Variant report

Variant	rs17536734
Chromosome Location	chr21:27904447-27904448
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs17002241	0.93[EUR][1000 genomes]
rs2830267	0.93[EUR][1000 genomes]
rs2830268	1.00[EUR][1000 genomes]
rs2830272	0.93[EUR][1000 genomes]
rs35821450	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:27880600-27911600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr21:27884800-27915400	Weak transcription	Left Ventricle	heart
3	chr21:27886000-27904800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr21:27886000-27905800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr21:27886000-27923000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr21:27886200-27944200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr21:27891200-27905800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr21:27891800-27906600	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr21:27892000-27930400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr21:27893000-27908200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr21:27901800-27931400	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr21:27902000-27916400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr21:27902800-27904800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr21:27903000-27921000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr21:27903400-27932800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr21:27903600-27905400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr21:27903600-27908200	Weak transcription	Primary hematopoietic stem cells	blood
18	chr21:27903800-27905200	Strong transcription	Fetal Lung	lung
19	chr21:27903800-27909000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr21:27904200-27905800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr21:27904200-27906600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr21:27904400-27907400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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