Variant report

Variant	rs13147600
Chromosome Location	chr4:10160489-10160490
allele	C/T
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:10159584..10164126-chr4:10173679..10176923,6	K562	blood:
2	chr4:10159186..10164011-chr4:10164137..10169302,8	K562	blood:
3	chr4:10117824..10124820-chr4:10157230..10164396,13	K562	blood:
4	chr4:10159426..10161534-chr4:10457764..10459581,2	K562	blood:
5	chr4:10159453..10161794-chr4:10166917..10170966,3	MCF-7	breast:
6	chr4:10117458..10122489-chr4:10158161..10162241,5	MCF-7	breast:
7	chr4:10118185..10123341-chr4:10157230..10162785,8	K562	blood:
8	chr4:10153604..10155530-chr4:10159159..10161032,2	K562	blood:
9	chr4:10151902..10153544-chr4:10159740..10162552,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000223086	Chromatin interaction
ENSG00000178163	Chromatin interaction
ENSG00000071127	Chromatin interaction
ENSG00000251296	Chromatin interaction

Extended variants
information (count: 135 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs1001218	1.00[CEU][hapmap];0.86[CHB][hapmap]
rs10016136	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10020720	0.85[CHB][hapmap];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10027448	1.00[CEU][hapmap];0.82[CHB][hapmap]
rs10031699	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10155145	0.81[ASN][1000 genomes]
rs10489075	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[YRI][hapmap]
rs10516202	0.85[CHB][hapmap]
rs10516203	0.83[ASN][1000 genomes]
rs10939741	0.93[ASN][1000 genomes]
rs10939762	0.82[AMR][1000 genomes]
rs10939820	0.85[CHB][hapmap]
rs11722643	0.82[ASN][1000 genomes]
rs11723503	0.81[ASN][1000 genomes]
rs11724184	0.83[ASN][1000 genomes]
rs11726425	0.81[AMR][1000 genomes]
rs11727367	0.81[ASN][1000 genomes]
rs11735463	0.85[CHB][hapmap];1.00[YRI][hapmap];0.88[ASN][1000 genomes]
rs11736560	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11945358	0.85[CHB][hapmap]
rs12499527	0.82[ASN][1000 genomes]
rs12502342	0.81[ASN][1000 genomes]
rs12502368	0.81[ASN][1000 genomes]
rs12511548	1.00[CEU][hapmap];0.82[CHB][hapmap]
rs12642426	0.82[ASN][1000 genomes]
rs12642543	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13114828	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs13118272	0.82[CHB][hapmap];1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs13118647	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs13119002	0.85[AMR][1000 genomes]
rs13126688	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[YRI][hapmap]
rs13134726	0.81[CHB][hapmap];1.00[YRI][hapmap]
rs13135578	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes]
rs13148836	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs1541522	0.80[AMR][1000 genomes]
rs16893993	0.81[ASN][1000 genomes]
rs2003566	0.82[AMR][1000 genomes]
rs2005859	0.86[AMR][1000 genomes]
rs2068466	0.85[CHB][hapmap]
rs2110023	0.87[AMR][1000 genomes]
rs2159866	0.86[AMR][1000 genomes]
rs2192087	1.00[CEU][hapmap];0.82[CHB][hapmap];0.85[AMR][1000 genomes]
rs2192089	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs2192097	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs2192100	0.81[CHB][hapmap]
rs2215690	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs2215692	0.86[AMR][1000 genomes]
rs2215693	1.00[CEU][hapmap];0.82[CHB][hapmap]
rs2241466	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28502741	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs28600873	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2868419	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs34426660	0.82[ASN][1000 genomes]
rs34448220	0.83[ASN][1000 genomes]
rs35411115	0.82[ASN][1000 genomes]
rs35865690	0.85[ASN][1000 genomes]
rs3756216	0.83[ASN][1000 genomes]
rs3756217	0.81[CHB][hapmap];0.83[ASN][1000 genomes]
rs3756231	1.00[CEU][hapmap]
rs3796840	1.00[CEU][hapmap]
rs4140695	1.00[CEU][hapmap];0.81[CHB][hapmap];0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4235358	0.88[ASN][1000 genomes]
rs4393996	0.84[ASN][1000 genomes]
rs4406017	0.81[CHB][hapmap]
rs4472137	0.87[ASN][1000 genomes]
rs4572881	0.82[CHB][hapmap];0.84[ASN][1000 genomes]
rs4697723	1.00[CEU][hapmap];0.81[CHB][hapmap];0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4697725	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4697733	1.00[CEU][hapmap];0.82[CHB][hapmap]
rs4697736	0.81[CHB][hapmap]
rs4697942	1.00[CEU][hapmap];0.81[CHB][hapmap];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4697943	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4697944	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4697945	1.00[CEU][hapmap];0.92[AMR][1000 genomes]
rs4697953	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4697959	0.90[AMR][1000 genomes]
rs4697970	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs4697976	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs4697987	1.00[CEU][hapmap];0.84[AMR][1000 genomes]
rs4697988	0.88[CHB][hapmap]
rs6449341	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[AMR][1000 genomes]
rs6449423	1.00[CEU][hapmap];0.82[CHB][hapmap]
rs6449441	0.86[JPT][hapmap]
rs6814532	0.81[CHB][hapmap];0.90[ASN][1000 genomes]
rs6816102	1.00[CEU][hapmap];0.84[AMR][1000 genomes]
rs6850167	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs715259	0.85[ASN][1000 genomes]
rs71603991	0.81[ASN][1000 genomes]
rs7671856	0.82[AMR][1000 genomes]
rs7691156	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs887726	1.00[CEU][hapmap];0.81[CHB][hapmap];0.87[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs929576	0.88[AMR][1000 genomes]
rs9991911	0.93[ASN][1000 genomes]
rs9998005	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533218	chr4:9371016-10252290	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	74 gene(s)	inside rSNPs	diseases
2	nsv530090	chr4:9383695-10165033	Enhancers Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
3	nsv1014216	chr4:9713612-10223836	Transcr. at gene 5' and 3' Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
4	nsv878681	chr4:9802853-10397327	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
5	nsv997941	chr4:9805223-10493388	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
6	nsv1008649	chr4:9805223-10589802	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
7	nsv1000587	chr4:9805223-10610752	Flanking Active TSS Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
8	nsv537022	chr4:9805223-10610752	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS 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	56 gene(s)	inside rSNPs	diseases
9	nsv1003454	chr4:9805223-10710990	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers 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 miRNA	58 gene(s)	inside rSNPs	diseases
10	nsv537023	chr4:9805223-10710990	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
11	nsv1004801	chr4:9814720-10674528	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
12	nsv537024	chr4:9814720-10674528	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
13	nsv931483	chr4:9814721-10716463	Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
14	nsv537026	chr4:9903566-10262258	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
15	nsv1009972	chr4:9903566-10710990	Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
16	nsv537027	chr4:9903566-10710990	Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription 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	58 gene(s)	inside rSNPs	diseases
17	esv2752052	chr4:9911872-10313111	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
18	nsv1010620	chr4:9937123-10686682	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
19	nsv530280	chr4:9947818-10940041	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
20	nsv532706	chr4:9948018-10451450	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
21	nsv1013022	chr4:9961220-10230042	Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
22	nsv537028	chr4:9961220-10230042	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
23	nsv537029	chr4:9961220-10262258	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats 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	47 gene(s)	inside rSNPs	diseases
24	nsv878691	chr4:9966477-10418078	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription 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	50 gene(s)	inside rSNPs	diseases
25	nsv1013487	chr4:9972011-10320963	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
26	nsv1008067	chr4:10004664-10262258	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
27	nsv537030	chr4:10004664-10262258	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
28	nsv869057	chr4:10013411-10875454	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
29	nsv537031	chr4:10040713-10262258	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
30	nsv997936	chr4:10040713-11009045	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
31	nsv428438	chr4:10058226-10273779	Flanking Active TSS Genic enhancers Strong transcription Active TSS Weak transcription 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	46 gene(s)	inside rSNPs	diseases
32	nsv537032	chr4:10069805-10262258	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
33	nsv537033	chr4:10069805-10297561	Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	49 gene(s)	inside rSNPs	diseases
34	nsv1003286	chr4:10082156-10230606	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
35	esv16807	chr4:10099819-10234566	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
36	nsv537034	chr4:10103058-10262258	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
37	nsv537035	chr4:10103058-10297561	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
38	esv2752053	chr4:10124819-10270300	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
39	esv1000327	chr4:10135604-10192545	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
40	nsv593695	chr4:10138470-10345548	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
41	nsv593696	chr4:10140551-10168849	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10151200-10164400	Weak transcription	Right Atrium	heart
2	chr4:10157600-10160800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr4:10158000-10160800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr4:10158600-10165600	Enhancers	Fetal Thymus	thymus
5	chr4:10158800-10161000	Enhancers	Fetal Stomach	stomach
6	chr4:10158800-10161200	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr4:10159000-10160800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr4:10159000-10160800	Enhancers	Brain Hippocampus Middle	brain
9	chr4:10159000-10160800	Enhancers	Brain Substantia Nigra	brain
10	chr4:10159200-10160800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr4:10159200-10160800	Enhancers	Fetal Lung	lung
12	chr4:10159200-10160800	Enhancers	Rectal Smooth Muscle	rectum
13	chr4:10159200-10161000	Enhancers	Primary T cells fromperipheralblood	blood
14	chr4:10159200-10161000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr4:10159200-10161200	Enhancers	Colon Smooth Muscle	Colon
16	chr4:10159400-10160600	Enhancers	HUVEC	blood vessel
17	chr4:10159600-10160800	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr4:10159600-10161000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:10159600-10161800	Enhancers	HMEC	breast
20	chr4:10159800-10160600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr4:10159800-10161600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:10159800-10161600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:10159800-10161800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr4:10159800-10163800	Weak transcription	Fetal Intestine Large	intestine
25	chr4:10159800-10163800	Weak transcription	Stomach Mucosa	stomach
26	chr4:10159800-10164200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr4:10159800-10172600	Weak transcription	NHEK	skin
28	chr4:10160000-10160600	Enhancers	K562	blood
29	chr4:10160200-10160800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:10160200-10161000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr4:10160200-10161600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr4:10160200-10169400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:10160400-10160600	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr4:10160400-10161000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr4:10160400-10161600	Weak transcription	Primary T cells from cord blood	blood
36	chr4:10160400-10162200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr4:10160400-10163400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr4:10160400-10164400	Enhancers	Thymus	Thymus
39	chr4:10160400-10164600	Weak transcription	Stomach Smooth Muscle	stomach

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