Variant report

Variant	rs11155227
Chromosome Location	chr6:142336801-142336802
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11155228	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11155229	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11155230	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11155232	0.86[EUR][1000 genomes]
rs11155233	0.83[EUR][1000 genomes]
rs11968035	0.83[EUR][1000 genomes]
rs12193129	0.86[EUR][1000 genomes]
rs12213080	0.86[EUR][1000 genomes]
rs13192891	0.85[EUR][1000 genomes]
rs13193057	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13201184	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17071344	0.82[ASN][1000 genomes]
rs17071365	1.00[CHB][hapmap]
rs17071369	1.00[CHB][hapmap]
rs17071371	1.00[CHB][hapmap]
rs28421672	0.85[EUR][1000 genomes]
rs34933058	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35664031	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35999198	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7450527	0.85[EUR][1000 genomes]
rs7744927	0.83[EUR][1000 genomes]
rs7754673	1.00[CHB][hapmap]
rs7764878	0.83[EUR][1000 genomes]
rs9496231	0.83[EUR][1000 genomes]
rs9496232	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv604792	chr6:142192725-142399251	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1019170	chr6:142234933-142397088	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv886731	chr6:142287143-142364628	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv886732	chr6:142290338-142536049	Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv886733	chr6:142316672-142514226	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv464069	chr6:142322456-142407741	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv604794	chr6:142322456-142407741	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv1027489	chr6:142336722-142429903	Bivalent Enhancer Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142331600-142343000	Weak transcription	K562	blood
2	chr6:142334800-142337000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:142335400-142337000	Enhancers	H9 Cell Line	embryonic stem cell
4	chr6:142335600-142343000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:142335600-142351200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:142335800-142340200	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr6:142336000-142337000	Flanking Active TSS	HSMM	muscle
8	chr6:142336200-142337000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:142336200-142337000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:142336400-142337000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:142336400-142337000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:142336400-142337000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr6:142336400-142337000	Enhancers	NH-A	brain
14	chr6:142336400-142337000	Enhancers	NHDF-Ad	bronchial
15	chr6:142336400-142337000	Enhancers	Osteobl	bone
16	chr6:142336600-142337000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:142336600-142337000	Enhancers	HMEC	breast
18	chr6:142336600-142337000	Enhancers	HUVEC	blood vessel
19	chr6:142336600-142337000	Enhancers	NHEK	skin
20	chr6:142336800-142337400	Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr6:142336800-142339400	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr6:142336800-142346600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr6:142336800-142349200	Weak transcription	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links