Variant report

Variant	rs1435529
Chromosome Location	chr7:12237733-12237734
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	chr7:12237104..12239270-chr7:12329420..12331412,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12531818	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12531845	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12531860	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12538086	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13340498	0.91[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs13340544	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17165715	1.00[EUR][1000 genomes]
rs6960846	0.86[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs6977864	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6978367	0.91[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs6978546	0.86[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs6978768	0.86[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs6978857	0.91[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6978877	0.91[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6979046	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6979124	0.91[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7780083	0.91[AFR][1000 genomes]
rs7780093	0.91[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7780477	0.91[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7781919	0.91[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7799209	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799220	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799372	0.88[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs967125	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs967126	0.91[AFR][1000 genomes];0.92[ASN][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	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv1023608	chr7:12064114-12247520	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv534432	chr7:12148960-12693032	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1021710	chr7:12164993-12251790	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
5	nsv1024554	chr7:12214722-12967418	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
6	nsv538735	chr7:12214722-12967418	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers 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	58 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	chr7:12228400-12238600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:12236800-12239800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr7:12237000-12239600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:12237000-12239800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:12237600-12238600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr7:12237600-12238800	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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