Variant report

Variant	rs386770778
Chromosome Location	chr13:48419935-48419936
allele	AA/CG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3510679	chr13:48236624-48498185	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3510680	chr13:48236624-48498185	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv561589	chr13:48251736-48420218	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2383197	chr13:48419735-48420255	Enhancers	n/a	n/a	inside rSNPs	diseases
5	esv3521402	chr13:48419828-48420187	Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3521406	chr13:48419842-48420184	Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3521404	chr13:48419846-48420131	Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3521401	chr13:48419854-48420110	Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3510286	chr13:48419862-48420140	Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3510319	chr13:48419874-48420098	Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3521403	chr13:48419874-48420138	Enhancers	n/a	n/a	inside rSNPs	diseases
12	esv3510308	chr13:48419894-48420108	Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3510297	chr13:48419912-48420086	Enhancers	n/a	n/a	inside rSNPs	diseases
14	esv3521405	chr13:48419924-48420081	Enhancers	n/a	n/a	inside rSNPs	diseases
15	esv3510330	chr13:48419926-48420091	Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv3521407	chr13:48419926-48420091	Enhancers	n/a	n/a	inside rSNPs	diseases
17	esv1006301	chr13:48419932-48420087	Enhancers	n/a	n/a	inside rSNPs	diseases
18	esv1611410	chr13:48419934-48420090	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	chr13:48419000-48420400	Enhancers	HMEC	breast
2	chr13:48419000-48421400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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