Variant report

Variant	rs554567867
Chromosome Location	chr4:175626637-175626638
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:66 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1018390	chr4:175475505-175969742	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv880584	chr4:175505749-175644689	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv988593	chr4:175620441-175627158	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv596235	chr4:175621502-175626769	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3466671	chr4:175623177-175628675	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3359677	chr4:175623727-175628225	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3424636	chr4:175624427-175628125	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3466670	chr4:175624702-175627311	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv9678	chr4:175624896-175627187	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3466673	chr4:175625033-175627076	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3493568	chr4:175625062-175627079	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3466672	chr4:175625066-175627052	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3493567	chr4:175625069-175627052	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv821054	chr4:175625072-175627021	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv822844	chr4:175625072-175627021	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3493571	chr4:175625086-175627007	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3466669	chr4:175625089-175627046	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3466674	chr4:175625103-175626998	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3493570	chr4:175625112-175627018	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv3466676	chr4:175625151-175626978	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
22	esv3493569	chr4:175625165-175626970	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
23	esv3466677	chr4:175625167-175626974	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
24	esv3493572	chr4:175625167-175626974	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
25	nsv596236	chr4:175625180-175626769	Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv1836845	chr4:175625180-175626823	Weak transcription	n/a	n/a	inside rSNPs	diseases
27	esv12796	chr4:175625198-175626963	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
28	nsv822845	chr4:175625282-175627021	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
29	nsv596238	chr4:175625334-175626769	Weak transcription	n/a	n/a	inside rSNPs	diseases
30	esv1796005	chr4:175625334-175626823	Weak transcription	n/a	n/a	inside rSNPs	diseases
31	esv1801058	chr4:175625334-175626823	Weak transcription	n/a	n/a	inside rSNPs	diseases
32	esv1839259	chr4:175625334-175628121	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
33	esv1840041	chr4:175625334-175628121	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
34	nsv596241	chr4:175625493-175626718	Weak transcription	n/a	n/a	inside rSNPs	diseases
35	esv1792858	chr4:175625493-175626769	Weak transcription	n/a	n/a	inside rSNPs	diseases
36	esv1798789	chr4:175625493-175626769	Weak transcription	n/a	n/a	inside rSNPs	diseases
37	esv1801980	chr4:175625493-175626769	Weak transcription	n/a	n/a	inside rSNPs	diseases
38	esv1836794	chr4:175625493-175626769	Weak transcription	n/a	n/a	inside rSNPs	diseases
39	esv1837061	chr4:175625493-175626769	Weak transcription	n/a	n/a	inside rSNPs	diseases
40	esv1839771	chr4:175625493-175626769	Weak transcription	n/a	n/a	inside rSNPs	diseases
41	esv1841326	chr4:175625493-175626769	Weak transcription	n/a	n/a	inside rSNPs	diseases
42	nsv596242	chr4:175625493-175626769	Weak transcription	n/a	n/a	inside rSNPs	diseases
43	esv1799376	chr4:175625493-175626823	Weak transcription	n/a	n/a	inside rSNPs	diseases
44	esv1800333	chr4:175625493-175626823	Weak transcription	n/a	n/a	inside rSNPs	diseases
45	nsv596243	chr4:175625493-175626823	Weak transcription	n/a	n/a	inside rSNPs	diseases
46	esv1836376	chr4:175625493-175628121	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
47	nsv596244	chr4:175625493-175631711	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
48	nsv596246	chr4:175625561-175626661	Weak transcription	n/a	n/a	inside rSNPs	diseases
49	nsv596247	chr4:175625561-175626718	Weak transcription	n/a	n/a	inside rSNPs	diseases
50	esv1836823	chr4:175625561-175626769	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	chr4:175624600-175628400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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