Variant report

Variant	rs537278107
Chromosome Location	chr6:166719856-166719857
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886934	chr6:166642850-166747572	Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv886935	chr6:166704744-166726566	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv886936	chr6:166714024-166731289	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv3356004	chr6:166719787-166722335	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv823927	chr6:166719837-166722561	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166717000-166720200	Weak transcription	Pancreas	Pancrea
2	chr6:166718800-166722600	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr6:166719000-166720000	Bivalent Enhancer	Fetal Intestine Small	intestine
4	chr6:166719000-166720200	Bivalent Enhancer	Fetal Intestine Large	intestine
5	chr6:166719200-166720000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr6:166719200-166720000	Enhancers	GM12878-XiMat	blood
7	chr6:166719200-166722400	Active TSS	Brain Substantia Nigra	brain
8	chr6:166719400-166720200	Active TSS	Brain Anterior Caudate	brain
9	chr6:166719400-166720200	Active TSS	Brain Hippocampus Middle	brain
10	chr6:166719400-166720200	Bivalent Enhancer	HepG2	liver
11	chr6:166719400-166720400	Bivalent Enhancer	Adipose Nuclei	Adipose
12	chr6:166719400-166720400	Bivalent/Poised TSS	Brain Angular Gyrus	brain
13	chr6:166719400-166720400	Active TSS	Brain Inferior Temporal Lobe	brain
14	chr6:166719400-166722400	Active TSS	Brain Cingulate Gyrus	brain
15	chr6:166719800-166720600	Enhancers	Liver	Liver
16	chr6:166719800-166720800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
17	chr6:166719800-166722400	Bivalent Enhancer	Fetal Brain Male	brain

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