Variant report

Variant	nsv1030988
Chromosome Location	chr7:120636796-120672504
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:530)
CpG islands
(count:305)
Chromatin interactive
region (count:31)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:120661906-120661975	K562	blood:	n/a	n/a
2	ARID3A	chr7:120646050-120646078	K562	blood:	n/a	n/a
3	ARID3A	chr7:120670423-120670663	K562	blood:	n/a	n/a
4	ARID3A	chr7:120636448-120637008	K562	blood:	n/a	n/a
5	ARID3A	chr7:120659123-120659800	K562	blood:	n/a	n/a
6	ARID3A	chr7:120648443-120648852	K562	blood:	n/a	n/a
7	ARID3A	chr7:120638048-120641003	K562	blood:	n/a	chr7:120640489-120640505
8	ARID3A	chr7:120660910-120661207	K562	blood:	n/a	n/a
9	ARID3A	chr7:120664002-120664279	K562	blood:	n/a	n/a
10	ARID3A	chr7:120660577-120660593	K562	blood:	n/a	n/a
11	ARID3A	chr7:120646558-120647569	K562	blood:	n/a	n/a
12	ATF1	chr7:120643664-120644101	K562	blood:	n/a	n/a
13	ATF1	chr7:120640072-120640337	K562	blood:	n/a	n/a
14	ATF1	chr7:120636429-120636992	K562	blood:	n/a	n/a
15	ATF1	chr7:120637477-120637676	K562	blood:	n/a	n/a
16	ATF1	chr7:120640539-120640765	K562	blood:	n/a	n/a
17	ATF1	chr7:120658999-120659405	K562	blood:	n/a	n/a
18	BACH1	chr7:120640868-120641042	K562	blood:	n/a	n/a
19	BACH1	chr7:120644242-120644287	K562	blood:	n/a	n/a
20	BACH1	chr7:120664921-120665051	K562	blood:	n/a	n/a
21	BACH1	chr7:120646859-120646879	K562	blood:	n/a	n/a
22	BACH1	chr7:120664350-120664358	K562	blood:	n/a	n/a
23	BCLAF1	chr7:120640047-120640905	K562	blood:	n/a	n/a
24	BHLHE40	chr7:120636512-120637203	K562	blood:	n/a	n/a
25	BHLHE40	chr7:120638834-120638948	K562	blood:	n/a	n/a
26	BHLHE40	chr7:120663233-120663254	K562	blood:	n/a	n/a
27	BHLHE40	chr7:120640054-120640799	K562	blood:	n/a	n/a
28	BHLHE40	chr7:120641083-120641338	K562	blood:	n/a	n/a
29	BHLHE40	chr7:120646846-120647281	K562	blood:	n/a	n/a
30	BRCA1	chr7:120663498-120664536	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr7:120660284-120661088	Hela-S3	cervix:	n/a	n/a
32	CCNT2	chr7:120646977-120647211	K562	blood:	n/a	n/a
33	CCNT2	chr7:120653601-120653801	K562	blood:	n/a	n/a
34	CCNT2	chr7:120640493-120640702	K562	blood:	n/a	n/a
35	CCNT2	chr7:120651541-120651559	K562	blood:	n/a	n/a
36	CCNT2	chr7:120636860-120637060	K562	blood:	n/a	n/a
37	CEBPB	chr7:120659143-120659452	K562	blood:	n/a	n/a
38	CEBPB	chr7:120657096-120657397	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr7:120647089-120647385	A549	lung:	n/a	n/a
40	CEBPB	chr7:120663820-120664533	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:120660777-120661132	K562	blood:	n/a	chr7:120660939-120660950
42	CEBPB	chr7:120647179-120647307	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:120659089-120659643	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:120660763-120661128	HepG2	liver:	n/a	chr7:120660939-120660950
45	CEBPB	chr7:120642826-120643213	IMR90	lung:	n/a	chr7:120643068-120643079
46	CEBPB	chr7:120647073-120647395	K562	blood:	n/a	n/a
47	CEBPB	chr7:120668624-120668932	K562	blood:	n/a	n/a
48	CEBPB	chr7:120659116-120659475	K562	blood:	n/a	n/a
49	CEBPB	chr7:120647078-120647465	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:120659127-120659474	IMR90	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:120639815-120639865	HRCEpiC	kidney:	n/a
2	chr7:120662793-120662843	IMR90	lung:	fetal
3	chr7:120639815-120639865	Caco-2	colon:	n/a
4	chr7:120657213-120657263	HEEpiC	esophagus:	n/a
5	chr7:120657213-120657263	ECC-1	luminal epithelium:	n/a
6	chr7:120639815-120639865	AG04449	skin:	fetal
7	chr7:120657213-120657263	GM19239	blood:	n/a
8	chr7:120639815-120639865	HL-60	blood:	n/a
9	chr7:120644149-120644199	GM06990	blood:	n/a
10	chr7:120657213-120657263	HCPEpiC	choroid plexus:	n/a
11	chr7:120644149-120644199	NT2-D1	testis:	n/a
12	chr7:120657213-120657263	HIPEpiC	eye:	n/a
13	chr7:120639815-120639865	ProgFib	skin:	n/a
14	chr7:120657213-120657263	CMK	blood:	n/a
15	chr7:120657213-120657263	ovcar-3	ovarian:	n/a
16	chr7:120646878-120646928	HRPEpiC	eye:	n/a
17	chr7:120662793-120662843	NH-A	brain:	n/a
18	chr7:120644149-120644199	HRE	kidney:	n/a
19	chr7:120644149-120644199	LNCaP	prostate:	n/a
20	chr7:120662793-120662843	K562	blood:	n/a
21	chr7:120646878-120646928	LNCaP	prostate:	n/a
22	chr7:120644149-120644199	GM19239	blood:	n/a
23	chr7:120662793-120662843	Caco-2	colon:	n/a
24	chr7:120639815-120639865	Hela-S3	cervix:	n/a
25	chr7:120662793-120662843	HRE	kidney:	n/a
26	chr7:120644149-120644199	SKMC	muscle:	n/a
27	chr7:120662793-120662843	AG09319	gingival:	n/a
28	chr7:120644149-120644199	GM12891	blood:	n/a
29	chr7:120646878-120646928	MCF-7	breast:	n/a
30	chr7:120646878-120646928	HCT-116	colon:	n/a
31	chr7:120644149-120644199	T-47D	breast:	n/a
32	chr7:120646878-120646928	HCF	heart:	n/a
33	chr7:120657213-120657263	Caco-2	colon:	n/a
34	chr7:120662793-120662843	HCPEpiC	choroid plexus:	n/a
35	chr7:120644149-120644199	K562	blood:	n/a
36	chr7:120657213-120657263	A549	lung:	n/a
37	chr7:120644149-120644199	NHDF-neo	bronchial:	n/a
38	chr7:120639815-120639865	PFSK-1	brain:	n/a
39	chr7:120657213-120657263	HCF	heart:	n/a
40	chr7:120646878-120646928	NT2-D1	testis:	n/a
41	chr7:120644149-120644199	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:120657213-120657263	H1-hESC	embryonic stem cell:	embryo
43	chr7:120662793-120662843	MCF10A-Er-Src	breast:	n/a
44	chr7:120662793-120662843	A549	lung:	n/a
45	chr7:120646878-120646928	Hela-S3	cervix:	n/a
46	chr7:120646878-120646928	GM06990	blood:	n/a
47	chr7:120646878-120646928	GM12891	blood:	n/a
48	chr7:120644149-120644199	NB4	blood:	n/a
49	chr7:120646878-120646928	CMK	blood:	n/a
50	chr7:120639815-120639865	AG09319	gingival:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:120659278..120662150-chr7:120687240..120689583,2	K562	blood:
2	chr7:120608520..120610806-chr7:120667744..120669253,2	K562	blood:
3	chr7:120621518..120649031-chr7:120712706..120728931,108	K562	blood:
4	chr7:120624020..120645873-chr7:120713358..120727138,77	K562	blood:
5	chr7:120669733..120671373-chr7:120674950..120676635,2	K562	blood:
6	chr7:120651629..120654433-chr7:120773346..120775726,2	K562	blood:
7	chr7:120665801..120667354-chr7:120675569..120677821,2	K562	blood:
8	chr7:120649401..120651569-chr7:120679058..120681900,2	K562	blood:
9	chr7:120646710..120649505-chr7:120714634..120717834,3	K562	blood:
10	chr7:120662342..120664104-chr7:120692798..120695619,2	K562	blood:
11	chr7:120579519..120582035-chr7:120642680..120645197,2	K562	blood:
12	chr7:120616082..120617788-chr7:120647461..120650370,2	K562	blood:
13	chr7:120652112..120653722-chr7:120711850..120714681,2	K562	blood:
14	chr7:120668315..120670686-chr7:120720482..120722440,2	K562	blood:
15	chr7:120651556..120653799-chr7:120654229..120655864,2	K562	blood:
16	chr7:120590701..120593592-chr7:120658942..120660558,2	K562	blood:
17	chr7:120591020..120592724-chr7:120645056..120647672,3	K562	blood:
18	chr7:120658347..120660022-chr7:120787197..120789297,2	K562	blood:
19	chr7:120590701..120592712-chr7:120659058..120661712,2	K562	blood:
20	chr7:120660852..120665277-chr7:120680137..120683898,4	K562	blood:
21	chr7:120644958..120648520-chr7:120680179..120682620,4	K562	blood:
22	chr7:120650230..120651746-chr7:120654454..120656718,2	MCF-7	breast:
23	chr7:120651881..120654026-chr7:120689747..120692732,2	K562	blood:
24	chr7:120670213..120673148-chr7:120677345..120680325,2	K562	blood:
25	chr7:120590021..120592843-chr7:120639404..120643575,5	K562	blood:
26	chr7:120661476..120663248-chr7:120721625..120723394,2	K562	blood:
27	chr7:120658657..120661112-chr7:120743405..120745049,2	K562	blood:
28	chr7:120660560..120662573-chr7:120715794..120718811,3	K562	blood:
29	chr7:120589944..120591471-chr7:120664683..120667030,2	K562	blood:
30	chr7:120662581..120666417-chr7:120714540..120719894,6	K562	blood:
31	chr7:120646087..120648520-chr7:120680329..120682630,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ING3-5	chr7:120655798-120655902	NONHSAT122999
2	lnc-ING3-3	chr7:120671720-120671974	expReg_chr7_8572_+
3	lnc-ING3-4	chr7:120671993-120672337	expReg_chr7_8573_+

No data

Variant related genes	Relation type
CPED1	TF binding region
CPED1	CpG island
ENSG00000234927	chromatin interactions
ENSG00000212628	chromatin interactions
ENSG00000106034	chromatin interactions
ENSG00000071243	chromatin interactions

Extended variants
information (count: 1208 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1208 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs41697	chr7:120636796-120636797	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559626588	chr7:120636855-120636856	Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs528397566	chr7:120636858-120636859	Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs142169904	chr7:120636895-120636896	Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs571272587	chr7:120636923-120636924	Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536999403	chr7:120636924-120636925	Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs116806639	chr7:120636963-120636964	Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs145911195	chr7:120636969-120636970	Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369548234	chr7:120636970-120636971	Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs111577867	chr7:120637033-120637034	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs190088587	chr7:120637038-120637039	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs573360832	chr7:120637057-120637058	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs182146032	chr7:120637082-120637083	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs538981832	chr7:120637231-120637232	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs558776894	chr7:120637253-120637254	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs575279038	chr7:120637279-120637280	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs533751782	chr7:120637283-120637284	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs114581139	chr7:120637290-120637291	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs117470101	chr7:120637304-120637305	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs141411766	chr7:120637312-120637313	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs143593600	chr7:120637317-120637318	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs148308352	chr7:120637319-120637320	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs549990368	chr7:120637375-120637376	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs185878580	chr7:120637380-120637381	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs189432741	chr7:120637404-120637405	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs75601245	chr7:120637446-120637447	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs77087646	chr7:120637486-120637487	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs567385285	chr7:120637516-120637517	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs535988029	chr7:120637532-120637533	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs180996185	chr7:120637563-120637564	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs566953188	chr7:120637574-120637575	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs185226620	chr7:120637593-120637594	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs141411057	chr7:120637599-120637600	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs558862053	chr7:120637625-120637626	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs575514792	chr7:120637628-120637629	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs530245429	chr7:120637669-120637670	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs549309839	chr7:120637671-120637672	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs150863973	chr7:120637682-120637683	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs115986734	chr7:120637688-120637689	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs138272570	chr7:120637726-120637727	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs540380758	chr7:120637747-120637748	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs190330277	chr7:120637771-120637772	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs41698	chr7:120637844-120637845	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs371608465	chr7:120637869-120637870	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs181145684	chr7:120637886-120637887	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs555428677	chr7:120637889-120637890	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs530806587	chr7:120637903-120637904	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs186788264	chr7:120637915-120637916	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs571352912	chr7:120637940-120637941	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs560740053	chr7:120637981-120637982	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:948 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120631200-120640400	Weak transcription	Brain Anterior Caudate	brain
2	chr7:120632400-120641400	Transcr. at gene 5' and 3'	K562	blood
3	chr7:120633000-120636800	Enhancers	Liver	Liver
4	chr7:120633000-120636800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr7:120633600-120636800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr7:120634000-120637400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:120634200-120636800	Weak transcription	NH-A	brain
8	chr7:120634200-120644000	Weak transcription	Spleen	Spleen
9	chr7:120634600-120638400	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr7:120634800-120636800	Weak transcription	Right Atrium	heart
11	chr7:120634800-120636800	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr7:120634800-120637000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr7:120634800-120637200	Weak transcription	NHLF	lung
14	chr7:120634800-120637800	Enhancers	Primary hematopoietic stem cells	blood
15	chr7:120635000-120637400	Enhancers	Aorta	Aorta
16	chr7:120635000-120640800	Enhancers	Dnd41	blood
17	chr7:120635200-120636800	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr7:120635200-120637200	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr7:120635200-120637200	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr7:120635200-120638600	Weak transcription	Ovary	ovary
21	chr7:120635400-120637600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr7:120635800-120637200	Enhancers	Primary B cells from peripheral blood	blood
23	chr7:120635800-120637200	Enhancers	Primary T cells fromperipheralblood	blood
24	chr7:120635800-120637400	Enhancers	Primary B cells from cord blood	blood
25	chr7:120635800-120637400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr7:120635800-120639800	Enhancers	Colon Smooth Muscle	Colon
27	chr7:120636000-120637000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr7:120636000-120637200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr7:120636000-120637200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr7:120636000-120638200	Enhancers	Left Ventricle	heart
31	chr7:120636000-120639600	Enhancers	Fetal Stomach	stomach
32	chr7:120636000-120639600	Enhancers	NHDF-Ad	bronchial
33	chr7:120636200-120636800	Enhancers	Rectal Smooth Muscle	rectum
34	chr7:120636200-120637000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:120636200-120637000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr7:120636200-120637000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr7:120636200-120637000	Enhancers	Brain Hippocampus Middle	brain
38	chr7:120636200-120637000	Enhancers	Duodenum Mucosa	Duodenum
39	chr7:120636200-120637000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr7:120636200-120637000	Enhancers	Fetal Lung	lung
41	chr7:120636200-120637000	Enhancers	Fetal Muscle Leg	muscle
42	chr7:120636200-120637000	Enhancers	Placenta	Placenta
43	chr7:120636200-120637000	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr7:120636200-120637000	Enhancers	HUVEC	blood vessel
45	chr7:120636200-120637200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:120636200-120637200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr7:120636200-120637200	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr7:120636200-120637200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr7:120636200-120637200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr7:120636200-120637200	Enhancers	Psoas Muscle	Psoas

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