Variant report

Variant	rs545070057
Chromosome Location	chr1:215194761-215194762
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv468105	chr1:215167236-215248417	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv549182	chr1:215167236-215248417	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3330090	chr1:215194689-215194800	Weak transcription	n/a	n/a	inside rSNPs	diseases
4	esv3453472	chr1:215194714-215194785	Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3453473	chr1:215194728-215194781	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215177200-215211200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:215188800-215195200	Weak transcription	NHDF-Ad	bronchial
3	chr1:215192400-215195200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:215192400-215195200	Weak transcription	NHLF	lung
5	chr1:215192400-215195400	Weak transcription	Osteobl	bone
6	chr1:215193600-215195000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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