Variant report

Variant	rs2614781
Chromosome Location	chr15:51177049-51177050
allele	A/G
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:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:50977345..50980340-chr15:51175475..51179077,6	MCF-7	breast:
2	chr15:51173960..51175662-chr15:51175864..51177753,2	K562	blood:
3	chr15:51176099..51177660-chr15:51207519..51209221,2	K562	blood:
4	chr15:51176736..51179086-chr17:57924082..57925795,2	MCF-7	breast:
5	chr15:51176893..51178567-chr3:64222246..64223916,2	MCF-7	breast:
6	chr15:51169182..51171979-chr15:51176658..51178721,2	K562	blood:
7	chr15:51056324..51059354-chr15:51172484..51179110,10	MCF-7	breast:
8	chr15:51176297..51178705-chr15:51190226..51192825,2	MCF-7	breast:
9	chr15:51176979..51180496-chr15:51199774..51202562,4	MCF-7	breast:
10	chr15:50900703..50903174-chr15:51177027..51179659,2	K562	blood:
11	chr15:50977263..50981217-chr15:51174338..51179159,10	MCF-7	breast:
12	chr15:51056574..51058163-chr15:51177043..51179683,2	MCF-7	breast:
13	chr15:50854287..50856205-chr15:51176623..51178248,2	MCF-7	breast:
14	chr15:51147815..51150812-chr15:51176681..51178652,2	MCF-7	breast:
15	chr15:51176719..51180099-chr15:51197525..51202342,6	K562	blood:
16	chr15:51175847..51180099-chr15:51197260..51201772,6	K562	blood:
17	chr15:51166538..51169087-chr15:51176701..51178224,2	MCF-7	breast:
18	chr15:50976848..50980229-chr15:51173151..51177604,4	K562	blood:
19	chr15:51171742..51173328-chr15:51175943..51178564,2	MCF-7	breast:
20	chr15:50840397..50843164-chr15:51176115..51178210,2	MCF-7	breast:
21	chr15:51176620..51178151-chr15:51189371..51192335,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000201524	Chromatin interaction
ENSG00000081014	Chromatin interaction
ENSG00000243027	Chromatin interaction
ENSG00000138600	Chromatin interaction
ENSG00000092439	Chromatin interaction

Extended variants
information (count: 156 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:137)

rs_ID	r²[population]
rs10744956	0.86[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs11070809	0.82[JPT][hapmap]
rs11070824	0.87[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11070829	0.87[ASN][1000 genomes]
rs1147128	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1147129	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1147130	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1147131	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1147133	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1147135	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1147136	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1147139	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11632971	0.92[ASN][1000 genomes]
rs11635015	0.91[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.95[ASN][1000 genomes]
rs11635102	0.91[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.96[ASN][1000 genomes]
rs11855605	0.86[JPT][hapmap]
rs11856886	0.81[JPT][hapmap]
rs12438343	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12440387	0.95[CHB][hapmap]
rs12441714	0.95[ASN][1000 genomes]
rs12593469	0.86[JPT][hapmap]
rs12595034	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1276854	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12898208	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12898530	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12899459	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12900658	0.86[JPT][hapmap]
rs12902894	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12902899	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12904125	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12904382	0.86[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs12905611	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12906866	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12908516	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12912295	0.94[ASN][1000 genomes]
rs12916407	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12917005	0.81[JPT][hapmap]
rs12917408	0.81[JPT][hapmap]
rs1371058	0.87[ASN][1000 genomes]
rs1472946	0.86[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs1509423	0.88[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.95[ASN][1000 genomes]
rs1550336	0.95[JPT][hapmap];0.86[YRI][hapmap];0.82[ASN][1000 genomes]
rs1550340	0.87[ASN][1000 genomes]
rs17703090	0.87[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs2118785	0.83[ASN][1000 genomes]
rs2127366	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2127367	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2127368	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2170011	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2249535	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2306331	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2306332	0.95[ASN][1000 genomes]
rs2414078	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2414079	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2414080	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2414081	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2614763	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2614776	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2614779	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2614780	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2614782	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2614784	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2614789	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2614790	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2614791	0.86[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs2614792	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2614794	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2619686	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2619687	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2619688	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2619691	0.91[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs2619693	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2619694	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2663533	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2663534	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2663535	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2663537	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2663538	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2663541	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2663543	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2663544	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2663545	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2663546	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2663548	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2663550	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2663551	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2663553	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2663554	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2663555	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2663556	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28702388	0.82[ASN][1000 genomes]
rs3743045	0.86[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs3784301	0.89[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3784302	0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs3784303	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3809501	0.81[JPT][hapmap]
rs4438254	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4444282	0.89[ASN][1000 genomes]
rs4534781	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4775910	0.87[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs62018857	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6493469	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6493471	0.81[ASN][1000 genomes]
rs6493473	0.83[ASN][1000 genomes]
rs6493476	0.95[JPT][hapmap];0.86[YRI][hapmap];0.82[ASN][1000 genomes]
rs714784	0.86[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.88[ASN][1000 genomes]
rs7162209	0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.95[ASN][1000 genomes]
rs7168385	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7168846	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7169888	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7170311	0.94[ASN][1000 genomes]
rs7170365	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7170675	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7171085	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7177267	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7180258	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7181051	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7181201	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7181997	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7182957	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7184026	0.89[ASN][1000 genomes]
rs7494977	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8024247	0.86[JPT][hapmap]
rs8024428	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8026318	0.95[JPT][hapmap];0.86[YRI][hapmap];0.82[ASN][1000 genomes]
rs8029155	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8029369	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8030124	0.84[ASN][1000 genomes]
rs8030214	0.91[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.95[ASN][1000 genomes]
rs8031702	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8033934	0.87[ASN][1000 genomes]
rs8034236	0.88[ASN][1000 genomes]
rs8034576	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8035358	0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.95[ASN][1000 genomes]
rs8035452	0.86[JPT][hapmap]
rs8035635	0.86[JPT][hapmap]
rs8041824	0.86[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	nsv1043805	chr15:50715572-51208891	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS 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 target site	82 gene(s)	inside rSNPs	diseases
2	nsv542384	chr15:50715572-51208891	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic 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 target site	82 gene(s)	inside rSNPs	diseases
3	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv457134	chr15:50770868-51184583	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
5	nsv471242	chr15:50770868-51184583	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS 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 target site	54 gene(s)	inside rSNPs	diseases
6	nsv569396	chr15:50770868-51184583	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
7	nsv457135	chr15:50770868-51189707	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
8	nsv569397	chr15:50770868-51189707	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking 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 target site	54 gene(s)	inside rSNPs	diseases
9	nsv1047039	chr15:50782070-51187804	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
10	nsv542385	chr15:50782070-51187804	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
11	nsv457136	chr15:50789125-51294995	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
12	nsv569398	chr15:50789125-51294995	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
13	nsv1042372	chr15:50846461-51208891	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
14	nsv542386	chr15:50846461-51208891	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
15	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
16	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
17	nsv529339	chr15:51048579-51270372	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
18	nsv516168	chr15:51114437-51217361	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
19	nsv428636	chr15:51154834-51298044	Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers 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 target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51151200-51177400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr15:51169200-51178200	Weak transcription	Right Ventricle	heart
3	chr15:51169200-51180000	Weak transcription	Right Atrium	heart
4	chr15:51169400-51177400	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr15:51169600-51177400	Weak transcription	Brain Anterior Caudate	brain
6	chr15:51169600-51177400	Weak transcription	Fetal Muscle Leg	muscle
7	chr15:51169600-51177600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr15:51171000-51177800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr15:51171600-51177400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr15:51172600-51177400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr15:51173000-51177400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr15:51173600-51177600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr15:51173600-51177800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr15:51173800-51177400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr15:51175800-51177200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr15:51175800-51177400	Enhancers	Primary B cells from cord blood	blood
17	chr15:51175800-51177600	Enhancers	Primary hematopoietic stem cells	blood
18	chr15:51175800-51177600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr15:51175800-51177600	Enhancers	Liver	Liver
20	chr15:51175800-51177600	Enhancers	Placenta	Placenta
21	chr15:51175800-51177800	Enhancers	Dnd41	blood
22	chr15:51175800-51178200	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr15:51175800-51178200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr15:51175800-51178200	Flanking Active TSS	GM12878-XiMat	blood
25	chr15:51176000-51177400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:51176000-51177600	Enhancers	NHDF-Ad	bronchial
27	chr15:51176000-51177600	Enhancers	NHLF	lung
28	chr15:51176000-51178200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr15:51176000-51178200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr15:51176000-51178200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:51176000-51178600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr15:51176000-51179400	Enhancers	HUVEC	blood vessel
33	chr15:51176200-51177400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr15:51176200-51177400	Enhancers	Hela-S3	cervix
35	chr15:51176200-51177600	Enhancers	Adipose Nuclei	Adipose
36	chr15:51176200-51177600	Weak transcription	Spleen	Spleen
37	chr15:51176200-51177600	Flanking Active TSS	A549	lung
38	chr15:51176200-51178000	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr15:51176200-51178000	Enhancers	HSMMtube	muscle
40	chr15:51176200-51178200	Enhancers	Duodenum Mucosa	Duodenum
41	chr15:51176400-51177400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr15:51176400-51177400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr15:51176400-51177400	Weak transcription	Primary B cells from peripheral blood	blood
44	chr15:51176400-51177400	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr15:51176400-51177400	Flanking Active TSS	Osteobl	bone
46	chr15:51176400-51177600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr15:51176400-51177600	Weak transcription	Esophagus	oesophagus
48	chr15:51176600-51177200	Weak transcription	Psoas Muscle	Psoas
49	chr15:51176600-51177400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr15:51176600-51177400	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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