Variant report

Variant	rs73589795
Chromosome Location	chr6:161904184-161904185
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16892585	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16892615	0.94[AFR][1000 genomes]
rs55868193	1.00[AMR][1000 genomes]
rs73589786	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73589790	1.00[AMR][1000 genomes]
rs73589792	1.00[AMR][1000 genomes]
rs73589798	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73589800	1.00[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	nsv481931	chr6:161647026-161961906	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv1031234	chr6:161676768-162250726	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv886819	chr6:161712035-162520133	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv886820	chr6:161712880-162184932	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv830854	chr6:161739926-161927515	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv518931	chr6:161793319-162406335	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv481861	chr6:161802883-162160197	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv481981	chr6:161829077-162215745	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1033603	chr6:161844266-162001436	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv481750	chr6:161850976-161996586	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv481932	chr6:161862158-162097499	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv886822	chr6:161891388-161958898	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv886823	chr6:161891388-161971398	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv886824	chr6:161891388-161982988	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv886825	chr6:161891388-162184932	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161898000-161905600	Weak transcription	Pancreas	Pancrea
2	chr6:161898200-161910800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:161898800-161906400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:161900800-161904600	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr6:161900800-161905000	Enhancers	Adipose Nuclei	Adipose
6	chr6:161901200-161908000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:161901200-161914600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:161901600-161904200	Enhancers	Brain Anterior Caudate	brain
9	chr6:161901600-161904800	Enhancers	Fetal Kidney	kidney
10	chr6:161902200-161908000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:161902200-161908000	Weak transcription	Right Atrium	heart
12	chr6:161902600-161915200	Weak transcription	Psoas Muscle	Psoas
13	chr6:161902800-161904400	Enhancers	Brain Hippocampus Middle	brain
14	chr6:161902800-161905000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr6:161903200-161904200	Enhancers	Liver	Liver
16	chr6:161903200-161904200	Enhancers	Brain Substantia Nigra	brain
17	chr6:161903400-161904200	Enhancers	Brain Cingulate Gyrus	brain
18	chr6:161903400-161904400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr6:161903400-161904400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr6:161903400-161904600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:161903800-161904200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr6:161903800-161904600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr6:161903800-161907200	Weak transcription	A549	lung
24	chr6:161903800-161908000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr6:161904000-161904200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:161904000-161904400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr6:161904000-161904400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr6:161904000-161904400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr6:161904000-161904800	Active TSS	Fetal Brain Male	brain
30	chr6:161904000-161907200	Weak transcription	Muscle Satellite Cultured Cells	--

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