Variant report

Variant	rs138936780
Chromosome Location	chr1:57050983-57050984
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869295	chr1:56894955-57656562	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv528673	chr1:57048961-57059571	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv945966	chr1:57050677-57051793	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57045400-57051800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:57046200-57051400	Weak transcription	Osteobl	bone
3	chr1:57048000-57056000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:57050200-57052000	Enhancers	NHDF-Ad	bronchial
5	chr1:57050200-57052400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:57050400-57051000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr1:57050400-57051000	Enhancers	Brain Cingulate Gyrus	brain
8	chr1:57050400-57051000	Enhancers	HSMM	muscle
9	chr1:57050400-57052000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr1:57050600-57051000	Weak transcription	A549	lung
11	chr1:57050600-57051600	Weak transcription	NHLF	lung
12	chr1:57050800-57051800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:57050800-57052000	Enhancers	Liver	Liver
14	chr1:57050800-57052200	Enhancers	HepG2	liver

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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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