Variant report

Variant	esv1825684
Chromosome Location	chr18:44526351-44549177
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	ARID3A	chr18:44530288-44530439	K562	blood:	n/a	n/a
2	BHLHE40	chr18:44546870-44547457	HepG2	liver:	n/a	n/a
3	BHLHE40	chr18:44547816-44548107	HepG2	liver:	n/a	n/a
4	BRCA1	chr18:44526800-44527412	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr18:44533294-44533502	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr18:44540976-44541166	K562	blood:	n/a	n/a
7	CHD2	chr18:44526653-44526788	K562	blood:	n/a	n/a
8	CHD2	chr18:44526479-44527130	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr18:44547080-44547230	HepG2	liver:	n/a	n/a
10	CTCF	chr18:44529966-44530356	HepG2	liver:	n/a	chr18:44530204-44530222
11	CTCF	chr18:44530160-44530310	NHLF	lung:	n/a	chr18:44530204-44530222
12	CTCF	chr18:44530200-44530350	GM12868	blood:	n/a	chr18:44530204-44530222
13	CTCF	chr18:44529820-44529970	GM12865	blood:	n/a	n/a
14	CTCF	chr18:44527419-44527474	Medullo	brain:	n/a	n/a
15	CTCF	chr18:44530160-44530310	GM12872	blood:	n/a	chr18:44530204-44530222
16	CTCF	chr18:44530092-44530324	GM13977	blood:	n/a	chr18:44530204-44530222
17	CTCF	chr18:44530100-44530250	GM12878	blood:	n/a	chr18:44530204-44530222
18	CTCF	chr18:44530083-44530358	Medullo	brain:	n/a	chr18:44530204-44530222
19	CTCF	chr18:44530140-44530290	MCF-7	breast:	n/a	chr18:44530204-44530222
20	CTCF	chr18:44530135-44530294	SK-N-SH_RA	brain:	n/a	chr18:44530204-44530222
21	CTCF	chr18:44544960-44545110	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr18:44530120-44530270	HMF	breast:	n/a	chr18:44530204-44530222
23	CTCF	chr18:44529640-44529890	GM12864	blood:	n/a	n/a
24	CTCF	chr18:44529985-44530402	K562	blood:	n/a	chr18:44530204-44530222
25	CTCF	chr18:44530108-44530356	Hela-S3	cervix:	n/a	chr18:44530204-44530222
26	CTCF	chr18:44530100-44530250	GM12801	blood:	n/a	chr18:44530204-44530222
27	CTCF	chr18:44530100-44530389	GM12878	blood:	n/a	chr18:44530204-44530222
28	CTCF	chr18:44530155-44530313	GM20000	blood:	n/a	chr18:44530204-44530222
29	CTCF	chr18:44530204-44530332	A549	lung:	n/a	chr18:44530204-44530222
30	CTCF	chr18:44530140-44530290	GM12873	blood:	n/a	chr18:44530204-44530222
31	CTCF	chr18:44545561-44545716	LNCaP	prostate:	n/a	n/a
32	CTCF	chr18:44530203-44530338	Fibrobl	skin:	n/a	chr18:44530204-44530222
33	CTCF	chr18:44530152-44530311	Kidney_OC	kidney:	n/a	chr18:44530204-44530222
34	CTCF	chr18:44530160-44530310	MCF-7	breast:	n/a	chr18:44530204-44530222
35	CTCF	chr18:44530120-44530270	AG10803	skin:	n/a	chr18:44530204-44530222
36	CTCF	chr18:44530160-44530310	SAEC	small airway:	n/a	chr18:44530204-44530222
37	CTCF	chr18:44530140-44530290	AG04449	skin:	n/a	chr18:44530204-44530222
38	CTCF	chr18:44530100-44530250	HFF-Myc	foreskin:	n/a	chr18:44530204-44530222
39	CTCF	chr18:44530217-44530321	GM19240	blood:	n/a	n/a
40	CTCF	chr18:44530160-44530310	HPAF	blood vessel:	n/a	chr18:44530204-44530222
41	CTCF	chr18:44530160-44530310	GM12869	blood:	n/a	chr18:44530204-44530222
42	CTCF	chr18:44530140-44530290	HepG2	liver:	n/a	chr18:44530204-44530222
43	CTCF	chr18:44530120-44530270	HVMF	connective:	n/a	chr18:44530204-44530222
44	CTCF	chr18:44530200-44530350	HCT-116	colon:	n/a	chr18:44530204-44530222
45	CTCF	chr18:44530232-44530340	GM12892	blood:	n/a	n/a
46	CTCF	chr18:44530120-44530270	AG04449	skin:	n/a	chr18:44530204-44530222
47	CTCF	chr18:44530140-44530290	GM12865	blood:	n/a	chr18:44530204-44530222
48	CTCF	chr18:44530140-44530290	HFF	foreskin:	n/a	chr18:44530204-44530222
49	CTCF	chr18:44530140-44530290	WERI-Rb-1	eye:	n/a	chr18:44530204-44530222
50	CTCF	chr18:44530167-44530292	MCF-7	breast:	n/a	chr18:44530204-44530222

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44545807-44545857	NHDF-neo	bronchial:	n/a
2	chr18:44545807-44545857	NHDF-neo	bronchial:	n/a
3	chr18:44526743-44526793	HCM	heart:	n/a
4	chr18:44545794-44545844	U87	brain:	n/a
5	chr18:44526605-44526655	HRCEpiC	kidney:	n/a
6	chr18:44526756-44526806	NT2-D1	testis:	n/a
7	chr18:44526605-44526655	SKMC	muscle:	n/a
8	chr18:44545794-44545844	ECC-1	luminal epithelium:	n/a
9	chr18:44526867-44526917	U87	brain:	n/a
10	chr18:44527971-44528021	H1-hESC	embryonic stem cell:	embryo
11	chr18:44526756-44526806	SK-N-MC	brain:	n/a
12	chr18:44526700-44526750	AG09319	gingival:	n/a
13	chr18:44526707-44526757	NB4	blood:	n/a
14	chr18:44543612-44543662	AG09319	gingival:	n/a
15	chr18:44543612-44543662	HCM	heart:	n/a
16	chr18:44547161-44547211	HPAEpiC	pulmonary alveolar:	n/a
17	chr18:44543259-44543309	GM12891	blood:	n/a
18	chr18:44543612-44543662	NHBE	bronchial:	n/a
19	chr18:44543259-44543309	HEK293	kidney:	embryo
20	chr18:44543259-44543309	MCF10A-Er-Src	breast:	n/a
21	chr18:44527971-44528021	NT2-D1	testis:	n/a
22	chr18:44526430-44526480	ECC-1	luminal epithelium:	n/a
23	chr18:44544982-44545032	HepG2	liver:	n/a
24	chr18:44526756-44526806	HepG2	liver:	n/a
25	chr18:44543612-44543662	SKMC	muscle:	n/a
26	chr18:44527971-44528021	HCPEpiC	choroid plexus:	n/a
27	chr18:44530218-44530268	HPAEpiC	pulmonary alveolar:	n/a
28	chr18:44526700-44526750	NHBE	bronchial:	n/a
29	chr18:44545807-44545857	MCF-7	breast:	n/a
30	chr18:44541383-44541433	IMR90	lung:	fetal
31	chr18:44526707-44526757	NT2-D1	testis:	n/a
32	chr18:44526707-44526757	AG04449	skin:	fetal
33	chr18:44545807-44545857	HIPEpiC	eye:	n/a
34	chr18:44540890-44540940	HRPEpiC	eye:	n/a
35	chr18:44547161-44547211	MCF10A-Er-Src	breast:	n/a
36	chr18:44545794-44545844	Caco-2	colon:	n/a
37	chr18:44526867-44526917	CMK	blood:	n/a
38	chr18:44526430-44526480	HPAEpiC	pulmonary alveolar:	n/a
39	chr18:44527971-44528021	GM12892	blood:	n/a
40	chr18:44526867-44526917	LNCaP	prostate:	n/a
41	chr18:44526430-44526480	HCF	heart:	n/a
42	chr18:44530218-44530268	HRE	kidney:	n/a
43	chr18:44547161-44547211	MCF-7	breast:	n/a
44	chr18:44527026-44527076	PrEC	prostate:	n/a
45	chr18:44541383-44541433	MCF-7	breast:	n/a
46	chr18:44526707-44526757	Hepatocyte	liver:	n/a
47	chr18:44543259-44543309	Hepatocyte	liver:	n/a
48	chr18:44526430-44526480	HIPEpiC	eye:	n/a
49	chr18:44526700-44526750	GM06990	blood:	n/a
50	chr18:44547161-44547211	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:44529742..44530665-chr18:44562546..44563169,2	MCF-7	breast:
2	chr18:44526928..44528966-chr18:44543505..44545090,2	MCF-7	breast:
3	chr18:44494535..44496872-chr18:44526864..44529810,3	MCF-7	breast:
4	chr18:44497069..44499203-chr18:44524229..44526403,2	MCF-7	breast:

Variant related genes	Relation type
TCEB3CL2	TF binding region
KATNAL2	TF binding region
TCEB3CL2	CpG island
KATNAL2	CpG island
ENSG00000266996	chromatin interactions
ENSG00000078043	chromatin interactions
ENSG00000167216	chromatin interactions

Extended variants
information (count: 766 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:766 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182452691	chr18:44526453-44526454	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs536881811	chr18:44526498-44526499	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs148332628	chr18:44526535-44526536	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563124336	chr18:44526580-44526581	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs9304340	chr18:44526582-44526583	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs539350025	chr18:44526636-44526637	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs117601679	chr18:44526741-44526742	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs552906545	chr18:44526766-44526767	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs2187092	chr18:44526798-44526799	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs377608846	chr18:44526827-44526828	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs542308583	chr18:44526828-44526829	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs562071271	chr18:44526836-44526837	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs9973035	chr18:44526837-44526838	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs544784476	chr18:44526897-44526898	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs143094010	chr18:44526901-44526902	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
16	rs533620407	chr18:44526903-44526904	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
17	rs147040526	chr18:44526957-44526958	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs559297253	chr18:44526958-44526959	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs187086995	chr18:44526991-44526992	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs190259435	chr18:44527035-44527036	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568028341	chr18:44527098-44527099	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181511338	chr18:44527099-44527100	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs8095351	chr18:44527147-44527148	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs185641491	chr18:44527158-44527159	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs138267867	chr18:44527161-44527162	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552898582	chr18:44527267-44527268	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs118189636	chr18:44527277-44527278	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535518088	chr18:44527278-44527279	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs143732900	chr18:44527324-44527325	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575623081	chr18:44527368-44527369	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs8094654	chr18:44527397-44527398	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs532471052	chr18:44527407-44527408	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558343546	chr18:44527471-44527472	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs578235159	chr18:44527506-44527507	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190012010	chr18:44527547-44527548	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs72917200	chr18:44527549-44527550	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs569056381	chr18:44527582-44527583	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs541432045	chr18:44527602-44527603	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs114400351	chr18:44527613-44527614	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs537609744	chr18:44527641-44527642	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs530480008	chr18:44527645-44527646	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs550298857	chr18:44527660-44527661	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs570307581	chr18:44527661-44527662	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532989977	chr18:44527693-44527694	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs548711135	chr18:44527741-44527742	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182302348	chr18:44527835-44527836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566623149	chr18:44527852-44527853	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs72917202	chr18:44527854-44527855	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs555429535	chr18:44527875-44527876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs8095373	chr18:44527895-44527896	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
small cell lung cancer	17426248	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44520200-44526800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr18:44520400-44526400	Weak transcription	Osteobl	bone
3	chr18:44520800-44526400	Weak transcription	NHDF-Ad	bronchial
4	chr18:44520800-44526400	Weak transcription	NHLF	lung
5	chr18:44521000-44526400	Weak transcription	Psoas Muscle	Psoas
6	chr18:44521000-44526400	Weak transcription	HSMMtube	muscle
7	chr18:44523200-44526400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr18:44525400-44526600	Enhancers	Gastric	stomach
9	chr18:44526000-44527600	Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr18:44526200-44526400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr18:44526200-44526400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr18:44526200-44526400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr18:44526200-44526400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
14	chr18:44526200-44526400	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr18:44526200-44526400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr18:44526200-44526400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr18:44526200-44526400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
18	chr18:44526200-44526400	Enhancers	Primary B cells from cord blood	blood
19	chr18:44526200-44526400	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr18:44526200-44526400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr18:44526200-44526400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr18:44526200-44526400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr18:44526200-44526400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr18:44526200-44526400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr18:44526200-44526400	Enhancers	Adipose Nuclei	Adipose
26	chr18:44526200-44526400	Active TSS	Brain Germinal Matrix	brain
27	chr18:44526200-44526400	Enhancers	Fetal Thymus	thymus
28	chr18:44526200-44526400	Enhancers	HMEC	breast
29	chr18:44526200-44526400	Bivalent Enhancer	HUVEC	blood vessel
30	chr18:44526200-44526400	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr18:44526200-44526600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
32	chr18:44526200-44526600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr18:44526200-44526600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr18:44526200-44526600	Enhancers	Primary B cells from peripheral blood	blood
35	chr18:44526200-44526600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr18:44526200-44526600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
37	chr18:44526200-44526600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr18:44526200-44526600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
39	chr18:44526200-44526600	Flanking Active TSS	Fetal Brain Male	brain
40	chr18:44526200-44526600	Flanking Active TSS	Fetal Muscle Leg	muscle
41	chr18:44526200-44526600	Enhancers	Left Ventricle	heart
42	chr18:44526200-44526600	Flanking Active TSS	NH-A	brain
43	chr18:44526200-44527200	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr18:44526200-44527200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr18:44526200-44527200	Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr18:44526200-44527200	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr18:44526200-44527200	Active TSS	Liver	Liver
48	chr18:44526200-44527200	Active TSS	Brain Anterior Caudate	brain
49	chr18:44526200-44527200	Active TSS	Duodenum Smooth Muscle	Duodenum
50	chr18:44526200-44527200	Active TSS	Fetal Adrenal Gland	Adrenal Gland

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