Variant report

Variant	rs369728362
Chromosome Location	chr1:150700750-150700751
allele	C/T
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	nsv1006838	chr1:150440214-150722783	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
2	esv2829859	chr1:150608894-150937329	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv872417	chr1:150618632-150759979	Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv872418	chr1:150683512-150860471	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv872419	chr1:150699199-150738759	Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	esv3442070	chr1:150700278-150703526	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3397469	chr1:150700353-150703301	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150670600-150702600	Weak transcription	Hela-S3	cervix
2	chr1:150681600-150702600	Weak transcription	A549	lung
3	chr1:150690800-150702400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr1:150695000-150702600	Weak transcription	Primary B cells from cord blood	blood
5	chr1:150695200-150702800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr1:150696400-150702600	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr1:150697200-150704400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:150697400-150702800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr1:150697600-150705000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr1:150698600-150704400	Weak transcription	Lung	lung
11	chr1:150699200-150702600	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr1:150700600-150702600	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr1:150700600-150704000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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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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