Variant report

Variant	rs17153498
Chromosome Location	chr8:11446955-11446956
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:11411028..11411558-chr8:11446874..11447601,2	K562	blood:
2	chr8:11421719..11422643-chr8:11446645..11447610,4	K562	blood:
3	chr8:11446527..11447418-chr8:11587991..11588812,3	MCF-7	breast:
4	chr8:11446870..11447723-chr8:11603904..11604616,2	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 3 )

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

rs_ID	r²[population]
rs10097870	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10903340	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11250150	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11250151	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11774572	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11778830	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11780420	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11995206	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13270267	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2244648	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4841567	0.83[EUR][1000 genomes]
rs55896564	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56051089	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7823651	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[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	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	esv34097	chr8:11177372-11489894	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1017865	chr8:11377795-11579954	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1026837	chr8:11394466-11464127	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1018959	chr8:11395232-11455756	Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv890358	chr8:11396856-11448738	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv1033629	chr8:11401789-11466745	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv523827	chr8:11408401-11486220	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv1032195	chr8:11420541-11480692	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv1016749	chr8:11422571-11466745	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs17153498	C8orf13	Cis_1M	lymphoblastoid	RTeQTL
rs17153498	C8orf5	Cis_1M	lymphoblastoid	RTeQTL
rs17153498	BLK	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11444600-11447000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr8:11444600-11447600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:11444600-11449400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:11444800-11447600	Enhancers	Placenta	Placenta
5	chr8:11445400-11447000	Enhancers	Fetal Muscle Trunk	muscle
6	chr8:11445400-11447000	Enhancers	HSMMtube	muscle
7	chr8:11445600-11450800	Weak transcription	Right Ventricle	heart
8	chr8:11445600-11454000	Enhancers	Fetal Heart	heart
9	chr8:11445800-11447000	Weak transcription	Pancreas	Pancrea
10	chr8:11445800-11447400	Bivalent Enhancer	Fetal Muscle Leg	muscle
11	chr8:11446200-11447000	Enhancers	Stomach Smooth Muscle	stomach
12	chr8:11446200-11450800	Weak transcription	Right Atrium	heart
13	chr8:11446400-11447200	Enhancers	Stomach Mucosa	stomach
14	chr8:11446400-11447400	Weak transcription	Left Ventricle	heart
15	chr8:11446600-11447000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
16	chr8:11446600-11447200	Enhancers	Primary B cells from peripheral blood	blood
17	chr8:11446600-11447400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr8:11446600-11448400	Enhancers	Liver	Liver
19	chr8:11446800-11447000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr8:11446800-11447000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:11446800-11447000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
22	chr8:11446800-11447000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr8:11446800-11447000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
24	chr8:11446800-11447000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr8:11446800-11447000	Bivalent Enhancer	Fetal Thymus	thymus
26	chr8:11446800-11447000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
27	chr8:11446800-11447000	Enhancers	A549	lung
28	chr8:11446800-11447000	Flanking Active TSS	GM12878-XiMat	blood
29	chr8:11446800-11447200	Enhancers	Primary B cells from cord blood	blood
30	chr8:11446800-11447200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
31	chr8:11446800-11447200	Bivalent Enhancer	NHEK	skin
32	chr8:11446800-11447400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr8:11446800-11447400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
34	chr8:11446800-11447400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr8:11446800-11447400	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr8:11446800-11447400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
37	chr8:11446800-11447400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr8:11446800-11447600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr8:11446800-11447600	Enhancers	Fetal Intestine Small	intestine
40	chr8:11446800-11448000	Flanking Active TSS	HepG2	liver

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