Variant report

Variant	rs372106915
Chromosome Location	chr4:28421938-28421939
allele	G/T
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	nsv878775	chr4:28163856-28473048	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1000514	chr4:28192982-28445194	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1010133	chr4:28273244-28642942	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1014938	chr4:28277683-28642942	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv3419889	chr4:28419654-28423852	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv513125	chr4:28420204-28422934	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv2470633	chr4:28420772-28422433	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3515363	chr4:28420904-28423002	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv8649	chr4:28421325-28422187	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv1974343	chr4:28421398-28422132	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv10865	chr4:28421456-28422091	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3515365	chr4:28421487-28422049	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3515361	chr4:28421488-28422041	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	nsv593889	chr4:28421503-28421940	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	nsv511260	chr4:28421503-28432456	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
16	nsv593890	chr4:28421503-28432456	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
17	esv3464961	chr4:28421504-28422022	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3515360	chr4:28421505-28421977	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3464962	chr4:28421512-28422013	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
20	esv3464960	chr4:28421514-28422010	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv3464959	chr4:28421530-28421968	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv3515366	chr4:28421532-28421990	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
23	esv3515368	chr4:28421544-28421988	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
24	esv3515364	chr4:28421546-28421942	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
25	esv3966	chr4:28421550-28422065	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv3400354	chr4:28421552-28421960	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
27	nsv593891	chr4:28421565-28421940	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
28	esv3464958	chr4:28421576-28421946	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
29	esv3515367	chr4:28421589-28421940	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
30	nsv293683	chr4:28421591-28421940	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
31	esv3464963	chr4:28421591-28421942	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
32	esv3515369	chr4:28421591-28421942	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
33	nsv593892	chr4:28421667-28421940	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	chr4:28421600-28426000	Weak transcription	Placenta Amnion	Placenta Amnion

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