Variant report

Variant	rs587706576
Chromosome Location	chr14:105635700-105635701
allele	A/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	SMC3	chr14:105635492-105635824	K562	blood:	n/a	chr14:105635653-105635667 chr14:105635657-105635667
2	CTCF	chr14:105635600-105635750	MCF-7	breast:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
3	CTCF	chr14:105635390-105635915	K562	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
4	CTCF	chr14:105635528-105635804	GM19238	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
5	CTCF	chr14:105635580-105635730	WI-38	lung:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
6	CTCF	chr14:105635560-105635710	RPTEC	kidney:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
7	CCNT2	chr14:105634944-105635778	K562	blood:	n/a	chr14:105635426-105635435
8	CTCF	chr14:105635546-105635733	SK-N-SH_RA	brain:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
9	CTCF	chr14:105635535-105635773	MCF-7	breast:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
10	RAD21	chr14:105635377-105635788	A549	lung:	n/a	chr14:105635657-105635669 chr14:105635657-105635667 chr14:105635565-105635579
11	CTCF	chr14:105635620-105635770	HBMEC	blood vessel:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
12	CTCF	chr14:105635580-105635730	HUVEC	blood vessel:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
13	CTCF	chr14:105635537-105635830	HepG2	liver:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
14	RCOR1	chr14:105635440-105635729	K562	blood:	n/a	n/a
15	CTCF	chr14:105635494-105635804	NHEK	skin:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
16	SIN3A	chr14:105635406-105635786	H1-hESC	embryonic stem cell:	n/a	chr14:105635551-105635564 chr14:105635572-105635585 chr14:105635654-105635665
17	CTCFL	chr14:105635520-105635751	K562	blood:	n/a	chr14:105635658-105635667
18	FOXA1	chr14:105635536-105635779	T-47D	breast:	n/a	n/a
19	CTCF	chr14:105635640-105635790	GM12865	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
20	RAD21	chr14:105635586-105635729	GM12878	blood:	n/a	chr14:105635657-105635669 chr14:105635657-105635667
21	CTCF	chr14:105635568-105635745	HepG2	liver:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
22	TCF12	chr14:105634937-105635738	ECC-1	luminal epithelium:	n/a	n/a
23	CTCF	chr14:105635600-105635750	AG09319	gingival:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
24	CTCF	chr14:105635579-105635745	MCF-7	breast:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
25	POLR2A	chr14:105635262-105635856	HUVEC	blood vessel:	n/a	n/a
26	ZBTB7A	chr14:105635108-105635782	K562	blood:	n/a	chr14:105635659-105635668
27	CTCF	chr14:105635640-105635790	GM12864	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
28	CTCF	chr14:105635600-105635750	GM12870	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
29	YY1	chr14:105635411-105635921	H1-hESC	embryonic stem cell:	n/a	chr14:105635657-105635671
30	RAD21	chr14:105635601-105635786	K562	blood:	n/a	chr14:105635657-105635669 chr14:105635657-105635667
31	HMGN3	chr14:105635266-105635810	K562	blood:	n/a	n/a
32	CTCF	chr14:105635580-105635730	HVMF	connective:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
33	UBTF	chr14:105634906-105635778	K562	blood:	n/a	n/a
34	CTCF	chr14:105635620-105635770	BJ	skin:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
35	SMC3	chr14:105635595-105635739	GM12878	blood:	n/a	chr14:105635653-105635667 chr14:105635657-105635667
36	CTCF	chr14:105635600-105635750	GM12865	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
37	GABPA	chr14:105635365-105635827	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr14:105635567-105635739	GM20000	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
39	CTCF	chr14:105635600-105635750	GM12875	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
40	RAD21	chr14:105635524-105635735	GM12878	blood:	n/a	chr14:105635657-105635669 chr14:105635657-105635667 chr14:105635565-105635579
41	CTCF	chr14:105635561-105635764	A549	lung:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
42	CTCF	chr14:105635580-105635730	HCM	heart:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
43	CTCF	chr14:105635620-105635770	HEK293	kidney:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
44	CTCF	chr14:105635600-105635750	AG04450	lung:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
45	CTCF	chr14:105635600-105635750	HRPEpiC	eye:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
46	CTCF	chr14:105635600-105635750	K562	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
47	CTCF	chr14:105635557-105635756	GM13977	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
48	CTCF	chr14:105635560-105635710	HCM	heart:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
49	CTCF	chr14:105635586-105635730	HepG2	liver:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
50	POLR2A	chr14:105635371-105635712	H1-neurons	neurons:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105635593..105636402-chr14:105818301..105819224,3	K562	blood:
2	chr14:105450462..105452951-chr14:105633617..105637647,3	MCF-7	breast:
3	chr14:105635510..105639334-chr14:105658974..105662269,3	K562	blood:
4	chr14:105635244..105636129-chr14:105665708..105667054,3	K562	blood:
5	chr14:105631465..105635896-chr14:105645452..105649219,9	MCF-7	breast:
6	chr14:105633273..105637288-chr14:105642227..105645314,5	MCF-7	breast:
7	chr14:105632764..105636922-chr14:105637769..105642057,5	MCF-7	breast:
8	chr14:105633510..105636132-chr14:105956968..105959602,2	K562	blood:
9	chr14:105268465..105270651-chr14:105635461..105637238,2	K562	blood:
10	chr14:105635176..105636125-chr14:105747875..105748809,5	K562	blood:

Variant related genes	Relation type
JAG2	TF binding region
ENSG00000140104	Chromatin interaction
ENSG00000257622	Chromatin interaction
ENSG00000183828	Chromatin interaction
ENSG00000185347	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 0)

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	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
2	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
3	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
4	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
5	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
6	nsv1052190	chr14:105423761-105722653	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
7	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
8	nsv456458	chr14:105435649-105690092	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
9	nsv566150	chr14:105435649-105690092	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
10	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS 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	86 gene(s)	inside rSNPs	diseases
11	nsv902425	chr14:105463936-105690092	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
12	nsv9175	chr14:105496509-105688941	Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
13	esv2758369	chr14:105513346-105803170	Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
14	esv2760014	chr14:105513346-105803170	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
15	nsv902430	chr14:105587644-105682527	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
16	nsv902431	chr14:105587644-105685865	Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
17	nsv902432	chr14:105587644-105690092	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active 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	16 gene(s)	inside rSNPs	diseases
18	esv1797182	chr14:105590971-105696174	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
19	esv1836064	chr14:105590971-105696174	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers 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	16 gene(s)	inside rSNPs	diseases
20	nsv456464	chr14:105591377-105654606	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
21	nsv456465	chr14:105591377-105654606	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
22	nsv566156	chr14:105591377-105654606	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
23	nsv902433	chr14:105596054-105719306	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
24	nsv902434	chr14:105602619-105654606	ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
25	nsv902435	chr14:105602619-105654606	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
26	nsv902436	chr14:105602619-105672794	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
27	nsv902437	chr14:105602619-105679055	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
28	nsv902438	chr14:105602619-105682527	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
29	nsv902439	chr14:105602619-105690092	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
30	nsv902440	chr14:105602619-105699630	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
31	nsv902441	chr14:105602619-105803170	Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
32	nsv902442	chr14:105602619-105803170	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
33	esv1817919	chr14:105605199-105803170	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
34	nsv530813	chr14:105607701-106453697	Strong transcription Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
35	nsv902447	chr14:105608564-105654606	Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
36	nsv817646	chr14:105615648-105654606	Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
37	nsv456466	chr14:105615648-105685865	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
38	nsv456467	chr14:105615648-105685865	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
39	nsv566159	chr14:105615648-105685865	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
40	esv1794421	chr14:105617042-105635756	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	12 gene(s)	inside rSNPs	diseases
41	nsv902448	chr14:105617042-105682527	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
42	nsv902449	chr14:105617891-105682527	Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
43	nsv566160	chr14:105617891-105685865	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
44	nsv902450	chr14:105624693-105682527	Bivalent Enhancer Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
45	nsv902451	chr14:105624693-105690092	Bivalent/Poised TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
46	nsv902452	chr14:105625743-105654606	Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
47	nsv902453	chr14:105625743-105660766	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
48	esv3424809	chr14:105633332-105636080	Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
49	esv3487376	chr14:105633457-105635855	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
50	esv3487377	chr14:105633457-105635855	Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105633600-105635800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:105633800-105635800	Bivalent/Poised TSS	Thymus	Thymus
3	chr14:105633800-105635800	Active TSS	K562	blood
4	chr14:105634400-105635800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr14:105634400-105635800	Active TSS	Fetal Brain Female	brain
6	chr14:105634400-105635800	Active TSS	Right Atrium	heart
7	chr14:105634400-105636400	Weak transcription	Fetal Heart	heart
8	chr14:105634400-105637000	Weak transcription	HSMMtube	muscle
9	chr14:105634800-105635800	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr14:105635000-105635800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
11	chr14:105635200-105635800	Enhancers	Esophagus	oesophagus
12	chr14:105635200-105635800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
13	chr14:105635200-105636200	Enhancers	Placenta	Placenta
14	chr14:105635200-105637400	Weak transcription	Hela-S3	cervix
15	chr14:105635200-105637800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:105635200-105642200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr14:105635400-105635800	Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr14:105635400-105635800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:105635400-105635800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
20	chr14:105635400-105635800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
21	chr14:105635400-105635800	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
22	chr14:105635400-105635800	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
23	chr14:105635400-105635800	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr14:105635400-105635800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr14:105635400-105635800	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
26	chr14:105635400-105635800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr14:105635400-105635800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr14:105635400-105635800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr14:105635400-105635800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr14:105635400-105635800	Enhancers	Liver	Liver
31	chr14:105635400-105635800	Active TSS	Brain Anterior Caudate	brain
32	chr14:105635400-105635800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
33	chr14:105635400-105635800	Bivalent Enhancer	Rectal Smooth Muscle	rectum
34	chr14:105635400-105635800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
35	chr14:105635400-105635800	Bivalent Enhancer	Spleen	Spleen
36	chr14:105635400-105636000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr14:105635400-105636000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
38	chr14:105635400-105636000	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
39	chr14:105635400-105636000	Enhancers	Brain Angular Gyrus	brain
40	chr14:105635400-105636000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
41	chr14:105635400-105636400	Enhancers	Fetal Brain Male	brain
42	chr14:105635400-105636800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
43	chr14:105635400-105637600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
44	chr14:105635400-105637800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
45	chr14:105635400-105637800	Bivalent Enhancer	Stomach Mucosa	stomach
46	chr14:105635400-105638200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr14:105635400-105638200	Bivalent Enhancer	Fetal Thymus	thymus
48	chr14:105635400-105638600	Enhancers	HUVEC	blood vessel
49	chr14:105635600-105635800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr14:105635600-105635800	Enhancers	Primary B cells from cord blood	blood

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