Variant report

Variant	rs376380126
Chromosome Location	chr4:120244583-120244584
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	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1012868	chr4:120014630-120464880	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv537232	chr4:120014630-120464880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv428769	chr4:120205572-120363323	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv879840	chr4:120227419-120257417	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	esv2525765	chr4:120243529-120245168	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
7	esv3346833	chr4:120243754-120245852	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
8	nsv879841	chr4:120244085-120388406	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv879842	chr4:120244085-120424087	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	esv2018154	chr4:120244361-120245100	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv8767	chr4:120244404-120245164	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3466094	chr4:120244454-120245001	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3517491	chr4:120244459-120245048	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3517489	chr4:120244463-120245007	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	esv3517487	chr4:120244484-120244968	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3466092	chr4:120244496-120244976	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3466091	chr4:120244498-120245049	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
18	esv3517490	chr4:120244507-120244968	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3432674	chr4:120244508-120244961	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
20	esv3466095	chr4:120244512-120244933	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv3466093	chr4:120244543-120244911	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv3517488	chr4:120244558-120244904	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
23	nsv290888	chr4:120244559-120244903	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
24	esv3466096	chr4:120244559-120244919	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv3517492	chr4:120244559-120244919	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
26	nsv290094	chr4:120244574-120244918	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120222000-120251000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr4:120222200-120244600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:120235600-120251000	Weak transcription	Left Ventricle	heart
4	chr4:120243600-120245200	Enhancers	Fetal Intestine Large	intestine
5	chr4:120244000-120245400	Enhancers	Fetal Intestine Small	intestine
6	chr4:120244400-120244800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr4:120244400-120249800	Weak transcription	Duodenum Mucosa	Duodenum

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