Variant report

Variant	esv3422045
Chromosome Location	chr15:78110122-78112870
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	chr15:78112561-78112947	K562	blood:	n/a	n/a
4	CCNT2	chr15:78112531-78112910	K562	blood:	n/a	n/a
5	CHD1	chr15:78111718-78111742	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr15:78112731-78112878	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr15:78112768-78112882	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr15:78112210-78112963	A549	lung:	n/a	n/a
9	CTBP2	chr15:78111581-78112011	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr15:78112680-78112830	HUVEC	blood vessel:	n/a	chr15:78112771-78112781
11	CTCF	chr15:78112740-78112890	HRPEpiC	eye:	n/a	chr15:78112771-78112781
12	CTCF	chr15:78112693-78112845	LNCaP	prostate:	n/a	chr15:78112771-78112781
13	CTCF	chr15:78112601-78112851	T-47D	breast:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781
14	CTCF	chr15:78112669-78112888	GM12892	blood:	n/a	chr15:78112771-78112781
15	CTCF	chr15:78112685-78112875	GM19238	blood:	n/a	chr15:78112771-78112781
16	CTCF	chr15:78112800-78112950	GM12873	blood:	n/a	n/a
17	CTCF	chr15:78112680-78112830	HCPEpiC	choroid plexus:	n/a	chr15:78112771-78112781
18	CTCF	chr15:78112640-78112790	HCM	heart:	n/a	chr15:78112771-78112781
19	CTCF	chr15:78112620-78112770	HVMF	connective:	n/a	n/a
20	CTCF	chr15:78112692-78112820	Pancreas_OC	pancreas:	n/a	chr15:78112771-78112781
21	CTCF	chr15:78111763-78111842	GM12891	blood:	n/a	n/a
22	CTCF	chr15:78112505-78112550	MCF-7	breast:	n/a	n/a
23	CTCF	chr15:78112720-78112870	HAc	cerebellar:	n/a	chr15:78112771-78112781
24	CTCF	chr15:78112720-78112870	HMF	breast:	n/a	chr15:78112771-78112781
25	CTCF	chr15:78112699-78112843	GM10248	blood:	n/a	chr15:78112771-78112781
26	CTCF	chr15:78112680-78112830	GM12875	blood:	n/a	chr15:78112771-78112781
27	CTCF	chr15:78112720-78112870	HRE	kidney:	n/a	chr15:78112771-78112781
28	CTCF	chr15:78112680-78112830	AG09309	skin:	n/a	chr15:78112771-78112781
29	CTCF	chr15:78112720-78112870	HCPEpiC	choroid plexus:	n/a	chr15:78112771-78112781
30	CTCF	chr15:78112700-78112850	GM12874	blood:	n/a	chr15:78112771-78112781
31	CTCF	chr15:78112643-78112913	MCF-7	breast:	n/a	chr15:78112771-78112781
32	CTCF	chr15:78112640-78112790	GM12864	blood:	n/a	chr15:78112771-78112781
33	CTCF	chr15:78112223-78114736	SK-N-SH	brain:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781 chr15:78113982-78114000
34	CTCF	chr15:78112660-78112810	GM12873	blood:	n/a	chr15:78112771-78112781
35	CTCF	chr15:78112657-78112912	A549	lung:	n/a	chr15:78112771-78112781
36	CTCF	chr15:78112700-78112850	WERI-Rb-1	eye:	n/a	chr15:78112771-78112781
37	CTCF	chr15:78112760-78112910	RPTEC	kidney:	n/a	chr15:78112771-78112781
38	CTCF	chr15:78112672-78112878	ProgFib	skin:	n/a	chr15:78112771-78112781
39	CTCF	chr15:78112580-78112730	GM12865	blood:	n/a	chr15:78112615-78112628 chr15:78112615-78112624
40	CTCF	chr15:78112714-78112825	HUVEC	blood vessel:	n/a	chr15:78112771-78112781
41	CTCF	chr15:78112753-78112790	GM20000	blood:	n/a	chr15:78112771-78112781
42	CTCF	chr15:78112626-78112946	K562	blood:	n/a	chr15:78112771-78112781
43	CTCF	chr15:78112666-78112857	HepG2	liver:	n/a	chr15:78112771-78112781
44	CTCF	chr15:78112660-78112810	NB4	blood:	n/a	chr15:78112771-78112781
45	CTCF	chr15:78112680-78112830	HBMEC	blood vessel:	n/a	chr15:78112771-78112781
46	CTCF	chr15:78112720-78112870	HEK293	kidney:	n/a	chr15:78112771-78112781
47	CTCF	chr15:78112720-78112870	HFF-Myc	foreskin:	n/a	chr15:78112771-78112781
48	CTCF	chr15:78112720-78112870	HepG2	liver:	n/a	chr15:78112771-78112781
49	CTCF	chr15:78112780-78112930	AG09309	skin:	n/a	n/a
50	CTCF	chr15:78112615-78112856	SK-N-SH_RA	brain:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78110857-78110907	SK-N-SH_RA	brain:	n/a
2	chr15:78111830-78111880	HRE	kidney:	n/a
3	chr15:78110106-78110156	NHBE	bronchial:	n/a
4	chr15:78110106-78110156	GM06990	blood:	n/a
5	chr15:78112818-78112868	AG09319	gingival:	n/a
6	chr15:78111390-78111440	GM12878	blood:	n/a
7	chr15:78110903-78110953	ovcar-3	ovarian:	n/a
8	chr15:78111390-78111440	ProgFib	skin:	n/a
9	chr15:78110857-78110907	AG10803	skin:	n/a
10	chr15:78111390-78111440	HPAEpiC	pulmonary alveolar:	n/a
11	chr15:78111390-78111440	HRE	kidney:	n/a
12	chr15:78110106-78110156	A549	lung:	n/a
13	chr15:78111830-78111880	BE2_C	brain:	n/a
14	chr15:78110857-78110907	PFSK-1	brain:	n/a
15	chr15:78112818-78112868	SK-N-SH_RA	brain:	n/a
16	chr15:78111196-78111246	SK-N-MC	brain:	n/a
17	chr15:78110857-78110907	RPTEC	kidney:	n/a
18	chr15:78110106-78110156	U87	brain:	n/a
19	chr15:78112026-78112076	PrEC	prostate:	n/a
20	chr15:78110903-78110953	HPAEpiC	pulmonary alveolar:	n/a
21	chr15:78112818-78112868	GM12878	blood:	n/a
22	chr15:78112847-78112897	BE2_C	brain:	n/a
23	chr15:78110903-78110953	HEK293	kidney:	embryo
24	chr15:78110857-78110907	HNPCEpiC	eye:	n/a
25	chr15:78112818-78112868	CMK	blood:	n/a
26	chr15:78112818-78112868	GM06990	blood:	n/a
27	chr15:78110903-78110953	HRPEpiC	eye:	n/a
28	chr15:78110106-78110156	PrEC	prostate:	n/a
29	chr15:78111830-78111880	Hela-S3	cervix:	n/a
30	chr15:78111830-78111880	HCT-116	colon:	n/a
31	chr15:78112847-78112897	Caco-2	colon:	n/a
32	chr15:78110903-78110953	H1-hESC	embryonic stem cell:	embryo
33	chr15:78111830-78111880	NHBE	bronchial:	n/a
34	chr15:78112847-78112897	ProgFib	skin:	n/a
35	chr15:78111830-78111880	HCM	heart:	n/a
36	chr15:78110857-78110907	NHBE	bronchial:	n/a
37	chr15:78112818-78112868	Hepatocyte	liver:	n/a
38	chr15:78111830-78111880	SK-N-SH	brain:	n/a
39	chr15:78111390-78111440	GM19239	blood:	n/a
40	chr15:78111390-78111440	NHBE	bronchial:	n/a
41	chr15:78111196-78111246	Hela-S3	cervix:	n/a
42	chr15:78111390-78111440	AG04450	lung:	fetal
43	chr15:78110857-78110907	GM12878	blood:	n/a
44	chr15:78110857-78110907	HIPEpiC	eye:	n/a
45	chr15:78112818-78112868	GM19239	blood:	n/a
46	chr15:78112847-78112897	PANC-1	pancreas:	n/a
47	chr15:78111830-78111880	SK-N-SH_RA	brain:	n/a
48	chr15:78112026-78112076	AoSMC	blood vessel:	n/a
49	chr15:78111196-78111246	GM12878	blood:	n/a
50	chr15:78112818-78112868	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:77923251..77928296-chr15:78111448..78115771,8	MCF-7	breast:
2	chr15:77925397..77928069-chr15:78112259..78116246,3	K562	blood:
3	chr15:78093726..78095482-chr15:78109302..78111368,2	K562	blood:
4	chr15:77925435..77927439-chr15:78112259..78115090,22	K562	blood:
5	chr15:77925072..77927787-chr15:78111223..78115888,59	MCF-7	breast:
6	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
7	chr15:77925397..77927315-chr15:78112259..78115116,2	K562	blood:
8	chr15:77925299..77927652-chr15:78112444..78114100,3	MCF-7	breast:
9	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:

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

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

Extended variants
information (count: 84 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:84 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	rs78281737	chr15:78110832-78110833	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556522160	chr15:78110845-78110846	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs139123602	chr15:78110892-78110893	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs538911312	chr15:78110946-78110947	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs376166106	chr15:78110959-78110960	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553531029	chr15:78110981-78110982	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs73457784	chr15:78111000-78111001	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs542366280	chr15:78111027-78111028	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs554601760	chr15:78111034-78111035	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573916797	chr15:78111042-78111043	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201879176	chr15:78111048-78111049	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs544364701	chr15:78111095-78111096	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs147212157	chr15:78111097-78111098	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559663613	chr15:78111121-78111122	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs4243054	chr15:78111156-78111157	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs372545549	chr15:78111163-78111164	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs4243055	chr15:78111216-78111217	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs527646951	chr15:78111274-78111275	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs145382349	chr15:78111295-78111296	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs180908784	chr15:78111359-78111360	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs35981882	chr15:78111402-78111403	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372088592	chr15:78111519-78111520	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12911998	chr15:78111563-78111564	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs531822614	chr15:78111598-78111599	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs550026719	chr15:78111630-78111631	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs571460945	chr15:78111643-78111644	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs185470896	chr15:78111669-78111670	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs372187360	chr15:78111723-78111724	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	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:284 , 50 per page) page: 1 2 3 4 5 6

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

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