Variant report

Variant	rs7614404
Chromosome Location	chr3:68748264-68748265
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11128088	0.92[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs1504295	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1504296	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6764338	0.95[ASN][1000 genomes]
rs971381	0.92[AFR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9813609	0.82[AFR][1000 genomes]
rs9826485	0.90[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9878555	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9878718	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007418	chr3:68720455-68748774	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv2760802	chr3:68720845-68749351	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv3863	chr3:68720921-68769064	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv508224	chr3:68724528-68762976	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv1816839	chr3:68725221-68748772	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2763723	chr3:68725751-68748786	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1011301	chr3:68732016-68749067	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv1801449	chr3:68732028-68748758	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv236	chr3:68733871-68757344	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv1797952	chr3:68736176-68748559	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv1816943	chr3:68736176-68748559	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv1818526	chr3:68736176-68748559	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv1846986	chr3:68736176-68748559	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv1792254	chr3:68736176-68748891	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv10279	chr3:68736204-68748919	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3500727	chr3:68737662-68748960	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3461105	chr3:68737762-68749760	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3461103	chr3:68738687-68749235	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3500723	chr3:68738862-68748860	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv1011180	chr3:68738940-68749025	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv511214	chr3:68739025-68748667	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
22	esv2432036	chr3:68739103-68748515	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
23	esv3461107	chr3:68739412-68748410	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv436359	chr3:68739549-68749079	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv2536446	chr3:68739659-68748602	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
26	nsv590594	chr3:68740238-68748667	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
27	esv1800963	chr3:68741337-68748559	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
28	esv1803332	chr3:68741337-68748559	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
29	esv1817284	chr3:68741337-68748559	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
30	esv1822496	chr3:68741337-68748559	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
31	esv1825556	chr3:68741337-68748559	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
32	esv1827102	chr3:68741337-68748559	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
33	esv1843541	chr3:68741337-68748559	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
34	esv1851241	chr3:68741337-68748559	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
35	esv1848116	chr3:68746259-68748758	Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68748200-68748600	Enhancers	Fetal Lung	lung

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