Variant report

Variant	rs35607692
Chromosome Location	chr12:121542027-121542028
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	chr12:121540942..121542575-chr12:121550109..121552835,2	K562	blood:

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs12810503	0.87[AMR][1000 genomes]
rs12813980	0.87[AMR][1000 genomes]
rs12814235	0.87[AMR][1000 genomes]
rs12816966	0.87[AMR][1000 genomes]
rs12817169	0.84[AMR][1000 genomes]
rs12819523	0.87[AMR][1000 genomes]
rs12819930	0.84[AMR][1000 genomes]
rs12820593	0.87[AMR][1000 genomes]
rs12824585	0.87[AMR][1000 genomes]
rs12830584	0.87[AMR][1000 genomes]
rs12832396	0.87[AMR][1000 genomes]
rs1718153	0.80[AMR][1000 genomes]
rs17432871	0.87[AMR][1000 genomes]
rs17434640	0.87[AMR][1000 genomes]
rs17525809	0.84[AMR][1000 genomes]
rs2260138	0.80[AMR][1000 genomes]
rs28969465	0.87[AMR][1000 genomes]
rs28969469	0.87[AMR][1000 genomes]
rs34185850	0.87[AMR][1000 genomes]
rs34325588	0.87[AMR][1000 genomes]
rs34480856	0.87[AMR][1000 genomes]
rs34811727	0.87[AMR][1000 genomes]
rs34934130	0.87[AMR][1000 genomes]
rs35018823	0.80[AMR][1000 genomes]
rs35076950	0.87[AMR][1000 genomes]
rs35237790	0.87[AMR][1000 genomes]
rs35362296	0.87[AMR][1000 genomes]
rs35455367	0.87[AMR][1000 genomes]
rs35579189	0.80[AMR][1000 genomes]
rs35605477	0.87[AMR][1000 genomes]
rs35869834	0.87[AMR][1000 genomes]
rs35940217	0.87[AMR][1000 genomes]
rs494986	0.84[AMR][1000 genomes]
rs513113	0.80[AMR][1000 genomes]
rs514109	0.80[AMR][1000 genomes]
rs585847	0.80[AMR][1000 genomes]
rs588130	0.80[AMR][1000 genomes]
rs588510	0.80[AMR][1000 genomes]
rs588573	0.80[AMR][1000 genomes]
rs599785	0.80[AMR][1000 genomes]
rs603891	0.80[AMR][1000 genomes]
rs618201	0.80[AMR][1000 genomes]
rs657172	0.84[AMR][1000 genomes]
rs66570654	0.87[AMR][1000 genomes]
rs66811517	0.87[AMR][1000 genomes]
rs67691679	0.87[AMR][1000 genomes]
rs67739439	0.87[AMR][1000 genomes]
rs67881993	0.95[AMR][1000 genomes]
rs67898046	0.87[AMR][1000 genomes]
rs71454676	0.84[AMR][1000 genomes]
rs71454679	0.87[AMR][1000 genomes]
rs71454680	0.87[AMR][1000 genomes]
rs73214191	0.87[AMR][1000 genomes]
rs73214199	0.87[AMR][1000 genomes]
rs73216114	0.87[AMR][1000 genomes]
rs73218241	0.87[AMR][1000 genomes]
rs934353	0.80[AMR][1000 genomes]
rs934354	0.80[AMR][1000 genomes]
rs934355	0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521928	chr12:121041728-121761800	Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	nsv899559	chr12:121324727-121592689	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv899560	chr12:121371233-121560581	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers 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 target site	23 gene(s)	inside rSNPs	diseases
4	nsv899562	chr12:121376416-121565870	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	esv2758318	chr12:121415845-121584813	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	esv2759917	chr12:121415845-121584813	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	nsv832531	chr12:121440495-121604232	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv560454	chr12:121457073-121745742	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
9	nsv430537	chr12:121487632-121579955	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv1054878	chr12:121519880-121761800	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
11	nsv455729	chr12:121525591-121761800	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
12	nsv560455	chr12:121525591-121761800	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
13	esv3498663	chr12:121535725-121542472	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	esv3498674	chr12:121535832-121542370	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	nsv973130	chr12:121541847-121547563	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121534000-121545200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:121541800-121542200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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