Variant report

Variant	rs73706936
Chromosome Location	chr7:87467146-87467147
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:10)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:10 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr7:87467127-87467183	LNCaP	prostate:	n/a	n/a
2	CTCF	chr7:87467080-87467230	MCF-7	breast:	n/a	n/a
3	CTCF	chr7:87467091-87467156	Hela-S3	cervix:	n/a	n/a
4	RAD21	chr7:87466964-87467260	MCF-7	breast:	n/a	n/a
5	CTCF	chr7:87466980-87467259	MCF-7	breast:	n/a	n/a
6	CTCF	chr7:87467140-87467290	HPAF	blood vessel:	n/a	n/a
7	CTCF	chr7:87467099-87467173	MCF-7	breast:	n/a	n/a
8	CTCF	chr7:87467118-87467190	GM12878	blood:	n/a	n/a
9	CTCF	chr7:87467076-87467178	MCF-7	breast:	n/a	n/a
10	CTCF	chr7:87467000-87467150	AG04450	lung:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:87465363..87467362-chr7:87470380..87471981,2	K562	blood:
2	chr7:87466437..87468274-chr7:87505862..87508203,2	K562	blood:
3	chr7:87465363..87469135-chr7:87470380..87473582,3	K562	blood:
4	chr7:87466308..87468274-chr7:87505770..87508203,3	K562	blood:

No data

Variant related genes	Relation type
SLC25A40	TF binding region
ENSG00000075303	Chromatin interaction
ENSG00000006634	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs28381790	1.00[AMR][1000 genomes]
rs28381791	1.00[AMR][1000 genomes]
rs28381792	1.00[AMR][1000 genomes]
rs28381795	1.00[AMR][1000 genomes]
rs28381800	1.00[AMR][1000 genomes]
rs55990608	0.92[AFR][1000 genomes]
rs56208559	1.00[AFR][1000 genomes]
rs56225435	0.92[AFR][1000 genomes]
rs56397035	1.00[AFR][1000 genomes]
rs57593184	1.00[AMR][1000 genomes]
rs59075963	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59696208	0.84[AFR][1000 genomes]
rs59965458	1.00[AMR][1000 genomes]
rs60521777	1.00[AMR][1000 genomes]
rs61056962	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61232411	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6950539	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6974534	0.92[AFR][1000 genomes]
rs73705274	1.00[AMR][1000 genomes]
rs73705275	1.00[AMR][1000 genomes]
rs73706908	1.00[AFR][1000 genomes]
rs73706920	1.00[AFR][1000 genomes]
rs73706928	1.00[AFR][1000 genomes]
rs73706931	1.00[AMR][1000 genomes]
rs73706933	1.00[AMR][1000 genomes]
rs73706934	1.00[AMR][1000 genomes]
rs73706937	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73706938	1.00[AMR][1000 genomes]
rs73706939	1.00[AMR][1000 genomes]
rs73706943	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73706945	1.00[AMR][1000 genomes]
rs73706946	1.00[AMR][1000 genomes]
rs73706947	1.00[AMR][1000 genomes]
rs73706949	1.00[AMR][1000 genomes]
rs7801454	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888677	chr7:86802025-87781111	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv464622	chr7:86832603-87541248	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv607725	chr7:86832603-87541248	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv1015862	chr7:87075394-88049798	Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	nsv1023352	chr7:87418818-88192925	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv539005	chr7:87418818-88192925	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:87455000-87474200	Weak transcription	Left Ventricle	heart
2	chr7:87455200-87473000	Weak transcription	Liver	Liver
3	chr7:87455200-87486600	Weak transcription	Brain Germinal Matrix	brain
4	chr7:87455400-87474200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr7:87457400-87474200	Weak transcription	Aorta	Aorta
6	chr7:87457800-87474200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr7:87458200-87478400	Weak transcription	Adipose Nuclei	Adipose
8	chr7:87458400-87478600	Weak transcription	Brain Anterior Caudate	brain
9	chr7:87458600-87469400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr7:87458600-87474400	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr7:87458600-87480400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:87458800-87467600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr7:87459000-87474200	Weak transcription	Primary B cells from cord blood	blood
14	chr7:87459000-87474400	Weak transcription	Duodenum Mucosa	Duodenum
15	chr7:87459200-87482400	Weak transcription	A549	lung
16	chr7:87459400-87474200	Weak transcription	Fetal Stomach	stomach
17	chr7:87459400-87474400	Weak transcription	HUVEC	blood vessel
18	chr7:87459600-87471600	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr7:87459600-87473200	Weak transcription	Fetal Thymus	thymus
20	chr7:87459600-87474200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:87459600-87474600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:87459600-87474600	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr7:87459800-87474800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr7:87459800-87478600	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr7:87459800-87480600	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr7:87460000-87474400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr7:87460000-87474400	Weak transcription	Fetal Brain Female	brain
28	chr7:87460200-87471800	Weak transcription	Fetal Brain Male	brain
29	chr7:87460200-87478800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr7:87460400-87487200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr7:87460600-87474400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:87460600-87474400	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr7:87460600-87481200	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr7:87460600-87481600	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr7:87460600-87498000	Weak transcription	Fetal Heart	heart
36	chr7:87460800-87474400	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr7:87461000-87471400	Weak transcription	GM12878-XiMat	blood
38	chr7:87461000-87473400	Weak transcription	Primary B cells from peripheral blood	blood
39	chr7:87461200-87471600	Weak transcription	K562	blood
40	chr7:87461200-87474200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr7:87461200-87474200	Weak transcription	Ovary	ovary
42	chr7:87461200-87478200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr7:87461200-87486600	Weak transcription	Psoas Muscle	Psoas
44	chr7:87461400-87474400	Weak transcription	Rectal Smooth Muscle	rectum
45	chr7:87461400-87486800	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr7:87461600-87472400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr7:87461600-87473200	Weak transcription	HSMM	muscle
48	chr7:87461600-87474200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr7:87461600-87481600	Weak transcription	Fetal Lung	lung
50	chr7:87462400-87474600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links