Variant report

Variant	rs2959646
Chromosome Location	chr8:98935189-98935190
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10091886	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs1020654	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs1020655	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs12548243	0.94[CEU][hapmap];0.80[EUR][1000 genomes]
rs1378123	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs1378124	0.87[CEU][hapmap];0.82[MEX][hapmap];0.80[EUR][1000 genomes]
rs1378125	0.91[CEU][hapmap];0.80[EUR][1000 genomes]
rs1378126	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs1454714	0.87[CEU][hapmap];0.82[MEX][hapmap]
rs1840372	0.80[EUR][1000 genomes]
rs1968721	0.81[EUR][1000 genomes]
rs2256367	0.91[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];0.88[MEX][hapmap];0.83[TSI][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2444900	0.94[EUR][1000 genomes]
rs2444903	0.91[CEU][hapmap];1.00[CHB][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2444904	1.00[CHB][hapmap]
rs2444906	0.82[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2512068	1.00[CHB][hapmap]
rs2512072	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs2513835	0.91[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2513836	0.81[EUR][1000 genomes]
rs2513837	1.00[CEU][hapmap];0.95[GIH][hapmap];0.88[MEX][hapmap];0.94[EUR][1000 genomes]
rs2513838	0.91[CEU][hapmap];0.88[MEX][hapmap];0.81[EUR][1000 genomes]
rs2513839	0.87[CEU][hapmap];0.81[EUR][1000 genomes]
rs4298468	0.80[EUR][1000 genomes]
rs4469426	0.86[CEU][hapmap];0.80[EUR][1000 genomes]
rs4512352	0.86[CEU][hapmap];0.80[EUR][1000 genomes]
rs5012370	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs6468603	0.95[CEU][hapmap];0.93[EUR][1000 genomes]
rs9693435	0.82[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 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	nsv1028055	chr8:98780445-98977746	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv891214	chr8:98849303-98990399	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv891215	chr8:98910287-98980663	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:98929200-98944800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr8:98929600-98938000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr8:98929800-98936600	Weak transcription	Fetal Lung	lung
4	chr8:98929800-98937800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr8:98930800-98950000	Weak transcription	Right Ventricle	heart
6	chr8:98931000-98938600	Weak transcription	Placenta	Placenta
7	chr8:98931000-98940800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:98931200-98938000	Weak transcription	NH-A	brain
9	chr8:98931200-98938400	Weak transcription	Left Ventricle	heart
10	chr8:98931200-98944200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr8:98931600-98937800	Weak transcription	Fetal Intestine Large	intestine
12	chr8:98931600-98938200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:98931800-98943200	Enhancers	Fetal Muscle Leg	muscle
14	chr8:98932000-98940800	Weak transcription	Ovary	ovary
15	chr8:98932200-98943400	Weak transcription	Pancreas	Pancrea
16	chr8:98932400-98936400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:98932400-98940600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:98932800-98935400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr8:98933000-98935400	Enhancers	Brain Anterior Caudate	brain
20	chr8:98933000-98935400	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr8:98933000-98935800	Enhancers	Brain Cingulate Gyrus	brain
22	chr8:98933000-98936800	Enhancers	Brain Hippocampus Middle	brain
23	chr8:98933200-98935200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:98933200-98935200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:98933200-98935400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:98933200-98935800	Enhancers	Brain Angular Gyrus	brain
27	chr8:98933200-98936400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr8:98933800-98935200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr8:98933800-98935400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr8:98934000-98935400	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr8:98934000-98935400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr8:98934000-98935800	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr8:98934000-98937600	Weak transcription	Fetal Stomach	stomach
34	chr8:98934200-98935200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr8:98934200-98943400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr8:98934600-98935200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:98934600-98936000	Enhancers	Right Atrium	heart
38	chr8:98934600-98936800	Weak transcription	Fetal Muscle Trunk	muscle
39	chr8:98934600-98938400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr8:98934800-98935200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr8:98934800-98935200	Flanking Active TSS	Brain Substantia Nigra	brain
42	chr8:98934800-98935200	Enhancers	Placenta Amnion	Placenta Amnion
43	chr8:98934800-98935400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr8:98934800-98935600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:98934800-98935800	Enhancers	Osteobl	bone
46	chr8:98934800-98936200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:98934800-98936400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr8:98934800-98938800	Enhancers	Adipose Nuclei	Adipose
49	chr8:98935000-98935200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr8:98935000-98935200	Enhancers	Rectal Mucosa Donor 31	rectum

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