Variant report

Variant	esv2757921
Chromosome Location	chr4:10343699-10545800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1722)
CpG islands
(count:2201)
Chromatin interactive
region (count:187)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1722 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10459741-10459919	K562	blood:	n/a	n/a
2	ARID3A	chr4:10416844-10416961	K562	blood:	n/a	n/a
3	ARID3A	chr4:10405152-10405708	K562	blood:	n/a	n/a
4	ARID3A	chr4:10460913-10461399	K562	blood:	n/a	n/a
5	ARID3A	chr4:10539745-10539913	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:10539570-10539891	K562	blood:	n/a	n/a
7	ARID3A	chr4:10373102-10373103	HepG2	liver:	n/a	n/a
8	ATF3	chr4:10462880-10463147	K562	blood:	n/a	n/a
9	ATF3	chr4:10497303-10497547	K562	blood:	n/a	n/a
10	BACH1	chr4:10462736-10463370	K562	blood:	n/a	n/a
11	BACH1	chr4:10446374-10446389	K562	blood:	n/a	n/a
12	BACH1	chr4:10461300-10461416	K562	blood:	n/a	n/a
13	BACH1	chr4:10462826-10463788	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:10444197-10445521	K562	blood:	n/a	n/a
15	BACH1	chr4:10458630-10459108	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr4:10537480-10537757	GM12878	blood:	n/a	n/a
17	BATF	chr4:10537483-10537720	GM12878	blood:	n/a	n/a
18	BATF	chr4:10440575-10440842	GM12878	blood:	n/a	chr4:10440756-10440766
19	BATF	chr4:10461948-10462177	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:10511488-10511709	K562	blood:	n/a	n/a
21	BHLHE40	chr4:10460967-10461712	K562	blood:	n/a	n/a
22	BHLHE40	chr4:10405415-10405586	K562	blood:	n/a	n/a
23	BHLHE40	chr4:10458951-10459247	GM12878	blood:	n/a	chr4:10459125-10459141
24	BHLHE40	chr4:10458017-10458645	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:10531035-10531100	K562	blood:	n/a	n/a
26	BHLHE40	chr4:10353695-10353726	K562	blood:	n/a	n/a
27	BHLHE40	chr4:10459217-10460106	K562	blood:	n/a	n/a
28	BHLHE40	chr4:10376277-10376477	K562	blood:	n/a	n/a
29	BHLHE40	chr4:10387822-10388106	K562	blood:	n/a	n/a
30	BHLHE40	chr4:10497245-10497653	K562	blood:	n/a	n/a
31	BHLHE40	chr4:10462903-10463146	GM12878	blood:	n/a	chr4:10462953-10462969 chr4:10462950-10462966 chr4:10462947-10462963 chr4:10462949-10462965
32	BHLHE40	chr4:10418648-10418697	GM12878	blood:	n/a	n/a
33	BHLHE40	chr4:10462844-10463255	K562	blood:	n/a	chr4:10462953-10462969 chr4:10462950-10462966 chr4:10462947-10462963 chr4:10462949-10462965 chr4:10463133-10463149
34	BHLHE40	chr4:10497301-10497575	HepG2	liver:	n/a	n/a
35	BRCA1	chr4:10462928-10463022	GM12878	blood:	n/a	n/a
36	BRCA1	chr4:10463085-10463106	HepG2	liver:	n/a	n/a
37	CBX3	chr4:10462629-10463372	K562	blood:	n/a	n/a
38	CBX3	chr4:10444650-10444918	K562	blood:	n/a	n/a
39	CBX3	chr4:10462293-10463603	K562	blood:	n/a	n/a
40	CBX3	chr4:10458207-10458558	K562	blood:	n/a	n/a
41	CBX3	chr4:10527957-10529036	HCT-116	colon:	n/a	n/a
42	CBX3	chr4:10459827-10460193	K562	blood:	n/a	n/a
43	CCNT2	chr4:10346894-10347462	K562	blood:	n/a	n/a
44	CCNT2	chr4:10405344-10405663	K562	blood:	n/a	n/a
45	CCNT2	chr4:10387632-10388049	K562	blood:	n/a	n/a
46	CCNT2	chr4:10419643-10419843	K562	blood:	n/a	n/a
47	CCNT2	chr4:10532044-10532251	K562	blood:	n/a	n/a
48	CCNT2	chr4:10462773-10463268	K562	blood:	n/a	n/a
49	CCNT2	chr4:10459488-10460006	K562	blood:	n/a	chr4:10459969-10459978
50	CCNT2	chr4:10368408-10368665	K562	blood:	n/a	n/a

(count:2201 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10463620-10463670	H1-hESC	embryonic stem cell:	embryo
2	chr4:10372870-10372920	SK-N-SH_RA	brain:	n/a
3	chr4:10458918-10458968	Hepatocyte	liver:	n/a
4	chr4:10458667-10458717	HL-60	blood:	n/a
5	chr4:10463350-10463400	SKMC	muscle:	n/a
6	chr4:10463620-10463670	H1-hESC	embryonic stem cell:	embryo
7	chr4:10372870-10372920	SK-N-SH_RA	brain:	n/a
8	chr4:10458918-10458968	Hepatocyte	liver:	n/a
9	chr4:10458667-10458717	HL-60	blood:	n/a
10	chr4:10463350-10463400	SKMC	muscle:	n/a
11	chr4:10405694-10405744	MCF10A-Er-Src	breast:	n/a
12	chr4:10463749-10463799	RPTEC	kidney:	n/a
13	chr4:10459929-10459979	Hepatocyte	liver:	n/a
14	chr4:10459219-10459269	AG09309	skin:	n/a
15	chr4:10459836-10459886	NHDF-neo	bronchial:	n/a
16	chr4:10459228-10459278	HL-60	blood:	n/a
17	chr4:10459128-10459178	HEEpiC	esophagus:	n/a
18	chr4:10462849-10462899	HCPEpiC	choroid plexus:	n/a
19	chr4:10459836-10459886	Hela-S3	cervix:	n/a
20	chr4:10459929-10459979	HAEpiC	amniotic membrane:	n/a
21	chr4:10458918-10458968	AG09319	gingival:	n/a
22	chr4:10458531-10458581	HRE	kidney:	n/a
23	chr4:10459183-10459233	ECC-1	luminal epithelium:	n/a
24	chr4:10531768-10531818	U87	brain:	n/a
25	chr4:10459132-10459182	IMR90	lung:	fetal
26	chr4:10463749-10463799	HepG2	liver:	n/a
27	chr4:10459141-10459191	NHDF-neo	bronchial:	n/a
28	chr4:10531768-10531818	HEK293	kidney:	embryo
29	chr4:10459141-10459191	SK-N-MC	brain:	n/a
30	chr4:10458667-10458717	GM12878	blood:	n/a
31	chr4:10459163-10459213	HL-60	blood:	n/a
32	chr4:10372870-10372920	SK-N-MC	brain:	n/a
33	chr4:10463590-10463640	NHDF-neo	bronchial:	n/a
34	chr4:10531768-10531818	MCF-7	breast:	n/a
35	chr4:10459352-10459402	LNCaP	prostate:	n/a
36	chr4:10462849-10462899	NT2-D1	testis:	n/a
37	chr4:10467319-10467369	Hepatocyte	liver:	n/a
38	chr4:10461465-10461515	AG09309	skin:	n/a
39	chr4:10463350-10463400	ProgFib	skin:	n/a
40	chr4:10459228-10459278	K562	blood:	n/a
41	chr4:10531768-10531818	SK-N-SH	brain:	n/a
42	chr4:10498037-10498087	SK-N-SH	brain:	n/a
43	chr4:10459132-10459182	PrEC	prostate:	n/a
44	chr4:10456597-10456647	AG09319	gingival:	n/a
45	chr4:10458049-10458099	H1-hESC	embryonic stem cell:	embryo
46	chr4:10462849-10462899	LNCaP	prostate:	n/a
47	chr4:10459163-10459213	HNPCEpiC	eye:	n/a
48	chr4:10458918-10458968	HRE	kidney:	n/a
49	chr4:10405694-10405744	SK-N-SH	brain:	n/a
50	chr4:10459228-10459278	HCPEpiC	choroid plexus:	n/a

(count:187 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr4:10166490..10167101-chr4:10539409..10540077,2	MCF-7	breast:
2	chr4:10463521..10466499-chr4:10467971..10469908,2	K562	blood:
3	chr4:10366541..10368710-chr4:10369302..10371481,3	K562	blood:
4	chr4:10117292..10119185-chr4:10371644..10373221,2	K562	blood:
5	chr4:10346990..10348791-chr4:10349503..10352332,2	K562	blood:
6	chr4:10116151..10120402-chr4:10440722..10445122,4	K562	blood:
7	chr4:10439495..10442453-chr4:10454853..10458527,4	K562	blood:
8	chr4:10370932..10373880-chr4:10390683..10392321,2	K562	blood:
9	chr4:10338266..10339875-chr4:10342241..10344480,2	K562	blood:
10	chr4:10414281..10417254-chr4:10441057..10442576,2	K562	blood:
11	chr4:10374180..10377123-chr4:10380489..10383795,3	K562	blood:
12	chr4:10481628..10483228-chr4:10483399..10484967,2	K562	blood:
13	chr4:10431804..10434625-chr4:10441827..10447697,5	K562	blood:
14	chr4:10529511..10531855-chr4:10533474..10535069,2	K562	blood:
15	chr4:10441301..10442802-chr4:10444428..10446278,2	K562	blood:
16	chr4:10419551..10421094-chr4:10421815..10424714,2	K562	blood:
17	chr4:10116897..10119989-chr4:10451461..10454968,3	K562	blood:
18	chr4:10362193..10364438-chr4:10456296..10459241,2	K562	blood:
19	chr4:10117123..10120331-chr4:10451418..10454682,4	K562	blood:
20	chr4:10349621..10351967-chr4:10356635..10358807,2	K562	blood:
21	chr4:10390019..10393146-chr4:10400722..10404569,4	K562	blood:
22	chr4:10351809..10354070-chr4:10359322..10360898,2	K562	blood:
23	chr4:10122860..10124582-chr4:10454402..10456296,2	K562	blood:
24	chr4:10374180..10377123-chr4:10380489..10383795,3	K562	blood:
25	chr17:59945131..59945952-chr4:10405006..10405538,2	MCF-7	breast:
26	chr4:10462498..10464981-chr4:10471870..10474447,2	K562	blood:
27	chr4:10427499..10429493-chr4:10443184..10445146,2	K562	blood:
28	chr4:10413005..10416502-chr4:10417554..10421094,3	K562	blood:
29	chr4:10436735..10439258-chr4:10444645..10446611,2	K562	blood:
30	chr4:10509410..10511877-chr4:10515360..10517382,2	K562	blood:
31	chr4:10414281..10417254-chr4:10441057..10442576,2	K562	blood:
32	chr4:10385942..10388810-chr4:10389542..10391176,2	K562	blood:
33	chr17:34890127..34891028-chr4:10458093..10458597,2	HCT-116	colon:
34	chr4:10364753..10366272-chr4:10370398..10372088,2	K562	blood:
35	chr4:10436820..10442109-chr4:10453962..10457876,6	K562	blood:
36	chr4:10182435..10184114-chr4:10441654..10444481,2	K562	blood:
37	chr4:10119630..10121541-chr4:10538034..10541032,2	K562	blood:
38	chr4:10168181..10169847-chr4:10460956..10462626,2	K562	blood:
39	chr4:10439495..10442453-chr4:10454853..10458527,4	K562	blood:
40	chr4:10119097..10123564-chr4:10520690..10524781,5	K562	blood:
41	chr4:10303834..10305662-chr4:10370006..10372655,2	K562	blood:
42	chr4:10427499..10429493-chr4:10443184..10445146,2	K562	blood:
43	chr4:10109397..10110994-chr4:10487986..10490652,2	K562	blood:
44	chr4:10377322..10379936-chr4:10386087..10389023,2	K562	blood:
45	chr4:10534187..10535776-chr4:10538246..10540113,2	K562	blood:
46	chr4:10116877..10119746-chr4:10350370..10353025,2	K562	blood:
47	chr4:10186739..10189194-chr4:10403510..10406450,4	K562	blood:
48	chr4:10182377..10184143-chr4:10453503..10455042,2	K562	blood:
49	chr4:10483820..10485837-chr4:10490038..10492249,2	K562	blood:
50	chr4:10405058..10406722-chr4:10414024..10415781,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLNK-1	chr4:10480148-10480547	NONHSAT095504
2	lnc-DRD5-20	chr4:10439848-10440173	NONHSAT095499
3	lnc-CLNK-2	chr4:10458941-10459032	NONHSAT095501
4	lnc-DRD5-18	chr4:10369809-10369975	l_2604_chr4:10348296-10419642_testes
5	lnc-CLNK-2	chr4:10458941-10459034	NONHSAT095502
6	lnc-CLNK-2	chr4:10452511-10456612	NONHSAT095502
7	lnc-DRD5-19	chr4:10437730-10438054	NONHSAT095500
8	lnc-DRD5-18	chr4:10359894-10360314	l_2604_chr4:10348296-10419642_testes
9	lnc-DRD5-21	chr4:10486610-10487079	NONHSAT095505
10	lnc-DRD5-4	chr4:10404495-10404649	NONHSAT095495
11	lnc-DRD5-18	chr4:10352660-10352812	l_2604_chr4:10348296-10419642_testes
12	lnc-ZNF518B-1	chr4:10433041-10433567	NONHSAT095498
13	lnc-DRD5-18	chr4:10348828-10349271	l_2604_chr4:10348296-10419642_testes
14	lnc-CLNK-2	chr4:10458758-10458800	NONHSAT095503
15	lnc-DRD5-4	chr4:10409553-10409610	FPKM1_group_22843_transcript_2
16	lnc-DRD5-18	chr4:10419449-10419642	l_2604_chr4:10348296-10419642_testes
17	lnc-DRD5-4	chr4:10404495-10404649	FPKM1_group_22843_transcript_2
18	lnc-CLNK-2	chr4:10452511-10456612	NONHSAT095503
19	lnc-DRD5-18	chr4:10348297-10348499	l_2604_chr4:10348296-10419642_testes
20	lnc-CLNK-2	chr4:10452511-10454646	NONHSAT095501
21	lnc-DRD5-4	chr4:10409553-10410132	NONHSAT095495
22	lnc-DRD5-20	chr4:10436252-10437668	NONHSAT095499
23	lnc-CLNK-2	chr4:10456218-10456612	NONHSAT095501

No data

Variant related genes	Relation type
ZNF518B	TF binding region
CLNK	TF binding region
ENSG00000250613	TF binding region
ENSG00000248419	TF binding region
ZNF518B	CpG island
CLNK	CpG island
ENSG00000250613	CpG island
ENSG00000248419	CpG island
ENSG00000141140	chromatin interactions
ENSG00000250505	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000184886	chromatin interactions
ENSG00000248777	chromatin interactions
ENSG00000251296	chromatin interactions
ENSG00000109684	chromatin interactions
ENSG00000250074	chromatin interactions
ENSG00000248419	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000250613	chromatin interactions

Extended variants
information (count: 8936 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:8936 , 50 per page) page: 1 2 3 4 5 6 7 ... 179

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557799929	chr4:10343713-10343714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551904402	chr4:10343737-10343738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143019112	chr4:10343758-10343759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528306110	chr4:10343767-10343768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546854625	chr4:10343771-10343772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78277567	chr4:10343775-10343776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566530116	chr4:10343789-10343790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535421386	chr4:10343809-10343810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556692071	chr4:10343816-10343817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533875697	chr4:10343828-10343829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145164134	chr4:10343842-10343843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370129809	chr4:10343843-10343844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138693964	chr4:10343864-10343865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6856833	chr4:10343891-10343892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs17419975	chr4:10343911-10343912	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs577496087	chr4:10343916-10343917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541674058	chr4:10343917-10343918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559672664	chr4:10343937-10343938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs59083556	chr4:10343939-10343940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149354938	chr4:10343951-10343952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575067793	chr4:10343991-10343992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542164067	chr4:10343992-10343993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181117566	chr4:10344002-10344003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372496706	chr4:10344012-10344013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs60739271	chr4:10344023-10344024	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs530881359	chr4:10344034-10344035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545879203	chr4:10344099-10344100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542141453	chr4:10344109-10344110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528269353	chr4:10344113-10344114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115879201	chr4:10344148-10344149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144697618	chr4:10344159-10344160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61230832	chr4:10344165-10344166	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs535726906	chr4:10344167-10344168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568885134	chr4:10344169-10344170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539473289	chr4:10344176-10344177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184478341	chr4:10344212-10344213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537525194	chr4:10344220-10344221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571107760	chr4:10344250-10344251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76880000	chr4:10344260-10344261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189151198	chr4:10344284-10344285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182003666	chr4:10344287-10344288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76180948	chr4:10344300-10344301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542178171	chr4:10344308-10344309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369903727	chr4:10344349-10344350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373321963	chr4:10344351-10344352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557672558	chr4:10344356-10344357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575214662	chr4:10344358-10344359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545842638	chr4:10344362-10344363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7654423	chr4:10344431-10344432	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs186202895	chr4:10344432-10344433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21990379	CNVD

Chromatin state (count:2112 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10338800-10346800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:10339200-10346800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:10339400-10346800	Weak transcription	NHEK	skin
4	chr4:10339800-10345400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:10340000-10346400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:10343400-10345800	Weak transcription	K562	blood
7	chr4:10345200-10346000	Enhancers	HMEC	breast
8	chr4:10345400-10345800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:10345400-10348600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:10345800-10347000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:10345800-10347200	Enhancers	K562	blood
12	chr4:10346000-10347000	Weak transcription	HMEC	breast
13	chr4:10346200-10348200	Enhancers	Placenta	Placenta
14	chr4:10346400-10348800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:10346800-10347200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr4:10346800-10347600	Enhancers	Lung	lung
17	chr4:10346800-10348600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:10346800-10348600	Enhancers	Placenta Amnion	Placenta Amnion
19	chr4:10346800-10348600	Enhancers	NHEK	skin
20	chr4:10347000-10348600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:10347000-10349400	Enhancers	HMEC	breast
22	chr4:10347200-10347800	Flanking Active TSS	K562	blood
23	chr4:10347200-10348400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr4:10347200-10348600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr4:10347800-10349600	Enhancers	K562	blood
26	chr4:10348400-10351600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr4:10348600-10354400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:10348600-10355000	Weak transcription	NHEK	skin
29	chr4:10348600-10355400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:10348800-10349200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:10349200-10349400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:10349200-10351600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:10349400-10350600	Weak transcription	HMEC	breast
34	chr4:10349400-10355600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:10349600-10353400	Weak transcription	K562	blood
36	chr4:10353400-10353800	Enhancers	K562	blood
37	chr4:10353800-10355000	Weak transcription	HMEC	breast
38	chr4:10353800-10356200	Weak transcription	K562	blood
39	chr4:10354400-10355000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:10354600-10357000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:10355000-10355200	Enhancers	NHEK	skin
42	chr4:10355000-10355400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr4:10355000-10356600	Enhancers	HMEC	breast
44	chr4:10355200-10356000	Weak transcription	NHEK	skin
45	chr4:10355400-10357000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr4:10355400-10357600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:10355600-10356400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:10355600-10356800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr4:10356000-10356800	Enhancers	NHEK	skin
50	chr4:10356200-10356800	Enhancers	K562	blood

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