Variant report

Variant	nsv887443
Chromosome Location	chr7:6753286-6832265
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1125)
CpG islands
(count:1100)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6769330-6769549	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:6769148-6769268	K562	blood:	n/a	n/a
3	ATF2	chr7:6769041-6769427	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:6764660-6765106	GM12878	blood:	n/a	n/a
5	ATF2	chr7:6768932-6769576	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:6764577-6765116	GM12878	blood:	n/a	n/a
7	ATF2	chr7:6765435-6765872	GM12878	blood:	n/a	n/a
8	BATF	chr7:6770212-6770532	GM12878	blood:	n/a	n/a
9	BATF	chr7:6764386-6765017	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:6764490-6765004	GM12878	blood:	n/a	n/a
11	BCL3	chr7:6765434-6765865	GM12878	blood:	n/a	n/a
12	BCL3	chr7:6764602-6765093	GM12878	blood:	n/a	n/a
13	BCLAF1	chr7:6769053-6769626	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:6768933-6769605	GM12878	blood:	n/a	chr7:6768960-6768969
15	BCLAF1	chr7:6765486-6765849	GM12878	blood:	n/a	n/a
16	BCLAF1	chr7:6764543-6765036	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:6769137-6769602	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:6769211-6769538	K562	blood:	n/a	n/a
19	BHLHE40	chr7:6769947-6770143	K562	blood:	n/a	n/a
20	BHLHE40	chr7:6765444-6765862	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:6832136-6832415	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:6764639-6765044	GM12878	blood:	n/a	n/a
23	BRCA1	chr7:6769345-6769648	HepG2	liver:	n/a	n/a
24	BRCA1	chr7:6769210-6769550	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr7:6768880-6769635	K562	blood:	n/a	n/a
26	CBX3	chr7:6803410-6803703	K562	blood:	n/a	n/a
27	CBX3	chr7:6769851-6770383	K562	blood:	n/a	n/a
28	CBX3	chr7:6809662-6809823	K562	blood:	n/a	n/a
29	CBX3	chr7:6768879-6769361	K562	blood:	n/a	n/a
30	CCNT2	chr7:6769175-6769724	K562	blood:	n/a	n/a
31	CEBPB	chr7:6769943-6769977	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:6807101-6807394	K562	blood:	n/a	n/a
33	CEBPB	chr7:6808935-6809247	K562	blood:	n/a	n/a
34	CEBPB	chr7:6808876-6809289	K562	blood:	n/a	n/a
35	CEBPD	chr7:6808904-6809347	K562	blood:	n/a	n/a
36	CHD1	chr7:6764785-6765290	GM12878	blood:	n/a	n/a
37	CHD1	chr7:6769255-6769940	GM12878	blood:	n/a	n/a
38	CHD2	chr7:6769108-6770024	HepG2	liver:	n/a	n/a
39	CHD2	chr7:6769152-6769942	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr7:6769061-6769581	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr7:6769156-6770092	K562	blood:	n/a	n/a
42	CHD2	chr7:6769097-6769650	GM12878	blood:	n/a	n/a
43	CREB1	chr7:6769086-6769579	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr7:6769002-6769580	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr7:6769195-6769646	A549	lung:	n/a	n/a
46	CTCF	chr7:6757897-6758012	H1-hESC	embryonic stem cell:	n/a	chr7:6757947-6757965
47	CTCF	chr7:6757900-6758050	GM12873	blood:	n/a	chr7:6757947-6757965
48	CTCF	chr7:6780077-6780234	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:6769280-6769430	GM12874	blood:	n/a	n/a
50	CTCF	chr7:6757840-6757990	GM12869	blood:	n/a	chr7:6757947-6757965

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6770940-6770990	HNPCEpiC	eye:	n/a
2	chr7:6800488-6800538	GM12878	blood:	n/a
3	chr7:6770940-6770990	HNPCEpiC	eye:	n/a
4	chr7:6800488-6800538	GM12878	blood:	n/a
5	chr7:6800488-6800538	SK-N-MC	brain:	n/a
6	chr7:6803522-6803572	IMR90	lung:	fetal
7	chr7:6800488-6800538	ovcar-3	ovarian:	n/a
8	chr7:6769322-6769372	AG09309	skin:	n/a
9	chr7:6797497-6797547	HL-60	blood:	n/a
10	chr7:6774720-6774770	RPTEC	kidney:	n/a
11	chr7:6770940-6770990	HMEC	breast:	n/a
12	chr7:6803522-6803572	Hepatocyte	liver:	n/a
13	chr7:6766092-6766142	AG09309	skin:	n/a
14	chr7:6774169-6774219	NHDF-neo	bronchial:	n/a
15	chr7:6817550-6817600	AG09309	skin:	n/a
16	chr7:6769406-6769456	GM06990	blood:	n/a
17	chr7:6769322-6769372	BJ	skin:	n/a
18	chr7:6769406-6769456	AG04450	lung:	fetal
19	chr7:6769409-6769459	Hela-S3	cervix:	n/a
20	chr7:6774169-6774219	AG04449	skin:	fetal
21	chr7:6766092-6766142	IMR90	lung:	fetal
22	chr7:6774720-6774770	PrEC	prostate:	n/a
23	chr7:6769322-6769372	LNCaP	prostate:	n/a
24	chr7:6770940-6770990	HEK293	kidney:	embryo
25	chr7:6770013-6770063	GM19239	blood:	n/a
26	chr7:6790012-6790062	GM06990	blood:	n/a
27	chr7:6769322-6769372	U87	brain:	n/a
28	chr7:6774169-6774219	HRE	kidney:	n/a
29	chr7:6819532-6819582	HMEC	breast:	n/a
30	chr7:6797497-6797547	ECC-1	luminal epithelium:	n/a
31	chr7:6770940-6770990	AG04450	lung:	fetal
32	chr7:6793977-6794027	GM12892	blood:	n/a
33	chr7:6772985-6773035	Hepatocyte	liver:	n/a
34	chr7:6769409-6769459	ProgFib	skin:	n/a
35	chr7:6797497-6797547	GM19239	blood:	n/a
36	chr7:6817550-6817600	GM06990	blood:	n/a
37	chr7:6774720-6774770	NH-A	brain:	n/a
38	chr7:6770013-6770063	NHBE	bronchial:	n/a
39	chr7:6770013-6770063	AG04449	skin:	fetal
40	chr7:6774169-6774219	HCF	heart:	n/a
41	chr7:6774169-6774219	A549	lung:	n/a
42	chr7:6819532-6819582	AG04450	lung:	fetal
43	chr7:6790012-6790062	HNPCEpiC	eye:	n/a
44	chr7:6770013-6770063	HRPEpiC	eye:	n/a
45	chr7:6797497-6797547	HCPEpiC	choroid plexus:	n/a
46	chr7:6772985-6773035	HepG2	liver:	n/a
47	chr7:6772985-6773035	AG09309	skin:	n/a
48	chr7:6803522-6803572	AG09309	skin:	n/a
49	chr7:6793977-6794027	NH-A	brain:	n/a
50	chr7:6774169-6774219	AG09319	gingival:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6746161..6747688-chr7:6768318..6771249,2	MCF-7	breast:
2	chr7:6755281..6757989-chr7:6768169..6769805,2	K562	blood:
3	chr7:6745224..6747442-chr7:6767898..6770902,3	MCF-7	breast:
4	chr7:6744871..6747873-chr7:6767656..6771321,4	K562	blood:
5	chr7:6768428..6771621-chr7:6773707..6775724,3	MCF-7	breast:
6	chr7:6767588..6769922-chr7:6774691..6777140,2	MCF-7	breast:
7	chr7:6745040..6747820-chr7:6753016..6755979,2	K562	blood:
8	chr7:6745463..6748475-chr7:6767656..6769994,3	K562	blood:
9	chr7:6616941..6618678-chr7:6767339..6769412,2	MCF-7	breast:
10	chr7:6766860..6769459-chr7:6864426..6866111,2	MCF-7	breast:
11	chr7:6675529..6677980-chr7:6768487..6770695,2	K562	blood:
12	chr7:6768428..6771621-chr7:6773707..6775724,3	MCF-7	breast:
13	chr7:6767588..6769922-chr7:6774691..6777140,2	MCF-7	breast:
14	chr2:85554880..85555877-chr7:6769205..6770035,2	Hela-S3	cervix:
15	chr7:6745105..6747702-chr7:6760857..6762901,2	MCF-7	breast:
16	chr7:6048395..6048947-chr7:6768981..6769924,2	NB4	blood:
17	chr7:6761698..6764136-chr7:6769053..6770920,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RSPH10B2-1	chr7:6771528-6771586	NONHSAT119063
2	lnc-RSPH10B2-1	chr7:6792653-6793492	NONHSAT119063

No data

Variant related genes	Relation type
RSPH10B2	TF binding region
PMS2CL	TF binding region
RSPH10B2	CpG island
PMS2CL	CpG island
ENSG00000205903	chromatin interactions
ENSG00000152291	chromatin interactions
ENSG00000146574	chromatin interactions
ENSG00000122512	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000106305	chromatin interactions

Extended variants
information (count: 1944 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1944 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2346236	chr7:6753286-6753287	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535534602	chr7:6753317-6753318	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547880594	chr7:6753343-6753344	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565902865	chr7:6753362-6753363	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs539797828	chr7:6753383-6753384	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs558215383	chr7:6753399-6753400	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577197627	chr7:6753428-6753429	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs56288394	chr7:6753475-6753476	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs2881352	chr7:6753511-6753512	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs528506978	chr7:6753530-6753531	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs540350819	chr7:6753531-6753532	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs574583775	chr7:6753532-6753533	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs578234837	chr7:6753541-6753542	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs184491125	chr7:6753561-6753562	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10247600	chr7:6753605-6753606	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs187052442	chr7:6753644-6753645	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545379895	chr7:6753680-6753681	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs191861776	chr7:6753687-6753688	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184365662	chr7:6753688-6753689	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs1830075	chr7:6753694-6753695	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs562104036	chr7:6753736-6753737	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs562564797	chr7:6753762-6753763	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs189118908	chr7:6753795-6753796	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs11979878	chr7:6753803-6753804	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs10247888	chr7:6753811-6753812	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs11979883	chr7:6753815-6753816	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs569100460	chr7:6753870-6753871	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs368250653	chr7:6753891-6753892	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs143293796	chr7:6753896-6753897	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs181893329	chr7:6753900-6753901	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs367674365	chr7:6753908-6753909	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538098032	chr7:6753919-6753920	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185587356	chr7:6753920-6753921	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs568134103	chr7:6753934-6753935	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs375266675	chr7:6753948-6753949	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs190512579	chr7:6753961-6753962	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs528557915	chr7:6753962-6753963	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572097868	chr7:6753976-6753977	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs6972017	chr7:6754034-6754035	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs73674174	chr7:6754039-6754040	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs575644049	chr7:6754053-6754054	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140495185	chr7:6754065-6754066	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs558123246	chr7:6754071-6754072	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs180734778	chr7:6754072-6754073	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs556433302	chr7:6754077-6754078	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs377172356	chr7:6754078-6754079	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529592209	chr7:6754081-6754082	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564926826	chr7:6754110-6754111	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs185159164	chr7:6754118-6754119	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs550368340	chr7:6754119-6754120	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1056 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6747000-6768600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:6747400-6757400	Weak transcription	Fetal Brain Female	brain
3	chr7:6752200-6754600	Strong transcription	Liver	Liver
4	chr7:6754600-6768600	Weak transcription	Liver	Liver
5	chr7:6759400-6759600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:6763600-6766600	Enhancers	Primary B cells from cord blood	blood
7	chr7:6764000-6765800	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr7:6764000-6766200	Enhancers	Primary B cells from peripheral blood	blood
9	chr7:6764200-6764600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:6764200-6765800	Enhancers	Primary hematopoietic stem cells	blood
11	chr7:6764200-6766200	Enhancers	GM12878-XiMat	blood
12	chr7:6764400-6765200	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr7:6764400-6765400	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr7:6764400-6765800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:6764600-6764800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr7:6764600-6764800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:6764600-6764800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr7:6764600-6765200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:6764600-6765200	Enhancers	Spleen	Spleen
20	chr7:6764600-6765800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:6764800-6765000	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr7:6765000-6765200	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr7:6765000-6768600	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr7:6765200-6765800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:6765200-6766000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr7:6765200-6768600	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr7:6765200-6769000	Weak transcription	Spleen	Spleen
28	chr7:6765400-6768600	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr7:6765800-6768400	Weak transcription	Primary hematopoietic stem cells	blood
30	chr7:6765800-6768400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr7:6765800-6768600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr7:6765800-6768600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr7:6765800-6768600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr7:6766000-6766400	Enhancers	NHEK	skin
35	chr7:6766200-6766400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr7:6766200-6766400	Enhancers	Placenta	Placenta
37	chr7:6766200-6768400	Weak transcription	GM12878-XiMat	blood
38	chr7:6766200-6768800	Weak transcription	Primary B cells from peripheral blood	blood
39	chr7:6766200-6769000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr7:6766400-6768600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr7:6766400-6769000	Weak transcription	NHEK	skin
42	chr7:6766600-6768600	Weak transcription	Primary B cells from cord blood	blood
43	chr7:6766600-6768800	Weak transcription	Placenta	Placenta
44	chr7:6767400-6767600	Enhancers	HSMMtube	muscle
45	chr7:6767400-6767600	Enhancers	K562	blood
46	chr7:6767600-6769000	Weak transcription	HSMMtube	muscle
47	chr7:6767600-6769000	Weak transcription	K562	blood
48	chr7:6768200-6770600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:6768400-6768600	Active TSS	Primary hematopoietic stem cells	blood
50	chr7:6768400-6768600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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