Variant report

Variant	rs7121157
Chromosome Location	chr11:10002359-10002360
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:10000703..10003036-chr11:10327811..10330632,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000133805	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs11042575	0.93[ASN][1000 genomes]
rs11042586	0.80[ASN][1000 genomes]
rs11824183	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11825114	0.90[ASN][1000 genomes]
rs12099014	0.90[ASN][1000 genomes]
rs12574585	0.91[ASN][1000 genomes]
rs12577989	0.90[ASN][1000 genomes]
rs16907318	0.94[ASN][1000 genomes]
rs16907329	0.94[ASN][1000 genomes]
rs16907334	0.90[ASN][1000 genomes]
rs2403261	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2403263	0.84[ASN][1000 genomes]
rs2896513	0.81[ASN][1000 genomes]
rs2896514	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2896515	0.83[ASN][1000 genomes]
rs4910090	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4910091	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4910092	0.91[ASN][1000 genomes]
rs55927206	0.91[ASN][1000 genomes]
rs56850765	0.80[ASN][1000 genomes]
rs57017265	0.94[ASN][1000 genomes]
rs57180563	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58419649	0.90[ASN][1000 genomes]
rs58687525	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61877012	0.83[ASN][1000 genomes]
rs61877018	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61877043	0.84[ASN][1000 genomes]
rs61877045	0.80[ASN][1000 genomes]
rs67011375	0.86[ASN][1000 genomes]
rs67132348	0.81[AFR][1000 genomes]
rs67404901	0.81[AMR][1000 genomes]
rs7103902	0.91[ASN][1000 genomes]
rs7106234	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7107302	0.91[ASN][1000 genomes]
rs7107916	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7113715	0.84[ASN][1000 genomes]
rs7114031	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7128234	0.82[ASN][1000 genomes]
rs7128838	0.83[ASN][1000 genomes]
rs7130610	0.83[ASN][1000 genomes]
rs713402	0.94[ASN][1000 genomes]
rs72855628	0.90[ASN][1000 genomes]
rs72855633	0.90[ASN][1000 genomes]
rs72855635	0.90[ASN][1000 genomes]
rs72855636	0.90[ASN][1000 genomes]
rs72855639	0.90[ASN][1000 genomes]
rs72855643	0.91[ASN][1000 genomes]
rs72855678	0.90[ASN][1000 genomes]
rs7925889	0.84[ASN][1000 genomes]
rs7926141	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7930920	0.84[ASN][1000 genomes]
rs7932484	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7935297	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7936461	0.83[ASN][1000 genomes]
rs7940348	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7949164	0.84[ASN][1000 genomes]
rs7949322	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933855	chr11:9645441-10130519	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS 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 miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv896988	chr11:9912052-10012511	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv896989	chr11:9951968-10059623	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
4	esv1819684	chr11:9973062-10012511	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9973800-10010600	Weak transcription	Fetal Brain Male	brain
2	chr11:9981000-10020000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr11:9981200-10004200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:9981200-10009200	Weak transcription	Brain Germinal Matrix	brain
5	chr11:9981400-10003400	Weak transcription	Brain Anterior Caudate	brain
6	chr11:9981400-10003400	Weak transcription	NHEK	skin
7	chr11:9981400-10003600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:9981400-10004200	Weak transcription	Esophagus	oesophagus
9	chr11:9981400-10004200	Weak transcription	Lung	lung
10	chr11:9981400-10004400	Weak transcription	HepG2	liver
11	chr11:9981400-10008800	Weak transcription	Primary T cells from cord blood	blood
12	chr11:9981400-10010200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr11:9981400-10014800	Weak transcription	Dnd41	blood
14	chr11:9981400-10017000	Weak transcription	Stomach Smooth Muscle	stomach
15	chr11:9981400-10051600	Weak transcription	Aorta	Aorta
16	chr11:9981600-10003400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr11:9981800-10003400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr11:9981800-10004800	Weak transcription	Ovary	ovary
19	chr11:9983600-10004800	Weak transcription	Fetal Lung	lung
20	chr11:9983600-10023200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr11:9984600-10010200	Weak transcription	Fetal Kidney	kidney
22	chr11:9985800-10004000	Weak transcription	Placenta	Placenta
23	chr11:9985800-10004200	Weak transcription	Fetal Muscle Leg	muscle
24	chr11:9985800-10004400	Weak transcription	Fetal Muscle Trunk	muscle
25	chr11:9985800-10021600	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr11:9985800-10023600	Weak transcription	Primary B cells from cord blood	blood
27	chr11:9985800-10049000	Weak transcription	Left Ventricle	heart
28	chr11:9986000-10006000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr11:9987200-10003600	Weak transcription	Hela-S3	cervix
30	chr11:9987600-10002600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr11:9989400-10004000	Weak transcription	Fetal Stomach	stomach
32	chr11:9990000-10002600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:9990000-10004800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:9990000-10012600	Weak transcription	Liver	Liver
35	chr11:9990000-10018200	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr11:9990200-10006200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:9990400-10028200	Weak transcription	Fetal Brain Female	brain
38	chr11:9990600-10003800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr11:9991200-10060000	Weak transcription	Colon Smooth Muscle	Colon
40	chr11:9994800-10041800	Weak transcription	Rectal Smooth Muscle	rectum
41	chr11:9995000-10003600	Weak transcription	Brain Hippocampus Middle	brain
42	chr11:9995000-10008800	Weak transcription	Primary B cells from peripheral blood	blood
43	chr11:9995400-10004200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr11:9996000-10004200	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr11:9996000-10024600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr11:9996200-10002400	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr11:9999000-10004000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr11:9999200-10003600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:9999400-10004200	Weak transcription	Fetal Intestine Large	intestine
50	chr11:9999600-10002800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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