Variant report

Variant	rs111588073
Chromosome Location	chr4:69790983-69790984
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005513	chr4:69446718-69890307	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv999654	chr4:69661415-70132110	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	esv3420586	chr4:69680878-70322918	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
4	esv3398036	chr4:69700493-69841391	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1067773	chr4:69718248-70715727	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	esv3468151	chr4:69718675-70322776	Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
7	esv3468153	chr4:69718675-70322776	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
8	nsv436447	chr4:69743339-69851390	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv4372	chr4:69764499-69810115	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv967758	chr4:69780530-69870183	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv829962	chr4:69786869-69910283	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	esv3448476	chr4:69790113-69792511	Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases
13	esv3339141	chr4:69790613-69792061	Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
14	esv6299	chr4:69790614-69791335	Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3414761	chr4:69790708-69791268	Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3467171	chr4:69790728-69791282	Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3490280	chr4:69790769-69791275	Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3467173	chr4:69790790-69791246	Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3467172	chr4:69790791-69791252	Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv3337155	chr4:69790822-69791200	Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv3829	chr4:69790837-69791262	Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv3467176	chr4:69790841-69791181	Weak transcription	n/a	n/a	inside rSNPs	diseases
23	esv3467177	chr4:69790856-69791195	Weak transcription	n/a	n/a	inside rSNPs	diseases
24	esv3490281	chr4:69790856-69791195	Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv1002295	chr4:69790860-69791179	Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv1486252	chr4:69790874-69791194	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69790600-69792800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr4:69790600-69793800	Weak transcription	HepG2	liver

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