Variant report

Variant	rs546661507
Chromosome Location	chr14:85138499-85138500
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751288	chr14:84815330-85704047	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1046875	chr14:84993510-85193250	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv565378	chr14:85070611-85140984	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv1829021	chr14:85106009-85196163	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3530368	chr14:85137199-85141497	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv2516457	chr14:85138146-85139948	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv1820152	chr14:85138430-85139498	Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv1831944	chr14:85138430-85139498	Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv1835010	chr14:85138430-85139498	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv1835631	chr14:85138430-85139498	Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv1840823	chr14:85138430-85139498	Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv1841671	chr14:85138430-85139498	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3516593	chr14:85138449-85140647	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85135600-85143600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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

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