Variant report

Variant	rs547970749
Chromosome Location	chr7:136851581-136851582
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	esv2753059	chr7:136633745-136893745	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1028902	chr7:136727136-136858804	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv464730	chr7:136825522-136882925	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv608463	chr7:136825522-136882925	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv831149	chr7:136831665-137006468	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1034546	chr7:136832263-136858804	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	esv2563049	chr7:136850762-136852698	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
9	esv9074	chr7:136851355-136852174	Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases
10	esv3388206	chr7:136851412-136852460	Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases
11	esv2126350	chr7:136851426-136852127	Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
12	esv3476816	chr7:136851512-136852026	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3515376	chr7:136851518-136852031	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	esv3515372	chr7:136851527-136852045	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3515374	chr7:136851539-136851958	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv3476818	chr7:136851545-136851992	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
17	esv3476817	chr7:136851549-136852004	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3515377	chr7:136851557-136851976	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3476821	chr7:136851559-136851949	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136850400-136854000	Weak transcription	Fetal Kidney	kidney
2	chr7:136850600-136851600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:136850800-136851600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:136851200-136853800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:136851200-136853800	Weak transcription	Fetal Stomach	stomach

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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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