Variant report

Variant	rs6831381
Chromosome Location	chr4:7904431-7904432
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10938695	0.89[ASN][1000 genomes]
rs13115283	0.95[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13127935	0.94[CHB][hapmap];0.85[ASN][1000 genomes]
rs16841407	0.81[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs28376859	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28410206	0.84[AMR][1000 genomes]
rs28500712	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28503942	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28572044	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28681260	0.84[ASN][1000 genomes]
rs4447866	0.88[CHB][hapmap]
rs4549363	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59283470	0.84[AMR][1000 genomes]
rs59521811	0.91[ASN][1000 genomes]
rs62289323	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62289332	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6824410	0.94[CHB][hapmap];0.93[CHD][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap];0.87[ASN][1000 genomes]
rs6824700	0.88[CHB][hapmap];0.90[CHD][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.96[MEX][hapmap];0.82[TSI][hapmap]
rs6839119	0.82[ASN][1000 genomes]
rs6844956	0.94[CHB][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs6845653	0.90[ASN][1000 genomes]
rs7375284	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7376648	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7378106	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7441783	0.83[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491712	chr4:7582506-8155069	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	esv34140	chr4:7787936-8172491	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS 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	18 gene(s)	inside rSNPs	diseases
3	esv2754386	chr4:7822449-7992909	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2756298	chr4:7822449-7992909	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv878578	chr4:7841833-7969594	Enhancers Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6831381	AFAP1	cis	cerebellum	SCAN

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7893200-7905600	Weak transcription	Brain Angular Gyrus	brain
2	chr4:7894200-7912400	Weak transcription	Fetal Intestine Large	intestine
3	chr4:7894400-7906200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr4:7895600-7907600	Weak transcription	Colonic Mucosa	Colon
5	chr4:7896800-7907600	Weak transcription	Fetal Intestine Small	intestine
6	chr4:7897000-7907400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:7897400-7905800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:7898800-7905200	Enhancers	Colon Smooth Muscle	Colon
9	chr4:7899200-7905800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr4:7899600-7907000	Enhancers	Fetal Brain Male	brain
11	chr4:7899800-7930600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:7900000-7905000	Weak transcription	HMEC	breast
13	chr4:7900000-7906400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr4:7900000-7907400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:7900200-7905400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr4:7900200-7905600	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr4:7900200-7912400	Weak transcription	NHEK	skin
18	chr4:7900400-7904600	Enhancers	H1 Cell Line	embryonic stem cell
19	chr4:7900400-7905800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:7900800-7905000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr4:7900800-7906000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:7900800-7914400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr4:7901000-7905200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr4:7901000-7905600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr4:7901000-7905800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:7901000-7907400	Enhancers	HSMMtube	muscle
27	chr4:7901000-7909000	Enhancers	Fetal Brain Female	brain
28	chr4:7901200-7905200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr4:7901400-7909400	Enhancers	Fetal Lung	lung
30	chr4:7901600-7905000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr4:7901600-7905800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr4:7901600-7907400	Enhancers	Duodenum Smooth Muscle	Duodenum
33	chr4:7901600-7914400	Enhancers	Fetal Muscle Leg	muscle
34	chr4:7901800-7905400	Genic enhancers	Osteobl	bone
35	chr4:7901800-7905800	Enhancers	Muscle Satellite Cultured Cells	--
36	chr4:7901800-7905800	Enhancers	HUVEC	blood vessel
37	chr4:7902000-7904600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr4:7902000-7905000	Genic enhancers	NH-A	brain
39	chr4:7902000-7909200	Enhancers	Fetal Heart	heart
40	chr4:7902000-7909400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr4:7902200-7905600	Enhancers	NHDF-Ad	bronchial
42	chr4:7902200-7906200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:7902400-7907600	Enhancers	Rectal Smooth Muscle	rectum
44	chr4:7902600-7905200	Enhancers	Aorta	Aorta
45	chr4:7902600-7905800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr4:7902600-7906400	Genic enhancers	HSMM	muscle
47	chr4:7902800-7905000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr4:7903000-7905800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr4:7903000-7906000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr4:7903000-7906600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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