Variant report

Variant	rs10229491
Chromosome Location	chr7:105480279-105480280
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:105470129..105472971-chr7:105479942..105482901,2	MCF-7	breast:
2	chr7:105467716..105469978-chr7:105478235..105481087,2	MCF-7	breast:
3	chr7:105480095..105482542-chr7:105492125..105494142,2	K562	blood:
4	chr7:105471516..105474316-chr7:105479305..105481935,2	MCF-7	breast:
5	chr7:105475286..105478263-chr7:105479596..105482018,2	MCF-7	breast:

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs2108324	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs212412	0.98[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs212413	0.98[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs4727628	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs740307	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs740309	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7781203	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7792471	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs886797	0.87[AMR][1000 genomes];0.98[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	nsv1027213	chr7:105438610-106022869	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 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	chr7:105465400-105506600	Weak transcription	Fetal Intestine Large	intestine
2	chr7:105471800-105483600	Weak transcription	Pancreas	Pancrea
3	chr7:105471800-105484000	Weak transcription	Primary T cells from cord blood	blood
4	chr7:105472400-105489800	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr7:105473000-105494400	Weak transcription	Fetal Lung	lung
6	chr7:105473200-105490000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr7:105473400-105484400	Weak transcription	Hela-S3	cervix
8	chr7:105473800-105480400	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr7:105473800-105481000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:105477600-105480800	Enhancers	Fetal Brain Male	brain
11	chr7:105478000-105480400	Enhancers	Fetal Muscle Leg	muscle
12	chr7:105478000-105481000	Enhancers	Lung	lung
13	chr7:105478000-105481800	Enhancers	Fetal Muscle Trunk	muscle
14	chr7:105478000-105482200	Enhancers	Rectal Smooth Muscle	rectum
15	chr7:105478400-105480400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:105478400-105481000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:105478400-105481600	Weak transcription	Psoas Muscle	Psoas
18	chr7:105478600-105482000	Enhancers	NHEK	skin
19	chr7:105478600-105483200	Enhancers	HMEC	breast
20	chr7:105478600-105483400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:105478800-105480600	Enhancers	H9 Cell Line	embryonic stem cell
22	chr7:105478800-105480600	Enhancers	Brain Cingulate Gyrus	brain
23	chr7:105478800-105482600	Enhancers	NHLF	lung
24	chr7:105478800-105484200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr7:105479000-105480800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr7:105479000-105481600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:105479000-105482200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:105479000-105483400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr7:105479200-105480600	Enhancers	Brain Germinal Matrix	brain
30	chr7:105479200-105481000	Enhancers	Fetal Brain Female	brain
31	chr7:105479200-105481800	Enhancers	Fetal Thymus	thymus
32	chr7:105479200-105482600	Enhancers	Esophagus	oesophagus
33	chr7:105479400-105480600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr7:105479400-105480600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr7:105479400-105481000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr7:105479400-105481200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr7:105479400-105482000	Weak transcription	Colonic Mucosa	Colon
38	chr7:105479400-105482200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr7:105479400-105482400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr7:105479400-105483800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr7:105479400-105490000	Weak transcription	NHDF-Ad	bronchial
42	chr7:105479400-105494400	Weak transcription	Brain Angular Gyrus	brain
43	chr7:105479600-105481400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:105479600-105483600	Weak transcription	Fetal Intestine Small	intestine
45	chr7:105479600-105487600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr7:105479600-105489600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:105479600-105489600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:105479600-105489800	Weak transcription	HSMM	muscle
49	chr7:105479600-105494400	Weak transcription	Fetal Kidney	kidney
50	chr7:105479600-105506200	Weak transcription	Duodenum Mucosa	Duodenum

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