Variant report

Variant	rs632621
Chromosome Location	chr6:161381835-161381836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10945710	1.00[ASN][1000 genomes]
rs1464780	1.00[AMR][1000 genomes]
rs4559074	1.00[AMR][1000 genomes]
rs645718	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6925800	1.00[AMR][1000 genomes]
rs6937526	0.91[AMR][1000 genomes]
rs7738762	1.00[AMR][1000 genomes]
rs7753585	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422347	chr6:161211171-161442377	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1030045	chr6:161359075-161562255	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv886817	chr6:161371621-161846654	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	esv3381361	chr6:161373617-161864101	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161372800-161394000	Weak transcription	Right Atrium	heart
2	chr6:161378200-161386600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:161380000-161382400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:161380000-161382600	Enhancers	Fetal Brain Male	brain
5	chr6:161380200-161382400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:161380200-161382600	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr6:161380200-161382600	Enhancers	Brain Germinal Matrix	brain
8	chr6:161380200-161382600	Enhancers	Pancreas	Pancrea
9	chr6:161380600-161382600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr6:161380600-161382600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:161380800-161382200	Enhancers	Fetal Brain Female	brain
12	chr6:161380800-161382600	Enhancers	Fetal Lung	lung
13	chr6:161381000-161382400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr6:161381200-161382000	Enhancers	Brain Anterior Caudate	brain
15	chr6:161381200-161382200	Enhancers	Brain Hippocampus Middle	brain
16	chr6:161381200-161382600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr6:161381200-161382800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr6:161381600-161382000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr6:161381800-161382200	Enhancers	Brain Angular Gyrus	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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