Variant report

Variant	rs35746992
Chromosome Location	chr15:77996984-77996985
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:77996121..77999450-chr15:78013163..78015366,3	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs12907305	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12911431	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12912165	0.92[EUR][1000 genomes]
rs12913905	0.92[EUR][1000 genomes]
rs12914069	0.92[EUR][1000 genomes]
rs28409660	0.92[EUR][1000 genomes]
rs28457682	0.92[EUR][1000 genomes]
rs28470773	0.92[EUR][1000 genomes]
rs28482107	0.90[EUR][1000 genomes]
rs28502093	0.90[EUR][1000 genomes]
rs28534807	0.92[EUR][1000 genomes]
rs28544452	0.92[EUR][1000 genomes]
rs28558809	0.92[EUR][1000 genomes]
rs28577113	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28640971	0.92[EUR][1000 genomes]
rs28676831	0.92[EUR][1000 genomes]
rs28698962	0.92[EUR][1000 genomes]
rs28835040	0.92[EUR][1000 genomes]
rs34332318	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34543037	0.92[EUR][1000 genomes]
rs34606680	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34772139	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34828064	0.90[EUR][1000 genomes]
rs35303947	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35722051	0.90[EUR][1000 genomes]
rs36067074	0.92[EUR][1000 genomes]
rs4076997	0.90[EUR][1000 genomes]
rs4076999	0.90[EUR][1000 genomes]
rs58395512	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs66701160	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs67228710	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7174507	0.86[EUR][1000 genomes]
rs7174547	0.89[EUR][1000 genomes]
rs7179534	0.86[EUR][1000 genomes]

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	nsv1040852	chr15:77160237-78137541	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv916323	chr15:77485765-78121259	Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv833060	chr15:77816654-78035204	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
5	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
6	nsv570141	chr15:77985554-78017361	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv570142	chr15:77993282-78010746	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv570143	chr15:77993282-78017361	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv3311437	chr15:77996541-77997081	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3311436	chr15:77996550-77997061	Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3510235	chr15:77996566-77997051	Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3311435	chr15:77996611-77997045	Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77969200-78007600	Weak transcription	Right Atrium	heart
2	chr15:77992200-77998800	Weak transcription	Brain Angular Gyrus	brain
3	chr15:77992200-77999200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr15:77992200-78002200	Weak transcription	Fetal Brain Male	brain
5	chr15:77994800-78002000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:77995400-78004200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr15:77996800-77997000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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