Variant report

Variant	rs190228243
Chromosome Location	chr9:92786874-92786875
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	nsv893561	chr9:92732368-92802101	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv482303	chr9:92752928-92890226	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv614852	chr9:92786722-93100550	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr9:92776800-92787200	Weak transcription	Esophagus	oesophagus
2	chr9:92781400-92790400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:92783000-92789000	Enhancers	Primary B cells from cord blood	blood
4	chr9:92783400-92787000	Enhancers	Primary B cells from peripheral blood	blood
5	chr9:92783400-92787800	Weak transcription	HSMMtube	muscle
6	chr9:92783600-92787200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr9:92784800-92788600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr9:92785000-92787200	Weak transcription	Gastric	stomach
9	chr9:92785400-92787600	Weak transcription	NHEK	skin
10	chr9:92786000-92787800	Enhancers	Duodenum Mucosa	Duodenum
11	chr9:92786000-92787800	Enhancers	GM12878-XiMat	blood
12	chr9:92786200-92787000	Weak transcription	Lung	lung
13	chr9:92786200-92788400	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr9:92786600-92787000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr9:92786600-92788200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr9:92786800-92787600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr9:92786800-92788000	Enhancers	Fetal Intestine Small	intestine
18	chr9:92786800-92788200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr9:92786800-92788400	Enhancers	Adipose Nuclei	Adipose

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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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