Variant report

Variant	rs3735885
Chromosome Location	chr8:99205111-99205112
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr8:99205035-99205279	NB4	blood:	n/a	chr8:99205100-99205110 chr8:99205142-99205152
2	MAX	chr8:99204985-99205214	NB4	blood:	n/a	chr8:99205100-99205110 chr8:99205142-99205152
3	TEAD4	chr8:99204753-99205125	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:99184801..99187794-chr8:99204671..99207468,2	MCF-7	breast:

Variant related genes	Relation type
RNU6-914P	TF binding region

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10086902	0.98[ASN][1000 genomes]
rs10095850	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1129891	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs13264255	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13276153	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1542289	0.81[ASW][hapmap]
rs2002424	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2053935	0.81[ASW][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs2122928	1.00[CHB][hapmap];0.95[JPT][hapmap];0.80[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs3735887	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.90[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4734391	1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4734392	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4735536	1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs4735538	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs62522244	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6991266	0.86[ASW][hapmap];0.96[CEU][hapmap];0.83[CHB][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.83[LWK][hapmap];0.90[MEX][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6996271	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7005080	0.80[JPT][hapmap]
rs7833247	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7838769	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs896416	0.81[ASW][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs9642948	0.83[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032904	chr8:98756076-99476925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv539687	chr8:98756076-99476925	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv831405	chr8:99095239-99260934	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv891216	chr8:99153160-99209248	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99191600-99243800	Weak transcription	Spleen	Spleen
2	chr8:99192200-99205800	Weak transcription	Fetal Intestine Small	intestine
3	chr8:99192200-99210600	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr8:99192200-99214400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr8:99192800-99210400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:99193400-99206400	Weak transcription	Pancreas	Pancrea
7	chr8:99194800-99216600	Weak transcription	Colonic Mucosa	Colon
8	chr8:99197000-99209200	Weak transcription	HSMMtube	muscle
9	chr8:99197000-99210400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr8:99197000-99219000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:99197400-99206200	Weak transcription	Aorta	Aorta
12	chr8:99197400-99206200	Weak transcription	Rectal Smooth Muscle	rectum
13	chr8:99197800-99215400	Weak transcription	Fetal Stomach	stomach
14	chr8:99198000-99210400	Weak transcription	Osteobl	bone
15	chr8:99198000-99217000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr8:99198200-99207200	Weak transcription	Esophagus	oesophagus
17	chr8:99198200-99215200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr8:99198200-99239200	Weak transcription	Lung	lung
19	chr8:99201800-99214400	Weak transcription	Left Ventricle	heart
20	chr8:99202000-99215200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr8:99202000-99215200	Weak transcription	NHDF-Ad	bronchial
22	chr8:99203600-99210600	Weak transcription	Adipose Nuclei	Adipose
23	chr8:99203800-99205200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr8:99203800-99252600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr8:99204000-99214200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr8:99204400-99206800	Enhancers	K562	blood
27	chr8:99204600-99205400	Enhancers	Fetal Heart	heart
28	chr8:99204600-99214800	Weak transcription	Gastric	stomach
29	chr8:99204800-99205200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:99204800-99205200	Strong transcription	Fetal Intestine Large	intestine
31	chr8:99204800-99205200	Enhancers	Right Atrium	heart
32	chr8:99204800-99205400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:99204800-99205600	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr8:99204800-99206600	Strong transcription	Ovary	ovary
35	chr8:99205000-99205600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr8:99205000-99206400	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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