Variant report

Variant	esv16622
Chromosome Location	chr9:139662736-139665108
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	chr9:139664383-139664584	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr9:139662376-139662882	GM12878	blood:	n/a	chr9:139662543-139662552 chr9:139662543-139662552
3	BHLHE40	chr9:139664520-139664614	GM12878	blood:	n/a	n/a
4	BHLHE40	chr9:139664410-139664615	K562	blood:	n/a	n/a
5	CBX3	chr9:139664352-139664698	K562	blood:	n/a	n/a
6	CEBPB	chr9:139664485-139664618	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr9:139662932-139663042	IMR90	lung:	n/a	n/a
8	CHD2	chr9:139664436-139664568	H1-hESC	embryonic stem cell:	n/a	n/a
9	CREB1	chr9:139664368-139664674	A549	lung:	n/a	n/a
10	CTCF	chr9:139664460-139664610	GM12873	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
11	CTCF	chr9:139664520-139664670	NHLF	lung:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
12	CTCF	chr9:139664480-139664630	HPAF	blood vessel:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
13	CTCF	chr9:139664500-139664650	A549	lung:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
14	CTCF	chr9:139664444-139664683	GM12878	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
15	CTCF	chr9:139664456-139664694	Pancreas_OC	pancreas:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
16	CTCF	chr9:139664477-139664674	GM10248	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
17	CTCF	chr9:139664478-139664678	Hela-S3	cervix:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
18	CTCF	chr9:139664460-139664610	HRPEpiC	eye:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
19	CTCF	chr9:139664462-139664672	GM13976	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
20	CTCF	chr9:139664500-139664650	AG04450	lung:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
21	CTCF	chr9:139664500-139664650	K562	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
22	CTCF	chr9:139664460-139664610	HEK293	kidney:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
23	CTCF	chr9:139664480-139664630	HBMEC	blood vessel:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
24	CTCF	chr9:139664233-139664713	SK-N-SH	brain:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
25	CTCF	chr9:139664500-139664650	GM12875	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
26	CTCF	chr9:139664480-139664630	NHDF-neo	bronchial:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
27	CTCF	chr9:139664437-139664691	K562	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
28	CTCF	chr9:139664413-139664738	IMR90	lung:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
29	CTCF	chr9:139664445-139664694	Fibrobl	skin:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
30	CTCF	chr9:139664421-139664634	SK-N-SH_RA	brain:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
31	CTCF	chr9:139664360-139664510	HFF-Myc	foreskin:	n/a	chr9:139664483-139664493 chr9:139664481-139664494
32	CTCF	chr9:139664434-139664698	MCF-7	breast:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
33	CTCF	chr9:139664460-139664663	MCF-7	breast:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
34	CTCF	chr9:139664471-139664674	Spleen_OC	spleen:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
35	CTCF	chr9:139665080-139665230	RPTEC	kidney:	n/a	n/a
36	CTCF	chr9:139664271-139664724	K562	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
37	CTCF	chr9:139664328-139664691	MCF-7	breast:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
38	CTCF	chr9:139664480-139664630	AG09319	gingival:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
39	CTCF	chr9:139664500-139664650	GM12871	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
40	CTCF	chr9:139664500-139664650	HVMF	connective:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
41	CTCF	chr9:139664500-139664650	GM12868	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
42	CTCF	chr9:139664460-139664610	GM12868	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
43	CTCF	chr9:139664460-139664610	HEEpiC	esophagus:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
44	CTCF	chr9:139664415-139664705	Gliobla	brain:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
45	CTCF	chr9:139664500-139664650	GM12869	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
46	CTCF	chr9:139664480-139664630	Hela-S3	cervix:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
47	CTCF	chr9:139664480-139664630	HUVEC	blood vessel:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
48	CTCF	chr9:139664440-139664590	WI-38	lung:	n/a	chr9:139664483-139664493 chr9:139664481-139664494
49	CTCF	chr9:139664421-139664714	GM12891	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
50	CTCF	chr9:139664480-139664630	HAc	cerebellar:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603

No.	Distal block	Cell Line	Cell type
1	chr9:139621278..139624827-chr9:139660350..139665047,5	K562	blood:
2	chr9:139640588..139643273-chr9:139662768..139664600,2	K562	blood:
3	chr9:139615454..139618647-chr9:139663629..139666598,3	MCF-7	breast:
4	chr9:139664152..139666690-chr9:139684867..139687116,2	MCF-7	breast:
5	chr9:139617845..139623838-chr9:139660350..139667246,10	K562	blood:
6	chr8:134883443..134884944-chr9:139662718..139664230,2	K562	blood:
7	chr9:139662310..139665146-chr9:139700169..139702660,2	K562	blood:
8	chr9:139662206..139666130-chr9:139666450..139670889,6	K562	blood:
9	chr9:139656220..139657844-chr9:139664541..139666356,2	K562	blood:
10	chr9:139663599..139665182-chr9:139742980..139744994,2	MCF-7	breast:
11	chr9:139663003..139666035-chr9:139678378..139681076,3	MCF-7	breast:
12	chr9:139662596..139664291-chr9:139666561..139668575,2	K562	blood:

Variant related genes	Relation type
LCN15	TF binding region
ENSG00000272896	chromatin interactions
ENSG00000213213	chromatin interactions
ENSG00000054148	chromatin interactions
ENSG00000233016	chromatin interactions
ENSG00000273066	chromatin interactions
ENSG00000196642	chromatin interactions
ENSG00000267206	chromatin interactions
ENSG00000244187	chromatin interactions
ENSG00000204003	chromatin interactions

Extended variants
information (count: 90 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:90 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188651927	chr9:139662737-139662738	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs566551555	chr9:139662742-139662743	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs12349641	chr9:139662779-139662780	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs375891906	chr9:139662784-139662785	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs568993322	chr9:139662790-139662791	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs182475200	chr9:139662882-139662883	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs554878574	chr9:139662889-139662890	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs28634988	chr9:139662922-139662923	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs13298473	chr9:139662929-139662930	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs112979277	chr9:139662933-139662934	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs537889173	chr9:139662942-139662943	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs28469533	chr9:139662944-139662945	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs60814940	chr9:139662949-139662950	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs28392637	chr9:139662953-139662954	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs144096256	chr9:139662955-139662956	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs148813041	chr9:139662964-139662965	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs4256669	chr9:139662976-139662977	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs553921172	chr9:139662988-139662989	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs577266785	chr9:139662990-139662991	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs61541150	chr9:139662994-139662995	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs573623899	chr9:139663001-139663002	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs59511277	chr9:139663002-139663003	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs59961482	chr9:139663006-139663007	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs542483525	chr9:139663008-139663009	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs56943002	chr9:139663010-139663011	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs191783035	chr9:139663013-139663014	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs59938720	chr9:139663016-139663017	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs377111006	chr9:139663017-139663018	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs4549865	chr9:139663031-139663032	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	mRNA abundance
30	rs183471637	chr9:139663062-139663063	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs377630815	chr9:139663065-139663066	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs562002235	chr9:139663086-139663087	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs4256670	chr9:139663122-139663123	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs187631364	chr9:139663169-139663170	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs193248671	chr9:139663173-139663174	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs4534210	chr9:139663175-139663176	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs551954530	chr9:139663204-139663205	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs568958224	chr9:139663213-139663214	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs4610845	chr9:139663235-139663236	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs144744095	chr9:139663236-139663237	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs147871249	chr9:139663250-139663251	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs562205372	chr9:139663299-139663300	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs539692524	chr9:139663379-139663380	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs554119258	chr9:139663413-139663414	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs570721202	chr9:139663455-139663456	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs11145876	chr9:139663458-139663459	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs556335848	chr9:139663484-139663485	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs80109460	chr9:139663556-139663557	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs11145877	chr9:139663632-139663633	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs547305655	chr9:139663634-139663635	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Hepatocellular carcinoma	22174799	CNVD
Idiopathic chronic pancreatitis	21572526	CNVD
Kleefstra syndrome	22670141	CNVD
Schizophrenia	22241247	CNVD
9q deletion syndrome	16826528	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	19293338	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Mantle cell lymphoma	19029149	CNVD
Autism	20808228	CNVD
Epilepsy	22083797	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Developmental delay	20877625	CNVD
Hypoplastic	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
Palpebral fissures	20877625	CNVD
Melanoma	20877625	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:139655600-139664400	Weak transcription	Pancreas	Pancrea
2	chr9:139657600-139664200	Weak transcription	Right Ventricle	heart
3	chr9:139657800-139667800	Weak transcription	Right Atrium	heart
4	chr9:139658400-139664200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:139658400-139664200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr9:139658800-139662800	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr9:139659200-139667800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:139659400-139663600	Enhancers	Primary B cells from peripheral blood	blood
9	chr9:139660200-139663000	Enhancers	Primary B cells from cord blood	blood
10	chr9:139660600-139662800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr9:139660800-139663000	Enhancers	GM12878-XiMat	blood
12	chr9:139661400-139664200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr9:139661600-139662800	Enhancers	K562	blood
14	chr9:139662200-139662800	Enhancers	Fetal Thymus	thymus
15	chr9:139662400-139662800	Flanking Active TSS	HepG2	liver
16	chr9:139662600-139662800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr9:139662600-139662800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr9:139662600-139662800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
19	chr9:139662600-139662800	Bivalent Enhancer	Placenta	Placenta
20	chr9:139662600-139662800	Enhancers	Spleen	Spleen
21	chr9:139662800-139664200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr9:139662800-139664200	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr9:139662800-139664200	Weak transcription	HepG2	liver
24	chr9:139662800-139664200	Weak transcription	K562	blood
25	chr9:139662800-139664400	Weak transcription	Fetal Thymus	thymus
26	chr9:139663000-139664200	Weak transcription	Primary B cells from cord blood	blood
27	chr9:139663600-139664000	Weak transcription	Primary B cells from peripheral blood	blood
28	chr9:139664000-139664600	Enhancers	Primary B cells from peripheral blood	blood
29	chr9:139664200-139664400	Active TSS	H1 Cell Line	embryonic stem cell
30	chr9:139664200-139664400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
31	chr9:139664200-139664400	Enhancers	Primary B cells from cord blood	blood
32	chr9:139664200-139664400	Enhancers	Primary hematopoietic stem cells	blood
33	chr9:139664200-139664400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
34	chr9:139664200-139664400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr9:139664200-139664400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr9:139664200-139664400	Active TSS	Brain Inferior Temporal Lobe	brain
37	chr9:139664200-139664400	Active TSS	Rectal Mucosa Donor 31	rectum
38	chr9:139664200-139664600	Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr9:139664200-139664600	Active TSS	H9 Cell Line	embryonic stem cell
40	chr9:139664200-139664600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr9:139664200-139664600	Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr9:139664200-139664600	Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr9:139664200-139664600	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr9:139664200-139664600	Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr9:139664200-139664600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr9:139664200-139664600	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr9:139664200-139664600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr9:139664200-139664600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:139664200-139664600	Enhancers	Primary T cells from cord blood	blood
50	chr9:139664200-139664600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood

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