Variant report

Variant	rs2765043
Chromosome Location	chr14:103989655-103989656
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	REST	chr14:103986945-103989959	H1-neurons	neurons:	n/a	chr14:103989743-103989752 chr14:103988064-103988074 chr14:103989793-103989800
2	POLR2A	chr14:103984036-103989875	H1-hESC	embryonic stem cell:	n/a	n/a
3	MXI1	chr14:103986803-103990569	SK-N-SH	brain:	n/a	n/a
4	SIN3A	chr14:103987054-103989756	H1-hESC	embryonic stem cell:	n/a	chr14:103988976-103988989 chr14:103989142-103989151 chr14:103989135-103989148
5	E2F6	chr14:103989042-103989873	H1-hESC	embryonic stem cell:	n/a	chr14:103989439-103989446 chr14:103989436-103989451 chr14:103989686-103989698 chr14:103989436-103989447 chr14:103989435-103989447 chr14:103989439-103989446 chr14:103989439-103989446 chr14:103989438-103989447
6	MAX	chr14:103989143-103989767	H1-hESC	embryonic stem cell:	n/a	chr14:103989597-103989607
7	ZBTB7A	chr14:103988383-103989658	K562	blood:	n/a	chr14:103988522-103988531 chr14:103989036-103989045 chr14:103988625-103988634
8	E2F6	chr14:103988214-103989777	A549	lung:	n/a	chr14:103989439-103989446 chr14:103989436-103989451 chr14:103989686-103989698 chr14:103989436-103989447 chr14:103988544-103988553 chr14:103988834-103988843 chr14:103989435-103989447 chr14:103988832-103988842 chr14:103988524-103988539 chr14:103989439-103989446 chr14:103988542-103988551 chr14:103989439-103989446 chr14:103988523-103988532 chr14:103989438-103989447
9	TBP	chr14:103988545-103989709	H1-hESC	embryonic stem cell:	n/a	n/a
10	MAX	chr14:103989084-103989847	H1-hESC	embryonic stem cell:	n/a	chr14:103989597-103989607
11	MAX	chr14:103986799-103989700	A549	lung:	n/a	chr14:103987326-103987336 chr14:103989597-103989607 chr14:103987076-103987086
12	POLR2A	chr14:103987154-103989659	H1-neurons	neurons:	n/a	n/a
13	E2F6	chr14:103989134-103989661	A549	lung:	n/a	chr14:103989439-103989446 chr14:103989436-103989451 chr14:103989436-103989447 chr14:103989435-103989447 chr14:103989439-103989446 chr14:103989439-103989446 chr14:103989438-103989447
14	E2F6	chr14:103988974-103990621	H1-hESC	embryonic stem cell:	n/a	chr14:103989439-103989446 chr14:103989436-103989451 chr14:103989686-103989698 chr14:103989436-103989447 chr14:103989435-103989447 chr14:103989439-103989446 chr14:103989439-103989446 chr14:103989438-103989447
15	GABPA	chr14:103989469-103989793	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:103989629-103989679	NB4	blood:	n/a
2	chr14:103989629-103989679	GM12892	blood:	n/a
3	chr14:103989629-103989679	HUVEC	blood vessel:	n/a
4	chr14:103989629-103989679	K562	blood:	n/a
5	chr14:103989629-103989679	HEEpiC	esophagus:	n/a
6	chr14:103989629-103989679	HRCEpiC	kidney:	n/a
7	chr14:103989629-103989679	ovcar-3	ovarian:	n/a
8	chr14:103989629-103989679	AG04450	lung:	fetal
9	chr14:103989629-103989679	HMEC	breast:	n/a
10	chr14:103989629-103989679	MCF10A-Er-Src	breast:	n/a
11	chr14:103989629-103989679	GM06990	blood:	n/a
12	chr14:103989629-103989679	H1-hESC	embryonic stem cell:	embryo
13	chr14:103989629-103989679	NHBE	bronchial:	n/a
14	chr14:103989629-103989679	HAEpiC	amniotic membrane:	n/a
15	chr14:103989629-103989679	IMR90	lung:	fetal
16	chr14:103989629-103989679	HCM	heart:	n/a
17	chr14:103989629-103989679	Jurkat	blood:	n/a
18	chr14:103989629-103989679	HEK293	kidney:	embryo
19	chr14:103989629-103989679	HCF	heart:	n/a
20	chr14:103989629-103989679	CMK	blood:	n/a
21	chr14:103989629-103989679	NHDF-neo	bronchial:	n/a
22	chr14:103989629-103989679	HIPEpiC	eye:	n/a
23	chr14:103989629-103989679	Hepatocyte	liver:	n/a
24	chr14:103989629-103989679	GM12878	blood:	n/a
25	chr14:103989629-103989679	PFSK-1	brain:	n/a
26	chr14:103989629-103989679	HRPEpiC	eye:	n/a
27	chr14:103989629-103989679	PANC-1	pancreas:	n/a
28	chr14:103989629-103989679	RPTEC	kidney:	n/a
29	chr14:103989629-103989679	SK-N-MC	brain:	n/a
30	chr14:103989629-103989679	SK-N-SH_RA	brain:	n/a
31	chr14:103989629-103989679	AG09319	gingival:	n/a
32	chr14:103989629-103989679	BE2_C	brain:	n/a
33	chr14:103989629-103989679	NH-A	brain:	n/a
34	chr14:103989629-103989679	GM12891	blood:	n/a
35	chr14:103989629-103989679	T-47D	breast:	n/a
36	chr14:103989629-103989679	HepG2	liver:	n/a
37	chr14:103989629-103989679	GM19239	blood:	n/a
38	chr14:103989629-103989679	ECC-1	luminal epithelium:	n/a
39	chr14:103989629-103989679	Caco-2	colon:	n/a
40	chr14:103989629-103989679	Hela-S3	cervix:	n/a
41	chr14:103989629-103989679	SAEC	small airway:	n/a
42	chr14:103989629-103989679	AoSMC	blood vessel:	n/a
43	chr14:103989629-103989679	AG04449	skin:	fetal
44	chr14:103989629-103989679	HRE	kidney:	n/a
45	chr14:103989629-103989679	AG09309	skin:	n/a
46	chr14:103989629-103989679	SKMC	muscle:	n/a
47	chr14:103989629-103989679	HNPCEpiC	eye:	n/a
48	chr14:103989629-103989679	PrEC	prostate:	n/a
49	chr14:103989629-103989679	NT2-D1	testis:	n/a
50	chr14:103989629-103989679	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:103986778..103989691-chr14:104095238..104098302,4	K562	blood:
2	chr14:103799200..103803060-chr14:103987408..103990865,9	K562	blood:
3	chr14:103985364..103989946-chr14:104026445..104030227,8	MCF-7	breast:
4	chr14:103963760..103966397-chr14:103985638..103989760,5	K562	blood:
5	chr14:103989521..103992471-chr14:104020578..104022117,2	K562	blood:
6	chr14:103893677..103895539-chr14:103987804..103990047,2	K562	blood:
7	chr14:103798500..103802639-chr14:103987592..103992121,9	K562	blood:
8	chr14:103987454..103990068-chr14:104178702..104181671,2	K562	blood:

Variant related genes	Relation type
CKB	TF binding region
CKB	CpG island
ENSG00000126215	Chromatin interaction
ENSG00000100664	Chromatin interaction
ENSG00000269963	Chromatin interaction
ENSG00000166170	Chromatin interaction
ENSG00000256053	Chromatin interaction
ENSG00000075413	Chromatin interaction
ENSG00000259775	Chromatin interaction
ENSG00000126214	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs2756120	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2756126	1.00[AFR][1000 genomes]
rs2765037	1.00[AFR][1000 genomes]
rs2765039	1.00[AFR][1000 genomes]
rs754288	0.85[AFR][1000 genomes]
rs941836	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:71 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534254	chr14:103470073-104023906	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
2	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
3	nsv832883	chr14:103927687-104120953	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	esv1835815	chr14:103942991-103989757	Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	29 gene(s)	inside rSNPs	diseases
5	nsv1044967	chr14:103954727-104007051	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong 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	36 gene(s)	inside rSNPs	diseases
6	esv1807091	chr14:103956182-104020454	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
7	esv1835824	chr14:103956182-104020454	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv902297	chr14:103956182-104061646	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
9	nsv902298	chr14:103959289-104061646	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
10	esv1818859	chr14:103967299-103989757	Active TSS Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	28 gene(s)	inside rSNPs	diseases
11	esv1833254	chr14:103967299-103989757	Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	28 gene(s)	inside rSNPs	diseases
12	esv1835374	chr14:103967299-103989757	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Bivalent Enhancer 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	28 gene(s)	inside rSNPs	diseases
13	nsv902299	chr14:103967504-104061646	Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
14	nsv902300	chr14:103967504-104205811	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
15	esv1834605	chr14:103969909-104003091	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
16	nsv902301	chr14:103979953-104003094	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
17	esv1850440	chr14:103979953-104007555	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
18	nsv902302	chr14:103979953-104018455	Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
19	nsv902303	chr14:103979953-104034746	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
20	nsv902304	chr14:103979953-104061646	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
21	nsv902305	chr14:103979953-104073551	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
22	nsv827068	chr14:103982866-104021347	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
23	nsv902306	chr14:103984294-104003094	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
24	esv1835145	chr14:103984294-104014935	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
25	nsv902307	chr14:103986155-104003094	Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
26	esv1824096	chr14:103986255-103999371	Active TSS Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
27	esv1842368	chr14:103986255-103999371	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
28	nsv565989	chr14:103986457-103989655	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
29	nsv565990	chr14:103986457-103989757	Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
30	nsv565992	chr14:103986805-103989655	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
31	nsv565993	chr14:103986805-103989757	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
32	esv1802117	chr14:103987140-103989757	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
33	esv1838510	chr14:103987140-103989757	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
34	esv1844858	chr14:103987140-103989757	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
35	nsv565995	chr14:103987140-103989757	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
36	esv1799108	chr14:103987140-103990026	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
37	esv1800826	chr14:103987140-103990026	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
38	esv1835694	chr14:103987140-103990026	Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
39	esv1838769	chr14:103987140-103990026	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
40	esv1839208	chr14:103987140-103990026	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
41	esv1850033	chr14:103987140-103990026	Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
42	esv1834274	chr14:103987140-103996205	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
43	esv1834291	chr14:103987140-103999371	Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
44	esv1839917	chr14:103987140-103999371	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
45	esv1845597	chr14:103987140-103999371	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
46	esv1851656	chr14:103987140-104007555	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
47	esv1839595	chr14:103987140-104034746	Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
48	nsv565996	chr14:103987305-103989757	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
49	esv20822	chr14:103988029-103989824	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	24 gene(s)	inside rSNPs	diseases
50	esv1795529	chr14:103988059-103989757	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103987000-103989800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:103987000-103989800	Active TSS	K562	blood
3	chr14:103987000-103990000	Active TSS	Brain Anterior Caudate	brain
4	chr14:103987200-103989800	Active TSS	H9 Cell Line	embryonic stem cell
5	chr14:103987400-103989800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:103987400-103989800	Active TSS	Brain Angular Gyrus	brain
7	chr14:103987600-103990200	Active TSS	Fetal Brain Female	brain
8	chr14:103987800-103989800	Enhancers	Spleen	Spleen
9	chr14:103987800-103990000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr14:103988200-103989800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr14:103988400-103989800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
12	chr14:103988400-103989800	Flanking Active TSS	Colonic Mucosa	Colon
13	chr14:103988600-103989800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
14	chr14:103988600-103989800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
15	chr14:103988600-103990400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
16	chr14:103988800-103989800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
17	chr14:103988800-103989800	Active TSS	Brain Germinal Matrix	brain
18	chr14:103988800-103989800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
19	chr14:103988800-103989800	Bivalent/Poised TSS	NHEK	skin
20	chr14:103988800-103990000	Enhancers	Liver	Liver
21	chr14:103989000-103989800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr14:103989200-103989800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr14:103989200-103989800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr14:103989200-103989800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr14:103989200-103989800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr14:103989200-103989800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr14:103989200-103989800	Flanking Active TSS	Ovary	ovary
28	chr14:103989200-103989800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr14:103989200-103989800	Flanking Active TSS	Stomach Smooth Muscle	stomach
30	chr14:103989200-103989800	Bivalent Enhancer	NH-A	brain
31	chr14:103989200-103990000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
32	chr14:103989200-103990000	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr14:103989200-103990200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
34	chr14:103989400-103989800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
35	chr14:103989400-103989800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr14:103989400-103989800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
37	chr14:103989400-103989800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr14:103989400-103989800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
39	chr14:103989400-103989800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr14:103989400-103989800	Flanking Active TSS	Brain Cingulate Gyrus	brain
41	chr14:103989400-103989800	Flanking Active TSS	Brain Hippocampus Middle	brain
42	chr14:103989400-103989800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr14:103989400-103989800	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
44	chr14:103989400-103989800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
45	chr14:103989400-103989800	Enhancers	Pancreas	Pancrea
46	chr14:103989400-103989800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
47	chr14:103989400-103989800	Flanking Active TSS	Right Atrium	heart
48	chr14:103989400-103989800	Flanking Active TSS	Right Ventricle	heart
49	chr14:103989400-103989800	Flanking Active TSS	A549	lung
50	chr14:103989400-103989800	Bivalent Enhancer	HMEC	breast

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