Variant report

Variant	rs537095196
Chromosome Location	chr1:191920076-191920077
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UCHL5-7	chr1:191919999-191920464	NONHSAT008526

Extended variants
information (count: 20 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007060	chr1:191577303-192141825	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv548592	chr1:191623693-191936556	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv548593	chr1:191624744-191936556	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv999147	chr1:191633993-191944853	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv428279	chr1:191689246-192014612	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv548610	chr1:191805526-191953675	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv430047	chr1:191811587-192203678	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv872825	chr1:191868441-191975137	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv872826	chr1:191868441-192074894	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	esv1835685	chr1:191913535-191922347	Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	esv3319472	chr1:191914929-191920327	Enhancers	lncRNA	n/a	inside rSNPs	diseases
12	esv1836222	chr1:191916122-191924244	Inactive region	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	esv1840064	chr1:191916122-191924244	Inactive region	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	nsv825809	chr1:191916798-191922222	Inactive region	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
15	nsv825820	chr1:191916798-191922276	Inactive region	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
16	nsv825831	chr1:191916798-191922355	Inactive region	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
17	nsv548627	chr1:191917000-191924244	Inactive region	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
18	esv1812983	chr1:191917000-191953675	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
19	esv1836372	chr1:191917043-191922347	Inactive region	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
20	esv1805300	chr1:191917043-191922833	Inactive region	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links