Variant report

Variant	rs13440199
Chromosome Location	chr9:116107074-116107075
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:116102720..116107904-chr9:116161009..116164019,5	MCF-7	breast:
2	chr9:116106104..116109704-chr9:116111339..116114258,3	K562	blood:
3	chr9:116091449..116094429-chr9:116104938..116107109,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000119411	Chromatin interaction
ENSG00000148218	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10481639	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10817480	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981726	0.93[EUR][1000 genomes]
rs10981731	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10981733	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981740	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981741	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981742	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981743	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981744	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981745	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981746	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981747	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981748	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981750	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981751	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981752	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981760	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12006029	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12337552	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12338029	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12339382	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12344170	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12344525	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12351134	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12351296	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12351630	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1543535	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16932583	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16932649	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17764563	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28495580	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28607343	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs41276795	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4324980	0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4437724	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4442214	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4445296	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4560870	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4636275	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs5012573	0.95[EUR][1000 genomes]
rs60528957	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs60849153	0.93[ASN][1000 genomes]
rs66649870	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs67292897	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7025347	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7027445	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7041782	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7863485	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7865438	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7875945	0.95[EUR][1000 genomes];0.93[ASN][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	nsv530949	chr9:115821128-116487796	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv1042663	chr9:115920158-116167140	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv893744	chr9:115934852-116170227	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13440199	BSPRY	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116103000-116107200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr9:116103000-116111800	Weak transcription	Lung	lung
3	chr9:116103200-116107200	Weak transcription	Brain Angular Gyrus	brain
4	chr9:116103200-116107400	Weak transcription	Fetal Intestine Large	intestine
5	chr9:116103200-116108000	Enhancers	Fetal Heart	heart
6	chr9:116103200-116108200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr9:116103200-116108600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr9:116103200-116108800	Weak transcription	Placenta	Placenta
9	chr9:116103200-116110000	Weak transcription	Right Atrium	heart
10	chr9:116103200-116111400	Weak transcription	Stomach Mucosa	stomach
11	chr9:116103200-116111400	Weak transcription	GM12878-XiMat	blood
12	chr9:116104000-116108400	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr9:116105400-116108200	Enhancers	Brain Hippocampus Middle	brain
14	chr9:116105400-116108800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr9:116105600-116107600	Enhancers	Colon Smooth Muscle	Colon
16	chr9:116105600-116107800	Enhancers	Primary hematopoietic stem cells	blood
17	chr9:116105600-116107800	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr9:116105600-116107800	Enhancers	Rectal Smooth Muscle	rectum
19	chr9:116105600-116108200	Enhancers	Brain Substantia Nigra	brain
20	chr9:116105800-116107600	Enhancers	Fetal Lung	lung
21	chr9:116105800-116110200	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr9:116105800-116111400	Enhancers	Fetal Intestine Small	intestine
23	chr9:116105800-116111400	Weak transcription	Right Ventricle	heart
24	chr9:116106000-116107200	Weak transcription	Brain Anterior Caudate	brain
25	chr9:116106000-116107200	Weak transcription	Small Intestine	intestine
26	chr9:116106200-116107600	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr9:116106200-116111400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr9:116106400-116107400	Weak transcription	HepG2	liver
29	chr9:116106400-116108800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr9:116106400-116109200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr9:116106400-116110400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr9:116106600-116109400	Weak transcription	Colonic Mucosa	Colon
33	chr9:116106600-116110000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr9:116106600-116111400	Weak transcription	Liver	Liver
35	chr9:116106600-116111400	Weak transcription	Esophagus	oesophagus
36	chr9:116106600-116111400	Weak transcription	Pancreas	Pancrea
37	chr9:116106600-116111800	Weak transcription	K562	blood
38	chr9:116106800-116107200	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr9:116107000-116108000	Enhancers	Duodenum Mucosa	Duodenum
40	chr9:116107000-116108200	Enhancers	Brain Cingulate Gyrus	brain
41	chr9:116107000-116108200	Enhancers	Rectal Mucosa Donor 29	rectum

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