Variant report

Variant	rs528631509
Chromosome Location	chr14:82123765-82123766
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047694	chr14:81831147-82534026	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv542145	chr14:81831147-82534026	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv565299	chr14:81983027-82586324	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1052666	chr14:82069162-83028382	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv902121	chr14:82075469-82146538	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1375	chr14:82116362-82138158	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1037114	chr14:82123315-82241676	Bivalent Enhancer Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:82121800-82123800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr14:82121800-82124800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr14:82122000-82124000	Enhancers	Brain Cingulate Gyrus	brain
4	chr14:82122200-82124600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr14:82122200-82124800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr14:82122400-82124600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr14:82122600-82124800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr14:82123200-82123800	Enhancers	Brain Substantia Nigra	brain
9	chr14:82123200-82126200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr14:82123400-82124000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr14:82123400-82124400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr14:82123400-82124800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr14:82123600-82124400	Enhancers	Brain Germinal Matrix	brain
14	chr14:82123600-82124400	Enhancers	Brain Hippocampus Middle	brain
15	chr14:82123600-82124400	Weak transcription	Ovary	ovary
16	chr14:82123600-82124800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr14:82123600-82124800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr14:82123600-82126200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr14:82123600-82128600	Weak transcription	Aorta	Aorta

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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