Variant report

Variant	rs527843092
Chromosome Location	chr19:35588164-35588165
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:35581232..35583047-chr19:35586945..35589675,2	MCF-7	breast:
2	chr19:35581971..35584009-chr19:35587170..35589088,2	K562	blood:

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911611	chr19:35483679-35589920	Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv911612	chr19:35501051-35602498	Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
4	nsv911614	chr19:35570307-35648365	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	41 gene(s)	inside rSNPs	diseases
5	nsv525108	chr19:35577870-35589920	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv911615	chr19:35577870-35648365	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
7	nsv911616	chr19:35577870-35669071	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
8	nsv960759	chr19:35587586-35590800	Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv911617	chr19:35587791-35642297	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35582000-35589800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr19:35582200-35591600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr19:35582200-35605600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr19:35582400-35591600	Weak transcription	Brain Anterior Caudate	brain
5	chr19:35582600-35601600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr19:35585200-35589000	Weak transcription	Pancreas	Pancrea
7	chr19:35585600-35589600	Weak transcription	Stomach Mucosa	stomach
8	chr19:35587200-35589800	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr19:35587200-35596200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr19:35587400-35589600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr19:35587600-35588200	Strong transcription	Brain Cingulate Gyrus	brain
12	chr19:35587600-35588200	Enhancers	NHEK	skin
13	chr19:35587600-35589400	Weak transcription	Brain Angular Gyrus	brain
14	chr19:35587600-35589400	Weak transcription	Brain Hippocampus Middle	brain
15	chr19:35587600-35589400	Weak transcription	Brain Substantia Nigra	brain
16	chr19:35587600-35590200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr19:35587600-35596400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr19:35587800-35589600	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr19:35588000-35589000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr19:35588000-35589000	Weak transcription	HMEC	breast
21	chr19:35588000-35589200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr19:35588000-35589400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr19:35588000-35589600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr19:35588000-35589600	Weak transcription	Esophagus	oesophagus

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