Variant report

Variant	rs570367684
Chromosome Location	chr14:77722391-77722392
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431017	chr14:76938089-77854647	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
2	nsv832834	chr14:77554987-77724357	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv1361	chr14:77707417-77753024	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
4	nsv902104	chr14:77720741-77756321	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
5	esv3372720	chr14:77722362-77722587	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77697600-77726800	Weak transcription	Brain Substantia Nigra	brain
2	chr14:77709800-77729600	Weak transcription	Fetal Brain Male	brain
3	chr14:77711200-77731000	Weak transcription	Spleen	Spleen
4	chr14:77713200-77726800	Weak transcription	Brain Cingulate Gyrus	brain
5	chr14:77714000-77723400	Weak transcription	Fetal Intestine Large	intestine
6	chr14:77716200-77724200	Weak transcription	Brain Angular Gyrus	brain
7	chr14:77718400-77726800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr14:77720000-77724600	Weak transcription	Fetal Intestine Small	intestine
9	chr14:77720400-77724000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:77720600-77725000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr14:77720800-77723400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr14:77720800-77724600	Weak transcription	Brain Germinal Matrix	brain
13	chr14:77720800-77725600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr14:77720800-77725800	Weak transcription	Esophagus	oesophagus
15	chr14:77720800-77726800	Weak transcription	Brain Anterior Caudate	brain
16	chr14:77720800-77727000	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr14:77721800-77725000	Strong transcription	Fetal Brain Female	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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