Variant report

Variant	rs6751359
Chromosome Location	chr2:111787307-111787308
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:111785222..111792269-chr2:111873385..111881089,20	MCF-7	breast:
2	chr2:111786662..111788456-chr2:111876359..111879256,2	MCF-7	breast:
3	chr2:111786327..111787920-chr2:111880079..111881845,2	MCF-7	breast:
4	chr2:111785810..111788620-chr2:111868172..111870697,2	MCF-7	breast:
5	chr2:111786376..111787935-chr2:111803727..111805483,2	MCF-7	breast:
6	chr2:111786604..111788790-chr2:111806791..111809985,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000153094	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10181859	0.84[ASN][1000 genomes]
rs10191949	0.84[ASN][1000 genomes]
rs1157454	0.80[ASN][1000 genomes]
rs11894723	0.84[ASN][1000 genomes]
rs13035209	0.84[ASN][1000 genomes]
rs1483534	0.80[ASN][1000 genomes]
rs1483536	0.84[ASN][1000 genomes]
rs1564706	0.85[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs17041773	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1976058	0.94[ASN][1000 genomes]
rs2306583	0.94[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3789078	0.83[AFR][1000 genomes]
rs4848366	0.80[ASN][1000 genomes]
rs4849331	0.80[ASN][1000 genomes]
rs56304079	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56379112	1.00[EUR][1000 genomes]
rs57037141	1.00[EUR][1000 genomes]
rs6542250	0.80[ASN][1000 genomes]
rs6737041	0.84[ASN][1000 genomes]
rs7590779	1.00[EUR][1000 genomes]
rs958347	0.84[ASN][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	nsv874838	chr2:111376870-112046226	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv874839	chr2:111400934-111868010	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv834330	chr2:111593290-111789447	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111775200-111787800	Weak transcription	Spleen	Spleen
2	chr2:111784600-111787400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:111785000-111787600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr2:111785600-111790200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr2:111786000-111795800	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr2:111786200-111792400	Enhancers	Fetal Lung	lung
7	chr2:111786400-111788200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:111786400-111790400	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr2:111786600-111787800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:111786600-111788000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr2:111786600-111788200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr2:111786600-111788600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr2:111786600-111790600	Enhancers	Duodenum Mucosa	Duodenum
14	chr2:111786800-111787800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr2:111786800-111788000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr2:111786800-111788000	Enhancers	Primary B cells from cord blood	blood
17	chr2:111786800-111788200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr2:111786800-111788200	Enhancers	Placenta	Placenta
19	chr2:111786800-111790000	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr2:111786800-111792800	Enhancers	Fetal Intestine Small	intestine
21	chr2:111787000-111787400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr2:111787000-111787400	Enhancers	Dnd41	blood
23	chr2:111787000-111788000	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr2:111787000-111788200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr2:111787000-111788200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:111787000-111788200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr2:111787000-111788200	Enhancers	Fetal Thymus	thymus
28	chr2:111787000-111788600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr2:111787000-111788600	Enhancers	Colonic Mucosa	Colon
30	chr2:111787000-111789000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr2:111787000-111789200	Enhancers	Fetal Heart	heart
32	chr2:111787000-111789800	Enhancers	Fetal Stomach	stomach
33	chr2:111787000-111792000	Enhancers	Stomach Mucosa	stomach
34	chr2:111787000-111792800	Enhancers	Fetal Intestine Large	intestine
35	chr2:111787200-111787400	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr2:111787200-111787600	Enhancers	Primary T cells from cord blood	blood
37	chr2:111787200-111787800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr2:111787200-111788000	Enhancers	Small Intestine	intestine
39	chr2:111787200-111788200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr2:111787200-111788200	Enhancers	Fetal Muscle Trunk	muscle

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