Variant report

Variant	rs2609351
Chromosome Location	chr1:223190346-223190347
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:223190301..223192365-chr1:223194147..223196886,3	MCF-7	breast:
2	chr1:223190305..223191926-chr1:223196099..223197954,2	K562	blood:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1048209	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2255147	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2609352	0.92[EUR][1000 genomes]
rs2609353	0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2609355	0.93[EUR][1000 genomes]
rs2789912	0.94[EUR][1000 genomes]
rs2789948	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2789949	0.98[EUR][1000 genomes]
rs2789951	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2971990	0.97[EUR][1000 genomes];0.98[ASN][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	nsv999185	chr1:222500725-223278032	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv535304	chr1:222500725-223278032	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv1012537	chr1:222755091-223512243	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	nsv1014896	chr1:223070446-223327185	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv873207	chr1:223078802-223292632	Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv917330	chr1:223141547-223225893	Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223178800-223191400	Weak transcription	Right Atrium	heart
2	chr1:223178800-223194600	Weak transcription	Gastric	stomach
3	chr1:223179200-223195400	Weak transcription	Spleen	Spleen
4	chr1:223184800-223204800	Weak transcription	Stomach Mucosa	stomach
5	chr1:223185000-223196800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr1:223185200-223190600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr1:223185200-223196000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:223185400-223190400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr1:223186200-223193200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
10	chr1:223186600-223192200	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:223186600-223195400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr1:223186800-223193000	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:223187600-223190400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:223187600-223193400	Weak transcription	Fetal Kidney	kidney
15	chr1:223187800-223193400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
16	chr1:223188400-223191800	Strong transcription	H9 Cell Line	embryonic stem cell
17	chr1:223189000-223192200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
18	chr1:223189600-223190400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:223189600-223190600	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr1:223189600-223192000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:223189600-223192200	Enhancers	Left Ventricle	heart
22	chr1:223189600-223192400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr1:223189800-223190400	Genic enhancers	H1 Cell Line	embryonic stem cell
24	chr1:223189800-223190400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:223189800-223190400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr1:223189800-223190400	Enhancers	Brain Cingulate Gyrus	brain
27	chr1:223189800-223190400	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr1:223189800-223190600	Enhancers	Right Ventricle	heart
29	chr1:223189800-223190600	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr1:223189800-223190800	Enhancers	Lung	lung
31	chr1:223189800-223190800	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr1:223189800-223191600	Weak transcription	Esophagus	oesophagus
33	chr1:223189800-223193000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr1:223190000-223190600	Genic enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr1:223190200-223190600	Genic enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:223190200-223190600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr1:223190200-223190600	Enhancers	Adipose Nuclei	Adipose
38	chr1:223190200-223191600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr1:223190200-223195600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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