Variant report

Variant	rs112979667
Chromosome Location	chr14:105265948-105265949
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:64)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:64 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZBTB7A	chr14:105265894-105267034	ECC-1	luminal epithelium:	n/a	chr14:105266444-105266455
2	RAD21	chr14:105265915-105266220	HepG2	liver:	n/a	n/a
3	MAZ	chr14:105265714-105267436	HepG2	liver:	n/a	n/a
4	CTCF	chr14:105265933-105266195	IMR90	lung:	n/a	n/a
5	UBTF	chr14:105265899-105266248	K562	blood:	n/a	n/a
6	CTCF	chr14:105265920-105266070	HCFaa	heart:	n/a	n/a
7	SMC3	chr14:105265918-105266213	HepG2	liver:	n/a	n/a
8	CTCF	chr14:105265920-105266070	HFF-Myc	foreskin:	n/a	n/a
9	CTCF	chr14:105265920-105266070	GM12874	blood:	n/a	n/a
10	RAD21	chr14:105265925-105266135	HepG2	liver:	n/a	n/a
11	CTCF	chr14:105265940-105266090	GM12873	blood:	n/a	n/a
12	MAZ	chr14:105265934-105267784	K562	blood:	n/a	n/a
13	RXRA	chr14:105265896-105266242	HepG2	liver:	n/a	n/a
14	CTCF	chr14:105265940-105266090	HVMF	connective:	n/a	n/a
15	RAD21	chr14:105265908-105266229	H1-hESC	embryonic stem cell:	n/a	n/a
16	MAX	chr14:105265886-105268098	HepG2	liver:	n/a	n/a
17	CTCF	chr14:105265936-105266122	GM19239	blood:	n/a	n/a
18	CHD2	chr14:105265778-105266868	H1-hESC	embryonic stem cell:	n/a	chr14:105266658-105266667 chr14:105266855-105266865
19	CTCF	chr14:105265944-105266153	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr14:105265337-105266718	K562	blood:	n/a	n/a
21	HEY1	chr14:105265897-105267588	HepG2	liver:	n/a	chr14:105267327-105267342 chr14:105267153-105267168 chr14:105267290-105267305 chr14:105267324-105267339 chr14:105267127-105267142 chr14:105266860-105266875
22	CTCF	chr14:105265948-105266184	H1-hESC	embryonic stem cell:	n/a	n/a
23	GTF2F1	chr14:105265886-105266172	H1-hESC	embryonic stem cell:	n/a	n/a
24	TBP	chr14:105265803-105267429	K562	blood:	n/a	n/a
25	CTCF	chr14:105265920-105266070	SAEC	small airway:	n/a	n/a
26	CTBP2	chr14:105265584-105266198	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr14:105265920-105266070	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr14:105265940-105266090	WI-38	lung:	n/a	n/a
29	CTCF	chr14:105265940-105266090	AG04450	lung:	n/a	n/a
30	CTCF	chr14:105265940-105266090	AG09309	skin:	n/a	n/a
31	POLR2A	chr14:105265414-105267635	HepG2	liver:	n/a	n/a
32	SP1	chr14:105265780-105266306	H1-hESC	embryonic stem cell:	n/a	n/a
33	ZNF143	chr14:105265673-105266254	H1-hESC	embryonic stem cell:	n/a	n/a
34	YY1	chr14:105265859-105266442	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr14:105265940-105266090	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr14:105265947-105266154	K562	blood:	n/a	n/a
37	ZBTB7A	chr14:105265853-105266249	K562	blood:	n/a	n/a
38	EP300	chr14:105265945-105266879	K562	blood:	n/a	chr14:105266870-105266879
39	RAD21	chr14:105265832-105266334	H1-hESC	embryonic stem cell:	n/a	n/a
40	YY1	chr14:105265809-105266834	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUND	chr14:105265888-105266221	H1-hESC	embryonic stem cell:	n/a	n/a
42	RCOR1	chr14:105265881-105266220	HepG2	liver:	n/a	n/a
43	RAD21	chr14:105265848-105266230	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr14:105265920-105266070	GM12871	blood:	n/a	n/a
45	CTCF	chr14:105265940-105266090	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr14:105265880-105266030	GM12864	blood:	n/a	n/a
47	MAX	chr14:105265936-105266296	K562	blood:	n/a	n/a
48	ZBTB7A	chr14:105265896-105266257	HepG2	liver:	n/a	n/a
49	CTCF	chr14:105265897-105266146	HepG2	liver:	n/a	n/a
50	BACH1	chr14:105265908-105266571	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105265909-105265959	CMK	blood:	n/a
2	chr14:105265909-105265959	HCM	heart:	n/a
3	chr14:105265909-105265959	Jurkat	blood:	n/a
4	chr14:105265909-105265959	MCF-7	breast:	n/a
5	chr14:105265909-105265959	MCF10A-Er-Src	breast:	n/a
6	chr14:105265909-105265959	GM12891	blood:	n/a
7	chr14:105265909-105265959	AG10803	skin:	n/a
8	chr14:105265909-105265959	PFSK-1	brain:	n/a
9	chr14:105265909-105265959	HMEC	breast:	n/a
10	chr14:105265909-105265959	Hepatocyte	liver:	n/a
11	chr14:105265909-105265959	Caco-2	colon:	n/a
12	chr14:105265909-105265959	BJ	skin:	n/a
13	chr14:105265909-105265959	AG09309	skin:	n/a
14	chr14:105265909-105265959	NHBE	bronchial:	n/a
15	chr14:105265909-105265959	GM12892	blood:	n/a
16	chr14:105265909-105265959	HepG2	liver:	n/a
17	chr14:105265909-105265959	SKMC	muscle:	n/a
18	chr14:105265909-105265959	AG04450	lung:	fetal
19	chr14:105265909-105265959	HUVEC	blood vessel:	n/a
20	chr14:105265909-105265959	AG09319	gingival:	n/a
21	chr14:105265909-105265959	SAEC	small airway:	n/a
22	chr14:105265909-105265959	NH-A	brain:	n/a
23	chr14:105265909-105265959	GM06990	blood:	n/a
24	chr14:105265909-105265959	BE2_C	brain:	n/a
25	chr14:105265909-105265959	GM19239	blood:	n/a
26	chr14:105265909-105265959	AoSMC	blood vessel:	n/a
27	chr14:105265909-105265959	NHDF-neo	bronchial:	n/a
28	chr14:105265909-105265959	SK-N-SH	brain:	n/a
29	chr14:105265909-105265959	T-47D	breast:	n/a
30	chr14:105265909-105265959	H1-hESC	embryonic stem cell:	embryo
31	chr14:105265909-105265959	IMR90	lung:	fetal
32	chr14:105265909-105265959	HL-60	blood:	n/a
33	chr14:105265909-105265959	SK-N-SH_RA	brain:	n/a
34	chr14:105265909-105265959	SK-N-MC	brain:	n/a
35	chr14:105265909-105265959	HRPEpiC	eye:	n/a
36	chr14:105265909-105265959	HRE	kidney:	n/a
37	chr14:105265909-105265959	HAEpiC	amniotic membrane:	n/a
38	chr14:105265909-105265959	HNPCEpiC	eye:	n/a
39	chr14:105265909-105265959	K562	blood:	n/a
40	chr14:105265909-105265959	ProgFib	skin:	n/a
41	chr14:105265909-105265959	HCF	heart:	n/a
42	chr14:105265909-105265959	NB4	blood:	n/a
43	chr14:105265909-105265959	HEK293	kidney:	embryo
44	chr14:105265909-105265959	LNCaP	prostate:	n/a
45	chr14:105265909-105265959	ovcar-3	ovarian:	n/a
46	chr14:105265909-105265959	HRCEpiC	kidney:	n/a
47	chr14:105265909-105265959	HIPEpiC	eye:	n/a
48	chr14:105265909-105265959	ECC-1	luminal epithelium:	n/a
49	chr14:105265909-105265959	HCT-116	colon:	n/a
50	chr14:105265909-105265959	HEEpiC	esophagus:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105264148..105266055-chr14:105338238..105340290,2	K562	blood:
2	chr14:105217901..105222027-chr14:105264438..105269623,6	K562	blood:
3	chr14:105188315..105194275-chr14:105263600..105268559,9	MCF-7	breast:
4	chr14:105259095..105269353-chr14:105280422..105289302,26	K562	blood:
5	chr14:105151580..105154010-chr14:105263839..105266807,2	MCF-7	breast:
6	chr14:105217632..105222660-chr14:105263642..105269157,6	K562	blood:
7	chr14:104576831..104579461-chr14:105265082..105267856,2	MCF-7	breast:
8	chr14:105265057..105267677-chr3:49054198..49056753,2	MCF-7	breast:
9	chr14:105264532..105267379-chr14:105360102..105364298,4	MCF-7	breast:
10	chr14:105265825..105268360-chr14:105330933..105332611,2	K562	blood:
11	chr14:105190071..105193724-chr14:105262102..105266779,4	K562	blood:
12	chr14:105188668..105192164-chr14:105264427..105268088,6	MCF-7	breast:
13	chr14:105265912..105268902-chr14:105329301..105333250,7	MCF-7	breast:
14	chr14:105265110..105267765-chr14:105766806..105769681,2	K562	blood:
15	chr14:105264903..105267195-chr14:105323456..105325361,2	MCF-7	breast:
16	chr14:105216947..105220630-chr14:105265563..105270028,6	MCF-7	breast:

No data

Variant related genes	Relation type
AKT1	TF binding region
ZBTB42	TF binding region
ZBTB42	CpG island
AKT1	CpG island
ENSG00000179364	Chromatin interaction
ENSG00000185024	Chromatin interaction
ENSG00000178149	Chromatin interaction
ENSG00000184990	Chromatin interaction
ENSG00000258701	Chromatin interaction
ENSG00000166183	Chromatin interaction
ENSG00000258593	Chromatin interaction
ENSG00000099814	Chromatin interaction
ENSG00000185100	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

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	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	nsv902412	chr14:105238701-105361934	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers 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	53 gene(s)	inside rSNPs	diseases
32	nsv566071	chr14:105242831-105274763	Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
33	nsv566072	chr14:105245251-105274712	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
34	esv1836552	chr14:105246686-105348552	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
35	nsv902413	chr14:105246686-105366499	Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
36	nsv902414	chr14:105246989-105274093	Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
37	nsv902415	chr14:105250045-105270554	Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
38	esv3379257	chr14:105265732-105268280	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105261400-105266000	Weak transcription	Fetal Kidney	kidney
2	chr14:105262400-105266400	Enhancers	Spleen	Spleen
3	chr14:105262600-105266000	Enhancers	Fetal Muscle Leg	muscle
4	chr14:105262600-105266000	Weak transcription	Osteobl	bone
5	chr14:105262600-105266200	Enhancers	Stomach Mucosa	stomach
6	chr14:105262600-105266200	Weak transcription	HMEC	breast
7	chr14:105262600-105266200	Weak transcription	HUVEC	blood vessel
8	chr14:105262600-105266400	Enhancers	Placenta	Placenta
9	chr14:105262800-105266000	Enhancers	Adipose Nuclei	Adipose
10	chr14:105262800-105266000	Weak transcription	Brain Cingulate Gyrus	brain
11	chr14:105262800-105266000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr14:105262800-105266200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr14:105262800-105266200	Weak transcription	Brain Angular Gyrus	brain
14	chr14:105262800-105266200	Weak transcription	Brain Anterior Caudate	brain
15	chr14:105262800-105266200	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr14:105262800-105266200	Enhancers	Fetal Intestine Small	intestine
17	chr14:105262800-105266200	Weak transcription	Psoas Muscle	Psoas
18	chr14:105262800-105266200	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr14:105262800-105266200	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr14:105262800-105266200	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr14:105262800-105266200	Weak transcription	NHDF-Ad	bronchial
22	chr14:105262800-105266400	Weak transcription	Ovary	ovary
23	chr14:105262800-105266400	Weak transcription	Small Intestine	intestine
24	chr14:105263000-105266000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:105263000-105266000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr14:105263000-105266000	Weak transcription	Brain Hippocampus Middle	brain
27	chr14:105263000-105266000	Enhancers	Duodenum Mucosa	Duodenum
28	chr14:105263000-105266200	Weak transcription	Primary T cells from cord blood	blood
29	chr14:105263000-105266200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr14:105263000-105266200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr14:105263000-105266200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr14:105263000-105266200	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr14:105263000-105266200	Weak transcription	Dnd41	blood
34	chr14:105263000-105267200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr14:105263200-105266200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr14:105263200-105266200	Weak transcription	Brain Substantia Nigra	brain
37	chr14:105263400-105266000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:105263600-105266000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr14:105263600-105266000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr14:105263600-105266200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr14:105264000-105266000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr14:105264200-105266000	Weak transcription	Left Ventricle	heart
43	chr14:105264400-105266200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr14:105264400-105266200	Weak transcription	HSMMtube	muscle
45	chr14:105264600-105266000	Weak transcription	Lung	lung
46	chr14:105264600-105266200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr14:105264600-105266200	Weak transcription	NHLF	lung
48	chr14:105264800-105266000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:105264800-105266400	Weak transcription	HSMM	muscle
50	chr14:105264800-105267200	Weak transcription	Gastric	stomach

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