Variant report

Variant	rs75844411
Chromosome Location	chr15:30396121-30396122
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	CTCF	chr15:30395623-30396207	A549	lung:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
2	POLR2A	chr15:30395438-30396641	A549	lung:	n/a	n/a
3	CTCF	chr15:30396020-30396170	GM12875	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
4	CTCF	chr15:30396121-30396134	Gliobla	brain:	n/a	n/a
5	FOSL2	chr15:30395778-30396245	HepG2	liver:	n/a	chr15:30396170-30396181
6	SP1	chr15:30395622-30396246	A549	lung:	n/a	chr15:30395785-30395795 chr15:30395786-30395795 chr15:30395786-30395795 chr15:30395785-30395794
7	CTCF	chr15:30396000-30396150	GM12864	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
8	NR3C1	chr15:30395287-30396676	A549	lung:	n/a	n/a
9	CTCF	chr15:30396000-30396150	HCM	heart:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
10	CTCF	chr15:30396000-30396150	HCPEpiC	choroid plexus:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
11	YY1	chr15:30395938-30396222	HepG2	liver:	n/a	chr15:30395988-30395997 chr15:30396082-30396093 chr15:30396021-30396035
12	POLR2A	chr15:30395742-30396513	Hela-S3	cervix:	n/a	n/a
13	SIN3AK20	chr15:30395822-30396179	A549	lung:	n/a	n/a
14	CTCF	chr15:30395654-30396255	K562	blood:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
15	CTCF	chr15:30396020-30396170	RPTEC	kidney:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
16	POLR2A	chr15:30395524-30396832	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr15:30395995-30396164	A549	lung:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
18	POLR2A	chr15:30395597-30396607	A549	lung:	n/a	n/a
19	YY1	chr15:30395964-30396128	H1-hESC	embryonic stem cell:	n/a	chr15:30395988-30395997 chr15:30396082-30396093 chr15:30396021-30396035
20	CTCF	chr15:30395980-30396130	K562	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
21	SP1	chr15:30395651-30396460	A549	lung:	n/a	chr15:30396317-30396324 chr15:30396312-30396321 chr15:30395785-30395795 chr15:30396313-30396322 chr15:30395786-30395795 chr15:30396311-30396323 chr15:30395786-30395795 chr15:30395785-30395794 chr15:30396312-30396321 chr15:30396365-30396379
22	CTCF	chr15:30396000-30396150	AG09319	gingival:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
23	YY1	chr15:30395763-30396549	A549	lung:	n/a	chr15:30395988-30395997 chr15:30396082-30396093 chr15:30396464-30396478 chr15:30396021-30396035
24	CTCF	chr15:30395980-30396130	HRE	kidney:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
25	CTCF	chr15:30395980-30396130	WI-38	lung:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
26	CTCF	chr15:30396000-30396150	GM12874	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
27	CTCF	chr15:30396020-30396170	HAc	cerebellar:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
28	CTCF	chr15:30396000-30396150	HMEC	breast:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
29	CTCF	chr15:30396000-30396150	BJ	skin:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
30	CTCF	chr15:30395980-30396130	AG09319	gingival:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
31	CTCF	chr15:30395980-30396130	HL-60	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
32	CTCF	chr15:30395570-30396241	A549	lung:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
33	RXRA	chr15:30395634-30396374	HepG2	liver:	n/a	chr15:30396274-30396288
34	TAF1	chr15:30395665-30396349	H1-hESC	embryonic stem cell:	n/a	n/a
35	TAF1	chr15:30395555-30396743	H1-hESC	embryonic stem cell:	n/a	n/a
36	JUND	chr15:30395701-30396222	A549	lung:	n/a	chr15:30396170-30396181
37	TAF1	chr15:30395797-30396300	A549	lung:	n/a	n/a
38	CTCF	chr15:30396020-30396170	GM12869	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
39	TCF3	chr15:30396119-30396563	GM12878	blood:	n/a	chr15:30396514-30396527 chr15:30396510-30396524
40	CTCF	chr15:30396020-30396170	HFF-Myc	foreskin:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
41	POLR2A	chr15:30395407-30396278	H1-hESC	embryonic stem cell:	n/a	n/a
42	EBF1	chr15:30396101-30396589	GM12878	blood:	n/a	n/a
43	POLR2A	chr15:30395737-30396142	A549	lung:	n/a	n/a
44	CTCF	chr15:30396000-30396150	AG04450	lung:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
45	POLR2A	chr15:30395590-30396592	A549	lung:	n/a	n/a
46	CTCF	chr15:30396020-30396170	GM12867	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
47	CTCF	chr15:30396000-30396150	A549	lung:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
48	POLR2A	chr15:30396044-30396270	A549	lung:	n/a	n/a
49	CTCF	chr15:30395980-30396130	HepG2	liver:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
50	CTCF	chr15:30396000-30396150	SK-N-SH_RA	brain:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30396121-30396171	HEEpiC	esophagus:	n/a
2	chr15:30396121-30396171	NT2-D1	testis:	n/a
3	chr15:30396121-30396171	AG04450	lung:	fetal
4	chr15:30396121-30396171	HCF	heart:	n/a
5	chr15:30396121-30396171	HRPEpiC	eye:	n/a
6	chr15:30396121-30396171	AG04449	skin:	fetal
7	chr15:30396121-30396171	GM12878	blood:	n/a
8	chr15:30396121-30396171	H1-hESC	embryonic stem cell:	embryo
9	chr15:30396121-30396171	HRCEpiC	kidney:	n/a
10	chr15:30396121-30396171	A549	lung:	n/a
11	chr15:30396121-30396171	HPAEpiC	pulmonary alveolar:	n/a
12	chr15:30396121-30396171	GM12891	blood:	n/a
13	chr15:30396121-30396171	SK-N-SH_RA	brain:	n/a
14	chr15:30396121-30396171	AG09309	skin:	n/a
15	chr15:30396121-30396171	HCM	heart:	n/a
16	chr15:30396121-30396171	ECC-1	luminal epithelium:	n/a
17	chr15:30396121-30396171	HUVEC	blood vessel:	n/a
18	chr15:30396121-30396171	ProgFib	skin:	n/a
19	chr15:30396121-30396171	HEK293	kidney:	embryo
20	chr15:30396121-30396171	AG10803	skin:	n/a
21	chr15:30396121-30396171	GM19239	blood:	n/a
22	chr15:30396121-30396171	NB4	blood:	n/a
23	chr15:30396121-30396171	GM12892	blood:	n/a
24	chr15:30396121-30396171	MCF10A-Er-Src	breast:	n/a
25	chr15:30396121-30396171	SK-N-SH	brain:	n/a
26	chr15:30396121-30396171	Jurkat	blood:	n/a
27	chr15:30396121-30396171	Caco-2	colon:	n/a
28	chr15:30396121-30396171	ovcar-3	ovarian:	n/a
29	chr15:30396121-30396171	T-47D	breast:	n/a
30	chr15:30396121-30396171	SAEC	small airway:	n/a
31	chr15:30396121-30396171	HRE	kidney:	n/a
32	chr15:30396121-30396171	HAEpiC	amniotic membrane:	n/a
33	chr15:30396121-30396171	PrEC	prostate:	n/a
34	chr15:30396121-30396171	LNCaP	prostate:	n/a
35	chr15:30396121-30396171	HNPCEpiC	eye:	n/a
36	chr15:30396121-30396171	Hepatocyte	liver:	n/a
37	chr15:30396121-30396171	HMEC	breast:	n/a
38	chr15:30396121-30396171	MCF-7	breast:	n/a
39	chr15:30396121-30396171	AG09319	gingival:	n/a
40	chr15:30396121-30396171	BE2_C	brain:	n/a
41	chr15:30396121-30396171	PFSK-1	brain:	n/a
42	chr15:30396121-30396171	RPTEC	kidney:	n/a
43	chr15:30396121-30396171	NHDF-neo	bronchial:	n/a
44	chr15:30396121-30396171	HepG2	liver:	n/a
45	chr15:30396121-30396171	PANC-1	pancreas:	n/a
46	chr15:30396121-30396171	K562	blood:	n/a
47	chr15:30396121-30396171	HL-60	blood:	n/a
48	chr15:30396121-30396171	IMR90	lung:	fetal
49	chr15:30396121-30396171	AoSMC	blood vessel:	n/a
50	chr15:30396121-30396171	BJ	skin:	n/a

Variant related genes	Relation type
DNM1P28	TF binding region
DNM1P28	CpG island

Extended variants
information (count: 57 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:57 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431371	chr15:30193316-31012794	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
2	esv2751527	chr15:30245808-30605836	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv427954	chr15:30292944-30458813	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv1819007	chr15:30292944-31018462	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
5	esv1824179	chr15:30292944-31051705	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
6	nsv428300	chr15:30292944-31051705	ZNF genes & repeats Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
7	esv2758374	chr15:30292944-31152491	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
8	esv2760022	chr15:30292944-31177476	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
9	esv1823206	chr15:30308088-30858486	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
10	nsv832946	chr15:30318810-30507542	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
11	nsv518720	chr15:30346230-31106826	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases
12	esv1821764	chr15:30348514-30926365	Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
13	esv1816989	chr15:30352811-30910092	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
14	esv1820957	chr15:30353491-30901911	Bivalent Enhancer Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
15	esv1822745	chr15:30358034-30399178	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	esv1817932	chr15:30362487-30950529	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
17	nsv869831	chr15:30366124-31115047	Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases
18	esv1008245	chr15:30366457-30445008	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
19	nsv903757	chr15:30369153-31179534	Strong transcription Active TSS Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
20	nsv1044368	chr15:30369914-30900866	Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island lncRNA	40 gene(s)	inside rSNPs	diseases
21	nsv1053277	chr15:30369914-31087321	Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
22	nsv1053894	chr15:30369914-31088465	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
23	esv2760396	chr15:30369914-31099626	Strong transcription Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
24	nsv1039789	chr15:30370019-30900866	Genic enhancers Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	40 gene(s)	inside rSNPs	diseases
25	nsv1040604	chr15:30370019-30920612	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
26	esv1821800	chr15:30370548-30682265	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island lncRNA	21 gene(s)	inside rSNPs	diseases
27	esv1821978	chr15:30372082-30954110	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
28	esv1822009	chr15:30372082-30956242	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
29	esv1821068	chr15:30372282-30685516	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	21 gene(s)	inside rSNPs	diseases
30	esv1820651	chr15:30372282-30910092	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	41 gene(s)	inside rSNPs	diseases
31	nsv974545	chr15:30373033-30401482	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island lncRNA	6 gene(s)	inside rSNPs	diseases
32	nsv568717	chr15:30382120-30760974	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	25 gene(s)	inside rSNPs	diseases
33	nsv568718	chr15:30382120-30918248	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
34	nsv9232	chr15:30384844-31090547	Strong transcription Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
35	nsv1040151	chr15:30386399-30505750	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	10 gene(s)	inside rSNPs	diseases
36	nsv1043128	chr15:30386399-30545018	Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	11 gene(s)	inside rSNPs	diseases
37	nsv1051897	chr15:30386399-30596631	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	13 gene(s)	inside rSNPs	diseases
38	nsv1044014	chr15:30386399-30605841	ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	13 gene(s)	inside rSNPs	diseases
39	nsv1050209	chr15:30386399-30732267	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	22 gene(s)	inside rSNPs	diseases
40	nsv1035201	chr15:30386399-30734745	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island lncRNA	22 gene(s)	inside rSNPs	diseases
41	nsv1047974	chr15:30386399-30780651	Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	24 gene(s)	inside rSNPs	diseases
42	nsv1048557	chr15:30386399-30807930	Active TSS Bivalent/Poised TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island lncRNA	25 gene(s)	inside rSNPs	diseases
43	nsv1047669	chr15:30386399-30821746	Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island lncRNA	25 gene(s)	inside rSNPs	diseases
44	nsv1052282	chr15:30386399-30900866	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island lncRNA	36 gene(s)	inside rSNPs	diseases
45	nsv1050658	chr15:30386399-30920612	Strong transcription Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
46	nsv1035535	chr15:30386399-30925593	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
47	nsv1048881	chr15:30386399-30933522	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
48	nsv1042426	chr15:30386399-30936285	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
49	nsv1039382	chr15:30386399-31080276	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
50	nsv1049639	chr15:30386399-31087321	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30395800-30396200	Active TSS	Primary neutrophils fromperipheralblood	blood
2	chr15:30395800-30396200	Active TSS	Primary B cells from peripheral blood	blood
3	chr15:30395800-30396200	Active TSS	Colonic Mucosa	Colon
4	chr15:30395800-30396200	Active TSS	Gastric	stomach
5	chr15:30395800-30396400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr15:30395800-30396400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr15:30395800-30396400	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr15:30395800-30396400	Active TSS	Breast Myoepithelial Primary Cells	Breast
9	chr15:30395800-30396400	Active TSS	Muscle Satellite Cultured Cells	--
10	chr15:30395800-30396400	Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr15:30395800-30396400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr15:30395800-30396400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr15:30395800-30396400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:30395800-30396400	Active TSS	Adipose Nuclei	Adipose
15	chr15:30395800-30396400	Active TSS	Esophagus	oesophagus
16	chr15:30395800-30396400	Active TSS	Fetal Brain Female	brain
17	chr15:30395800-30396400	Bivalent/Poised TSS	Fetal Stomach	stomach
18	chr15:30395800-30396400	Active TSS	Left Ventricle	heart
19	chr15:30395800-30396400	Active TSS	Rectal Mucosa Donor 31	rectum
20	chr15:30395800-30396400	Active TSS	Right Atrium	heart
21	chr15:30395800-30396400	Active TSS	Right Ventricle	heart
22	chr15:30395800-30396400	Active TSS	Thymus	Thymus
23	chr15:30395800-30396400	Active TSS	Spleen	Spleen
24	chr15:30395800-30396400	Active TSS	HepG2	liver
25	chr15:30395800-30396400	Active TSS	Monocytes-CD14+_RO01746	blood
26	chr15:30395800-30396600	Active TSS	H1 Cell Line	embryonic stem cell
27	chr15:30395800-30396600	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr15:30395800-30396600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr15:30395800-30396600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr15:30395800-30396600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
31	chr15:30395800-30396600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr15:30395800-30396600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr15:30395800-30396600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr15:30395800-30396600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr15:30395800-30396600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr15:30395800-30396600	Active TSS	Pancreas	Pancrea
37	chr15:30395800-30396600	Active TSS	HUVEC	blood vessel
38	chr15:30395800-30396800	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr15:30395800-30396800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr15:30396000-30396200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr15:30396000-30396200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
42	chr15:30396000-30396200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr15:30396000-30396200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
44	chr15:30396000-30396200	Enhancers	Ovary	ovary
45	chr15:30396000-30396200	Enhancers	Small Intestine	intestine
46	chr15:30396000-30396200	Flanking Active TSS	HMEC	breast
47	chr15:30396000-30396400	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr15:30396000-30396400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr15:30396000-30396400	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr15:30396000-30396400	Active TSS	iPS-18 Cell Line	embryonic stem cell

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