Variant report

Variant	rs62445887
Chromosome Location	chr7:21925417-21925418
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10238697	0.92[EUR][1000 genomes]
rs6958820	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6976590	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73279884	0.92[EUR][1000 genomes]
rs73279886	1.00[EUR][1000 genomes]
rs73281732	0.92[EUR][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	nsv1018133	chr7:21740118-22055283	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv830922	chr7:21793386-21964675	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv1027453	chr7:21918474-21982448	Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:21907400-21937200	Weak transcription	Fetal Thymus	thymus
2	chr7:21908400-21936600	Weak transcription	Primary T cells from cord blood	blood
3	chr7:21910000-21939400	Weak transcription	Left Ventricle	heart
4	chr7:21911200-21938400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr7:21916400-21933800	Weak transcription	Thymus	Thymus
6	chr7:21916800-21927400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr7:21916800-21935000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr7:21916800-21936600	Weak transcription	Primary B cells from cord blood	blood
9	chr7:21917000-21925600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr7:21917000-21936600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr7:21917000-21938400	Weak transcription	Fetal Intestine Small	intestine
12	chr7:21917800-21926400	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr7:21922000-21926400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr7:21923000-21937800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr7:21923200-21938600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr7:21924000-21937600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr7:21924400-21937800	Weak transcription	NHEK	skin
18	chr7:21924400-21945400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:21924800-21936400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:21925000-21928200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:21925200-21926400	Enhancers	Fetal Heart	heart
22	chr7:21925400-21928000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr7:21925400-21928200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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