Variant report

Variant	rs1251487
Chromosome Location	chr1:76519880-76519881
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs1251477	0.90[AFR][1000 genomes]

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	nsv998499	chr1:76361784-76598712	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2754129	chr1:76489579-76529279	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv870968	chr1:76490234-76552475	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv947186	chr1:76512447-76530843	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1477	chr1:76515963-76534339	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76517600-76521400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:76517800-76520000	Enhancers	Fetal Stomach	stomach
3	chr1:76518000-76520200	Enhancers	Colon Smooth Muscle	Colon
4	chr1:76518400-76520600	Enhancers	Rectal Smooth Muscle	rectum
5	chr1:76518600-76520000	Enhancers	Placenta Amnion	Placenta Amnion
6	chr1:76519000-76520000	Enhancers	Primary hematopoietic stem cells	blood
7	chr1:76519200-76521200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr1:76519200-76524600	Weak transcription	Brain Hippocampus Middle	brain
9	chr1:76519200-76524600	Weak transcription	Brain Substantia Nigra	brain
10	chr1:76519400-76521200	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr1:76519400-76521200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:76519400-76521200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:76519400-76521200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:76519400-76521600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr1:76519400-76524800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:76519600-76521200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr1:76519600-76524800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr1:76519800-76520000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

Quick Search:

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

what's new

Quick links