Variant report

Variant	rs11790147
Chromosome Location	chr9:95824554-95824555
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:95822333..95825278-chr9:95837106..95839130,2	K562	blood:
2	chr9:95818455..95825266-chr9:95831322..95836031,9	K562	blood:
3	chr9:95816364..95826268-chr9:95852309..95863275,20	MCF-7	breast:
4	chr9:95820029..95822398-chr9:95824222..95826137,2	MCF-7	breast:
5	chr9:95823748..95825552-chr9:95838160..95839835,2	MCF-7	breast:
6	chr9:95824479..95826328-chr9:95840688..95842946,2	K562	blood:
7	chr9:95823455..95825994-chr9:96212209..96214573,2	MCF-7	breast:
8	chr9:95812448..95814756-chr9:95824271..95826609,2	K562	blood:
9	chr9:95819521..95827100-chr9:95855273..95859349,14	K562	blood:
10	chr9:95819208..95822509-chr9:95822531..95826993,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000157303	Chromatin interaction
ENSG00000223446	Chromatin interaction
ENSG00000165233	Chromatin interaction
ENSG00000048828	Chromatin interaction
ENSG00000188938	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11790662	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11794425	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56988496	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs60481048	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62573565	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7859904	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526296	chr9:95708192-96030392	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1054767	chr9:95738134-95875977	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1035230	chr9:95770249-95934982	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv893575	chr9:95781040-95854013	Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv893576	chr9:95789960-96158277	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	esv1824329	chr9:95811604-95921347	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv893577	chr9:95812707-95872216	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv893578	chr9:95818641-95887320	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95820800-95827600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
2	chr9:95821000-95827400	Flanking Active TSS	GM12878-XiMat	blood
3	chr9:95821600-95824800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
4	chr9:95821600-95827400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
5	chr9:95821600-95827600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
6	chr9:95821800-95824800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
7	chr9:95821800-95824800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr9:95821800-95825000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
9	chr9:95821800-95825000	Flanking Active TSS	HepG2	liver
10	chr9:95821800-95825400	Flanking Active TSS	Primary T cells from cord blood	blood
11	chr9:95821800-95827400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
12	chr9:95822000-95824600	Enhancers	Gastric	stomach
13	chr9:95822000-95825000	Enhancers	Spleen	Spleen
14	chr9:95822000-95825200	Enhancers	Liver	Liver
15	chr9:95822000-95825600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
16	chr9:95822000-95825600	Enhancers	Fetal Intestine Small	intestine
17	chr9:95822000-95826200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr9:95822000-95834200	Weak transcription	Esophagus	oesophagus
19	chr9:95822000-95834200	Weak transcription	Right Atrium	heart
20	chr9:95822200-95825200	Enhancers	Pancreas	Pancrea
21	chr9:95822200-95825800	Enhancers	Fetal Intestine Large	intestine
22	chr9:95822400-95824600	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr9:95822400-95824600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr9:95822400-95826200	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr9:95822400-95828600	Enhancers	Primary hematopoietic stem cells	blood
26	chr9:95822600-95825000	Enhancers	Fetal Muscle Leg	muscle
27	chr9:95822600-95834400	Weak transcription	Brain Hippocampus Middle	brain
28	chr9:95822800-95825600	Enhancers	Fetal Thymus	thymus
29	chr9:95822800-95826000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr9:95822800-95831000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr9:95823000-95825000	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr9:95823000-95825800	Enhancers	Colonic Mucosa	Colon
33	chr9:95823000-95826000	Enhancers	Dnd41	blood
34	chr9:95823200-95824600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr9:95823200-95824800	Enhancers	Stomach Mucosa	stomach
36	chr9:95823200-95826200	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr9:95823400-95824800	Enhancers	Primary B cells from cord blood	blood
38	chr9:95823400-95826400	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr9:95823400-95827800	Weak transcription	Right Ventricle	heart
40	chr9:95823600-95826200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr9:95823600-95826600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr9:95823800-95826800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr9:95824000-95824800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr9:95824000-95824800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr9:95824000-95825400	Flanking Active TSS	Thymus	Thymus
46	chr9:95824000-95826600	Weak transcription	HSMM	muscle
47	chr9:95824000-95826800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr9:95824000-95827000	Weak transcription	Placenta	Placenta
49	chr9:95824000-95833800	Weak transcription	Ovary	ovary
50	chr9:95824200-95824600	Enhancers	Primary T killer memory cells from peripheral blood	blood

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