Variant report

Variant	rs60821881
Chromosome Location	chr21:15405648-15405649
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs13046630	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13048438	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2525599	0.85[EUR][1000 genomes]
rs2822383	0.85[EUR][1000 genomes]
rs2822384	0.84[EUR][1000 genomes]
rs34338538	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35178815	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35827720	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4611722	0.89[EUR][1000 genomes]
rs6516571	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7364079	0.83[EUR][1000 genomes]
rs8129930	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1058202	chr21:14706767-15628668	Weak transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
2	nsv1067433	chr21:14736298-15507502	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1055396	chr21:14756514-15507502	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS 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 miRNA	32 gene(s)	inside rSNPs	diseases
4	nsv1062639	chr21:14775729-15507502	Enhancers ZNF genes & repeats Strong transcription Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
5	nsv587015	chr21:14957973-15448560	Genic enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
6	nsv1058072	chr21:15372509-15568171	Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs60821881	ANKRD20A18P	cis	Esophagus Mucosa	GTEx

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15400200-15407000	Weak transcription	Ovary	ovary
2	chr21:15400200-15409000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr21:15400400-15407000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr21:15400400-15407200	Weak transcription	Fetal Lung	lung
5	chr21:15400400-15407400	Weak transcription	Thymus	Thymus
6	chr21:15400400-15411000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr21:15400400-15412200	Weak transcription	Fetal Thymus	thymus
8	chr21:15400600-15407000	Weak transcription	Fetal Muscle Leg	muscle
9	chr21:15401000-15410800	Weak transcription	Colon Smooth Muscle	Colon
10	chr21:15401200-15405800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr21:15401200-15406000	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr21:15401200-15408800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr21:15401200-15412000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr21:15401200-15412200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr21:15401200-15414000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr21:15401800-15407200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr21:15401800-15423000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr21:15401800-15452000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr21:15402000-15412200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr21:15402200-15407200	Weak transcription	Stomach Smooth Muscle	stomach
21	chr21:15402600-15407000	Weak transcription	GM12878-XiMat	blood
22	chr21:15402600-15442400	Weak transcription	Dnd41	blood
23	chr21:15402800-15419200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr21:15404600-15406400	Weak transcription	Brain Germinal Matrix	brain
25	chr21:15404600-15407200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr21:15404600-15410000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr21:15405400-15409200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr21:15405400-15415000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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