Variant report

Variant	rs7147744
Chromosome Location	chr14:105143579-105143580
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAZ	chr14:105143538-105144783	K562	blood:	n/a	chr14:105143577-105143587 chr14:105144497-105144507
2	POLR2A	chr14:105143303-105144923	GM12878	blood:	n/a	n/a
3	ZNF143	chr14:105143278-105144644	GM12878	blood:	n/a	chr14:105143486-105143504
4	BHLHE40	chr14:105143271-105144899	K562	blood:	n/a	chr14:105143538-105143547 chr14:105144268-105144284
5	MAX	chr14:105143433-105144651	H1-hESC	embryonic stem cell:	n/a	chr14:105143577-105143587 chr14:105143491-105143501 chr14:105144497-105144507
6	POLR2A	chr14:105142890-105145187	H1-hESC	embryonic stem cell:	n/a	n/a
7	RUNX3	chr14:105143330-105144598	GM12878	blood:	n/a	n/a
8	MAZ	chr14:105143290-105144960	GM12878	blood:	n/a	chr14:105143577-105143587 chr14:105143491-105143501 chr14:105144497-105144507
9	MAX	chr14:105143378-105143615	K562	blood:	n/a	chr14:105143577-105143587 chr14:105143491-105143501
10	POLR2A	chr14:105143532-105145036	K562	blood:	n/a	n/a
11	RELA	chr14:105143322-105144515	GM19193	blood:	n/a	n/a
12	POLR2A	chr14:105143226-105144801	GM19099	blood:	n/a	n/a
13	CHD2	chr14:105143556-105144590	GM12878	blood:	n/a	chr14:105143743-105143753
14	E2F6	chr14:105143563-105144724	A549	lung:	n/a	chr14:105144442-105144449 chr14:105144441-105144453 chr14:105144442-105144449 chr14:105144442-105144449 chr14:105144441-105144450
15	USF1	chr14:105143395-105143701	H1-hESC	embryonic stem cell:	n/a	chr14:105143538-105143547
16	ZBTB7A	chr14:105143410-105143831	K562	blood:	n/a	chr14:105143501-105143509 chr14:105143700-105143709
17	ELF1	chr14:105143000-105144668	GM12878	blood:	n/a	chr14:105144320-105144332 chr14:105144271-105144283
18	EP300	chr14:105143573-105144690	A549	lung:	n/a	chr14:105144493-105144509 chr14:105144476-105144492
19	POLR2A	chr14:105143122-105143650	ECC-1	luminal epithelium:	n/a	n/a
20	RELA	chr14:105143203-105145071	GM18951	blood:	n/a	n/a
21	POLR2A	chr14:105143201-105144755	GM18526	blood:	n/a	n/a
22	MAX	chr14:105143481-105144681	H1-hESC	embryonic stem cell:	n/a	chr14:105143577-105143587 chr14:105143491-105143501 chr14:105144497-105144507
23	MAX	chr14:105143387-105144835	GM12878	blood:	n/a	chr14:105143577-105143587 chr14:105143491-105143501 chr14:105144497-105144507
24	STAT5A	chr14:105143446-105144674	GM12878	blood:	n/a	chr14:105144088-105144100 chr14:105143493-105143505 chr14:105144601-105144613 chr14:105143962-105143974
25	CTCF	chr14:105143540-105143690	HRE	kidney:	n/a	n/a
26	TCF12	chr14:105143500-105144964	A549	lung:	n/a	chr14:105144062-105144072
27	RELA	chr14:105143393-105144859	GM15510	blood:	n/a	n/a
28	EP300	chr14:105143412-105144625	GM12878	blood:	n/a	chr14:105144493-105144509 chr14:105144476-105144492
29	POLR2A	chr14:105143507-105144718	GM12878	blood:	n/a	n/a
30	ZBTB7A	chr14:105143497-105145240	ECC-1	luminal epithelium:	n/a	chr14:105145168-105145177 chr14:105143501-105143509 chr14:105143700-105143709
31	POLR2A	chr14:105143522-105144762	GM12892	blood:	n/a	n/a
32	BHLHE40	chr14:105143507-105143704	A549	lung:	n/a	chr14:105143538-105143547
33	BHLHE40	chr14:105143200-105144847	GM12878	blood:	n/a	chr14:105143538-105143547 chr14:105144268-105144284
34	TCF3	chr14:105143434-105143763	GM12878	blood:	n/a	n/a
35	MXI1	chr14:105143383-105144737	GM12878	blood:	n/a	chr14:105144062-105144071 chr14:105144491-105144500
36	POLR2A	chr14:105143484-105144659	A549	lung:	n/a	n/a
37	POLR2A	chr14:105143574-105145070	Hela-S3	cervix:	n/a	n/a
38	TCF12	chr14:105143462-105143654	GM12878	blood:	n/a	n/a
39	MAX	chr14:105143575-105144730	ECC-1	luminal epithelium:	n/a	chr14:105143577-105143587 chr14:105144497-105144507
40	POLR2A	chr14:105143466-105145142	A549	lung:	n/a	n/a
41	POLR2A	chr14:105143376-105144843	GM15510	blood:	n/a	n/a
42	MTA3	chr14:105143168-105144543	GM12878	blood:	n/a	n/a
43	RELA	chr14:105143373-105144689	GM19099	blood:	n/a	n/a
44	POLR2A	chr14:105143209-105144816	GM19193	blood:	n/a	n/a
45	POLR2A	chr14:105143131-105144787	GM18505	blood:	n/a	n/a
46	USF2	chr14:105143384-105143749	GM12878	blood:	n/a	chr14:105143538-105143547
47	MAX	chr14:105143454-105149192	A549	lung:	n/a	chr14:105147697-105147707 chr14:105148821-105148831 chr14:105143577-105143587 chr14:105147699-105147706 chr14:105147373-105147382 chr14:105145703-105145713 chr14:105147696-105147704 chr14:105148098-105148108 chr14:105143491-105143501 chr14:105147698-105147707 chr14:105146998-105147007 chr14:105148306-105148316 chr14:105144497-105144507
48	POLR2A	chr14:105143524-105144664	A549	lung:	n/a	n/a
49	BATF	chr14:105143425-105143730	GM12878	blood:	n/a	n/a
50	EBF1	chr14:105143370-105144947	GM12878	blood:	n/a	chr14:105143855-105143866 chr14:105144830-105144840 chr14:105144831-105144840

No.	Distal block	Cell Line	Cell type
1	chr14:105138099..105140345-chr14:105142107..105143661,2	K562	blood:
2	chr14:105141722..105146086-chr14:105153894..105158180,8	K562	blood:
3	chr14:105141667..105144301-chr14:105219073..105221089,2	K562	blood:
4	chr14:105143562..105144379-chr3:138553432..138553985,2	HCT-116	colon:
5	chr14:105143237..105145709-chr14:105189737..105191924,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000256050	TF binding region
ENSG00000203485	Chromatin interaction
ENSG00000184990	Chromatin interaction
ENSG00000258858	Chromatin interaction
ENSG00000185100	Chromatin interaction
ENSG00000051382	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10135029	0.96[ASN][1000 genomes]
rs10139247	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10143904	0.96[ASN][1000 genomes]
rs28661507	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs28676628	0.96[ASN][1000 genomes]
rs28729119	0.96[ASN][1000 genomes]
rs3935916	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4075355	0.96[ASN][1000 genomes]
rs4078242	1.00[ASN][1000 genomes]
rs5015594	0.96[ASN][1000 genomes]
rs55880426	0.91[EUR][1000 genomes]
rs56275181	0.80[ASN][1000 genomes]
rs56385415	0.80[ASN][1000 genomes]
rs7145744	1.00[ASN][1000 genomes]
rs72713850	0.80[ASN][1000 genomes]
rs72713852	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:43 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530812	chr14:104775571-105364883	Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1051647	chr14:104983302-105153720	Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
3	nsv542223	chr14:104983302-105153720	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
4	nsv902372	chr14:105011436-105200377	Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	nsv456445	chr14:105023512-105170003	Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
6	nsv566047	chr14:105023512-105170003	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
7	nsv1053591	chr14:105024558-105475931	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
8	nsv542224	chr14:105024558-105475931	Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
9	esv2830002	chr14:105078251-105348552	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
10	nsv902378	chr14:105086475-105200377	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
11	nsv902379	chr14:105086475-105274093	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
12	nsv902380	chr14:105092479-105166002	Genic enhancers Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription 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	36 gene(s)	inside rSNPs	diseases
13	nsv902381	chr14:105092479-105168414	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
14	nsv902382	chr14:105092479-105185666	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
15	nsv902383	chr14:105092479-105200377	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
16	nsv902384	chr14:105092479-105208567	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription 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 miRNA target site	45 gene(s)	inside rSNPs	diseases
17	nsv902385	chr14:105092479-105215351	Enhancers Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
18	nsv902386	chr14:105092479-105233095	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
19	nsv902387	chr14:105092479-105274093	Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
20	nsv902388	chr14:105092479-105311249	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
21	nsv902389	chr14:105092479-105366499	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
22	nsv902390	chr14:105100021-105185666	Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
23	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS 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 miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
24	nsv902391	chr14:105105769-105185666	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
25	nsv902392	chr14:105105769-105274093	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
26	nsv902393	chr14:105116232-105200377	Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
27	nsv902394	chr14:105116232-105274093	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
28	nsv902395	chr14:105119897-105215351	Strong transcription Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
29	nsv902396	chr14:105119897-105274093	Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
30	nsv566048	chr14:105126354-105185666	Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
31	nsv456446	chr14:105126354-105189504	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
32	nsv566049	chr14:105126354-105189504	Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
33	nsv456447	chr14:105126354-105200377	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
34	nsv566050	chr14:105126354-105200377	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers 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	44 gene(s)	inside rSNPs	diseases
35	nsv456448	chr14:105126354-105208567	Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
36	nsv566051	chr14:105126354-105208567	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
37	nsv470678	chr14:105126354-105246686	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
38	nsv566052	chr14:105126354-105268228	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
39	nsv470677	chr14:105126354-105348552	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
40	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
41	nsv984482	chr14:105134201-105159338	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
42	nsv566053	chr14:105139894-105268228	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
43	nsv902397	chr14:105139894-105268228	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105133600-105143600	Weak transcription	Gastric	stomach
2	chr14:105140200-105143600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr14:105140800-105143600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr14:105140800-105143600	Weak transcription	HMEC	breast
5	chr14:105142400-105143600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr14:105142600-105143600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:105142600-105143600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr14:105142600-105143600	Enhancers	Fetal Intestine Small	intestine
9	chr14:105142600-105143600	Enhancers	Placenta	Placenta
10	chr14:105142600-105143600	Enhancers	Fetal Thymus	thymus
11	chr14:105142600-105143800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr14:105142600-105143800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:105142600-105143800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr14:105142600-105143800	Enhancers	HSMMtube	muscle
15	chr14:105142600-105144000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr14:105142800-105143600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr14:105142800-105143600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr14:105142800-105143600	Bivalent Enhancer	Fetal Muscle Leg	muscle
19	chr14:105142800-105144400	Flanking Active TSS	HepG2	liver
20	chr14:105143000-105143600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr14:105143000-105143600	Enhancers	Primary B cells from peripheral blood	blood
22	chr14:105143000-105143600	Enhancers	Primary hematopoietic stem cells	blood
23	chr14:105143000-105143600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr14:105143000-105143600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr14:105143000-105143600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr14:105143000-105143600	Enhancers	Brain Germinal Matrix	brain
27	chr14:105143000-105143600	Enhancers	Colonic Mucosa	Colon
28	chr14:105143000-105143600	Bivalent Enhancer	Fetal Stomach	stomach
29	chr14:105143000-105143600	Enhancers	A549	lung
30	chr14:105143000-105143800	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr14:105143000-105143800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr14:105143000-105143800	Enhancers	Esophagus	oesophagus
33	chr14:105143000-105143800	Enhancers	Fetal Heart	heart
34	chr14:105143000-105143800	Enhancers	Left Ventricle	heart
35	chr14:105143000-105143800	Enhancers	Right Ventricle	heart
36	chr14:105143000-105143800	Enhancers	K562	blood
37	chr14:105143000-105143800	Enhancers	NH-A	brain
38	chr14:105143000-105143800	Enhancers	NHEK	skin
39	chr14:105143000-105144000	Enhancers	Placenta Amnion	Placenta Amnion
40	chr14:105143000-105144200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
41	chr14:105143000-105144200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr14:105143000-105144600	Active TSS	H9 Cell Line	embryonic stem cell
43	chr14:105143000-105145000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr14:105143200-105143600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr14:105143200-105143600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr14:105143200-105143600	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr14:105143200-105143600	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr14:105143200-105143600	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr14:105143200-105143600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr14:105143200-105143600	Enhancers	Adipose Nuclei	Adipose

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