Variant report

Variant	rs7549883
Chromosome Location	chr1:77479230-77479231
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs12084940	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7555422	0.88[AFR][1000 genomes]
rs9661805	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003826	chr1:76965331-77656929	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv535006	chr1:76965331-77656929	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv830292	chr1:77425571-77584307	Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	3 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	chr1:77465200-77480200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:77465200-77483600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:77465200-77484200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:77465200-77484200	Weak transcription	NHEK	skin
5	chr1:77471600-77484200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr1:77472800-77487600	Weak transcription	Aorta	Aorta
7	chr1:77475400-77486000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr1:77476800-77484200	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr1:77477000-77484000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:77477000-77484600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:77477000-77491400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:77477200-77481200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr1:77477200-77481200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr1:77477200-77483800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr1:77477200-77484000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr1:77478000-77482000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:77478000-77489000	Weak transcription	Fetal Stomach	stomach
18	chr1:77478200-77479600	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr1:77478200-77484200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr1:77478400-77484000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr1:77478600-77479400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr1:77478600-77485600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:77479000-77481400	Weak transcription	Fetal Brain Male	brain
24	chr1:77479200-77480200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links