Variant report

Variant	rs8027297
Chromosome Location	chr15:93042897-93042898
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs2306842	1.00[YRI][hapmap]
rs8026367	1.00[YRI][hapmap]

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	nsv948621	chr15:92688981-93158095	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1049561	chr15:92758434-93097965	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1037972	chr15:92804908-93270761	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
4	nsv904499	chr15:92914795-93472582	Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	163 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:93039200-93043200	Weak transcription	Brain Anterior Caudate	brain
2	chr15:93040000-93045600	Weak transcription	HSMMtube	muscle
3	chr15:93042600-93043200	Enhancers	Brain Germinal Matrix	brain
4	chr15:93042600-93043400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr15:93042600-93044000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
6	chr15:93042600-93044000	Enhancers	Fetal Brain Male	brain
7	chr15:93042600-93044000	Enhancers	Fetal Brain Female	brain
8	chr15:93042600-93044200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr15:93042800-93043200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:93042800-93043600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr15:93042800-93044000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:93042800-93044000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:93042800-93044000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr15:93042800-93044200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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Input of quick search could be:

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

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