Variant report

Variant	rs7181825
Chromosome Location	chr15:93339357-93339358
allele	C/T
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:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:93337836..93370220-chr15:93420085..93452591,332	K562	blood:
2	chr15:93339283..93342293-chr15:93459393..93462402,3	MCF-7	breast:
3	chr15:93338892..93343222-chr15:93422830..93428061,5	MCF-7	breast:
4	chr15:93337242..93342192-chr15:93350779..93355697,6	MCF-7	breast:
5	chr15:93336742..93338839-chr15:93339129..93341121,2	K562	blood:
6	chr15:93339018..93342191-chr15:93351438..93355555,4	MCF-7	breast:
7	chr15:93338780..93342194-chr15:93442202..93446226,4	MCF-7	breast:
8	chr15:93338607..93340953-chr15:93442127..93443801,2	MCF-7	breast:
9	chr15:93333327..93367027-chr15:93419774..93462750,363	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHD2-8	chr15:93338714-93340338	NR_033769

No data

Variant related genes	Relation type
ENSG00000185442	Chromatin interaction
ENSG00000264173	Chromatin interaction
ENSG00000173575	Chromatin interaction
ENSG00000258922	Chromatin interaction
ENSG00000272888	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12101782	0.83[YRI][hapmap];0.87[AMR][1000 genomes]
rs28574593	0.89[EUR][1000 genomes]
rs28660596	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28685637	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28754851	1.00[EUR][1000 genomes]
rs28805897	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28881565	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7182474	0.83[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv904499	chr15:92914795-93472582	Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	163 gene(s)	inside rSNPs	diseases
2	nsv948738	chr15:93070742-93728147	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
3	nsv1049490	chr15:93134405-93591660	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
4	nsv1042292	chr15:93286333-93374887	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
5	nsv984199	chr15:93288362-93381522	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
6	nsv530846	chr15:93323949-94030462	Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	153 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:93304800-93344800	Weak transcription	Aorta	Aorta
2	chr15:93315400-93340200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr15:93315400-93340400	Weak transcription	Pancreas	Pancrea
4	chr15:93315400-93340600	Weak transcription	Ovary	ovary
5	chr15:93323400-93340400	Weak transcription	Hela-S3	cervix
6	chr15:93324200-93344600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr15:93324400-93340000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr15:93324400-93340600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr15:93325400-93340000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr15:93325400-93351000	Weak transcription	Primary T cells from cord blood	blood
11	chr15:93325600-93340200	Weak transcription	Brain Germinal Matrix	brain
12	chr15:93325600-93347400	Weak transcription	Right Ventricle	heart
13	chr15:93325800-93340600	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr15:93331200-93340600	Weak transcription	Lung	lung
15	chr15:93331200-93346800	Weak transcription	Psoas Muscle	Psoas
16	chr15:93332000-93340200	Weak transcription	Brain Angular Gyrus	brain
17	chr15:93332400-93340200	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr15:93334200-93340600	Weak transcription	Fetal Intestine Small	intestine
19	chr15:93338200-93339600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr15:93338200-93340600	Weak transcription	NHLF	lung
21	chr15:93338800-93339800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr15:93338800-93340600	Flanking Active TSS	HepG2	liver
23	chr15:93338800-93341000	Enhancers	Liver	Liver
24	chr15:93339200-93340400	Weak transcription	Fetal Kidney	kidney

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