Variant report

Variant	esv16466
Chromosome Location	chr8:96206151-96243934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1109)
CpG islands
(count:183)
Chromatin interactive
region (count:142)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1109 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:96222407-96222791	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:96238736-96239118	K562	blood:	n/a	n/a
3	ARID3A	chr8:96235911-96236248	K562	blood:	n/a	n/a
4	ARID3A	chr8:96237312-96237625	K562	blood:	n/a	n/a
5	ARID3A	chr8:96224165-96224531	K562	blood:	n/a	n/a
6	ARID3A	chr8:96212521-96212598	K562	blood:	n/a	n/a
7	ARID3A	chr8:96237833-96237936	K562	blood:	n/a	n/a
8	ARID3A	chr8:96223744-96224151	HepG2	liver:	n/a	chr8:96223906-96223922 chr8:96223905-96223921
9	ARID3A	chr8:96212726-96212965	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:96237680-96238075	HepG2	liver:	n/a	n/a
11	ATF1	chr8:96238705-96239049	K562	blood:	n/a	n/a
12	ATF1	chr8:96211938-96212282	K562	blood:	n/a	n/a
13	ATF1	chr8:96221867-96222148	K562	blood:	n/a	n/a
14	ATF1	chr8:96241079-96241401	K562	blood:	n/a	n/a
15	ATF1	chr8:96235725-96236095	K562	blood:	n/a	n/a
16	ATF2	chr8:96226054-96226497	GM12878	blood:	n/a	n/a
17	ATF2	chr8:96240481-96240886	GM12878	blood:	n/a	n/a
18	ATF2	chr8:96240355-96240989	GM12878	blood:	n/a	n/a
19	ATF3	chr8:96241002-96241334	K562	blood:	n/a	n/a
20	ATF3	chr8:96241832-96242128	K562	blood:	n/a	n/a
21	ATF3	chr8:96238640-96239042	K562	blood:	n/a	n/a
22	ATF3	chr8:96241845-96242061	GM12878	blood:	n/a	n/a
23	ATF3	chr8:96241722-96242193	GM12878	blood:	n/a	n/a
24	BACH1	chr8:96237741-96238307	K562	blood:	n/a	n/a
25	BACH1	chr8:96238683-96239045	K562	blood:	n/a	n/a
26	BACH1	chr8:96237898-96237955	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr8:96240535-96240805	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:96240489-96240847	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:96240502-96240757	GM12878	blood:	n/a	n/a
30	BCL3	chr8:96229221-96229625	GM12878	blood:	n/a	n/a
31	BCLAF1	chr8:96240458-96241034	GM12878	blood:	n/a	n/a
32	BHLHE40	chr8:96240570-96240977	GM12878	blood:	n/a	n/a
33	BHLHE40	chr8:96243632-96243648	K562	blood:	n/a	n/a
34	BHLHE40	chr8:96235734-96236401	K562	blood:	n/a	n/a
35	BHLHE40	chr8:96207428-96207567	K562	blood:	n/a	n/a
36	BHLHE40	chr8:96224599-96224903	K562	blood:	n/a	n/a
37	BHLHE40	chr8:96226960-96227142	K562	blood:	n/a	n/a
38	BHLHE40	chr8:96238650-96239057	K562	blood:	n/a	n/a
39	BHLHE40	chr8:96241057-96241691	K562	blood:	n/a	n/a
40	BHLHE40	chr8:96237572-96238122	K562	blood:	n/a	n/a
41	BRCA1	chr8:96238870-96238884	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr8:96210432-96210870	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr8:96214094-96214463	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr8:96237889-96238027	HepG2	liver:	n/a	n/a
45	CBX3	chr8:96238613-96239203	K562	blood:	n/a	n/a
46	CBX3	chr8:96241028-96242353	K562	blood:	n/a	n/a
47	CCNT2	chr8:96241063-96241528	K562	blood:	n/a	chr8:96241245-96241265
48	CCNT2	chr8:96211922-96212232	K562	blood:	n/a	n/a
49	CCNT2	chr8:96224640-96225068	K562	blood:	n/a	chr8:96224871-96224891 chr8:96224829-96224849 chr8:96224778-96224787
50	CCNT2	chr8:96238569-96239100	K562	blood:	n/a	chr8:96238680-96238689

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:96213626-96213676	NHDF-neo	bronchial:	n/a
2	chr8:96226844-96226894	GM12892	blood:	n/a
3	chr8:96213626-96213676	K562	blood:	n/a
4	chr8:96214079-96214129	RPTEC	kidney:	n/a
5	chr8:96213626-96213676	PFSK-1	brain:	n/a
6	chr8:96226844-96226894	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:96214079-96214129	T-47D	breast:	n/a
8	chr8:96213626-96213676	H1-hESC	embryonic stem cell:	embryo
9	chr8:96213626-96213676	HCPEpiC	choroid plexus:	n/a
10	chr8:96214079-96214129	ECC-1	luminal epithelium:	n/a
11	chr8:96213626-96213676	NB4	blood:	n/a
12	chr8:96214079-96214129	HL-60	blood:	n/a
13	chr8:96213626-96213676	RPTEC	kidney:	n/a
14	chr8:96213626-96213676	HPAEpiC	pulmonary alveolar:	n/a
15	chr8:96214079-96214129	K562	blood:	n/a
16	chr8:96226844-96226894	AG04449	skin:	fetal
17	chr8:96214079-96214129	SKMC	muscle:	n/a
18	chr8:96226844-96226894	H1-hESC	embryonic stem cell:	embryo
19	chr8:96213626-96213676	MCF10A-Er-Src	breast:	n/a
20	chr8:96213626-96213676	HCM	heart:	n/a
21	chr8:96213626-96213676	GM12891	blood:	n/a
22	chr8:96214079-96214129	NH-A	brain:	n/a
23	chr8:96213626-96213676	HL-60	blood:	n/a
24	chr8:96213626-96213676	Hepatocyte	liver:	n/a
25	chr8:96214079-96214129	HNPCEpiC	eye:	n/a
26	chr8:96214079-96214129	NHDF-neo	bronchial:	n/a
27	chr8:96214079-96214129	GM12878	blood:	n/a
28	chr8:96226844-96226894	GM06990	blood:	n/a
29	chr8:96213626-96213676	T-47D	breast:	n/a
30	chr8:96213626-96213676	ovcar-3	ovarian:	n/a
31	chr8:96214079-96214129	NT2-D1	testis:	n/a
32	chr8:96214079-96214129	HAEpiC	amniotic membrane:	n/a
33	chr8:96213626-96213676	SAEC	small airway:	n/a
34	chr8:96214079-96214129	GM19239	blood:	n/a
35	chr8:96213626-96213676	BE2_C	brain:	n/a
36	chr8:96226844-96226894	HNPCEpiC	eye:	n/a
37	chr8:96226844-96226894	K562	blood:	n/a
38	chr8:96226844-96226894	AG09319	gingival:	n/a
39	chr8:96213626-96213676	HRCEpiC	kidney:	n/a
40	chr8:96214079-96214129	U87	brain:	n/a
41	chr8:96226844-96226894	SK-N-MC	brain:	n/a
42	chr8:96214079-96214129	HMEC	breast:	n/a
43	chr8:96226844-96226894	HIPEpiC	eye:	n/a
44	chr8:96213626-96213676	NT2-D1	testis:	n/a
45	chr8:96213626-96213676	HRE	kidney:	n/a
46	chr8:96214079-96214129	PFSK-1	brain:	n/a
47	chr8:96226844-96226894	T-47D	breast:	n/a
48	chr8:96214079-96214129	HEK293	kidney:	embryo
49	chr8:96213626-96213676	NHBE	bronchial:	n/a
50	chr8:96214079-96214129	ovcar-3	ovarian:	n/a

(count:142 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:96145188..96147902-chr8:96236051..96240393,4	K562	blood:
2	chr8:96233041..96235359-chr8:96238288..96241007,3	K562	blood:
3	chr8:96087772..96089911-chr8:96238508..96240959,2	MCF-7	breast:
4	chr8:96123068..96125522-chr8:96208069..96210345,2	MCF-7	breast:
5	chr8:96236807..96240008-chr8:96246119..96247780,3	MCF-7	breast:
6	chr8:96224254..96224982-chr8:96236085..96236596,2	MCF-7	breast:
7	chr8:96147448..96150087-chr8:96233164..96235373,2	MCF-7	breast:
8	chr8:96163106..96166154-chr8:96205325..96207933,3	MCF-7	breast:
9	chr8:96203164..96205455-chr8:96217318..96219508,3	MCF-7	breast:
10	chr8:96221874..96223119-chr8:96235797..96236784,7	MCF-7	breast:
11	chr8:96145749..96147825-chr8:96236619..96239498,2	MCF-7	breast:
12	chr8:96228952..96231247-chr8:96237951..96240683,3	MCF-7	breast:
13	chr8:96214009..96217041-chr8:96227079..96229399,3	K562	blood:
14	chr8:96205065..96207467-chr8:96211843..96213815,3	MCF-7	breast:
15	chr8:96202933..96207621-chr8:96217016..96224905,7	MCF-7	breast:
16	chr8:96220160..96222982-chr8:96225240..96226907,2	K562	blood:
17	chr8:96145268..96146858-chr8:96230035..96232960,2	MCF-7	breast:
18	chr8:96222260..96224188-chr8:96237998..96239656,2	MCF-7	breast:
19	chr8:96205463..96207920-chr8:96210246..96213783,6	MCF-7	breast:
20	chr8:96206515..96208115-chr8:96256638..96258375,2	MCF-7	breast:
21	chr8:96114675..96115219-chr8:96215202..96216074,2	MCF-7	breast:
22	chr8:96205463..96207920-chr8:96210246..96213783,6	MCF-7	breast:
23	chr8:96124242..96126154-chr8:96223005..96225325,2	MCF-7	breast:
24	chr8:96223779..96226497-chr8:96236467..96238844,2	K562	blood:
25	chr8:96229120..96231629-chr8:96232251..96235212,3	MCF-7	breast:
26	chr8:96109979..96112421-chr8:96207106..96209124,2	MCF-7	breast:
27	chr8:96230420..96235229-chr8:96280327..96282960,4	MCF-7	breast:
28	chr8:96201546..96203086-chr8:96222450..96224514,2	MCF-7	breast:
29	chr8:96219891..96220818-chr8:96235921..96236731,3	MCF-7	breast:
30	chr8:96221874..96223119-chr8:96235797..96236784,7	MCF-7	breast:
31	chr8:96224814..96227323-chr8:96239460..96241166,3	MCF-7	breast:
32	chr8:96111749..96114066-chr8:96234612..96236782,2	K562	blood:
33	chr8:96218443..96220891-chr8:96249353..96251227,2	MCF-7	breast:
34	chr8:96204194..96207440-chr8:96236906..96239736,3	MCF-7	breast:
35	chr8:96241997..96243931-chr8:96244182..96247053,2	MCF-7	breast:
36	chr8:96234981..96237972-chr8:97273758..97275615,2	MCF-7	breast:
37	chr8:96204194..96207440-chr8:96236906..96239736,3	MCF-7	breast:
38	chr8:96228560..96230239-chr8:96242060..96244919,2	MCF-7	breast:
39	chr8:96145520..96147593-chr8:96211677..96214625,3	MCF-7	breast:
40	chr8:96241566..96243964-chr8:96265502..96267289,2	K562	blood:
41	chr8:96222260..96224188-chr8:96237998..96239656,2	MCF-7	breast:
42	chr8:96204685..96206421-chr8:96234538..96236078,2	MCF-7	breast:
43	chr8:96224254..96224982-chr8:96236085..96236596,2	MCF-7	breast:
44	chr8:96219891..96220754-chr8:96235921..96236812,8	MCF-7	breast:
45	chr8:96236752..96238827-chr8:128748699..128750665,2	MCF-7	breast:
46	chr8:96086865..96087716-chr8:96235978..96236892,2	MCF-7	breast:
47	chr8:96171786..96172477-chr8:96211697..96212423,2	MCF-7	breast:
48	chr8:96243081..96246840-chr8:96248821..96252281,5	K562	blood:
49	chr8:96220160..96222982-chr8:96225240..96226907,2	K562	blood:
50	chr8:96232022..96234358-chr8:96242400..96245249,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf37-1	chr8:96220647-96220806	ENSG00000253351
2	lnc-C8orf37-1	chr8:96220713-96220767	NONHSAT127827
3	lnc-PLEKHF2-2	chr8:96217488-96217540	ENSG00000253773.1
4	lnc-C8orf37-1	chr8:96219235-96219536	ENSG00000253351
5	lnc-C8orf37-1	chr8:96228546-96228743	NONHSAT127827
6	lnc-PLEKHF2-2	chr8:96216684-96217151	ENSG00000253773.1
7	lnc-C8orf37-1	chr8:96228546-96228602	ENSG00000253351

No data

Variant related genes	Relation type
ENSG00000253351	TF binding region
ENSG00000253773	TF binding region
ENSG00000253351	CpG island
ENSG00000253773	CpG island
ENSG00000156471	chromatin interactions
ENSG00000175895	chromatin interactions
ENSG00000156170	chromatin interactions
ENSG00000254248	chromatin interactions
ENSG00000245080	chromatin interactions
ENSG00000253351	chromatin interactions
ENSG00000156172	chromatin interactions
ENSG00000156469	chromatin interactions
ENSG00000253773	chromatin interactions
ENSG00000175305	chromatin interactions

Extended variants
information (count: 1437 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1437 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542513058	chr8:96206165-96206166	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs138934133	chr8:96206181-96206182	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs369929759	chr8:96206182-96206183	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs530928689	chr8:96206219-96206220	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs550726048	chr8:96206232-96206233	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs141985635	chr8:96206258-96206259	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs554659120	chr8:96206259-96206260	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs568541800	chr8:96206320-96206321	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs567524776	chr8:96206322-96206323	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs145761529	chr8:96206369-96206370	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs557146125	chr8:96206414-96206415	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs565539467	chr8:96206441-96206442	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs534572205	chr8:96206442-96206443	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs554838407	chr8:96206464-96206465	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs568311801	chr8:96206486-96206487	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs537031202	chr8:96206504-96206505	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs556718738	chr8:96206510-96206511	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs564182993	chr8:96206514-96206515	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs531255033	chr8:96206515-96206516	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs552157808	chr8:96206526-96206527	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs78833911	chr8:96206527-96206528	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs79946012	chr8:96206528-96206529	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs62524831	chr8:96206530-96206531	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs142758003	chr8:96206531-96206532	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs576980975	chr8:96206546-96206547	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs2439641	chr8:96206553-96206554	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs545965507	chr8:96206558-96206559	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs553558891	chr8:96206656-96206657	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs573486797	chr8:96206674-96206675	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs144471588	chr8:96206681-96206682	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs536407988	chr8:96206698-96206699	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs78926339	chr8:96206704-96206705	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs531142974	chr8:96206712-96206713	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs78757567	chr8:96206715-96206716	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs564161711	chr8:96206718-96206719	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs533205206	chr8:96206735-96206736	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs184184239	chr8:96206736-96206737	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs16917408	chr8:96206740-96206741	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs370431343	chr8:96206744-96206745	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs62524832	chr8:96206745-96206746	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs568331572	chr8:96206788-96206789	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs2439640	chr8:96206789-96206790	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs16917410	chr8:96206803-96206804	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs148040560	chr8:96206831-96206832	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs374324139	chr8:96206918-96206919	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs144617658	chr8:96206923-96206924	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539502374	chr8:96206936-96206937	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs553095836	chr8:96206937-96206938	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs572878425	chr8:96206941-96206942	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs141718944	chr8:96206957-96206958	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:866 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96201800-96206800	Enhancers	Fetal Thymus	thymus
2	chr8:96202600-96206200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:96203600-96208200	Weak transcription	Right Ventricle	heart
4	chr8:96203800-96206400	Enhancers	Hela-S3	cervix
5	chr8:96204400-96206400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr8:96204400-96208200	Weak transcription	Gastric	stomach
7	chr8:96204600-96206600	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr8:96204600-96212400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr8:96204800-96206600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr8:96205000-96206400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr8:96205000-96208000	Weak transcription	Primary B cells from peripheral blood	blood
12	chr8:96205000-96213400	Weak transcription	Lung	lung
13	chr8:96205600-96210200	Weak transcription	HMEC	breast
14	chr8:96205600-96213800	Weak transcription	Thymus	Thymus
15	chr8:96205800-96207000	Weak transcription	Esophagus	oesophagus
16	chr8:96205800-96207000	Weak transcription	HSMMtube	muscle
17	chr8:96205800-96207600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:96205800-96208200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:96205800-96208200	Weak transcription	NHEK	skin
20	chr8:96206000-96208200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:96206000-96208200	Weak transcription	Placenta	Placenta
22	chr8:96206200-96210000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:96206400-96206800	Weak transcription	Hela-S3	cervix
24	chr8:96206400-96215000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr8:96206600-96207000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:96206600-96208200	Weak transcription	Right Atrium	heart
27	chr8:96206800-96208000	Weak transcription	Fetal Thymus	thymus
28	chr8:96206800-96208800	Enhancers	Hela-S3	cervix
29	chr8:96207000-96207200	Enhancers	HSMMtube	muscle
30	chr8:96207000-96207400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:96207000-96209200	Enhancers	Esophagus	oesophagus
32	chr8:96207400-96208000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr8:96207400-96212800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:96207600-96207800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:96207800-96208400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:96208000-96208400	Enhancers	Primary B cells from peripheral blood	blood
37	chr8:96208200-96208600	Enhancers	Gastric	stomach
38	chr8:96208200-96208600	Enhancers	Right Atrium	heart
39	chr8:96208200-96209000	Enhancers	Placenta	Placenta
40	chr8:96208200-96209000	Enhancers	Right Ventricle	heart
41	chr8:96208200-96209000	Enhancers	Stomach Mucosa	stomach
42	chr8:96208200-96209200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr8:96208200-96211000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr8:96208200-96211200	Enhancers	NHEK	skin
45	chr8:96208400-96209000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:96208400-96209200	Enhancers	Pancreas	Pancrea
47	chr8:96208400-96212000	Weak transcription	Primary B cells from peripheral blood	blood
48	chr8:96208600-96211800	Weak transcription	Right Atrium	heart
49	chr8:96208600-96216400	Weak transcription	Gastric	stomach
50	chr8:96208800-96210200	Weak transcription	Hela-S3	cervix

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