Variant report

Variant	nsv5783
Chromosome Location	chr7:69048608-69066760
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:331)
CpG islands
(count:855)
Chromatin interactive
region (count:4)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:69063053-69063343	GM12878	blood:	n/a	chr7:69063178-69063187
2	ATF3	chr7:69063100-69063327	H1-hESC	embryonic stem cell:	n/a	chr7:69063178-69063187
3	ATF3	chr7:69063091-69063322	HepG2	liver:	n/a	chr7:69063178-69063187
4	BACH1	chr7:69062461-69063013	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:69063820-69063967	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:69063035-69063521	GM12878	blood:	n/a	chr7:69063474-69063490 chr7:69063469-69063485
7	CEBPB	chr7:69062466-69062544	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr7:69048924-69049021	A549	lung:	n/a	chr7:69049001-69049012
9	CEBPB	chr7:69048881-69049081	HepG2	liver:	n/a	chr7:69049001-69049012
10	CEBPB	chr7:69048976-69049078	K562	blood:	n/a	chr7:69049001-69049012
11	CHD1	chr7:69066219-69066779	GM12878	blood:	n/a	n/a
12	CHD1	chr7:69064701-69065396	GM12878	blood:	n/a	chr7:69065096-69065106
13	CHD1	chr7:69063410-69064343	GM12878	blood:	n/a	chr7:69063817-69063827
14	CHD1	chr7:69063642-69064040	H1-hESC	embryonic stem cell:	n/a	chr7:69063817-69063827
15	CHD1	chr7:69064359-69064746	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr7:69065964-69066235	GM12878	blood:	n/a	n/a
17	CHD2	chr7:69064381-69064464	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr7:69065142-69065392	GM12878	blood:	n/a	n/a
19	CHD2	chr7:69062787-69062910	GM12878	blood:	n/a	n/a
20	CHD2	chr7:69064482-69064590	GM12878	blood:	n/a	n/a
21	CHD2	chr7:69062506-69062596	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr7:69065047-69065303	H1-hESC	embryonic stem cell:	n/a	chr7:69065096-69065106
23	CHD2	chr7:69062219-69062472	GM12878	blood:	n/a	n/a
24	CHD2	chr7:69063122-69063531	GM12878	blood:	n/a	chr7:69063259-69063269 chr7:69063183-69063193
25	CHD2	chr7:69063133-69063284	HepG2	liver:	n/a	chr7:69063259-69063269 chr7:69063183-69063193
26	CREB1	chr7:69063060-69063625	A549	lung:	n/a	n/a
27	CTBP2	chr7:69064293-69065439	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTBP2	chr7:69062218-69062982	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:69065183-69065207	GM19240	blood:	n/a	n/a
30	CTCF	chr7:69065140-69065290	SK-N-SH_RA	brain:	n/a	chr7:69065182-69065198
31	CTCF	chr7:69063521-69063656	Fibrobl	skin:	n/a	n/a
32	CTCF	chr7:69064960-69065110	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr7:69062590-69062657	A549	lung:	n/a	n/a
34	CTCF	chr7:69061370-69061408	GM20000	blood:	n/a	n/a
35	CTCF	chr7:69064480-69064630	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr7:69062584-69062763	GM12878	blood:	n/a	n/a
37	CTCF	chr7:69062560-69062710	AG04449	skin:	n/a	n/a
38	CTCF	chr7:69062600-69062750	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr7:69065180-69065330	GM12865	blood:	n/a	chr7:69065182-69065198
40	CTCF	chr7:69062636-69062676	GM19240	blood:	n/a	n/a
41	CTCF	chr7:69062540-69062690	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr7:69065080-69065230	GM12866	blood:	n/a	chr7:69065182-69065198 chr7:69065100-69065113
43	CTCF	chr7:69064520-69064670	AG04449	skin:	n/a	n/a
44	CTCF	chr7:69065254-69065283	ProgFib	skin:	n/a	n/a
45	CTCF	chr7:69065080-69065230	AG04449	skin:	n/a	chr7:69065182-69065198 chr7:69065100-69065113
46	CTCF	chr7:69065221-69065286	Fibrobl	skin:	n/a	n/a
47	CTCF	chr7:69062678-69062683	GM19240	blood:	n/a	n/a
48	CTCF	chr7:69062637-69062678	GM12891	blood:	n/a	n/a
49	CTCF	chr7:69061960-69062110	GM06990	blood:	n/a	n/a
50	CTCF	chr7:69062640-69062790	GM12874	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:69062621-69062671	Jurkat	blood:	n/a
2	chr7:69062621-69062671	Jurkat	blood:	n/a
3	chr7:69065031-69065081	Jurkat	blood:	n/a
4	chr7:69063971-69064021	NHDF-neo	bronchial:	n/a
5	chr7:69064801-69064851	GM19239	blood:	n/a
6	chr7:69058543-69058593	ECC-1	luminal epithelium:	n/a
7	chr7:69065031-69065081	SK-N-SH	brain:	n/a
8	chr7:69065031-69065081	GM06990	blood:	n/a
9	chr7:69062621-69062671	ProgFib	skin:	n/a
10	chr7:69064868-69064918	GM12891	blood:	n/a
11	chr7:69064801-69064851	PrEC	prostate:	n/a
12	chr7:69062082-69062132	LNCaP	prostate:	n/a
13	chr7:69062534-69062584	HRCEpiC	kidney:	n/a
14	chr7:69064884-69064934	HRPEpiC	eye:	n/a
15	chr7:69062887-69062937	A549	lung:	n/a
16	chr7:69064801-69064851	SK-N-SH_RA	brain:	n/a
17	chr7:69062082-69062132	H1-hESC	embryonic stem cell:	embryo
18	chr7:69065031-69065081	AG04450	lung:	fetal
19	chr7:69064801-69064851	HCPEpiC	choroid plexus:	n/a
20	chr7:69062887-69062937	PFSK-1	brain:	n/a
21	chr7:69064884-69064934	K562	blood:	n/a
22	chr7:69063475-69063525	HIPEpiC	eye:	n/a
23	chr7:69065351-69065401	HCF	heart:	n/a
24	chr7:69058543-69058593	SK-N-SH	brain:	n/a
25	chr7:69063475-69063525	AG09309	skin:	n/a
26	chr7:69065031-69065081	NB4	blood:	n/a
27	chr7:69064868-69064918	PFSK-1	brain:	n/a
28	chr7:69065031-69065081	PFSK-1	brain:	n/a
29	chr7:69063404-69063454	K562	blood:	n/a
30	chr7:69062621-69062671	GM06990	blood:	n/a
31	chr7:69064801-69064851	HAEpiC	amniotic membrane:	n/a
32	chr7:69062621-69062671	Hela-S3	cervix:	n/a
33	chr7:69064801-69064851	GM06990	blood:	n/a
34	chr7:69064868-69064918	NHBE	bronchial:	n/a
35	chr7:69065031-69065081	HL-60	blood:	n/a
36	chr7:69065351-69065401	SAEC	small airway:	n/a
37	chr7:69062082-69062132	SK-N-SH	brain:	n/a
38	chr7:69064884-69064934	SKMC	muscle:	n/a
39	chr7:69062082-69062132	HNPCEpiC	eye:	n/a
40	chr7:69063404-69063454	H1-hESC	embryonic stem cell:	embryo
41	chr7:69062082-69062132	NT2-D1	testis:	n/a
42	chr7:69062887-69062937	U87	brain:	n/a
43	chr7:69062887-69062937	BJ	skin:	n/a
44	chr7:69063404-69063454	AG10803	skin:	n/a
45	chr7:69064093-69064143	BE2_C	brain:	n/a
46	chr7:69065351-69065401	MCF10A-Er-Src	breast:	n/a
47	chr7:69063475-69063525	HEEpiC	esophagus:	n/a
48	chr7:69062082-69062132	BE2_C	brain:	n/a
49	chr7:69064868-69064918	CMK	blood:	n/a
50	chr7:69065031-69065081	ECC-1	luminal epithelium:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:69064794..69066719-chr7:69068260..69070601,2	MCF-7	breast:
2	chr10:104261951..104262527-chr7:69062342..69063007,2	NB4	blood:
3	chr17:73150080..73150778-chr7:69062421..69063092,2	NB4	blood:
4	chr1:198906160..198906960-chr7:69062272..69062955,2	NB4	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CALN1-1	chr7:69062220-69062803	NONHSAT121322
2	lnc-CALN1-1	chr7:69061500-69061677	XLOC_006493
3	lnc-AUTS2-1	chr7:69061156-69063004	XLOC_006142
4	lnc-CALN1-1	chr7:69057888-69058140	XLOC_006493
5	lnc-CALN1-1	chr7:69061124-69061419	NR_108105
6	lnc-CALN1-1	chr7:69062220-69062546	XLOC_006493
7	lnc-CALN1-1	chr7:69060944-69061419	ENSG00000234215.2
8	lnc-CALN1-1	chr7:69062220-69063004	XLOC_006493
9	lnc-CALN1-1	chr7:69062220-69063004	XLOC_006493
10	lnc-CALN1-1	chr7:69061641-69061677	XLOC_006493
11	lnc-CALN1-1	chr7:69061144-69061419	XLOC_006493
12	lnc-CALN1-1	chr7:69062220-69062803	NONHSAT121323
13	lnc-CALN1-1	chr7:69060765-69061419	XLOC_006493
14	lnc-CALN1-1	chr7:69062220-69062434	ENSG00000234215.2
15	lnc-CALN1-1	chr7:69061742-69061918	XLOC_006493
16	lnc-CALN1-1	chr7:69062220-69062434	XLOC_006493
17	lnc-CALN1-1	chr7:69061641-69061679	XLOC_006493
18	lnc-CALN1-1	chr7:69057888-69058140	XLOC_006493
19	lnc-CALN1-1	chr7:69057888-69058140	XLOC_006493
20	lnc-CALN1-1	chr7:69061144-69061419	XLOC_006493
21	lnc-CALN1-1	chr7:69062220-69062481	NR_108105
22	lnc-CALN1-1	chr7:69059791-69061419	NONHSAT121323
23	lnc-CALN1-1	chr7:69061144-69061419	XLOC_006493
24	lnc-CALN1-1	chr7:69061641-69061677	NONHSAT121323
25	lnc-CALN1-1	chr7:69059791-69061419	NONHSAT121322
26	lnc-CALN1-1	chr7:69057924-69058140	XLOC_006493
27	lnc-AUTS2-1	chr7:69054796-69054845	XLOC_006142
28	lnc-CALN1-1	chr7:69061133-69061419	XLOC_006493
29	lnc-CALN1-1	chr7:69061144-69061419	XLOC_006493

No data

Variant related genes	Relation type
ENSG00000234215	TF binding region
AUTS2	TF binding region
ENSG00000234215	CpG island
AUTS2	CpG island
ENSG00000189159	chromatin interactions
ENSG00000138107	chromatin interactions
ENSG00000229989	chromatin interactions
PDGFRA	miRNA target sites
PDE4D	miRNA target sites
PROK2	miRNA target sites
CTDSPL2	miRNA target sites
CTGF	miRNA target sites

Extended variants
information (count: 569 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534659941	chr7:69048616-69048617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs10268221	chr7:69048690-69048691	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs568499122	chr7:69048753-69048754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565551386	chr7:69048781-69048782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535927290	chr7:69048782-69048783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143756171	chr7:69048811-69048812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2851493	chr7:69048815-69048816	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs377423884	chr7:69048818-69048819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546385890	chr7:69048835-69048836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146816538	chr7:69048894-69048895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10256309	chr7:69048942-69048943	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs4403308	chr7:69048951-69048952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540610324	chr7:69049023-69049024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558901731	chr7:69049043-69049044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529663167	chr7:69049064-69049065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148967010	chr7:69049082-69049083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112977695	chr7:69049103-69049104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs367876605	chr7:69049105-69049106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563054777	chr7:69049119-69049120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530575628	chr7:69049138-69049139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552348330	chr7:69049183-69049184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570598354	chr7:69049184-69049185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528369732	chr7:69049190-69049191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs118191965	chr7:69049194-69049195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs530327332	chr7:69049278-69049279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550286973	chr7:69049291-69049292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185278378	chr7:69049330-69049331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114249614	chr7:69049387-69049388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142866054	chr7:69049388-69049389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538999455	chr7:69049396-69049397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73701367	chr7:69049398-69049399	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs151045508	chr7:69049399-69049400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191912251	chr7:69049445-69049446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183603232	chr7:69049451-69049452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540894252	chr7:69049461-69049462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555657768	chr7:69049462-69049463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574055354	chr7:69049475-69049476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188649412	chr7:69049487-69049488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs9692258	chr7:69049578-69049579	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs12113755	chr7:69049586-69049587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373963294	chr7:69049674-69049675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs193129216	chr7:69049702-69049703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs12112985	chr7:69049724-69049725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532992795	chr7:69049726-69049727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200154853	chr7:69049727-69049728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs71097486	chr7:69049757-69049758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs375558030	chr7:69049758-69049759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545616817	chr7:69049809-69049810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183322952	chr7:69049810-69049811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs60949943	chr7:69049824-69049825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
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
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	22102821	CNVD
Basal cell lymphoma	21115979	CNVD

Chromatin state (count:643 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:69048400-69051000	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr7:69048800-69051400	Enhancers	Fetal Intestine Small	intestine
3	chr7:69048800-69052400	Enhancers	Fetal Intestine Large	intestine
4	chr7:69051000-69051400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr7:69051400-69053000	Weak transcription	Fetal Intestine Small	intestine
6	chr7:69052400-69053200	Weak transcription	Fetal Intestine Large	intestine
7	chr7:69053000-69053400	Enhancers	Fetal Intestine Small	intestine
8	chr7:69053000-69054800	Enhancers	Brain Hippocampus Middle	brain
9	chr7:69053000-69055000	Enhancers	Brain Cingulate Gyrus	brain
10	chr7:69053200-69053400	Enhancers	Fetal Intestine Large	intestine
11	chr7:69053200-69053800	Enhancers	Brain Anterior Caudate	brain
12	chr7:69053400-69053600	Enhancers	Brain Substantia Nigra	brain
13	chr7:69053600-69054200	Weak transcription	Brain Substantia Nigra	brain
14	chr7:69053600-69054800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr7:69054000-69054200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr7:69054000-69054200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr7:69054200-69054800	Enhancers	Brain Substantia Nigra	brain
18	chr7:69054400-69056000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr7:69055600-69056000	Weak transcription	Brain Anterior Caudate	brain
20	chr7:69056000-69057000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr7:69056800-69057000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr7:69057000-69061800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr7:69058000-69058400	Enhancers	Fetal Intestine Small	intestine
24	chr7:69058400-69062000	Weak transcription	Fetal Intestine Small	intestine
25	chr7:69059800-69060000	Enhancers	Brain Anterior Caudate	brain
26	chr7:69060000-69061600	Weak transcription	Brain Anterior Caudate	brain
27	chr7:69061000-69061800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:69061200-69061600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr7:69061200-69061800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:69061200-69062000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:69061200-69062000	Enhancers	Primary hematopoietic stem cells	blood
32	chr7:69061400-69062000	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr7:69061600-69061800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:69061600-69061800	Enhancers	Adipose Nuclei	Adipose
35	chr7:69061600-69061800	Bivalent Enhancer	Colonic Mucosa	Colon
36	chr7:69061600-69062000	Enhancers	Brain Cingulate Gyrus	brain
37	chr7:69061600-69062000	Enhancers	Colon Smooth Muscle	Colon
38	chr7:69061600-69062000	Enhancers	Dnd41	blood
39	chr7:69061600-69062200	Flanking Active TSS	Brain Anterior Caudate	brain
40	chr7:69061600-69062400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:69061600-69065800	Active TSS	Brain Angular Gyrus	brain
42	chr7:69061800-69062000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:69061800-69062000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
44	chr7:69061800-69062000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
45	chr7:69061800-69062000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr7:69061800-69062000	Enhancers	Primary B cells from peripheral blood	blood
47	chr7:69061800-69062000	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
48	chr7:69061800-69062000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr7:69061800-69062000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:69061800-69062000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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