Variant report

Variant	esv2758262
Chromosome Location	chr11:32714643-33049940
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4574)
CpG islands
(count:3601)
Chromatin interactive
region (count:201)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4574 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33039311-33039873	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:32913427-32913694	HepG2	liver:	n/a	chr11:32913597-32913613
3	ARID3A	chr11:33037131-33037894	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:32814471-32814880	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:32851965-32852404	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:32850824-32851272	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:32975953-32975956	K562	blood:	n/a	n/a
8	ARID3A	chr11:32906515-32906528	K562	blood:	n/a	n/a
9	ARID3A	chr11:32728312-32729190	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:32913132-32913996	K562	blood:	n/a	chr11:32913597-32913613
11	ARID3A	chr11:33040791-33040796	HepG2	liver:	n/a	n/a
12	ARID3A	chr11:32728333-32728791	K562	blood:	n/a	n/a
13	ARID3A	chr11:33040233-33040432	HepG2	liver:	n/a	n/a
14	ARID3A	chr11:32915738-32916200	HepG2	liver:	n/a	n/a
15	ARID3A	chr11:32720244-32720392	HepG2	liver:	n/a	n/a
16	ATF1	chr11:32888538-32888562	K562	blood:	n/a	n/a
17	ATF1	chr11:32878012-32878101	K562	blood:	n/a	n/a
18	ATF1	chr11:33046458-33046503	K562	blood:	n/a	n/a
19	ATF1	chr11:32915664-32916142	K562	blood:	n/a	n/a
20	ATF1	chr11:32728632-32728832	K562	blood:	n/a	n/a
21	ATF2	chr11:32913292-32914128	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr11:32728438-32728961	GM12878	blood:	n/a	n/a
23	ATF2	chr11:32913700-32914254	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr11:32850594-32851339	GM12878	blood:	n/a	n/a
25	ATF2	chr11:32913742-32914213	GM12878	blood:	n/a	n/a
26	ATF2	chr11:32915625-32916189	GM12878	blood:	n/a	n/a
27	ATF2	chr11:33033025-33033631	GM12878	blood:	n/a	n/a
28	ATF2	chr11:32913808-32914188	GM12878	blood:	n/a	n/a
29	ATF2	chr11:32914760-32915526	GM12878	blood:	n/a	n/a
30	ATF2	chr11:32850720-32851321	GM12878	blood:	n/a	n/a
31	ATF2	chr11:32728471-32728962	GM12878	blood:	n/a	n/a
32	ATF2	chr11:32915613-32916188	GM12878	blood:	n/a	n/a
33	ATF3	chr11:32728578-32728824	K562	blood:	n/a	n/a
34	ATF3	chr11:33037243-33037511	HepG2	liver:	n/a	chr11:33037392-33037401
35	ATF3	chr11:33037116-33037523	H1-hESC	embryonic stem cell:	n/a	chr11:33037392-33037401
36	ATF3	chr11:33037237-33037556	H1-hESC	embryonic stem cell:	n/a	chr11:33037392-33037401
37	ATF3	chr11:33037205-33037643	K562	blood:	n/a	chr11:33037392-33037401
38	ATF3	chr11:32915769-32916187	K562	blood:	n/a	n/a
39	BACH1	chr11:33037926-33038067	K562	blood:	n/a	n/a
40	BACH1	chr11:32935881-32935887	K562	blood:	n/a	n/a
41	BACH1	chr11:32862150-32862517	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr11:32728557-32728875	K562	blood:	n/a	chr11:32728711-32728725
43	BACH1	chr11:32915078-32915472	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr11:33037095-33037637	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr11:32913665-32914328	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr11:32791060-32791286	K562	blood:	n/a	n/a
47	BACH1	chr11:32928699-32928715	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr11:32913936-32914116	K562	blood:	n/a	n/a
49	BACH1	chr11:32791164-32791439	H1-hESC	embryonic stem cell:	n/a	n/a
50	BATF	chr11:33033446-33033786	GM12878	blood:	n/a	n/a

(count:3601 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:32851177-32851227	HRPEpiC	eye:	n/a
2	chr11:33038313-33038363	GM12891	blood:	n/a
3	chr11:32851177-32851227	HRPEpiC	eye:	n/a
4	chr11:33038313-33038363	GM12891	blood:	n/a
5	chr11:33023005-33023055	HCM	heart:	n/a
6	chr11:32915823-32915873	RPTEC	kidney:	n/a
7	chr11:32914818-32914868	NHBE	bronchial:	n/a
8	chr11:32959933-32959983	PFSK-1	brain:	n/a
9	chr11:33037397-33037447	T-47D	breast:	n/a
10	chr11:32851260-32851310	HRCEpiC	kidney:	n/a
11	chr11:32914605-32914655	A549	lung:	n/a
12	chr11:32915131-32915181	NHDF-neo	bronchial:	n/a
13	chr11:32816080-32816130	Caco-2	colon:	n/a
14	chr11:32816885-32816935	AG09309	skin:	n/a
15	chr11:32915903-32915953	NHBE	bronchial:	n/a
16	chr11:32851240-32851290	PANC-1	pancreas:	n/a
17	chr11:32851346-32851396	HEK293	kidney:	embryo
18	chr11:32914648-32914698	T-47D	breast:	n/a
19	chr11:32926880-32926930	ovcar-3	ovarian:	n/a
20	chr11:32915131-32915181	AoSMC	blood vessel:	n/a
21	chr11:33037397-33037447	MCF-7	breast:	n/a
22	chr11:32851378-32851428	K562	blood:	n/a
23	chr11:32815865-32815915	SAEC	small airway:	n/a
24	chr11:32851361-32851411	Hela-S3	cervix:	n/a
25	chr11:33038313-33038363	Caco-2	colon:	n/a
26	chr11:33000491-33000541	AG09319	gingival:	n/a
27	chr11:32914618-32914668	GM12892	blood:	n/a
28	chr11:33037530-33037580	SK-N-MC	brain:	n/a
29	chr11:32914648-32914698	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:32916120-32916170	SK-N-SH	brain:	n/a
31	chr11:32913990-32914040	HRE	kidney:	n/a
32	chr11:32816227-32816277	SK-N-SH_RA	brain:	n/a
33	chr11:32909110-32909160	AG09319	gingival:	n/a
34	chr11:33037792-33037842	HRPEpiC	eye:	n/a
35	chr11:32851177-32851227	U87	brain:	n/a
36	chr11:33000491-33000541	HRE	kidney:	n/a
37	chr11:32915497-32915547	ECC-1	luminal epithelium:	n/a
38	chr11:33036574-33036624	CMK	blood:	n/a
39	chr11:32854320-32854370	Hela-S3	cervix:	n/a
40	chr11:33038313-33038363	SAEC	small airway:	n/a
41	chr11:32851371-32851421	HL-60	blood:	n/a
42	chr11:32919083-32919133	HAEpiC	amniotic membrane:	n/a
43	chr11:32851361-32851411	AG10803	skin:	n/a
44	chr11:33037624-33037674	A549	lung:	n/a
45	chr11:32851371-32851421	Hepatocyte	liver:	n/a
46	chr11:32851378-32851428	ECC-1	luminal epithelium:	n/a
47	chr11:32851177-32851227	HEK293	kidney:	embryo
48	chr11:32851950-32852000	HCF	heart:	n/a
49	chr11:33000491-33000541	BE2_C	brain:	n/a
50	chr11:32909418-32909468	IMR90	lung:	fetal

(count:201 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr11:32808269..32810578-chr11:32811401..32813892,2	K562	blood:
2	chr11:32911547..32917607-chr11:32930395..32938117,12	K562	blood:
3	chr11:32945489..32947897-chr11:32951878..32954086,3	MCF-7	breast:
4	chr11:33038166..33041060-chr11:33046643..33049387,2	MCF-7	breast:
5	chr11:32912801..32916780-chr11:33060030..33062962,4	MCF-7	breast:
6	chr11:32935648..32937235-chr11:32951020..32953921,2	MCF-7	breast:
7	chr11:32900766..32903313-chr11:32912451..32914688,2	K562	blood:
8	chr11:32982056..32982733-chr11:33350989..33351739,2	K562	blood:
9	chr11:32941568..32943265-chr11:33077961..33080633,2	MCF-7	breast:
10	chr11:33043473..33045913-chr11:33047452..33049632,3	K562	blood:
11	chr11:32851461..32852210-chr3:49058647..49059440,2	NB4	blood:
12	chr11:33043473..33045913-chr11:33047452..33049632,3	K562	blood:
13	chr11:32851501..32854370-chr11:32879596..32881538,2	MCF-7	breast:
14	chr11:32850001..32854483-chr11:32912810..32915962,5	MCF-7	breast:
15	chr11:32915892..32917470-chr11:32980726..32982282,2	K562	blood:
16	chr11:32919542..32926976-chr11:32927671..32932534,9	K562	blood:
17	chr11:32913447..32916787-chr11:32944160..32946280,4	K562	blood:
18	chr11:32914066..32915835-chr11:33278115..33280779,2	K562	blood:
19	chr11:32850001..32854483-chr11:32912810..32915962,5	MCF-7	breast:
20	chr11:32911083..32916400-chr11:33180278..33184105,5	K562	blood:
21	chr11:32982353..32983263-chr11:33086839..33087416,2	MCF-7	breast:
22	chr11:32916175..32919465-chr11:32932228..32934625,3	K562	blood:
23	chr11:32946755..32948347-chr11:32949662..32952100,2	MCF-7	breast:
24	chr11:32734751..32735852-chr11:32814047..32815123,4	K562	blood:
25	chr11:32914076..32914799-chr6:26123502..26124171,2	Hela-S3	cervix:
26	chr11:32770910..32771799-chr11:32813954..32815012,4	MCF-7	breast:
27	chr11:32914073..32914891-chr6:27858213..27859098,2	HCT-116	colon:
28	chr11:32912444..32914191-chr11:32997049..32998828,2	K562	blood:
29	chr11:32849868..32852880-chr11:32911360..32916794,6	MCF-7	breast:
30	chr11:32723875..32726854-chr11:32913788..32916126,2	K562	blood:
31	chr11:32892015..32892872-chr11:32914554..32915403,2	MCF-7	breast:
32	chr11:32913172..32915250-chr11:32939039..32941847,3	K562	blood:
33	chr11:32925698..32927365-chr11:32931913..32934059,2	K562	blood:
34	chr11:32924828..32927562-chr11:32932566..32935396,2	MCF-7	breast:
35	chr11:32862368..32865112-chr11:32868900..32870710,2	K562	blood:
36	chr11:33043183..33045594-chr11:33046266..33049632,4	K562	blood:
37	chr11:32996304..32999169-chr11:33001880..33003438,2	MCF-7	breast:
38	chr11:32862368..32865112-chr11:32868900..32870710,2	K562	blood:
39	chr11:32994287..32996312-chr11:32999002..33001854,3	K562	blood:
40	chr11:32904524..32910209-chr11:32910222..32915650,10	MCF-7	breast:
41	chr11:32913434..32915654-chr11:32937933..32940006,3	MCF-7	breast:
42	chr11:32770910..32771799-chr11:32813954..32815012,4	MCF-7	breast:
43	chr11:32996304..32999169-chr11:33001880..33003438,2	MCF-7	breast:
44	chr11:32913437..32915867-chr11:32930703..32933783,3	MCF-7	breast:
45	chr11:32914058..32916371-chr11:32975765..32977557,2	MCF-7	breast:
46	chr11:32933148..32935266-chr11:32937418..32940169,3	K562	blood:
47	chr11:32925698..32927365-chr11:32931913..32934059,2	K562	blood:
48	chr11:32955247..32956983-chr11:32962122..32964180,2	K562	blood:
49	chr11:32949447..32951560-chr11:32996072..32998442,2	K562	blood:
50	chr11:32950716..32952924-chr11:32954824..32956515,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSTF3-1	chr11:33036823-33036899	NONHSAT018681
2	lnc-QSER1-1	chr11:32878980-32879666	NONHSAT018678
3	lnc-PRRG4-3	chr11:32823241-32823497	NONHSAT018675
4	lnc-CCDC73-1	chr11:32878982-32879665	ENSG00000248689
5	lnc-PRRG4-2	chr11:32839176-32839252	NONHSAT018676
6	lnc-PRRG4-2	chr11:32839485-32839664	NONHSAT018676
7	lnc-CCDC73-2	chr11:32817536-32817819	NONHSAT018674
8	lnc-PRRG4-4	chr11:32779814-32780160	NONHSAT018673
9	lnc-PRRG4-1	chr11:32846016-32846832	NONHSAT018677
10	lnc-CCDC73-1	chr11:32875249-32875810	ENSG00000248689
11	lnc-QSER1-1	chr11:32875249-32875808	NONHSAT018678
12	lnc-CSTF3-1	chr11:32978271-32978312	NONHSAT018681
13	lnc-CSTF3-1	chr11:33025345-33025436	NONHSAT018681
14	lnc-CSTF3-1	chr11:32977870-32978000	NONHSAT018681

No data

Variant related genes	Relation type
CCDC73	TF binding region
DEPDC7	TF binding region
ENSG00000244535	TF binding region
QSER1	TF binding region
ENSG00000200615	TF binding region
PRRG4	TF binding region
CCDC73	CpG island
DEPDC7	CpG island
ENSG00000244535	CpG island
QSER1	CpG island
ENSG00000200615	CpG island
PRRG4	CpG island
ENSG00000184937	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000231770	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000176148	chromatin interactions
ENSG00000248489	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000086189	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000247151	chromatin interactions
ENSG00000201403	chromatin interactions
ENSG00000110422	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000257337	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000260259	chromatin interactions
ENSG00000153207	chromatin interactions
ENSG00000125740	chromatin interactions
ENSG00000153015	chromatin interactions
ENSG00000186714	chromatin interactions
ENSG00000184445	chromatin interactions
ENSG00000151849	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000200615	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000121690	chromatin interactions
ENSG00000079215	chromatin interactions
ENSG00000135378	chromatin interactions
ENSG00000165006	chromatin interactions
ENSG00000086200	chromatin interactions
ENSG00000152256	chromatin interactions
ENSG00000176102	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000185324	chromatin interactions
ENSG00000188846	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000183242	chromatin interactions
ENSG00000228265	chromatin interactions
LMAN2L	miRNA target sites
FBXW7	miRNA target sites

Extended variants
information (count: 9328 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:9328 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142655085	chr11:32714656-32714657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs144155339	chr11:32714685-32714686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562596001	chr11:32714687-32714688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531402714	chr11:32714688-32714689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551614296	chr11:32714721-32714722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571370588	chr11:32714760-32714761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533742886	chr11:32714777-32714778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147774590	chr11:32714793-32714794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567431589	chr11:32714811-32714812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141170658	chr11:32714897-32714898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150323197	chr11:32714900-32714901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537753381	chr11:32714921-32714922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568211983	chr11:32714947-32714948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556009987	chr11:32714995-32714996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567929308	chr11:32714997-32714998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12289390	chr11:32715092-32715093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs558780360	chr11:32715161-32715162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs137999714	chr11:32715175-32715176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555273012	chr11:32715196-32715197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575159999	chr11:32715245-32715246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542661754	chr11:32715256-32715257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562430954	chr11:32715272-32715273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201273951	chr11:32715315-32715316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531435141	chr11:32715338-32715339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545133599	chr11:32715391-32715392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190619874	chr11:32715411-32715412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554594712	chr11:32715412-32715413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149076084	chr11:32715420-32715421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567244496	chr11:32715454-32715455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182835126	chr11:32715455-32715456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549772198	chr11:32715472-32715473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569762679	chr11:32715488-32715489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186426673	chr11:32715504-32715505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111580695	chr11:32715524-32715525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192283940	chr11:32715550-32715551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373912974	chr11:32715564-32715565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572908296	chr11:32715570-32715571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183652170	chr11:32715623-32715624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187924903	chr11:32715639-32715640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535244452	chr11:32715651-32715652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143141697	chr11:32715684-32715685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190665913	chr11:32715716-32715717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544085362	chr11:32715728-32715729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182778508	chr11:32715755-32715756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576144432	chr11:32715809-32715810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187101960	chr11:32715952-32715953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375710559	chr11:32715955-32715956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138724015	chr11:32716005-32716006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192307876	chr11:32716017-32716018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138936109	chr11:32716081-32716082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4272 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32711000-32725600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:32714600-32716400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr11:32716200-32717800	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr11:32716400-32717800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr11:32716800-32717800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr11:32717200-32717800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr11:32719800-32720600	Flanking Active TSS	A549	lung
8	chr11:32720000-32720400	Enhancers	HepG2	liver
9	chr11:32720600-32721000	Enhancers	A549	lung
10	chr11:32722800-32724200	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr11:32722800-32724600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr11:32723000-32723600	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr11:32723000-32723600	Enhancers	Primary hematopoietic stem cells	blood
14	chr11:32723000-32723800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr11:32723200-32723800	Enhancers	Dnd41	blood
16	chr11:32723400-32723800	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr11:32723600-32724600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr11:32723800-32725600	Weak transcription	Dnd41	blood
19	chr11:32724600-32724800	Enhancers	Primary hematopoietic stem cells	blood
20	chr11:32725600-32725800	Enhancers	Gastric	stomach
21	chr11:32725600-32726200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr11:32725600-32727200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:32725600-32727200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr11:32725600-32727200	ZNF genes & repeats	Dnd41	blood
25	chr11:32725800-32726400	ZNF genes & repeats	Gastric	stomach
26	chr11:32726800-32727200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr11:32727000-32727200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr11:32727000-32729800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr11:32727600-32728400	Enhancers	A549	lung
30	chr11:32727800-32729600	Enhancers	Hela-S3	cervix
31	chr11:32728200-32728800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:32728200-32729200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:32728200-32729400	Enhancers	GM12878-XiMat	blood
34	chr11:32728200-32729400	Enhancers	HMEC	breast
35	chr11:32728200-32729400	Enhancers	NHLF	lung
36	chr11:32728400-32729000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr11:32728400-32729000	Enhancers	Osteobl	bone
38	chr11:32728400-32729200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr11:32728400-32729400	Enhancers	Muscle Satellite Cultured Cells	--
40	chr11:32728400-32729400	Flanking Active TSS	A549	lung
41	chr11:32728400-32729400	Enhancers	HepG2	liver
42	chr11:32728400-32729600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:32728400-32729600	Enhancers	NHEK	skin
44	chr11:32728600-32728800	Enhancers	NH-A	brain
45	chr11:32728800-32729000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr11:32728800-32729000	Enhancers	Colon Smooth Muscle	Colon
47	chr11:32728800-32729200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:32728800-32729200	Enhancers	Rectal Smooth Muscle	rectum
49	chr11:32728800-32729200	Flanking Active TSS	NH-A	brain
50	chr11:32728800-32729400	Enhancers	HSMM	muscle

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