Variant report

Variant	rs7783424
Chromosome Location	chr7:110719583-110719584
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs1014269	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1014270	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1014271	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10237613	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs10241771	1.00[CEU][hapmap];0.86[YRI][hapmap];0.96[EUR][1000 genomes]
rs10257531	0.96[EUR][1000 genomes]
rs10257931	0.88[YRI][hapmap]
rs10269177	1.00[CEU][hapmap];0.83[YRI][hapmap];0.91[EUR][1000 genomes]
rs12705758	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs13238719	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs214841	1.00[CEU][hapmap];0.93[YRI][hapmap];0.96[EUR][1000 genomes]
rs214842	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs214844	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs214845	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs214846	1.00[CEU][hapmap];1.00[YRI][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214847	0.91[EUR][1000 genomes]
rs214848	1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs214849	0.96[EUR][1000 genomes]
rs214850	0.96[EUR][1000 genomes]
rs214851	0.96[EUR][1000 genomes]
rs214853	1.00[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214854	0.96[EUR][1000 genomes]
rs214855	1.00[CEU][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214856	1.00[CEU][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214857	1.00[CEU][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214858	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs214859	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs214860	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs214861	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs214862	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs214863	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.89[LWK][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214864	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs214865	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs214866	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214867	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs214868	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs214869	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214870	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs214871	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs214872	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs214873	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214874	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214877	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs214878	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214879	0.96[EUR][1000 genomes]
rs214880	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs214881	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs214882	0.96[EUR][1000 genomes]
rs214886	0.96[EUR][1000 genomes]
rs214887	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs214894	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2160024	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2396302	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28590134	0.96[EUR][1000 genomes]
rs37745	1.00[CEU][hapmap]
rs4236594	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4730474	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57817514	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57971786	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs58799975	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59902560	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60913915	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6466372	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6945175	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6964177	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7790427	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7801913	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7801960	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7802954	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7808895	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs799639	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs996595	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs996597	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][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	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

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110714600-110720200	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr7:110714800-110720800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr7:110714800-110720800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr7:110714800-110720800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr7:110714800-110722200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr7:110715000-110720800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr7:110715000-110721800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr7:110715000-110721800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:110715200-110722000	Weak transcription	Fetal Lung	lung
10	chr7:110715200-110722400	Weak transcription	Brain Hippocampus Middle	brain
11	chr7:110716400-110722000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:110716800-110719800	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr7:110716800-110721400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:110716800-110721800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr7:110716800-110722000	Weak transcription	NHLF	lung
16	chr7:110716800-110722200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:110717000-110722200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr7:110717200-110721800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr7:110717200-110721800	Weak transcription	NH-A	brain
20	chr7:110717600-110720800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr7:110717600-110721400	Weak transcription	Fetal Thymus	thymus
22	chr7:110717600-110721800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr7:110717800-110720000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr7:110717800-110721600	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr7:110718000-110719600	Weak transcription	Primary T cells from cord blood	blood
26	chr7:110718000-110720600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr7:110718200-110720800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr7:110718200-110722000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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