Variant report

Variant	rs115792797
Chromosome Location	chr7:144921475-144921476
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031071	chr7:144318082-145125392	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv539169	chr7:144318082-145125392	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv831179	chr7:144830077-144998851	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1026420	chr7:144902627-145020612	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv3506044	chr7:144915719-144922517	Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3506043	chr7:144916169-144922467	Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv1007031	chr7:144916246-144921563	Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3476905	chr7:144916750-144921511	Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3420768	chr7:144916798-144921494	Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3476903	chr7:144916801-144921483	Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3476904	chr7:144916812-144921500	Enhancers	n/a	n/a	inside rSNPs	diseases
12	esv15162	chr7:144916993-144921583	Enhancers	n/a	n/a	inside rSNPs	diseases
13	nsv608915	chr7:144917817-144923298	Enhancers	n/a	n/a	inside rSNPs	diseases
14	nsv608918	chr7:144918207-144923298	Enhancers	n/a	n/a	inside rSNPs	diseases
15	nsv608921	chr7:144919485-144923298	Enhancers	n/a	n/a	inside rSNPs	diseases
16	nsv608924	chr7:144920025-144923298	Enhancers	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	chr7:144921000-144923000	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr7:144921200-144922400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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