Variant report

Variant	rs17011858
Chromosome Location	chr4:87307227-87307228
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs17011708	0.84[AFR][1000 genomes]
rs17011764	0.84[AFR][1000 genomes]
rs17011766	0.84[AFR][1000 genomes]
rs17011767	0.84[AFR][1000 genomes]
rs17011774	0.84[AFR][1000 genomes]
rs17011806	0.84[AFR][1000 genomes]
rs17011819	0.84[AFR][1000 genomes]
rs17011845	0.89[AFR][1000 genomes]
rs17011853	0.89[AFR][1000 genomes]
rs17011872	0.89[AFR][1000 genomes]
rs7661679	0.84[AFR][1000 genomes]
rs7667204	0.84[AFR][1000 genomes]
rs7675381	0.84[AFR][1000 genomes]
rs7691277	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv594786	chr4:87076360-87609320	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv999470	chr4:87165663-87514552	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537164	chr4:87165663-87514552	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv934210	chr4:87197339-87325578	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv594787	chr4:87221827-87888667	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv1012836	chr4:87279206-87643558	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 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	chr4:87281600-87315800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr4:87290400-87308200	Weak transcription	Ovary	ovary
3	chr4:87301800-87307400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr4:87302600-87307600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:87302600-87308400	Weak transcription	Fetal Brain Male	brain
6	chr4:87302600-87310800	Weak transcription	Pancreas	Pancrea
7	chr4:87302600-87334000	Weak transcription	Fetal Stomach	stomach
8	chr4:87302800-87312600	Weak transcription	Esophagus	oesophagus
9	chr4:87303000-87307400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:87303200-87312800	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr4:87305800-87307400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:87305800-87311200	Weak transcription	Aorta	Aorta
13	chr4:87305800-87311600	Weak transcription	Gastric	stomach
14	chr4:87307200-87307600	Enhancers	H9 Cell Line	embryonic stem cell
15	chr4:87307200-87307600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr4:87307200-87307800	Enhancers	H1 Cell Line	embryonic stem cell
17	chr4:87307200-87308200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:87307200-87308400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:87307200-87309000	Enhancers	HUES64 Cell Line	embryonic stem cell

Quick Search:

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

what's new

Quick links