378952-34732704	Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
26	nsv960018	chr16:34386660-34409650	Weak transcription ZNF genes & repeats	TF binding region CpG island	3 gene(s)	inside rSNPs	diseases
27	nsv144	chr16:34390796-34715796	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
28	esv3416829	chr16:34403801-34405799	Inactive region	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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