Variant report

Variant	nsv891447
Chromosome Location	chr8:130724556-130754719
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	chr8:130738547-130738921	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:130740874-130741037	K562	blood:	n/a	n/a
3	ARID3A	chr8:130738533-130738902	K562	blood:	n/a	n/a
4	ARID3A	chr8:130734277-130734292	K562	blood:	n/a	n/a
5	ARID3A	chr8:130740929-130741022	HepG2	liver:	n/a	n/a
6	BACH1	chr8:130738640-130738754	K562	blood:	n/a	n/a
7	BHLHE40	chr8:130738532-130738794	K562	blood:	n/a	n/a
8	CBX3	chr8:130728107-130728639	HCT-116	colon:	n/a	n/a
9	CBX3	chr8:130728169-130728691	HCT-116	colon:	n/a	n/a
10	CBX3	chr8:130730566-130730821	K562	blood:	n/a	n/a
11	CBX3	chr8:130728209-130728650	K562	blood:	n/a	n/a
12	CBX3	chr8:130728253-130728570	K562	blood:	n/a	n/a
13	CEBPB	chr8:130741824-130742759	IMR90	lung:	n/a	n/a
14	CEBPB	chr8:130741902-130742188	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:130737676-130737782	K562	blood:	n/a	n/a
16	CEBPB	chr8:130735180-130735458	IMR90	lung:	n/a	n/a
17	CEBPB	chr8:130741823-130742196	A549	lung:	n/a	n/a
18	CEBPB	chr8:130734703-130734833	K562	blood:	n/a	n/a
19	CEBPB	chr8:130741910-130742100	K562	blood:	n/a	n/a
20	CTCF	chr8:130738680-130738830	HMF	breast:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
21	CTCF	chr8:130744140-130744290	AG09309	skin:	n/a	n/a
22	CTCF	chr8:130738620-130738770	GM12870	blood:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
23	CTCF	chr8:130741300-130741450	HMF	breast:	n/a	n/a
24	CTCF	chr8:130738584-130738819	GM19240	blood:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
25	CTCF	chr8:130738650-130738753	H1-hESC	embryonic stem cell:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
26	CTCF	chr8:130740920-130741070	HMEC	breast:	n/a	n/a
27	CTCF	chr8:130738660-130738810	HPAF	blood vessel:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
28	CTCF	chr8:130740911-130741033	GM12892	blood:	n/a	n/a
29	CTCF	chr8:130744113-130744327	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:130738660-130738810	SK-N-SH_RA	brain:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
31	CTCF	chr8:130738524-130738939	IMR90	lung:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
32	CTCF	chr8:130740860-130741010	HCT-116	colon:	n/a	n/a
33	CTCF	chr8:130738566-130738818	HepG2	liver:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
34	CTCF	chr8:130744163-130744306	Fibrobl	skin:	n/a	n/a
35	CTCF	chr8:130738660-130738810	AG09309	skin:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
36	CTCF	chr8:130738720-130738870	GM12866	blood:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
37	CTCF	chr8:130739380-130739530	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr8:130738680-130738830	A549	lung:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
39	CTCF	chr8:130740900-130741050	A549	lung:	n/a	n/a
40	CTCF	chr8:130738960-130739110	HMF	breast:	n/a	n/a
41	CTCF	chr8:130744120-130744270	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr8:130740873-130741061	LNCaP	prostate:	n/a	n/a
43	CTCF	chr8:130740900-130741050	AG10803	skin:	n/a	n/a
44	CTCF	chr8:130738600-130738883	Medullo	brain:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
45	CTCF	chr8:130738680-130738830	AG10803	skin:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
46	CTCF	chr8:130740860-130741010	AG04449	skin:	n/a	n/a
47	CTCF	chr8:130738628-130738855	Lung_OC	lung:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750
48	CTCF	chr8:130744140-130744290	AG04450	lung:	n/a	n/a
49	CTCF	chr8:130740781-130741285	K562	blood:	n/a	n/a
50	CTCF	chr8:130738496-130738901	HepG2	liver:	n/a	chr8:130738735-130738753 chr8:130738730-130738751 chr8:130738737-130738750

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:130738823-130738873	AG04449	skin:	fetal
2	chr8:130738823-130738873	SAEC	small airway:	n/a
3	chr8:130738823-130738873	HNPCEpiC	eye:	n/a
4	chr8:130738823-130738873	GM12892	blood:	n/a
5	chr8:130738823-130738873	HUVEC	blood vessel:	n/a
6	chr8:130738823-130738873	HepG2	liver:	n/a
7	chr8:130738823-130738873	HCF	heart:	n/a
8	chr8:130738823-130738873	GM19239	blood:	n/a
9	chr8:130738823-130738873	T-47D	breast:	n/a
10	chr8:130738823-130738873	A549	lung:	n/a
11	chr8:130738823-130738873	SK-N-SH	brain:	n/a
12	chr8:130738823-130738873	GM12891	blood:	n/a
13	chr8:130738823-130738873	PFSK-1	brain:	n/a
14	chr8:130738823-130738873	H1-hESC	embryonic stem cell:	embryo
15	chr8:130738823-130738873	NB4	blood:	n/a
16	chr8:130738823-130738873	HRE	kidney:	n/a
17	chr8:130738823-130738873	HEEpiC	esophagus:	n/a
18	chr8:130738823-130738873	ProgFib	skin:	n/a
19	chr8:130738823-130738873	HRPEpiC	eye:	n/a
20	chr8:130738823-130738873	BE2_C	brain:	n/a
21	chr8:130738823-130738873	Hepatocyte	liver:	n/a
22	chr8:130738823-130738873	U87	brain:	n/a
23	chr8:130738823-130738873	AG04450	lung:	fetal
24	chr8:130738823-130738873	IMR90	lung:	fetal
25	chr8:130738823-130738873	AG10803	skin:	n/a
26	chr8:130738823-130738873	K562	blood:	n/a
27	chr8:130738823-130738873	NHBE	bronchial:	n/a
28	chr8:130738823-130738873	MCF10A-Er-Src	breast:	n/a
29	chr8:130738823-130738873	Caco-2	colon:	n/a
30	chr8:130738823-130738873	SK-N-SH_RA	brain:	n/a
31	chr8:130738823-130738873	HMEC	breast:	n/a
32	chr8:130738823-130738873	MCF-7	breast:	n/a
33	chr8:130738823-130738873	RPTEC	kidney:	n/a
34	chr8:130738823-130738873	Hela-S3	cervix:	n/a
35	chr8:130738823-130738873	PrEC	prostate:	n/a
36	chr8:130738823-130738873	AG09309	skin:	n/a
37	chr8:130738823-130738873	HAEpiC	amniotic membrane:	n/a
38	chr8:130738823-130738873	AG09319	gingival:	n/a
39	chr8:130738823-130738873	AoSMC	blood vessel:	n/a
40	chr8:130738823-130738873	HIPEpiC	eye:	n/a
41	chr8:130738823-130738873	SK-N-MC	brain:	n/a
42	chr8:130738823-130738873	ECC-1	luminal epithelium:	n/a
43	chr8:130738823-130738873	SKMC	muscle:	n/a
44	chr8:130738823-130738873	ovcar-3	ovarian:	n/a
45	chr8:130738823-130738873	CMK	blood:	n/a
46	chr8:130738823-130738873	BJ	skin:	n/a
47	chr8:130738823-130738873	NHDF-neo	bronchial:	n/a
48	chr8:130738823-130738873	HPAEpiC	pulmonary alveolar:	n/a
49	chr8:130738823-130738873	GM06990	blood:	n/a
50	chr8:130738823-130738873	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr8:128747171..128749323-chr8:130738753..130740305,2	MCF-7	breast:
2	chr8:130699941..130700716-chr8:130738329..130738842,2	MCF-7	breast:
3	chr8:130593091..130595640-chr8:130733142..130736387,3	K562	blood:
4	chr8:130732259..130735444-chr8:130737069..130741081,4	K562	blood:
5	chr8:130717459..130720769-chr8:130721541..130726036,4	MCF-7	breast:
6	chr8:130724777..130726937-chr8:130738994..130740773,2	K562	blood:
7	chr8:130685068..130686753-chr8:130736730..130739405,2	K562	blood:
8	chr8:128748320..128750405-chr8:130724803..130726595,2	K562	blood:
9	chr8:128747251..128749651-chr8:130737243..130738948,2	K562	blood:
10	chr8:130694163..130694944-chr8:130737903..130739156,3	MCF-7	breast:
11	chr8:130721029..130723097-chr8:130725235..130727750,2	K562	blood:
12	chr8:130738688..130740229-chr8:130741129..130743486,2	K562	blood:
13	chr8:128748018..128748536-chr8:130738676..130739207,2	K562	blood:
14	chr8:130709093..130710072-chr8:130738277..130738889,2	MCF-7	breast:
15	chr8:130685068..130688410-chr8:130735715..130739405,3	K562	blood:
16	chr8:130699541..130700041-chr8:130738268..130738843,2	K562	blood:
17	chr8:130724777..130726937-chr8:130738994..130740773,2	K562	blood:
18	chr8:130719927..130722565-chr8:130723755..130726675,2	MCF-7	breast:
19	chr8:130738688..130740229-chr8:130741129..130743486,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYC-16	chr8:130740990-130741553	NONHSAT129131
2	lnc-MYC-16	chr8:130742037-130742257	NONHSAT129131
3	lnc-MYC-16	chr8:130742355-130742691	NONHSAT129131

Variant related genes	Relation type
ENSG00000224110	TF binding region
ENSG00000224110	CpG island
ENSG00000136997	chromatin interactions
ENSG00000224110	chromatin interactions

Extended variants
information (count: 1158 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:1158 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12679359	chr8:130724556-130724557	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554994411	chr8:130724566-130724567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143439011	chr8:130724610-130724611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546420532	chr8:130724727-130724728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564327723	chr8:130724743-130724744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182603573	chr8:130724760-130724761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573396527	chr8:130724797-130724798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576353895	chr8:130724807-130724808	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543725118	chr8:130724816-130724817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562008604	chr8:130724823-130724824	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs12547506	chr8:130724921-130724922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs4467908	chr8:130724937-130724938	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs540664039	chr8:130724943-130724944	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs559068723	chr8:130725009-130725010	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs187311057	chr8:130725013-130725014	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192126885	chr8:130725071-130725072	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10094846	chr8:130725082-130725083	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570682181	chr8:130725124-130725125	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs538004344	chr8:130725139-130725140	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550109924	chr8:130725182-130725183	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs147992918	chr8:130725190-130725191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs372509038	chr8:130725209-130725210	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs183200179	chr8:130725257-130725258	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs62523852	chr8:130725280-130725281	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs563918659	chr8:130725304-130725305	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs116354977	chr8:130725320-130725321	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs140584342	chr8:130725339-130725340	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs576241946	chr8:130725370-130725371	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs543567176	chr8:130725375-130725376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188678108	chr8:130725417-130725418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs150487936	chr8:130725442-130725443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs574246118	chr8:130725465-130725466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs138394007	chr8:130725471-130725472	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs193020940	chr8:130725488-130725489	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533331651	chr8:130725519-130725520	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs115510166	chr8:130725522-130725523	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs563733514	chr8:130725543-130725544	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531538192	chr8:130725554-130725555	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs62523853	chr8:130725557-130725558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs549999997	chr8:130725559-130725560	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs142936610	chr8:130725560-130725561	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535373720	chr8:130725590-130725591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs547399987	chr8:130725606-130725607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565558883	chr8:130725632-130725633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539009504	chr8:130725639-130725640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs148846943	chr8:130725652-130725653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11407061	chr8:130725653-130725654	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs78338480	chr8:130725654-130725655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs557439062	chr8:130725662-130725663	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs6470764	chr8:130725665-130725666	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease

Variant related diseases (count:154)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	16620391	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130719800-130725600	Enhancers	K562	blood
2	chr8:130720600-130724800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:130720800-130725600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:130721000-130724600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:130721600-130725400	Weak transcription	HSMMtube	muscle
6	chr8:130721600-130725600	Weak transcription	Fetal Stomach	stomach
7	chr8:130722200-130724600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:130722400-130725000	Weak transcription	Fetal Lung	lung
9	chr8:130723200-130734600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:130723400-130725000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr8:130723400-130725000	Weak transcription	Placenta	Placenta
12	chr8:130723400-130725400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr8:130723400-130726800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr8:130723400-130740400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr8:130723600-130725200	Weak transcription	NHDF-Ad	bronchial
16	chr8:130723600-130725600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr8:130723800-130725200	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr8:130724000-130725400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:130724000-130726200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:130724600-130726800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr8:130724600-130727800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr8:130724800-130726600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr8:130725000-130725400	Enhancers	Fetal Lung	lung
24	chr8:130725000-130725600	Enhancers	Placenta	Placenta
25	chr8:130725000-130725800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr8:130725200-130725400	Enhancers	HSMM	muscle
27	chr8:130725200-130726000	Enhancers	Placenta Amnion	Placenta Amnion
28	chr8:130725200-130726200	Enhancers	NHDF-Ad	bronchial
29	chr8:130725400-130725600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr8:130725400-130725600	Enhancers	HSMMtube	muscle
31	chr8:130725400-130726200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr8:130725600-130725800	Weak transcription	HSMMtube	muscle
33	chr8:130725600-130726200	Enhancers	Fetal Stomach	stomach
34	chr8:130725600-130726200	Enhancers	A549	lung
35	chr8:130725600-130726600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:130726400-130726600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr8:130733800-130734800	Enhancers	K562	blood
38	chr8:130734000-130735000	Enhancers	HSMMtube	muscle
39	chr8:130734600-130735400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr8:130734600-130735400	Enhancers	Osteobl	bone
41	chr8:130734800-130735600	Enhancers	A549	lung
42	chr8:130734800-130737200	Weak transcription	K562	blood
43	chr8:130735400-130738400	Weak transcription	Osteobl	bone
44	chr8:130735400-130742600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:130735600-130737200	Weak transcription	A549	lung
46	chr8:130737200-130739200	Enhancers	A549	lung
47	chr8:130737200-130740800	Enhancers	K562	blood
48	chr8:130737800-130738600	Enhancers	Fetal Heart	heart
49	chr8:130738000-130739200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr8:130738200-130738400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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