Variant report

Variant	rs73372908
Chromosome Location	chr21:46937872-46937873
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RUNX3	chr21:46937625-46938198	GM12878	blood:	n/a	n/a
2	CEBPB	chr21:46937666-46938031	HepG2	liver:	n/a	n/a
3	FOXP2	chr21:46937660-46937959	PFSK-1	brain:	n/a	n/a
4	RUNX3	chr21:46937634-46938123	GM12878	blood:	n/a	n/a
5	EP300	chr21:46937799-46938022	GM12878	blood:	n/a	n/a
6	MYC	chr21:46937722-46937920	NB4	blood:	n/a	n/a
7	FOS	chr21:46937737-46937961	MCF10A-Er-Src	breast:	n/a	n/a
8	CEBPB	chr21:46937687-46938083	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr21:46937699-46938014	K562	blood:	n/a	n/a
10	CEBPB	chr21:46937759-46937923	HepG2	liver:	n/a	n/a
11	CEBPB	chr21:46937672-46938028	Hela-S3	cervix:	n/a	n/a
12	BATF	chr21:46937688-46938003	GM12878	blood:	n/a	n/a
13	POLR2A	chr21:46937637-46937980	HL-60	blood:	n/a	n/a
14	CEBPB	chr21:46937632-46938080	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr21:46937750-46937929	H1-hESC	embryonic stem cell:	n/a	n/a
16	FOS	chr21:46937742-46937933	MCF10A-Er-Src	breast:	n/a	n/a
17	CEBPB	chr21:46937685-46938012	K562	blood:	n/a	n/a
18	CEBPB	chr21:46937580-46938088	MCF-7	breast:	n/a	n/a
19	STAT3	chr21:46937826-46937989	MCF10A-Er-Src	breast:	n/a	n/a
20	JUND	chr21:46937758-46937958	HepG2	liver:	n/a	n/a
21	FOS	chr21:46937770-46937942	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr21:46937659-46938122	HUVEC	blood vessel:	n/a	n/a
23	EP300	chr21:46937836-46937903	HepG2	liver:	n/a	n/a
24	CEBPB	chr21:46937731-46938030	HepG2	liver:	n/a	n/a
25	MYC	chr21:46937760-46938046	MCF10A-Er-Src	breast:	n/a	n/a
26	MYC	chr21:46937775-46937985	MCF10A-Er-Src	breast:	n/a	n/a
27	MYC	chr21:46937752-46937897	HUVEC	blood vessel:	n/a	n/a
28	NFIC	chr21:46937699-46938185	GM12878	blood:	n/a	n/a
29	CEBPB	chr21:46937714-46938019	A549	lung:	n/a	n/a
30	CEBPB	chr21:46937657-46938009	HepG2	liver:	n/a	n/a
31	ATF2	chr21:46937701-46938102	GM12878	blood:	n/a	n/a
32	CREB1	chr21:46937597-46938197	GM12878	blood:	n/a	n/a
33	POLR2A	chr21:46937864-46937915	HUVEC	blood vessel:	n/a	n/a
34	FOS	chr21:46937763-46938034	MCF10A-Er-Src	breast:	n/a	n/a
35	ATF2	chr21:46937684-46938084	GM12878	blood:	n/a	n/a
36	CEBPB	chr21:46937685-46938015	IMR90	lung:	n/a	n/a
37	CEBPB	chr21:46937629-46938135	MCF-7	breast:	n/a	n/a
38	CREB1	chr21:46937733-46938089	GM12878	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:46929866..46938044-chr21:46958345..46966843,19	MCF-7	breast:
2	chr21:46931307..46938554-chr21:46948936..46957386,13	MCF-7	breast:
3	chr21:46932082..46938082-chr21:46958527..46965997,11	MCF-7	breast:
4	chr21:46937157..46942745-chr21:46943220..46951744,10	K562	blood:
5	chr21:46493551..46495324-chr21:46936558..46938317,2	K562	blood:
6	chr21:46934806..46937902-chr21:46950852..46955377,4	MCF-7	breast:
7	chr21:46936312..46939945-chr21:46959313..46962987,4	K562	blood:

No data

Variant related genes	Relation type
SLC19A1	TF binding region
ENSG00000173638	Chromatin interaction
ENSG00000235374	Chromatin interaction
ENSG00000197381	Chromatin interaction

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12106284	1.00[AMR][1000 genomes]
rs17004784	1.00[AMR][1000 genomes]
rs17004786	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28413786	1.00[AMR][1000 genomes]
rs57287584	1.00[AMR][1000 genomes]
rs73370896	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73370901	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73372904	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73372917	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73372920	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73372923	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73372934	1.00[AMR][1000 genomes]
rs73372947	1.00[AMR][1000 genomes]
rs73907569	1.00[AMR][1000 genomes]
rs9306133	1.00[AMR][1000 genomes]
rs9306134	1.00[AMR][1000 genomes]
rs9984419	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:79 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531546	chr21:46504151-47411772	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
2	nsv914001	chr21:46647078-46944113	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
3	nsv914002	chr21:46655638-46945024	Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS 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	57 gene(s)	inside rSNPs	diseases
4	nsv1057807	chr21:46656346-47077374	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
5	esv2762114	chr21:46680202-47067744	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
6	nsv1057661	chr21:46687476-46961041	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
7	nsv914012	chr21:46695039-47015661	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
8	nsv1058665	chr21:46719445-47634282	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	91 gene(s)	inside rSNPs	diseases
9	nsv544486	chr21:46719445-47634282	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	91 gene(s)	inside rSNPs	diseases
10	esv1799934	chr21:46737751-46959154	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	42 gene(s)	inside rSNPs	diseases
11	nsv914027	chr21:46765580-46982335	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
12	esv1794926	chr21:46781404-46965534	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
13	nsv914031	chr21:46802952-46952750	Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
14	nsv914037	chr21:46816363-46982335	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
15	nsv914038	chr21:46817380-46964378	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
16	nsv1058685	chr21:46819364-46967996	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
17	nsv914044	chr21:46821907-46982335	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
18	nsv1056917	chr21:46822253-46976682	Enhancers Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
19	nsv1061626	chr21:46830542-46961041	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
20	nsv914046	chr21:46830873-46982335	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
21	nsv516407	chr21:46830873-47040656	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
22	nsv1066282	chr21:46839570-46966180	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
23	nsv1057447	chr21:46839570-46976682	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
24	nsv914048	chr21:46839904-47032872	Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS 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	34 gene(s)	inside rSNPs	diseases
25	nsv834111	chr21:46843086-47005244	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
26	esv1841607	chr21:46846944-46970385	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
27	nsv1062107	chr21:46847759-46976682	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats 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	29 gene(s)	inside rSNPs	diseases
28	esv1822272	chr21:46848326-47038855	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
29	nsv914049	chr21:46848589-46982335	Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
30	nsv1059083	chr21:46855788-46964378	Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
31	nsv914054	chr21:46859717-46964378	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
32	esv1816583	chr21:46859717-46982335	Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
33	nsv1064303	chr21:46873869-46959142	Flanking Active TSS Genic enhancers Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
34	nsv914058	chr21:46876083-46952750	Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
35	nsv1065190	chr21:46882278-46961041	Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
36	nsv1067396	chr21:46882278-46967996	Genic enhancers Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
37	nsv544490	chr21:46882278-46967996	Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Enhancers 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	23 gene(s)	inside rSNPs	diseases
38	nsv1064667	chr21:46882647-46976682	Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
39	nsv1064108	chr21:46882647-46979776	Flanking Active TSS Strong transcription Bivalent/Poised TSS Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
40	nsv914059	chr21:46883153-46964378	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
41	nsv1056757	chr21:46886710-46970498	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer 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	23 gene(s)	inside rSNPs	diseases
42	nsv1065126	chr21:46886710-46976682	Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
43	nsv1060416	chr21:46886710-46979776	Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
44	nsv914060	chr21:46889666-47015661	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
45	nsv1056986	chr21:46890759-46976682	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
46	nsv1056039	chr21:46891310-46961041	Weak transcription Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
47	nsv1057386	chr21:46891554-46959142	Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
48	nsv1055493	chr21:46894021-46966180	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
49	nsv1065095	chr21:46894736-46976682	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
50	nsv1062243	chr21:46894736-46979776	Active TSS Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46898200-46939600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr21:46898200-46945000	Weak transcription	Right Atrium	heart
3	chr21:46899600-46940400	Weak transcription	Rectal Smooth Muscle	rectum
4	chr21:46911200-46938200	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr21:46916000-46938200	Weak transcription	Fetal Heart	heart
6	chr21:46916000-46939600	Weak transcription	Fetal Kidney	kidney
7	chr21:46918200-46938400	Weak transcription	Brain Hippocampus Middle	brain
8	chr21:46919400-46945000	Weak transcription	Left Ventricle	heart
9	chr21:46920200-46946800	Weak transcription	NHEK	skin
10	chr21:46926200-46938000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr21:46929200-46938800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr21:46929400-46946600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr21:46931200-46938000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr21:46931600-46938200	Strong transcription	A549	lung
15	chr21:46931600-46938400	Strong transcription	Dnd41	blood
16	chr21:46932000-46938000	Strong transcription	Primary T cells from cord blood	blood
17	chr21:46932400-46948600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr21:46932800-46938200	Strong transcription	Fetal Brain Female	brain
19	chr21:46932800-46939000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr21:46933200-46938000	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr21:46933200-46938200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr21:46933400-46940400	Weak transcription	Aorta	Aorta
23	chr21:46933600-46938000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr21:46933600-46939600	Weak transcription	HMEC	breast
25	chr21:46933800-46938200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr21:46934000-46938200	Weak transcription	Brain Anterior Caudate	brain
27	chr21:46934000-46938200	Weak transcription	Brain Substantia Nigra	brain
28	chr21:46934000-46938400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr21:46934000-46938400	Weak transcription	Brain Cingulate Gyrus	brain
30	chr21:46934200-46938000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr21:46934200-46938000	Weak transcription	Stomach Smooth Muscle	stomach
32	chr21:46934400-46939000	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr21:46934800-46938400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr21:46934800-46940400	Weak transcription	Ovary	ovary
35	chr21:46934800-46945200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr21:46935000-46939400	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr21:46935000-46942400	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr21:46935000-46949200	Weak transcription	Brain Angular Gyrus	brain
39	chr21:46935200-46938400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr21:46935200-46938800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr21:46935200-46938800	Weak transcription	Fetal Lung	lung
42	chr21:46935800-46939400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr21:46935800-46944800	Weak transcription	Pancreas	Pancrea
44	chr21:46936000-46939600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr21:46936600-46938200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr21:46936600-46939600	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr21:46936800-46938200	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr21:46936800-46938200	Weak transcription	Adipose Nuclei	Adipose
49	chr21:46936800-46938600	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr21:46936800-46938600	Weak transcription	Brain Inferior Temporal Lobe	brain

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