Variant report

Variant	rs28410896
Chromosome Location	chr12:123901143-123901144
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123899774..123903276-chr12:123906131..123908571,3	K562	blood:
2	chr12:123876805..123878620-chr12:123900011..123901536,2	MCF-7	breast:
3	chr12:123889675..123891640-chr12:123898975..123901256,2	MCF-7	breast:
4	chr12:123745148..123747831-chr12:123900027..123902729,2	K562	blood:
5	chr12:123882533..123885309-chr12:123899138..123901801,2	MCF-7	breast:
6	chr12:123900528..123903276-chr12:123907055..123908571,2	K562	blood:
7	chr12:123873545..123876441-chr12:123898825..123901741,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000269980	Chromatin interaction
ENSG00000183955	Chromatin interaction
ENSG00000235423	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs28376121	0.88[EUR][1000 genomes]
rs28406193	0.80[EUR][1000 genomes]
rs28472704	0.80[EUR][1000 genomes]
rs28481863	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28569885	0.88[EUR][1000 genomes]
rs28576953	0.80[EUR][1000 genomes]
rs28625019	0.90[EUR][1000 genomes]
rs28676499	0.90[EUR][1000 genomes]
rs28706696	0.90[EUR][1000 genomes]
rs28715490	0.91[EUR][1000 genomes]
rs4930718	0.83[EUR][1000 genomes]
rs4930719	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038841	chr12:123757305-124087671	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	nsv541622	chr12:123757305-124087671	Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv1035223	chr12:123795559-123991706	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	nsv899579	chr12:123843017-123901480	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs28410896	MPHOSPH9	Cis_1M	lymphoblastoid	RTeQTL
rs28410896	RP11-282O18.3	cis	Esophagus Mucosa	GTEx
rs28410896	ARL6IP4	Cis_1M	lymphoblastoid	RTeQTL
rs28410896	CDK2AP1	Cis_1M	lymphoblastoid	RTeQTL
rs28410896	SBNO1	Cis_1M	lymphoblastoid	RTeQTL
rs28410896	LOC283378	Cis_1M	lymphoblastoid	RTeQTL
rs28410896	CDK2AP1	cis	Esophagus Mucosa	GTEx

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123882000-123911600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr12:123889600-123902600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:123889600-123917000	Weak transcription	K562	blood
4	chr12:123889800-123902800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr12:123890800-123917200	Weak transcription	Fetal Kidney	kidney
6	chr12:123891200-123920400	Weak transcription	Psoas Muscle	Psoas
7	chr12:123891400-123908600	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr12:123891600-123919800	Weak transcription	Colon Smooth Muscle	Colon
9	chr12:123891600-123920000	Weak transcription	Small Intestine	intestine
10	chr12:123892000-123903800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr12:123892000-123911400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr12:123892200-123901200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:123892200-123905200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr12:123892200-123905200	Weak transcription	Brain Angular Gyrus	brain
15	chr12:123892200-123905200	Weak transcription	HMEC	breast
16	chr12:123892200-123910000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr12:123892200-123916800	Weak transcription	NHEK	skin
18	chr12:123892200-123920200	Weak transcription	NH-A	brain
19	chr12:123892600-123907000	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr12:123892800-123920000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr12:123893400-123905200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr12:123893400-123918200	Weak transcription	Hela-S3	cervix
23	chr12:123893600-123905200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr12:123893600-123905200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr12:123893800-123905200	Weak transcription	Gastric	stomach
26	chr12:123893800-123908200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr12:123893800-123909600	Weak transcription	Brain Germinal Matrix	brain
28	chr12:123894000-123907800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr12:123894000-123920600	Weak transcription	HSMMtube	muscle
30	chr12:123894200-123905200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr12:123894200-123905400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:123894200-123908000	Weak transcription	Fetal Intestine Large	intestine
33	chr12:123894200-123911600	Weak transcription	Esophagus	oesophagus
34	chr12:123894200-123917000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr12:123894200-123917000	Weak transcription	HUVEC	blood vessel
36	chr12:123894400-123905200	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr12:123894400-123905200	Weak transcription	Osteobl	bone
38	chr12:123894400-123907000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr12:123894800-123908200	Weak transcription	Fetal Intestine Small	intestine
40	chr12:123894800-123911600	Weak transcription	Colonic Mucosa	Colon
41	chr12:123894800-123920000	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr12:123895000-123905200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:123895000-123905800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr12:123895000-123907200	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr12:123895200-123901200	Weak transcription	Brain Hippocampus Middle	brain
46	chr12:123895200-123904600	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr12:123895200-123905200	Weak transcription	Right Ventricle	heart
48	chr12:123895200-123905400	Weak transcription	Brain Cingulate Gyrus	brain
49	chr12:123895200-123905800	Weak transcription	NHDF-Ad	bronchial
50	chr12:123895200-123907000	Weak transcription	Fetal Muscle Leg	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links