Variant report

Variant	rs2185972
Chromosome Location	chr9:95922790-95922791
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:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:95922016..95922887-chr9:96067232..96067822,2	K562	blood:
2	chr9:95921846..95923192-chr9:96065668..96067944,24	MCF-7	breast:
3	chr9:95922383..95922884-chr9:96328410..96328999,2	K562	blood:
4	chr9:95921974..95922852-chr9:96725322..96725880,3	K562	blood:
5	chr9:95921958..95922909-chr9:96066342..96067827,12	MCF-7	breast:
6	chr9:95921857..95922911-chr9:96064779..96065588,5	MCF-7	breast:
7	chr9:95920898..95923528-chr9:96327939..96330398,2	MCF-7	breast:
8	chr9:95922346..95922872-chr9:96038951..96039532,2	MCF-7	breast:
9	chr9:95921993..95922867-chr9:96074788..96075566,3	K562	blood:
10	chr9:95922348..95922941-chr9:96193576..96194466,2	MCF-7	breast:
11	chr9:95922407..95924638-chr9:96036435..96038460,2	MCF-7	breast:
12	chr9:95921936..95922821-chr9:96064640..96065645,10	MCF-7	breast:
13	chr9:95921928..95922819-chr9:96190315..96190930,2	K562	blood:
14	chr9:95922249..95924729-chr9:95929251..95932279,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000237385	Chromatin interaction
ENSG00000263875	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs2154076	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2154078	0.85[ASN][1000 genomes]
rs7028251	0.86[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	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
3	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
4	nsv893579	chr9:95855100-95923091	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv893580	chr9:95855100-96099377	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv893581	chr9:95872216-95930334	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv824983	chr9:95902154-95978408	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	nsv430082	chr9:95905745-96095045	Genic enhancers Enhancers Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95907200-95944400	Weak transcription	Right Atrium	heart
2	chr9:95913400-95929000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:95919000-95925000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr9:95921800-95922800	Flanking Active TSS	HepG2	liver
5	chr9:95922000-95922800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:95922000-95922800	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr9:95922000-95922800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr9:95922000-95922800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr9:95922000-95922800	Enhancers	Adipose Nuclei	Adipose
10	chr9:95922000-95922800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr9:95922000-95922800	Enhancers	Fetal Heart	heart
12	chr9:95922000-95922800	Enhancers	Fetal Intestine Small	intestine
13	chr9:95922000-95923000	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr9:95922000-95923200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr9:95922000-95923200	Enhancers	Brain Substantia Nigra	brain
16	chr9:95922000-95923200	Enhancers	Colon Smooth Muscle	Colon
17	chr9:95922000-95925400	Enhancers	Fetal Brain Male	brain
18	chr9:95922000-95925400	Enhancers	Fetal Stomach	stomach
19	chr9:95922200-95922800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr9:95922200-95922800	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr9:95922200-95923000	Enhancers	Pancreas	Pancrea
22	chr9:95922200-95923200	Enhancers	Rectal Smooth Muscle	rectum
23	chr9:95922200-95925600	Enhancers	Fetal Muscle Trunk	muscle
24	chr9:95922200-95925600	Enhancers	Fetal Muscle Leg	muscle
25	chr9:95922400-95922800	Weak transcription	Brain Germinal Matrix	brain
26	chr9:95922400-95923400	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr9:95922400-95923800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr9:95922400-95924000	Weak transcription	Brain Hippocampus Middle	brain
29	chr9:95922400-95924200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr9:95922400-95924200	Weak transcription	Brain Anterior Caudate	brain
31	chr9:95922400-95930600	Weak transcription	Right Ventricle	heart
32	chr9:95922600-95922800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr9:95922600-95923000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr9:95922600-95923400	Weak transcription	Fetal Brain Female	brain
35	chr9:95922600-95923600	Weak transcription	Fetal Lung	lung
36	chr9:95922600-95923600	Enhancers	Stomach Smooth Muscle	stomach
37	chr9:95922600-95924200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr9:95922600-95925200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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