Variant report

Variant	nsv429801
Chromosome Location	chr7:112434049-112477049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:133)
CpG islands
(count:122)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:12)

(count:133 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:112438984-112439353	K562	blood:	n/a	n/a
2	ARID3A	chr7:112434541-112434790	K562	blood:	n/a	n/a
3	ATF1	chr7:112438902-112439403	K562	blood:	n/a	n/a
4	ATF1	chr7:112434525-112434784	K562	blood:	n/a	n/a
5	BACH1	chr7:112460008-112460010	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:112470316-112470356	K562	blood:	n/a	n/a
7	BATF	chr7:112473188-112473388	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:112438964-112439324	K562	blood:	n/a	n/a
9	BHLHE40	chr7:112474845-112474879	K562	blood:	n/a	n/a
10	CBX3	chr7:112434186-112434880	K562	blood:	n/a	n/a
11	CCNT2	chr7:112438951-112439251	K562	blood:	n/a	n/a
12	CEBPB	chr7:112433826-112434387	HCT-116	colon:	n/a	n/a
13	CEBPB	chr7:112439115-112439210	K562	blood:	n/a	n/a
14	CEBPB	chr7:112445990-112446241	HepG2	liver:	n/a	chr7:112446082-112446093 chr7:112446080-112446091 chr7:112446082-112446091
15	CEBPB	chr7:112433914-112434189	K562	blood:	n/a	n/a
16	CEBPB	chr7:112433976-112434123	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:112442550-112442808	HepG2	liver:	n/a	chr7:112442702-112442713
18	CEBPB	chr7:112473142-112473402	A549	lung:	n/a	chr7:112473235-112473246
19	CEBPB	chr7:112433661-112434400	HCT-116	colon:	n/a	n/a
20	CEBPB	chr7:112449716-112449880	HepG2	liver:	n/a	chr7:112449746-112449757
21	CEBPB	chr7:112443862-112444034	HepG2	liver:	n/a	chr7:112443957-112443968
22	CEBPB	chr7:112473083-112473430	MCF-7	breast:	n/a	chr7:112473235-112473246
23	CEBPB	chr7:112473139-112473362	HepG2	liver:	n/a	chr7:112473235-112473246
24	CEBPB	chr7:112433918-112434218	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:112473138-112473370	K562	blood:	n/a	chr7:112473235-112473246
26	CEBPB	chr7:112446002-112446259	IMR90	lung:	n/a	chr7:112446082-112446093 chr7:112446080-112446091 chr7:112446082-112446091
27	CEBPB	chr7:112445960-112446247	A549	lung:	n/a	chr7:112446082-112446093 chr7:112446080-112446091 chr7:112446082-112446091
28	CTCF	chr7:112463660-112463915	GM12878	blood:	n/a	n/a
29	CTCF	chr7:112449880-112450030	GM12872	blood:	n/a	n/a
30	CUX1	chr7:112438996-112439287	K562	blood:	n/a	n/a
31	CUX1	chr7:112434531-112434692	K562	blood:	n/a	n/a
32	E2F4	chr7:112465164-112465168	MCF10A-Er-Src	breast:	n/a	n/a
33	EBF1	chr7:112463657-112463930	GM12878	blood:	n/a	n/a
34	ELF1	chr7:112434434-112434841	K562	blood:	n/a	n/a
35	EP300	chr7:112433966-112434781	K562	blood:	n/a	n/a
36	EP300	chr7:112438894-112439313	K562	blood:	n/a	n/a
37	FAM48A	chr7:112462023-112462126	GM12878	blood:	n/a	n/a
38	FAM48A	chr7:112450688-112450802	GM12878	blood:	n/a	n/a
39	FOS	chr7:112434547-112434806	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr7:112434606-112434806	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr7:112434526-112434844	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr7:112434089-112434108	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr7:112434101-112434105	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr7:112461373-112461608	MCF10A-Er-Src	breast:	n/a	n/a
45	FOXA1	chr7:112446245-112446437	T-47D	breast:	n/a	n/a
46	FOXA1	chr7:112446231-112446445	T-47D	breast:	n/a	n/a
47	GATA1	chr7:112438390-112439391	PBDE	blood:	n/a	n/a
48	GATA2	chr7:112440451-112440940	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr7:112468343-112468526	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr7:112449914-112450153	SH-SY5Y	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:112434498-112434548	AoSMC	blood vessel:	n/a
2	chr7:112459177-112459227	AG09309	skin:	n/a
3	chr7:112434498-112434548	SK-N-SH_RA	brain:	n/a
4	chr7:112434498-112434548	PANC-1	pancreas:	n/a
5	chr7:112434498-112434548	HRCEpiC	kidney:	n/a
6	chr7:112459177-112459227	GM12892	blood:	n/a
7	chr7:112434498-112434548	SK-N-MC	brain:	n/a
8	chr7:112434498-112434548	MCF10A-Er-Src	breast:	n/a
9	chr7:112459177-112459227	PrEC	prostate:	n/a
10	chr7:112459177-112459227	RPTEC	kidney:	n/a
11	chr7:112434498-112434548	HCT-116	colon:	n/a
12	chr7:112434498-112434548	HEEpiC	esophagus:	n/a
13	chr7:112459177-112459227	Hepatocyte	liver:	n/a
14	chr7:112459177-112459227	MCF-7	breast:	n/a
15	chr7:112459177-112459227	SAEC	small airway:	n/a
16	chr7:112459177-112459227	MCF10A-Er-Src	breast:	n/a
17	chr7:112434498-112434548	RPTEC	kidney:	n/a
18	chr7:112434498-112434548	HL-60	blood:	n/a
19	chr7:112434498-112434548	LNCaP	prostate:	n/a
20	chr7:112434498-112434548	NB4	blood:	n/a
21	chr7:112459177-112459227	NHBE	bronchial:	n/a
22	chr7:112459177-112459227	HUVEC	blood vessel:	n/a
23	chr7:112459177-112459227	A549	lung:	n/a
24	chr7:112459177-112459227	HL-60	blood:	n/a
25	chr7:112434498-112434548	NH-A	brain:	n/a
26	chr7:112434498-112434548	AG09319	gingival:	n/a
27	chr7:112459177-112459227	HMEC	breast:	n/a
28	chr7:112434498-112434548	IMR90	lung:	fetal
29	chr7:112434498-112434548	NHDF-neo	bronchial:	n/a
30	chr7:112434498-112434548	AG10803	skin:	n/a
31	chr7:112459177-112459227	AG10803	skin:	n/a
32	chr7:112434498-112434548	ovcar-3	ovarian:	n/a
33	chr7:112434498-112434548	NT2-D1	testis:	n/a
34	chr7:112434498-112434548	AG04450	lung:	fetal
35	chr7:112459177-112459227	BE2_C	brain:	n/a
36	chr7:112434498-112434548	HCPEpiC	choroid plexus:	n/a
37	chr7:112459177-112459227	HEK293	kidney:	embryo
38	chr7:112459177-112459227	HepG2	liver:	n/a
39	chr7:112459177-112459227	PFSK-1	brain:	n/a
40	chr7:112459177-112459227	SK-N-SH_RA	brain:	n/a
41	chr7:112459177-112459227	SK-N-SH	brain:	n/a
42	chr7:112459177-112459227	Caco-2	colon:	n/a
43	chr7:112459177-112459227	NT2-D1	testis:	n/a
44	chr7:112459177-112459227	HRE	kidney:	n/a
45	chr7:112459177-112459227	HRPEpiC	eye:	n/a
46	chr7:112459177-112459227	HEEpiC	esophagus:	n/a
47	chr7:112459177-112459227	HIPEpiC	eye:	n/a
48	chr7:112459177-112459227	HNPCEpiC	eye:	n/a
49	chr7:112434498-112434548	H1-hESC	embryonic stem cell:	embryo
50	chr7:112434498-112434548	K562	blood:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:112431532..112434194-chr7:112463729..112466329,2	K562	blood:
2	chr7:112429386..112431628-chr7:112438433..112441266,2	MCF-7	breast:
3	chr7:112427720..112431505-chr7:112447113..112451957,4	K562	blood:
4	chr7:112445350..112448501-chr7:112449970..112452849,3	K562	blood:
5	chr7:112469510..112471987-chr7:112486621..112488702,2	K562	blood:
6	chr7:112445350..112448501-chr7:112449970..112452849,3	K562	blood:
7	chr7:112457341..112459401-chr7:112460833..112463216,2	K562	blood:
8	chr7:112460967..112462582-chr7:112467318..112468834,2	MCF-7	breast:
9	chr7:112457341..112459401-chr7:112460833..112463216,2	K562	blood:
10	chr7:112429949..112431702-chr7:112439578..112441274,2	MCF-7	breast:
11	chr7:112440427..112442573-chr7:112447288..112451136,3	K562	blood:
12	chr7:112464327..112467031-chr7:112469420..112472125,2	K562	blood:
13	chr7:112428959..112431266-chr7:112462884..112465767,2	K562	blood:
14	chr7:112430477..112433385-chr7:112446391..112449066,2	K562	blood:
15	chr7:112440427..112442573-chr7:112447288..112451136,3	K562	blood:
16	chr7:112431532..112434194-chr7:112463729..112466329,2	K562	blood:
17	chr7:112439935..112445178-chr7:112445414..112449539,5	K562	blood:
18	chr7:112464327..112467031-chr7:112469420..112472125,2	K562	blood:
19	chr7:112399378..112401790-chr7:112440568..112442211,2	K562	blood:
20	chr7:112442436..112445188-chr7:112575668..112578638,2	K562	blood:
21	chr7:112439935..112445178-chr7:112445414..112449539,5	K562	blood:
22	chr7:112460967..112462582-chr7:112467318..112468834,2	MCF-7	breast:
23	chr7:112469172..112470968-chr7:112479580..112481135,2	K562	blood:
24	chr7:112429019..112430745-chr7:112433310..112435464,2	MCF-7	breast:
25	chr7:112432334..112434564-chr7:112518600..112520396,2	K562	blood:
26	chr7:112429306..112431701-chr7:112443388..112445678,2	MCF-7	breast:

No data

(count:12 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	C7orf60	hsa-miR-186-5p	chr7:112461232-112461253
2	C7orf60	hsa-miR-130b-3p	chr7:112461411-112461432
3	C7orf60	hsa-miR-186-5p	chr7:112461629-112461648
4	C7orf60	hsa-miR-130b-3p	chr7:112460947-112460941
5	C7orf60	hsa-miR-186-5p	chr7:112460090-112460113
6	C7orf60	hsa-miR-130b-3p	chr7:112460941-112460966
7	C7orf60	hsa-let-7a-5p	chr7:112460505-112460499
8	C7orf60	hsa-let-7a-5p	chr7:112460500-112460523
9	C7orf60	hsa-miR-130b-3p	chr7:112459535-112459557
10	C7orf60	hsa-miR-130b-3p	chr7:112461417-112461411
11	C7orf60	hsa-miR-130b-3p	chr7:112460487-112460481
12	C7orf60	hsa-miR-130b-3p	chr7:112460481-112460502

Variant related genes	Relation type
TMEM168	TF binding region
TMEM168	CpG island
ENSG00000146802	chromatin interactions

Extended variants
information (count: 1433 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1433 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532293760	chr7:112434078-112434079	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs550815253	chr7:112434087-112434088	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs568966557	chr7:112434109-112434110	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573241808	chr7:112434167-112434168	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs144327279	chr7:112434169-112434170	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs36107002	chr7:112434170-112434171	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs113906276	chr7:112434171-112434172	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs10254076	chr7:112434173-112434174	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs71155070	chr7:112434210-112434211	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs3082862	chr7:112434211-112434212	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs190110777	chr7:112434321-112434322	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs75147308	chr7:112434401-112434402	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs1718954	chr7:112434413-112434414	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534213591	chr7:112434427-112434428	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs546918157	chr7:112434441-112434442	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs559015062	chr7:112434453-112434454	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs149569829	chr7:112434459-112434460	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs181881042	chr7:112434460-112434461	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs61393265	chr7:112434490-112434491	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs139371854	chr7:112434501-112434502	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs186569387	chr7:112434502-112434503	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560851857	chr7:112434522-112434523	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs528150604	chr7:112434534-112434535	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs142683432	chr7:112434568-112434569	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs189510335	chr7:112434573-112434574	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs34404619	chr7:112434676-112434677	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs531940505	chr7:112434677-112434678	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550602654	chr7:112434736-112434737	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs181829072	chr7:112434745-112434746	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs145984806	chr7:112434767-112434768	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs62472527	chr7:112434778-112434779	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs367667845	chr7:112434910-112434911	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs142110303	chr7:112434917-112434918	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs534302666	chr7:112434923-112434924	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs76796991	chr7:112434936-112434937	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs570860833	chr7:112434995-112434996	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs538233061	chr7:112435070-112435071	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs556622449	chr7:112435075-112435076	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs185369274	chr7:112435094-112435095	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs542089458	chr7:112435099-112435100	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs139015219	chr7:112435140-112435141	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs189772452	chr7:112435148-112435149	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs7803405	chr7:112435163-112435164	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs62472528	chr7:112435169-112435170	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs116592912	chr7:112435173-112435174	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs532058233	chr7:112435182-112435183	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs544187133	chr7:112435194-112435195	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs1796501	chr7:112435209-112435210	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs530023498	chr7:112435236-112435237	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs548149811	chr7:112435351-112435352	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Acute myeloid leukemia	16864856	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	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
Autism	19401682	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	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112430800-112440400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:112432400-112434800	Enhancers	K562	blood
3	chr7:112432800-112434400	Enhancers	NHEK	skin
4	chr7:112434000-112434200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:112434800-112438400	Weak transcription	K562	blood
6	chr7:112438400-112440800	Enhancers	Fetal Heart	heart
7	chr7:112438400-112440800	Enhancers	K562	blood
8	chr7:112438400-112441800	Enhancers	Fetal Lung	lung
9	chr7:112438800-112439200	Active TSS	Fetal Brain Male	brain
10	chr7:112438800-112439400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr7:112438800-112439600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr7:112438800-112439600	Enhancers	Ovary	ovary
13	chr7:112439000-112441000	Enhancers	Fetal Stomach	stomach
14	chr7:112440400-112440600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:112440400-112441000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr7:112440600-112441200	Enhancers	Fetal Muscle Leg	muscle
17	chr7:112441000-112442400	Weak transcription	Fetal Stomach	stomach
18	chr7:112441000-112443000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:112441800-112442800	Enhancers	Lung	lung
20	chr7:112442400-112442600	ZNF genes & repeats	Fetal Stomach	stomach
21	chr7:112442600-112443000	Weak transcription	Fetal Stomach	stomach
22	chr7:112442800-112472800	Weak transcription	Lung	lung
23	chr7:112443000-112443200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:112449200-112449800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr7:112449600-112450000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr7:112449600-112450000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr7:112449600-112450200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr7:112449800-112450000	Enhancers	H9 Cell Line	embryonic stem cell
29	chr7:112450000-112452800	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr7:112450000-112453000	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr7:112451200-112469200	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr7:112452800-112453000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr7:112454800-112458600	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr7:112454800-112463200	Weak transcription	HUVEC	blood vessel
35	chr7:112455400-112457600	Weak transcription	Primary B cells from cord blood	blood
36	chr7:112455400-112467600	Weak transcription	Primary T cells from cord blood	blood
37	chr7:112455800-112458600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr7:112456000-112461800	Weak transcription	Fetal Intestine Large	intestine
39	chr7:112456000-112461800	Weak transcription	Left Ventricle	heart
40	chr7:112456000-112465800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:112456200-112459600	Weak transcription	Fetal Lung	lung
42	chr7:112456200-112461600	Weak transcription	Primary B cells from peripheral blood	blood
43	chr7:112456200-112467800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr7:112456200-112468600	Weak transcription	Duodenum Mucosa	Duodenum
45	chr7:112456400-112458000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:112456400-112467800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:112456400-112470000	Weak transcription	Right Ventricle	heart
48	chr7:112456600-112461600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:112456600-112468000	Weak transcription	HSMMtube	muscle
50	chr7:112456600-112470200	Weak transcription	Stomach Smooth Muscle	stomach

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