Variant report

Variant	rs114093285
Chromosome Location	chr7:117894269-117894270
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:117893799..117896241-chr7:117904650..117906874,2	K562	blood:

Extended variants
information (count: 20 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869971	chr7:117420583-118274149	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	nsv889088	chr7:117744660-117913648	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv889089	chr7:117865940-117921267	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv889090	chr7:117865940-118067460	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv2432841	chr7:117893381-117895064	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv3362740	chr7:117893541-117895689	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
7	esv1993322	chr7:117893760-117894466	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
8	esv3476668	chr7:117893859-117894339	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
9	esv3496070	chr7:117893868-117894365	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
10	esv3496073	chr7:117893875-117894354	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
11	esv3496071	chr7:117893889-117894289	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
12	esv4194	chr7:117893891-117894297	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
13	esv3476669	chr7:117893894-117894305	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
14	esv3496069	chr7:117893900-117894310	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
15	esv3476666	chr7:117893900-117894320	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
16	esv3496068	chr7:117893913-117894299	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
17	esv3383648	chr7:117893916-117894276	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
18	esv3496072	chr7:117893947-117894272	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
19	esv3476670	chr7:117893951-117894270	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
20	esv3496075	chr7:117893951-117894270	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117893200-117894600	Enhancers	HUES48 Cell Line	embryonic stem cell

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