Variant report

Variant	rs41374744
Chromosome Location	chr7:26227855-26227856
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr1:224594903..224596626-chr7:26226850..26229013,2	K562	blood:
2	chr7:26152221..26157308-chr7:26225005..26229751,7	K562	blood:
3	chr6:26157751..26159704-chr7:26225924..26228352,2	K562	blood:
4	chr15:65821799..65824575-chr7:26227378..26229024,2	K562	blood:
5	chr7:26014155..26016824-chr7:26226230..26228691,2	K562	blood:
6	chr7:26127085..26136794-chr7:26224123..26230309,16	K562	blood:
7	chr7:26224902..26232884-chr7:26322008..26332976,29	K562	blood:
8	chr7:26184369..26187148-chr7:26227369..26229065,2	K562	blood:
9	chr20:42086338..42086868-chr7:26227227..26227873,2	NB4	blood:
10	chr7:26226466..26228099-chr7:26385363..26387499,2	K562	blood:
11	chr7:26187891..26202612-chr7:26221953..26234536,42	K562	blood:
12	chr7:26226202..26228605-chr7:26311727..26314300,2	K562	blood:
13	chr7:26226324..26228907-chr7:26403420..26405277,2	K562	blood:
14	chr7:26123870..26125696-chr7:26226783..26229178,2	MCF-7	breast:
15	chr7:26136960..26140512-chr7:26226454..26229545,3	K562	blood:
16	chr7:26118254..26119023-chr7:26227436..26228387,2	MCF-7	breast:
17	chr7:25930064..25934864-chr7:26225414..26230890,12	K562	blood:
18	chr7:26227531..26229073-chr7:27198944..27201412,2	K562	blood:
19	chr7:26110644..26115952-chr7:26225900..26230055,7	K562	blood:
20	chr7:26181706..26184362-chr7:26226921..26229070,2	K562	blood:
21	chr5:137803047..137805590-chr7:26225142..26227880,2	K562	blood:
22	chr11:62609056..62609626-chr7:26227177..26227982,3	NB4	blood:
23	chr7:26225967..26229689-chr7:26296962..26299546,3	K562	blood:
24	chr7:26171147..26177551-chr7:26225022..26228862,6	K562	blood:
25	chr7:26187762..26202698-chr7:26218693..26233402,42	K562	blood:
26	chr7:26225358..26228940-chr7:26318718..26321554,4	K562	blood:
27	chr15:66789294..66791666-chr7:26226759..26229465,2	K562	blood:
28	chr7:23510320..23511244-chr7:26227489..26228174,2	NB4	blood:
29	chr7:26152455..26156873-chr7:26226826..26229761,5	K562	blood:
30	chr6:27102918..27104491-chr7:26227359..26229692,2	K562	blood:
31	chr7:26111985..26114950-chr7:26225900..26229450,4	K562	blood:
32	chr7:26174186..26178287-chr7:26225672..26229068,5	K562	blood:
33	chr7:26204327..26208311-chr7:26225894..26230203,6	K562	blood:
34	chr7:26224549..26228496-chr7:26395464..26399879,4	K562	blood:
35	chr7:26076616..26078985-chr7:26226158..26229090,2	K562	blood:
36	chr7:26225358..26228144-chr7:26318718..26321292,4	K562	blood:
37	chr7:26224710..26231544-chr7:26402048..26407320,8	K562	blood:
38	chr7:26212218..26214993-chr7:26226282..26231933,7	K562	blood:
39	chr16:68118132..68120641-chr7:26227231..26229928,2	K562	blood:
40	chr7:26224902..26232884-chr7:26322942..26334107,28	K562	blood:

No data

Variant related genes	Relation type
ENSG00000072736	Chromatin interaction
ENSG00000174446	Chromatin interaction
ENSG00000074696	Chromatin interaction
ENSG00000086300	Chromatin interaction
ENSG00000050344	Chromatin interaction
ENSG00000266589	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000124193	Chromatin interaction
ENSG00000273237	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10499573	1.00[CHB][hapmap];0.94[JPT][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10951126	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10951127	0.94[CHB][hapmap];0.93[JPT][hapmap];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11978377	0.94[EUR][1000 genomes]
rs11979154	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12533620	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12537093	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12538280	1.00[MEX][hapmap]
rs12539124	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1864241	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2070601	1.00[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2237329	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2237330	0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2237332	0.94[EUR][1000 genomes]
rs2237333	1.00[ASW][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];0.94[JPT][hapmap];0.87[LWK][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2237334	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4273	1.00[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58438239	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs58914793	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6960012	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9638832	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9639531	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[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	nsv887849	chr7:26075094-26234302	Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1021308	chr7:26116605-26419720	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
3	nsv1018971	chr7:26161228-26380361	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	165 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26199400-26230200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:26207000-26228000	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr7:26207200-26228200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr7:26213800-26228400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr7:26214400-26228200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr7:26215600-26228800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr7:26217200-26228000	Weak transcription	Fetal Brain Male	brain
8	chr7:26217400-26234800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr7:26218200-26236000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr7:26218600-26228600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:26218800-26231800	Weak transcription	Fetal Intestine Small	intestine
12	chr7:26219000-26233800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:26219600-26228200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr7:26219600-26228200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:26220000-26228000	Weak transcription	Fetal Kidney	kidney
16	chr7:26220600-26234200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr7:26221400-26228000	Weak transcription	Colon Smooth Muscle	Colon
18	chr7:26221800-26228000	Weak transcription	Fetal Lung	lung
19	chr7:26222200-26233200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:26222600-26228200	Weak transcription	Ovary	ovary
21	chr7:26222600-26232000	Weak transcription	Right Atrium	heart
22	chr7:26223200-26233200	Strong transcription	Fetal Thymus	thymus
23	chr7:26223800-26231800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:26223800-26232200	Strong transcription	Primary neutrophils fromperipheralblood	blood
25	chr7:26223800-26232400	Genic enhancers	A549	lung
26	chr7:26223800-26233200	Strong transcription	HMEC	breast
27	chr7:26224000-26229400	Weak transcription	HepG2	liver
28	chr7:26224000-26235000	Strong transcription	NH-A	brain
29	chr7:26224200-26228000	Weak transcription	Primary B cells from cord blood	blood
30	chr7:26224200-26228200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr7:26224200-26232600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr7:26224200-26232800	Weak transcription	Fetal Stomach	stomach
33	chr7:26224200-26235000	Strong transcription	NHEK	skin
34	chr7:26224400-26228800	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr7:26224400-26232000	Strong transcription	Brain Anterior Caudate	brain
36	chr7:26224400-26234400	Strong transcription	Muscle Satellite Cultured Cells	--
37	chr7:26224600-26231200	Strong transcription	HUVEC	blood vessel
38	chr7:26224800-26228000	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr7:26224800-26228400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:26224800-26231600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
41	chr7:26224800-26236000	Strong transcription	HSMM	muscle
42	chr7:26224800-26236800	Strong transcription	HSMMtube	muscle
43	chr7:26225000-26228000	Enhancers	K562	blood
44	chr7:26225200-26228200	Weak transcription	Fetal Heart	heart
45	chr7:26225800-26234800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:26226000-26228600	Genic enhancers	Primary T cells fromperipheralblood	blood
47	chr7:26226000-26231600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr7:26226000-26231600	Strong transcription	Brain Germinal Matrix	brain
49	chr7:26226000-26231800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:26226000-26232000	Strong transcription	Brain Inferior Temporal Lobe	brain

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