Variant report

Variant	rs1911749
Chromosome Location	chr7:50105771-50105772
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10234768	0.83[EUR][1000 genomes]
rs10245556	0.84[EUR][1000 genomes]
rs1351692	0.85[ASN][1000 genomes]
rs1379174	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1379175	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1456907	0.83[EUR][1000 genomes]
rs1466292	0.86[EUR][1000 genomes]
rs1508412	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1911748	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1911750	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1911757	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1911758	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2174929	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2202772	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2221657	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2247539	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2247628	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2366027	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2366028	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2366029	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2886552	0.85[ASN][1000 genomes]
rs3807323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3807324	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3823541	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4019793	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4244228	0.85[EUR][1000 genomes]
rs4917107	0.83[ASN][1000 genomes]
rs4917109	0.93[ASN][1000 genomes]
rs4917110	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4917111	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4917112	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6583423	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6583426	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6583432	0.80[EUR][1000 genomes]
rs6944215	0.85[ASN][1000 genomes]
rs6956098	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6973828	0.83[EUR][1000 genomes]
rs897695	0.80[EUR][1000 genomes]
rs897696	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv464444	chr7:49671882-50454736	Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv606897	chr7:49671883-50454736	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv498090	chr7:49708644-50427714	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1020869	chr7:49712860-50457544	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv830997	chr7:49970866-50136498	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv830998	chr7:50103183-50156564	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv3487863	chr7:50103956-50107154	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv2547949	chr7:50104135-50106830	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3477215	chr7:50104630-50106181	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv1958519	chr7:50104649-50106249	Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3487866	chr7:50104668-50106426	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
12	esv3487867	chr7:50104679-50106186	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3477213	chr7:50104684-50106149	Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3477214	chr7:50104697-50106142	Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3487868	chr7:50104699-50106186	Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3487865	chr7:50104699-50106223	Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3489860	chr7:50104718-50106162	Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3477216	chr7:50104757-50106079	Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3477217	chr7:50104771-50106076	Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv3489861	chr7:50104771-50106076	Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv16471	chr7:50104797-50106153	Weak transcription	n/a	n/a	inside rSNPs	diseases
22	nsv606901	chr7:50104821-50105786	Weak transcription	n/a	n/a	inside rSNPs	diseases
23	nsv606902	chr7:50104874-50105786	Weak transcription	n/a	n/a	inside rSNPs	diseases
24	nsv606903	chr7:50104874-50105956	Weak transcription	n/a	n/a	inside rSNPs	diseases
25	nsv606904	chr7:50104926-50105786	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50103400-50106800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr7:50105000-50107400	Weak transcription	H1 Cell Line	embryonic stem cell

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