Variant report

Variant	rs10444872
Chromosome Location	chr15:93072232-93072233
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11856532	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12148722	0.90[EUR][1000 genomes]
rs12904001	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12905243	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12905251	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12906057	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12907344	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12912164	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12916155	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17522532	0.86[AFR][1000 genomes]
rs17600892	0.86[AFR][1000 genomes]
rs34054075	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34315625	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34449011	0.88[AMR][1000 genomes]
rs34864143	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4778001	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs74031607	0.83[AFR][1000 genomes]
rs9646231	0.86[AFR][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	nsv948621	chr15:92688981-93158095	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1049561	chr15:92758434-93097965	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1037972	chr15:92804908-93270761	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
4	nsv904499	chr15:92914795-93472582	Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	163 gene(s)	inside rSNPs	diseases
5	esv2751542	chr15:93053681-93091815	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv948738	chr15:93070742-93728147	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:93067800-93072400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:93069800-93073800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
3	chr15:93070600-93072800	Enhancers	HSMM	muscle
4	chr15:93071400-93073600	Weak transcription	Gastric	stomach
5	chr15:93072200-93072600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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