Variant report

Variant	rs61734364
Chromosome Location	chr12:48110150-48110151
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr12:48110000-48110150	AG04449	skin:	n/a	n/a
2	ZNF263	chr12:48109131-48110377	HEK293-T-REx	kidney:	n/a	chr12:48109667-48109676
3	CTCF	chr12:48108771-48110151	SK-N-SH	brain:	n/a	chr12:48109258-48109276 chr12:48109887-48109900 chr12:48109259-48109275 chr12:48109261-48109274 chr12:48109260-48109281

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:48107776..48110722-chr12:48159579..48161577,2	K562	blood:
2	chr12:48108449..48110795-chr12:48232871..48234613,2	K562	blood:
3	chr12:48109212..48111939-chr12:48164649..48166863,2	MCF-7	breast:
4	chr12:48108161..48111101-chr12:48229795..48232541,2	K562	blood:
5	chr12:48108886..48110989-chr12:48118546..48121224,2	MCF-7	breast:
6	chr12:48109985..48110534-chr12:48152833..48153829,2	MCF-7	breast:
7	chr12:48110039..48113166-chr12:48116140..48121059,8	MCF-7	breast:
8	chr12:48108739..48111513-chr12:48143992..48146721,2	MCF-7	breast:
9	chr12:48109596..48111288-chr12:48213761..48215553,2	MCF-7	breast:
10	chr12:48108389..48110707-chr12:48231215..48233864,2	MCF-7	breast:
11	chr12:48109324..48111684-chr12:48163704..48166114,2	K562	blood:
12	chr12:48108354..48111166-chr12:48231258..48232998,20	K562	blood:
13	chr12:48098499..48101428-chr12:48108711..48111511,2	MCF-7	breast:
14	chr12:48108589..48112284-chr12:48169450..48173129,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000257433	TF binding region
ENSG00000079337	Chromatin interaction
ENSG00000005175	Chromatin interaction
ENSG00000257433	Chromatin interaction
ENSG00000061273	Chromatin interaction
ENSG00000211584	Chromatin interaction
ENSG00000111405	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1859256	1.00[AMR][1000 genomes]
rs57162394	1.00[AMR][1000 genomes]
rs57691959	1.00[AMR][1000 genomes]
rs58237186	1.00[AMR][1000 genomes]
rs58280987	1.00[AMR][1000 genomes]
rs58348653	1.00[AMR][1000 genomes]
rs58350284	1.00[AMR][1000 genomes]
rs58636268	1.00[AMR][1000 genomes]
rs59421933	1.00[AMR][1000 genomes]
rs60045275	1.00[AMR][1000 genomes]
rs60608560	1.00[AMR][1000 genomes]
rs61033936	1.00[AMR][1000 genomes]
rs61288073	1.00[AMR][1000 genomes]
rs61327127	1.00[AMR][1000 genomes]
rs61446607	1.00[AMR][1000 genomes]
rs61739888	1.00[AMR][1000 genomes]
rs7300107	1.00[AMR][1000 genomes]
rs7314320	1.00[AMR][1000 genomes]
rs73300649	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73300689	1.00[AMR][1000 genomes]
rs73300701	1.00[AMR][1000 genomes]
rs73302603	1.00[AMR][1000 genomes]
rs73302628	1.00[AMR][1000 genomes]
rs73302629	1.00[AMR][1000 genomes]
rs73302650	1.00[AMR][1000 genomes]
rs73302653	1.00[AMR][1000 genomes]
rs73302662	1.00[AMR][1000 genomes]
rs73302664	1.00[AMR][1000 genomes]
rs73302673	1.00[AMR][1000 genomes]
rs73302677	1.00[AMR][1000 genomes]
rs73302679	1.00[AMR][1000 genomes]
rs73302681	1.00[AMR][1000 genomes]
rs73302682	1.00[AMR][1000 genomes]
rs757283	1.00[AMR][1000 genomes]
rs7965816	1.00[AMR][1000 genomes]
rs877196	1.00[AMR][1000 genomes]
rs877197	1.00[AMR][1000 genomes]
rs877198	1.00[AMR][1000 genomes]
rs879177	1.00[AMR][1000 genomes]
rs879178	1.00[AMR][1000 genomes]
rs879179	1.00[AMR][1000 genomes]
rs9738787	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751101	chr12:47940858-48126885	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	esv1813565	chr12:48097697-48177858	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48100000-48111200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:48101400-48111000	Weak transcription	Colonic Mucosa	Colon
3	chr12:48101400-48111200	Weak transcription	Small Intestine	intestine
4	chr12:48101800-48111200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:48102800-48125000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr12:48103200-48111200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr12:48103400-48111000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr12:48104600-48113000	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr12:48105600-48111200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr12:48106200-48112600	Enhancers	Ovary	ovary
11	chr12:48106600-48111200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr12:48108200-48112400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr12:48108600-48112400	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr12:48108800-48111200	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr12:48108800-48111200	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr12:48108800-48112200	Enhancers	Brain Angular Gyrus	brain
17	chr12:48108800-48112200	Enhancers	Fetal Muscle Trunk	muscle
18	chr12:48108800-48112600	Enhancers	Brain Cingulate Gyrus	brain
19	chr12:48108800-48112600	Enhancers	Fetal Muscle Leg	muscle
20	chr12:48108800-48112600	Enhancers	Fetal Stomach	stomach
21	chr12:48108800-48112600	Enhancers	Left Ventricle	heart
22	chr12:48108800-48112600	Enhancers	Right Atrium	heart
23	chr12:48108800-48112600	Enhancers	Right Ventricle	heart
24	chr12:48108800-48112800	Enhancers	Brain Hippocampus Middle	brain
25	chr12:48108800-48112800	Enhancers	Brain Substantia Nigra	brain
26	chr12:48108800-48113000	Enhancers	Rectal Smooth Muscle	rectum
27	chr12:48109000-48110200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr12:48109000-48110200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr12:48109000-48110200	Enhancers	Fetal Heart	heart
30	chr12:48109000-48110200	Enhancers	Stomach Mucosa	stomach
31	chr12:48109000-48110200	Enhancers	HMEC	breast
32	chr12:48109000-48110400	Enhancers	Esophagus	oesophagus
33	chr12:48109000-48110400	Enhancers	Psoas Muscle	Psoas
34	chr12:48109000-48112200	Enhancers	Primary T cells fromperipheralblood	blood
35	chr12:48109000-48112200	Enhancers	Fetal Thymus	thymus
36	chr12:48109000-48112400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr12:48109000-48112400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr12:48109000-48112600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr12:48109000-48112600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:48109000-48112600	Enhancers	Lung	lung
41	chr12:48109200-48110400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
42	chr12:48109400-48110800	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr12:48109400-48110800	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr12:48109400-48112200	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr12:48109400-48112400	Enhancers	Primary hematopoietic stem cells	blood
46	chr12:48109600-48110200	Weak transcription	Fetal Intestine Small	intestine
47	chr12:48109600-48110400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr12:48109600-48110600	Weak transcription	Primary B cells from cord blood	blood
49	chr12:48109600-48110600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr12:48109600-48110600	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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