Variant report

Variant	rs568865560
Chromosome Location	chr14:103989135-103989136
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	MAX	chr14:103988971-103989576	K562	blood:	n/a	n/a
4	CEBPD	chr14:103988979-103989314	HepG2	liver:	n/a	n/a
5	TCF12	chr14:103989031-103989276	GM12878	blood:	n/a	n/a
6	TAF1	chr14:103989051-103989309	PFSK-1	brain:	n/a	n/a
7	HCFC1	chr14:103986832-103989529	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr14:103988488-103989375	ProgFib	skin:	n/a	n/a
9	POLR2A	chr14:103988702-103989341	HepG2	liver:	n/a	n/a
10	TAF7	chr14:103987154-103989562	H1-hESC	embryonic stem cell:	n/a	n/a
11	CCNT2	chr14:103986744-103989391	K562	blood:	n/a	chr14:103988517-103988526 chr14:103987325-103987334 chr14:103987516-103987525 chr14:103988030-103988050
12	POLR2A	chr14:103988958-103989393	PFSK-1	brain:	n/a	n/a
13	MAZ	chr14:103986938-103989516	IMR90	lung:	n/a	chr14:103987326-103987336 chr14:103987076-103987086
14	POLR2A	chr14:103989029-103989284	HepG2	liver:	n/a	n/a
15	SIN3AK20	chr14:103988993-103989285	K562	blood:	n/a	n/a
16	JUND	chr14:103988988-103989439	H1-hESC	embryonic stem cell:	n/a	n/a
17	TCF7L2	chr14:103989124-103989280	PANC-1	pancreas:	n/a	n/a
18	CHD2	chr14:103989124-103989465	H1-hESC	embryonic stem cell:	n/a	n/a
19	TAF1	chr14:103988964-103989301	HepG2	liver:	n/a	n/a
20	MXI1	chr14:103986803-103990569	SK-N-SH	brain:	n/a	n/a
21	IRF1	chr14:103989005-103989472	K562	blood:	n/a	n/a
22	TBP	chr14:103988994-103989378	HepG2	liver:	n/a	n/a
23	SIN3A	chr14:103987054-103989756	H1-hESC	embryonic stem cell:	n/a	chr14:103988976-103988989 chr14:103989142-103989151 chr14:103989135-103989148
24	TAF1	chr14:103989057-103989327	SK-N-SH	brain:	n/a	n/a
25	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
26	EGR1	chr14:103988935-103989223	K562	blood:	n/a	n/a
27	E2F6	chr14:103989033-103989555	K562	blood:	n/a	chr14:103989439-103989446 chr14:103989436-103989451 chr14:103989436-103989447 chr14:103989435-103989447 chr14:103989439-103989446 chr14:103989439-103989446 chr14:103989438-103989447
28	TAL1	chr14:103988931-103989147	K562	blood:	n/a	n/a
29	MXI1	chr14:103989075-103989293	HepG2	liver:	n/a	n/a
30	POLR2A	chr14:103988325-103989377	A549	lung:	n/a	n/a
31	POLR2A	chr14:103988933-103989332	K562	blood:	n/a	n/a
32	GTF2F1	chr14:103989031-103989311	K562	blood:	n/a	n/a
33	TBL1XR1	chr14:103988957-103989266	K562	blood:	n/a	n/a
34	POLR2A	chr14:103988977-103989357	SK-N-MC	brain:	n/a	n/a
35	POLR2A	chr14:103989039-103989274	HepG2	liver:	n/a	n/a
36	CHD2	chr14:103989115-103989238	K562	blood:	n/a	n/a
37	POLR2A	chr14:103988979-103989283	HepG2	liver:	n/a	n/a
38	REST	chr14:103988911-103989573	H1-neurons	neurons:	n/a	n/a
39	TCF12	chr14:103989047-103989228	H1-hESC	embryonic stem cell:	n/a	n/a
40	NFYA	chr14:103989037-103989498	Hela-S3	cervix:	n/a	chr14:103989214-103989229 chr14:103989214-103989229
41	HCFC1	chr14:103989097-103989317	K562	blood:	n/a	n/a
42	POLR2A	chr14:103988938-103989339	ECC-1	luminal epithelium:	n/a	n/a
43	TCF7L2	chr14:103988964-103989479	HCT-116	colon:	n/a	n/a
44	EP300	chr14:103989012-103989492	H1-hESC	embryonic stem cell:	n/a	chr14:103989169-103989185 chr14:103989287-103989296 chr14:103989173-103989189
45	YY1	chr14:103988968-103989304	K562	blood:	n/a	chr14:103988969-103988983 chr14:103989291-103989302 chr14:103989254-103989268
46	TAF1	chr14:103988963-103989308	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr14:103988637-103989341	HepG2	liver:	n/a	n/a
48	HEY1	chr14:103988837-103989399	HepG2	liver:	n/a	chr14:103989175-103989190 chr14:103989007-103989022
49	POLR2A	chr14:103984058-103989460	A549	lung:	n/a	n/a
50	POLR2A	chr14:103988440-103989470	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:103986778..103989691-chr14:104095238..104098302,4	K562	blood:
2	chr14:103988730..103989594-chr5:40834707..40835350,2	Hela-S3	cervix:
3	chr14:103986881..103989564-chr14:104195653..104197565,2	K562	blood:
4	chr14:103799200..103803060-chr14:103987408..103990865,9	K562	blood:
5	chr14:103985364..103989946-chr14:104026445..104030227,8	MCF-7	breast:
6	chr14:103963760..103966397-chr14:103985638..103989760,5	K562	blood:
7	chr14:54907336..54908126-chr14:103988325..103989307,2	Hela-S3	cervix:
8	chr14:103893677..103895539-chr14:103987804..103990047,2	K562	blood:
9	chr14:103988878..103989543-chr7:39662895..39663568,2	Hela-S3	cervix:
10	chr14:103988720..103989231-chr16:18812317..18812925,2	Hela-S3	cervix:
11	chr14:103988216..103989188-chr3:156543435..156544222,2	HCT-116	colon:
12	chr10:102820580..102821244-chr14:103988608..103989371,2	Hela-S3	cervix:
13	chr14:103988618..103989155-chr2:27632066..27633031,2	Hela-S3	cervix:
14	chr14:103522157..103524674-chr14:103987667..103989193,2	K562	blood:
15	chr14:103798500..103802639-chr14:103987592..103992121,9	K562	blood:
16	chr1:25256344..25257214-chr14:103988746..103989611,2	HCT-116	colon:
17	chr14:103987454..103990068-chr14:104178702..104181671,2	K562	blood:
18	chr14:103988769..103989622-chr3:43327887..43328473,2	HCT-116	colon:

Variant related genes	Relation type
CKB	TF binding region
ENSG00000115241	Chromatin interaction
ENSG00000198752	Chromatin interaction
ENSG00000126214	Chromatin interaction
ENSG00000260342	Chromatin interaction
ENSG00000259775	Chromatin interaction
ENSG00000100711	Chromatin interaction
ENSG00000273162	Chromatin interaction
ENSG00000145592	Chromatin interaction
ENSG00000100664	Chromatin interaction
ENSG00000163788	Chromatin interaction
ENSG00000075413	Chromatin interaction
ENSG00000256053	Chromatin interaction
ENSG00000269963	Chromatin interaction
ENSG00000170540	Chromatin interaction
ENSG00000006451	Chromatin interaction
ENSG00000126215	Chromatin interaction
ENSG00000166170	Chromatin interaction
ENSG00000020633	Chromatin interaction
ENSG00000197980	Chromatin interaction
ENSG00000100528	Chromatin interaction

Extended variants
information (count: 83 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:83 , 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	esv3340255	chr14:103986824-103989372	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
33	esv1834374	chr14:103987140-103989172	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
34	nsv565994	chr14:103987140-103989172	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
35	esv1848068	chr14:103987140-103989639	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
36	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
37	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
38	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
39	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
40	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
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103986800-103989400	Active TSS	HepG2	liver
2	chr14:103986800-103989600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr14:103987000-103989200	Active TSS	Ovary	ovary
4	chr14:103987000-103989200	Active TSS	Sigmoid Colon	Sigmoid Colon
5	chr14:103987000-103989400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr14:103987000-103989400	Active TSS	Rectal Smooth Muscle	rectum
7	chr14:103987000-103989400	Active TSS	Right Atrium	heart
8	chr14:103987000-103989400	Active TSS	HSMM	muscle
9	chr14:103987000-103989600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr14:103987000-103989600	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr14:103987000-103989600	Active TSS	Colon Smooth Muscle	Colon
12	chr14:103987000-103989600	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr14:103987000-103989600	Active TSS	Hela-S3	cervix
14	chr14:103987000-103989800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr14:103987000-103989800	Active TSS	K562	blood
16	chr14:103987000-103990000	Active TSS	Brain Anterior Caudate	brain
17	chr14:103987200-103989200	Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr14:103987200-103989200	Active TSS	Aorta	Aorta
19	chr14:103987200-103989200	Active TSS	Pancreas	Pancrea
20	chr14:103987200-103989200	Active TSS	Stomach Smooth Muscle	stomach
21	chr14:103987200-103989400	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr14:103987200-103989400	Active TSS	Brain Cingulate Gyrus	brain
23	chr14:103987200-103989400	Active TSS	Gastric	stomach
24	chr14:103987200-103989600	Flanking Active TSS	Primary B cells from cord blood	blood
25	chr14:103987200-103989600	Active TSS	Brain Inferior Temporal Lobe	brain
26	chr14:103987200-103989600	Active TSS	Left Ventricle	heart
27	chr14:103987200-103989600	Active TSS	HSMMtube	muscle
28	chr14:103987200-103989800	Active TSS	H9 Cell Line	embryonic stem cell
29	chr14:103987400-103989200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr14:103987400-103989200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr14:103987400-103989200	Active TSS	Rectal Mucosa Donor 31	rectum
32	chr14:103987400-103989400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr14:103987400-103989400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr14:103987400-103989400	Active TSS	Fetal Intestine Large	intestine
35	chr14:103987400-103989400	Active TSS	Rectal Mucosa Donor 29	rectum
36	chr14:103987400-103989400	Active TSS	A549	lung
37	chr14:103987400-103989400	Active TSS	NHDF-Ad	bronchial
38	chr14:103987400-103989600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr14:103987400-103989800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:103987400-103989800	Active TSS	Brain Angular Gyrus	brain
41	chr14:103987600-103989400	Active TSS	H1 Cell Line	embryonic stem cell
42	chr14:103987600-103989400	Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr14:103987600-103989400	Active TSS	Brain Hippocampus Middle	brain
44	chr14:103987600-103989400	Active TSS	NHLF	lung
45	chr14:103987600-103989600	Bivalent Enhancer	HUVEC	blood vessel
46	chr14:103987600-103990200	Active TSS	Fetal Brain Female	brain
47	chr14:103987800-103989400	Active TSS	Fetal Intestine Small	intestine
48	chr14:103987800-103989400	Bivalent/Poised TSS	Fetal Stomach	stomach
49	chr14:103987800-103989600	Active TSS	Brain Substantia Nigra	brain
50	chr14:103987800-103989800	Enhancers	Spleen	Spleen

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