Variant report

Variant	rs17084104
Chromosome Location	chr6:153761404-153761405
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10485215	0.95[ASN][1000 genomes]
rs10485216	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11752411	0.96[ASN][1000 genomes]
rs11757575	0.96[ASN][1000 genomes]
rs11757608	0.95[ASN][1000 genomes]
rs12526771	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2125636	0.96[ASN][1000 genomes]
rs34496708	0.96[ASN][1000 genomes]
rs35073837	0.96[ASN][1000 genomes]
rs35249387	0.96[ASN][1000 genomes]
rs35969076	0.96[ASN][1000 genomes]
rs4870196	0.96[ASN][1000 genomes]
rs4870201	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs503414	0.83[ASN][1000 genomes]
rs59067214	0.93[ASN][1000 genomes]
rs6557290	0.96[ASN][1000 genomes]
rs6557291	0.96[ASN][1000 genomes]
rs6557292	0.96[ASN][1000 genomes]
rs6557293	0.96[ASN][1000 genomes]
rs6941385	0.94[ASN][1000 genomes]
rs73016408	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73018433	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs791433	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916080	chr6:153650242-153881059	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv915884	chr6:153717053-153979225	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3529752	chr6:153733306-154425819	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	esv3529753	chr6:153733306-154425819	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv886777	chr6:153748334-153798384	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv886778	chr6:153748334-153801170	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv886779	chr6:153748334-153804853	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv886780	chr6:153748334-153822736	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv886781	chr6:153748334-153844303	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv604915	chr6:153753285-153830536	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv886782	chr6:153757736-153855165	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:153758000-153764000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr6:153758000-153764200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:153759200-153761600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr6:153759200-153762600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr6:153759200-153762800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr6:153760600-153762600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr6:153760800-153762800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr6:153761200-153761600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr6:153761200-153761800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr6:153761400-153761600	Enhancers	H9 Cell Line	embryonic stem cell
11	chr6:153761400-153762000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:153761400-153762000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr6:153761400-153763200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr6:153761400-153764800	Enhancers	HUES64 Cell Line	embryonic stem cell

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