Variant report

Variant	rs922221
Chromosome Location	chr9:6399588-6399589
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:6398344..6401128-chr9:6407574..6409551,2	K562	blood:
2	chr1:11968667..11972683-chr9:6399248..6402268,5	K562	blood:

Variant related genes	Relation type
ENSG00000201801	Chromatin interaction

Extended variants
information (count: 126 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:112)

rs_ID	r²[population]
rs10115294	1.00[EUR][1000 genomes]
rs10123132	1.00[YRI][hapmap]
rs10123605	1.00[EUR][1000 genomes]
rs10125313	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1037885	0.83[TSI][hapmap];0.96[EUR][1000 genomes]
rs1048279	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10491838	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10739096	1.00[EUR][1000 genomes]
rs10739101	0.96[EUR][1000 genomes]
rs10739103	1.00[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10739104	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10758762	0.96[EUR][1000 genomes]
rs10758763	1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10758768	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10815400	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10815401	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10815429	1.00[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs10815430	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs10815441	1.00[YRI][hapmap]
rs1156869	1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs12346381	0.84[EUR][1000 genomes]
rs1322170	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13283631	1.00[YRI][hapmap]
rs13283687	1.00[YRI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13284032	0.87[TSI][hapmap];1.00[YRI][hapmap]
rs13284392	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13285152	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13285458	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13286720	1.00[YRI][hapmap]
rs13288875	1.00[YRI][hapmap]
rs13290126	1.00[YRI][hapmap]
rs13291494	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13291887	1.00[YRI][hapmap]
rs13292030	1.00[YRI][hapmap]
rs13293015	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13293673	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13296481	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13298872	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13299896	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13300059	1.00[YRI][hapmap]
rs13302032	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1330381	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1381038	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1407357	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1407358	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1412420	0.87[TSI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1563	1.00[YRI][hapmap]
rs16924678	1.00[YRI][hapmap]
rs16924682	1.00[YRI][hapmap]
rs1854709	1.00[YRI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1855022	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2000198	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2019737	0.96[EUR][1000 genomes]
rs2051003	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2150964	0.85[EUR][1000 genomes]
rs2150971	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2282158	1.00[YRI][hapmap]
rs2297443	1.00[YRI][hapmap]
rs2381438	0.87[EUR][1000 genomes]
rs28615746	1.00[EUR][1000 genomes]
rs2890707	0.85[TSI][hapmap];0.96[EUR][1000 genomes]
rs34530211	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34581400	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35301257	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35408061	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs36089474	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3818705	1.00[YRI][hapmap]
rs3847262	0.85[TSI][hapmap];0.96[EUR][1000 genomes]
rs3858051	0.96[EUR][1000 genomes]
rs4008347	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs424119	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4475552	0.87[EUR][1000 genomes]
rs4742172	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs4742177	0.96[EUR][1000 genomes]
rs4742180	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4742198	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4742200	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4742203	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs503315	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs553048	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6477060	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6477067	0.96[EUR][1000 genomes]
rs67541153	0.96[EUR][1000 genomes]
rs7021445	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7031407	1.00[EUR][1000 genomes]
rs7031967	0.96[EUR][1000 genomes]
rs7032411	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7035574	0.92[EUR][1000 genomes]
rs7036990	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7037276	1.00[MKK][hapmap]
rs7039968	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7040374	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7041863	0.85[TSI][hapmap]
rs7043824	1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7043887	1.00[EUR][1000 genomes]
rs7044749	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7045164	1.00[ASW][hapmap];1.00[MKK][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap]
rs7048431	0.87[EUR][1000 genomes]
rs72693587	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7350177	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7851921	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7852138	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7853322	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7858373	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7859139	0.96[EUR][1000 genomes]
rs7864212	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7869419	0.87[TSI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7873206	1.00[EUR][1000 genomes]
rs898673	0.96[EUR][1000 genomes]
rs980849	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs980850	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs993952	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948847	chr9:5712626-6417677	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1031086	chr9:5806949-6630686	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv539967	chr9:5806949-6630686	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv933124	chr9:6099101-6644738	Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv1029000	chr9:6188652-6687205	Enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
6	nsv1031459	chr9:6216913-6657192	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
7	nsv948562	chr9:6222553-6684955	Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
8	nsv1024324	chr9:6308178-6408875	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1032350	chr9:6328167-6630686	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
10	nsv1019222	chr9:6328242-6402856	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv892160	chr9:6364449-6506038	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
12	nsv892161	chr9:6364449-6523056	Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
13	nsv831497	chr9:6377501-6612402	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
14	nsv1023419	chr9:6393886-6415025	Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6398600-6400200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr9:6398800-6399800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:6398800-6399800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr9:6398800-6399800	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr9:6398800-6399800	Enhancers	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links