Variant report

Variant	rs7277524
Chromosome Location	chr21:27942187-27942188
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs13433431	0.96[YRI][hapmap]
rs13433470	0.90[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1543775	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1893573	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2135305	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2830275	0.80[YRI][hapmap];0.83[AMR][1000 genomes]
rs2830280	0.87[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2830282	1.00[AMR][1000 genomes]
rs2830295	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2830296	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2830298	1.00[AMR][1000 genomes]
rs2830299	1.00[AMR][1000 genomes]
rs2830300	1.00[AMR][1000 genomes]
rs2830301	1.00[AMR][1000 genomes]
rs28401356	1.00[AMR][1000 genomes]
rs28525622	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28572488	0.83[AMR][1000 genomes]
rs28624518	0.83[AMR][1000 genomes]
rs28678819	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57821067	1.00[AMR][1000 genomes]
rs7283190	0.90[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73351185	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73351190	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73353008	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8127446	0.83[AMR][1000 genomes]
rs8128689	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8129932	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8129933	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8130654	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8133538	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs9974221	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9975467	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9975732	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs9978127	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9979986	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9980194	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9980419	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9984233	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs9984431	0.89[AFR][1000 genomes]
rs9989934	1.00[AFR][1000 genomes];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	nsv1056506	chr21:27332898-28049880	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv544412	chr21:27332898-28049880	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv587335	chr21:27715263-27955385	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv544413	chr21:27942060-28065995	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:27886200-27944200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr21:27912600-27942600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr21:27914600-27944200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr21:27923000-27944200	Weak transcription	Fetal Stomach	stomach
5	chr21:27923200-27944200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr21:27923400-27944800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr21:27929000-27944800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr21:27930200-27942600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr21:27931400-27943000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr21:27931400-27944400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr21:27931600-27944400	Weak transcription	Left Ventricle	heart
12	chr21:27933200-27942400	Weak transcription	Right Atrium	heart
13	chr21:27933200-27945000	Weak transcription	Spleen	Spleen
14	chr21:27934000-27944400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr21:27934200-27943200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr21:27935200-27944800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr21:27938000-27942200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr21:27938000-27942200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr21:27938200-27942400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr21:27938200-27942400	Weak transcription	Fetal Kidney	kidney
21	chr21:27938200-27943200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr21:27938600-27942400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr21:27938600-27942800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr21:27938800-27942200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr21:27938800-27942400	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr21:27938800-27942400	Weak transcription	Fetal Lung	lung
27	chr21:27938800-27942600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr21:27938800-27943600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr21:27939000-27942400	Weak transcription	Primary hematopoietic stem cells	blood
30	chr21:27939200-27942200	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr21:27939200-27942600	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr21:27939200-27944400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr21:27940800-27943200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr21:27941800-27942200	Enhancers	HUVEC	blood vessel
35	chr21:27942000-27942400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr21:27942000-27944400	Active TSS	Adipose Nuclei	Adipose

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