Variant report

Variant	rs28582722
Chromosome Location	chr14:34895713-34895714
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10142314	1.00[AMR][1000 genomes]
rs10143373	0.86[AFR][1000 genomes]
rs10144769	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10147869	0.81[AFR][1000 genomes]
rs10149214	1.00[AMR][1000 genomes]
rs10150887	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2383631	1.00[AMR][1000 genomes]
rs28418627	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28448660	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28603155	0.87[AMR][1000 genomes]
rs28687504	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28716315	0.81[AFR][1000 genomes]
rs28722131	1.00[AMR][1000 genomes]
rs7144173	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8006226	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040980	chr14:34345018-35255592	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
2	nsv1051104	chr14:34592378-35007083	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv949738	chr14:34616331-34990688	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv564192	chr14:34725233-34996507	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv564193	chr14:34728127-35000188	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv528989	chr14:34744426-34998705	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv1054949	chr14:34834260-34992049	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
8	nsv542025	chr14:34834260-34992049	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
9	nsv1050218	chr14:34851521-34969433	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
10	nsv1048369	chr14:34886956-34974774	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 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	chr14:34890800-34905800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:34891200-34902400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr14:34892600-34895800	Enhancers	Placenta	Placenta
4	chr14:34892800-34905400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr14:34893800-34896800	Enhancers	Pancreas	Pancrea
6	chr14:34894200-34914000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr14:34894400-34897600	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr14:34894600-34897000	Enhancers	Liver	Liver
9	chr14:34894600-34902400	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr14:34894600-34913400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr14:34895200-34896400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr14:34895200-34906400	Weak transcription	Hela-S3	cervix
13	chr14:34895400-34895800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr14:34895600-34896000	Enhancers	Psoas Muscle	Psoas
15	chr14:34895600-34897000	Enhancers	Duodenum Mucosa	Duodenum
16	chr14:34895600-34897000	Enhancers	Gastric	stomach
17	chr14:34895600-34897000	Enhancers	Stomach Mucosa	stomach

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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