Variant report

Variant	rs7015777
Chromosome Location	chr8:10277635-10277636
allele	C/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:7)

rs_ID	r²[population]
rs10112584	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.83[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs10113408	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12677754	0.96[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4311657	0.83[AMR][1000 genomes]
rs6997671	0.81[AMR][1000 genomes]
rs7009513	0.82[JPT][hapmap]
rs7821432	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030934	chr8:10065169-10561161	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv890347	chr8:10153082-10331636	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv527326	chr8:10199548-10320019	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1025557	chr8:10216726-10555187	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv465460	chr8:10241411-10290566	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
9	nsv610265	chr8:10241411-10290566	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
10	nsv610266	chr8:10250758-10294330	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
11	nsv1019701	chr8:10254709-10279269	Enhancers Weak transcription Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv890348	chr8:10265712-10289663	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
13	nsv610267	chr8:10268736-10526742	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10192600-10282400	Weak transcription	Gastric	stomach
2	chr8:10263600-10283400	Weak transcription	Fetal Intestine Small	intestine
3	chr8:10271000-10281200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr8:10275000-10280400	Weak transcription	Fetal Brain Female	brain
5	chr8:10276000-10280400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:10276000-10281200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr8:10276000-10281800	Weak transcription	Brain Germinal Matrix	brain
8	chr8:10276000-10282400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr8:10276000-10282400	Weak transcription	Pancreas	Pancrea
10	chr8:10276000-10282400	Weak transcription	Spleen	Spleen
11	chr8:10276000-10282600	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr8:10276000-10282600	Weak transcription	Duodenum Mucosa	Duodenum
13	chr8:10276000-10282600	Weak transcription	Lung	lung
14	chr8:10276000-10282600	Weak transcription	Right Atrium	heart
15	chr8:10276000-10282600	Weak transcription	NHLF	lung
16	chr8:10276000-10283800	Weak transcription	Psoas Muscle	Psoas
17	chr8:10276000-10290400	Weak transcription	Fetal Intestine Large	intestine
18	chr8:10276000-10293600	Weak transcription	Brain Substantia Nigra	brain
19	chr8:10276200-10282200	Weak transcription	Fetal Lung	lung
20	chr8:10276200-10282200	Weak transcription	Fetal Stomach	stomach
21	chr8:10276200-10283800	Weak transcription	Liver	Liver
22	chr8:10277200-10277800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
23	chr8:10277200-10281000	Weak transcription	Fetal Brain Male	brain
24	chr8:10277400-10277800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
25	chr8:10277400-10277800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
26	chr8:10277400-10277800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
27	chr8:10277400-10277800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
28	chr8:10277400-10282400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:10277400-10282400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr8:10277600-10277800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
31	chr8:10277600-10277800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
32	chr8:10277600-10277800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
33	chr8:10277600-10280400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr8:10277600-10282400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links