Variant report

Variant	rs574383285
Chromosome Location	chr2:11824370-11824371
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv1003899	chr2:11789374-12248081	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
4	nsv469449	chr2:11808654-11854012	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv580972	chr2:11808654-11854012	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv527025	chr2:11823585-11833459	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11818000-11828200	Weak transcription	Right Atrium	heart
2	chr2:11818400-11828400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr2:11818400-11828400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr2:11820800-11824400	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr2:11821400-11825600	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr2:11821400-11827800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr2:11822600-11828200	Weak transcription	Pancreas	Pancrea
8	chr2:11822800-11827600	Weak transcription	Hela-S3	cervix
9	chr2:11823000-11828200	Weak transcription	Psoas Muscle	Psoas
10	chr2:11823600-11824400	Enhancers	Brain Cingulate Gyrus	brain
11	chr2:11823600-11826800	Enhancers	Ovary	ovary
12	chr2:11823800-11824400	Enhancers	Brain Substantia Nigra	brain
13	chr2:11824000-11824400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr2:11824200-11824400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:11824200-11824400	Enhancers	Brain Angular Gyrus	brain
16	chr2:11824200-11824400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
17	chr2:11824200-11827800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr2:11824200-11828200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr2:11824200-11828200	Weak transcription	Brain Anterior Caudate	brain

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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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