Variant report

Variant	nsv891247
Chromosome Location	chr8:104090979-104121862
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	chr8:104095541-104095587	K562	blood:	n/a	n/a
2	ATF2	chr8:104090445-104091042	GM12878	blood:	n/a	n/a
3	ATF2	chr8:104090545-104091021	GM12878	blood:	n/a	n/a
4	BACH1	chr8:104107337-104107371	K562	blood:	n/a	n/a
5	BACH1	chr8:104102486-104102493	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:104117631-104117890	GM12878	blood:	n/a	chr8:104117695-104117705
7	BCL11A	chr8:104108917-104109093	GM12878	blood:	n/a	n/a
8	BCL3	chr8:104094887-104095295	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:104091076-104091557	K562	blood:	n/a	n/a
10	BHLHE40	chr8:104090462-104091056	GM12878	blood:	n/a	n/a
11	CCNT2	chr8:104091071-104091401	K562	blood:	n/a	n/a
12	CEBPB	chr8:104106860-104106978	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr8:104109141-104109320	IMR90	lung:	n/a	chr8:104109217-104109228 chr8:104109217-104109228 chr8:104109215-104109228
14	CEBPB	chr8:104102872-104103081	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr8:104103318-104103496	IMR90	lung:	n/a	n/a
16	CEBPB	chr8:104102946-104103016	K562	blood:	n/a	n/a
17	CEBPB	chr8:104117226-104117934	IMR90	lung:	n/a	n/a
18	CHD1	chr8:104115947-104118691	IMR90	lung:	n/a	n/a
19	CTBP2	chr8:104118185-104118659	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:104116500-104116650	HFF	foreskin:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
21	CTCF	chr8:104116100-104116250	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr8:104116497-104116679	HepG2	liver:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
23	CTCF	chr8:104116520-104116670	HPAF	blood vessel:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
24	CTCF	chr8:104116200-104116350	SAEC	small airway:	n/a	n/a
25	CTCF	chr8:104116390-104116768	SK-N-SH_RA	brain:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
26	CTCF	chr8:104116511-104116675	ProgFib	skin:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
27	CTCF	chr8:104116490-104116726	Spleen_OC	spleen:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
28	CTCF	chr8:104116520-104116670	HPF	lung:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
29	CTCF	chr8:104116513-104116668	SK-N-SH_RA	brain:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
30	CTCF	chr8:104116560-104116710	HCT-116	colon:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
31	CTCF	chr8:104116560-104116710	HAc	cerebellar:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
32	CTCF	chr8:104116500-104116650	WI-38	lung:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
33	CTCF	chr8:104116480-104116630	HEK293	kidney:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
34	CTCF	chr8:104116511-104116678	GM10248	blood:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
35	CTCF	chr8:104116435-104116706	Gliobla	brain:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
36	CTCF	chr8:104116480-104116630	HRE	kidney:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
37	CTCF	chr8:104116437-104116756	A549	lung:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
38	CTCF	chr8:104116540-104116690	HCT-116	colon:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
39	CTCF	chr8:104116479-104116677	LNCaP	prostate:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
40	CTCF	chr8:104116540-104116690	GM12864	blood:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
41	CTCF	chr8:104116520-104116670	HA-sp	spinal cord:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
42	CTCF	chr8:104116520-104116670	SK-N-SH_RA	brain:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
43	CTCF	chr8:104116500-104116650	GM12874	blood:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
44	CTCF	chr8:104116505-104116683	MCF-7	breast:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
45	CTCF	chr8:104116520-104116670	HCPEpiC	choroid plexus:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
46	CTCF	chr8:104116508-104116510	ProgFib	skin:	n/a	n/a
47	CTCF	chr8:104116289-104116816	MCF-7	breast:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
48	CTCF	chr8:104116540-104116690	A549	lung:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
49	CTCF	chr8:104116540-104116690	HBMEC	blood vessel:	n/a	chr8:104116591-104116604 chr8:104116588-104116606
50	CTCF	chr8:104116486-104116791	H1-hESC	embryonic stem cell:	n/a	chr8:104116591-104116604 chr8:104116588-104116606

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:104117866-104117916	Jurkat	blood:	n/a
2	chr8:104117866-104117916	PANC-1	pancreas:	n/a
3	chr8:104117866-104117916	HCF	heart:	n/a
4	chr8:104117866-104117916	BJ	skin:	n/a
5	chr8:104117866-104117916	CMK	blood:	n/a
6	chr8:104117866-104117916	HMEC	breast:	n/a
7	chr8:104117866-104117916	HCPEpiC	choroid plexus:	n/a
8	chr8:104117866-104117916	HAEpiC	amniotic membrane:	n/a
9	chr8:104117866-104117916	NHBE	bronchial:	n/a
10	chr8:104117866-104117916	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:104117866-104117916	HepG2	liver:	n/a
12	chr8:104117866-104117916	ECC-1	luminal epithelium:	n/a
13	chr8:104117866-104117916	U87	brain:	n/a
14	chr8:104117866-104117916	IMR90	lung:	fetal
15	chr8:104117866-104117916	SK-N-MC	brain:	n/a
16	chr8:104117866-104117916	Hepatocyte	liver:	n/a
17	chr8:104117866-104117916	HUVEC	blood vessel:	n/a
18	chr8:104117866-104117916	MCF-7	breast:	n/a
19	chr8:104117866-104117916	AG09319	gingival:	n/a
20	chr8:104117866-104117916	GM12892	blood:	n/a
21	chr8:104117866-104117916	AG04449	skin:	fetal
22	chr8:104117866-104117916	SK-N-SH_RA	brain:	n/a
23	chr8:104117866-104117916	SAEC	small airway:	n/a
24	chr8:104117866-104117916	K562	blood:	n/a
25	chr8:104117866-104117916	NB4	blood:	n/a
26	chr8:104117866-104117916	HNPCEpiC	eye:	n/a
27	chr8:104117866-104117916	HEK293	kidney:	embryo
28	chr8:104117866-104117916	NT2-D1	testis:	n/a
29	chr8:104117866-104117916	H1-hESC	embryonic stem cell:	embryo
30	chr8:104117866-104117916	Hela-S3	cervix:	n/a
31	chr8:104117866-104117916	BE2_C	brain:	n/a
32	chr8:104117866-104117916	Caco-2	colon:	n/a
33	chr8:104117866-104117916	HCM	heart:	n/a
34	chr8:104117866-104117916	NHDF-neo	bronchial:	n/a
35	chr8:104117866-104117916	GM12891	blood:	n/a
36	chr8:104117866-104117916	SKMC	muscle:	n/a
37	chr8:104117866-104117916	HIPEpiC	eye:	n/a
38	chr8:104117866-104117916	GM12878	blood:	n/a
39	chr8:104117866-104117916	HL-60	blood:	n/a
40	chr8:104117866-104117916	A549	lung:	n/a
41	chr8:104117866-104117916	T-47D	breast:	n/a
42	chr8:104117866-104117916	ovcar-3	ovarian:	n/a
43	chr8:104117866-104117916	PrEC	prostate:	n/a
44	chr8:104117866-104117916	AG04450	lung:	fetal
45	chr8:104117866-104117916	HRCEpiC	kidney:	n/a
46	chr8:104117866-104117916	PFSK-1	brain:	n/a
47	chr8:104117866-104117916	GM06990	blood:	n/a
48	chr8:104117866-104117916	SK-N-SH	brain:	n/a
49	chr8:104117866-104117916	HRE	kidney:	n/a
50	chr8:104117866-104117916	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:104110807..104113342-chr8:104119604..104121157,2	K562	blood:
2	chr8:104085770..104086578-chr8:104116221..104116962,2	K562	blood:
3	chr8:104117433..104118172-chr9:117001760..117002366,2	MCF-7	breast:
4	chr8:104090004..104092160-chr8:104092634..104094909,2	MCF-7	breast:
5	chr8:104121135..104121844-chr8:104148279..104149267,2	MCF-7	breast:
6	chr8:104098045..104100056-chr8:104425768..104428502,2	MCF-7	breast:
7	chr8:104114771..104116295-chr8:104145426..104148111,2	K562	blood:
8	chr8:104110807..104113342-chr8:104119604..104121157,2	K562	blood:
9	chr8:104110222..104113167-chr8:104144712..104147363,2	K562	blood:
10	chr8:104110536..104112989-chr8:104114800..104117513,2	MCF-7	breast:
11	chr8:104116215..104117089-chr8:104524009..104524511,2	K562	blood:
12	chr8:104116308..104117555-chr8:104219520..104220293,3	MCF-7	breast:
13	chr8:104093989..104095614-chr8:104098040..104099547,2	MCF-7	breast:
14	chr8:104093989..104095614-chr8:104098040..104099547,2	MCF-7	breast:
15	chr8:104090004..104092160-chr8:104092634..104094909,2	MCF-7	breast:
16	chr8:104092100..104094274-chr8:104097821..104101418,3	K562	blood:
17	chr8:104116094..104117635-chr8:104276900..104277894,4	MCF-7	breast:
18	chr8:104094593..104096552-chr8:104098718..104100840,2	K562	blood:
19	chr8:104116132..104116726-chr8:104523965..104524539,2	MCF-7	breast:
20	chr8:104115954..104116689-chr8:104276929..104277840,2	MCF-7	breast:
21	chr8:104094593..104096552-chr8:104098718..104100840,2	K562	blood:
22	chr8:104110536..104112989-chr8:104114800..104117513,2	MCF-7	breast:
23	chr8:104082725..104084383-chr8:104095090..104097237,2	MCF-7	breast:
24	chr8:104116271..104117073-chr8:104385047..104386147,6	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V1C1-5	chr8:104103491-104103737	NONHSAT128153
2	lnc-ATP6V1C1-3	chr8:104097879-104098818	NONHSAT128151

Variant related genes	Relation type
ENSG00000253977	TF binding region
ENSG00000253556	TF binding region
MTND1P5	TF binding region
ENSG00000265667	TF binding region
ENSG00000253977	CpG island
ENSG00000253556	CpG island
MTND1P5	CpG island
ENSG00000265667	CpG island
ENSG00000253795	chromatin interactions
ENSG00000164933	chromatin interactions
ENSG00000253556	chromatin interactions
ENSG00000164934	chromatin interactions

Extended variants
information (count: 1231 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1231 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2453999	chr8:104090979-104090980	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs530018803	chr8:104090998-104090999	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs548375190	chr8:104091059-104091060	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs376926574	chr8:104091060-104091061	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs181693595	chr8:104091087-104091088	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs371194019	chr8:104091159-104091160	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs77160666	chr8:104091160-104091161	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs17790746	chr8:104091195-104091196	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs142931883	chr8:104091215-104091216	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs370597931	chr8:104091238-104091239	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs555890441	chr8:104091254-104091255	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs574766576	chr8:104091256-104091257	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs549394826	chr8:104091289-104091290	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs551840812	chr8:104091399-104091400	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs150686260	chr8:104091424-104091425	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs376311913	chr8:104091431-104091432	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs572281897	chr8:104091434-104091435	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs546124149	chr8:104091437-104091438	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs1497448	chr8:104091440-104091441	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs185636275	chr8:104091477-104091478	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs191474024	chr8:104091514-104091515	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs56112091	chr8:104091527-104091528	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs141028329	chr8:104091559-104091560	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs78650943	chr8:104091566-104091567	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs566820055	chr8:104091571-104091572	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs552755800	chr8:104091577-104091578	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs182447939	chr8:104091591-104091592	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs144580535	chr8:104091608-104091609	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs537567513	chr8:104091621-104091622	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs371566775	chr8:104091638-104091639	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs549717808	chr8:104091657-104091658	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs79631591	chr8:104091664-104091665	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs535110180	chr8:104091683-104091684	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs539489986	chr8:104091691-104091692	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs375489155	chr8:104091724-104091725	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs572443046	chr8:104091798-104091799	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs553099489	chr8:104091806-104091807	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs539980788	chr8:104091823-104091824	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs147887066	chr8:104091898-104091899	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs576452620	chr8:104091927-104091928	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs372416723	chr8:104091960-104091961	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs562197724	chr8:104092072-104092073	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs574060885	chr8:104092113-104092114	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs541479415	chr8:104092122-104092123	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs572933090	chr8:104092130-104092131	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs74416168	chr8:104092154-104092155	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs112541807	chr8:104092169-104092170	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs552321997	chr8:104092178-104092179	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs530547702	chr8:104092247-104092248	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs202173778	chr8:104092258-104092259	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
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
Sezary syndrome	18413736	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Bladder cancer	21909424	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104066800-104091200	Weak transcription	Stomach Mucosa	stomach
2	chr8:104080400-104091200	Weak transcription	Small Intestine	intestine
3	chr8:104081200-104091000	Weak transcription	Ovary	ovary
4	chr8:104083600-104093000	Weak transcription	Placenta	Placenta
5	chr8:104084200-104091000	Weak transcription	Thymus	Thymus
6	chr8:104086800-104091000	Weak transcription	Fetal Brain Male	brain
7	chr8:104087600-104093200	Weak transcription	Brain Germinal Matrix	brain
8	chr8:104088200-104091200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr8:104088400-104091600	Enhancers	Primary B cells from peripheral blood	blood
10	chr8:104088600-104091000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr8:104088600-104092000	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr8:104089000-104091600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
13	chr8:104089200-104091200	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr8:104089200-104091200	Weak transcription	Brain Cingulate Gyrus	brain
15	chr8:104089400-104091600	Enhancers	Liver	Liver
16	chr8:104089800-104091200	Enhancers	Colon Smooth Muscle	Colon
17	chr8:104090000-104091000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:104090000-104091200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:104090200-104091000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr8:104090200-104091000	Enhancers	HMEC	breast
21	chr8:104090200-104091400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr8:104090200-104091400	Enhancers	NHEK	skin
23	chr8:104090200-104091600	Enhancers	Primary B cells from cord blood	blood
24	chr8:104090200-104091600	Enhancers	K562	blood
25	chr8:104090400-104091000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr8:104090400-104091000	Weak transcription	Fetal Muscle Leg	muscle
27	chr8:104090400-104091000	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr8:104090400-104091200	Weak transcription	Spleen	Spleen
29	chr8:104090400-104091400	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr8:104090400-104091400	Weak transcription	Pancreas	Pancrea
31	chr8:104090400-104091600	Enhancers	Fetal Stomach	stomach
32	chr8:104090400-104091800	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr8:104090400-104093000	Weak transcription	Gastric	stomach
34	chr8:104090400-104093000	Weak transcription	Lung	lung
35	chr8:104090600-104091000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:104090600-104091200	Active TSS	Right Atrium	heart
37	chr8:104090600-104091200	Active TSS	Osteobl	bone
38	chr8:104090600-104091400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr8:104090600-104091400	Active TSS	Brain Angular Gyrus	brain
40	chr8:104090600-104091400	Active TSS	Colonic Mucosa	Colon
41	chr8:104090600-104091400	Flanking Active TSS	GM12878-XiMat	blood
42	chr8:104090600-104091400	Flanking Active TSS	HUVEC	blood vessel
43	chr8:104090600-104091600	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr8:104090800-104091000	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr8:104090800-104091000	Enhancers	Rectal Smooth Muscle	rectum
46	chr8:104090800-104091000	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
47	chr8:104090800-104091000	Flanking Active TSS	Stomach Smooth Muscle	stomach
48	chr8:104090800-104091000	Active TSS	NHDF-Ad	bronchial
49	chr8:104090800-104091200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr8:104090800-104091200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood

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