Variant report

Variant	nsv971698
Chromosome Location	chr8:124409783-124416455
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:84)
CpG islands
(count:183)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:84 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:124415851-124416343	HepG2	liver:	n/a	n/a
2	BHLHE40	chr8:124409783-124409928	GM12878	blood:	n/a	n/a
3	BHLHE40	chr8:124415931-124416283	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:124414956-124414982	IMR90	lung:	n/a	n/a
5	CEBPB	chr8:124414942-124415026	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:124415958-124416290	HepG2	liver:	n/a	n/a
7	CEBPD	chr8:124415892-124416310	HepG2	liver:	n/a	n/a
8	CTCF	chr8:124414240-124414390	GM12874	blood:	n/a	n/a
9	CTCF	chr8:124414184-124414215	LNCaP	prostate:	n/a	n/a
10	CTCF	chr8:124416080-124416230	Caco-2	colon:	n/a	n/a
11	CTCF	chr8:124414360-124414510	HepG2	liver:	n/a	n/a
12	E2F4	chr8:124407644-124410228	MCF10A-Er-Src	breast:	n/a	chr8:124409072-124409084 chr8:124408970-124408981 chr8:124408746-124408758 chr8:124408685-124408696 chr8:124408971-124408978 chr8:124409016-124409025 chr8:124408971-124408979 chr8:124408971-124408982 chr8:124408665-124408680 chr8:124408971-124408979 chr8:124408970-124408978 chr8:124408984-124408993 chr8:124408682-124408699 chr8:124408972-124408987 chr8:124408970-124408980
13	E2F6	chr8:124409830-124410403	H1-hESC	embryonic stem cell:	n/a	n/a
14	E2F6	chr8:124410066-124410233	H1-hESC	embryonic stem cell:	n/a	n/a
15	ELF1	chr8:124415948-124416270	HepG2	liver:	n/a	n/a
16	ELF1	chr8:124415960-124416309	HepG2	liver:	n/a	n/a
17	EP300	chr8:124415867-124416416	HepG2	liver:	n/a	n/a
18	EP300	chr8:124415927-124416407	HepG2	liver:	n/a	n/a
19	EP300	chr8:124409749-124409800	GM12878	blood:	n/a	n/a
20	EP300	chr8:124415712-124416337	HepG2	liver:	n/a	n/a
21	FOSL2	chr8:124415802-124416272	HepG2	liver:	n/a	n/a
22	FOXA1	chr8:124415763-124416325	HepG2	liver:	n/a	n/a
23	FOXA1	chr8:124415809-124416469	HepG2	liver:	n/a	n/a
24	FOXA1	chr8:124415890-124416394	HepG2	liver:	n/a	n/a
25	FOXA1	chr8:124415837-124416402	HepG2	liver:	n/a	n/a
26	FOXA2	chr8:124415933-124416273	A549	lung:	n/a	n/a
27	FOXA2	chr8:124415897-124416320	HepG2	liver:	n/a	n/a
28	FOXA2	chr8:124415538-124418528	HepG2	liver:	n/a	n/a
29	HDAC2	chr8:124415826-124416355	HepG2	liver:	n/a	n/a
30	HDAC2	chr8:124415831-124416265	HepG2	liver:	n/a	n/a
31	HEY1	chr8:124415748-124416788	HepG2	liver:	n/a	n/a
32	HEY1	chr8:124415852-124416376	HepG2	liver:	n/a	n/a
33	HNF4A	chr8:124415892-124416233	HepG2	liver:	n/a	n/a
34	HNF4A	chr8:124415846-124416304	HepG2	liver:	n/a	n/a
35	HNF4G	chr8:124415922-124416316	HepG2	liver:	n/a	n/a
36	HNF4G	chr8:124415876-124416242	HepG2	liver:	n/a	n/a
37	JUND	chr8:124415974-124416229	HepG2	liver:	n/a	n/a
38	JUND	chr8:124415967-124416277	HepG2	liver:	n/a	n/a
39	MAFF	chr8:124415997-124416373	HepG2	liver:	n/a	n/a
40	MAFK	chr8:124415901-124416321	HepG2	liver:	n/a	n/a
41	MAFK	chr8:124416012-124416357	HepG2	liver:	n/a	n/a
42	MAX	chr8:124415662-124416461	HepG2	liver:	n/a	chr8:124415902-124415911
43	MBD4	chr8:124415689-124416404	HepG2	liver:	n/a	n/a
44	MBD4	chr8:124415621-124416385	HepG2	liver:	n/a	n/a
45	MXI1	chr8:124415858-124416324	HepG2	liver:	n/a	n/a
46	MYBL2	chr8:124415497-124416737	HepG2	liver:	n/a	n/a
47	MYBL2	chr8:124415662-124416376	HepG2	liver:	n/a	n/a
48	MYC	chr8:124416075-124416078	NB4	blood:	n/a	n/a
49	MYC	chr8:124415967-124415968	HepG2	liver:	n/a	n/a
50	MYC	chr8:124415976-124416273	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:124412914-124412964	HAEpiC	amniotic membrane:	n/a
2	chr8:124412845-124412895	PrEC	prostate:	n/a
3	chr8:124413003-124413053	HepG2	liver:	n/a
4	chr8:124412914-124412964	ovcar-3	ovarian:	n/a
5	chr8:124412845-124412895	CMK	blood:	n/a
6	chr8:124412914-124412964	AG04449	skin:	fetal
7	chr8:124413003-124413053	NB4	blood:	n/a
8	chr8:124412845-124412895	AG09309	skin:	n/a
9	chr8:124412845-124412895	SK-N-SH	brain:	n/a
10	chr8:124413003-124413053	GM19239	blood:	n/a
11	chr8:124412914-124412964	NB4	blood:	n/a
12	chr8:124413003-124413053	K562	blood:	n/a
13	chr8:124413003-124413053	IMR90	lung:	fetal
14	chr8:124412845-124412895	BJ	skin:	n/a
15	chr8:124412914-124412964	NT2-D1	testis:	n/a
16	chr8:124412845-124412895	HL-60	blood:	n/a
17	chr8:124412914-124412964	T-47D	breast:	n/a
18	chr8:124412845-124412895	Hepatocyte	liver:	n/a
19	chr8:124413003-124413053	HL-60	blood:	n/a
20	chr8:124413003-124413053	NHBE	bronchial:	n/a
21	chr8:124413003-124413053	ovcar-3	ovarian:	n/a
22	chr8:124412914-124412964	LNCaP	prostate:	n/a
23	chr8:124412845-124412895	GM12878	blood:	n/a
24	chr8:124412914-124412964	NH-A	brain:	n/a
25	chr8:124413003-124413053	HEEpiC	esophagus:	n/a
26	chr8:124412845-124412895	SK-N-MC	brain:	n/a
27	chr8:124412914-124412964	HCT-116	colon:	n/a
28	chr8:124413003-124413053	HNPCEpiC	eye:	n/a
29	chr8:124412914-124412964	PrEC	prostate:	n/a
30	chr8:124412845-124412895	HCF	heart:	n/a
31	chr8:124413003-124413053	GM12878	blood:	n/a
32	chr8:124413003-124413053	SAEC	small airway:	n/a
33	chr8:124412914-124412964	HRE	kidney:	n/a
34	chr8:124413003-124413053	AG04449	skin:	fetal
35	chr8:124412914-124412964	ProgFib	skin:	n/a
36	chr8:124412914-124412964	AoSMC	blood vessel:	n/a
37	chr8:124412914-124412964	SK-N-MC	brain:	n/a
38	chr8:124413003-124413053	Caco-2	colon:	n/a
39	chr8:124412914-124412964	HIPEpiC	eye:	n/a
40	chr8:124413003-124413053	T-47D	breast:	n/a
41	chr8:124412914-124412964	CMK	blood:	n/a
42	chr8:124412845-124412895	HNPCEpiC	eye:	n/a
43	chr8:124412845-124412895	HCT-116	colon:	n/a
44	chr8:124412914-124412964	IMR90	lung:	fetal
45	chr8:124412845-124412895	A549	lung:	n/a
46	chr8:124412914-124412964	Hepatocyte	liver:	n/a
47	chr8:124412845-124412895	H1-hESC	embryonic stem cell:	embryo
48	chr8:124412845-124412895	AG04449	skin:	fetal
49	chr8:124412914-124412964	HEEpiC	esophagus:	n/a
50	chr8:124413003-124413053	CMK	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:124406625..124409750-chr8:124412518..124416367,5	K562	blood:
2	chr8:124406688..124410730-chr8:124426992..124430866,9	K562	blood:
3	chr8:124406056..124410111-chr8:124427174..124433258,8	MCF-7	breast:
4	chr8:124408566..124410301-chr8:124410632..124412919,2	MCF-7	breast:
5	chr8:124286665..124288585-chr8:124408066..124410491,3	K562	blood:
6	chr8:124405499..124410730-chr8:124426606..124431705,19	K562	blood:
7	chr8:124415153..124417409-chr8:124424066..124426465,2	K562	blood:
8	chr8:124283826..124290020-chr8:124406062..124410538,8	MCF-7	breast:
9	chr8:124412641..124414334-chr8:124426914..124428862,2	K562	blood:
10	chr8:124283412..124288800-chr8:124404176..124410687,11	K562	blood:
11	chr8:124416051..124418848-chr8:124419770..124421913,2	MCF-7	breast:
12	chr8:124408566..124410301-chr8:124410632..124412919,2	MCF-7	breast:
13	chr8:124411247..124413629-chr8:124428301..124430441,2	K562	blood:
14	chr8:124409346..124411086-chr8:124417132..124419397,2	K562	blood:
15	chr8:124404505..124411576-chr8:124423647..124430734,19	MCF-7	breast:

No data

Variant related genes	Relation type
ATAD2	TF binding region
IMPDH1P6	TF binding region
ATAD2	CpG island
IMPDH1P6	CpG island
ENSG00000254294	chromatin interactions
ENSG00000156795	chromatin interactions
ENSG00000165156	chromatin interactions
ENSG00000156802	chromatin interactions

Extended variants
information (count: 256 )
Associated
traits (count: 143 )

Variant overlapped rSNPs/rCNVs (count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78448759	chr8:124409805-124409806	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs566396946	chr8:124409815-124409816	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs536092960	chr8:124409911-124409912	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs555987655	chr8:124409972-124409973	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs576041981	chr8:124410019-124410020	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs185599412	chr8:124410037-124410038	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs558459443	chr8:124410096-124410097	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs577981661	chr8:124410137-124410138	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs16898263	chr8:124410142-124410143	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs560684200	chr8:124410160-124410161	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs73323704	chr8:124410172-124410173	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs183113546	chr8:124410255-124410256	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs114763914	chr8:124410275-124410276	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs187849224	chr8:124410304-124410305	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs115767754	chr8:124410332-124410333	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs116804374	chr8:124410333-124410334	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs577030442	chr8:124410415-124410416	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs190941763	chr8:124410431-124410432	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs371082958	chr8:124410452-124410453	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs546274760	chr8:124410497-124410498	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs566601029	chr8:124410515-124410516	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs183893401	chr8:124410534-124410535	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs139699836	chr8:124410563-124410564	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs369058236	chr8:124410583-124410584	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs7000034	chr8:124410587-124410588	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs538406067	chr8:124410653-124410654	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs558496762	chr8:124410659-124410660	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs187759025	chr8:124410706-124410707	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs534240198	chr8:124410730-124410731	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs112324590	chr8:124410731-124410732	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs574107467	chr8:124410783-124410784	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs7000575	chr8:124410820-124410821	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs556207594	chr8:124410821-124410822	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs191956518	chr8:124410847-124410848	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556221528	chr8:124410855-124410856	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs543958269	chr8:124410896-124410897	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs111228606	chr8:124410943-124410944	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs564450514	chr8:124410944-124410945	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs533066233	chr8:124411034-124411035	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs542572305	chr8:124411045-124411046	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs560755353	chr8:124411097-124411098	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs75461903	chr8:124411122-124411123	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs528866161	chr8:124411143-124411144	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs184384579	chr8:124411182-124411183	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs13252796	chr8:124411269-124411270	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs56029347	chr8:124411273-124411274	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs531991643	chr8:124411279-124411280	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs374179542	chr8:124411303-124411304	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs367837426	chr8:124411329-124411330	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs551674532	chr8:124411333-124411334	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:143)

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
Acute myeloid leukemia	20729466	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
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
Carcinoma ex pleomorphic adenoma	18828159	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
Congenital diaphragmatic hernia	21085971	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
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	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
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164919	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124407000-124409800	Active TSS	Rectal Mucosa Donor 29	rectum
2	chr8:124408200-124409800	Active TSS	Brain Cingulate Gyrus	brain
3	chr8:124409000-124409800	Flanking Active TSS	Dnd41	blood
4	chr8:124409000-124412800	Weak transcription	Gastric	stomach
5	chr8:124409000-124412800	Weak transcription	Pancreas	Pancrea
6	chr8:124409200-124409800	Enhancers	Hela-S3	cervix
7	chr8:124409200-124413000	Weak transcription	Esophagus	oesophagus
8	chr8:124409200-124413000	Weak transcription	Lung	lung
9	chr8:124409200-124415600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr8:124409400-124409800	Enhancers	H9 Cell Line	embryonic stem cell
11	chr8:124409400-124409800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chr8:124409400-124409800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr8:124409400-124409800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:124409400-124409800	Enhancers	Primary B cells from peripheral blood	blood
15	chr8:124409400-124409800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr8:124409400-124409800	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr8:124409400-124409800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr8:124409400-124409800	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr8:124409400-124409800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:124409400-124409800	Enhancers	Fetal Kidney	kidney
21	chr8:124409400-124409800	Enhancers	NHDF-Ad	bronchial
22	chr8:124409400-124410200	Enhancers	K562	blood
23	chr8:124409400-124412800	Weak transcription	Fetal Intestine Small	intestine
24	chr8:124409400-124412800	Weak transcription	Fetal Stomach	stomach
25	chr8:124409400-124413000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr8:124409400-124413200	Weak transcription	Colon Smooth Muscle	Colon
27	chr8:124409400-124413600	Weak transcription	Fetal Brain Male	brain
28	chr8:124409400-124414000	Weak transcription	Primary hematopoietic stem cells	blood
29	chr8:124409400-124415400	Weak transcription	Liver	Liver
30	chr8:124409400-124415800	Weak transcription	Fetal Intestine Large	intestine
31	chr8:124409400-124415800	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr8:124409400-124419200	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr8:124409400-124421400	Weak transcription	Right Ventricle	heart
34	chr8:124409400-124424800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr8:124409400-124427600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr8:124409400-124427600	Weak transcription	A549	lung
37	chr8:124409400-124428000	Weak transcription	Brain Anterior Caudate	brain
38	chr8:124409600-124409800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
39	chr8:124409600-124409800	Active TSS	Primary T cells from cord blood	blood
40	chr8:124409600-124409800	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr8:124409600-124409800	Active TSS	Thymus	Thymus
42	chr8:124409600-124410000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
43	chr8:124409600-124412600	Weak transcription	HepG2	liver
44	chr8:124409600-124414800	Weak transcription	Fetal Heart	heart
45	chr8:124409600-124417800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr8:124409600-124424600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr8:124409600-124424800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr8:124409800-124410200	Enhancers	Dnd41	blood
49	chr8:124409800-124415800	Weak transcription	Hela-S3	cervix
50	chr8:124409800-124424600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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