Variant report

Variant	esv3321779
Chromosome Location	chr15:78109497-78113895
allele	n/a
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	BACH1	chr15:78111596-78111934	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr15:78112581-78112794	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr15:78113211-78113483	K562	blood:	n/a	chr15:78113370-78113391 chr15:78113374-78113387
4	BHLHE40	chr15:78112561-78112947	K562	blood:	n/a	n/a
5	BHLHE40	chr15:78113815-78114121	K562	blood:	n/a	chr15:78113828-78113844
6	CCNT2	chr15:78112531-78112910	K562	blood:	n/a	n/a
7	CHD1	chr15:78111718-78111742	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr15:78112768-78112882	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr15:78112731-78112878	Hela-S3	cervix:	n/a	n/a
10	CREB1	chr15:78112210-78112963	A549	lung:	n/a	n/a
11	CTBP2	chr15:78111581-78112011	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr15:78113871-78114151	GM10266	blood:	n/a	chr15:78113982-78114000
13	CTCF	chr15:78112720-78112870	HEK293	kidney:	n/a	chr15:78112771-78112781
14	CTCF	chr15:78112700-78112850	GM12870	blood:	n/a	chr15:78112771-78112781
15	CTCF	chr15:78112511-78112987	K562	blood:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781
16	CTCF	chr15:78112666-78112857	HepG2	liver:	n/a	chr15:78112771-78112781
17	CTCF	chr15:78112740-78112890	GM12864	blood:	n/a	chr15:78112771-78112781
18	CTCF	chr15:78112627-78112951	MCF-7	breast:	n/a	chr15:78112771-78112781
19	CTCF	chr15:78112740-78112890	MCF-7	breast:	n/a	chr15:78112771-78112781
20	CTCF	chr15:78112680-78112830	GM12865	blood:	n/a	chr15:78112771-78112781
21	CTCF	chr15:78112640-78112790	HAc	cerebellar:	n/a	chr15:78112771-78112781
22	CTCF	chr15:78112682-78112863	LNCaP	prostate:	n/a	chr15:78112771-78112781
23	CTCF	chr15:78112699-78112843	GM10248	blood:	n/a	chr15:78112771-78112781
24	CTCF	chr15:78113855-78114146	MCF-7	breast:	n/a	chr15:78113982-78114000
25	CTCF	chr15:78113859-78114137	ProgFib	skin:	n/a	chr15:78113982-78114000
26	CTCF	chr15:78113606-78114288	MCF-7	breast:	n/a	chr15:78113982-78114000
27	CTCF	chr15:78113749-78114162	HepG2	liver:	n/a	chr15:78113982-78114000
28	CTCF	chr15:78112680-78112830	GM12875	blood:	n/a	chr15:78112771-78112781
29	CTCF	chr15:78112680-78112830	GM12878	blood:	n/a	chr15:78112771-78112781
30	CTCF	chr15:78112680-78112830	RPTEC	kidney:	n/a	chr15:78112771-78112781
31	CTCF	chr15:78112820-78112970	HVMF	connective:	n/a	n/a
32	CTCF	chr15:78112615-78112856	SK-N-SH_RA	brain:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781
33	CTCF	chr15:78112920-78113070	HVMF	connective:	n/a	n/a
34	CTCF	chr15:78113840-78113990	HAc	cerebellar:	n/a	n/a
35	CTCF	chr15:78113746-78114209	H1-hESC	embryonic stem cell:	n/a	chr15:78113982-78114000
36	CTCF	chr15:78112680-78112830	AG09309	skin:	n/a	chr15:78112771-78112781
37	CTCF	chr15:78112700-78112850	GM06990	blood:	n/a	chr15:78112771-78112781
38	CTCF	chr15:78113861-78114132	MCF-7	breast:	n/a	chr15:78113982-78114000
39	CTCF	chr15:78112760-78112910	AoAF	blood vessel:	n/a	chr15:78112771-78112781
40	CTCF	chr15:78113871-78114134	MCF-7	breast:	n/a	chr15:78113982-78114000
41	CTCF	chr15:78112693-78112845	LNCaP	prostate:	n/a	chr15:78112771-78112781
42	CTCF	chr15:78112660-78112810	NB4	blood:	n/a	chr15:78112771-78112781
43	CTCF	chr15:78112720-78112870	Caco-2	colon:	n/a	chr15:78112771-78112781
44	CTCF	chr15:78112753-78112790	GM20000	blood:	n/a	chr15:78112771-78112781
45	CTCF	chr15:78112740-78112890	HRPEpiC	eye:	n/a	chr15:78112771-78112781
46	CTCF	chr15:78112669-78112888	GM12892	blood:	n/a	chr15:78112771-78112781
47	CTCF	chr15:78112690-78112852	Medullo	brain:	n/a	chr15:78112771-78112781
48	CTCF	chr15:78112362-78114448	A549	lung:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781 chr15:78113982-78114000
49	CTCF	chr15:78112720-78112870	HRE	kidney:	n/a	chr15:78112771-78112781
50	CTCF	chr15:78113400-78113690	GM12873	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78111830-78111880	PFSK-1	brain:	n/a
2	chr15:78110106-78110156	SK-N-SH_RA	brain:	n/a
3	chr15:78111830-78111880	PFSK-1	brain:	n/a
4	chr15:78110106-78110156	SK-N-SH_RA	brain:	n/a
5	chr15:78113237-78113287	HEK293	kidney:	embryo
6	chr15:78110903-78110953	GM12878	blood:	n/a
7	chr15:78112847-78112897	HCT-116	colon:	n/a
8	chr15:78111390-78111440	GM19239	blood:	n/a
9	chr15:78111830-78111880	HCM	heart:	n/a
10	chr15:78111196-78111246	IMR90	lung:	fetal
11	chr15:78110857-78110907	AG09319	gingival:	n/a
12	chr15:78110857-78110907	U87	brain:	n/a
13	chr15:78110857-78110907	SAEC	small airway:	n/a
14	chr15:78113237-78113287	HRPEpiC	eye:	n/a
15	chr15:78109450-78109500	CMK	blood:	n/a
16	chr15:78113667-78113717	NHBE	bronchial:	n/a
17	chr15:78110106-78110156	GM19239	blood:	n/a
18	chr15:78112847-78112897	ECC-1	luminal epithelium:	n/a
19	chr15:78112026-78112076	HUVEC	blood vessel:	n/a
20	chr15:78110857-78110907	MCF-7	breast:	n/a
21	chr15:78111830-78111880	AG09309	skin:	n/a
22	chr15:78111196-78111246	MCF10A-Er-Src	breast:	n/a
23	chr15:78110903-78110953	HRE	kidney:	n/a
24	chr15:78112847-78112897	Hepatocyte	liver:	n/a
25	chr15:78111390-78111440	H1-hESC	embryonic stem cell:	embryo
26	chr15:78111390-78111440	K562	blood:	n/a
27	chr15:78110106-78110156	HIPEpiC	eye:	n/a
28	chr15:78110903-78110953	Hela-S3	cervix:	n/a
29	chr15:78110106-78110156	SKMC	muscle:	n/a
30	chr15:78113667-78113717	Jurkat	blood:	n/a
31	chr15:78111196-78111246	GM12892	blood:	n/a
32	chr15:78111196-78111246	ProgFib	skin:	n/a
33	chr15:78110857-78110907	NT2-D1	testis:	n/a
34	chr15:78110903-78110953	PFSK-1	brain:	n/a
35	chr15:78112026-78112076	A549	lung:	n/a
36	chr15:78111390-78111440	HPAEpiC	pulmonary alveolar:	n/a
37	chr15:78112026-78112076	AG10803	skin:	n/a
38	chr15:78112818-78112868	HRCEpiC	kidney:	n/a
39	chr15:78113667-78113717	HAEpiC	amniotic membrane:	n/a
40	chr15:78110903-78110953	AoSMC	blood vessel:	n/a
41	chr15:78111390-78111440	SK-N-SH_RA	brain:	n/a
42	chr15:78112026-78112076	NHBE	bronchial:	n/a
43	chr15:78112026-78112076	IMR90	lung:	fetal
44	chr15:78110903-78110953	HCT-116	colon:	n/a
45	chr15:78113667-78113717	GM12878	blood:	n/a
46	chr15:78110106-78110156	GM12892	blood:	n/a
47	chr15:78113237-78113287	GM12891	blood:	n/a
48	chr15:78110903-78110953	HCPEpiC	choroid plexus:	n/a
49	chr15:78113667-78113717	GM19239	blood:	n/a
50	chr15:78111390-78111440	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:77925435..77927439-chr15:78112259..78115090,22	K562	blood:
2	chr15:77925072..77927787-chr15:78111223..78115888,59	MCF-7	breast:
3	chr15:78093726..78095482-chr15:78109302..78111368,2	K562	blood:
4	chr15:77925397..77928069-chr15:78112259..78116246,3	K562	blood:
5	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
6	chr15:77925299..77927652-chr15:78112444..78114100,3	MCF-7	breast:
7	chr15:77950482..77951067-chr15:78113646..78114389,2	K562	blood:
8	chr15:77835732..77836546-chr15:78113747..78114395,2	MCF-7	breast:
9	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
10	chr15:77925397..77927315-chr15:78112259..78115116,2	K562	blood:
11	chr15:77951738..77952728-chr15:78113529..78114461,5	K562	blood:
12	chr15:77925249..77927257-chr15:78113205..78115049,24	MCF-7	breast:
13	chr15:77951785..77952749-chr15:78113535..78114168,4	MCF-7	breast:
14	chr15:77951840..77952665-chr15:78112887..78114250,4	MCF-7	breast:
15	chr15:77923251..77928296-chr15:78111448..78115771,8	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBC1D2B-7	chr15:78112376-78112566	NONHSAT047460
2	lnc-TBC1D2B-7	chr15:78111613-78111870	NONHSAT047458
3	lnc-TBC1D2B-7	chr15:78113121-78113196	NONHSAT047459

Variant related genes	Relation type
LINGO1	TF binding region
LINGO1	CpG island
ENSG00000259281	chromatin interactions
ENSG00000169783	chromatin interactions

Extended variants
information (count: 147 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:147 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115296171	chr15:78109607-78109608	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs555650685	chr15:78109616-78109617	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs573886421	chr15:78109638-78109639	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs540501615	chr15:78109663-78109664	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs544497305	chr15:78109687-78109688	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs77235588	chr15:78109689-78109690	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577705392	chr15:78109727-78109728	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs4304989	chr15:78109751-78109752	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs181516363	chr15:78109797-78109798	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs74026871	chr15:78109800-78109801	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559947880	chr15:78109807-78109808	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541882879	chr15:78109808-78109809	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs144595235	chr15:78109812-78109813	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540905582	chr15:78109819-78109820	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113673032	chr15:78109830-78109831	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs115199929	chr15:78109855-78109856	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs369675448	chr15:78109862-78109863	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs529604271	chr15:78109881-78109882	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562563819	chr15:78109899-78109900	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs114347661	chr15:78109909-78109910	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs34073889	chr15:78109911-78109912	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs367768082	chr15:78109997-78109998	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs184253746	chr15:78110047-78110048	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs575256139	chr15:78110064-78110065	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544018317	chr15:78110090-78110091	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551480007	chr15:78110096-78110097	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs566818994	chr15:78110106-78110107	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs116975357	chr15:78110108-78110109	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs555300687	chr15:78110181-78110182	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs138620334	chr15:78110191-78110192	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs538185331	chr15:78110219-78110220	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs114939267	chr15:78110275-78110276	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577717658	chr15:78110282-78110283	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs544984590	chr15:78110300-78110301	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs560076128	chr15:78110304-78110305	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559532640	chr15:78110330-78110331	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs542701506	chr15:78110335-78110336	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs188488556	chr15:78110345-78110346	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs141201155	chr15:78110466-78110467	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs529406613	chr15:78110506-78110507	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550863805	chr15:78110586-78110587	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562812907	chr15:78110595-78110596	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs533171790	chr15:78110619-78110620	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551397538	chr15:78110622-78110623	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs62007854	chr15:78110748-78110749	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566836844	chr15:78110761-78110762	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376449595	chr15:78110773-78110774	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs527830508	chr15:78110776-78110777	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs549450161	chr15:78110783-78110784	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150772004	chr15:78110792-78110793	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78101600-78110400	Weak transcription	Brain Angular Gyrus	brain
2	chr15:78105800-78109800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr15:78107400-78111600	Weak transcription	Gastric	stomach
4	chr15:78108200-78109600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:78108800-78109800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr15:78108800-78110600	Bivalent Enhancer	Fetal Brain Male	brain
7	chr15:78109000-78110600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:78109000-78110800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr15:78109200-78109600	Bivalent Enhancer	Fetal Muscle Leg	muscle
10	chr15:78109200-78109800	Enhancers	H9 Cell Line	embryonic stem cell
11	chr15:78109200-78110200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr15:78109200-78110600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:78109200-78110600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr15:78109400-78109800	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr15:78109400-78110400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
16	chr15:78109400-78110400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr15:78109400-78110600	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
18	chr15:78109400-78110800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
19	chr15:78109600-78109800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr15:78109600-78109800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
21	chr15:78109600-78109800	Active TSS	Spleen	Spleen
22	chr15:78109600-78110000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
23	chr15:78109600-78110000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
24	chr15:78109600-78110600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
25	chr15:78109600-78110600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr15:78109600-78110800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr15:78109600-78110800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
28	chr15:78109800-78110000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr15:78109800-78110200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr15:78109800-78110400	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr15:78109800-78111800	Bivalent Enhancer	Spleen	Spleen
32	chr15:78110000-78110800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
33	chr15:78110000-78110800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr15:78110200-78110400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
35	chr15:78110200-78110400	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
36	chr15:78110200-78111000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
37	chr15:78110400-78110600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
38	chr15:78110400-78110600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr15:78110400-78110600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
40	chr15:78110400-78110600	Flanking Active TSS	Brain Angular Gyrus	brain
41	chr15:78110400-78110600	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
42	chr15:78110400-78111000	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
43	chr15:78110400-78111200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
44	chr15:78110400-78111200	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
45	chr15:78110600-78110800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:78110600-78110800	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr15:78110600-78110800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
48	chr15:78110600-78110800	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
49	chr15:78110600-78110800	Bivalent Enhancer	Fetal Intestine Small	intestine
50	chr15:78110600-78110800	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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