Variant report

Variant	esv3427035
Chromosome Location	chr7:150862769-150866067
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:150865277-150865440	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr7:150865448-150865561	K562	blood:	n/a	n/a
3	CCNT2	chr7:150865180-150865617	K562	blood:	n/a	chr7:150865351-150865360
4	CREB1	chr7:150865213-150865579	A549	lung:	n/a	n/a
5	CTBP2	chr7:150863930-150864684	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr7:150864440-150864590	HCM	heart:	n/a	n/a
7	CTCF	chr7:150865400-150865550	AG04449	skin:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
8	CTCF	chr7:150864420-150864570	AG04450	lung:	n/a	n/a
9	CTCF	chr7:150865460-150865610	GM06990	blood:	n/a	chr7:150865474-150865490 chr7:150865473-150865491
10	CTCF	chr7:150865400-150865550	NHDF-neo	bronchial:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
11	CTCF	chr7:150865440-150865590	HCFaa	heart:	n/a	chr7:150865474-150865490 chr7:150865473-150865491
12	CTCF	chr7:150865420-150865570	AG04449	skin:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
13	CTCF	chr7:150865420-150865570	HCM	heart:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
14	CTCF	chr7:150865327-150865603	MCF-7	breast:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
15	CTCF	chr7:150865420-150865570	GM12801	blood:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
16	CTCF	chr7:150865400-150865550	GM12864	blood:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
17	CTCF	chr7:150865440-150865590	HBMEC	blood vessel:	n/a	chr7:150865474-150865490 chr7:150865473-150865491
18	CTCF	chr7:150865163-150866020	A549	lung:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
19	CTCF	chr7:150865400-150865550	GM12870	blood:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
20	CTCF	chr7:150865400-150865550	HRPEpiC	eye:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
21	CTCF	chr7:150865429-150865518	LNCaP	prostate:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
22	CTCF	chr7:150864940-150865090	HRPEpiC	eye:	n/a	chr7:150865077-150865090
23	CTCF	chr7:150865400-150865550	AG09319	gingival:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
24	CTCF	chr7:150865400-150865550	HepG2	liver:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
25	CTCF	chr7:150864460-150864610	K562	blood:	n/a	n/a
26	CTCF	chr7:150865308-150865606	MCF-7	breast:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
27	CTCF	chr7:150864580-150864762	T-47D	breast:	n/a	n/a
28	CTCF	chr7:150864480-150864630	HAc	cerebellar:	n/a	n/a
29	CTCF	chr7:150864284-150864630	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr7:150864400-150864550	GM12870	blood:	n/a	n/a
31	CTCF	chr7:150865440-150865590	GM12878	blood:	n/a	chr7:150865474-150865490 chr7:150865473-150865491
32	CTCF	chr7:150865309-150865602	HepG2	liver:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
33	CTCF	chr7:150865331-150865604	GM10266	blood:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
34	CTCF	chr7:150865290-150865641	A549	lung:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
35	CTCF	chr7:150864736-150864739	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr7:150865400-150865550	HMEC	breast:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
37	CTCF	chr7:150865420-150865570	GM12867	blood:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
38	CTCF	chr7:150865354-150865578	LNCaP	prostate:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
39	CTCF	chr7:150865182-150865260	A549	lung:	n/a	n/a
40	CTCF	chr7:150865460-150865610	HPAF	blood vessel:	n/a	chr7:150865474-150865490 chr7:150865473-150865491
41	CTCF	chr7:150864620-150864770	GM12869	blood:	n/a	n/a
42	CTCF	chr7:150864620-150864781	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:150865400-150865550	HVMF	connective:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
44	CTCF	chr7:150865322-150865585	Fibrobl	skin:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
45	CTCF	chr7:150865400-150865550	HCT-116	colon:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
46	CTCF	chr7:150864444-150864815	K562	blood:	n/a	n/a
47	CTCF	chr7:150865400-150865550	GM12878	blood:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
48	CTCF	chr7:150864460-150864610	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr7:150865380-150865530	GM12865	blood:	n/a	chr7:150865474-150865490 chr7:150865473-150865491 chr7:150865430-150865443
50	CTCF	chr7:150864513-150864750	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150864994-150865044	ovcar-3	ovarian:	n/a
2	chr7:150864987-150865037	GM12878	blood:	n/a
3	chr7:150864994-150865044	ovcar-3	ovarian:	n/a
4	chr7:150864987-150865037	GM12878	blood:	n/a
5	chr7:150864974-150865024	GM12878	blood:	n/a
6	chr7:150865207-150865257	NH-A	brain:	n/a
7	chr7:150865207-150865257	HRPEpiC	eye:	n/a
8	chr7:150864395-150864445	CMK	blood:	n/a
9	chr7:150865207-150865257	GM06990	blood:	n/a
10	chr7:150865930-150865980	AG09319	gingival:	n/a
11	chr7:150864521-150864571	AG10803	skin:	n/a
12	chr7:150863969-150864019	BE2_C	brain:	n/a
13	chr7:150864974-150865024	HCF	heart:	n/a
14	chr7:150864994-150865044	AG10803	skin:	n/a
15	chr7:150864885-150864935	HL-60	blood:	n/a
16	chr7:150865060-150865110	AG04449	skin:	fetal
17	chr7:150864521-150864571	ProgFib	skin:	n/a
18	chr7:150864974-150865024	BE2_C	brain:	n/a
19	chr7:150865291-150865341	H1-hESC	embryonic stem cell:	embryo
20	chr7:150864395-150864445	NT2-D1	testis:	n/a
21	chr7:150864521-150864571	SK-N-SH	brain:	n/a
22	chr7:150864996-150865046	A549	lung:	n/a
23	chr7:150864961-150865011	GM19239	blood:	n/a
24	chr7:150864885-150864935	HEK293	kidney:	embryo
25	chr7:150864996-150865046	HCF	heart:	n/a
26	chr7:150865186-150865236	BE2_C	brain:	n/a
27	chr7:150863969-150864019	K562	blood:	n/a
28	chr7:150864521-150864571	Hepatocyte	liver:	n/a
29	chr7:150864994-150865044	Jurkat	blood:	n/a
30	chr7:150865291-150865341	HNPCEpiC	eye:	n/a
31	chr7:150864395-150864445	SKMC	muscle:	n/a
32	chr7:150865930-150865980	HMEC	breast:	n/a
33	chr7:150864961-150865011	MCF-7	breast:	n/a
34	chr7:150864994-150865044	AoSMC	blood vessel:	n/a
35	chr7:150865186-150865236	SK-N-SH	brain:	n/a
36	chr7:150865930-150865980	Hela-S3	cervix:	n/a
37	chr7:150865930-150865980	NT2-D1	testis:	n/a
38	chr7:150865207-150865257	LNCaP	prostate:	n/a
39	chr7:150864395-150864445	GM12892	blood:	n/a
40	chr7:150864521-150864571	NHBE	bronchial:	n/a
41	chr7:150865207-150865257	PrEC	prostate:	n/a
42	chr7:150864961-150865011	GM12892	blood:	n/a
43	chr7:150862828-150862878	Hepatocyte	liver:	n/a
44	chr7:150864996-150865046	H1-hESC	embryonic stem cell:	embryo
45	chr7:150864987-150865037	ovcar-3	ovarian:	n/a
46	chr7:150864961-150865011	HNPCEpiC	eye:	n/a
47	chr7:150864987-150865037	AG10803	skin:	n/a
48	chr7:150865186-150865236	MCF-7	breast:	n/a
49	chr7:150864521-150864571	HCPEpiC	choroid plexus:	n/a
50	chr7:150865060-150865110	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:150865075..150865984-chr7:151000597..151001184,2	MCF-7	breast:
2	chr7:150865510..150867888-chr7:150868111..150870105,3	MCF-7	breast:
3	chr7:150820141..150822604-chr7:150863393..150866266,2	MCF-7	breast:
4	chr7:150862132..150865299-chr7:150928833..150931121,3	MCF-7	breast:
5	chr7:150865945..150868557-chr7:150928822..150930653,2	MCF-7	breast:
6	chr7:150824108..150825865-chr7:150861440..150864326,2	K562	blood:
7	chr7:150839778..150841717-chr7:150865578..150867319,2	K562	blood:
8	chr7:150864964..150867853-chr7:150903647..150905737,2	K562	blood:
9	chr7:150859717..150863159-chr7:150864095..150867866,6	K562	blood:
10	chr7:150864670..150867629-chr7:150867737..150869840,2	MCF-7	breast:
11	chr7:150865018..150866330-chr7:150941109..150942155,6	K562	blood:
12	chr7:150863436..150865058-chr7:150871430..150873448,2	MCF-7	breast:
13	chr7:150855142..150857552-chr7:150862337..150864254,3	MCF-7	breast:
14	chr7:150852560..150855237-chr7:150861683..150864566,2	MCF-7	breast:
15	chr7:150865011..150865946-chr7:151000191..151001152,4	K562	blood:
16	chr7:150857151..150859740-chr7:150859852..150862844,3	K562	blood:
17	chr7:150823153..150825845-chr7:150864127..150866768,5	MCF-7	breast:
18	chr7:150849801..150850474-chr7:150865426..150865984,2	MCF-7	breast:
19	chr7:150864964..150867853-chr7:150902641..150905737,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GBX1-1	chr7:150864098-150864278	NONHSAT124198

Variant related genes	Relation type
GBX1	TF binding region
GBX1	CpG island
ENSG00000164900	chromatin interactions
ENSG00000133612	chromatin interactions
ENSG00000033100	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183382246	chr7:150862800-150862801	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs559236278	chr7:150862864-150862865	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs553458242	chr7:150862994-150862995	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs74965800	chr7:150863006-150863007	Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs143775534	chr7:150863058-150863059	Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs530496497	chr7:150863066-150863067	Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs550523676	chr7:150863105-150863106	Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs73478605	chr7:150863156-150863157	Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567715512	chr7:150863178-150863179	Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs545560985	chr7:150863236-150863237	Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs567270088	chr7:150863242-150863243	Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs529711836	chr7:150863259-150863260	Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs546675876	chr7:150863270-150863271	Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs566137289	chr7:150863340-150863341	Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs534925576	chr7:150863358-150863359	Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs558009381	chr7:150863424-150863425	Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs17173717	chr7:150863456-150863457	Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs571583130	chr7:150863493-150863494	Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs537366536	chr7:150863539-150863540	Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs376110409	chr7:150863562-150863563	Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs376902580	chr7:150863565-150863566	Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs571698053	chr7:150863567-150863568	Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs560422086	chr7:150863568-150863569	Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs542752918	chr7:150863570-150863571	Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs542260816	chr7:150863572-150863573	Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs397889076	chr7:150863573-150863574	Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs553474143	chr7:150863609-150863610	Bivalent/Poised TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs573060037	chr7:150863631-150863632	Bivalent/Poised TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs545251046	chr7:150863676-150863677	Bivalent/Poised TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs188364314	chr7:150863751-150863752	Bivalent/Poised TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs530790121	chr7:150863783-150863784	Bivalent/Poised TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs527777221	chr7:150864012-150864013	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs544526359	chr7:150864015-150864016	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs560672553	chr7:150864018-150864019	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs529738402	chr7:150864027-150864028	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs542666192	chr7:150864043-150864044	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs546366739	chr7:150864044-150864045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs58304055	chr7:150864057-150864058	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs532100212	chr7:150864066-150864067	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs551527003	chr7:150864069-150864070	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs200640367	chr7:150864083-150864084	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs371770525	chr7:150864095-150864096	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs375522842	chr7:150864099-150864100	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs369810012	chr7:150864100-150864101	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs372158178	chr7:150864104-150864105	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs201756310	chr7:150864117-150864118	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs531566127	chr7:150864159-150864160	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs370046549	chr7:150864172-150864173	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs537304457	chr7:150864175-150864176	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs201650225	chr7:150864179-150864180	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150841400-150862800	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr7:150863000-150864800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr7:150863400-150863800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:150863400-150864200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
5	chr7:150863600-150863800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
6	chr7:150863600-150863800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
7	chr7:150863600-150863800	Bivalent Enhancer	Primary B cells from cord blood	blood
8	chr7:150863600-150863800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
9	chr7:150863600-150864000	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:150863600-150864000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:150863600-150864000	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
12	chr7:150863600-150864000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
13	chr7:150863600-150864000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:150863600-150864000	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
15	chr7:150863600-150864000	Active TSS	Ovary	ovary
16	chr7:150863600-150864200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:150863600-150864200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:150863600-150864200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:150863600-150864200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
20	chr7:150863600-150864400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
21	chr7:150863600-150865000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
22	chr7:150863600-150865600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
23	chr7:150863800-150864000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
24	chr7:150863800-150864000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
25	chr7:150863800-150864000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
26	chr7:150863800-150864000	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
27	chr7:150863800-150864000	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
28	chr7:150863800-150864000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
29	chr7:150863800-150864000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
30	chr7:150863800-150864000	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
31	chr7:150863800-150864000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
32	chr7:150863800-150864000	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
33	chr7:150863800-150864000	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr7:150863800-150864000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
35	chr7:150863800-150864000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr7:150863800-150864000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr7:150863800-150864000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr7:150863800-150864000	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
39	chr7:150863800-150864000	Bivalent Enhancer	Adipose Nuclei	Adipose
40	chr7:150863800-150864000	Bivalent Enhancer	Liver	Liver
41	chr7:150863800-150864000	Bivalent Enhancer	Brain Anterior Caudate	brain
42	chr7:150863800-150864000	Bivalent Enhancer	Brain Cingulate Gyrus	brain
43	chr7:150863800-150864000	Bivalent Enhancer	Brain Germinal Matrix	brain
44	chr7:150863800-150864000	Bivalent Enhancer	Brain Hippocampus Middle	brain
45	chr7:150863800-150864000	Bivalent Enhancer	Brain Substantia Nigra	brain
46	chr7:150863800-150864000	Bivalent Enhancer	Duodenum Mucosa	Duodenum
47	chr7:150863800-150864000	Bivalent Enhancer	Fetal Heart	heart
48	chr7:150863800-150864000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr7:150863800-150864000	Bivalent Enhancer	Fetal Muscle Leg	muscle
50	chr7:150863800-150864000	Bivalent Enhancer	Fetal Stomach	stomach

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