Variant report

Variant	rs190152125
Chromosome Location	chr7:127766352-127766353
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022385	chr7:127246656-127971194	Weak transcription Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv539120	chr7:127246656-127971194	Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	esv3377181	chr7:127765666-127767764	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2591981	chr7:127765924-127767382	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv8422	chr7:127766222-127766853	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2306945	chr7:127766232-127766933	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3476750	chr7:127766293-127766827	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3523425	chr7:127766318-127766835	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3523422	chr7:127766323-127766818	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3523421	chr7:127766342-127766763	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3476752	chr7:127766349-127766800	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3476754	chr7:127766350-127766797	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127762400-127772000	Weak transcription	Right Atrium	heart
2	chr7:127764200-127769000	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr7:127766000-127766400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr7:127766200-127769200	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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