Variant report

Variant	rs61687771
Chromosome Location	chr9:96444934-96444935
allele	C/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:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:96444128..96445167-chr9:96724637..96725907,10	K562	blood:
2	chr9:96442742..96446259-chr9:96719078..96722660,3	MCF-7	breast:
3	chr9:96444762..96447288-chr9:96447833..96449686,2	MCF-7	breast:
4	chr9:96443766..96445914-chr9:96765340..96767005,2	MCF-7	breast:
5	chr9:96444176..96445839-chr9:96582616..96583550,7	MCF-7	breast:
6	chr9:96444213..96445067-chr9:96670972..96672102,3	MCF-7	breast:
7	chr9:96443866..96445187-chr9:96726929..96728716,7	MCF-7	breast:
8	chr9:96444144..96445247-chr9:96764543..96765553,7	MCF-7	breast:
9	chr9:96443546..96446066-chr9:96715342..96717948,2	MCF-7	breast:
10	chr9:96444155..96444970-chr9:96725446..96726134,3	MCF-7	breast:
11	chr9:96444184..96445089-chr9:96724737..96725876,7	MCF-7	breast:
12	chr10:78850015..78850515-chr9:96444142..96445078,2	MCF-7	breast:
13	chr9:96444131..96445035-chr9:96705927..96707008,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000131668	Chromatin interaction
ENSG00000235601	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs16909308	1.00[AMR][1000 genomes]
rs16912641	0.90[EUR][1000 genomes]
rs2001587	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2001588	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2398854	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35505758	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs41274432	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41276200	1.00[AMR][1000 genomes]
rs57824368	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59044538	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60016166	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7030805	1.00[AMR][1000 genomes]
rs73522240	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73522243	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73522252	0.84[EUR][1000 genomes]
rs73522271	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73522273	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73522292	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73522296	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523904	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523906	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523907	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523908	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523910	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523917	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523922	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523932	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523933	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523934	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523942	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523944	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523946	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73527828	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7870558	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	nsv893586	chr9:96363859-96493773	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv1036609	chr9:96375217-96477641	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv893587	chr9:96383605-96451784	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96412600-96445000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:96436800-96447000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr9:96440600-96447600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr9:96440800-96445600	Weak transcription	NHLF	lung
5	chr9:96440800-96447400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr9:96441000-96446400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr9:96441000-96447200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr9:96442200-96446200	Weak transcription	Lung	lung
9	chr9:96442400-96446200	Weak transcription	Thymus	Thymus
10	chr9:96442400-96447400	Weak transcription	Adipose Nuclei	Adipose
11	chr9:96442400-96447600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr9:96442600-96447600	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr9:96442800-96449200	Weak transcription	Fetal Muscle Leg	muscle
14	chr9:96443600-96445200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr9:96444000-96445000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
16	chr9:96444000-96445600	Enhancers	Placenta	Placenta
17	chr9:96444200-96449400	Enhancers	Fetal Stomach	stomach
18	chr9:96444600-96445000	Enhancers	HepG2	liver
19	chr9:96444800-96445000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr9:96444800-96445000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr9:96444800-96445000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr9:96444800-96445000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr9:96444800-96445000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr9:96444800-96445200	Enhancers	Stomach Smooth Muscle	stomach
25	chr9:96444800-96446000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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