Variant report

Variant	rs201628853
Chromosome Location	chr3:34892113-34892114
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834654	chr3:34747802-34916657	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv834655	chr3:34752929-34898824	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3415700	chr3:34806371-34914306	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv432407	chr3:34869616-34898125	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv3330911	chr3:34891649-34892508	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv2219743	chr3:34891802-34892289	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
7	esv3417006	chr3:34891863-34892201	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
8	esv3496370	chr3:34891898-34892160	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
9	esv3496371	chr3:34891898-34892160	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
10	esv3413855	chr3:34891922-34892149	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
11	esv3461756	chr3:34891924-34892155	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
12	esv3461757	chr3:34891924-34892155	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
13	nsv236553	chr3:34891992-34892113	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
14	nsv236291	chr3:34892006-34892127	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34885600-34897400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:34886000-34897000	Weak transcription	Fetal Muscle Leg	muscle
3	chr3:34888800-34892600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:34891400-34896200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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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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