Variant report

Variant	rs35055383
Chromosome Location	chr6:134154546-134154547
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830812	chr6:133993897-134165407	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv34122	chr6:134089019-134378252	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	esv3435508	chr6:134153809-134155707	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	inside rSNPs	n/a
4	esv2011634	chr6:134154361-134154888	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
5	esv3391009	chr6:134154441-134154776	Weak transcription	n/a	n/a	inside rSNPs	n/a
6	esv3521540	chr6:134154449-134154773	Weak transcription	n/a	n/a	inside rSNPs	n/a
7	esv3521543	chr6:134154468-134154716	Weak transcription	n/a	n/a	inside rSNPs	n/a
8	esv3521542	chr6:134154488-134154724	Weak transcription	n/a	n/a	inside rSNPs	n/a
9	esv3473395	chr6:134154490-134154702	Weak transcription	n/a	n/a	inside rSNPs	n/a
10	esv3473398	chr6:134154490-134154702	Weak transcription	n/a	n/a	inside rSNPs	n/a
11	esv3347244	chr6:134154508-134154694	Weak transcription	n/a	n/a	inside rSNPs	n/a
12	esv3521544	chr6:134154526-134154698	Weak transcription	n/a	n/a	inside rSNPs	n/a
13	esv994787	chr6:134154546-134154673	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134152200-134154800	Weak transcription	Fetal Lung	lung
2	chr6:134152200-134155000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:134152200-134155000	Weak transcription	Ovary	ovary
4	chr6:134152400-134154800	Weak transcription	A549	lung
5	chr6:134152600-134154800	Weak transcription	Fetal Kidney	kidney

Quick Search:

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

what's new

Quick links