Variant report

Variant	rs10992135
Chromosome Location	chr9:94617450-94617451
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:94611262..94612833-chr9:94616740..94619706,2	K562	blood:

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs10761133	0.81[CEU][hapmap]
rs10761135	0.81[CEU][hapmap]
rs10820906	0.95[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10820907	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10820910	0.88[CEU][hapmap]
rs10992123	0.84[CEU][hapmap];0.80[EUR][1000 genomes]
rs10992124	0.87[CEU][hapmap]
rs10992128	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs10992129	0.91[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10992130	0.92[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10992131	0.96[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992132	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10992134	0.96[CEU][hapmap];0.89[YRI][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10992136	0.88[CEU][hapmap];0.80[AMR][1000 genomes]
rs10992137	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10992139	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10992140	0.83[EUR][1000 genomes]
rs10992142	0.92[CEU][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10992143	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs10992144	0.92[CEU][hapmap];0.83[AMR][1000 genomes]
rs10992145	0.92[CEU][hapmap]
rs11789730	0.83[CEU][hapmap]
rs11790144	0.88[CEU][hapmap]
rs11791450	0.87[CEU][hapmap]
rs12376130	0.84[CEU][hapmap]
rs12376231	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12376539	0.92[CEU][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12378938	0.85[CEU][hapmap]
rs12551140	0.87[CEU][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12552292	0.82[CEU][hapmap];0.80[EUR][1000 genomes]
rs12552858	0.95[CEU][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12555334	0.86[CEU][hapmap]
rs12684524	0.92[CEU][hapmap]
rs1528363	0.92[CEU][hapmap]
rs1528364	0.92[CEU][hapmap]
rs1534531	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1534533	0.88[CEU][hapmap]
rs16907887	0.88[CEU][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1881385	0.83[CEU][hapmap]
rs1881387	0.92[CEU][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1881392	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1997286	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2312732	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2312734	0.87[CEU][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2312735	0.83[CEU][hapmap]
rs2841691	0.81[EUR][1000 genomes]
rs4322068	0.92[CEU][hapmap];0.89[YRI][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4639579	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs4743857	0.96[CEU][hapmap];0.86[YRI][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4744107	0.92[CEU][hapmap]
rs4744108	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4744109	0.88[CEU][hapmap]
rs4744110	0.83[CEU][hapmap]
rs4744111	0.88[CEU][hapmap]
rs4744112	0.81[CEU][hapmap]
rs4744113	0.81[CEU][hapmap]
rs55864279	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56088447	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56308784	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62564595	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62564597	0.83[EUR][1000 genomes]
rs62564598	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62564599	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62565674	0.82[EUR][1000 genomes]
rs6479374	0.92[CEU][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6479375	0.92[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6479376	0.88[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs67944481	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7019210	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7029950	0.92[CEU][hapmap];0.89[YRI][hapmap]
rs7030661	0.88[CEU][hapmap];0.80[AMR][1000 genomes]
rs7031562	1.00[CEU][hapmap];0.89[YRI][hapmap];0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7033819	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs7039406	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7045226	0.88[CEU][hapmap];0.80[AMR][1000 genomes]
rs7045333	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7048756	1.00[CEU][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72746206	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7850118	0.92[CEU][hapmap];0.80[AMR][1000 genomes]
rs7850636	0.83[EUR][1000 genomes]
rs7855417	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs7856144	0.92[CEU][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7859331	0.92[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7863061	0.88[CEU][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7867707	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs7870049	0.84[CEU][hapmap]
rs7874148	0.92[CEU][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]

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	nsv1045332	chr9:94352661-94656016	Active TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1047426	chr9:94363211-94758114	Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv531631	chr9:94373847-94633213	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers 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	5 gene(s)	inside rSNPs	diseases
4	nsv1036176	chr9:94500213-94639367	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv540171	chr9:94500213-94639367	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv949008	chr9:94500776-95182133	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94601800-94618400	Weak transcription	K562	blood
2	chr9:94606800-94619600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr9:94607200-94619600	Weak transcription	Fetal Intestine Large	intestine
4	chr9:94607600-94619600	Weak transcription	Fetal Intestine Small	intestine
5	chr9:94608400-94619000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:94609600-94617800	Weak transcription	Colon Smooth Muscle	Colon
7	chr9:94610200-94619000	Weak transcription	Ovary	ovary
8	chr9:94610400-94618600	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr9:94610600-94618800	Weak transcription	Fetal Kidney	kidney
10	chr9:94611400-94619000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr9:94615200-94621000	Enhancers	Fetal Heart	heart
12	chr9:94615400-94618000	Strong transcription	Fetal Stomach	stomach
13	chr9:94615600-94618000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr9:94616000-94620400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr9:94616400-94621400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:94616600-94617600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:94616600-94617600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:94616600-94617800	Weak transcription	Esophagus	oesophagus
19	chr9:94616600-94618800	Weak transcription	Right Atrium	heart
20	chr9:94616800-94617600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr9:94616800-94617600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr9:94616800-94619600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr9:94616800-94621400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr9:94617000-94618800	Weak transcription	Fetal Lung	lung
25	chr9:94617400-94618000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr9:94617400-94618600	Enhancers	Stomach Smooth Muscle	stomach
27	chr9:94617400-94621400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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