Variant report

Variant	rs552794833
Chromosome Location	chr7:126051983-126051984
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429810	chr7:125488049-126131049	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv529300	chr7:125669493-126587858	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1023465	chr7:125873329-126191422	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1028204	chr7:125897362-126225444	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv539118	chr7:125897362-126225444	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv1033349	chr7:126010250-126168918	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv508480	chr7:126034101-126058203	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv5937	chr7:126036436-126076012	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	esv2764050	chr7:126039714-126058773	Enhancers Active TSS Flanking Active TSS Weak transcription	lncRNA	n/a	inside rSNPs	diseases
10	esv1798300	chr7:126040117-126052078	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
11	nsv1024506	chr7:126043644-126058773	Active TSS Enhancers Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
12	nsv1018179	chr7:126043644-126063008	Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
13	nsv1025757	chr7:126043644-126063431	Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	inside rSNPs	diseases
14	nsv1030866	chr7:126044001-126063431	Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
15	nsv1026094	chr7:126044131-126055409	Active TSS Enhancers Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
16	nsv1020879	chr7:126044148-126063431	Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
17	nsv435855	chr7:126045295-126052385	Active TSS Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
18	esv989913	chr7:126045296-126052397	Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
19	nsv1023102	chr7:126045470-126067406	Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	inside rSNPs	diseases
20	esv2450596	chr7:126045519-126052366	Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
21	nsv1024234	chr7:126045639-126066742	Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
22	esv3523778	chr7:126045916-126052464	Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
23	esv3523777	chr7:126046066-126052564	Active TSS Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
24	esv3475384	chr7:126046716-126053414	Flanking Active TSS Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
25	esv3520567	chr7:126047466-126052464	Active TSS Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
26	esv3475383	chr7:126047541-126052689	Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
27	esv1800345	chr7:126048572-126052078	Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
28	esv1837644	chr7:126048572-126052078	Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
29	esv1842987	chr7:126048572-126052078	Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
30	esv1844893	chr7:126048572-126052078	Active TSS Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
31	esv1837519	chr7:126048572-126055187	Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
32	esv1842942	chr7:126048572-126055187	Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
33	esv1845454	chr7:126048572-126055187	Active TSS Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126051400-126052000	Active TSS	Brain Angular Gyrus	brain
2	chr7:126051600-126052000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr7:126051600-126052200	Flanking Active TSS	GM12878-XiMat	blood

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