Variant report

Variant	rs138046634
Chromosome Location	chr2:212771437-212771438
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv834525	chr2:212693190-212860356	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv584323	chr2:212731514-212783175	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv584324	chr2:212766614-212773932	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv584325	chr2:212768779-212772954	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv584326	chr2:212768779-212773495	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv584327	chr2:212768779-212773569	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
8	esv1848923	chr2:212768779-212774540	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
9	esv1847998	chr2:212768779-212774751	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
10	esv1851182	chr2:212768779-212774751	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
11	esv3459090	chr2:212771110-212775328	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
12	esv3459091	chr2:212771155-212775274	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
13	esv3459093	chr2:212771183-212775353	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
14	esv3459092	chr2:212771225-212775161	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
15	esv3459094	chr2:212771225-212775161	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212766400-212771600	Weak transcription	Brain Anterior Caudate	brain
2	chr2:212769200-212772000	Weak transcription	Fetal Heart	heart
3	chr2:212771400-212771800	Enhancers	Brain Substantia Nigra	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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