Variant report

Variant	rs10257437
Chromosome Location	chr7:27065705-27065706
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:27061277-27071265..7:27203007-27207968	H1-hESC	embryonic stem cell:	embryo
2	7:27061277-27071265..7:27238414-27242313	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SKAP2-4	chr7:27065646-27065719	NONHSAT119659

Variant related genes	Relation type
ENSG00000243766	Chromatin interaction
ENSG00000078399	Chromatin interaction
ENSG00000106031	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10081212	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs10242380	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10257464	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10259208	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10267689	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1082312	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1082315	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11974418	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11977871	0.82[CEU][hapmap]
rs12700785	0.82[CEU][hapmap]
rs13221446	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17500459	0.86[AMR][1000 genomes]
rs1874924	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs213515	0.93[CEU][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs213516	0.82[CEU][hapmap]
rs213518	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs213521	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs213536	0.87[CEU][hapmap]
rs2140998	0.93[CEU][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2693661	0.82[CEU][hapmap]
rs2936423	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34889704	0.87[AMR][1000 genomes]
rs591895	0.87[CEU][hapmap]
rs6461982	0.86[AMR][1000 genomes]
rs659131	0.87[CEU][hapmap]
rs6974705	0.92[AMR][1000 genomes]
rs774246	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs774247	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs774252	1.00[CEU][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs774253	0.82[CEU][hapmap]
rs774257	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs774258	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs774260	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs774261	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs774262	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs774265	0.93[CEU][hapmap];0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs774268	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7776505	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7791056	1.00[CEU][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7797624	0.86[AMR][1000 genomes]
rs954051	0.87[CEU][hapmap]

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	nsv1025538	chr7:26482342-27376045	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
2	nsv538805	chr7:26482342-27376045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
3	nsv1018709	chr7:26990384-27216552	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
4	nsv538806	chr7:26990384-27216552	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
5	nsv966768	chr7:27063598-27066773	Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10257437	HOXA2	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27065200-27070200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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