Variant report

Variant	rs59901297
Chromosome Location	chr21:15465633-15465634
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12482507	0.80[ASN][1000 genomes]
rs12627691	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2226730	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2822397	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4816227	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4816961	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56812774	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58025195	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58841158	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59808785	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67981257	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73151515	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73151533	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73338200	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73340110	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8131959	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8133169	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][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	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	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
6	nsv1056787	chr21:15407504-15530291	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv1831533	chr21:15442382-15477876	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	n/a
8	esv1827667	chr21:15442582-15521121	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv1827538	chr21:15446711-15472381	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	inside rSNPs	n/a
10	esv990249	chr21:15446864-15471276	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
11	esv1830377	chr21:15446911-15477676	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	inside rSNPs	n/a
12	esv1830288	chr21:15448891-15474325	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	inside rSNPs	n/a
13	esv32571	chr21:15456265-15467954	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15441000-15470200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr21:15444200-15475400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr21:15455800-15479800	Weak transcription	Colon Smooth Muscle	Colon
4	chr21:15456000-15470000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr21:15456800-15470200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr21:15457000-15467600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr21:15457600-15465800	Weak transcription	Hela-S3	cervix
8	chr21:15457600-15470000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr21:15457600-15470200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr21:15457600-15470200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr21:15457600-15470200	Weak transcription	Adipose Nuclei	Adipose
12	chr21:15457600-15470200	Weak transcription	Esophagus	oesophagus
13	chr21:15457600-15472800	Weak transcription	Fetal Muscle Leg	muscle
14	chr21:15457600-15473800	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr21:15457600-15487400	Weak transcription	Fetal Brain Male	brain
16	chr21:15457800-15467800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr21:15457800-15486200	Weak transcription	Thymus	Thymus
18	chr21:15458000-15466000	Weak transcription	Fetal Intestine Small	intestine
19	chr21:15459200-15466000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr21:15459600-15469000	Weak transcription	Brain Germinal Matrix	brain
21	chr21:15459800-15470200	Weak transcription	Ovary	ovary
22	chr21:15460000-15470200	Weak transcription	Fetal Lung	lung
23	chr21:15460200-15467400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr21:15461000-15470200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr21:15462200-15465800	Strong transcription	Dnd41	blood
26	chr21:15462400-15471400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr21:15463000-15465800	ZNF genes & repeats	GM12878-XiMat	blood
28	chr21:15463200-15470200	Weak transcription	Stomach Smooth Muscle	stomach
29	chr21:15463200-15472200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr21:15463400-15470200	Weak transcription	Gastric	stomach
31	chr21:15463800-15465800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr21:15464200-15468000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr21:15464400-15470200	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr21:15464600-15466000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr21:15464600-15467400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr21:15464600-15469800	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr21:15464600-15470000	Weak transcription	Fetal Brain Female	brain
38	chr21:15464600-15470200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr21:15464800-15466200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr21:15464800-15466200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr21:15464800-15470200	Weak transcription	K562	blood
42	chr21:15465200-15465800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr21:15465200-15465800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr21:15465400-15465800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr21:15465400-15465800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr21:15465400-15466000	ZNF genes & repeats	Fetal Stomach	stomach
47	chr21:15465400-15466200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr21:15465600-15465800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr21:15465600-15467600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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