Variant report

Variant	rs10955307
Chromosome Location	chr8:104127328-104127329
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs12677471	0.82[EUR][1000 genomes]
rs13253566	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs13275878	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831413	chr8:104085141-104269789	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104119000-104127800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr8:104119400-104134000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:104121800-104127800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr8:104122000-104134600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr8:104122400-104131200	Weak transcription	NH-A	brain
6	chr8:104123400-104127800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr8:104123600-104132600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:104123800-104128200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr8:104124200-104127600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr8:104124200-104127800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr8:104126200-104127400	Enhancers	HSMMtube	muscle
12	chr8:104126400-104128000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr8:104126400-104128200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:104126600-104127400	Enhancers	Osteobl	bone
15	chr8:104126600-104132000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr8:104127000-104127400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr8:104127000-104127400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr8:104127200-104132000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte 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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