Variant report

Variant	esv3361772
Chromosome Location	chr4:15666732-15684418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1041)
CpG islands
(count:612)
Chromatin interactive
region (count:42)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:15671764-15671961	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:15682685-15683480	K562	blood:	n/a	n/a
3	ARID3A	chr4:15681520-15681997	K562	blood:	n/a	n/a
4	ARID3A	chr4:15678570-15678731	K562	blood:	n/a	n/a
5	ARID3A	chr4:15677903-15678084	K562	blood:	n/a	n/a
6	ARID3A	chr4:15679102-15680659	K562	blood:	n/a	chr4:15680344-15680360 chr4:15680345-15680361
7	ARID3A	chr4:15679048-15679681	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:15681140-15681298	K562	blood:	n/a	n/a
9	ATF1	chr4:15679256-15679597	K562	blood:	n/a	n/a
10	ATF2	chr4:15682845-15683733	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:15682720-15683739	GM12878	blood:	n/a	n/a
12	ATF2	chr4:15682900-15683624	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:15682925-15683476	GM12878	blood:	n/a	n/a
14	ATF3	chr4:15683205-15683492	K562	blood:	n/a	n/a
15	ATF3	chr4:15678850-15679197	K562	blood:	n/a	n/a
16	ATF3	chr4:15682964-15683764	A549	lung:	n/a	n/a
17	ATF3	chr4:15683084-15683514	A549	lung:	n/a	n/a
18	BCL3	chr4:15682906-15683659	A549	lung:	n/a	n/a
19	BCL3	chr4:15682932-15683657	A549	lung:	n/a	n/a
20	BCL3	chr4:15682872-15683441	K562	blood:	n/a	n/a
21	BCLAF1	chr4:15682817-15683515	K562	blood:	n/a	n/a
22	BCLAF1	chr4:15682879-15683736	GM12878	blood:	n/a	n/a
23	BCLAF1	chr4:15682790-15683713	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:15682828-15683673	K562	blood:	n/a	n/a
25	BHLHE40	chr4:15679136-15679611	K562	blood:	n/a	n/a
26	BHLHE40	chr4:15682954-15683796	HepG2	liver:	n/a	n/a
27	BHLHE40	chr4:15682664-15683530	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:15683926-15684173	K562	blood:	n/a	n/a
29	BHLHE40	chr4:15680783-15681149	K562	blood:	n/a	n/a
30	BHLHE40	chr4:15681538-15682061	K562	blood:	n/a	n/a
31	BRCA1	chr4:15667486-15667686	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr4:15682998-15683654	HepG2	liver:	n/a	n/a
33	BRCA1	chr4:15682826-15683622	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr4:15682957-15683823	GM12878	blood:	n/a	n/a
35	BRCA1	chr4:15682878-15683779	H1-hESC	embryonic stem cell:	n/a	n/a
36	CBX3	chr4:15682844-15683719	K562	blood:	n/a	n/a
37	CBX3	chr4:15667309-15667865	HCT-116	colon:	n/a	n/a
38	CBX3	chr4:15683012-15683371	K562	blood:	n/a	n/a
39	CCNT2	chr4:15682806-15683987	K562	blood:	n/a	n/a
40	CEBPB	chr4:15680294-15680624	K562	blood:	n/a	chr4:15680456-15680467
41	CEBPB	chr4:15677721-15678018	A549	lung:	n/a	chr4:15677848-15677861 chr4:15677849-15677860
42	CEBPB	chr4:15677667-15678039	K562	blood:	n/a	chr4:15677848-15677861 chr4:15677849-15677860
43	CEBPB	chr4:15677700-15677977	Hela-S3	cervix:	n/a	chr4:15677848-15677861 chr4:15677849-15677860
44	CEBPB	chr4:15677687-15678035	IMR90	lung:	n/a	chr4:15677848-15677861 chr4:15677849-15677860
45	CEBPB	chr4:15682975-15683479	K562	blood:	n/a	n/a
46	CEBPB	chr4:15667392-15667758	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr4:15679326-15679597	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:15679897-15680071	A549	lung:	n/a	n/a
49	CEBPB	chr4:15667225-15667861	HCT-116	colon:	n/a	n/a
50	CEBPB	chr4:15682164-15682389	H1-hESC	embryonic stem cell:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:15683284-15683334	K562	blood:	n/a
2	chr4:15682941-15682991	HCPEpiC	choroid plexus:	n/a
3	chr4:15683284-15683334	K562	blood:	n/a
4	chr4:15682941-15682991	HCPEpiC	choroid plexus:	n/a
5	chr4:15683497-15683547	SAEC	small airway:	n/a
6	chr4:15679598-15679648	HEK293	kidney:	embryo
7	chr4:15683206-15683256	MCF10A-Er-Src	breast:	n/a
8	chr4:15682922-15682972	PrEC	prostate:	n/a
9	chr4:15683206-15683256	HEEpiC	esophagus:	n/a
10	chr4:15683124-15683174	SK-N-SH_RA	brain:	n/a
11	chr4:15679598-15679648	AG04450	lung:	fetal
12	chr4:15683124-15683174	HRPEpiC	eye:	n/a
13	chr4:15683224-15683274	ovcar-3	ovarian:	n/a
14	chr4:15683284-15683334	BE2_C	brain:	n/a
15	chr4:15683224-15683274	Caco-2	colon:	n/a
16	chr4:15682922-15682972	ProgFib	skin:	n/a
17	chr4:15683224-15683274	HAEpiC	amniotic membrane:	n/a
18	chr4:15683224-15683274	GM12891	blood:	n/a
19	chr4:15683497-15683547	AG10803	skin:	n/a
20	chr4:15683224-15683274	NH-A	brain:	n/a
21	chr4:15683124-15683174	NB4	blood:	n/a
22	chr4:15683497-15683547	HMEC	breast:	n/a
23	chr4:15682941-15682991	HEEpiC	esophagus:	n/a
24	chr4:15682922-15682972	MCF10A-Er-Src	breast:	n/a
25	chr4:15683218-15683268	HCM	heart:	n/a
26	chr4:15683206-15683256	NH-A	brain:	n/a
27	chr4:15683224-15683274	PFSK-1	brain:	n/a
28	chr4:15683284-15683334	Jurkat	blood:	n/a
29	chr4:15679598-15679648	AG09319	gingival:	n/a
30	chr4:15683124-15683174	HEEpiC	esophagus:	n/a
31	chr4:15683284-15683334	MCF-7	breast:	n/a
32	chr4:15679598-15679648	GM19239	blood:	n/a
33	chr4:15683124-15683174	NT2-D1	testis:	n/a
34	chr4:15682922-15682972	HL-60	blood:	n/a
35	chr4:15683218-15683268	T-47D	breast:	n/a
36	chr4:15683691-15683741	LNCaP	prostate:	n/a
37	chr4:15682941-15682991	HMEC	breast:	n/a
38	chr4:15679598-15679648	HRCEpiC	kidney:	n/a
39	chr4:15682941-15682991	IMR90	lung:	fetal
40	chr4:15683224-15683274	HepG2	liver:	n/a
41	chr4:15683691-15683741	AG09319	gingival:	n/a
42	chr4:15683124-15683174	AoSMC	blood vessel:	n/a
43	chr4:15683206-15683256	MCF-7	breast:	n/a
44	chr4:15683691-15683741	T-47D	breast:	n/a
45	chr4:15683206-15683256	SK-N-MC	brain:	n/a
46	chr4:15683284-15683334	Hela-S3	cervix:	n/a
47	chr4:15683206-15683256	H1-hESC	embryonic stem cell:	embryo
48	chr4:15682922-15682972	LNCaP	prostate:	n/a
49	chr4:15683206-15683256	NB4	blood:	n/a
50	chr4:15683691-15683741	A549	lung:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:15652080..15658606-chr4:15677363..15685579,17	MCF-7	breast:
2	chr4:15651703..15660794-chr4:15677607..15686235,25	K562	blood:
3	chr4:15681714..15684664-chr4:16226494..16229781,3	K562	blood:
4	chr4:15673240..15674969-chr4:15677739..15681015,3	MCF-7	breast:
5	chr4:15681636..15683511-chr4:15686226..15688652,2	K562	blood:
6	chr4:15480315..15482682-chr4:15674758..15677054,2	MCF-7	breast:
7	chr1:206858096..206858827-chr4:15682769..15683336,2	Hela-S3	cervix:
8	chr4:15662285..15665284-chr4:15678264..15680948,2	MCF-7	breast:
9	chr4:15003674..15005700-chr4:15682740..15684585,3	K562	blood:
10	chr4:15664444..15667043-chr4:15668246..15669921,2	K562	blood:
11	chr4:15673240..15674969-chr4:15677739..15681015,3	MCF-7	breast:
12	chr4:15668976..15670549-chr4:15675107..15677746,2	MCF-7	breast:
13	chr4:15656601..15660282-chr4:15674023..15676952,3	MCF-7	breast:
14	chr4:15663938..15667635-chr4:15670287..15673065,4	K562	blood:
15	chr4:15669572..15671315-chr4:15723195..15724968,2	MCF-7	breast:
16	chr3:134204301..134205283-chr4:15682678..15683336,2	Hela-S3	cervix:
17	chr4:15659405..15662406-chr4:15663977..15668803,5	MCF-7	breast:
18	chr4:15652202..15654659-chr4:15668639..15670937,2	MCF-7	breast:
19	chr4:15664653..15666973-chr4:15669930..15673591,3	MCF-7	breast:
20	chr4:15669270..15672127-chr4:15677094..15678755,2	MCF-7	breast:
21	chr4:15681678..15685124-chr4:15685309..15687808,5	MCF-7	breast:
22	chr4:15668976..15670549-chr4:15675107..15677746,2	MCF-7	breast:
23	chr4:15655595..15658742-chr4:15680185..15687360,10	MCF-7	breast:
24	chr4:15650206..15660298-chr4:15677140..15687517,25	K562	blood:
25	chr4:15682398..15684850-chr8:101964333..101966529,2	MCF-7	breast:
26	chr4:15656755..15658996-chr4:15665833..15667600,3	MCF-7	breast:
27	chr4:15664444..15667043-chr4:15668246..15669921,2	K562	blood:
28	chr1:53685929..53686881-chr4:15682646..15683566,2	HCT-116	colon:
29	chr4:15663938..15667635-chr4:15670287..15673065,4	K562	blood:
30	chr4:15664653..15666973-chr4:15669930..15673591,3	MCF-7	breast:
31	chr4:15667185..15670762-chr4:15673659..15675755,3	K562	blood:
32	chr4:15659126..15661222-chr4:15677719..15679356,2	MCF-7	breast:
33	chr4:15669222..15672294-chr4:15681695..15684873,3	K562	blood:
34	chr4:15479910..15482087-chr4:15683434..15685124,3	MCF-7	breast:
35	chr4:15669176..15670885-chr4:15682529..15684654,2	MCF-7	breast:
36	chr4:15667185..15670762-chr4:15673659..15675755,3	K562	blood:
37	chr4:15669270..15672127-chr4:15677094..15678755,2	MCF-7	breast:
38	chr4:15655677..15658651-chr4:15671837..15675305,4	MCF-7	breast:
39	chr4:15666992..15669093-chr4:15681918..15684119,2	MCF-7	breast:
40	chr4:15653293..15659319-chr4:15668815..15673574,11	MCF-7	breast:
41	chr4:15654775..15659231-chr4:15659761..15666940,9	K562	blood:
42	chr4:15655910..15661308-chr4:15665213..15668611,5	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM200B-1	chr4:15683292-15683407	NONHSAT095628
2	lnc-FAM200B-1	chr4:15683446-15683524	NONHSAT095640
3	lnc-FAM200B-1	chr4:15683458-15683591	NONHSAT095642
4	lnc-FBXL5-5	chr4:15682903-15683302	NONHSAT095626
5	lnc-FAM200B-1	chr4:15683285-15683407	NONHSAT095627
6	lnc-FAM200B-1	chr4:15683419-15683591	NONHSAT095638
7	lnc-FAM200B-1	chr4:15683448-15683524	NONHSAT095641
8	lnc-FAM200B-1	chr4:15683429-15683644	NONHSAT095639
9	lnc-FAM200B-1	chr4:15683379-15683524	NONHSAT095633
10	lnc-FAM200B-1	chr4:15683414-15683524	NONHSAT095637
11	lnc-FAM200B-1	chr4:15683380-15683524	NONHSAT095636
12	lnc-FAM200B-1	chr4:15683377-15683644	NONHSAT095631
13	lnc-FAM200B-1	chr4:15683379-15683407	NONHSAT095634
14	lnc-FAM200B-1	chr4:15683379-15683591	NONHSAT095635
15	lnc-FAM200B-1	chr4:15683356-15683524	NONHSAT095630

No data

Variant related genes	Relation type
FAM200B	TF binding region
FBXL5	TF binding region
FAM200B	CpG island
FBXL5	CpG island
ENSG00000237765	chromatin interactions
ENSG00000137449	chromatin interactions
ENSG00000169762	chromatin interactions
ENSG00000118564	chromatin interactions
ENSG00000259818	chromatin interactions
ENSG00000048342	chromatin interactions
ENSG00000162384	chromatin interactions
ENSG00000164924	chromatin interactions
ENSG00000263327	chromatin interactions
ENSG00000162889	chromatin interactions
ENSG00000129055	chromatin interactions
ENSG00000182923	chromatin interactions

Extended variants
information (count: 618 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:618 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200357320	chr4:15666782-15666783	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs73243114	chr4:15666816-15666817	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs562118437	chr4:15666829-15666830	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs202154896	chr4:15666869-15666870	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs376295816	chr4:15666873-15666874	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs531179378	chr4:15666890-15666891	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs145633477	chr4:15666959-15666960	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs138263182	chr4:15666961-15666962	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs187207314	chr4:15667017-15667018	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs191242333	chr4:15667084-15667085	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs113451527	chr4:15667178-15667179	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs559536899	chr4:15667190-15667191	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs566488574	chr4:15667336-15667337	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs529155184	chr4:15667349-15667350	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs76632768	chr4:15667382-15667383	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs373786843	chr4:15667384-15667385	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs568948519	chr4:15667400-15667401	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs538005298	chr4:15667462-15667463	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs557535414	chr4:15667463-15667464	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531603863	chr4:15667469-15667470	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539563174	chr4:15667471-15667472	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs115226713	chr4:15667512-15667513	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs35939471	chr4:15667514-15667515	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs573215703	chr4:15667537-15667538	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs542153651	chr4:15667567-15667568	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs556062942	chr4:15667621-15667622	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs200674716	chr4:15667639-15667640	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs12507207	chr4:15667646-15667647	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs371311564	chr4:15667647-15667648	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs544768576	chr4:15667648-15667649	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs11939541	chr4:15667724-15667725	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs183769906	chr4:15667747-15667748	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs540363443	chr4:15667750-15667751	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs527875475	chr4:15667852-15667853	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs188417002	chr4:15667885-15667886	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs113522548	chr4:15667889-15667890	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs113362594	chr4:15667890-15667891	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs548711959	chr4:15667904-15667905	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs569086987	chr4:15667930-15667931	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs142643028	chr4:15667941-15667942	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs146040133	chr4:15667977-15667978	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs138653428	chr4:15667980-15667981	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs185637638	chr4:15668008-15668009	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs190101222	chr4:15668114-15668115	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs117244396	chr4:15668127-15668128	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs149913260	chr4:15668133-15668134	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs549948370	chr4:15668161-15668162	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs137957142	chr4:15668168-15668169	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs376005155	chr4:15668172-15668173	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs374182047	chr4:15668178-15668179	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
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
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
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Breast cancer	22522925	CNVD
Non-small cell lung cancer	21829676	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:848 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15657600-15681400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr4:15657800-15666800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:15657800-15667800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr4:15658000-15666800	Weak transcription	Thymus	Thymus
5	chr4:15658000-15667400	Weak transcription	Fetal Muscle Leg	muscle
6	chr4:15658000-15667800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:15658000-15672200	Weak transcription	Fetal Muscle Trunk	muscle
8	chr4:15658000-15673800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:15658000-15675200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:15658000-15679000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr4:15658000-15681400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr4:15658200-15666800	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr4:15658200-15667200	Weak transcription	Fetal Thymus	thymus
14	chr4:15658200-15667400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr4:15658200-15667400	Weak transcription	NH-A	brain
16	chr4:15658200-15667800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr4:15658200-15667800	Weak transcription	NHLF	lung
18	chr4:15658200-15668000	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr4:15658200-15670600	Weak transcription	Brain Cingulate Gyrus	brain
20	chr4:15658200-15679200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:15658200-15679200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr4:15658200-15682200	Weak transcription	Fetal Stomach	stomach
23	chr4:15658400-15667000	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr4:15658400-15667400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr4:15658400-15668400	Weak transcription	Dnd41	blood
26	chr4:15658400-15668600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr4:15658600-15673000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:15658600-15679000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr4:15659600-15668200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr4:15659800-15678600	Weak transcription	K562	blood
31	chr4:15660000-15667400	Weak transcription	HSMMtube	muscle
32	chr4:15660000-15667400	Weak transcription	NHDF-Ad	bronchial
33	chr4:15660000-15668600	Weak transcription	HepG2	liver
34	chr4:15660200-15670600	Weak transcription	Fetal Lung	lung
35	chr4:15660400-15679200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr4:15661200-15668000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:15661400-15667400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr4:15661600-15667200	Weak transcription	A549	lung
39	chr4:15661600-15667600	Weak transcription	Osteobl	bone
40	chr4:15661600-15668400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr4:15661600-15668800	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr4:15661600-15678600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:15661800-15667200	Weak transcription	HSMM	muscle
44	chr4:15662000-15667000	Weak transcription	Adipose Nuclei	Adipose
45	chr4:15662000-15667400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:15662000-15667400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr4:15662000-15668200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr4:15662200-15668600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:15662400-15667400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr4:15662400-15667400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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