Variant report

Variant	rs372681289
Chromosome Location	chr4:98133693-98133694
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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	nsv879640	chr4:97711707-98697586	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3439430	chr4:98132679-98134702	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
3	esv2480456	chr4:98132887-98134284	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
4	esv1984913	chr4:98133190-98133882	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv8127	chr4:98133255-98133978	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3465788	chr4:98133258-98133795	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3506817	chr4:98133264-98133800	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3506816	chr4:98133275-98133779	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3465784	chr4:98133290-98133758	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3506820	chr4:98133304-98133754	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3367913	chr4:98133319-98133741	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3465787	chr4:98133321-98133761	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3465785	chr4:98133330-98133717	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3506819	chr4:98133332-98133739	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	esv3465783	chr4:98133361-98133695	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv3465789	chr4:98133376-98133705	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3506821	chr4:98133376-98133705	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98132200-98134000	Enhancers	Placenta Amnion	Placenta Amnion
2	chr4:98133200-98136400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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