Variant report

Variant	rs189680533
Chromosome Location	chr7:103463011-103463012
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv523031	chr7:103457789-103470499	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3431631	chr7:103462366-103464364	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv934055	chr7:103462527-103473944	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv7153	chr7:103462846-103463549	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2236652	chr7:103462877-103463603	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3476505	chr7:103462953-103463491	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3501808	chr7:103462971-103463500	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3501806	chr7:103462980-103463486	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3364581	chr7:103462992-103464405	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3501805	chr7:103462996-103463424	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3716	chr7:103463000-103463509	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3476503	chr7:103463005-103463457	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3476504	chr7:103463007-103463460	Weak transcription	Chromatin interactive region	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	chr7:103457800-103472000	Weak transcription	HepG2	liver
2	chr7:103461200-103482400	Weak transcription	H1 BMP4 Derived Mesendoderm 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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