Variant report

Variant	rs190915192
Chromosome Location	chr14:72266145-72266146
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3398985	chr14:71927884-72404676	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1047559	chr14:72151736-72282151	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1342	chr14:72260578-72305563	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72265000-72268200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr14:72265200-72267200	Enhancers	Fetal Stomach	stomach
3	chr14:72265400-72266200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr14:72265400-72266200	Enhancers	Lung	lung
5	chr14:72265400-72266200	Enhancers	Spleen	Spleen
6	chr14:72265800-72266200	Enhancers	Placenta	Placenta
7	chr14:72265800-72266600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr14:72265800-72267000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr14:72266000-72266200	Enhancers	A549	lung
10	chr14:72266000-72266200	Enhancers	NHLF	lung
11	chr14:72266000-72266400	Enhancers	Colon Smooth Muscle	Colon
12	chr14:72266000-72266600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr14:72266000-72266800	Enhancers	Brain Hippocampus Middle	brain
14	chr14:72266000-72267000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr14:72266000-72270200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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