Variant report

Variant	rs197602
Chromosome Location	chr1:57680247-57680248
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1053	0.92[CEU][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs155284	0.92[CEU][hapmap];0.96[EUR][1000 genomes]
rs155285	0.93[CEU][hapmap];0.96[EUR][1000 genomes]
rs197101	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs197103	0.86[CEU][hapmap];0.89[EUR][1000 genomes]
rs197105	0.92[CEU][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs197598	0.93[CEU][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs197600	0.98[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs197601	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs197610	0.92[CEU][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs264037	0.93[CEU][hapmap];0.95[EUR][1000 genomes]
rs264038	0.90[EUR][1000 genomes]
rs502350	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461628	chr1:57463326-57816489	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv546305	chr1:57463326-57816489	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57672400-57680600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:57672400-57680800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr1:57672600-57680800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr1:57675600-57692600	Weak transcription	Fetal Intestine Large	intestine
5	chr1:57675800-57680800	Weak transcription	Fetal Heart	heart
6	chr1:57676000-57689800	Weak transcription	Fetal Intestine Small	intestine
7	chr1:57678600-57684600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:57678800-57680600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr1:57678800-57681000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:57679200-57695000	Weak transcription	Fetal Brain Female	brain
11	chr1:57679400-57681000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:57679800-57681400	Weak transcription	hESC Derived CD56+ Mesoderm 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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