Variant report

Variant	rs575158421
Chromosome Location	chr14:103987842-103987843
allele	A/C
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	SIN3AK20	chr14:103987008-103988094	PANC-1	pancreas:	n/a	n/a
4	CHD2	chr14:103986970-103988080	Hela-S3	cervix:	n/a	n/a
5	MAX	chr14:103987392-103988197	K562	blood:	n/a	n/a
6	CREB1	chr14:103987028-103988249	K562	blood:	n/a	n/a
7	EGR1	chr14:103986973-103988007	K562	blood:	n/a	chr14:103987326-103987336 chr14:103987324-103987334 chr14:103987075-103987085 chr14:103987482-103987496 chr14:103987518-103987527 chr14:103987838-103987851 chr14:103987979-103987989 chr14:103987517-103987530 chr14:103987839-103987848 chr14:103986975-103986988 chr14:103987326-103987339 chr14:103987838-103987851 chr14:103987514-103987528
8	HCFC1	chr14:103986832-103989529	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr14:103986986-103988289	H1-hESC	embryonic stem cell:	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	HEY1	chr14:103987251-103987906	K562	blood:	n/a	chr14:103987794-103987809
13	MAZ	chr14:103986938-103989516	IMR90	lung:	n/a	chr14:103987326-103987336 chr14:103987076-103987086
14	MXI1	chr14:103986803-103990569	SK-N-SH	brain:	n/a	n/a
15	E2F6	chr14:103987396-103988265	K562	blood:	n/a	chr14:103987803-103987812 chr14:103987438-103987447 chr14:103987837-103987846
16	SIN3A	chr14:103987054-103989756	H1-hESC	embryonic stem cell:	n/a	chr14:103988976-103988989 chr14:103989142-103989151 chr14:103989135-103989148
17	REST	chr14:103987634-103987861	K562	blood:	n/a	n/a
18	NFIC	chr14:103986732-103987883	ECC-1	luminal epithelium:	n/a	n/a
19	ZBTB7A	chr14:103987319-103988382	K562	blood:	n/a	n/a
20	MAX	chr14:103986959-103988180	Hela-S3	cervix:	n/a	chr14:103987326-103987336 chr14:103987076-103987086
21	POLR2A	chr14:103987014-103988185	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr14:103987027-103987885	Hela-S3	cervix:	n/a	n/a
23	MAX	chr14:103987325-103987858	SK-N-SH	brain:	n/a	chr14:103987326-103987336
24	MAX	chr14:103986944-103988137	ECC-1	luminal epithelium:	n/a	chr14:103987326-103987336 chr14:103987076-103987086
25	MYC	chr14:103987111-103988194	K562	blood:	n/a	chr14:103987326-103987336
26	PML	chr14:103987483-103987902	K562	blood:	n/a	n/a
27	MAX	chr14:103987153-103987890	MCF-7	breast:	n/a	chr14:103987326-103987336
28	UBTF	chr14:103987416-103988191	K562	blood:	n/a	n/a
29	MAZ	chr14:103986968-103988801	K562	blood:	n/a	chr14:103987326-103987336 chr14:103987076-103987086
30	EP300	chr14:103986720-103988062	ECC-1	luminal epithelium:	n/a	chr14:103987803-103987812
31	POLR2A	chr14:103987122-103988324	K562	blood:	n/a	n/a
32	POLR2A	chr14:103987273-103988184	NB4	blood:	n/a	n/a
33	CREB1	chr14:103987478-103988279	K562	blood:	n/a	n/a
34	ATF2	chr14:103987498-103987915	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr14:103984058-103989460	A549	lung:	n/a	n/a
36	CREB1	chr14:103987004-103988977	H1-hESC	embryonic stem cell:	n/a	chr14:103988541-103988554
37	MAX	chr14:103986913-103988961	K562	blood:	n/a	chr14:103987326-103987336 chr14:103987076-103987086
38	POLR2A	chr14:103983976-103988326	H1-hESC	embryonic stem cell:	n/a	n/a
39	TBL1XR1	chr14:103987387-103988119	K562	blood:	n/a	n/a
40	SIN3AK20	chr14:103987835-103988155	K562	blood:	n/a	n/a
41	REST	chr14:103987200-103987894	A549	lung:	n/a	n/a
42	BHLHE40	chr14:103987177-103988209	K562	blood:	n/a	chr14:103988055-103988071 chr14:103987797-103987813
43	MAX	chr14:103987223-103987876	H1-hESC	embryonic stem cell:	n/a	chr14:103987326-103987336
44	E2F6	chr14:103987025-103987958	A549	lung:	n/a	chr14:103987325-103987334 chr14:103987310-103987321 chr14:103987149-103987159 chr14:103987076-103987085 chr14:103987803-103987812 chr14:103987438-103987447 chr14:103987837-103987846
45	POLR2A	chr14:103987065-103987886	ProgFib	skin:	n/a	n/a
46	NFIC	chr14:103986774-103987842	ECC-1	luminal epithelium:	n/a	n/a
47	SP1	chr14:103987469-103987872	H1-hESC	embryonic stem cell:	n/a	chr14:103987837-103987846 chr14:103987516-103987525 chr14:103987515-103987524 chr14:103987515-103987525 chr14:103987515-103987525 chr14:103987514-103987526 chr14:103987514-103987526
48	POLR2A	chr14:103986539-103989395	Hela-S3	cervix:	n/a	n/a
49	TEAD4	chr14:103987383-103987872	ECC-1	luminal epithelium:	n/a	n/a
50	EGR1	chr14:103986887-103988103	HCT-116	colon:	n/a	chr14:103987326-103987336 chr14:103987324-103987334 chr14:103987075-103987085 chr14:103987482-103987496 chr14:103987518-103987527 chr14:103987838-103987851 chr14:103987979-103987989 chr14:103987517-103987530 chr14:103987839-103987848 chr14:103986975-103986988 chr14:103987326-103987339 chr14:103987838-103987851 chr14:103987514-103987528

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:103987810-103987860	HL-60	blood:	n/a
2	chr14:103987810-103987860	AG04449	skin:	fetal
3	chr14:103987810-103987860	ovcar-3	ovarian:	n/a
4	chr14:103987810-103987860	HEEpiC	esophagus:	n/a
5	chr14:103987810-103987860	Hela-S3	cervix:	n/a
6	chr14:103987810-103987860	AG09309	skin:	n/a
7	chr14:103987810-103987860	PANC-1	pancreas:	n/a
8	chr14:103987810-103987860	ProgFib	skin:	n/a
9	chr14:103987810-103987860	HRCEpiC	kidney:	n/a
10	chr14:103987810-103987860	H1-hESC	embryonic stem cell:	embryo
11	chr14:103987810-103987860	SK-N-SH_RA	brain:	n/a
12	chr14:103987810-103987860	AG04450	lung:	fetal
13	chr14:103987810-103987860	CMK	blood:	n/a
14	chr14:103987810-103987860	PrEC	prostate:	n/a
15	chr14:103987810-103987860	Caco-2	colon:	n/a
16	chr14:103987810-103987860	SAEC	small airway:	n/a
17	chr14:103987810-103987860	HCT-116	colon:	n/a
18	chr14:103987810-103987860	HUVEC	blood vessel:	n/a
19	chr14:103987810-103987860	T-47D	breast:	n/a
20	chr14:103987810-103987860	AoSMC	blood vessel:	n/a
21	chr14:103987810-103987860	HAEpiC	amniotic membrane:	n/a
22	chr14:103987810-103987860	PFSK-1	brain:	n/a
23	chr14:103987810-103987860	AG10803	skin:	n/a
24	chr14:103987810-103987860	SKMC	muscle:	n/a
25	chr14:103987810-103987860	LNCaP	prostate:	n/a
26	chr14:103987810-103987860	NHDF-neo	bronchial:	n/a
27	chr14:103987810-103987860	GM12892	blood:	n/a
28	chr14:103987810-103987860	HCF	heart:	n/a
29	chr14:103987810-103987860	MCF-7	breast:	n/a
30	chr14:103987810-103987860	SK-N-MC	brain:	n/a
31	chr14:103987810-103987860	GM19239	blood:	n/a
32	chr14:103987810-103987860	Hepatocyte	liver:	n/a
33	chr14:103987810-103987860	HepG2	liver:	n/a
34	chr14:103987810-103987860	HNPCEpiC	eye:	n/a
35	chr14:103987810-103987860	HCPEpiC	choroid plexus:	n/a
36	chr14:103987810-103987860	NB4	blood:	n/a
37	chr14:103987810-103987860	HPAEpiC	pulmonary alveolar:	n/a
38	chr14:103987810-103987860	HRPEpiC	eye:	n/a
39	chr14:103987810-103987860	AG09319	gingival:	n/a
40	chr14:103987810-103987860	GM06990	blood:	n/a
41	chr14:103987810-103987860	Jurkat	blood:	n/a
42	chr14:103987810-103987860	GM12878	blood:	n/a
43	chr14:103987810-103987860	HRE	kidney:	n/a
44	chr14:103987810-103987860	HEK293	kidney:	embryo
45	chr14:103987810-103987860	NH-A	brain:	n/a
46	chr14:103987810-103987860	BE2_C	brain:	n/a
47	chr14:103987810-103987860	GM12891	blood:	n/a
48	chr14:103987810-103987860	BJ	skin:	n/a
49	chr14:103987810-103987860	SK-N-SH	brain:	n/a
50	chr14:103987810-103987860	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:103587793..103589963-chr14:103986359..103988722,2	K562	blood:
2	chr14:103986778..103989691-chr14:104095238..104098302,4	K562	blood:
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	chr14:103893677..103895539-chr14:103987804..103990047,2	K562	blood:
8	chr14:103522157..103524674-chr14:103987667..103989193,2	K562	blood:
9	chr14:103983696..103988397-chr14:104026059..104029809,6	K562	blood:
10	chr14:103798500..103802639-chr14:103987592..103992121,9	K562	blood:
11	chr14:103987454..103990068-chr14:104178702..104181671,2	K562	blood:

Variant related genes	Relation type
CKB	TF binding region
CKB	CpG island
ENSG00000269963	Chromatin interaction
ENSG00000126214	Chromatin interaction
ENSG00000256053	Chromatin interaction
ENSG00000075413	Chromatin interaction
ENSG00000100711	Chromatin interaction
ENSG00000185215	Chromatin interaction
ENSG00000166170	Chromatin interaction
ENSG00000126215	Chromatin interaction
ENSG00000259717	Chromatin interaction
ENSG00000198752	Chromatin interaction
ENSG00000100664	Chromatin interaction
ENSG00000259775	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:56 , 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	nsv565987	chr14:103986155-103988707	Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
26	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
27	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
28	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
29	nsv565988	chr14:103986456-103988444	Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
30	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
31	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
32	nsv565991	chr14:103986805-103988650	Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
33	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
34	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
35	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
36	esv1842013	chr14:103987140-103988650	Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
37	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
38	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
39	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
40	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
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103980000-103988400	Weak transcription	Fetal Kidney	kidney
2	chr14:103985200-103988000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:103986200-103988600	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:103986200-103988800	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr14:103986400-103988400	Active TSS	Primary T cells from cord blood	blood
6	chr14:103986600-103988400	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
7	chr14:103986800-103988200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr14:103986800-103988400	Active TSS	Duodenum Smooth Muscle	Duodenum
9	chr14:103986800-103989000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:103986800-103989400	Active TSS	HepG2	liver
11	chr14:103986800-103989600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr14:103987000-103988000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr14:103987000-103988200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr14:103987000-103988400	Active TSS	Small Intestine	intestine
15	chr14:103987000-103988600	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr14:103987000-103988600	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr14:103987000-103988600	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr14:103987000-103988800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr14:103987000-103988800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
20	chr14:103987000-103989000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr14:103987000-103989000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr14:103987000-103989200	Active TSS	Ovary	ovary
23	chr14:103987000-103989200	Active TSS	Sigmoid Colon	Sigmoid Colon
24	chr14:103987000-103989400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr14:103987000-103989400	Active TSS	Rectal Smooth Muscle	rectum
26	chr14:103987000-103989400	Active TSS	Right Atrium	heart
27	chr14:103987000-103989400	Active TSS	HSMM	muscle
28	chr14:103987000-103989600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr14:103987000-103989600	Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr14:103987000-103989600	Active TSS	Colon Smooth Muscle	Colon
31	chr14:103987000-103989600	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr14:103987000-103989600	Active TSS	Hela-S3	cervix
33	chr14:103987000-103989800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr14:103987000-103989800	Active TSS	K562	blood
35	chr14:103987000-103990000	Active TSS	Brain Anterior Caudate	brain
36	chr14:103987200-103988000	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
37	chr14:103987200-103988000	Active TSS	Placenta Amnion	Placenta Amnion
38	chr14:103987200-103988000	Bivalent/Poised TSS	Thymus	Thymus
39	chr14:103987200-103988200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
40	chr14:103987200-103988400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr14:103987200-103988400	Active TSS	iPS-18 Cell Line	embryonic stem cell
42	chr14:103987200-103988400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr14:103987200-103988400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
44	chr14:103987200-103988400	Active TSS	Lung	lung
45	chr14:103987200-103988400	Bivalent/Poised TSS	Psoas Muscle	Psoas
46	chr14:103987200-103988400	Bivalent/Poised TSS	NHEK	skin
47	chr14:103987200-103988800	Bivalent/Poised TSS	Brain Germinal Matrix	brain
48	chr14:103987200-103988800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
49	chr14:103987200-103989200	Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr14:103987200-103989200	Active TSS	Aorta	Aorta

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