Variant report

Variant	rs13135351
Chromosome Location	chr4:10033525-10033526
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:8 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA2	chr4:10033288-10033733	HepG2	liver:	n/a	n/a
2	RXRA	chr4:10033326-10033644	HepG2	liver:	n/a	chr4:10033505-10033521
3	FOXA1	chr4:10033348-10033771	HepG2	liver:	n/a	n/a
4	KAP1	chr4:10033334-10033837	U2OS	brain:	n/a	n/a
5	RCOR1	chr4:10033454-10033724	HepG2	liver:	n/a	n/a
6	REST	chr4:10033280-10033587	PFSK-1	brain:	n/a	chr4:10033404-10033418
7	NR3C1	chr4:10033355-10033629	A549	lung:	n/a	n/a
8	KAP1	chr4:10033366-10033786	HEK293	kidney:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:10020627..10022375-chr4:10032476..10035233,2	K562	blood:
2	chr4:10031896..10034212-chr4:10409451..10411616,2	K562	blood:
3	chr4:10033030..10034868-chr4:10118461..10119964,2	MCF-7	breast:
4	chr4:10031202..10033907-chr4:10037747..10039900,2	K562	blood:
5	chr4:10020691..10022205-chr4:10031735..10034033,2	K562	blood:
6	chr4:10032509..10034533-chr4:10096806..10099727,2	K562	blood:

No data

Variant related genes	Relation type
SLC2A9	TF binding region
ENSG00000071127	Chromatin interaction
ENSG00000109667	Chromatin interaction

Extended variants
information (count: 124 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10004571	0.84[ASN][1000 genomes]
rs10006397	0.82[CHB][hapmap];0.85[JPT][hapmap];0.95[ASN][1000 genomes]
rs10016075	0.91[CHB][hapmap];0.89[JPT][hapmap]
rs10022499	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs10023068	0.91[CHB][hapmap];0.89[JPT][hapmap]
rs10033088	0.83[ASN][1000 genomes]
rs10516196	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10516197	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10939650	0.86[CHB][hapmap];0.89[JPT][hapmap]
rs10939679	0.90[ASN][1000 genomes]
rs10939680	0.90[ASN][1000 genomes]
rs10939681	0.86[ASN][1000 genomes]
rs12108388	0.90[ASN][1000 genomes]
rs12499734	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12642537	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13106922	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13112782	0.90[ASN][1000 genomes]
rs13113006	0.89[JPT][hapmap]
rs13114106	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13122112	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13125476	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs13127630	0.90[ASN][1000 genomes]
rs13129697	0.83[JPT][hapmap]
rs13132625	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs13139970	0.84[JPT][hapmap]
rs13142273	0.83[JPT][hapmap]
rs13144899	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs13148476	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13151331	0.90[JPT][hapmap]
rs16891285	0.89[JPT][hapmap]
rs16891489	0.90[JPT][hapmap]
rs16892419	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16892420	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16892449	0.85[AFR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16892474	1.00[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16892475	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.84[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16892493	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2240723	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2276963	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35201034	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs35249656	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35334203	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35782952	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs36036984	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3756231	0.86[CHB][hapmap]
rs3756233	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3756234	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3775939	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3775941	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3775942	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3775943	0.82[EUR][1000 genomes]
rs3796829	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs3822250	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4312756	0.90[JPT][hapmap]
rs4333184	0.82[CHB][hapmap];0.89[JPT][hapmap]
rs4364264	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs4467565	0.89[JPT][hapmap]
rs4549382	0.84[ASN][1000 genomes]
rs4608811	0.90[ASN][1000 genomes]
rs55668232	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57897925	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59234705	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6812851	0.84[ASN][1000 genomes]
rs6813650	0.83[ASN][1000 genomes]
rs6820616	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6820756	0.83[ASN][1000 genomes]
rs6821843	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6822023	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6826764	0.95[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs6834555	0.84[ASN][1000 genomes]
rs6837659	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6846692	0.88[ASN][1000 genomes]
rs6853437	0.91[CHB][hapmap];0.89[JPT][hapmap]
rs714871	0.84[ASN][1000 genomes]
rs714873	0.86[CHB][hapmap];0.84[ASN][1000 genomes]
rs733175	0.90[ASN][1000 genomes]
rs7349721	0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs7657096	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs7659924	0.90[ASN][1000 genomes]
rs7663032	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs7664225	0.82[ASN][1000 genomes]
rs7669090	0.88[ASN][1000 genomes]
rs7677430	0.89[ASN][1000 genomes]
rs7678211	0.84[ASN][1000 genomes]
rs7678346	0.90[ASN][1000 genomes]
rs7683832	0.90[ASN][1000 genomes]
rs7685958	1.00[CEU][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9291640	0.91[CHB][hapmap];0.89[JPT][hapmap]
rs938558	0.80[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:35 , 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	nsv1010249	chr4:9716101-10086188	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	esv2763339	chr4:9858426-10056376	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	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
17	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
18	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
19	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
20	nsv878688	chr4:9915850-10038112	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	nsv829857	chr4:9982514-10155835	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking 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	43 gene(s)	inside rSNPs	diseases
30	nsv469621	chr4:9987670-10142287	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
31	nsv482719	chr4:9987670-10142287	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
32	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
33	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
34	nsv593691	chr4:10013173-10050141	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
35	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

No data

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10021600-10035200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:10025800-10034200	Weak transcription	Colonic Mucosa	Colon
3	chr4:10030200-10034200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:10030800-10033800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:10030800-10034000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr4:10030800-10034400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr4:10031000-10033600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:10031000-10033600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr4:10031000-10033600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:10031000-10033600	Weak transcription	HMEC	breast
11	chr4:10031200-10034000	Weak transcription	NHEK	skin
12	chr4:10031800-10037200	Enhancers	Fetal Muscle Leg	muscle
13	chr4:10032000-10033800	Enhancers	Brain Hippocampus Middle	brain
14	chr4:10032000-10034400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:10032000-10034800	Enhancers	Fetal Heart	heart
16	chr4:10032200-10033600	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr4:10032200-10034200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:10032200-10034400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr4:10032200-10035200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr4:10032200-10035400	Enhancers	Right Ventricle	heart
21	chr4:10032200-10036000	Enhancers	Psoas Muscle	Psoas
22	chr4:10032400-10033800	Enhancers	Brain Cingulate Gyrus	brain
23	chr4:10032400-10033800	Enhancers	Brain Substantia Nigra	brain
24	chr4:10032400-10033800	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr4:10032400-10034800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr4:10032400-10035200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:10032400-10035400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr4:10032400-10035800	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr4:10032400-10036000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr4:10032400-10036200	Enhancers	Right Atrium	heart
31	chr4:10032400-10036400	Enhancers	Brain Angular Gyrus	brain
32	chr4:10032400-10036400	Enhancers	Left Ventricle	heart
33	chr4:10032400-10037000	Enhancers	Fetal Muscle Trunk	muscle
34	chr4:10032400-10037000	Enhancers	Placenta	Placenta
35	chr4:10032400-10037000	Enhancers	Fetal Stomach	stomach
36	chr4:10032600-10033600	Weak transcription	Pancreas	Pancrea
37	chr4:10032600-10034000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:10032600-10034200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:10032600-10034600	Enhancers	HSMM	muscle
40	chr4:10032600-10036200	Enhancers	Osteobl	bone
41	chr4:10032800-10033800	Enhancers	Brain Anterior Caudate	brain
42	chr4:10032800-10034000	Weak transcription	Small Intestine	intestine
43	chr4:10032800-10034400	Enhancers	A549	lung
44	chr4:10032800-10035200	Enhancers	Fetal Kidney	kidney
45	chr4:10032800-10035400	Enhancers	Fetal Intestine Small	intestine
46	chr4:10032800-10035600	Enhancers	Adipose Nuclei	Adipose
47	chr4:10033000-10033600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr4:10033000-10033600	Flanking Active TSS	HepG2	liver
49	chr4:10033000-10034000	Weak transcription	Liver	Liver
50	chr4:10033000-10034600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links