Variant report

Variant	rs10174787
Chromosome Location	chr2:114866431-114866432
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10172143	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10187225	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10197950	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58107161	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874904	chr2:114751691-115605062	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv829624	chr2:114791945-115119926	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv3381703	chr2:114794745-114989429	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114860000-114866600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:114865400-114867400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr2:114865600-114866600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr2:114866000-114867200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:114866000-114867400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr2:114866000-114867400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:114866000-114867600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr2:114866200-114866600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr2:114866200-114867400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr2:114866200-114867400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr2:114866200-114867400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr2:114866400-114866800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr2:114866400-114867400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:114866400-114867400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr2:114866400-114867400	Enhancers	Aorta	Aorta

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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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