Variant report

Variant	rs56324843
Chromosome Location	chr14:103993875-103993876
allele	A/C
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	POLR2A	chr14:103993643-103994932	U87	brain:	n/a	n/a
2	POLR2A	chr14:103993629-103994989	GM12878	blood:	n/a	n/a
3	BATF	chr14:103993662-103994102	GM12878	blood:	n/a	n/a
4	BHLHE40	chr14:103993765-103994050	GM12878	blood:	n/a	n/a
5	MXI1	chr14:103993661-103994180	GM12878	blood:	n/a	n/a
6	EBF1	chr14:103993669-103994279	GM12878	blood:	n/a	chr14:103993946-103993955 chr14:103993943-103993954
7	PAX5	chr14:103993442-103994132	GM12878	blood:	n/a	chr14:103993910-103993919 chr14:103993669-103993696 chr14:103993673-103993692
8	NFIC	chr14:103993619-103994159	GM12878	blood:	n/a	n/a
9	STAT1	chr14:103993554-103993906	GM12878	blood:	n/a	chr14:103993728-103993740
10	RUNX3	chr14:103993595-103994138	GM12878	blood:	n/a	n/a
11	FOS	chr14:103993788-103994015	MCF10A-Er-Src	breast:	n/a	chr14:103993965-103993976 chr14:103993966-103993976 chr14:103993968-103993979 chr14:103993967-103993975 chr14:103993966-103993976
12	SPI1	chr14:103993582-103994083	GM12891	blood:	n/a	chr14:103993753-103993766
13	CUX1	chr14:103993710-103994070	GM12878	blood:	n/a	n/a
14	SPI1	chr14:103993438-103994258	GM12878	blood:	n/a	chr14:103993753-103993766
15	STAT3	chr14:103993823-103994045	GM12878	blood:	n/a	chr14:103993910-103993921
16	POLR2A	chr14:103993851-103994230	GM12878	blood:	n/a	n/a
17	STAT5A	chr14:103993659-103994228	GM12878	blood:	n/a	chr14:103993728-103993740 chr14:103993910-103993921
18	FOXM1	chr14:103993684-103994076	GM12878	blood:	n/a	n/a
19	POU2F2	chr14:103993700-103994215	GM12878	blood:	n/a	n/a
20	YY1	chr14:103993596-103994052	GM12892	blood:	n/a	n/a
21	SPI1	chr14:103993596-103994078	GM12878	blood:	n/a	chr14:103993753-103993766
22	MAZ	chr14:103993751-103994183	GM12878	blood:	n/a	n/a
23	POLR2A	chr14:103993820-103993946	K562	blood:	n/a	n/a
24	BCL11A	chr14:103993692-103993969	GM12878	blood:	n/a	chr14:103993910-103993919
25	EP300	chr14:103993678-103994228	GM12878	blood:	n/a	chr14:103994182-103994198
26	MTA3	chr14:103993274-103994237	GM12878	blood:	n/a	n/a
27	SPI1	chr14:103993544-103994135	GM12891	blood:	n/a	chr14:103993753-103993766
28	ELF1	chr14:103993575-103994459	GM12878	blood:	n/a	n/a
29	CEBPB	chr14:103993666-103994100	GM12878	blood:	n/a	n/a
30	SPI1	chr14:103993689-103993919	GM12878	blood:	n/a	chr14:103993753-103993766
31	ZNF143	chr14:103993584-103994433	GM12878	blood:	n/a	n/a
32	ELK1	chr14:103993794-103993945	GM12878	blood:	n/a	n/a
33	BCLAF1	chr14:103993689-103994140	GM12878	blood:	n/a	chr14:103994023-103994031 chr14:103993910-103993919
34	EP300	chr14:103993796-103994077	GM12878	blood:	n/a	n/a
35	WRNIP1	chr14:103993688-103994047	GM12878	blood:	n/a	n/a
36	IKZF1	chr14:103993615-103994079	GM12878	blood:	n/a	n/a
37	RELA	chr14:103993714-103994078	GM19099	blood:	n/a	n/a
38	POLR2A	chr14:103993672-103994252	GM19193	blood:	n/a	n/a
39	EBF1	chr14:103993608-103994159	GM12878	blood:	n/a	chr14:103993946-103993955 chr14:103993943-103993954
40	POLR2A	chr14:103993577-103995852	U87	brain:	n/a	n/a
41	NFATC1	chr14:103993677-103994113	GM12878	blood:	n/a	n/a
42	PAX5	chr14:103993610-103994184	GM12878	blood:	n/a	chr14:103993910-103993919 chr14:103993669-103993696 chr14:103993673-103993692
43	TBL1XR1	chr14:103993728-103994011	GM12878	blood:	n/a	n/a
44	ATF2	chr14:103993464-103994168	GM12878	blood:	n/a	n/a
45	POLR2A	chr14:103993732-103994233	GM12878	blood:	n/a	n/a
46	FOS	chr14:103993663-103994062	MCF10A-Er-Src	breast:	n/a	chr14:103993965-103993976 chr14:103993966-103993976 chr14:103993968-103993979 chr14:103993967-103993975 chr14:103993966-103993976
47	BCL11A	chr14:103993701-103994105	GM12878	blood:	n/a	chr14:103994023-103994031 chr14:103993910-103993919
48	RFX5	chr14:103993733-103993936	GM12878	blood:	n/a	n/a
49	POLR2A	chr14:103993503-103995855	U87	brain:	n/a	n/a
50	PML	chr14:103993562-103994140	GM12878	blood:	n/a	chr14:103993913-103993921

No.	Distal block	Cell Line	Cell type
1	chr14:103992721..103998040-chr14:104027797..104030842,4	MCF-7	breast:
2	chr14:103991343..103994487-chr14:104021014..104023570,3	MCF-7	breast:
3	chr14:103992298..103994293-chr14:104026567..104028145,2	K562	blood:
4	chr14:103993654..103996154-chr14:104180669..104183057,2	K562	blood:
5	chr14:103992666..103995489-chr14:104177229..104179572,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CKB-1	chr14:103991347-103995409	ENSG00000260285.1
2	lnc-TRMT61A-1	chr14:103993557-103994281	NONHSAT040175

Variant related genes	Relation type
CKB	TF binding region
TRMT61A	TF binding region
ENSG00000256053	Chromatin interaction
ENSG00000100711	Chromatin interaction
ENSG00000126215	Chromatin interaction
ENSG00000166170	Chromatin interaction
ENSG00000224997	Chromatin interaction
ENSG00000126214	Chromatin interaction

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10129401	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10129621	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10130887	1.00[AMR][1000 genomes]
rs10134819	1.00[AMR][1000 genomes]
rs10138787	1.00[AMR][1000 genomes]
rs10139205	1.00[AMR][1000 genomes]
rs10145934	1.00[AMR][1000 genomes]
rs10149860	1.00[AMR][1000 genomes]
rs10220595	1.00[AMR][1000 genomes]
rs12100454	1.00[AMR][1000 genomes]
rs28524598	1.00[AMR][1000 genomes]
rs28701683	1.00[AMR][1000 genomes]
rs28701880	1.00[AMR][1000 genomes]
rs28711428	1.00[AMR][1000 genomes]
rs56666624	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57987958	1.00[AMR][1000 genomes]
rs58869129	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60349773	1.00[AMR][1000 genomes]
rs61733762	1.00[AMR][1000 genomes]
rs7141712	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7148427	1.00[AMR][1000 genomes]
rs7150651	1.00[AMR][1000 genomes]
rs7155401	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7158326	1.00[AMR][1000 genomes]
rs7158972	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73353046	1.00[AMR][1000 genomes]
rs73359246	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73359248	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73359263	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73359284	0.92[AFR][1000 genomes]
rs73359299	1.00[AMR][1000 genomes]
rs73359301	1.00[AMR][1000 genomes]
rs73361317	1.00[AMR][1000 genomes]
rs73361323	1.00[AMR][1000 genomes]
rs73361328	1.00[AMR][1000 genomes]
rs73361331	1.00[AMR][1000 genomes]
rs73361334	1.00[AMR][1000 genomes]
rs73361335	1.00[AMR][1000 genomes]
rs73361345	1.00[AMR][1000 genomes]
rs73361349	1.00[AMR][1000 genomes]
rs73365132	1.00[AMR][1000 genomes]
rs8006030	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8009277	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8015505	1.00[AMR][1000 genomes]
rs879551	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534254	chr14:103470073-104023906	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
2	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
3	nsv832883	chr14:103927687-104120953	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1044967	chr14:103954727-104007051	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	esv1807091	chr14:103956182-104020454	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
6	esv1835824	chr14:103956182-104020454	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
7	nsv902297	chr14:103956182-104061646	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
8	nsv902298	chr14:103959289-104061646	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
9	nsv902299	chr14:103967504-104061646	Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Weak transcription 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 target site	43 gene(s)	inside rSNPs	diseases
10	nsv902300	chr14:103967504-104205811	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
11	esv1834605	chr14:103969909-104003091	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
12	nsv902301	chr14:103979953-104003094	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
13	esv1850440	chr14:103979953-104007555	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
14	nsv902302	chr14:103979953-104018455	Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
15	nsv902303	chr14:103979953-104034746	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
16	nsv902304	chr14:103979953-104061646	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
17	nsv902305	chr14:103979953-104073551	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
18	nsv827068	chr14:103982866-104021347	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
19	nsv902306	chr14:103984294-104003094	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
20	esv1835145	chr14:103984294-104014935	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
21	nsv902307	chr14:103986155-104003094	Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
22	esv1824096	chr14:103986255-103999371	Active TSS Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
23	esv1842368	chr14:103986255-103999371	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
24	esv1834274	chr14:103987140-103996205	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
25	esv1834291	chr14:103987140-103999371	Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
26	esv1839917	chr14:103987140-103999371	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
27	esv1845597	chr14:103987140-103999371	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
28	esv1851656	chr14:103987140-104007555	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
29	esv1839595	chr14:103987140-104034746	Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
30	esv1809007	chr14:103988059-103999371	Enhancers Genic enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
31	esv1818214	chr14:103988059-103999371	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
32	esv1837939	chr14:103988059-103999371	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
33	esv1846909	chr14:103988059-103999371	Flanking Active TSS Active TSS Genic enhancers Enhancers Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
34	esv1794331	chr14:103988059-104004311	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
35	nsv566020	chr14:103989279-103996396	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
36	nsv566021	chr14:103989639-104012982	Active TSS Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
37	esv1819920	chr14:103989971-104018096	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103989600-103994000	Weak transcription	Left Ventricle	heart
2	chr14:103989600-103994600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr14:103989800-103994000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr14:103989800-103994000	Weak transcription	Esophagus	oesophagus
5	chr14:103989800-103994000	Weak transcription	Ovary	ovary
6	chr14:103989800-103994000	Weak transcription	Right Atrium	heart
7	chr14:103989800-103994600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr14:103990000-103994000	Weak transcription	Brain Angular Gyrus	brain
9	chr14:103990000-103994200	Enhancers	Fetal Intestine Large	intestine
10	chr14:103990200-103994200	Weak transcription	Fetal Brain Female	brain
11	chr14:103990200-103994400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr14:103990200-103994600	Enhancers	Pancreas	Pancrea
13	chr14:103990400-103994200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr14:103990600-103994400	Enhancers	K562	blood
15	chr14:103990800-103994400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr14:103990800-103994600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:103990800-103994600	Enhancers	Fetal Stomach	stomach
18	chr14:103991000-103994200	Weak transcription	HSMMtube	muscle
19	chr14:103991000-103994600	Enhancers	Liver	Liver
20	chr14:103991000-103994600	Enhancers	Fetal Muscle Leg	muscle
21	chr14:103991400-103994200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr14:103991400-103994600	Enhancers	Fetal Muscle Trunk	muscle
23	chr14:103991800-103994200	Weak transcription	Rectal Smooth Muscle	rectum
24	chr14:103991800-103994800	Enhancers	Fetal Heart	heart
25	chr14:103991800-103994800	Enhancers	Placenta	Placenta
26	chr14:103992000-103994200	Enhancers	Colonic Mucosa	Colon
27	chr14:103992200-103994600	Enhancers	Right Ventricle	heart
28	chr14:103992200-103995000	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr14:103992400-103994200	Genic enhancers	Fetal Intestine Small	intestine
30	chr14:103992400-103994400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr14:103992400-103994400	Enhancers	Brain Anterior Caudate	brain
32	chr14:103992400-103994400	Weak transcription	Fetal Kidney	kidney
33	chr14:103992400-103994600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr14:103992400-103994600	Enhancers	Lung	lung
35	chr14:103992400-103994800	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr14:103992400-103995000	Enhancers	Spleen	Spleen
37	chr14:103992600-103994200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:103992600-103994200	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr14:103992600-103994200	Enhancers	A549	lung
40	chr14:103992600-103994400	Enhancers	Adipose Nuclei	Adipose
41	chr14:103992600-103994600	Enhancers	Primary B cells from cord blood	blood
42	chr14:103992600-103994600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr14:103992600-103994800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr14:103992800-103994000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr14:103992800-103994000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr14:103992800-103994000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr14:103992800-103994600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr14:103992800-103994800	Enhancers	Primary B cells from peripheral blood	blood
49	chr14:103993000-103994000	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr14:103993000-103994200	Weak transcription	Fetal Lung	lung

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