Variant report

Variant	rs193190450
Chromosome Location	chr14:103994972-103994973
allele	C/G
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	SRF	chr14:103994589-103995858	MCF-7	breast:	n/a	chr14:103995479-103995489
2	MAZ	chr14:103994539-103995735	K562	blood:	n/a	n/a
3	POLR2A	chr14:103994599-103995893	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr14:103994859-103995779	K562	blood:	n/a	n/a
5	REST	chr14:103994799-103995914	H1-neurons	neurons:	n/a	chr14:103995670-103995683
6	POLR2A	chr14:103993629-103994989	GM12878	blood:	n/a	n/a
7	ELF1	chr14:103994419-103997638	MCF-7	breast:	n/a	chr14:103995523-103995532 chr14:103995487-103995496 chr14:103995544-103995553 chr14:103995522-103995533 chr14:103995540-103995552 chr14:103995488-103995500 chr14:103995541-103995550
8	POLR2A	chr14:103994677-103995814	GM19193	blood:	n/a	n/a
9	MTA3	chr14:103994458-103996055	GM12878	blood:	n/a	n/a
10	ELF1	chr14:103994596-103996014	GM12878	blood:	n/a	chr14:103995523-103995532 chr14:103995487-103995496 chr14:103995544-103995553 chr14:103995522-103995533 chr14:103995540-103995552 chr14:103995488-103995500 chr14:103995541-103995550
11	POLR2A	chr14:103994449-103996359	MCF10A-Er-Src	breast:	n/a	n/a
12	FOXA2	chr14:103994837-103995680	HepG2	liver:	n/a	n/a
13	YY1	chr14:103994861-103995040	K562	blood:	n/a	n/a
14	MYC	chr14:103994935-103995827	K562	blood:	n/a	chr14:103995561-103995571
15	POLR2A	chr14:103994080-103996288	SK-N-MC	brain:	n/a	n/a
16	SIN3AK20	chr14:103994884-103995886	MCF-7	breast:	n/a	n/a
17	HEY1	chr14:103994239-103995825	HepG2	liver:	n/a	chr14:103995540-103995555 chr14:103995539-103995554
18	E2F6	chr14:103994786-103995770	K562	blood:	n/a	chr14:103995513-103995522 chr14:103995542-103995552 chr14:103995427-103995439 chr14:103995539-103995549 chr14:103995490-103995499
19	MAX	chr14:103994457-103996062	HepG2	liver:	n/a	chr14:103995561-103995571
20	MAX	chr14:103994440-103996416	A549	lung:	n/a	chr14:103995561-103995571
21	MAX	chr14:103994928-103995823	HepG2	liver:	n/a	chr14:103995561-103995571
22	TAF1	chr14:103994950-103995826	HepG2	liver:	n/a	n/a
23	SIN3AK20	chr14:103994734-103996279	MCF-7	breast:	n/a	n/a
24	PML	chr14:103994956-103995756	MCF-7	breast:	n/a	n/a
25	POLR2A	chr14:103993577-103995852	U87	brain:	n/a	n/a
26	ESRRA	chr14:103994512-103996444	GM12878	blood:	n/a	chr14:103994819-103994832 chr14:103995633-103995652 chr14:103995617-103995630 chr14:103994792-103994806 chr14:103994787-103994806 chr14:103995633-103995647 chr14:103995632-103995648 chr14:103995638-103995647 chr14:103995628-103995647
27	HCFC1	chr14:103994712-103996096	Hela-S3	cervix:	n/a	n/a
28	ZBTB7A	chr14:103994938-103995309	K562	blood:	n/a	n/a
29	POLR2A	chr14:103994096-103996062	H1-hESC	embryonic stem cell:	n/a	n/a
30	MAX	chr14:103994910-103995935	A549	lung:	n/a	chr14:103995561-103995571
31	YY1	chr14:103994828-103995752	HepG2	liver:	n/a	chr14:103995541-103995552 chr14:103995487-103995496 chr14:103995541-103995550 chr14:103995538-103995552 chr14:103995544-103995553 chr14:103995539-103995553 chr14:103995538-103995547
32	POLR2A	chr14:103993503-103995855	U87	brain:	n/a	n/a
33	MXI1	chr14:103994392-103997122	SK-N-SH	brain:	n/a	n/a
34	MXI1	chr14:103994501-103997427	IMR90	lung:	n/a	n/a
35	POLR2A	chr14:103990643-103996520	HepG2	liver:	n/a	n/a
36	ZMIZ1	chr14:103994967-103995469	K562	blood:	n/a	n/a
37	POLR2A	chr14:103994336-103996408	K562	blood:	n/a	n/a
38	MAX	chr14:103994246-103996064	HepG2	liver:	n/a	chr14:103995561-103995571
39	CREB1	chr14:103994966-103996103	HepG2	liver:	n/a	chr14:103995499-103995512
40	MAZ	chr14:103994550-103995797	IMR90	lung:	n/a	n/a
41	FOXA2	chr14:103994969-103995926	A549	lung:	n/a	n/a
42	MAX	chr14:103994933-103996602	MCF-7	breast:	n/a	chr14:103995561-103995571
43	POLR2A	chr14:103994554-103995756	K562	blood:	n/a	n/a
44	E2F6	chr14:103994866-103995892	A549	lung:	n/a	chr14:103995513-103995522 chr14:103995542-103995552 chr14:103995427-103995439 chr14:103995539-103995549 chr14:103995490-103995499
45	POLR2A	chr14:103994388-103995782	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:103994927-103994977	AG09319	gingival:	n/a
2	chr14:103994927-103994977	Hela-S3	cervix:	n/a
3	chr14:103994927-103994977	CMK	blood:	n/a
4	chr14:103994927-103994977	GM12892	blood:	n/a
5	chr14:103994927-103994977	HCPEpiC	choroid plexus:	n/a
6	chr14:103994927-103994977	SKMC	muscle:	n/a
7	chr14:103994927-103994977	LNCaP	prostate:	n/a
8	chr14:103994927-103994977	HMEC	breast:	n/a
9	chr14:103994927-103994977	NT2-D1	testis:	n/a
10	chr14:103994927-103994977	SK-N-MC	brain:	n/a
11	chr14:103994927-103994977	HepG2	liver:	n/a
12	chr14:103994927-103994977	HL-60	blood:	n/a
13	chr14:103994927-103994977	GM12891	blood:	n/a
14	chr14:103994927-103994977	H1-hESC	embryonic stem cell:	embryo
15	chr14:103994927-103994977	HUVEC	blood vessel:	n/a
16	chr14:103994927-103994977	BE2_C	brain:	n/a
17	chr14:103994927-103994977	PrEC	prostate:	n/a
18	chr14:103994927-103994977	Jurkat	blood:	n/a
19	chr14:103994927-103994977	AG04450	lung:	fetal
20	chr14:103994927-103994977	HCF	heart:	n/a
21	chr14:103994927-103994977	HPAEpiC	pulmonary alveolar:	n/a
22	chr14:103994927-103994977	MCF10A-Er-Src	breast:	n/a
23	chr14:103994927-103994977	HIPEpiC	eye:	n/a
24	chr14:103994927-103994977	MCF-7	breast:	n/a
25	chr14:103994927-103994977	SK-N-SH	brain:	n/a
26	chr14:103994927-103994977	IMR90	lung:	fetal
27	chr14:103994927-103994977	BJ	skin:	n/a
28	chr14:103994927-103994977	ECC-1	luminal epithelium:	n/a
29	chr14:103994927-103994977	HRCEpiC	kidney:	n/a
30	chr14:103994927-103994977	NH-A	brain:	n/a
31	chr14:103994927-103994977	ovcar-3	ovarian:	n/a
32	chr14:103994927-103994977	GM19239	blood:	n/a
33	chr14:103994927-103994977	GM06990	blood:	n/a
34	chr14:103994927-103994977	U87	brain:	n/a
35	chr14:103994927-103994977	SK-N-SH_RA	brain:	n/a
36	chr14:103994927-103994977	PANC-1	pancreas:	n/a
37	chr14:103994927-103994977	AG10803	skin:	n/a
38	chr14:103994927-103994977	ProgFib	skin:	n/a
39	chr14:103994927-103994977	HCM	heart:	n/a
40	chr14:103994927-103994977	HCT-116	colon:	n/a
41	chr14:103994927-103994977	PFSK-1	brain:	n/a
42	chr14:103994927-103994977	HEEpiC	esophagus:	n/a
43	chr14:103994927-103994977	HRE	kidney:	n/a
44	chr14:103994927-103994977	NHDF-neo	bronchial:	n/a
45	chr14:103994927-103994977	AoSMC	blood vessel:	n/a
46	chr14:103994927-103994977	RPTEC	kidney:	n/a
47	chr14:103994927-103994977	AG04449	skin:	fetal
48	chr14:103994927-103994977	Caco-2	colon:	n/a
49	chr14:103994927-103994977	HAEpiC	amniotic membrane:	n/a
50	chr14:103994927-103994977	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:103994796..103995496-chr19:18392061..18392693,2	HCT-116	colon:
2	chr14:103994810..103997176-chr14:104176629..104178794,2	MCF-7	breast:
3	chr14:103851236..103854697-chr14:103993929..103996210,3	MCF-7	breast:
4	chr14:103992721..103998040-chr14:104027797..104030842,4	MCF-7	breast:
5	chr14:103993654..103996154-chr14:104180669..104183057,2	K562	blood:
6	chr14:103992666..103995489-chr14:104177229..104179572,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CKB-1	chr14:103991347-103995409	ENSG00000260285.1

Variant related genes	Relation type
TRMT61A	TF binding region
TRMT61A	CpG island
ENSG00000256053	Chromatin interaction
ENSG00000100711	Chromatin interaction
ENSG00000126215	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000166170	Chromatin interaction
ENSG00000224997	Chromatin interaction
ENSG00000075413	Chromatin interaction
ENSG00000126214	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	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	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	esv1809007	chr14:103988059-103999371	Enhancers Genic enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
31	esv1818214	chr14:103988059-103999371	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
32	esv1837939	chr14:103988059-103999371	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
33	esv1846909	chr14:103988059-103999371	Flanking Active TSS Active TSS Genic enhancers Enhancers Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
34	esv1794331	chr14:103988059-104004311	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
35	nsv566020	chr14:103989279-103996396	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
36	nsv566021	chr14:103989639-104012982	Active TSS Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Bivalent Enhancer 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	20 gene(s)	inside rSNPs	diseases
37	esv1819920	chr14:103989971-104018096	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
38	nsv9170	chr14:103994260-104017971	Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription 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	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103992200-103995000	Enhancers	Sigmoid Colon	Sigmoid Colon
2	chr14:103992400-103995000	Enhancers	Spleen	Spleen
3	chr14:103993200-103995200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
4	chr14:103993400-103995200	Flanking Active TSS	Osteobl	bone
5	chr14:103993600-103995000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr14:103993600-103995200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
7	chr14:103993600-103995200	Flanking Active TSS	GM12878-XiMat	blood
8	chr14:103994000-103995000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr14:103994000-103995000	Enhancers	Ovary	ovary
10	chr14:103994000-103995200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
11	chr14:103994000-103995200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
12	chr14:103994000-103995200	Flanking Active TSS	Dnd41	blood
13	chr14:103994000-103995200	Flanking Active TSS	Hela-S3	cervix
14	chr14:103994200-103995000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr14:103994200-103995000	Flanking Active TSS	Brain Germinal Matrix	brain
16	chr14:103994200-103995000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
17	chr14:103994200-103995000	Flanking Active TSS	A549	lung
18	chr14:103994200-103995200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:103994200-103995200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr14:103994200-103995200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr14:103994200-103995200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr14:103994200-103995200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr14:103994200-103995200	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr14:103994200-103995200	Flanking Active TSS	Fetal Intestine Large	intestine
25	chr14:103994200-103995200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
26	chr14:103994200-103995200	Flanking Active TSS	Thymus	Thymus
27	chr14:103994200-103995200	Flanking Active TSS	HMEC	breast
28	chr14:103994200-103995200	Flanking Active TSS	NHDF-Ad	bronchial
29	chr14:103994200-103995400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr14:103994200-103995400	Flanking Active TSS	Colonic Mucosa	Colon
31	chr14:103994200-103995400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr14:103994400-103995000	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr14:103994400-103995000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr14:103994400-103995000	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr14:103994400-103995200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr14:103994400-103995200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr14:103994400-103995200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr14:103994400-103995200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr14:103994400-103995200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr14:103994400-103995200	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr14:103994400-103995200	Flanking Active TSS	Brain Anterior Caudate	brain
42	chr14:103994400-103995200	Flanking Active TSS	Brain Hippocampus Middle	brain
43	chr14:103994400-103995200	Flanking Active TSS	Brain Substantia Nigra	brain
44	chr14:103994400-103995200	Flanking Active TSS	Fetal Brain Female	brain
45	chr14:103994400-103995200	Flanking Active TSS	Rectal Smooth Muscle	rectum
46	chr14:103994400-103995400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
47	chr14:103994400-103995400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
48	chr14:103994400-103996400	Active TSS	Fetal Kidney	kidney
49	chr14:103994400-103996600	Flanking Active TSS	Stomach Smooth Muscle	stomach
50	chr14:103994400-103996800	Active TSS	HUES64 Cell Line	embryonic stem cell

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