Variant report

Variant	rs62004270
Chromosome Location	chr15:42294316-42294317
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	chr15:42285666..42287289-chr15:42294090..42296244,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1668555	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1668556	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1668560	0.90[ASN][1000 genomes]
rs1668561	0.92[ASN][1000 genomes]
rs1668567	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1668580	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1668581	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1668582	0.95[ASN][1000 genomes]
rs1668583	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1668584	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1704353	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1704359	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1704362	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1704366	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1704367	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1704373	0.92[ASN][1000 genomes]
rs1704376	0.92[ASN][1000 genomes]
rs1823552	0.80[ASN][1000 genomes]
rs2598465	0.90[ASN][1000 genomes]
rs2598466	0.80[ASN][1000 genomes]
rs2598467	0.80[ASN][1000 genomes]
rs2665200	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2665202	0.90[ASN][1000 genomes]
rs2665203	0.87[ASN][1000 genomes]
rs2665207	0.80[ASN][1000 genomes]
rs2665210	0.80[ASN][1000 genomes]
rs2665211	0.80[ASN][1000 genomes]
rs2724935	0.90[ASN][1000 genomes]
rs2724937	0.87[ASN][1000 genomes]
rs2724939	0.87[ASN][1000 genomes]
rs2724940	0.87[ASN][1000 genomes]
rs2724944	0.80[ASN][1000 genomes]
rs2724945	0.80[ASN][1000 genomes]
rs34595238	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs35670495	0.87[ASN][1000 genomes]
rs937991	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs937992	0.95[ASN][1000 genomes]
rs937993	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931223	chr15:41989960-42781757	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
2	nsv427958	chr15:42051317-42301283	Strong transcription Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv1035998	chr15:42098896-42434254	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
4	nsv1038933	chr15:42138456-42309087	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
5	nsv529687	chr15:42157320-42621682	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
6	nsv1054728	chr15:42177772-42310009	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
7	nsv1049445	chr15:42239738-42830484	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
8	nsv542366	chr15:42239738-42830484	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42273000-42301800	Weak transcription	Fetal Intestine Small	intestine
2	chr15:42273800-42301800	Weak transcription	Esophagus	oesophagus
3	chr15:42288200-42303400	Weak transcription	Pancreas	Pancrea
4	chr15:42289400-42297400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:42290200-42294800	Weak transcription	Right Ventricle	heart
6	chr15:42290400-42310400	Weak transcription	Right Atrium	heart

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