Variant report

Variant	rs11770525
Chromosome Location	chr7:3158988-3158989
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:3154011..3155575-chr7:3158921..3161053,2	K562	blood:
2	chr7:3153512..3155575-chr7:3157437..3160421,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10215661	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10276557	1.00[CEU][hapmap]
rs10281495	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10807823	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10951040	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs12155183	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12700596	1.00[ASN][1000 genomes]
rs1825820	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1825821	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1825822	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1976137	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs4719792	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs4719802	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs4719803	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs4722401	1.00[AFR][1000 genomes]
rs4722442	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6461836	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6461840	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6461844	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6949557	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6967557	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6972403	0.87[EUR][1000 genomes]
rs7799188	1.00[CEU][hapmap]
rs9986888	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv605873	chr7:2920067-3204177	Bivalent Enhancer Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv1026476	chr7:2965034-3311344	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv538656	chr7:2965034-3311344	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv464260	chr7:2966138-3315572	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv605874	chr7:2966138-3315572	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1018287	chr7:2967524-3298539	Genic enhancers Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv538657	chr7:2967524-3298539	Bivalent/Poised TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv1020680	chr7:3125512-3204521	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv1027945	chr7:3125512-3208071	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv1015656	chr7:3131821-3321353	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv1023566	chr7:3134090-3159323	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1027009	chr7:3141609-3311344	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv538658	chr7:3141609-3311344	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
14	nsv433013	chr7:3148898-3191654	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv605878	chr7:3149419-3183657	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv464263	chr7:3151177-3169494	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv605879	chr7:3151177-3169494	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3157400-3160400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:3157800-3159200	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr7:3157800-3161000	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr7:3157800-3161000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr7:3158000-3159400	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr7:3158000-3161000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr7:3158000-3161200	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr7:3158000-3161600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr7:3158200-3159800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr7:3158200-3160000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr7:3158400-3160400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr7:3158600-3159800	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr7:3158600-3160000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr7:3158800-3159200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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