Variant report

Variant	rs10991878
Chromosome Location	chr9:94074881-94074882
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:94066213..94070359-chr9:94073999..94077137,3	MCF-7	breast:
2	chr9:94072233..94075154-chr9:94185612..94187624,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000165030	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10820847	1.00[AMR][1000 genomes]
rs10991860	1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10991865	1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10991902	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10991920	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893570	chr9:93973938-94148084	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv482877	chr9:93979351-94157734	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv893571	chr9:94072113-94202927	Genic enhancers Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94029400-94080000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr9:94033800-94096400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:94039200-94089800	Weak transcription	Esophagus	oesophagus
4	chr9:94052000-94119200	Weak transcription	Small Intestine	intestine
5	chr9:94053400-94103800	Weak transcription	HSMMtube	muscle
6	chr9:94055600-94089600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr9:94056400-94089400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr9:94057600-94086400	Weak transcription	Fetal Brain Male	brain
9	chr9:94057600-94089400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:94058000-94088000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr9:94058400-94080400	Weak transcription	Fetal Kidney	kidney
12	chr9:94058400-94089400	Weak transcription	Brain Angular Gyrus	brain
13	chr9:94058800-94091800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr9:94059200-94089400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr9:94059400-94077600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr9:94059600-94077000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr9:94059600-94080400	Weak transcription	Fetal Muscle Trunk	muscle
18	chr9:94059600-94080600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr9:94059600-94082000	Weak transcription	Gastric	stomach
20	chr9:94059600-94103400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr9:94059800-94089400	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr9:94059800-94089400	Weak transcription	Dnd41	blood
23	chr9:94059800-94089600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr9:94059800-94101400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr9:94060000-94080200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr9:94060000-94080600	Weak transcription	Liver	Liver
27	chr9:94060000-94089200	Weak transcription	Primary B cells from peripheral blood	blood
28	chr9:94060200-94089400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr9:94060400-94089400	Weak transcription	Fetal Thymus	thymus
30	chr9:94061000-94084600	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr9:94061000-94089600	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr9:94063400-94089400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr9:94064000-94075600	Weak transcription	Fetal Intestine Small	intestine
34	chr9:94064000-94076200	Weak transcription	Fetal Stomach	stomach
35	chr9:94064000-94089400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr9:94064000-94089400	Weak transcription	Ovary	ovary
37	chr9:94064200-94078400	Weak transcription	Rectal Smooth Muscle	rectum
38	chr9:94065400-94082200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr9:94065400-94089400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr9:94065400-94101400	Weak transcription	K562	blood
41	chr9:94065600-94075600	Weak transcription	NH-A	brain
42	chr9:94065600-94077600	Weak transcription	Stomach Mucosa	stomach
43	chr9:94065600-94089400	Weak transcription	Brain Anterior Caudate	brain
44	chr9:94065600-94089400	Weak transcription	Stomach Smooth Muscle	stomach
45	chr9:94065600-94091400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr9:94065600-94102000	Weak transcription	Hela-S3	cervix
47	chr9:94065800-94075000	Weak transcription	HMEC	breast
48	chr9:94066000-94089600	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr9:94066400-94103400	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr9:94066600-94089600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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