Variant report

Variant	rs3899200
Chromosome Location	chr7:64710141-64710142
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:64699829..64702415-chr7:64709337..64710930,2	K562	blood:

Extended variants
information (count: 298 )
Associated
traits (count: 48 )

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10234467	0.89[CEU][hapmap];0.89[GIH][hapmap];0.84[TSI][hapmap]
rs10244630	0.96[CEU][hapmap];0.91[CHB][hapmap]
rs10263834	0.96[CEU][hapmap];0.85[CHB][hapmap]
rs10267741	0.81[CEU][hapmap];0.89[CHB][hapmap]
rs10277384	0.96[CEU][hapmap];0.91[CHB][hapmap]
rs10949982	0.81[AMR][1000 genomes]
rs10949983	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10949986	0.96[CEU][hapmap];0.90[CHB][hapmap]
rs10949991	0.96[CEU][hapmap];0.90[CHB][hapmap]
rs10949992	0.96[CEU][hapmap];0.90[CHB][hapmap]
rs10949993	0.96[CEU][hapmap];0.90[CHB][hapmap]
rs11761772	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs11769148	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11770225	0.96[CEU][hapmap];0.90[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.92[TSI][hapmap]
rs11773286	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12534769	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12535182	0.96[CEU][hapmap];0.91[CHB][hapmap];0.88[CHD][hapmap];0.98[GIH][hapmap];0.90[TSI][hapmap]
rs12536316	0.96[CEU][hapmap];0.91[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.90[TSI][hapmap]
rs12668784	0.96[CEU][hapmap];0.90[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];0.92[TSI][hapmap]
rs12669746	0.96[CEU][hapmap];0.90[CHB][hapmap]
rs12673478	0.95[CHB][hapmap]
rs13221806	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13223327	0.96[CEU][hapmap];0.98[GIH][hapmap];0.81[JPT][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13227242	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13227243	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13227507	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13229781	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[TSI][hapmap]
rs13234392	0.89[CEU][hapmap];0.93[GIH][hapmap];0.83[TSI][hapmap]
rs13240722	0.89[CEU][hapmap]
rs1543851	0.92[CEU][hapmap];0.91[CHB][hapmap]
rs17710097	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17782771	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2116213	0.88[CEU][hapmap]
rs2418470	0.85[CEU][hapmap];0.90[CHB][hapmap];0.81[CHD][hapmap];0.86[GIH][hapmap];0.90[TSI][hapmap]
rs2419281	0.89[CEU][hapmap]
rs2419417	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2419785	0.89[CEU][hapmap]
rs2419789	0.88[CEU][hapmap]
rs28496606	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28877001	0.89[CEU][hapmap];0.91[GIH][hapmap];0.82[TSI][hapmap]
rs2900858	1.00[CEU][hapmap];0.98[GIH][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2900982	0.89[CEU][hapmap];0.93[GIH][hapmap];0.83[TSI][hapmap]
rs34739196	1.00[CEU][hapmap];0.98[GIH][hapmap];0.81[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35513558	1.00[CEU][hapmap];0.98[GIH][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap]
rs3857677	0.96[CEU][hapmap];0.91[CHB][hapmap]
rs4082908	0.91[CHB][hapmap]
rs4717246	0.96[CEU][hapmap];0.91[CHB][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.88[MEX][hapmap];0.92[TSI][hapmap]
rs4717251	0.89[CEU][hapmap]
rs4717252	0.87[CEU][hapmap]
rs4717253	0.89[CEU][hapmap]
rs4717255	0.89[CEU][hapmap]
rs4717256	0.92[CEU][hapmap]
rs4718188	0.89[CEU][hapmap]
rs4718207	0.92[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.92[TSI][hapmap];0.80[ASN][1000 genomes]
rs4718208	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4718210	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4718211	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4718218	0.96[CEU][hapmap];0.91[CHB][hapmap]
rs4718221	0.96[CEU][hapmap];0.91[CHB][hapmap]
rs4718222	0.96[CEU][hapmap];0.91[CHB][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.92[TSI][hapmap]
rs4718224	0.96[CEU][hapmap];0.91[CHB][hapmap]
rs4718225	0.96[CEU][hapmap];0.91[CHB][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.92[TSI][hapmap]
rs4718239	0.88[CEU][hapmap]
rs4718240	0.89[CEU][hapmap];0.93[GIH][hapmap];0.83[TSI][hapmap]
rs474341	0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs495336	0.89[CEU][hapmap];0.91[GIH][hapmap];0.82[TSI][hapmap]
rs517258	0.96[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.90[TSI][hapmap]
rs532409	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs549970	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs58643803	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs593619	0.96[CEU][hapmap];0.95[GIH][hapmap];0.83[MEX][hapmap];0.97[TSI][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs594456	1.00[CEU][hapmap];0.95[GIH][hapmap];0.83[MEX][hapmap];0.97[TSI][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs608809	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs635028	0.81[ASN][1000 genomes]
rs6460230	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.93[GIH][hapmap];0.90[JPT][hapmap];0.97[TSI][hapmap]
rs6460232	0.96[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.84[MKK][hapmap];0.92[TSI][hapmap];0.80[AMR][1000 genomes]
rs6460246	0.81[CEU][hapmap]
rs6460247	0.81[CEU][hapmap]
rs6460248	0.88[CEU][hapmap];0.93[GIH][hapmap];0.83[TSI][hapmap]
rs657560	0.96[CEU][hapmap];0.95[GIH][hapmap];0.81[MEX][hapmap];0.97[TSI][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs658360	0.89[CEU][hapmap];0.89[GIH][hapmap];0.84[TSI][hapmap]
rs658606	0.88[CEU][hapmap];0.81[CHB][hapmap]
rs666389	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs66671129	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs673957	0.89[CEU][hapmap];0.91[GIH][hapmap];0.82[TSI][hapmap]
rs6948240	0.96[CEU][hapmap];0.90[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];0.95[TSI][hapmap]
rs6948955	0.80[ASN][1000 genomes]
rs6954951	0.96[CEU][hapmap];0.91[CHB][hapmap]
rs6956631	0.88[CEU][hapmap]
rs6973096	0.96[CEU][hapmap];0.91[CHB][hapmap]
rs6973539	0.83[CEU][hapmap]
rs6974876	0.96[CEU][hapmap];0.91[CHB][hapmap];0.88[CHD][hapmap];0.98[GIH][hapmap];0.83[MEX][hapmap];0.87[TSI][hapmap]
rs6978330	0.94[CHB][hapmap]
rs7778919	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7779837	0.88[CEU][hapmap]
rs7788253	0.88[CEU][hapmap]
rs7792874	0.89[CEU][hapmap];0.84[TSI][hapmap]
rs7796045	0.95[CHB][hapmap];0.98[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap]
rs7796077	0.89[CEU][hapmap];0.91[GIH][hapmap];0.82[TSI][hapmap]
rs7796833	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7799516	1.00[CEU][hapmap];0.98[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7802108	0.96[CEU][hapmap];0.86[CHB][hapmap]
rs7807271	0.88[CEU][hapmap]
rs7809513	0.91[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:194 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752165	chr7:64345822-65208605	Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv1033517	chr7:64443052-64942418	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv538893	chr7:64443052-64942418	Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv1034625	chr7:64456197-64850413	Genic enhancers Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	nsv1019089	chr7:64456197-64874187	Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
6	nsv1023699	chr7:64456197-64942418	Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv517778	chr7:64462326-65326821	ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
8	nsv429767	chr7:64473713-65415647	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
9	nsv917231	chr7:64478253-65300317	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
10	esv34341	chr7:64478386-65012082	Bivalent/Poised TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
11	esv2752166	chr7:64478386-65208605	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
12	nsv1029796	chr7:64494934-65302696	Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
13	nsv916005	chr7:64499811-65012082	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
14	nsv533081	chr7:64499945-65208605	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
15	esv3339156	chr7:64510176-65349050	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
16	nsv888286	chr7:64529883-64800432	Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
17	nsv888287	chr7:64537992-64990806	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
18	esv2758117	chr7:64551274-65208605	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
19	esv2759534	chr7:64551274-65373851	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
20	nsv427788	chr7:64551274-65390424	Weak transcription Active TSS Strong transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
21	esv2752167	chr7:64557394-65012082	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
22	esv2752168	chr7:64557394-65012082	Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
23	esv2752169	chr7:64557394-65012082	Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
24	nsv429768	chr7:64557394-65012082	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
25	nsv1021867	chr7:64565573-65012082	ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
26	nsv1032570	chr7:64565573-65184339	Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
27	nsv1029343	chr7:64566957-65208605	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
28	nsv538894	chr7:64566957-65208605	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
29	nsv869856	chr7:64567013-65196403	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
30	nsv607316	chr7:64582849-65208605	Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
31	nsv469565	chr7:64590611-64813395	Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
32	nsv482415	chr7:64590611-64813395	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
33	esv2761084	chr7:64594065-64967767	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
34	esv2764020	chr7:64594065-65351820	Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
35	nsv1032227	chr7:64594329-64917141	Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
36	nsv1016806	chr7:64594329-64941887	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
37	nsv1015575	chr7:64594329-64947974	Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
38	nsv1021106	chr7:64594329-64951818	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
39	nsv1016496	chr7:64594329-64960445	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
40	nsv1016392	chr7:64594329-64967755	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
41	nsv1020647	chr7:64594329-64997960	Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
42	nsv1019148	chr7:64594329-65002671	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
43	nsv1017973	chr7:64594329-65012082	Active TSS Weak transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
44	nsv1018590	chr7:64594329-65012082	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
45	nsv1021410	chr7:64594329-65012082	Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
46	nsv1034505	chr7:64594329-65012082	Strong transcription Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
47	nsv1029844	chr7:64594329-65094953	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
48	nsv1017365	chr7:64594329-65106792	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
49	nsv1032262	chr7:64594329-65161364	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
50	nsv1023425	chr7:64594329-65162170	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:48)

SNP	Gene	Cis/trans	Tissue	Source
rs3899200	INTS4L1	cis	Thyroid	GTEx
rs3899200	RP11-797H7.5	cis	Thyroid	GTEx
rs3899200	RP11-460N20.5	cis	Adipose Subcutaneous	GTEx
rs3899200	RP11-460N20.4	cis	lung	GTEx
rs3899200	RP11-797H7.3	cis	lung	GTEx
rs3899200	ZNF92	cis	cerebellum	SCAN
rs3899200	RP11-460N20.4	cis	Esophagus Muscularis	GTEx
rs3899200	INTS4L1	cis	Esophagus Muscularis	GTEx
rs3899200	RP11-797H7.3	cis	Nerve Tibial	GTEx
rs3899200	RP11-460N20.5	cis	Stomach	GTEx
rs3899200	ERV3	cis	multi-tissue	Pritchard
rs3899200	RP11-797H7.3	cis	Heart Left Ventricle	GTEx
rs3899200	RP11-460N20.4	cis	Nerve Tibial	GTEx
rs3899200	RP11-460N20.5	cis	lung	GTEx
rs3899200	RP11-460N20.4	cis	Artery Tibial	GTEx
rs3899200	RP11-460N20.5	cis	Nerve Tibial	GTEx
rs3899200	AC104057.1	cis	Esophagus Muscularis	GTEx
rs3899200	RP11-460N20.5	cis	Esophagus Mucosa	GTEx
rs3899200	ERV3	cis	cerebellum	SCAN
rs3899200	RP11-797H7.3	cis	Skin Sun Exposed Lower leg	GTEx
rs3899200	SEPHS1P1	cis	Nerve Tibial	GTEx
rs3899200	RP11-797H7.3	cis	Artery Aorta	GTEx
rs3899200	RP11-797H7.5	cis	lung	GTEx
rs3899200	RP11-797H7.3	cis	Adipose Subcutaneous	GTEx
rs3899200	ZNF273	cis	cerebellum	SCAN
rs3899200	RP11-460N20.4	cis	Adipose Subcutaneous	GTEx
rs3899200	RP11-797H7.5	cis	Heart Left Ventricle	GTEx
rs3899200	CCT6P3	cis	Adipose Subcutaneous	GTEx
rs3899200	RP11-460N20.5	cis	Skin Sun Exposed Lower leg	GTEx
rs3899200	ERV3	cis	parietal	SCAN
rs3899200	RP11-460N20.5	cis	Esophagus Muscularis	GTEx
rs3899200	RP11-460N20.5	cis	Thyroid	GTEx
rs3899200	INTS4L1	cis	Skin Sun Exposed Lower leg	GTEx
rs3899200	RP11-460N20.5	cis	Whole Blood	GTEx
rs3899200	INTS4L1	cis	Nerve Tibial	GTEx
rs3899200	RP11-460N20.5	cis	Artery Aorta	GTEx
rs3899200	ERV3-1	cis	Artery Aorta	GTEx
rs3899200	ZNF273	cis	Heart Left Ventricle	GTEx
rs3899200	RP11-797H7.3	cis	Thyroid	GTEx
rs3899200	RP11-460N20.5	cis	Artery Tibial	GTEx
rs3899200	RP11-667F9.1	cis	Adipose Subcutaneous	GTEx
rs3899200	AC104057.1	cis	Adipose Subcutaneous	GTEx
rs3899200	RP11-797H7.5	cis	Adipose Subcutaneous	GTEx
rs3899200	GUSB	cis	parietal	SCAN
rs3899200	RP11-460N20.4	cis	Esophagus Mucosa	GTEx
rs3899200	RP11-667F9.1	cis	Nerve Tibial	GTEx
rs3899200	RP11-797H7.3	cis	Artery Tibial	GTEx
rs3899200	ZNF273	cis	parietal	SCAN

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64700800-64710400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:64700800-64712000	Weak transcription	Right Atrium	heart
3	chr7:64704400-64710600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr7:64708000-64711000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:64708200-64710200	Weak transcription	Esophagus	oesophagus
6	chr7:64709000-64710600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr7:64709200-64710800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:64709600-64712200	Weak transcription	Spleen	Spleen
9	chr7:64710000-64710400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:64710000-64711000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr7:64710000-64711000	Enhancers	Placenta	Placenta

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