Variant report

Variant	rs191790455
Chromosome Location	chr11:105723458-105723459
allele	C/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	nsv832257	chr11:105662753-105817576	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv1825856	chr11:105672706-105775768	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv1825993	chr11:105698982-105762601	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2520318	chr11:105722956-105724455	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv9295	chr11:105723286-105724052	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv2000018	chr11:105723314-105724001	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3466108	chr11:105723347-105723931	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3496916	chr11:105723362-105723904	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3496915	chr11:105723392-105723934	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3466086	chr11:105723403-105723897	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3496917	chr11:105723406-105723862	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
12	esv3466097	chr11:105723410-105723897	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3466075	chr11:105723425-105723851	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	esv3496920	chr11:105723437-105723873	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105705200-105764600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr11:105716200-105728400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr11:105716400-105728000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr11:105723000-105723600	Enhancers	Fetal Lung	lung

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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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