Variant report

Variant	esv2764086
Chromosome Location	chr8:9216584-9334601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:913)
CpG islands
(count:183)
Chromatin interactive
region (count:12)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:913 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:9278878-9279410	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:9278102-9278582	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:9308180-9309361	HepG2	liver:	n/a	chr8:9309163-9309179
4	ARID3A	chr8:9291262-9291958	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:9334453-9334756	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:9221142-9221337	K562	blood:	n/a	n/a
7	ARID3A	chr8:9226585-9226862	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:9318207-9318547	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:9306103-9306534	HepG2	liver:	n/a	n/a
10	ATF1	chr8:9221037-9221355	K562	blood:	n/a	n/a
11	ATF1	chr8:9278166-9278351	K562	blood:	n/a	n/a
12	ATF2	chr8:9321110-9321873	GM12878	blood:	n/a	n/a
13	ATF2	chr8:9321026-9321933	GM12878	blood:	n/a	n/a
14	ATF3	chr8:9273451-9273572	K562	blood:	n/a	n/a
15	BACH1	chr8:9269856-9270069	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:9221030-9221358	K562	blood:	n/a	n/a
17	BACH1	chr8:9271926-9271967	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:9237674-9237953	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:9273684-9273878	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr8:9268141-9268184	K562	blood:	n/a	n/a
21	BACH1	chr8:9220327-9220372	K562	blood:	n/a	n/a
22	BACH1	chr8:9259998-9260555	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr8:9273578-9273842	K562	blood:	n/a	n/a
24	BACH1	chr8:9237732-9237985	K562	blood:	n/a	n/a
25	BACH1	chr8:9226532-9226872	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr8:9321011-9321638	GM12878	blood:	n/a	chr8:9321598-9321608
27	BATF	chr8:9321035-9321493	GM12878	blood:	n/a	n/a
28	BATF	chr8:9226494-9226823	GM12878	blood:	n/a	n/a
29	BATF	chr8:9268145-9268417	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:9321156-9321595	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:9321269-9321587	GM12878	blood:	n/a	n/a
32	BCLAF1	chr8:9321068-9321564	GM12878	blood:	n/a	n/a
33	BCLAF1	chr8:9226485-9226841	GM12878	blood:	n/a	n/a
34	BCLAF1	chr8:9321061-9321689	GM12878	blood:	n/a	chr8:9321596-9321605 chr8:9321597-9321606
35	BHLHE40	chr8:9321148-9321624	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:9279045-9279235	HepG2	liver:	n/a	n/a
37	BHLHE40	chr8:9308092-9309235	HepG2	liver:	n/a	n/a
38	BHLHE40	chr8:9259868-9260006	K562	blood:	n/a	chr8:9259912-9259933 chr8:9259916-9259929
39	BHLHE40	chr8:9221180-9221258	K562	blood:	n/a	n/a
40	BHLHE40	chr8:9237710-9238179	K562	blood:	n/a	n/a
41	BHLHE40	chr8:9308226-9308311	K562	blood:	n/a	n/a
42	BHLHE40	chr8:9259888-9259949	HepG2	liver:	n/a	chr8:9259912-9259933 chr8:9259916-9259929
43	BHLHE40	chr8:9261373-9261581	K562	blood:	n/a	n/a
44	BHLHE40	chr8:9334452-9334719	HepG2	liver:	n/a	n/a
45	BHLHE40	chr8:9273206-9273409	K562	blood:	n/a	chr8:9273312-9273321
46	BHLHE40	chr8:9226526-9226876	K562	blood:	n/a	n/a
47	BRCA1	chr8:9226519-9226761	HepG2	liver:	n/a	n/a
48	BRCA1	chr8:9226534-9226825	Hela-S3	cervix:	n/a	chr8:9226776-9226785
49	CBX3	chr8:9226579-9226779	K562	blood:	n/a	n/a
50	CBX3	chr8:9230323-9230652	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:9278742-9278792	HRPEpiC	eye:	n/a
2	chr8:9278742-9278792	PFSK-1	brain:	n/a
3	chr8:9260354-9260404	LNCaP	prostate:	n/a
4	chr8:9260354-9260404	AG10803	skin:	n/a
5	chr8:9278742-9278792	HNPCEpiC	eye:	n/a
6	chr8:9260335-9260385	NHBE	bronchial:	n/a
7	chr8:9260354-9260404	T-47D	breast:	n/a
8	chr8:9278742-9278792	NHBE	bronchial:	n/a
9	chr8:9278742-9278792	HAEpiC	amniotic membrane:	n/a
10	chr8:9260354-9260404	SKMC	muscle:	n/a
11	chr8:9260354-9260404	HL-60	blood:	n/a
12	chr8:9278742-9278792	RPTEC	kidney:	n/a
13	chr8:9260354-9260404	AG09309	skin:	n/a
14	chr8:9278742-9278792	T-47D	breast:	n/a
15	chr8:9260354-9260404	HUVEC	blood vessel:	n/a
16	chr8:9278742-9278792	IMR90	lung:	fetal
17	chr8:9260335-9260385	BE2_C	brain:	n/a
18	chr8:9278742-9278792	HEK293	kidney:	embryo
19	chr8:9260354-9260404	NH-A	brain:	n/a
20	chr8:9260335-9260385	HepG2	liver:	n/a
21	chr8:9278742-9278792	SKMC	muscle:	n/a
22	chr8:9278742-9278792	Jurkat	blood:	n/a
23	chr8:9278742-9278792	AG04449	skin:	fetal
24	chr8:9260335-9260385	PFSK-1	brain:	n/a
25	chr8:9278742-9278792	HCT-116	colon:	n/a
26	chr8:9260335-9260385	PANC-1	pancreas:	n/a
27	chr8:9260335-9260385	RPTEC	kidney:	n/a
28	chr8:9278742-9278792	HepG2	liver:	n/a
29	chr8:9278742-9278792	HUVEC	blood vessel:	n/a
30	chr8:9278742-9278792	AoSMC	blood vessel:	n/a
31	chr8:9260335-9260385	HCPEpiC	choroid plexus:	n/a
32	chr8:9278742-9278792	MCF-7	breast:	n/a
33	chr8:9278742-9278792	HCF	heart:	n/a
34	chr8:9278742-9278792	NT2-D1	testis:	n/a
35	chr8:9260354-9260404	GM12892	blood:	n/a
36	chr8:9260335-9260385	Caco-2	colon:	n/a
37	chr8:9260335-9260385	ProgFib	skin:	n/a
38	chr8:9278742-9278792	K562	blood:	n/a
39	chr8:9260354-9260404	RPTEC	kidney:	n/a
40	chr8:9260354-9260404	HNPCEpiC	eye:	n/a
41	chr8:9278742-9278792	ovcar-3	ovarian:	n/a
42	chr8:9260354-9260404	NHDF-neo	bronchial:	n/a
43	chr8:9260335-9260385	H1-hESC	embryonic stem cell:	embryo
44	chr8:9278742-9278792	A549	lung:	n/a
45	chr8:9260335-9260385	HRCEpiC	kidney:	n/a
46	chr8:9260354-9260404	K562	blood:	n/a
47	chr8:9278742-9278792	HRE	kidney:	n/a
48	chr8:9260335-9260385	HPAEpiC	pulmonary alveolar:	n/a
49	chr8:9260335-9260385	SK-N-MC	brain:	n/a
50	chr8:9260335-9260385	GM19239	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:9239070..9241481-chr8:9260327..9263090,2	MCF-7	breast:
2	chr8:9226621..9227308-chr8:9534051..9534690,2	MCF-7	breast:
3	chr8:9239070..9241481-chr8:9260327..9263090,2	MCF-7	breast:
4	chr8:9225162..9228698-chr8:9411632..9414803,4	MCF-7	breast:
5	chr8:9239162..9240719-chr8:9243045..9245390,2	K562	blood:
6	chr8:9226234..9227282-chr8:9688101..9689055,3	K562	blood:
7	chr8:9048939..9051745-chr8:9268709..9271649,2	K562	blood:
8	chr8:9243360..9245127-chr8:9412175..9414634,2	MCF-7	breast:
9	chr8:9239162..9240719-chr8:9243045..9245390,2	K562	blood:
10	chr8:9224923..9225494-chr8:9688129..9688755,2	MCF-7	breast:
11	chr8:9268719..9271294-chr8:9413214..9415247,2	MCF-7	breast:
12	chr8:9322565..9324066-chr8:9347698..9350401,2	K562	blood:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-10A14.4.1-4	chr8:9220822-9221223	ucscGeneNc_uc003wsq_1
2	lnc-TNKS-5	chr8:9314677-9314928	NONHSAT124956
3	lnc-TNKS-5	chr8:9313405-9314332	NONHSAT124956
4	lnc-PPP1R3B-4	chr8:9232444-9232475	ENSG00000254237
5	lnc-RP11-10A14.4.1-4	chr8:9227324-9230000	ucscGeneNc_uc003wsq_1
6	lnc-PPP1R3B-7	chr8:9266473-9267064	l_3547_chr8:9260263-9270085_testes
7	lnc-RP11-10A14.4.1-4	chr8:9218876-9218933	ENSG00000254235
8	lnc-TNKS-6	chr8:9233409-9235120	NONHSAT124952
9	lnc-PPP1R3B-4	chr8:9237490-9237882	ENSG00000254237
10	lnc-PPP1R3B-7	chr8:9267774-9268026	l_3547_chr8:9260263-9270085_testes
11	lnc-PPP1R3B-4	chr8:9230365-9230616	ENSG00000254237
12	lnc-RP11-10A14.4.1-4	chr8:9271159-9271386	NONHSAT124948
13	lnc-PPP1R3B-4	chr8:9241382-9241510	ENSG00000254237
14	lnc-PPP1R3B-6	chr8:9254520-9254602	l_3545_chr8:9246176-9254602_testes
15	lnc-PPP1R3B-9	chr8:9299027-9299099	NONHSAT124955
16	lnc-PPP1R3B-4	chr8:9273386-9273450	ENSG00000254237
17	lnc-RP11-10A14.4.1-4	chr8:9220768-9220892	NONHSAT124947
18	lnc-PPP1R3B-7	chr8:9269854-9270085	l_3547_chr8:9260263-9270085_testes
19	lnc-PPP1R3B-4	chr8:9261455-9261554	ENSG00000254237
20	lnc-TNKS-4	chr8:9318958-9319950	FPKM1_group_30860_transcript_4
21	lnc-PPP1R3B-8	chr8:9282245-9282386	NONHSAT124954
22	lnc-PPP1R3B-3	chr8:9217110-9217269	XLOC_007000
23	lnc-RP11-10A14.4.1-4	chr8:9218876-9218896	NONHSAT124940
24	lnc-PPP1R3B-4	chr8:9229480-9229649	ENSG00000254237
25	lnc-RP11-10A14.4.1-4	chr8:9249713-9250217	NONHSAT124947
26	lnc-TNKS-4	chr8:9318958-9319950	NONHSAT124957
27	lnc-PPP1R3B-7	chr8:9260264-9260351	l_3547_chr8:9260263-9270085_testes
28	lnc-RP11-10A14.4.1-4	chr8:9219971-9220333	ucscGeneNc_uc003wsq_1
29	lnc-PPP1R3B-4	chr8:9293542-9293715	ENSG00000254237
30	lnc-PPP1R3B-8	chr8:9280338-9281391	NONHSAT124954
31	lnc-PPP1R3B-8	chr8:9279664-9279765	NONHSAT124954
32	lnc-RP11-10A14.4.1-4	chr8:9220768-9220892	NONHSAT124948
33	lnc-RP11-10A14.4.1-4	chr8:9224971-9225402	ENSG00000254235
34	lnc-PPP1R3B-6	chr8:9246177-9246469	l_3545_chr8:9246176-9254602_testes
35	lnc-RP11-10A14.4.1-4	chr8:9220772-9220892	ENSG00000254235
36	lnc-TNKS-4	chr8:9319116-9319330	FPKM1_group_30860_transcript_4
37	lnc-TNKS-5	chr8:9311208-9311467	NONHSAT124956
38	lnc-PPP1R3B-4	chr8:9241382-9241510	ENSG00000254237
39	lnc-PPP1R3B-4	chr8:9232408-9232649	ENSG00000254237
40	lnc-PPP1R3B-9	chr8:9304981-9305257	NONHSAT124955
41	lnc-TNKS-4	chr8:9320538-9320752	NONHSAT124957
42	lnc-PPP1R3B-6	chr8:9253261-9253358	l_3545_chr8:9246176-9254602_testes
43	lnc-TNKS-5	chr8:9311815-9312409	NONHSAT124956

No data

Variant related genes	Relation type
ENSG00000249050	TF binding region
ENSG00000254237	TF binding region
RNU6-526P	TF binding region
ENSG00000253735	TF binding region
ENSG00000249050	CpG island
ENSG00000254237	CpG island
RNU6-526P	CpG island
ENSG00000253735	CpG island
ENSG00000173273	chromatin interactions
ENSG00000272267	chromatin interactions

Extended variants
information (count: 5175 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:5175 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9329191	chr8:9216584-9216585	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556961912	chr8:9216628-9216629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9329192	chr8:9216647-9216648	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs185689448	chr8:9216648-9216649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113474717	chr8:9216653-9216654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572167218	chr8:9216665-9216666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370887299	chr8:9216680-9216681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541130694	chr8:9216691-9216692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548173479	chr8:9216701-9216702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533171923	chr8:9216702-9216703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543832613	chr8:9216710-9216711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563806133	chr8:9216722-9216723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188684667	chr8:9216752-9216753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs28541420	chr8:9216759-9216760	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs28394733	chr8:9216764-9216765	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs369352857	chr8:9216766-9216767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs80329816	chr8:9216830-9216831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200911427	chr8:9216876-9216877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528143908	chr8:9216883-9216884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs180713016	chr8:9216906-9216907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571402571	chr8:9216907-9216908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12550199	chr8:9216924-9216925	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs367841494	chr8:9216928-9216929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556966897	chr8:9216934-9216935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs530648673	chr8:9216946-9216947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs78051589	chr8:9216948-9216949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186007234	chr8:9216960-9216961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148909394	chr8:9216962-9216963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2169384	chr8:9216986-9216987	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs541093913	chr8:9217037-9217038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557812738	chr8:9217076-9217077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192162054	chr8:9217111-9217112	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs4345557	chr8:9217123-9217124	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs370214265	chr8:9217127-9217128	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs563738937	chr8:9217144-9217145	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs141129892	chr8:9217147-9217148	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs186397779	chr8:9217150-9217151	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs559956986	chr8:9217191-9217192	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs1381350	chr8:9217195-9217196	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs570961419	chr8:9217216-9217217	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs111817600	chr8:9217219-9217220	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs190496045	chr8:9217225-9217226	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs540034708	chr8:9217265-9217266	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs552033598	chr8:9217280-9217281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553643954	chr8:9217295-9217296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182902054	chr8:9217308-9217309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4507762	chr8:9217339-9217340	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs554962536	chr8:9217342-9217343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550267533	chr8:9217347-9217348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150992886	chr8:9217348-9217349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9216000-9218400	Enhancers	Liver	Liver
2	chr8:9216800-9221200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:9217200-9218400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:9217400-9218200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:9218400-9218800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:9218400-9221200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:9218400-9226400	Weak transcription	Liver	Liver
8	chr8:9220600-9220800	Enhancers	K562	blood
9	chr8:9220800-9221200	Flanking Active TSS	K562	blood
10	chr8:9221000-9221400	Enhancers	Brain Germinal Matrix	brain
11	chr8:9221200-9221600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr8:9221200-9221800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:9221200-9221800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr8:9221200-9221800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:9221200-9221800	Enhancers	K562	blood
16	chr8:9221400-9221800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:9221800-9224800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:9226200-9226800	Weak transcription	Right Atrium	heart
19	chr8:9226200-9244400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:9226400-9226600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr8:9226400-9226600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr8:9226400-9226600	Enhancers	Primary B cells from peripheral blood	blood
23	chr8:9226400-9226600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr8:9226400-9226600	Enhancers	Brain Angular Gyrus	brain
25	chr8:9226400-9226600	Flanking Active TSS	Brain Anterior Caudate	brain
26	chr8:9226400-9226600	Enhancers	Brain Hippocampus Middle	brain
27	chr8:9226400-9226600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
28	chr8:9226400-9226600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr8:9226400-9226600	Enhancers	Fetal Intestine Small	intestine
30	chr8:9226400-9226600	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr8:9226400-9226800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr8:9226400-9226800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr8:9226400-9226800	Enhancers	Liver	Liver
34	chr8:9226400-9226800	Enhancers	Fetal Intestine Large	intestine
35	chr8:9226400-9226800	Bivalent Enhancer	HUVEC	blood vessel
36	chr8:9226400-9227000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr8:9226400-9227000	Active TSS	Brain Cingulate Gyrus	brain
38	chr8:9226400-9227200	Enhancers	Placenta	Placenta
39	chr8:9226600-9226800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:9226600-9226800	Active TSS	Primary hematopoietic stem cells	blood
41	chr8:9226600-9226800	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
42	chr8:9226600-9226800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr8:9226600-9226800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr8:9226600-9226800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr8:9226600-9226800	Active TSS	Brain Germinal Matrix	brain
46	chr8:9226600-9226800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
47	chr8:9226600-9226800	Bivalent Enhancer	Fetal Intestine Small	intestine
48	chr8:9226600-9226800	Active TSS	Skeletal Muscle Female	skeletal muscle
49	chr8:9226600-9226800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
50	chr8:9226600-9227000	Bivalent Enhancer	Primary B cells from peripheral blood	blood

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