Variant report

Variant	rs7907626
Chromosome Location	chr10:91351404-91351405
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	chr10:91349261..91351592-chr10:91402554..91405180,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000152782	Chromatin interaction
ENSG00000232936	Chromatin interaction
ENSG00000249962	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10748522	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10785889	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10785890	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10881605	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10881606	0.89[ASN][1000 genomes]
rs11185766	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11185785	0.89[ASN][1000 genomes]
rs11185803	0.89[ASN][1000 genomes]
rs11185807	0.89[ASN][1000 genomes]
rs11185813	0.89[ASN][1000 genomes]
rs11185814	0.89[ASN][1000 genomes]
rs11185815	0.89[ASN][1000 genomes]
rs11185817	0.89[ASN][1000 genomes]
rs11592441	0.89[ASN][1000 genomes]
rs1409354	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2038921	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2296616	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34369661	0.89[ASN][1000 genomes]
rs4313481	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6586203	0.89[ASN][1000 genomes]
rs6586205	0.89[ASN][1000 genomes]
rs7076277	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7077162	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7077189	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7089984	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs728056	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7893156	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7900297	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7901886	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7903124	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7905082	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7908686	0.81[EUR][1000 genomes]
rs7918120	0.82[AFR][1000 genomes];0.98[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	nsv1041964	chr10:90861380-91378356	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91334400-91352800	Weak transcription	Fetal Lung	lung
2	chr10:91335200-91352200	Weak transcription	NHDF-Ad	bronchial
3	chr10:91335400-91370800	Weak transcription	A549	lung
4	chr10:91335400-91375600	Weak transcription	NH-A	brain
5	chr10:91339000-91351600	Weak transcription	Aorta	Aorta
6	chr10:91340200-91352400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr10:91340600-91352400	Weak transcription	Fetal Muscle Leg	muscle
8	chr10:91342200-91352000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr10:91342400-91352200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr10:91343200-91352600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr10:91343200-91372600	Weak transcription	Primary B cells from cord blood	blood
12	chr10:91343400-91369200	Weak transcription	Brain Angular Gyrus	brain
13	chr10:91344000-91369200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr10:91344800-91352000	Weak transcription	Fetal Muscle Trunk	muscle
15	chr10:91345000-91392800	Weak transcription	Hela-S3	cervix
16	chr10:91346400-91352200	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr10:91346400-91357800	Weak transcription	Fetal Kidney	kidney
18	chr10:91346400-91358000	Weak transcription	Fetal Brain Female	brain
19	chr10:91346600-91352400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr10:91346600-91352400	Weak transcription	Brain Germinal Matrix	brain
21	chr10:91346600-91352600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr10:91347000-91359200	Weak transcription	Brain Cingulate Gyrus	brain
23	chr10:91347800-91352400	Weak transcription	HMEC	breast
24	chr10:91348400-91352200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr10:91348600-91373200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr10:91348800-91351600	Weak transcription	Right Ventricle	heart
27	chr10:91348800-91351600	Weak transcription	HepG2	liver
28	chr10:91348800-91351800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr10:91348800-91351800	Weak transcription	Primary hematopoietic stem cells	blood
30	chr10:91348800-91352400	Weak transcription	Duodenum Mucosa	Duodenum
31	chr10:91348800-91358000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr10:91349200-91352400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr10:91349200-91353400	Enhancers	Fetal Heart	heart
34	chr10:91349200-91367600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr10:91349400-91351600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr10:91349400-91351600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr10:91349400-91352400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr10:91349400-91357600	Weak transcription	HSMMtube	muscle
39	chr10:91349400-91372400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr10:91350200-91352400	Enhancers	Fetal Intestine Large	intestine
41	chr10:91350200-91353800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr10:91350200-91359800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr10:91350400-91352200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr10:91350400-91354600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr10:91350600-91353800	Strong transcription	Dnd41	blood
46	chr10:91350600-91354200	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr10:91350600-91355000	Strong transcription	HUES48 Cell Line	embryonic stem cell
48	chr10:91350800-91352400	Weak transcription	Brain Hippocampus Middle	brain
49	chr10:91350800-91363200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr10:91351000-91351600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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