Variant report

Variant	rs6851824
Chromosome Location	chr4:100566659-100566660
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs11097666	0.89[EUR][1000 genomes]
rs13107620	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13121590	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13129571	0.86[EUR][1000 genomes]
rs13135675	0.97[EUR][1000 genomes]
rs13135826	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs13142452	0.97[EUR][1000 genomes]
rs13146743	0.94[AFR][1000 genomes]
rs13151234	0.89[EUR][1000 genomes]
rs1491236	0.81[EUR][1000 genomes]
rs17029189	0.97[EUR][1000 genomes]
rs17029211	0.97[EUR][1000 genomes]
rs17029213	0.97[EUR][1000 genomes]
rs17029215	0.97[EUR][1000 genomes]
rs17029260	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17029263	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17029264	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17029267	0.91[AFR][1000 genomes]
rs34066136	0.85[AMR][1000 genomes]
rs34135026	0.89[EUR][1000 genomes]
rs34246356	0.89[EUR][1000 genomes]
rs34678000	0.97[EUR][1000 genomes]
rs34734558	0.97[EUR][1000 genomes]
rs34756677	0.97[EUR][1000 genomes]
rs34777713	0.87[EUR][1000 genomes]
rs34870956	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34874297	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35074439	0.89[EUR][1000 genomes]
rs35189300	0.93[EUR][1000 genomes]
rs35391161	0.97[EUR][1000 genomes]
rs35402611	0.86[EUR][1000 genomes]
rs35561084	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35595171	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35661838	0.93[EUR][1000 genomes]
rs35824615	0.97[EUR][1000 genomes]
rs35826214	0.93[EUR][1000 genomes]
rs35992230	0.89[EUR][1000 genomes]
rs41275719	0.97[EUR][1000 genomes]
rs6532821	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs6821960	1.00[CEU][hapmap]
rs6825904	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6830456	0.89[AFR][1000 genomes]
rs71612697	0.89[EUR][1000 genomes]
rs71612700	0.89[EUR][1000 genomes]
rs71612702	0.97[EUR][1000 genomes]
rs71614603	0.97[EUR][1000 genomes]
rs71614605	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs71614609	0.85[AMR][1000 genomes]
rs71619723	0.97[EUR][1000 genomes]
rs7665414	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs7667001	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs7667218	0.85[AMR][1000 genomes]
rs7688278	0.89[EUR][1000 genomes]
rs7695727	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs871320	0.87[YRI][hapmap];0.96[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933074	chr4:100460951-100630600	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100561800-100567400	Weak transcription	HSMMtube	muscle
2	chr4:100563400-100567000	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr4:100563400-100567600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:100564200-100567400	Weak transcription	Pancreas	Pancrea
5	chr4:100564400-100567800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
6	chr4:100564400-100569400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:100564600-100566800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:100564600-100567600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:100564800-100566800	Weak transcription	Stomach Smooth Muscle	stomach
10	chr4:100564800-100567400	Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr4:100565000-100566800	Weak transcription	Left Ventricle	heart
12	chr4:100565000-100567400	Weak transcription	Psoas Muscle	Psoas
13	chr4:100565000-100567600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:100565000-100567800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:100565000-100570200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr4:100565400-100567600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr4:100565400-100569400	Weak transcription	Fetal Intestine Small	intestine
18	chr4:100565400-100569400	Weak transcription	Fetal Lung	lung
19	chr4:100565400-100569800	Weak transcription	Fetal Intestine Large	intestine
20	chr4:100565800-100566800	Active TSS	Fetal Muscle Leg	muscle
21	chr4:100565800-100570400	Active TSS	Right Ventricle	heart
22	chr4:100566000-100566800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr4:100566000-100566800	Weak transcription	Fetal Muscle Trunk	muscle
24	chr4:100566000-100567600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr4:100566000-100568600	Enhancers	Ovary	ovary
26	chr4:100566200-100566800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
27	chr4:100566400-100567000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr4:100566400-100567600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:100566400-100568200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr4:100566400-100568600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr4:100566400-100569400	Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr4:100566600-100566800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
33	chr4:100566600-100575800	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links