Variant report

Variant	rs111827331
Chromosome Location	chr8:67671387-67671388
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv831346	chr8:67486555-67675324	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1026746	chr8:67639626-67794164	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv971317	chr8:67671241-67680064	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67652200-67672400	Weak transcription	Fetal Intestine Small	intestine
2	chr8:67656400-67679000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr8:67661000-67673400	Weak transcription	Brain Hippocampus Middle	brain
4	chr8:67664600-67686400	Weak transcription	Right Atrium	heart
5	chr8:67665000-67671600	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr8:67665800-67673000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr8:67666000-67673200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:67668600-67672800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr8:67670400-67671800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr8:67670800-67671400	Enhancers	Brain Cingulate Gyrus	brain
11	chr8:67671000-67671600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr8:67671200-67671600	Weak transcription	Brain Substantia Nigra	brain
13	chr8:67671200-67682800	Weak transcription	Brain Anterior Caudate	brain

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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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