Variant report

Variant	rs12901557
Chromosome Location	chr15:78202690-78202691
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11072692	0.82[AMR][1000 genomes]
rs11072693	0.80[AMR][1000 genomes]
rs11072697	0.80[AMR][1000 genomes]
rs11072698	0.80[AMR][1000 genomes]
rs11072699	0.82[AMR][1000 genomes]
rs11072700	0.82[AMR][1000 genomes]
rs11638419	0.82[AMR][1000 genomes]
rs11638589	0.81[AMR][1000 genomes]
rs12898476	0.86[AMR][1000 genomes]
rs12899237	0.81[AMR][1000 genomes]
rs12908305	0.82[AMR][1000 genomes]
rs12912453	0.82[AMR][1000 genomes]
rs12913449	0.82[AMR][1000 genomes]
rs12916128	0.81[AMR][1000 genomes]
rs4886538	0.83[AMR][1000 genomes]
rs4886539	0.82[AMR][1000 genomes]
rs4886540	0.82[AMR][1000 genomes]
rs4886542	0.80[AMR][1000 genomes]
rs57630695	0.81[AMR][1000 genomes]
rs57708464	0.81[AMR][1000 genomes]
rs58331113	0.82[AMR][1000 genomes]
rs59711627	0.82[AMR][1000 genomes]
rs61520355	0.88[AMR][1000 genomes]
rs67793790	0.82[AMR][1000 genomes]
rs73456876	0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
3	nsv833062	chr15:78035206-78220358	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv1833316	chr15:78081307-78328108	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv904426	chr15:78090630-78264164	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv904427	chr15:78129964-78251431	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv976954	chr15:78153346-78255825	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv1046383	chr15:78153850-78229596	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv904428	chr15:78156238-78230906	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv904429	chr15:78160362-78251431	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	esv1827357	chr15:78200594-78206047	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	esv1823600	chr15:78200594-78219757	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78180000-78215600	Weak transcription	Right Atrium	heart
2	chr15:78192000-78202800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr15:78200200-78203000	Enhancers	Colonic Mucosa	Colon
4	chr15:78200400-78202800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr15:78200400-78202800	Enhancers	Fetal Intestine Small	intestine
6	chr15:78200400-78203200	Enhancers	Esophagus	oesophagus
7	chr15:78200400-78203200	Enhancers	Stomach Mucosa	stomach
8	chr15:78200400-78203800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr15:78200600-78202800	Enhancers	Fetal Muscle Trunk	muscle
10	chr15:78200800-78202800	Enhancers	Fetal Intestine Large	intestine
11	chr15:78200800-78202800	Enhancers	A549	lung
12	chr15:78201000-78202800	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr15:78201000-78202800	Weak transcription	Fetal Thymus	thymus
14	chr15:78201200-78202800	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr15:78201200-78202800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr15:78201200-78202800	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr15:78201200-78202800	Weak transcription	NH-A	brain
18	chr15:78201400-78202800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr15:78201400-78202800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr15:78201400-78202800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr15:78201400-78202800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr15:78201400-78202800	Weak transcription	HSMM	muscle
23	chr15:78201600-78202800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:78201600-78202800	Enhancers	Duodenum Mucosa	Duodenum
25	chr15:78201800-78202800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr15:78201800-78202800	Enhancers	Placenta	Placenta
27	chr15:78201800-78202800	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr15:78202400-78202800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr15:78202400-78202800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr15:78202400-78202800	Enhancers	Fetal Muscle Leg	muscle
31	chr15:78202400-78203000	Flanking Active TSS	Hela-S3	cervix
32	chr15:78202600-78202800	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr15:78202600-78202800	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr15:78202600-78202800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr15:78202600-78202800	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr15:78202600-78202800	Enhancers	Dnd41	blood
37	chr15:78202600-78202800	Enhancers	HepG2	liver
38	chr15:78202600-78202800	Enhancers	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links