Variant report

Variant	rs4346145
Chromosome Location	chr14:84131185-84131186
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11626623	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1241909	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046869	chr14:83749048-84284813	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv542152	chr14:83749048-84284813	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1039276	chr14:83814378-84232588	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv902157	chr14:84058209-84172323	Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv902158	chr14:84087517-84172323	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv565374	chr14:84104059-84159334	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84129400-84137600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:84130400-84131400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr14:84130400-84131800	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr14:84130800-84131200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr14:84130800-84131200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr14:84130800-84131400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr14:84130800-84131600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr14:84130800-84131800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr14:84131000-84131200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr14:84131000-84131400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr14:84131000-84131400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr14:84131000-84131400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr14:84131000-84131400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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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