Variant report

Variant	rs10184246
Chromosome Location	chr2:86341328-86341329
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 153 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:134)

rs_ID	r²[population]
rs10175330	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10184462	0.92[CEU][hapmap];0.82[CHB][hapmap];0.84[EUR][1000 genomes]
rs10187150	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10188059	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10195199	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs10200018	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10202995	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10208602	0.84[EUR][1000 genomes]
rs10496318	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1057893	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10901	0.85[EUR][1000 genomes]
rs1124686	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11395	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11884038	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11885380	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11897696	0.90[EUR][1000 genomes]
rs11899254	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12151585	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12328100	0.93[JPT][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12465983	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12469363	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12469762	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12475079	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12475126	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12477274	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12478097	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12478369	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12714167	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12714169	0.85[EUR][1000 genomes]
rs12714170	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12714171	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12714172	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12714173	0.84[EUR][1000 genomes]
rs12714174	0.85[EUR][1000 genomes]
rs12714175	0.89[CEU][hapmap];0.82[CHB][hapmap];0.85[EUR][1000 genomes]
rs12714177	0.89[CEU][hapmap];0.82[CHB][hapmap];0.85[EUR][1000 genomes]
rs12994382	0.86[EUR][1000 genomes]
rs12994838	0.87[EUR][1000 genomes]
rs12996308	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12998025	0.88[EUR][1000 genomes]
rs12998164	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13001470	0.85[CEU][hapmap];0.82[CHB][hapmap];0.86[EUR][1000 genomes]
rs13010906	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13011139	0.81[EUR][1000 genomes]
rs13011498	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13013916	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13018652	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13019073	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13024123	1.00[CHB][hapmap];0.82[EUR][1000 genomes]
rs13024884	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13027248	0.89[CEU][hapmap];0.82[CHB][hapmap];0.86[EUR][1000 genomes]
rs13028023	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13035593	0.85[EUR][1000 genomes]
rs13403186	0.84[EUR][1000 genomes]
rs1424522	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1540391	0.82[CEU][hapmap];0.82[CHB][hapmap];0.81[EUR][1000 genomes]
rs17027013	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17551815	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2241438	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2278083	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2278536	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs2288113	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2288114	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2288115	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2289239	0.83[EUR][1000 genomes]
rs2367203	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2367204	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34263823	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34478066	0.82[EUR][1000 genomes]
rs35615768	0.86[EUR][1000 genomes]
rs3770060	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3770061	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3770062	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3770065	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3770067	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3770075	0.87[EUR][1000 genomes]
rs3821017	0.81[CEU][hapmap]
rs4374375	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4402761	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4422155	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4450596	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4544439	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4569473	0.85[EUR][1000 genomes]
rs4597526	0.81[EUR][1000 genomes]
rs4832236	0.82[EUR][1000 genomes]
rs62150072	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62150074	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6547660	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6547661	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6547662	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6547663	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6547665	0.89[CEU][hapmap];0.82[CHB][hapmap];0.85[EUR][1000 genomes]
rs6706204	0.84[EUR][1000 genomes]
rs6707029	0.92[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6719136	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6725372	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6729732	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6730226	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6731535	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6731995	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6735014	0.85[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs6737950	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6740044	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs6740287	0.86[EUR][1000 genomes]
rs6740666	0.85[ASN][1000 genomes]
rs6747474	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6749090	0.85[CEU][hapmap];0.84[EUR][1000 genomes]
rs6749439	0.84[EUR][1000 genomes]
rs6757387	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs715334	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs735738	1.00[CHB][hapmap]
rs7422930	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs7560376	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs7561589	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7563742	0.89[CEU][hapmap];0.82[CHB][hapmap];0.84[EUR][1000 genomes]
rs7566721	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7566961	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7569853	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7572386	1.00[CHB][hapmap];0.83[EUR][1000 genomes]
rs7588325	0.96[CEU][hapmap];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7590445	0.89[CEU][hapmap];0.82[CHB][hapmap];0.84[EUR][1000 genomes]
rs7608547	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7609008	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8244	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs876242	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9309632	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9309633	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9646999	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9653508	0.85[CEU][hapmap]
rs9653569	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9789526	0.83[EUR][1000 genomes]
rs9808316	0.81[EUR][1000 genomes]
rs9917140	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9973320	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751903	chr2:86253542-86505453	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv531380	chr2:86253552-86469217	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv870120	chr2:86265437-86343058	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
4	nsv1007474	chr2:86281967-86505453	Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv997563	chr2:86281967-86506132	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
6	nsv1008924	chr2:86282722-86499402	Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
7	nsv999956	chr2:86285944-86505453	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv1012768	chr2:86285944-86506132	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv1003207	chr2:86286314-86496732	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
10	nsv1000441	chr2:86286314-86508168	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
11	nsv535808	chr2:86286314-86508168	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
12	nsv1004442	chr2:86286480-86506132	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv916616	chr2:86289130-86509326	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
14	nsv458563	chr2:86292341-86507688	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
15	nsv582370	chr2:86292341-86507688	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
16	nsv1009140	chr2:86294939-86506132	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv582371	chr2:86296566-86507688	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
18	nsv531381	chr2:86301091-86478346	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
19	nsv1001157	chr2:86301440-86508168	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs10184246	MRPL35	cis	uninvolved skin	skin_eQTL
rs10184246	MRPL35	Cis_1M	lymphoblastoid	RTeQTL
rs10184246	IMMT	Cis_1M	lymphoblastoid	RTeQTL
rs10184246	IMMT	cis	Esophagus Mucosa	GTEx
rs10184246	IMMT	cis	Artery Aorta	GTEx
rs10184246	IMMT	cis	Whole Blood	GTEx
rs10184246	IMMT	cis	lung	GTEx
rs10184246	IMMT	cis	multi-tissue	Pritchard
rs10184246	IMMT	cis	Esophagus Muscularis	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86334200-86342000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:86334400-86342000	Weak transcription	Pancreas	Pancrea
3	chr2:86334400-86362800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:86334800-86341400	Weak transcription	Small Intestine	intestine
5	chr2:86334800-86344400	Weak transcription	Stomach Mucosa	stomach
6	chr2:86335000-86342400	Weak transcription	Fetal Kidney	kidney
7	chr2:86335000-86379000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
8	chr2:86335000-86409000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:86335200-86342200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr2:86335200-86344200	Strong transcription	Skeletal Muscle Female	skeletal muscle
11	chr2:86335200-86366600	Strong transcription	Primary T cells fromperipheralblood	blood
12	chr2:86335200-86380800	Strong transcription	Fetal Thymus	thymus
13	chr2:86335400-86342000	Weak transcription	Brain Substantia Nigra	brain
14	chr2:86335400-86346000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr2:86335400-86394000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:86335400-86408800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:86335600-86366600	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr2:86335600-86366800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr2:86335600-86368000	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr2:86335600-86369200	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr2:86335600-86373600	Strong transcription	K562	blood
22	chr2:86335600-86378800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr2:86335600-86379000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr2:86335600-86379000	Strong transcription	Duodenum Mucosa	Duodenum
25	chr2:86335600-86379000	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr2:86335600-86394000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr2:86335600-86401000	Strong transcription	Placenta	Placenta
28	chr2:86335600-86407400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr2:86335600-86408600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr2:86335800-86356400	Strong transcription	Primary B cells from peripheral blood	blood
31	chr2:86335800-86378600	Strong transcription	Fetal Brain Female	brain
32	chr2:86336000-86355600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr2:86336000-86365800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr2:86336000-86378600	Strong transcription	Brain Germinal Matrix	brain
35	chr2:86336000-86378800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr2:86336000-86378800	Strong transcription	Liver	Liver
37	chr2:86336000-86380800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr2:86336000-86401200	Strong transcription	Adipose Nuclei	Adipose
39	chr2:86336200-86366600	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr2:86336600-86353200	Strong transcription	Primary B cells from cord blood	blood
41	chr2:86336600-86363000	Strong transcription	Brain Inferior Temporal Lobe	brain
42	chr2:86336600-86369400	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr2:86336600-86378600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr2:86336600-86378600	Strong transcription	Fetal Muscle Leg	muscle
45	chr2:86336600-86378800	Strong transcription	Fetal Intestine Large	intestine
46	chr2:86336600-86378800	Strong transcription	Fetal Muscle Trunk	muscle
47	chr2:86336600-86378800	Strong transcription	Rectal Smooth Muscle	rectum
48	chr2:86336600-86394200	Strong transcription	Primary T cells from cord blood	blood
49	chr2:86336800-86344600	Weak transcription	Psoas Muscle	Psoas
50	chr2:86336800-86379200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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