Variant report

Variant	rs35945041
Chromosome Location	chr7:14250784-14250785
allele	-/A
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	nsv949467	chr7:13938464-14279074	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1015312	chr7:14092753-14266917	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1021056	chr7:14162525-14269443	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1025437	chr7:14226741-14295671	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	inside rSNPs	diseases
6	esv1794470	chr7:14246280-14253763	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
7	esv3400375	chr7:14249127-14253425	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3346834	chr7:14249627-14254175	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	nsv8053	chr7:14250271-14252610	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3342141	chr7:14250277-14253050	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3478406	chr7:14250422-14252285	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3478407	chr7:14250422-14252285	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3426554	chr7:14250452-14253300	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv18719	chr7:14250688-14252165	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	nsv821255	chr7:14250688-14252165	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv1799810	chr7:14250768-14251866	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv1802233	chr7:14250768-14252697	Enhancers Weak transcription	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	chr7:14249000-14250800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr7:14250000-14273400	Weak transcription	Left Ventricle	heart

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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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