Variant report

Variant	rs16900589
Chromosome Location	chr8:90795464-90795465
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:90795048..90796899-chr8:90901690..90903270,2	MCF-7	breast:
2	chr8:90772791..90774637-chr8:90794290..90797972,3	MCF-7	breast:
3	chr8:90790967..90797055-chr8:90994383..90998113,5	MCF-7	breast:
4	chr8:90768588..90770877-chr8:90794165..90796398,2	MCF-7	breast:
5	chr8:90794527..90798218-chr8:90801291..90805045,3	K562	blood:

Variant related genes	Relation type
ENSG00000104312	Chromatin interaction
ENSG00000104320	Chromatin interaction
ENSG00000251136	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10504882	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10504883	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16900025	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs16900480	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs16900484	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs16900581	1.00[ASN][1000 genomes]
rs16900592	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16900617	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16900677	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16900711	1.00[ASN][1000 genomes]
rs2293807	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs383592	0.95[YRI][hapmap]
rs39499	0.87[YRI][hapmap]
rs40544	0.95[YRI][hapmap]
rs42490	0.95[YRI][hapmap]
rs431264	0.89[YRI][hapmap]
rs55697113	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55702923	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs55881928	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55914077	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs55945927	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs56118532	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs56275901	0.87[ASN][1000 genomes]
rs56302550	0.90[ASN][1000 genomes]
rs56716125	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs56793332	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs57701764	0.90[ASN][1000 genomes]
rs58330617	0.90[ASN][1000 genomes]
rs58972679	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs59312383	0.90[ASN][1000 genomes]
rs59581432	0.90[ASN][1000 genomes]
rs59678171	0.90[ASN][1000 genomes]
rs59924471	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59941801	0.90[ASN][1000 genomes]
rs59988473	0.90[ASN][1000 genomes]
rs60183011	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs60327583	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs60651842	0.90[ASN][1000 genomes]
rs60691618	0.90[ASN][1000 genomes]
rs60772522	0.90[ASN][1000 genomes]
rs60959735	0.90[ASN][1000 genomes]
rs61017576	0.81[ASN][1000 genomes]
rs61044501	0.87[ASN][1000 genomes]
rs61258433	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61450435	0.90[ASN][1000 genomes]
rs61662505	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6998044	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7010806	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs73694459	0.87[ASN][1000 genomes]
rs73694461	0.87[ASN][1000 genomes]
rs73694462	0.87[ASN][1000 genomes]
rs73694463	0.85[ASN][1000 genomes]
rs73694485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs73694486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs73694487	1.00[ASN][1000 genomes]
rs73694488	1.00[ASN][1000 genomes]
rs73694490	1.00[ASN][1000 genomes]
rs73694492	1.00[ASN][1000 genomes]
rs73694493	1.00[ASN][1000 genomes]
rs73694496	0.95[ASN][1000 genomes]
rs7817339	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7829418	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7830914	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs7839470	0.87[ASN][1000 genomes]
rs7839478	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9721216	0.88[ASN][1000 genomes]

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	nsv891180	chr8:90697810-90802491	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv933502	chr8:90702392-91049100	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
3	nsv934114	chr8:90720182-90999106	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
4	nsv891181	chr8:90737258-90819998	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
5	nsv891182	chr8:90785685-90888786	Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90771000-90797000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:90771600-90803800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr8:90771800-90805000	Weak transcription	Esophagus	oesophagus
4	chr8:90772000-90796800	Weak transcription	Lung	lung
5	chr8:90772000-90797000	Weak transcription	Ovary	ovary
6	chr8:90772200-90802000	Weak transcription	Colonic Mucosa	Colon
7	chr8:90772200-90802400	Weak transcription	Spleen	Spleen
8	chr8:90772200-90805200	Weak transcription	Fetal Brain Male	brain
9	chr8:90772200-90807200	Weak transcription	Pancreas	Pancrea
10	chr8:90772200-90809400	Weak transcription	Small Intestine	intestine
11	chr8:90772400-90802200	Weak transcription	Colon Smooth Muscle	Colon
12	chr8:90773000-90806800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr8:90773000-90812400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr8:90773200-90799000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr8:90774200-90803600	Weak transcription	Fetal Heart	heart
16	chr8:90775800-90807200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:90776400-90799800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr8:90779000-90801200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr8:90779600-90802200	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr8:90781400-90806600	Weak transcription	Right Ventricle	heart
21	chr8:90781800-90805600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:90783600-90803600	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr8:90783800-90829000	Weak transcription	Aorta	Aorta
24	chr8:90784400-90799400	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr8:90785600-90797000	Weak transcription	Fetal Intestine Small	intestine
26	chr8:90785600-90799200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr8:90785600-90813800	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr8:90785800-90807200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr8:90785800-90810800	Weak transcription	Fetal Brain Female	brain
30	chr8:90786000-90796000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr8:90786000-90799000	Weak transcription	Brain Angular Gyrus	brain
32	chr8:90786000-90799600	Weak transcription	Brain Substantia Nigra	brain
33	chr8:90786000-90813000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr8:90786400-90809800	Weak transcription	HepG2	liver
35	chr8:90786800-90797000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr8:90786800-90797800	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr8:90786800-90798400	Weak transcription	HSMMtube	muscle
38	chr8:90787000-90797000	Weak transcription	Fetal Kidney	kidney
39	chr8:90787400-90796600	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr8:90787400-90799200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr8:90788400-90796400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr8:90788400-90796600	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr8:90788600-90799000	Weak transcription	Brain Anterior Caudate	brain
44	chr8:90789000-90797000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:90789400-90797000	Weak transcription	Fetal Stomach	stomach
46	chr8:90789400-90798400	Weak transcription	Brain Cingulate Gyrus	brain
47	chr8:90792000-90795600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
48	chr8:90792000-90804200	Strong transcription	HUES64 Cell Line	embryonic stem cell
49	chr8:90792200-90802600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr8:90792200-90805800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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