Variant report

Variant	rs144192670
Chromosome Location	chr4:107438143-107438144
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3518924	chr4:107436953-107439551	Weak transcription	n/a	n/a	inside rSNPs	diseases
2	esv3518925	chr4:107436953-107439551	Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv2512315	chr4:107437202-107438867	Weak transcription	n/a	n/a	inside rSNPs	diseases
4	esv3797	chr4:107437488-107438698	Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3468272	chr4:107437570-107438590	Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv2269047	chr4:107437593-107438635	Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3382522	chr4:107437608-107438449	Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3468273	chr4:107437639-107438588	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	chr4:107415200-107450200	Weak transcription	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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