Variant report

Variant	rs72716002
Chromosome Location	chr14:105287340-105287341
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:100)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:100 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAZ	chr14:105287084-105287403	HepG2	liver:	n/a	n/a
2	MXI1	chr14:105287035-105287381	HepG2	liver:	n/a	n/a
3	CTCF	chr14:105287070-105287394	K562	blood:	n/a	n/a
4	YY1	chr14:105286977-105287379	HepG2	liver:	n/a	n/a
5	RFX5	chr14:105287151-105287390	HepG2	liver:	n/a	n/a
6	SMC3	chr14:105286812-105287570	SK-N-SH	brain:	n/a	chr14:105287195-105287205
7	POLR2A	chr14:105287082-105287962	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr14:105287122-105287343	Pancreas_OC	pancreas:	n/a	n/a
9	CTCF	chr14:105287035-105287361	HepG2	liver:	n/a	n/a
10	MYBL2	chr14:105286934-105287501	HepG2	liver:	n/a	n/a
11	CTCF	chr14:105286709-105287706	SK-N-SH	brain:	n/a	n/a
12	CTCF	chr14:105287098-105287366	MCF-7	breast:	n/a	n/a
13	MXI1	chr14:105286691-105287681	SK-N-SH	brain:	n/a	n/a
14	CTCF	chr14:105287019-105287420	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr14:105287220-105287370	NHEK	skin:	n/a	n/a
16	CTCF	chr14:105287115-105287364	HepG2	liver:	n/a	n/a
17	TCF7L2	chr14:105287134-105287527	PANC-1	pancreas:	n/a	chr14:105287477-105287493 chr14:105287477-105287493 chr14:105287478-105287492 chr14:105287481-105287490 chr14:105287479-105287489
18	MYBL2	chr14:105286971-105287766	HepG2	liver:	n/a	n/a
19	CTCF	chr14:105286931-105287466	MCF-7	breast:	n/a	n/a
20	RAD21	chr14:105286947-105287505	MCF-7	breast:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
21	JUND	chr14:105287186-105287386	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr14:105287023-105287432	IMR90	lung:	n/a	n/a
23	EP300	chr14:105287014-105287451	HepG2	liver:	n/a	chr14:105287040-105287054 chr14:105287224-105287240 chr14:105287116-105287132
24	MAZ	chr14:105287189-105287363	K562	blood:	n/a	n/a
25	MYC	chr14:105287194-105287369	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr14:105287101-105287360	MCF-7	breast:	n/a	n/a
27	BHLHE40	chr14:105286963-105287348	HepG2	liver:	n/a	n/a
28	ZNF143	chr14:105287077-105287358	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr14:105287100-105287362	MCF-7	breast:	n/a	n/a
30	MAX	chr14:105287121-105287349	HepG2	liver:	n/a	n/a
31	GABPA	chr14:105287015-105287423	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr14:105286972-105287424	T-47D	breast:	n/a	n/a
33	HEY1	chr14:105286999-105287501	HepG2	liver:	n/a	n/a
34	MAX	chr14:105286969-105288097	HepG2	liver:	n/a	n/a
35	CTCF	chr14:105287118-105287348	ProgFib	skin:	n/a	n/a
36	RAD21	chr14:105287088-105287354	A549	lung:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
37	POLR2A	chr14:105287156-105287383	HepG2	liver:	n/a	n/a
38	RAD21	chr14:105286932-105287482	H1-hESC	embryonic stem cell:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
39	TBP	chr14:105287064-105287386	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr14:105287200-105287350	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr14:105287093-105287380	NHEK	skin:	n/a	n/a
42	RAD21	chr14:105287023-105287419	IMR90	lung:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
43	CTCF	chr14:105287153-105287354	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr14:105287111-105287352	A549	lung:	n/a	n/a
45	SMC3	chr14:105287124-105287368	Hela-S3	cervix:	n/a	chr14:105287195-105287205
46	RAD21	chr14:105286945-105287526	MCF-7	breast:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
47	RAD21	chr14:105287055-105287392	H1-hESC	embryonic stem cell:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
48	CTCF	chr14:105287086-105287501	K562	blood:	n/a	n/a
49	MAX	chr14:105286871-105287478	A549	lung:	n/a	n/a
50	RAD21	chr14:105286966-105287520	HCT-116	colon:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105287326-105287376	NHBE	bronchial:	n/a
2	chr14:105287326-105287376	Jurkat	blood:	n/a
3	chr14:105287326-105287376	IMR90	lung:	fetal
4	chr14:105287326-105287376	SKMC	muscle:	n/a
5	chr14:105287326-105287376	AG04450	lung:	fetal
6	chr14:105287326-105287376	A549	lung:	n/a
7	chr14:105287326-105287376	HRPEpiC	eye:	n/a
8	chr14:105287326-105287376	NHDF-neo	bronchial:	n/a
9	chr14:105287326-105287376	BJ	skin:	n/a
10	chr14:105287326-105287376	AG09309	skin:	n/a
11	chr14:105287326-105287376	SAEC	small airway:	n/a
12	chr14:105287326-105287376	T-47D	breast:	n/a
13	chr14:105287326-105287376	HepG2	liver:	n/a
14	chr14:105287326-105287376	HRE	kidney:	n/a
15	chr14:105287326-105287376	NB4	blood:	n/a
16	chr14:105287326-105287376	ProgFib	skin:	n/a
17	chr14:105287326-105287376	HAEpiC	amniotic membrane:	n/a
18	chr14:105287326-105287376	HL-60	blood:	n/a
19	chr14:105287326-105287376	AoSMC	blood vessel:	n/a
20	chr14:105287326-105287376	HRCEpiC	kidney:	n/a
21	chr14:105287326-105287376	CMK	blood:	n/a
22	chr14:105287326-105287376	Hepatocyte	liver:	n/a
23	chr14:105287326-105287376	H1-hESC	embryonic stem cell:	embryo
24	chr14:105287326-105287376	HMEC	breast:	n/a
25	chr14:105287326-105287376	GM19239	blood:	n/a
26	chr14:105287326-105287376	BE2_C	brain:	n/a
27	chr14:105287326-105287376	Hela-S3	cervix:	n/a
28	chr14:105287326-105287376	HEK293	kidney:	embryo
29	chr14:105287326-105287376	HEEpiC	esophagus:	n/a
30	chr14:105287326-105287376	PrEC	prostate:	n/a
31	chr14:105287326-105287376	LNCaP	prostate:	n/a
32	chr14:105287326-105287376	AG04449	skin:	fetal
33	chr14:105287326-105287376	PFSK-1	brain:	n/a
34	chr14:105287326-105287376	GM06990	blood:	n/a
35	chr14:105287326-105287376	GM12892	blood:	n/a
36	chr14:105287326-105287376	HCPEpiC	choroid plexus:	n/a
37	chr14:105287326-105287376	Caco-2	colon:	n/a
38	chr14:105287326-105287376	NH-A	brain:	n/a
39	chr14:105287326-105287376	MCF-7	breast:	n/a
40	chr14:105287326-105287376	HPAEpiC	pulmonary alveolar:	n/a
41	chr14:105287326-105287376	ovcar-3	ovarian:	n/a
42	chr14:105287326-105287376	RPTEC	kidney:	n/a
43	chr14:105287326-105287376	ECC-1	luminal epithelium:	n/a
44	chr14:105287326-105287376	HCF	heart:	n/a
45	chr14:105287326-105287376	SK-N-MC	brain:	n/a
46	chr14:105287326-105287376	K562	blood:	n/a
47	chr14:105287326-105287376	PANC-1	pancreas:	n/a
48	chr14:105287326-105287376	MCF10A-Er-Src	breast:	n/a
49	chr14:105287326-105287376	AG10803	skin:	n/a
50	chr14:105287326-105287376	HCM	heart:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105190451..105191132-chr14:105286694..105287658,2	MCF-7	breast:
2	chr14:105217398..105221846-chr14:105284355..105288810,4	MCF-7	breast:
3	chr14:105284603..105287527-chr14:105343615..105347092,3	MCF-7	breast:
4	chr14:105259095..105269353-chr14:105280422..105289302,26	K562	blood:
5	chr14:105234579..105236355-chr14:105286684..105287712,12	MCF-7	breast:
6	chr14:105266435..105267408-chr14:105286766..105287693,2	MCF-7	breast:
7	chr14:105234538..105236569-chr14:105286438..105288492,2	K562	blood:
8	chr14:105286488..105288795-chr17:79479840..79482559,2	MCF-7	breast:
9	chr14:105285820..105287586-chr14:105330282..105332678,2	MCF-7	breast:
10	chr14:105189864..105192391-chr14:105285849..105287579,2	MCF-7	breast:

No data

Variant related genes	Relation type
LINC00638	TF binding region
LINC00638	CpG island
ENSG00000184990	Chromatin interaction
ENSG00000184009	Chromatin interaction
ENSG00000099814	Chromatin interaction
ENSG00000258430	Chromatin interaction
ENSG00000179627	Chromatin interaction
ENSG00000142208	Chromatin interaction
ENSG00000229848	Chromatin interaction
ENSG00000185100	Chromatin interaction
ENSG00000229947	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10141861	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12050087	1.00[AFR][1000 genomes]
rs2841279	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34004095	1.00[AFR][1000 genomes]
rs3742938	1.00[AFR][1000 genomes]
rs41314519	1.00[AFR][1000 genomes]
rs57147900	1.00[AFR][1000 genomes]
rs57804458	1.00[AFR][1000 genomes]
rs58153756	1.00[AFR][1000 genomes]
rs58365272	1.00[AFR][1000 genomes]
rs61316883	1.00[AFR][1000 genomes]
rs61745186	1.00[AFR][1000 genomes]
rs61761195	1.00[AFR][1000 genomes]
rs7144557	1.00[AFR][1000 genomes]
rs72700126	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72700128	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72700150	1.00[AFR][1000 genomes]
rs72700170	1.00[AFR][1000 genomes]
rs72700172	1.00[AFR][1000 genomes]
rs72700175	1.00[AFR][1000 genomes]
rs72700176	1.00[AFR][1000 genomes]
rs72700183	1.00[AFR][1000 genomes]
rs72700187	1.00[AFR][1000 genomes]
rs72700189	1.00[AFR][1000 genomes]
rs72700192	1.00[AFR][1000 genomes]
rs72700202	1.00[AFR][1000 genomes]
rs72718103	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72718104	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72718105	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8012919	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 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	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	esv1833474	chr14:105268228-105332154	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
22	nsv566093	chr14:105274093-105321835	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
23	esv1840298	chr14:105274292-105366499	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
24	nsv902416	chr14:105277209-105366499	Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS 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	46 gene(s)	inside rSNPs	diseases
25	esv1803813	chr14:105285159-105293358	Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
26	nsv511540	chr14:105285159-105314093	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
27	nsv456456	chr14:105285159-105412541	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
28	nsv566099	chr14:105285159-105412541	Bivalent Enhancer Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers 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	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105283200-105292200	Weak transcription	Gastric	stomach
2	chr14:105283400-105287400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:105283400-105287400	Weak transcription	Duodenum Mucosa	Duodenum
4	chr14:105283400-105292000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr14:105283400-105292000	Weak transcription	Right Atrium	heart
6	chr14:105283600-105287600	Weak transcription	Brain Angular Gyrus	brain
7	chr14:105283600-105288800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr14:105283600-105292000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr14:105283600-105292000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr14:105283800-105292000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr14:105283800-105292200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr14:105284000-105287400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr14:105284000-105288000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr14:105284000-105288800	Weak transcription	Spleen	Spleen
15	chr14:105284000-105289400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:105284000-105292000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr14:105284200-105288200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr14:105284400-105287400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr14:105284400-105292200	Weak transcription	K562	blood
20	chr14:105284600-105290800	Weak transcription	Fetal Kidney	kidney
21	chr14:105285000-105287600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr14:105285000-105292200	Weak transcription	Dnd41	blood
23	chr14:105285200-105288400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr14:105286200-105288800	Enhancers	Fetal Stomach	stomach
25	chr14:105286400-105287600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr14:105286600-105287800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr14:105286600-105287800	Enhancers	A549	lung
28	chr14:105286800-105287400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr14:105286800-105287400	Enhancers	Brain Germinal Matrix	brain
30	chr14:105286800-105287600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr14:105286800-105287600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr14:105286800-105287600	Enhancers	Adipose Nuclei	Adipose
33	chr14:105286800-105287600	Enhancers	Liver	Liver
34	chr14:105286800-105287600	Enhancers	Fetal Intestine Small	intestine
35	chr14:105286800-105287600	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr14:105286800-105287600	Enhancers	HMEC	breast
37	chr14:105286800-105287600	Enhancers	HUVEC	blood vessel
38	chr14:105286800-105287800	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr14:105286800-105288000	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr14:105287000-105287400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr14:105287000-105287400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr14:105287000-105287400	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr14:105287000-105287400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr14:105287000-105287400	Enhancers	Brain Hippocampus Middle	brain
45	chr14:105287000-105287400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr14:105287000-105287400	Enhancers	Pancreas	Pancrea
47	chr14:105287000-105287400	Enhancers	Right Ventricle	heart
48	chr14:105287000-105287400	Active TSS	HepG2	liver
49	chr14:105287000-105287600	Enhancers	Fetal Muscle Leg	muscle
50	chr14:105287000-105287600	Enhancers	HSMM	muscle

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