Variant report

Variant	rs11632871
Chromosome Location	chr15:42341800-42341801
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11070359	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs11633219	0.96[ASN][1000 genomes]
rs11633296	0.96[ASN][1000 genomes]
rs11638531	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12902878	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12906047	0.81[AFR][1000 genomes]
rs12906547	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1517555	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17690138	1.00[ASN][1000 genomes]
rs1823551	0.83[EUR][1000 genomes]
rs2122674	0.99[ASN][1000 genomes]
rs2412657	0.81[EUR][1000 genomes]
rs2840153	1.00[ASN][1000 genomes]
rs4924612	0.88[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs8031547	1.00[ASN][1000 genomes]
rs938748	0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931223	chr15:41989960-42781757	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
2	nsv1035998	chr15:42098896-42434254	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
3	nsv529687	chr15:42157320-42621682	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
4	nsv1049445	chr15:42239738-42830484	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
5	nsv542366	chr15:42239738-42830484	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers 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 miRNA target site	73 gene(s)	inside rSNPs	diseases
6	nsv471683	chr15:42334375-42502982	Enhancers Bivalent Enhancer Genic enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv1043641	chr15:42336584-42381240	Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42339800-42342600	Weak transcription	Lung	lung
2	chr15:42340400-42342400	Enhancers	NHEK	skin
3	chr15:42340600-42343000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:42340800-42342200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr15:42340800-42342400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr15:42340800-42346400	Enhancers	Fetal Muscle Leg	muscle
7	chr15:42341000-42342600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr15:42341400-42342200	Weak transcription	Right Atrium	heart
9	chr15:42341400-42342200	Weak transcription	Right Ventricle	heart
10	chr15:42341400-42343000	Enhancers	Psoas Muscle	Psoas
11	chr15:42341400-42347000	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr15:42341400-42348800	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr15:42341400-42349000	Weak transcription	Esophagus	oesophagus
14	chr15:42341600-42342000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr15:42341600-42343200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
16	chr15:42341600-42343800	Enhancers	Fetal Heart	heart
17	chr15:42341600-42344200	Enhancers	Fetal Muscle Trunk	muscle

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links