Variant report

Variant	rs7358723
Chromosome Location	chr12:57329260-57329261
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10783813	1.00[CEU][hapmap]
rs725957	0.82[JPT][hapmap]

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	nsv1040850	chr12:57055011-57679209	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
2	nsv1043846	chr12:57323709-57377509	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
3	nsv428590	chr12:57329214-57527358	Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57325400-57329400	Enhancers	Placenta	Placenta
2	chr12:57325800-57335200	Weak transcription	Fetal Intestine Large	intestine
3	chr12:57326400-57335200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr12:57327000-57335200	Weak transcription	Spleen	Spleen
5	chr12:57327400-57330200	Enhancers	Esophagus	oesophagus
6	chr12:57327600-57329600	Weak transcription	K562	blood
7	chr12:57328000-57330000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:57328000-57330200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:57328200-57335000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr12:57328600-57329800	Enhancers	NHEK	skin
11	chr12:57328600-57330000	Enhancers	HMEC	breast
12	chr12:57328800-57329400	Enhancers	A549	lung
13	chr12:57328800-57329400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr12:57329200-57329800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	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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