Variant report

Variant	esv3401576
Chromosome Location	chr8:102640273-102724495
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1335)
CpG islands
(count:367)
Chromatin interactive
region (count:65)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1335 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:102689996-102690105	K562	blood:	n/a	n/a
2	ATF2	chr8:102714976-102715634	GM12878	blood:	n/a	n/a
3	ATF2	chr8:102712558-102713374	GM12878	blood:	n/a	n/a
4	ATF3	chr8:102658535-102658774	K562	blood:	n/a	n/a
5	BATF	chr8:102712494-102712819	GM12878	blood:	n/a	n/a
6	BATF	chr8:102656658-102657000	GM12878	blood:	n/a	n/a
7	BATF	chr8:102656546-102657040	GM12878	blood:	n/a	n/a
8	BATF	chr8:102715112-102715471	GM12878	blood:	n/a	n/a
9	BATF	chr8:102712479-102712793	GM12878	blood:	n/a	n/a
10	BATF	chr8:102719454-102719735	GM12878	blood:	n/a	n/a
11	BATF	chr8:102715138-102715499	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:102656589-102656993	GM12878	blood:	n/a	n/a
13	BCL11A	chr8:102715098-102715546	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:102656553-102657000	GM12878	blood:	n/a	n/a
15	BCL3	chr8:102715148-102715531	GM12878	blood:	n/a	n/a
16	BCLAF1	chr8:102715123-102715801	GM12878	blood:	n/a	n/a
17	BCLAF1	chr8:102658546-102658870	GM12878	blood:	n/a	chr8:102658686-102658694
18	BCLAF1	chr8:102715128-102715573	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:102644773-102645032	HepG2	liver:	n/a	n/a
20	BHLHE40	chr8:102658494-102658851	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:102712987-102713190	GM12878	blood:	n/a	n/a
22	BHLHE40	chr8:102715226-102715512	GM12878	blood:	n/a	n/a
23	BRCA1	chr8:102658635-102658824	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr8:102647666-102648348	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr8:102647652-102648420	HCT-116	colon:	n/a	n/a
26	CEBPB	chr8:102644621-102645229	HCT-116	colon:	n/a	n/a
27	CEBPB	chr8:102702638-102702919	HepG2	liver:	n/a	chr8:102702763-102702774
28	CEBPB	chr8:102644649-102645342	MCF-7	breast:	n/a	n/a
29	CEBPB	chr8:102713706-102714057	Hela-S3	cervix:	n/a	chr8:102713873-102713884 chr8:102713875-102713884 chr8:102713874-102713885
30	CEBPB	chr8:102647859-102648472	MCF-7	breast:	n/a	n/a
31	CEBPB	chr8:102647815-102648472	MCF-7	breast:	n/a	n/a
32	CEBPB	chr8:102713733-102714059	HepG2	liver:	n/a	chr8:102713873-102713884 chr8:102713875-102713884 chr8:102713874-102713885
33	CEBPB	chr8:102658437-102658779	K562	blood:	n/a	chr8:102658604-102658615 chr8:102658737-102658749
34	CEBPB	chr8:102713649-102714126	MCF-7	breast:	n/a	chr8:102713873-102713884 chr8:102713875-102713884 chr8:102713874-102713885
35	CEBPB	chr8:102713775-102714010	K562	blood:	n/a	chr8:102713873-102713884 chr8:102713875-102713884 chr8:102713874-102713885
36	CEBPB	chr8:102644658-102645311	A549	lung:	n/a	n/a
37	CEBPB	chr8:102644814-102645095	K562	blood:	n/a	n/a
38	CEBPB	chr8:102644774-102645157	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:102651079-102651286	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr8:102644774-102645158	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr8:102644742-102645161	K562	blood:	n/a	n/a
42	CEBPB	chr8:102658376-102658895	MCF-7	breast:	n/a	chr8:102658604-102658615 chr8:102658737-102658749
43	CEBPB	chr8:102651153-102651353	K562	blood:	n/a	n/a
44	CEBPB	chr8:102713641-102714163	ECC-1	luminal epithelium:	n/a	chr8:102713873-102713884 chr8:102713875-102713884 chr8:102713874-102713885
45	CEBPB	chr8:102651048-102651332	IMR90	lung:	n/a	n/a
46	CEBPB	chr8:102644778-102645130	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr8:102714802-102715555	MCF-7	breast:	n/a	n/a
48	CEBPB	chr8:102644511-102645295	HCT-116	colon:	n/a	n/a
49	CEBPB	chr8:102651042-102651377	HepG2	liver:	n/a	n/a
50	CEBPB	chr8:102658334-102658942	MCF-7	breast:	n/a	chr8:102658604-102658615 chr8:102658737-102658749

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:102669360-102669410	IMR90	lung:	fetal
2	chr8:102669360-102669410	IMR90	lung:	fetal
3	chr8:102680096-102680146	HCPEpiC	choroid plexus:	n/a
4	chr8:102701410-102701460	SK-N-MC	brain:	n/a
5	chr8:102680096-102680146	AG04450	lung:	fetal
6	chr8:102680096-102680146	GM19239	blood:	n/a
7	chr8:102669360-102669410	NHBE	bronchial:	n/a
8	chr8:102701410-102701460	HMEC	breast:	n/a
9	chr8:102669360-102669410	PrEC	prostate:	n/a
10	chr8:102701410-102701460	K562	blood:	n/a
11	chr8:102701376-102701426	SAEC	small airway:	n/a
12	chr8:102701410-102701460	HCPEpiC	choroid plexus:	n/a
13	chr8:102669360-102669410	HIPEpiC	eye:	n/a
14	chr8:102680096-102680146	AG09319	gingival:	n/a
15	chr8:102701410-102701460	MCF10A-Er-Src	breast:	n/a
16	chr8:102701376-102701426	A549	lung:	n/a
17	chr8:102702514-102702564	U87	brain:	n/a
18	chr8:102702514-102702564	MCF-7	breast:	n/a
19	chr8:102680096-102680146	NB4	blood:	n/a
20	chr8:102680096-102680146	RPTEC	kidney:	n/a
21	chr8:102701410-102701460	AG09309	skin:	n/a
22	chr8:102669360-102669410	Hela-S3	cervix:	n/a
23	chr8:102669360-102669410	GM19239	blood:	n/a
24	chr8:102702514-102702564	HepG2	liver:	n/a
25	chr8:102702514-102702564	GM06990	blood:	n/a
26	chr8:102701376-102701426	NT2-D1	testis:	n/a
27	chr8:102701410-102701460	NH-A	brain:	n/a
28	chr8:102699486-102699536	ProgFib	skin:	n/a
29	chr8:102699486-102699536	HAEpiC	amniotic membrane:	n/a
30	chr8:102702514-102702564	HEEpiC	esophagus:	n/a
31	chr8:102669360-102669410	HCT-116	colon:	n/a
32	chr8:102702514-102702564	HIPEpiC	eye:	n/a
33	chr8:102701410-102701460	Caco-2	colon:	n/a
34	chr8:102699486-102699536	ECC-1	luminal epithelium:	n/a
35	chr8:102702514-102702564	HAEpiC	amniotic membrane:	n/a
36	chr8:102702514-102702564	CMK	blood:	n/a
37	chr8:102680096-102680146	HEEpiC	esophagus:	n/a
38	chr8:102669360-102669410	HRE	kidney:	n/a
39	chr8:102701376-102701426	ECC-1	luminal epithelium:	n/a
40	chr8:102702514-102702564	HCPEpiC	choroid plexus:	n/a
41	chr8:102669360-102669410	PFSK-1	brain:	n/a
42	chr8:102702514-102702564	Hepatocyte	liver:	n/a
43	chr8:102701376-102701426	SKMC	muscle:	n/a
44	chr8:102699486-102699536	NH-A	brain:	n/a
45	chr8:102699486-102699536	HNPCEpiC	eye:	n/a
46	chr8:102680096-102680146	NHBE	bronchial:	n/a
47	chr8:102699486-102699536	A549	lung:	n/a
48	chr8:102680096-102680146	BE2_C	brain:	n/a
49	chr8:102701410-102701460	H1-hESC	embryonic stem cell:	embryo
50	chr8:102701410-102701460	ProgFib	skin:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:102676339..102678674-chr8:102680968..102682901,3	MCF-7	breast:
2	chr8:102620271..102621973-chr8:102646232..102648776,2	MCF-7	breast:
3	chr8:102518050..102520843-chr8:102644684..102646400,2	MCF-7	breast:
4	chr8:102703417..102705716-chr8:102712935..102714769,2	MCF-7	breast:
5	chr8:102672754..102675270-chr8:102680844..102682730,2	MCF-7	breast:
6	chr8:102652172..102654283-chr8:102658129..102660211,2	K562	blood:
7	chr8:102652218..102654020-chr8:102654403..102656656,2	MCF-7	breast:
8	chr8:102715403..102717842-chr8:102720455..102723118,2	K562	blood:
9	chr8:102719687..102721668-chr8:102834149..102836612,2	MCF-7	breast:
10	chr8:102703417..102705716-chr8:102712935..102714769,2	MCF-7	breast:
11	chr8:102667718..102669402-chr8:102670482..102672103,2	MCF-7	breast:
12	chr8:102699783..102701302-chr8:102702548..102704933,2	MCF-7	breast:
13	chr8:102658241..102659115-chr8:102982184..102983000,3	MCF-7	breast:
14	chr8:102652172..102654283-chr8:102658129..102660211,2	K562	blood:
15	chr8:102503159..102506071-chr8:102657015..102659448,3	MCF-7	breast:
16	chr8:102704561..102708348-chr8:102712896..102716376,5	MCF-7	breast:
17	chr8:102664916..102667894-chr8:102671918..102674454,2	MCF-7	breast:
18	chr8:102664289..102666765-chr8:102667718..102671185,4	MCF-7	breast:
19	chr8:102503148..102509288-chr8:102639386..102649682,19	MCF-7	breast:
20	chr8:102505361..102507168-chr8:102652647..102654652,2	MCF-7	breast:
21	chr8:102643444..102646539-chr8:102648297..102653448,5	MCF-7	breast:
22	chr8:102647973..102651609-chr8:102651902..102654799,4	MCF-7	breast:
23	chr8:102715403..102717842-chr8:102720455..102723118,2	K562	blood:
24	chr8:102671400..102672173-chr8:103209393..103210217,2	MCF-7	breast:
25	chr8:102517484..102520449-chr8:102641469..102644392,2	MCF-7	breast:
26	chr8:102673349..102676352-chr8:102676629..102679510,3	MCF-7	breast:
27	chr8:102649060..102651936-chr8:102661670..102663613,2	MCF-7	breast:
28	chr8:102338957..102339794-chr8:102644459..102645503,3	MCF-7	breast:
29	chr8:102501541..102504149-chr8:102653315..102655059,2	MCF-7	breast:
30	chr8:102646864..102649160-chr8:102652042..102653604,2	MCF-7	breast:
31	chr8:102557068..102559432-chr8:102644756..102646494,2	MCF-7	breast:
32	chr8:102657037..102659278-chr8:102659929..102662288,2	MCF-7	breast:
33	chr8:102578394..102580436-chr8:102646392..102647892,2	MCF-7	breast:
34	chr8:102338951..102340127-chr8:102644504..102645388,3	K562	blood:
35	chr8:102503246..102506384-chr8:102653850..102656829,3	MCF-7	breast:
36	chr8:102667718..102669402-chr8:102670482..102672103,2	MCF-7	breast:
37	chr8:102720592..102723059-chr8:102730767..102733650,2	MCF-7	breast:
38	chr8:102577611..102578416-chr8:102644647..102645261,2	MCF-7	breast:
39	chr8:102577206..102577740-chr8:102644735..102645456,2	MCF-7	breast:
40	chr8:102499850..102508532-chr8:102642696..102652505,26	MCF-7	breast:
41	chr8:102658165..102659183-chr8:103208962..103210318,7	MCF-7	breast:
42	chr8:102661081..102663898-chr8:102668064..102670538,3	MCF-7	breast:
43	chr8:102658241..102659174-chr8:103209354..103210263,6	MCF-7	breast:
44	chr8:102657037..102659278-chr8:102659929..102662288,2	MCF-7	breast:
45	chr8:102658411..102659082-chr8:103044751..103045545,2	MCF-7	breast:
46	chr8:102699783..102701302-chr8:102702548..102704933,2	MCF-7	breast:
47	chr8:102652218..102654020-chr8:102654403..102656656,2	MCF-7	breast:
48	chr8:102672754..102675270-chr8:102680844..102682730,2	MCF-7	breast:
49	chr8:102447454..102450323-chr8:102645181..102647136,2	MCF-7	breast:
50	chr8:102579608..102581495-chr8:102645973..102648635,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253629	TF binding region
GRHL2	TF binding region
NCALD	TF binding region
ENSG00000253629	CpG island
GRHL2	CpG island
NCALD	CpG island
ENSG00000104490	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000254024	chromatin interactions

Extended variants
information (count: 3576 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:3576 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375608102	chr8:102640292-102640293	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs574299606	chr8:102640384-102640385	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs535530003	chr8:102640391-102640392	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs554272216	chr8:102640449-102640450	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs534701165	chr8:102640455-102640456	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs572337620	chr8:102640461-102640462	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs546222050	chr8:102640539-102640540	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs564621387	chr8:102640589-102640590	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs10110084	chr8:102640623-102640624	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576763948	chr8:102640694-102640695	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs34311887	chr8:102640698-102640699	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs114872765	chr8:102640724-102640725	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs562230342	chr8:102640732-102640733	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs674011	chr8:102640767-102640768	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs111970759	chr8:102640781-102640782	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs140703267	chr8:102640823-102640824	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs559176981	chr8:102640903-102640904	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs527279882	chr8:102640999-102641000	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs568354847	chr8:102641015-102641016	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs552194744	chr8:102641018-102641019	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs144652525	chr8:102641021-102641022	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs557107623	chr8:102641065-102641066	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs116304010	chr8:102641091-102641092	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs549677660	chr8:102641161-102641162	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs567894659	chr8:102641167-102641168	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535675806	chr8:102641196-102641197	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs553968423	chr8:102641207-102641208	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs572549611	chr8:102641308-102641309	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs151268444	chr8:102641318-102641319	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs558092185	chr8:102641332-102641333	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs368941500	chr8:102641358-102641359	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs564361726	chr8:102641399-102641400	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs371872766	chr8:102641476-102641477	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs1573278	chr8:102641505-102641506	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs562393942	chr8:102641511-102641512	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs79487786	chr8:102641522-102641523	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs541650305	chr8:102641528-102641529	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs79800909	chr8:102641531-102641532	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs79003574	chr8:102641532-102641533	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs5893577	chr8:102641533-102641534	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559986239	chr8:102641567-102641568	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs527330518	chr8:102641594-102641595	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543576153	chr8:102641633-102641634	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs537589653	chr8:102641635-102641636	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs140510172	chr8:102641713-102641714	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs150131512	chr8:102641737-102641738	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531237367	chr8:102641763-102641764	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs75948897	chr8:102641768-102641769	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs568057234	chr8:102641771-102641772	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs145570409	chr8:102641780-102641781	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	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
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1245 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102616800-102643800	Weak transcription	Gastric	stomach
2	chr8:102618000-102640800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:102619800-102656200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr8:102627800-102643800	Weak transcription	Fetal Intestine Large	intestine
5	chr8:102628200-102643600	Weak transcription	Fetal Intestine Small	intestine
6	chr8:102630400-102644000	Weak transcription	Lung	lung
7	chr8:102630800-102641600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr8:102630800-102642800	Weak transcription	Fetal Stomach	stomach
9	chr8:102636200-102645000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr8:102636200-102646200	Weak transcription	Esophagus	oesophagus
11	chr8:102636400-102643400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr8:102636400-102647200	Weak transcription	HMEC	breast
13	chr8:102636400-102648200	Weak transcription	Fetal Lung	lung
14	chr8:102636600-102642400	Weak transcription	Rectal Smooth Muscle	rectum
15	chr8:102636600-102643800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:102636600-102643800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr8:102636600-102646200	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr8:102636800-102642800	Weak transcription	Fetal Kidney	kidney
19	chr8:102636800-102643800	Weak transcription	NHEK	skin
20	chr8:102636800-102645600	Weak transcription	Placenta	Placenta
21	chr8:102636800-102646000	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr8:102637000-102641200	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr8:102637000-102644000	Weak transcription	Pancreas	Pancrea
24	chr8:102637000-102646200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr8:102637200-102641000	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr8:102637200-102647000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr8:102637400-102646000	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr8:102637600-102646200	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr8:102638800-102643600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr8:102639000-102640800	Enhancers	Stomach Mucosa	stomach
31	chr8:102639400-102641200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr8:102639400-102642000	Weak transcription	Osteobl	bone
33	chr8:102639600-102640600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr8:102639600-102641400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:102639600-102642600	Weak transcription	NH-A	brain
36	chr8:102639800-102644600	Weak transcription	HUVEC	blood vessel
37	chr8:102640200-102640400	Enhancers	Duodenum Mucosa	Duodenum
38	chr8:102640200-102641200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr8:102640200-102643200	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr8:102640400-102644000	Weak transcription	Duodenum Mucosa	Duodenum
41	chr8:102640600-102643000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr8:102640800-102642800	Weak transcription	Stomach Mucosa	stomach
43	chr8:102641000-102641600	Strong transcription	HUES64 Cell Line	embryonic stem cell
44	chr8:102641200-102641600	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr8:102641200-102643600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr8:102641200-102643800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr8:102641400-102642000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr8:102641600-102643800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr8:102641600-102643800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr8:102641600-102644600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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