Variant report

Variant	rs13273698
Chromosome Location	chr8:96237160-96237161
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:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:96223779..96226497-chr8:96236467..96238844,2	K562	blood:
2	chr8:96234981..96237972-chr8:97273758..97275615,2	MCF-7	breast:
3	chr8:96204194..96207440-chr8:96236906..96239736,3	MCF-7	breast:
4	chr8:96145188..96147902-chr8:96236051..96240393,4	K562	blood:
5	chr8:96039470..96042211-chr8:96236701..96239677,2	K562	blood:
6	chr8:96222002..96228732-chr8:96228964..96237755,16	MCF-7	breast:
7	chr8:96078172..96080522-chr8:96236324..96239006,2	MCF-7	breast:
8	chr8:96145749..96147825-chr8:96236619..96239498,2	MCF-7	breast:
9	chr8:96236593..96238582-chr8:96243971..96246452,2	K562	blood:
10	chr8:96234462..96239842-chr8:96279058..96283088,6	K562	blood:
11	chr8:96143360..96148175-chr8:96235522..96240876,10	MCF-7	breast:
12	chr8:96236752..96238827-chr8:128748699..128750665,2	MCF-7	breast:
13	chr8:96148421..96149927-chr8:96235607..96238590,2	K562	blood:
14	chr8:96222030..96225621-chr8:96235538..96238037,4	MCF-7	breast:
15	chr8:96232323..96234888-chr8:96235835..96240054,4	MCF-7	breast:
16	chr8:96236807..96240008-chr8:96246119..96247780,3	MCF-7	breast:
17	chr8:96096993..96099961-chr8:96235932..96238973,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253773	Chromatin interaction
ENSG00000156172	Chromatin interaction
ENSG00000156471	Chromatin interaction
ENSG00000156469	Chromatin interaction
ENSG00000253351	Chromatin interaction
ENSG00000175895	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs55934128	0.86[ASN][1000 genomes]
rs6984009	0.86[ASN][1000 genomes]
rs7003496	0.86[ASN][1000 genomes]
rs73268339	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv523655	chr8:96205920-96239113	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv16466	chr8:96206151-96243934	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv6315	chr8:96216465-96261671	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv465741	chr8:96221122-96247835	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv611759	chr8:96221122-96247835	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96219800-96251800	Enhancers	Primary B cells from peripheral blood	blood
2	chr8:96223600-96237200	Weak transcription	Fetal Intestine Small	intestine
3	chr8:96228000-96238800	Weak transcription	Thymus	Thymus
4	chr8:96228800-96237600	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr8:96231600-96237600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr8:96231600-96241600	Enhancers	Fetal Thymus	thymus
7	chr8:96231800-96237600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:96233000-96237800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:96233200-96238800	Weak transcription	Spleen	Spleen
10	chr8:96233800-96237800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:96234000-96240000	Weak transcription	Primary T cells from cord blood	blood
12	chr8:96234200-96237400	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr8:96234200-96237600	Weak transcription	Fetal Lung	lung
14	chr8:96234200-96238000	Weak transcription	GM12878-XiMat	blood
15	chr8:96234200-96239000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:96235000-96239000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:96235000-96239600	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr8:96235000-96239600	Enhancers	Placenta	Placenta
19	chr8:96235000-96242200	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr8:96235200-96237600	Enhancers	HepG2	liver
21	chr8:96235200-96238600	Enhancers	Left Ventricle	heart
22	chr8:96235200-96238800	Enhancers	Fetal Heart	heart
23	chr8:96235200-96239000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr8:96235200-96239000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr8:96235200-96239000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr8:96235200-96239600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:96235200-96249200	Enhancers	Primary B cells from cord blood	blood
28	chr8:96235400-96238200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:96235400-96238800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr8:96235400-96239000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr8:96235400-96239000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr8:96235400-96239000	Enhancers	Brain Anterior Caudate	brain
33	chr8:96235400-96239400	Enhancers	Esophagus	oesophagus
34	chr8:96235400-96239400	Enhancers	Fetal Muscle Leg	muscle
35	chr8:96235400-96240000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr8:96235600-96239000	Enhancers	Right Ventricle	heart
37	chr8:96235600-96239200	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr8:96235600-96239600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr8:96235800-96239400	Enhancers	Placenta Amnion	Placenta Amnion
40	chr8:96235800-96240000	Enhancers	Brain Hippocampus Middle	brain
41	chr8:96236200-96237400	Enhancers	K562	blood
42	chr8:96236200-96237600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr8:96236200-96237600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr8:96236200-96237600	Weak transcription	Adipose Nuclei	Adipose
45	chr8:96236200-96237600	Weak transcription	Psoas Muscle	Psoas
46	chr8:96236200-96237600	Weak transcription	Stomach Smooth Muscle	stomach
47	chr8:96236200-96237800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr8:96236200-96238800	Enhancers	HMEC	breast
49	chr8:96236200-96238800	Enhancers	Osteobl	bone
50	chr8:96236200-96239000	Enhancers	NHDF-Ad	bronchial

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