Variant report

Variant	rs10873222
Chromosome Location	chr14:70370038-70370039
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1079903	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11158823	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12100496	0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1275848	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2766463	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4899322	0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7145070	0.81[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	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
3	nsv832824	chr14:70320639-70511401	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70364000-70370600	Weak transcription	HepG2	liver
2	chr14:70364000-70387600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:70367600-70370600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:70368600-70377400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr14:70368800-70371000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr14:70368800-70371000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr14:70368800-70379400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr14:70368800-70379600	Weak transcription	Liver	Liver
9	chr14:70369000-70375800	Weak transcription	Brain Hippocampus Middle	brain
10	chr14:70369200-70370600	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr14:70369200-70370600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr14:70369200-70370600	Weak transcription	Brain Substantia Nigra	brain
13	chr14:70369200-70376600	Weak transcription	Brain Cingulate Gyrus	brain
14	chr14:70369400-70370600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr14:70369400-70370800	Weak transcription	Hela-S3	cervix
16	chr14:70369600-70370400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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