Variant report

Variant	rs775251
Chromosome Location	chr12:57978740-57978741
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:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57976238..57978817-chr12:58135454..58137722,2	MCF-7	breast:
2	chr12:57977207..57980847-chr12:57996370..58000714,4	MCF-7	breast:
3	chr12:57911516..57914389-chr12:57978274..57982305,5	K562	blood:
4	chr12:57976772..57979526-chr12:58013170..58016217,4	MCF-7	breast:
5	chr12:57970575..57973134-chr12:57976795..57978927,2	K562	blood:
6	chr12:57976014..57978875-chr12:57984768..57986490,2	K562	blood:
7	chr12:57976485..57979398-chr12:58012165..58015688,3	MCF-7	breast:
8	chr12:57908786..57911403-chr12:57975787..57979264,3	K562	blood:
9	chr12:57978102..57980849-chr12:58144665..58146971,2	K562	blood:
10	chr12:57978631..57980822-chr12:58019393..58022185,2	MCF-7	breast:
11	chr12:57913180..57915409-chr12:57977178..57978948,2	K562	blood:
12	chr12:57977180..57979802-chr12:58003500..58006070,2	MCF-7	breast:
13	chr12:57907295..57911403-chr12:57977107..57980418,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIP4K2C-1	chr12:57978689-57980409	NONHSAT028938

No data

Variant related genes	Relation type
ENSG00000166986	Chromatin interaction
ENSG00000208028	Chromatin interaction
ENSG00000135446	Chromatin interaction
ENSG00000224713	Chromatin interaction
ENSG00000166987	Chromatin interaction
ENSG00000135502	Chromatin interaction
ENSG00000166908	Chromatin interaction
ENSG00000240771	Chromatin interaction
ENSG00000178498	Chromatin interaction
ENSG00000175197	Chromatin interaction
ENSG00000264046	Chromatin interaction
ENSG00000135439	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10783834	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11537654	0.91[CEU][hapmap]
rs2306390	0.82[CEU][hapmap]
rs2888334	1.00[CEU][hapmap];0.86[CHB][hapmap];0.90[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1812398	chr12:57829733-58001868	Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer 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	96 gene(s)	inside rSNPs	diseases
2	esv2758310	chr12:57829733-58001868	Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	esv2759901	chr12:57829733-58001868	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	nsv428283	chr12:57829733-58001868	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	nsv559034	chr12:57859932-58012233	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
6	nsv1038741	chr12:57877355-58174506	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
7	nsv541503	chr12:57877355-58174506	Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers 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	126 gene(s)	inside rSNPs	diseases
8	nsv541504	chr12:57958701-58062311	Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv725	chr12:57966549-57993808	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	n/a

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs775251	ITGB7	cis	cerebellum	SCAN
rs775251	FAM119B	cis	cerebellum	SCAN
rs775251	CDK4	cis	cerebellum	SCAN
rs775251	HOXC5	cis	cerebellum	SCAN
rs775251	TSPAN31	cis	cerebellum	SCAN
rs775251	FAM119B	Cis_1M	lymphoblastoid	RTeQTL
rs775251	TSFM	Cis_1M	lymphoblastoid	RTeQTL
rs775251	KIAA0748	cis	cerebellum	SCAN
rs775251	FAM119B	cis	lymphoblastoid	seeQTL
rs775251	METTL21B	cis	Esophagus Muscularis	GTEx

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57956600-57980600	Strong transcription	Brain Germinal Matrix	brain
2	chr12:57957000-57980800	Strong transcription	Fetal Brain Female	brain
3	chr12:57957200-57979200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:57961000-57982000	Weak transcription	Right Atrium	heart
5	chr12:57964400-57984400	Weak transcription	Pancreas	Pancrea
6	chr12:57966400-57984000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:57966600-57984000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:57966600-57984600	Weak transcription	Gastric	stomach
9	chr12:57966800-57984400	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr12:57967200-57982000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:57970600-57984200	Weak transcription	Fetal Brain Male	brain
12	chr12:57972200-57984200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:57972200-57984400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr12:57972600-57980800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr12:57975600-57984200	Weak transcription	Brain Substantia Nigra	brain
16	chr12:57975800-57979800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr12:57975800-57984200	Weak transcription	Brain Angular Gyrus	brain
18	chr12:57975800-57984400	Weak transcription	Aorta	Aorta
19	chr12:57976000-57980000	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr12:57976000-57980200	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr12:57976200-57984200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr12:57976400-57984400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr12:57976600-57984200	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr12:57976800-57984200	Weak transcription	Brain Anterior Caudate	brain
25	chr12:57977000-57981600	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr12:57977000-57981600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr12:57977000-57984200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr12:57977000-57984400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr12:57977200-57984200	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr12:57977400-57978800	Strong transcription	Brain Hippocampus Middle	brain
31	chr12:57977600-57979600	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr12:57977600-57980200	Weak transcription	Liver	Liver
33	chr12:57977600-57984200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr12:57977800-57979400	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr12:57977800-57979800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr12:57977800-57984200	Weak transcription	HepG2	liver
37	chr12:57978200-57979000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
38	chr12:57978200-57980400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
39	chr12:57978200-57981000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:57978400-57980000	Weak transcription	Spleen	Spleen
41	chr12:57978400-57980600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr12:57978600-57978800	Bivalent Enhancer	Primary B cells from cord blood	blood
43	chr12:57978600-57982800	Weak transcription	K562	blood

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