Variant report

Variant	rs574322998
Chromosome Location	chr11:106787731-106787732
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:87 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898362	chr11:106715879-106809457	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv556231	chr11:106737224-106815963	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv474	chr11:106757020-106795146	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv531938	chr11:106760733-107156814	Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv3466197	chr11:106784242-106789940	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv1819607	chr11:106784955-106789492	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
7	esv3486333	chr11:106785042-106790740	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
8	nsv556233	chr11:106785139-106787809	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
9	nsv556234	chr11:106785139-106788876	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
10	nsv556235	chr11:106785139-106789414	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
11	nsv556236	chr11:106785139-106789492	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
12	nsv556237	chr11:106785139-106795127	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
13	esv3486336	chr11:106785492-106790590	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
14	esv3466208	chr11:106785822-106789811	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
15	nsv826074	chr11:106786018-106789480	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
16	nsv826076	chr11:106786018-106789563	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv17689	chr11:106786102-106789524	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3466252	chr11:106786103-106789659	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3486337	chr11:106786107-106789651	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
20	esv3486335	chr11:106786107-106789662	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
21	esv3486334	chr11:106786149-106789651	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv3466241	chr11:106786159-106789642	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
23	esv3466219	chr11:106786166-106789637	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
24	esv3466230	chr11:106786174-106789593	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
25	nsv498770	chr11:106786237-106789571	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
26	esv3466263	chr11:106786239-106789573	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
27	nsv983210	chr11:106786319-106793649	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
28	nsv514589	chr11:106786374-106789470	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
29	nsv556238	chr11:106786428-106787757	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
30	nsv556239	chr11:106786428-106787809	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
31	nsv556240	chr11:106786428-106787987	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
32	nsv556241	chr11:106786428-106788739	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
33	nsv556242	chr11:106786428-106788876	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
34	nsv556243	chr11:106786428-106789062	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
35	nsv556244	chr11:106786428-106789227	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
36	esv1815489	chr11:106786428-106789414	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
37	esv1816755	chr11:106786428-106789414	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
38	esv1817109	chr11:106786428-106789414	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
39	esv1817196	chr11:106786428-106789414	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
40	esv1820844	chr11:106786428-106789414	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
41	esv1821094	chr11:106786428-106789414	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
42	esv1823464	chr11:106786428-106789414	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
43	esv1824878	chr11:106786428-106789414	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
44	nsv556245	chr11:106786428-106789414	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
45	esv1815319	chr11:106786428-106789492	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
46	esv1816679	chr11:106786428-106789492	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
47	esv1817227	chr11:106786428-106789492	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
48	esv1821129	chr11:106786428-106789492	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
49	esv1822778	chr11:106786428-106789492	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
50	esv1823554	chr11:106786428-106789492	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106786200-106806800	Weak transcription	Fetal Lung	lung

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