Variant report

Variant	esv3384926
Chromosome Location	chr8:100026040-100027833
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	ATF2	chr8:100024655-100026274	GM12878	blood:	n/a	n/a
2	BCLAF1	chr8:100024836-100026154	GM12878	blood:	n/a	chr8:100025253-100025262 chr8:100025599-100025612 chr8:100025221-100025234 chr8:100025419-100025432 chr8:100025201-100025214 chr8:100025210-100025223
3	BCLAF1	chr8:100024708-100026259	GM12878	blood:	n/a	chr8:100025253-100025262 chr8:100025599-100025612 chr8:100024802-100024811 chr8:100025221-100025234 chr8:100025419-100025432 chr8:100025201-100025214 chr8:100025210-100025223
4	BRCA1	chr8:100025226-100026216	Hela-S3	cervix:	n/a	n/a
5	CCNT2	chr8:100025079-100026178	K562	blood:	n/a	chr8:100025912-100025932 chr8:100025290-100025299
6	CHD1	chr8:100024865-100026237	GM12878	blood:	n/a	n/a
7	CREB1	chr8:100024910-100026059	K562	blood:	n/a	n/a
8	CUX1	chr8:100025008-100026070	K562	blood:	n/a	n/a
9	EBF1	chr8:100026032-100026065	GM12878	blood:	n/a	n/a
10	EGR1	chr8:100024787-100026086	HCT-116	colon:	n/a	chr8:100024798-100024811 chr8:100025285-100025295 chr8:100025253-100025262
11	ELF1	chr8:100024527-100026056	HCT-116	colon:	n/a	chr8:100025484-100025493 chr8:100025203-100025215 chr8:100025253-100025264 chr8:100025201-100025210
12	ELF1	chr8:100024665-100026193	HCT-116	colon:	n/a	chr8:100025484-100025493 chr8:100025203-100025215 chr8:100025253-100025264 chr8:100025201-100025210
13	ELF1	chr8:100024649-100026279	MCF-7	breast:	n/a	chr8:100025484-100025493 chr8:100025203-100025215 chr8:100025253-100025264 chr8:100025201-100025210
14	ELF1	chr8:100024896-100026206	SK-N-SH	brain:	n/a	chr8:100025484-100025493 chr8:100025203-100025215 chr8:100025253-100025264 chr8:100025201-100025210
15	ELF1	chr8:100024692-100026252	MCF-7	breast:	n/a	chr8:100025484-100025493 chr8:100025203-100025215 chr8:100025253-100025264 chr8:100025201-100025210
16	ELK1	chr8:100024848-100026145	Hela-S3	cervix:	n/a	chr8:100025253-100025262 chr8:100025253-100025262
17	FOS	chr8:100026046-100026053	MCF10A-Er-Src	breast:	n/a	n/a
18	GABPA	chr8:100024714-100026079	A549	lung:	n/a	chr8:100025202-100025216
19	GABPA	chr8:100024500-100026344	MCF-7	breast:	n/a	chr8:100025202-100025216
20	GABPA	chr8:100024784-100026273	SK-N-SH	brain:	n/a	chr8:100025202-100025216
21	GATA1	chr8:100024141-100026319	PBDE	blood:	n/a	chr8:100024663-100024679
22	GTF2F1	chr8:100024827-100026163	Hela-S3	cervix:	n/a	chr8:100025871-100025882
23	GTF2F1	chr8:100025995-100026150	H1-hESC	embryonic stem cell:	n/a	n/a
24	HA-E2F1	chr8:100024255-100026043	MCF-7	breast:	n/a	n/a
25	HDAC2	chr8:100024936-100026269	MCF-7	breast:	n/a	n/a
26	HMGN3	chr8:100025053-100026156	K562	blood:	n/a	n/a
27	IRF1	chr8:100024995-100026165	K562	blood:	n/a	n/a
28	IRF1	chr8:100024407-100026287	K562	blood:	n/a	n/a
29	JUND	chr8:100024870-100026112	H1-hESC	embryonic stem cell:	n/a	n/a
30	JUND	chr8:100024689-100026331	K562	blood:	n/a	n/a
31	KAP1	chr8:100024740-100026166	HEK293	kidney:	n/a	n/a
32	KAP1	chr8:100024839-100026157	U2OS	brain:	n/a	n/a
33	MAFK	chr8:100025038-100026137	Hela-S3	cervix:	n/a	n/a
34	MAX	chr8:100024762-100026176	NB4	blood:	n/a	chr8:100025597-100025607
35	MAX	chr8:100024598-100026302	MCF-7	breast:	n/a	chr8:100025597-100025607
36	MAX	chr8:100024891-100026179	Hela-S3	cervix:	n/a	chr8:100025597-100025607
37	MAZ	chr8:100024742-100026089	Hela-S3	cervix:	n/a	chr8:100025597-100025607
38	MAZ	chr8:100024647-100026137	K562	blood:	n/a	chr8:100025597-100025607
39	MAZ	chr8:100024684-100026174	GM12878	blood:	n/a	chr8:100025597-100025607
40	MAZ	chr8:100024120-100026176	IMR90	lung:	n/a	chr8:100025597-100025607
41	MTA3	chr8:100024230-100026277	GM12878	blood:	n/a	n/a
42	MTA3	chr8:100024570-100026171	GM12878	blood:	n/a	n/a
43	MXI1	chr8:100024783-100026132	GM12878	blood:	n/a	n/a
44	MYC	chr8:100024754-100026273	K562	blood:	n/a	chr8:100025597-100025607
45	MYC	chr8:100025945-100026139	MCF10A-Er-Src	breast:	n/a	n/a
46	MYC	chr8:100024352-100026261	K562	blood:	n/a	chr8:100025597-100025607
47	MYC	chr8:100024894-100026203	NB4	blood:	n/a	chr8:100025597-100025607
48	PML	chr8:100024711-100026278	GM12878	blood:	n/a	n/a
49	POLR2A	chr8:100024758-100026178	GM19099	blood:	n/a	n/a
50	POLR2A	chr8:100024859-100026226	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100026087-100026137	HIPEpiC	eye:	n/a
2	chr8:100026087-100026137	CMK	blood:	n/a
3	chr8:100026087-100026137	HCPEpiC	choroid plexus:	n/a
4	chr8:100026087-100026137	SAEC	small airway:	n/a
5	chr8:100026087-100026137	BE2_C	brain:	n/a
6	chr8:100026087-100026137	HNPCEpiC	eye:	n/a
7	chr8:100026087-100026137	NH-A	brain:	n/a
8	chr8:100026087-100026137	Caco-2	colon:	n/a
9	chr8:100026087-100026137	HCT-116	colon:	n/a
10	chr8:100026087-100026137	HEEpiC	esophagus:	n/a
11	chr8:100026087-100026137	U87	brain:	n/a
12	chr8:100026087-100026137	HCM	heart:	n/a
13	chr8:100026087-100026137	PrEC	prostate:	n/a
14	chr8:100026087-100026137	NHBE	bronchial:	n/a
15	chr8:100026087-100026137	HMEC	breast:	n/a
16	chr8:100026087-100026137	IMR90	lung:	fetal
17	chr8:100026087-100026137	T-47D	breast:	n/a
18	chr8:100026087-100026137	SK-N-MC	brain:	n/a
19	chr8:100026087-100026137	Hepatocyte	liver:	n/a
20	chr8:100026087-100026137	HRE	kidney:	n/a
21	chr8:100026087-100026137	GM19239	blood:	n/a
22	chr8:100026087-100026137	AG04449	skin:	fetal
23	chr8:100026087-100026137	HRCEpiC	kidney:	n/a
24	chr8:100026087-100026137	MCF-7	breast:	n/a
25	chr8:100026087-100026137	NHDF-neo	bronchial:	n/a
26	chr8:100026087-100026137	NT2-D1	testis:	n/a
27	chr8:100026087-100026137	MCF10A-Er-Src	breast:	n/a
28	chr8:100026087-100026137	PANC-1	pancreas:	n/a
29	chr8:100026087-100026137	HEK293	kidney:	embryo
30	chr8:100026087-100026137	ovcar-3	ovarian:	n/a
31	chr8:100026087-100026137	Jurkat	blood:	n/a
32	chr8:100026087-100026137	GM12891	blood:	n/a
33	chr8:100026087-100026137	AG09309	skin:	n/a
34	chr8:100026087-100026137	HAEpiC	amniotic membrane:	n/a
35	chr8:100026087-100026137	HUVEC	blood vessel:	n/a
36	chr8:100026087-100026137	NB4	blood:	n/a
37	chr8:100026087-100026137	HL-60	blood:	n/a
38	chr8:100026087-100026137	GM12878	blood:	n/a
39	chr8:100026087-100026137	ECC-1	luminal epithelium:	n/a
40	chr8:100026087-100026137	H1-hESC	embryonic stem cell:	embryo
41	chr8:100026087-100026137	LNCaP	prostate:	n/a
42	chr8:100026087-100026137	HRPEpiC	eye:	n/a
43	chr8:100026087-100026137	AoSMC	blood vessel:	n/a
44	chr8:100026087-100026137	AG10803	skin:	n/a
45	chr8:100026087-100026137	SKMC	muscle:	n/a
46	chr8:100026087-100026137	SK-N-SH	brain:	n/a
47	chr8:100026087-100026137	K562	blood:	n/a
48	chr8:100026087-100026137	AG09319	gingival:	n/a
49	chr8:100026087-100026137	HCF	heart:	n/a
50	chr8:100026087-100026137	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:100025901..100029663-chr8:100033487..100035486,3	K562	blood:
2	chr8:99952762..99963438-chr8:100019139..100031293,37	MCF-7	breast:
3	chr8:99677331..99680175-chr8:100027131..100030033,2	K562	blood:
4	chr8:100013186..100018258-chr8:100022769..100026424,8	MCF-7	breast:
5	chr15:66161556..66162059-chr8:100025171..100026075,2	HCT-116	colon:
6	chr8:100024284..100027084-chr8:100113982..100120280,5	MCF-7	breast:
7	chr8:100025833..100028756-chr8:100100624..100103335,2	MCF-7	breast:
8	chr8:100027143..100028710-chr8:100248941..100251194,2	MCF-7	breast:
9	chr8:100011149..100013712-chr8:100025594..100027308,2	K562	blood:
10	chr8:99953586..99962238-chr8:100023509..100028680,26	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253948	TF binding region
ENSG00000253948	CpG island
ENSG00000164920	chromatin interactions
ENSG00000103769	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000253180	chromatin interactions
ENSG00000104375	chromatin interactions
ENSG00000271930	chromatin interactions
ENSG00000263842	chromatin interactions

Extended variants
information (count: 63 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:63 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200327756	chr8:100026072-100026073	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs570877761	chr8:100026085-100026086	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs76932157	chr8:100026108-100026109	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs533575514	chr8:100026158-100026159	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs376108160	chr8:100026169-100026170	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs553809125	chr8:100026187-100026188	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs370810574	chr8:100026195-100026196	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs370135609	chr8:100026204-100026205	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs376340256	chr8:100026214-100026215	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs75894652	chr8:100026223-100026224	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs542402509	chr8:100026237-100026238	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs117681770	chr8:100026253-100026254	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs575915633	chr8:100026256-100026257	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs544881230	chr8:100026274-100026275	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs12547849	chr8:100026275-100026276	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs533336132	chr8:100026290-100026291	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs372136815	chr8:100026309-100026310	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs375146579	chr8:100026319-100026320	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs368125133	chr8:100026324-100026325	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs372638426	chr8:100026338-100026339	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs200536141	chr8:100026341-100026342	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs540300620	chr8:100026346-100026347	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs560622705	chr8:100026382-100026383	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs140602855	chr8:100026407-100026408	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs549068809	chr8:100026431-100026432	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs150463935	chr8:100026437-100026438	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs531416615	chr8:100026574-100026575	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs551235907	chr8:100026597-100026598	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs571480777	chr8:100026615-100026616	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs533766761	chr8:100026617-100026618	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs547118858	chr8:100026684-100026685	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs531558105	chr8:100026698-100026699	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs145333327	chr8:100026722-100026723	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs535922111	chr8:100026893-100026894	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs556304305	chr8:100026900-100026901	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs79241471	chr8:100026920-100026921	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs574786628	chr8:100026930-100026931	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs199642709	chr8:100026939-100026940	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs573450236	chr8:100026949-100026950	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs558471711	chr8:100026951-100026952	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs117956603	chr8:100026975-100026976	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs140297552	chr8:100026991-100026992	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs566708827	chr8:100027027-100027028	Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs560240569	chr8:100027031-100027032	Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs547243508	chr8:100027200-100027201	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs187313852	chr8:100027216-100027217	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs573986922	chr8:100027296-100027297	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs35213007	chr8:100027443-100027444	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs79417787	chr8:100027456-100027457	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs542676514	chr8:100027504-100027505	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	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
Cancer	20164919	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	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
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cohen syndrome	20461111	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:365 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100023200-100027200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:100023200-100027200	Active TSS	K562	blood
3	chr8:100023600-100027000	Active TSS	HUES64 Cell Line	embryonic stem cell
4	chr8:100023800-100026400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr8:100024000-100026800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr8:100024000-100026800	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr8:100024000-100027200	Active TSS	NHLF	lung
8	chr8:100024200-100026400	Active TSS	iPS-18 Cell Line	embryonic stem cell
9	chr8:100024200-100026400	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr8:100024200-100026400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:100024200-100026600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr8:100024200-100026600	Active TSS	NH-A	brain
13	chr8:100024200-100026800	Active TSS	Muscle Satellite Cultured Cells	--
14	chr8:100024200-100027000	Active TSS	HSMMtube	muscle
15	chr8:100024400-100026200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr8:100024400-100026200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr8:100024400-100026200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr8:100024400-100026200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr8:100024400-100026200	Bivalent/Poised TSS	HepG2	liver
20	chr8:100024400-100026400	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr8:100024400-100026400	Active TSS	H1 Cell Line	embryonic stem cell
22	chr8:100024400-100026400	Active TSS	H9 Cell Line	embryonic stem cell
23	chr8:100024400-100026400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
24	chr8:100024400-100026400	Active TSS	Aorta	Aorta
25	chr8:100024400-100026800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr8:100024400-100026800	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr8:100024400-100027000	Active TSS	Ovary	ovary
28	chr8:100024400-100027200	Active TSS	NHDF-Ad	bronchial
29	chr8:100024600-100026200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr8:100024600-100026200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr8:100024600-100026200	Active TSS	Esophagus	oesophagus
32	chr8:100024600-100026200	Active TSS	Fetal Muscle Trunk	muscle
33	chr8:100024600-100026200	Active TSS	Gastric	stomach
34	chr8:100024600-100026200	Active TSS	Left Ventricle	heart
35	chr8:100024600-100026200	Active TSS	Lung	lung
36	chr8:100024600-100026200	Active TSS	Placenta Amnion	Placenta Amnion
37	chr8:100024600-100026200	Active TSS	Sigmoid Colon	Sigmoid Colon
38	chr8:100024600-100026200	Active TSS	Small Intestine	intestine
39	chr8:100024600-100026200	Active TSS	Stomach Mucosa	stomach
40	chr8:100024600-100026200	Active TSS	NHEK	skin
41	chr8:100024600-100026400	Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr8:100024600-100026400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr8:100024600-100026400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr8:100024600-100026400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:100024600-100026400	Active TSS	Brain Anterior Caudate	brain
46	chr8:100024600-100026400	Active TSS	Brain Cingulate Gyrus	brain
47	chr8:100024600-100026400	Active TSS	Brain Hippocampus Middle	brain
48	chr8:100024600-100026400	Active TSS	Brain Inferior Temporal Lobe	brain
49	chr8:100024600-100026400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr8:100024600-100026400	Active TSS	Colonic Mucosa	Colon

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