Variant report

Variant	rs4983547
Chromosome Location	chr14:105215941-105215942
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:36)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:36 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MBD4	chr14:105215447-105215947	HepG2	liver:	n/a	n/a
2	HNF4A	chr14:105215495-105215982	HepG2	liver:	n/a	chr14:105215709-105215724
3	RAD21	chr14:105215348-105215957	HCT-116	colon:	n/a	n/a
4	GATA3	chr14:105215348-105216342	MCF-7	breast:	n/a	n/a
5	MYBL2	chr14:105215257-105216016	HepG2	liver:	n/a	n/a
6	FOSL2	chr14:105215293-105215961	HepG2	liver:	n/a	n/a
7	TEAD4	chr14:105215567-105216062	HepG2	liver:	n/a	n/a
8	HNF4A	chr14:105215499-105216020	HepG2	liver:	n/a	chr14:105215709-105215724
9	HEY1	chr14:105215398-105215994	HepG2	liver:	n/a	n/a
10	RAD21	chr14:105215436-105215999	MCF-7	breast:	n/a	n/a
11	MAZ	chr14:105215398-105216009	HepG2	liver:	n/a	n/a
12	HNF4G	chr14:105215500-105216014	HepG2	liver:	n/a	chr14:105215710-105215725
13	HDAC2	chr14:105215478-105216035	MCF-7	breast:	n/a	n/a
14	HNF4G	chr14:105215527-105215971	HepG2	liver:	n/a	chr14:105215710-105215725
15	SIN3AK20	chr14:105215298-105216287	MCF-7	breast:	n/a	n/a
16	GATA3	chr14:105215612-105216258	MCF-7	breast:	n/a	n/a
17	RAD21	chr14:105215483-105215970	HepG2	liver:	n/a	n/a
18	NFIC	chr14:105215610-105216290	ECC-1	luminal epithelium:	n/a	n/a
19	RCOR1	chr14:105215335-105215997	HepG2	liver:	n/a	n/a
20	GATA3	chr14:105215399-105216214	MCF-7	breast:	n/a	n/a
21	POLR2A	chr14:105215266-105216056	HepG2	liver:	n/a	n/a
22	ZNF217	chr14:105215610-105216151	MCF-7	breast:	n/a	n/a
23	RAD21	chr14:105215515-105215951	HepG2	liver:	n/a	n/a
24	ZNF143	chr14:105215669-105216173	H1-hESC	embryonic stem cell:	n/a	n/a
25	MAFK	chr14:105215571-105215970	HepG2	liver:	n/a	n/a
26	MAX	chr14:105215291-105216089	HepG2	liver:	n/a	n/a
27	POLR2A	chr14:105214412-105215982	HepG2	liver:	n/a	n/a
28	POLR2A	chr14:105215415-105215950	HepG2	liver:	n/a	n/a
29	POLR2A	chr14:105214791-105215967	HepG2	liver:	n/a	n/a
30	NR2F2	chr14:105215406-105216182	MCF-7	breast:	n/a	n/a
31	TCF12	chr14:105215203-105216395	MCF-7	breast:	n/a	n/a
32	POLR2A	chr14:105215131-105215972	HepG2	liver:	n/a	n/a
33	POLR2A	chr14:105215924-105215946	Hela-S3	cervix:	n/a	n/a
34	MAX	chr14:105215384-105216065	MCF-7	breast:	n/a	n/a
35	TEAD4	chr14:105215762-105216009	H1-hESC	embryonic stem cell:	n/a	n/a
36	NR2F2	chr14:105215338-105216436	MCF-7	breast:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105214906..105217436-chr14:105291555..105293979,2	K562	blood:
2	chr14:105215481..105217288-chr14:105225342..105227811,2	MCF-7	breast:
3	chr14:105212181..105214544-chr14:105215247..105218575,5	K562	blood:
4	chr14:105214138..105217932-chr14:105240840..105244138,4	MCF-7	breast:
5	chr14:105214906..105218911-chr14:105291555..105293979,3	K562	blood:
6	chr14:105189516..105190121-chr14:105215377..105216349,3	MCF-7	breast:
7	chr14:105195952..105198833-chr14:105214070..105216313,2	K562	blood:
8	chr14:105191198..105192100-chr14:105215255..105216111,2	MCF-7	breast:
9	chr14:105214288..105217812-chr14:105217866..105221644,6	MCF-7	breast:
10	chr14:105190272..105190941-chr14:105215673..105216221,2	MCF-7	breast:
11	chr14:105214166..105217064-chr14:105220903..105222419,2	K562	blood:
12	chr14:105214722..105217236-chr14:105281953..105283708,2	K562	blood:

No data

Variant related genes	Relation type
SIVA1	TF binding region
ENSG00000184990	Chromatin interaction
ENSG00000142208	Chromatin interaction
ENSG00000185100	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10142660	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1128866	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs11844508	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11850889	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12881199	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12885343	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12885496	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12887774	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12892858	0.94[EUR][1000 genomes]
rs12894569	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12896579	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12897418	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs28372998	0.85[ASN][1000 genomes]
rs28684636	0.85[ASN][1000 genomes]
rs35165446	0.94[EUR][1000 genomes]
rs35416681	0.85[ASN][1000 genomes]
rs35455320	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35550015	0.94[EUR][1000 genomes]
rs35590716	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35956117	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3730344	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3730346	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4381528	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4983542	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4983545	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58565216	0.85[ASN][1000 genomes]
rs59146350	0.85[ASN][1000 genomes]
rs61761200	0.85[ASN][1000 genomes]
rs61761256	0.85[ASN][1000 genomes]
rs71421880	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7146454	1.00[JPT][hapmap]
rs74090004	0.93[ASN][1000 genomes]
rs8192700	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:38 , 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	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	nsv517038	chr14:105146579-105311249	Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
21	nsv566057	chr14:105146579-105311249	Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
22	nsv566058	chr14:105148655-105233095	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers 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 target site	38 gene(s)	inside rSNPs	diseases
23	nsv902403	chr14:105148655-105233095	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
24	nsv820230	chr14:105148655-105246686	ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription 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 target site	38 gene(s)	inside rSNPs	diseases
25	nsv566059	chr14:105148655-105268228	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
26	nsv566060	chr14:105148655-105311249	Flanking Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS 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 target site	66 gene(s)	inside rSNPs	diseases
27	nsv902404	chr14:105148655-105311249	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
28	nsv902405	chr14:105148655-105340643	Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
29	nsv542226	chr14:105153660-105265857	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
30	nsv456455	chr14:105154105-105259734	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
31	nsv566062	chr14:105154105-105259734	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Weak 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	35 gene(s)	inside rSNPs	diseases
32	nsv902407	chr14:105154105-105268228	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
33	nsv902408	chr14:105154105-105274093	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
34	nsv902409	chr14:105154105-105311249	Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh 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 target site	63 gene(s)	inside rSNPs	diseases
35	nsv566063	chr14:105154105-105312935	Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
36	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
37	nsv902411	chr14:105163532-105268228	Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
38	nsv566069	chr14:105185666-105274538	Bivalent/Poised TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs4983547	SIVA1	Cis_1M	lymphoblastoid	RTeQTL
rs4983547	HCK	trans	lymphoblastoid	seeQTL
rs4983547	C14orf70	cis	parietal	SCAN
rs4983547	TRMT61A	cis	cerebellum	SCAN

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105191400-105218200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:105192000-105218200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr14:105192400-105218400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr14:105202600-105218400	Weak transcription	Ovary	ovary
5	chr14:105203800-105218400	Weak transcription	Psoas Muscle	Psoas
6	chr14:105204200-105219600	Weak transcription	Fetal Heart	heart
7	chr14:105211800-105216200	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr14:105211800-105217000	Enhancers	Fetal Thymus	thymus
9	chr14:105212000-105216200	Enhancers	Fetal Lung	lung
10	chr14:105212000-105216400	Enhancers	Fetal Kidney	kidney
11	chr14:105212000-105217000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr14:105212400-105216000	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr14:105212400-105216400	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr14:105212400-105216800	Enhancers	Liver	Liver
15	chr14:105212400-105217000	Enhancers	NHLF	lung
16	chr14:105212600-105218200	Weak transcription	Thymus	Thymus
17	chr14:105212800-105216800	Enhancers	Brain Cingulate Gyrus	brain
18	chr14:105212800-105218200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr14:105213000-105217200	Enhancers	Fetal Muscle Leg	muscle
20	chr14:105213000-105217400	Enhancers	Fetal Stomach	stomach
21	chr14:105213000-105218400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr14:105213200-105216400	Enhancers	Stomach Mucosa	stomach
23	chr14:105213200-105216800	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr14:105213200-105218400	Weak transcription	Pancreas	Pancrea
25	chr14:105213400-105216000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr14:105213400-105216200	Weak transcription	Rectal Smooth Muscle	rectum
27	chr14:105213400-105218200	Weak transcription	Right Ventricle	heart
28	chr14:105213600-105216000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr14:105213600-105217200	Enhancers	Esophagus	oesophagus
30	chr14:105213800-105216800	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr14:105213800-105217200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr14:105213800-105217200	Enhancers	Fetal Intestine Small	intestine
33	chr14:105213800-105217400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:105214200-105216200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr14:105214200-105216400	Enhancers	Brain Hippocampus Middle	brain
36	chr14:105214200-105216600	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr14:105214400-105216800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr14:105214400-105216800	Enhancers	Aorta	Aorta
39	chr14:105214400-105217200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr14:105214600-105216000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr14:105214600-105216000	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr14:105214600-105216600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr14:105214600-105217000	Enhancers	Osteobl	bone
44	chr14:105214600-105217800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr14:105214600-105218600	Weak transcription	Left Ventricle	heart
46	chr14:105214800-105216800	Enhancers	Brain Angular Gyrus	brain
47	chr14:105214800-105216800	Enhancers	Gastric	stomach
48	chr14:105214800-105218600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr14:105215000-105216600	Enhancers	Fetal Intestine Large	intestine
50	chr14:105215000-105216800	Enhancers	Brain Substantia Nigra	brain

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