Variant report

Variant	rs12537057
Chromosome Location	chr7:16449751-16449752
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:16447322..16450777-chr7:16450983..16453871,4	K562	blood:
2	chr7:16441360..16443090-chr7:16448119..16450606,2	K562	blood:
3	chr7:16446305..16449837-chr7:16459881..16462752,5	MCF-7	breast:
4	chr7:16448885..16451156-chr7:16453310..16455004,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000214960	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs55907655	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	esv2759514	chr7:16236162-16527390	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv2758105	chr7:16272822-16527390	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	esv2757215	chr7:16346139-16458474	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv1031019	chr7:16377519-16458474	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1034151	chr7:16415497-16578081	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16434400-16459000	Weak transcription	Stomach Mucosa	stomach
2	chr7:16439800-16450200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr7:16440200-16452600	Weak transcription	Pancreas	Pancrea
4	chr7:16440400-16450000	Weak transcription	Fetal Stomach	stomach
5	chr7:16440400-16450400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:16440400-16452400	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr7:16440400-16452600	Weak transcription	Gastric	stomach
8	chr7:16440400-16459600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:16443400-16451800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr7:16443400-16452400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr7:16443600-16450200	Weak transcription	Fetal Muscle Leg	muscle
12	chr7:16443600-16450200	Weak transcription	Left Ventricle	heart
13	chr7:16443600-16456400	Weak transcription	Primary hematopoietic stem cells	blood
14	chr7:16444000-16450800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:16444400-16450000	Weak transcription	K562	blood
16	chr7:16449000-16450000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:16449000-16450200	Enhancers	Brain Cingulate Gyrus	brain
18	chr7:16449000-16450600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:16449400-16450000	Enhancers	Brain Anterior Caudate	brain
20	chr7:16449400-16450400	Enhancers	Brain Substantia Nigra	brain
21	chr7:16449400-16450800	Enhancers	Fetal Lung	lung
22	chr7:16449600-16450200	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr7:16449600-16451600	Weak transcription	Rectal Smooth Muscle	rectum

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