Variant report

Variant	rs60793757
Chromosome Location	chr6:34475576-34475577
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	chr6:34475212..34479816-chr6:34480006..34482829,5	K562	blood:

Variant related genes	Relation type
ENSG00000124507	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs12660150	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12660470	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12661696	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12663061	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1409284	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1886980	1.00[EUR][1000 genomes]
rs2395596	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34603400	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3778069	1.00[EUR][1000 genomes]
rs3778071	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3778075	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3798546	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3798549	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3800468	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3800471	0.83[ASN][1000 genomes]
rs3822986	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3945698	1.00[EUR][1000 genomes]
rs55660517	1.00[EUR][1000 genomes]
rs56781192	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58067963	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58218720	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58741004	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59738570	1.00[EUR][1000 genomes]
rs60375159	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61453687	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7763757	1.00[EUR][1000 genomes]
rs913017	1.00[EUR][1000 genomes]
rs9791348	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022844	chr6:34317219-35060519	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv538195	chr6:34317219-35060519	Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv2758046	chr6:34382492-34714677	Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	esv2759418	chr6:34382492-34714677	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv885785	chr6:34404636-34874002	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv462904	chr6:34416388-34493012	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
7	nsv602903	chr6:34416388-34493012	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
8	nsv885786	chr6:34426884-34542662	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
9	esv1813536	chr6:34455242-34545123	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
10	nsv885787	chr6:34458533-34546560	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
11	nsv885788	chr6:34464010-34551912	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
12	nsv1033583	chr6:34471572-34828372	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats 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	38 gene(s)	inside rSNPs	diseases
13	nsv885789	chr6:34474939-34546560	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34441400-34494000	Weak transcription	Right Atrium	heart
2	chr6:34474600-34475600	Enhancers	K562	blood
3	chr6:34474800-34479600	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr6:34474800-34481400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr6:34474800-34481600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:34475000-34479800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr6:34475200-34479600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr6:34475200-34480400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr6:34475200-34480600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr6:34475200-34480800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:34475400-34475600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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