Variant report

Variant	rs370427943
Chromosome Location	chr14:103987552-103987553
allele	-/GGTAGCGGG
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	CTCF	chr14:103987445-103987698	LNCaP	prostate:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
2	REST	chr14:103986945-103989959	H1-neurons	neurons:	n/a	chr14:103989743-103989752 chr14:103988064-103988074 chr14:103989793-103989800
3	CTCF	chr14:103987520-103987670	GM12873	blood:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
4	CTCF	chr14:103987240-103987764	GM19238	blood:	n/a	chr14:103987432-103987445 chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
5	RCOR1	chr14:103987023-103987761	Hela-S3	cervix:	n/a	n/a
6	RAD21	chr14:103987511-103987709	A549	lung:	n/a	n/a
7	RAD21	chr14:103987417-103987705	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr14:103984036-103989875	H1-hESC	embryonic stem cell:	n/a	n/a
9	SMC3	chr14:103987483-103987751	K562	blood:	n/a	chr14:103987571-103987585
10	SIN3AK20	chr14:103987008-103988094	PANC-1	pancreas:	n/a	n/a
11	CHD2	chr14:103986970-103988080	Hela-S3	cervix:	n/a	n/a
12	MAX	chr14:103987392-103988197	K562	blood:	n/a	n/a
13	CTCF	chr14:103987440-103987590	HFF-Myc	foreskin:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
14	SIN3AK20	chr14:103987472-103987671	K562	blood:	n/a	n/a
15	MYC	chr14:103987525-103987780	MCF-7	breast:	n/a	n/a
16	CTCF	chr14:103987272-103987774	GM12892	blood:	n/a	chr14:103987432-103987445 chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
17	CTCF	chr14:103987500-103987650	HRE	kidney:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
18	CTCF	chr14:103987480-103987630	GM06990	blood:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
19	CTCFL	chr14:103987444-103987681	K562	blood:	n/a	n/a
20	CREB1	chr14:103987028-103988249	K562	blood:	n/a	n/a
21	ZKSCAN1	chr14:103987320-103987790	Hela-S3	cervix:	n/a	n/a
22	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
23	BACH1	chr14:103987332-103987746	H1-hESC	embryonic stem cell:	n/a	n/a
24	HCFC1	chr14:103986832-103989529	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr14:103986986-103988289	H1-hESC	embryonic stem cell:	n/a	n/a
26	GABPA	chr14:103987378-103987825	K562	blood:	n/a	chr14:103987803-103987812
27	CTCF	chr14:103987520-103987670	GM12867	blood:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
28	ZNF143	chr14:103987124-103987688	Hela-S3	cervix:	n/a	chr14:103987285-103987303
29	TAF7	chr14:103987154-103989562	H1-hESC	embryonic stem cell:	n/a	n/a
30	SPI1	chr14:103987548-103987729	GM12878	blood:	n/a	n/a
31	CCNT2	chr14:103986744-103989391	K562	blood:	n/a	chr14:103988517-103988526 chr14:103987325-103987334 chr14:103987516-103987525 chr14:103988030-103988050
32	HEY1	chr14:103987251-103987906	K562	blood:	n/a	chr14:103987794-103987809
33	CTCF	chr14:103987500-103987650	GM12867	blood:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
34	MAZ	chr14:103986938-103989516	IMR90	lung:	n/a	chr14:103987326-103987336 chr14:103987076-103987086
35	MXI1	chr14:103987426-103987763	GM12878	blood:	n/a	n/a
36	CTCF	chr14:103987500-103987650	NHDF-neo	bronchial:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
37	NR2F2	chr14:103987450-103987793	K562	blood:	n/a	n/a
38	CTCF	chr14:103987500-103987650	GM12870	blood:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
39	CTCF	chr14:103987010-103987834	HCT-116	colon:	n/a	chr14:103987432-103987445 chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
40	POLR2A	chr14:103987277-103987817	GM12878	blood:	n/a	n/a
41	CTCF	chr14:103987148-103987763	K562	blood:	n/a	chr14:103987432-103987445 chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
42	CTCF	chr14:103987500-103987650	SAEC	small airway:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
43	ELF1	chr14:103987323-103987799	K562	blood:	n/a	n/a
44	MXI1	chr14:103986803-103990569	SK-N-SH	brain:	n/a	n/a
45	CTCF	chr14:103987345-103987791	H1-hESC	embryonic stem cell:	n/a	chr14:103987432-103987445 chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
46	MAZ	chr14:103986885-103987774	GM12878	blood:	n/a	chr14:103987326-103987336 chr14:103987076-103987086
47	CTCF	chr14:103987540-103987690	HEK293	kidney:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
48	E2F6	chr14:103987396-103988265	K562	blood:	n/a	chr14:103987803-103987812 chr14:103987438-103987447 chr14:103987837-103987846
49	CTCF	chr14:103987500-103987650	GM12868	blood:	n/a	chr14:103987570-103987586 chr14:103987572-103987585 chr14:103987569-103987587
50	SP4	chr14:103987040-103987739	H1-hESC	embryonic stem cell:	n/a	chr14:103987142-103987158 chr14:103987321-103987337 chr14:103987323-103987339 chr14:103987176-103987192

No.	Distal block	Cell Line	Cell type
1	chr14:103587793..103589963-chr14:103986359..103988722,2	K562	blood:
2	chr1:151512166..151513141-chr14:103987052..103987573,2	Hela-S3	cervix:
3	chr14:103986778..103989691-chr14:104095238..104098302,4	K562	blood:
4	chr14:103986881..103989564-chr14:104195653..104197565,2	K562	blood:
5	chr14:103799200..103803060-chr14:103987408..103990865,9	K562	blood:
6	chr14:103985364..103989946-chr14:104026445..104030227,8	MCF-7	breast:
7	chr14:103963760..103966397-chr14:103985638..103989760,5	K562	blood:
8	chr14:103983696..103988397-chr14:104026059..104029809,6	K562	blood:
9	chr14:103987454..103990068-chr14:104178702..104181671,2	K562	blood:

Variant related genes	Relation type
CKB	TF binding region
ENSG00000256053	Chromatin interaction
ENSG00000126215	Chromatin interaction
ENSG00000232536	Chromatin interaction
ENSG00000166170	Chromatin interaction
ENSG00000100711	Chromatin interaction
ENSG00000126214	Chromatin interaction
ENSG00000185215	Chromatin interaction
ENSG00000075413	Chromatin interaction
ENSG00000143367	Chromatin interaction
ENSG00000269963	Chromatin interaction
ENSG00000100664	Chromatin interaction
ENSG00000259717	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:125 , 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	chr14:103982800-103987600	Enhancers	Fetal Brain Male	brain
3	chr14:103983000-103987600	Enhancers	Fetal Lung	lung
4	chr14:103985200-103987600	Transcr. at gene 5' and 3'	Cortex derived primary cultured neurospheres	brain
5	chr14:103985200-103988000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:103985400-103987600	Transcr. at gene 5' and 3'	Fetal Brain Female	brain
7	chr14:103985400-103987800	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
8	chr14:103986200-103988600	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr14:103986200-103988800	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr14:103986400-103988400	Active TSS	Primary T cells from cord blood	blood
11	chr14:103986600-103988400	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
12	chr14:103986800-103987600	Flanking Active TSS	Brain Hippocampus Middle	brain
13	chr14:103986800-103987800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
14	chr14:103986800-103987800	Flanking Active TSS	GM12878-XiMat	blood
15	chr14:103986800-103988200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr14:103986800-103988400	Active TSS	Duodenum Smooth Muscle	Duodenum
17	chr14:103986800-103989000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr14:103986800-103989400	Active TSS	HepG2	liver
19	chr14:103986800-103989600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr14:103987000-103987600	Transcr. at gene 5' and 3'	H1 Cell Line	embryonic stem cell
21	chr14:103987000-103987600	Transcr. at gene 5' and 3'	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:103987000-103987600	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
23	chr14:103987000-103987600	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
24	chr14:103987000-103987600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
25	chr14:103987000-103987600	Flanking Active TSS	Right Ventricle	heart
26	chr14:103987000-103987800	Transcr. at gene 5' and 3'	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr14:103987000-103987800	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
28	chr14:103987000-103987800	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
29	chr14:103987000-103987800	Flanking Active TSS	Primary hematopoietic stem cells	blood
30	chr14:103987000-103987800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr14:103987000-103987800	Flanking Active TSS	Adipose Nuclei	Adipose
32	chr14:103987000-103987800	Flanking Active TSS	Duodenum Mucosa	Duodenum
33	chr14:103987000-103987800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
34	chr14:103987000-103987800	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
35	chr14:103987000-103987800	Flanking Bivalent TSS/Enh	HMEC	breast
36	chr14:103987000-103988000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr14:103987000-103988200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
38	chr14:103987000-103988400	Active TSS	Small Intestine	intestine
39	chr14:103987000-103988600	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr14:103987000-103988600	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr14:103987000-103988600	Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr14:103987000-103988800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr14:103987000-103988800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
44	chr14:103987000-103989000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr14:103987000-103989000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:103987000-103989200	Active TSS	Ovary	ovary
47	chr14:103987000-103989200	Active TSS	Sigmoid Colon	Sigmoid Colon
48	chr14:103987000-103989400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:103987000-103989400	Active TSS	Rectal Smooth Muscle	rectum
50	chr14:103987000-103989400	Active TSS	Right Atrium	heart

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