Variant report

Variant	rs214865
Chromosome Location	chr7:110763563-110763564
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	chr7:110731481..110733049-chr7:110763510..110765094,2	K562	blood:

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs1014269	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs1014270	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs1014271	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs10237613	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10241771	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10257531	1.00[EUR][1000 genomes]
rs10269177	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs12705758	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13238719	0.91[EUR][1000 genomes]
rs214841	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs214842	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs214844	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214845	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214846	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs214847	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214848	0.96[EUR][1000 genomes]
rs214849	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214850	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214851	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214853	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs214854	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214855	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs214856	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs214857	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs214858	1.00[CEU][hapmap];0.82[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214859	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214860	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214861	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214862	1.00[CEU][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214863	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs214864	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214866	1.00[EUR][1000 genomes]
rs214867	1.00[CEU][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214868	1.00[CEU][hapmap];1.00[GIH][hapmap];0.81[LWK][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214869	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs214870	1.00[CEU][hapmap];0.82[YRI][hapmap];0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs214871	1.00[CEU][hapmap];0.95[YRI][hapmap];0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214872	1.00[CEU][hapmap];0.87[YRI][hapmap];1.00[EUR][1000 genomes]
rs214873	1.00[EUR][1000 genomes]
rs214874	1.00[EUR][1000 genomes]
rs214877	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs214878	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs214879	1.00[EUR][1000 genomes]
rs214880	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs214881	1.00[CEU][hapmap];0.83[YRI][hapmap];1.00[EUR][1000 genomes]
rs214882	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs214886	1.00[EUR][1000 genomes]
rs214887	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs214894	0.96[EUR][1000 genomes]
rs2160024	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs2396302	0.83[EUR][1000 genomes]
rs28590134	1.00[EUR][1000 genomes]
rs37745	1.00[CEU][hapmap]
rs4236594	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs4730474	0.91[EUR][1000 genomes]
rs57817514	1.00[EUR][1000 genomes]
rs57971786	0.96[EUR][1000 genomes]
rs58799975	1.00[EUR][1000 genomes]
rs59902560	0.91[EUR][1000 genomes]
rs60913915	1.00[EUR][1000 genomes]
rs6466372	0.83[EUR][1000 genomes]
rs6945175	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs6964177	0.83[EUR][1000 genomes]
rs7783424	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs7790427	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs7801913	0.83[EUR][1000 genomes]
rs7801960	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.83[EUR][1000 genomes]
rs7802954	1.00[CEU][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs7808895	0.91[EUR][1000 genomes]
rs996595	0.83[EUR][1000 genomes]
rs996597	1.00[CEU][hapmap]
rs9987043	1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531434	chr7:110310931-110839892	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3506497	chr7:110484691-111091738	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv3506498	chr7:110484750-111091689	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv2758129	chr7:110523298-110787849	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2759554	chr7:110523298-110787849	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1031546	chr7:110549137-110978256	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv817555	chr7:110564801-110990927	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1033286	chr7:110588021-110990928	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv539063	chr7:110588021-110990928	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv931978	chr7:110607590-111092490	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv1025987	chr7:110609568-111258501	Weak transcription Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
12	esv2830178	chr7:110645431-110778571	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv1024477	chr7:110660006-110944477	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv608154	chr7:110688993-110945501	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	nsv608155	chr7:110722482-111351512	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
16	nsv1035119	chr7:110745019-111258501	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110737400-110767000	Weak transcription	Brain Angular Gyrus	brain
2	chr7:110745600-110770000	Weak transcription	Brain Anterior Caudate	brain
3	chr7:110749200-110766400	Weak transcription	Brain Hippocampus Middle	brain
4	chr7:110752800-110763800	Weak transcription	Aorta	Aorta
5	chr7:110753000-110778000	Weak transcription	Ovary	ovary
6	chr7:110754800-110770800	Weak transcription	Fetal Brain Male	brain
7	chr7:110758400-110766600	Weak transcription	Fetal Thymus	thymus
8	chr7:110762200-110765000	Strong transcription	Cortex derived primary cultured neurospheres	brain
9	chr7:110762400-110763800	Strong transcription	Primary T helper cells PMA-I stimulated	--
10	chr7:110762400-110764800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:110762600-110763800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr7:110762600-110764200	Strong transcription	Brain Germinal Matrix	brain
13	chr7:110762600-110764400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr7:110762600-110764400	Strong transcription	Fetal Lung	lung
15	chr7:110762600-110764800	ZNF genes & repeats	Primary T cells from cord blood	blood
16	chr7:110762800-110764200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr7:110762800-110764400	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
18	chr7:110762800-110764600	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr7:110762800-110765400	Weak transcription	Fetal Muscle Leg	muscle
20	chr7:110763000-110766800	Weak transcription	Adipose Nuclei	Adipose
21	chr7:110763200-110763800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr7:110763400-110763800	Strong transcription	Fetal Brain Female	brain
23	chr7:110763400-110764800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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