Variant report

Variant	rs74828512
Chromosome Location	chr12:105680937-105680938
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899499	chr12:105616297-105722529	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1044450	chr12:105668451-105682822	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv510589	chr12:105670071-105743755	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv3492286	chr12:105680848-105681708	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3511409	chr12:105680886-105681685	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3511412	chr12:105680897-105681633	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3492274	chr12:105680905-105681674	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3656	chr12:105680909-105681748	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3492241	chr12:105680914-105681669	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3492252	chr12:105680917-105681633	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3511410	chr12:105680922-105681649	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3511411	chr12:105680926-105681647	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:105675800-105681200	Weak transcription	Stomach Mucosa	stomach
2	chr12:105676200-105681400	Weak transcription	HepG2	liver
3	chr12:105676400-105681400	Weak transcription	A549	lung

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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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