Variant report

Variant	rs542805695
Chromosome Location	chr1:159920122-159920123
allele	C/T
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	nsv872489	chr1:159844819-159940000	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv524006	chr1:159886422-159923111	Flanking Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv548055	chr1:159918418-159940000	Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159916200-159930600	Weak transcription	Right Atrium	heart
2	chr1:159916600-159920800	Weak transcription	Fetal Lung	lung
3	chr1:159916800-159923600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:159917000-159923400	Weak transcription	NHEK	skin
5	chr1:159918600-159920400	Enhancers	Sigmoid Colon	Sigmoid Colon
6	chr1:159918600-159921400	Enhancers	Placenta Amnion	Placenta Amnion
7	chr1:159919200-159920200	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr1:159919400-159923600	Weak transcription	K562	blood
9	chr1:159919600-159920400	Enhancers	Colonic Mucosa	Colon
10	chr1:159919600-159923000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:159919600-159923400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:159919800-159920200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr1:159919800-159920600	Weak transcription	Lung	lung
14	chr1:159919800-159923600	Weak transcription	Esophagus	oesophagus
15	chr1:159919800-159923800	Weak transcription	Fetal Intestine Small	intestine
16	chr1:159919800-159930400	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr1:159920000-159923800	Weak transcription	Rectal Mucosa Donor 29	rectum

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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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