Variant report

Variant	rs13224314
Chromosome Location	chr7:116756535-116756536
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA1	chr7:116756272-116756545	T-47D	breast:	n/a	chr7:116756404-116756419

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	7:116547624-116551247..7:116754962-116765597	GM12878	blood:
2	7:116754962-116765597..7:116894301-116914960	Hela-S3	cervix:
3	chr7:116755208..116758629-chr7:116767388..116769858,3	K562	blood:
4	7:116245779-116258944..7:116754962-116765597	Hela-S3	cervix:
5	7:116610596-116619447..7:116754962-116765597	GM12878	blood:
6	chr7:116727325..116729299-chr7:116756273..116758689,2	K562	blood:
7	chr7:116633872..116635793-chr7:116756393..116758415,2	K562	blood:
8	7:116580605-116585719..7:116754962-116765597	GM12878	blood:
9	7:116754962-116765597..7:117341506-117356953	Hela-S3	cervix:

No data

Variant related genes	Relation type
ST7	TF binding region
ENSG00000222150	Chromatin interaction
ENSG00000001626	Chromatin interaction
ENSG00000213050	Chromatin interaction
ENSG00000198898	Chromatin interaction
ENSG00000252115	Chromatin interaction
ENSG00000230605	Chromatin interaction
ENSG00000224042	Chromatin interaction
ENSG00000230785	Chromatin interaction
ENSG00000231210	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11762032	1.00[CHB][hapmap]
rs11764134	1.00[CHB][hapmap]
rs11773591	1.00[CHB][hapmap]
rs12706125	1.00[CHB][hapmap]
rs12706126	1.00[CHB][hapmap]
rs12706134	1.00[CHB][hapmap]
rs12706135	1.00[CHB][hapmap]
rs12706137	1.00[CHB][hapmap]
rs12706138	1.00[CHB][hapmap]
rs12706139	1.00[CHB][hapmap]
rs12706140	1.00[CHB][hapmap]
rs12706141	1.00[CHB][hapmap]
rs12706143	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12706144	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13221657	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13222576	1.00[CHB][hapmap]
rs13239447	1.00[CHB][hapmap]
rs13308921	1.00[CHB][hapmap]
rs2188693	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3808218	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.94[TSI][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3808222	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.85[JPT][hapmap];0.84[MEX][hapmap];0.92[TSI][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831108	chr7:116749534-116952011	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13224314	ANKRD7	cis	cerebellum	SCAN

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116725400-116766400	Weak transcription	Brain Germinal Matrix	brain
2	chr7:116737400-116758800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr7:116738400-116774200	Weak transcription	Ovary	ovary
4	chr7:116738400-116779600	Weak transcription	Esophagus	oesophagus
5	chr7:116738800-116760400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:116738800-116763400	Weak transcription	Hela-S3	cervix
7	chr7:116739400-116758800	Weak transcription	NH-A	brain
8	chr7:116743800-116760200	Weak transcription	Placenta	Placenta
9	chr7:116745600-116763600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:116750600-116758800	Weak transcription	Fetal Lung	lung
11	chr7:116750600-116759000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr7:116750800-116758800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr7:116750800-116758800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:116750800-116764600	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr7:116751200-116758400	Weak transcription	HUVEC	blood vessel
16	chr7:116751200-116758600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr7:116751200-116758800	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr7:116751200-116761400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:116751200-116762600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr7:116751200-116762600	Weak transcription	NHDF-Ad	bronchial
21	chr7:116751400-116763400	Weak transcription	Colon Smooth Muscle	Colon
22	chr7:116751400-116763600	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr7:116751400-116764600	Weak transcription	Duodenum Mucosa	Duodenum
24	chr7:116751400-116764600	Weak transcription	Lung	lung
25	chr7:116751400-116778600	Weak transcription	Stomach Smooth Muscle	stomach
26	chr7:116751800-116759400	Weak transcription	Primary hematopoietic stem cells	blood
27	chr7:116751800-116763800	Weak transcription	Fetal Intestine Small	intestine
28	chr7:116751800-116764400	Weak transcription	Fetal Intestine Large	intestine
29	chr7:116752000-116764600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:116752000-116764600	Weak transcription	Left Ventricle	heart
31	chr7:116753400-116757600	Enhancers	Fetal Brain Male	brain
32	chr7:116753800-116757000	Enhancers	Fetal Brain Female	brain
33	chr7:116754200-116758800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr7:116754200-116758800	Weak transcription	K562	blood
35	chr7:116754200-116763000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:116754200-116764400	Weak transcription	HSMM	muscle
37	chr7:116754200-116764600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:116754200-116764600	Weak transcription	Aorta	Aorta
39	chr7:116754200-116797400	Weak transcription	Fetal Stomach	stomach
40	chr7:116754600-116763400	Weak transcription	Fetal Heart	heart
41	chr7:116754800-116756600	Enhancers	Psoas Muscle	Psoas
42	chr7:116755000-116759800	Weak transcription	HSMMtube	muscle
43	chr7:116755200-116756800	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr7:116755200-116772000	Weak transcription	Fetal Muscle Trunk	muscle
45	chr7:116755400-116758600	Weak transcription	GM12878-XiMat	blood
46	chr7:116755400-116764600	Weak transcription	Fetal Muscle Leg	muscle
47	chr7:116755400-116764600	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr7:116756000-116756600	Enhancers	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links