Variant report

Variant	rs577457455
Chromosome Location	chr9:97464059-97464060
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893596	chr9:97321172-97598966	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1041922	chr9:97444976-97536753	Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv3502975	chr9:97461331-97466629	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3502973	chr9:97461395-97465947	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3405746	chr9:97461831-97466479	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3483152	chr9:97462401-97465687	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3483153	chr9:97462402-97465659	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3349687	chr9:97462414-97465642	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3502978	chr9:97462432-97465622	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3502976	chr9:97462449-97465560	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3502977	chr9:97462482-97465561	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3502972	chr9:97462525-97465513	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3483154	chr9:97462532-97465506	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3502979	chr9:97462532-97465506	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv10242	chr9:97462576-97464526	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv517074	chr9:97463435-97464381	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97457400-97465800	Weak transcription	Fetal Stomach	stomach
2	chr9:97460800-97465400	Weak transcription	Fetal Intestine Small	intestine
3	chr9:97461000-97465400	Weak transcription	Fetal Intestine Large	intestine
4	chr9:97461000-97465800	Weak transcription	Fetal Lung	lung
5	chr9:97461200-97465400	Weak transcription	HepG2	liver
6	chr9:97461200-97465800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr9:97463600-97467200	Weak transcription	Placenta	Placenta

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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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