Variant report

Variant	rs11484581
Chromosome Location	chr1:180431741-180431742
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:180431427..180433581-chr1:180456543..180458150,2	MCF-7	breast:

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10914013	0.86[AFR][1000 genomes]
rs12061731	0.86[AFR][1000 genomes]
rs12081607	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12084845	0.80[AFR][1000 genomes]
rs12087729	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003739	chr1:180027760-180483292	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv535217	chr1:180027760-180483292	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	nsv527918	chr1:180279710-180443808	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1013716	chr1:180287338-180477072	Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
5	nsv535221	chr1:180287338-180477072	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
6	esv2762200	chr1:180300936-180493841	ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
7	nsv1003359	chr1:180300936-180727561	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180392600-180446200	Weak transcription	K562	blood
2	chr1:180403400-180448000	Weak transcription	HMEC	breast
3	chr1:180404200-180431800	Weak transcription	NHEK	skin
4	chr1:180404400-180469000	Weak transcription	Pancreas	Pancrea
5	chr1:180421000-180431800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr1:180421000-180448000	Weak transcription	HSMM	muscle
7	chr1:180421200-180431800	Weak transcription	A549	lung
8	chr1:180421200-180451600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr1:180425800-180457600	Weak transcription	Aorta	Aorta
10	chr1:180427400-180448200	Weak transcription	Osteobl	bone
11	chr1:180428000-180470000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr1:180428600-180438000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:180429400-180435200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:180429600-180444600	Weak transcription	Esophagus	oesophagus
15	chr1:180429600-180455000	Weak transcription	Left Ventricle	heart
16	chr1:180430200-180431800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:180430200-180432600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:180430200-180454600	Weak transcription	Thymus	Thymus
19	chr1:180430400-180431800	ZNF genes & repeats	Fetal Lung	lung
20	chr1:180430400-180432000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:180430600-180432200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:180431000-180432000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
23	chr1:180431000-180432000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
24	chr1:180431000-180432200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:180431200-180432000	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
26	chr1:180431200-180432000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:180431200-180432400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
28	chr1:180431200-180432800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:180431200-180435200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
30	chr1:180431200-180470200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr1:180431400-180432000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:180431400-180432200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
33	chr1:180431400-180432800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
34	chr1:180431400-180447800	Weak transcription	Fetal Stomach	stomach
35	chr1:180431400-180448200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:180431600-180432000	ZNF genes & repeats	Dnd41	blood

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