Variant report

Variant	rs560897465
Chromosome Location	chr5:44876305-44876306
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027897	chr5:44695278-45061623	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
2	nsv881564	chr5:44783255-44914579	Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv880397	chr5:44800665-44939293	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
4	nsv880483	chr5:44827292-45038026	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv462129	chr5:44876288-44916789	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
6	nsv597935	chr5:44876288-44916789	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:44875000-44876400	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr5:44875000-44876400	Enhancers	HUVEC	blood vessel
3	chr5:44875000-44877000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr5:44875200-44876600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:44875800-44876400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:44875800-44876400	Flanking Active TSS	Hela-S3	cervix
7	chr5:44876000-44876400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr5:44876000-44876400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr5:44876000-44876400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr5:44876000-44876400	Flanking Active TSS	NH-A	brain
11	chr5:44876000-44876600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:44876000-44876600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:44876000-44877200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr5:44876200-44876600	Enhancers	A549	lung
15	chr5:44876200-44876600	ZNF genes & repeats	GM12878-XiMat	blood
16	chr5:44876200-44877000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:44876200-44877200	Enhancers	HMEC	breast
18	chr5:44876200-44877400	Enhancers	NHEK	skin

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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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