Variant report

Variant	rs12436635
Chromosome Location	chr14:105132647-105132648
allele	C/T
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	JUND	chr14:105132343-105132758	HepG2	liver:	n/a	chr14:105132401-105132412
2	MYBL2	chr14:105131647-105132878	HepG2	liver:	n/a	n/a
3	HDAC2	chr14:105132215-105132895	HepG2	liver:	n/a	n/a
4	TEAD4	chr14:105132284-105132885	ECC-1	luminal epithelium:	n/a	n/a
5	TCF12	chr14:105132072-105132926	ECC-1	luminal epithelium:	n/a	chr14:105132705-105132715 chr14:105132853-105132860
6	REST	chr14:105132415-105132873	HepG2	liver:	n/a	chr14:105132426-105132444 chr14:105132419-105132432
7	POLR2A	chr14:105132313-105132682	HepG2	liver:	n/a	n/a
8	POLR2A	chr14:105132027-105133016	HCT-116	colon:	n/a	n/a
9	TEAD4	chr14:105132217-105132991	HepG2	liver:	n/a	n/a
10	MAFF	chr14:105132534-105132750	HepG2	liver:	n/a	n/a
11	POLR2A	chr14:105131645-105132907	HepG2	liver:	n/a	n/a
12	RCOR1	chr14:105132029-105132820	HepG2	liver:	n/a	n/a
13	MAX	chr14:105131790-105133029	HepG2	liver:	n/a	n/a
14	YY1	chr14:105132525-105132885	HCT-116	colon:	n/a	n/a
15	ESR1	chr14:105132378-105132744	ECC-1	luminal epithelium:	n/a	n/a
16	ESR1	chr14:105132329-105132874	ECC-1	luminal epithelium:	n/a	n/a
17	MAX	chr14:105131960-105132820	ECC-1	luminal epithelium:	n/a	n/a
18	RAD21	chr14:105132056-105132660	HepG2	liver:	n/a	n/a
19	POLR2A	chr14:105132509-105132679	H1-hESC	embryonic stem cell:	n/a	n/a
20	SMC3	chr14:105131821-105132876	HepG2	liver:	n/a	chr14:105132056-105132063 chr14:105132307-105132314 chr14:105132238-105132246
21	POLR2A	chr14:105132034-105132898	HCT-116	colon:	n/a	n/a
22	MAX	chr14:105131519-105133018	HepG2	liver:	n/a	n/a
23	POLR2A	chr14:105132102-105132862	ECC-1	luminal epithelium:	n/a	n/a
24	FOSL2	chr14:105132377-105133135	HepG2	liver:	n/a	chr14:105132401-105132412
25	NFIC	chr14:105132197-105132862	HepG2	liver:	n/a	n/a
26	CEBPD	chr14:105132339-105132864	HepG2	liver:	n/a	n/a
27	TAF1	chr14:105132039-105132877	HepG2	liver:	n/a	n/a
28	SP1	chr14:105132302-105132812	H1-hESC	embryonic stem cell:	n/a	chr14:105132570-105132581 chr14:105132348-105132357
29	EP300	chr14:105132048-105132856	HepG2	liver:	n/a	chr14:105132776-105132792
30	CTCF	chr14:105132540-105132690	NHEK	skin:	n/a	n/a
31	CTCF	chr14:105132520-105132670	GM12874	blood:	n/a	n/a
32	NR3C1	chr14:105132373-105132792	ECC-1	luminal epithelium:	n/a	n/a
33	TCF12	chr14:105131239-105132831	A549	lung:	n/a	chr14:105132705-105132715
34	POLR2A	chr14:105132224-105132792	HepG2	liver:	n/a	n/a
35	ZBTB7A	chr14:105132348-105132804	HepG2	liver:	n/a	n/a
36	TEAD4	chr14:105132309-105132783	ECC-1	luminal epithelium:	n/a	n/a
37	POLR2A	chr14:105132064-105132902	HepG2	liver:	n/a	n/a
38	TBP	chr14:105131943-105132867	HepG2	liver:	n/a	n/a
39	MAX	chr14:105132091-105132876	HepG2	liver:	n/a	n/a
40	HEY1	chr14:105131698-105132993	HepG2	liver:	n/a	n/a
41	CHD2	chr14:105132027-105132743	HepG2	liver:	n/a	n/a
42	RFX5	chr14:105131730-105132970	HepG2	liver:	n/a	n/a
43	RXRA	chr14:105132343-105132788	HepG2	liver:	n/a	chr14:105132743-105132757
44	ESR1	chr14:105132272-105132777	ECC-1	luminal epithelium:	n/a	n/a
45	BHLHE40	chr14:105132438-105132866	HepG2	liver:	n/a	chr14:105132714-105132730
46	MAZ	chr14:105131946-105132880	HepG2	liver:	n/a	n/a
47	POLR2A	chr14:105131255-105132953	PANC-1	pancreas:	n/a	n/a
48	HNF4A	chr14:105132167-105132858	HepG2	liver:	n/a	chr14:105132740-105132762 chr14:105132607-105132622 chr14:105132609-105132621 chr14:105132608-105132623
49	BRCA1	chr14:105132319-105132700	HepG2	liver:	n/a	n/a
50	EP300	chr14:105131947-105132959	ECC-1	luminal epithelium:	n/a	chr14:105132038-105132048 chr14:105132776-105132792 chr14:105131982-105131991

No.	Distal block	Cell Line	Cell type
1	chr14:105132267..105134426-chr14:105148392..105150808,3	MCF-7	breast:
2	chr14:105129603..105135012-chr14:105153179..105156510,7	MCF-7	breast:
3	chr14:105132481..105134536-chr14:105189294..105191683,2	MCF-7	breast:
4	chr14:105132069..105135051-chr14:105166736..105168447,2	K562	blood:
5	chr14:105131813..105132691-chr14:105147357..105147890,2	MCF-7	breast:
6	chr14:105131134..105134373-chr14:105146178..105149539,6	MCF-7	breast:
7	chr14:105131727..105132946-chr14:105174165..105175944,9	MCF-7	breast:

Variant related genes	Relation type
ENSG00000260792	TF binding region
ENSG00000256050	Chromatin interaction
ENSG00000203485	Chromatin interaction
ENSG00000185100	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10873549	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12431388	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12433394	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12434207	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12436070	0.85[EUR][1000 genomes]
rs12436101	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28435446	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4371093	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4983377	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4983378	0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4983518	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4983524	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4983525	0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4983526	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs55639933	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57054585	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57515560	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs59699979	0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs59950617	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs72713869	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72713877	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72713881	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:40 , 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	nsv902375	chr14:105045524-105139894	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	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
37	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
38	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
39	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
40	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

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105122200-105132800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr14:105127200-105133000	Enhancers	Primary B cells from peripheral blood	blood
3	chr14:105129800-105133000	Enhancers	Fetal Thymus	thymus
4	chr14:105130000-105132800	Enhancers	Primary T cells from cord blood	blood
5	chr14:105130000-105132800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr14:105130000-105133000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr14:105130000-105133000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr14:105130200-105133000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr14:105130200-105133000	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr14:105130400-105133000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
11	chr14:105130400-105133200	Enhancers	Primary B cells from cord blood	blood
12	chr14:105130800-105132800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:105130800-105133200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:105131000-105132800	Enhancers	Spleen	Spleen
15	chr14:105131000-105133800	Enhancers	Brain Hippocampus Middle	brain
16	chr14:105131200-105133000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
17	chr14:105131200-105133600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr14:105131200-105133800	Enhancers	Brain Cingulate Gyrus	brain
19	chr14:105131200-105133800	Enhancers	Brain Substantia Nigra	brain
20	chr14:105131400-105133000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr14:105131400-105133000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr14:105131400-105133600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr14:105131400-105133600	Enhancers	Brain Angular Gyrus	brain
24	chr14:105131400-105133800	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr14:105131600-105132800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr14:105131600-105132800	Enhancers	Esophagus	oesophagus
27	chr14:105131600-105132800	Enhancers	Fetal Heart	heart
28	chr14:105131600-105132800	Enhancers	Pancreas	Pancrea
29	chr14:105131600-105133000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr14:105131600-105133000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr14:105131600-105133000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr14:105131600-105133000	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr14:105131600-105133000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr14:105131600-105133000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr14:105131600-105133000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr14:105131600-105133000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr14:105131600-105133000	Enhancers	Stomach Mucosa	stomach
38	chr14:105131600-105133000	Enhancers	HMEC	breast
39	chr14:105131600-105133600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr14:105131600-105133600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr14:105131600-105133800	Enhancers	Hela-S3	cervix
42	chr14:105131800-105132800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr14:105131800-105132800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr14:105131800-105132800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
45	chr14:105131800-105132800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr14:105131800-105132800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr14:105131800-105132800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr14:105131800-105132800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
49	chr14:105131800-105132800	Weak transcription	Fetal Kidney	kidney
50	chr14:105131800-105132800	Enhancers	Fetal Lung	lung

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