Variant report

Variant	nsv1018084
Chromosome Location	chr7:135901545-135983684
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:293)
CpG islands
(count:61)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:135931947-135932309	K562	blood:	n/a	n/a
2	ARID3A	chr7:135930122-135930423	K562	blood:	n/a	n/a
3	ATF1	chr7:135931923-135932438	K562	blood:	n/a	n/a
4	ATF1	chr7:135930049-135930441	K562	blood:	n/a	n/a
5	BACH1	chr7:135978827-135979087	H1-hESC	embryonic stem cell:	n/a	chr7:135978948-135978962
6	BACH1	chr7:135978995-135978996	K562	blood:	n/a	n/a
7	BCL11A	chr7:135914982-135915190	GM12878	blood:	n/a	chr7:135915177-135915186
8	BHLHE40	chr7:135930104-135930326	K562	blood:	n/a	n/a
9	CBX3	chr7:135938899-135939272	K562	blood:	n/a	n/a
10	CBX3	chr7:135949021-135949403	K562	blood:	n/a	n/a
11	CBX3	chr7:135929972-135930428	K562	blood:	n/a	n/a
12	CBX3	chr7:135945252-135945493	K562	blood:	n/a	n/a
13	CBX3	chr7:135949014-135949533	K562	blood:	n/a	n/a
14	CBX3	chr7:135916100-135916470	K562	blood:	n/a	n/a
15	CBX3	chr7:135920838-135921270	K562	blood:	n/a	n/a
16	CBX3	chr7:135929954-135930521	K562	blood:	n/a	n/a
17	CCNT2	chr7:135934694-135934784	K562	blood:	n/a	n/a
18	CCNT2	chr7:135930053-135930542	K562	blood:	n/a	n/a
19	CCNT2	chr7:135931929-135932232	K562	blood:	n/a	n/a
20	CCNT2	chr7:135925380-135925574	K562	blood:	n/a	n/a
21	CEBPB	chr7:135932979-135933054	K562	blood:	n/a	chr7:135932998-135933011 chr7:135932998-135933011
22	CEBPB	chr7:135944458-135944688	A549	lung:	n/a	chr7:135944546-135944557
23	CEBPB	chr7:135944458-135944712	K562	blood:	n/a	chr7:135944546-135944557
24	CEBPB	chr7:135933754-135933876	K562	blood:	n/a	n/a
25	CEBPB	chr7:135902717-135902907	K562	blood:	n/a	chr7:135902816-135902825 chr7:135902814-135902825
26	CEBPB	chr7:135929931-135930434	K562	blood:	n/a	n/a
27	CEBPB	chr7:135929999-135930429	K562	blood:	n/a	n/a
28	CEBPB	chr7:135944398-135944728	HepG2	liver:	n/a	chr7:135944546-135944557
29	CEBPD	chr7:135929988-135930518	K562	blood:	n/a	n/a
30	CEBPD	chr7:135929921-135930579	K562	blood:	n/a	n/a
31	CTCF	chr7:135979858-135979972	GM13977	blood:	n/a	n/a
32	CTCF	chr7:135979794-135980035	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:135954280-135954430	HRE	kidney:	n/a	chr7:135954408-135954429 chr7:135954406-135954424
34	CTCF	chr7:135979840-135979990	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr7:135979900-135980050	GM12872	blood:	n/a	n/a
36	CTCF	chr7:135979860-135980010	HepG2	liver:	n/a	n/a
37	CTCF	chr7:135979863-135979957	GM10266	blood:	n/a	n/a
38	CTCF	chr7:135979807-135980000	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr7:135979800-135979950	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr7:135980191-135980255	GM20000	blood:	n/a	n/a
41	CTCF	chr7:135979840-135979990	GM12873	blood:	n/a	n/a
42	CTCF	chr7:135979820-135979970	K562	blood:	n/a	n/a
43	CTCF	chr7:135920090-135920161	Lung_OC	lung:	n/a	n/a
44	CTCF	chr7:135979633-135980205	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:135979860-135980010	GM12868	blood:	n/a	n/a
46	CTCF	chr7:135932180-135932330	GM06990	blood:	n/a	n/a
47	CTCF	chr7:135979851-135979985	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr7:135954334-135954354	LNCaP	prostate:	n/a	n/a
49	CTCF	chr7:135979900-135980050	GM12868	blood:	n/a	n/a
50	CTCF	chr7:135979847-135980003	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:135938950-135939000	SAEC	small airway:	n/a
2	chr7:135938950-135939000	Caco-2	colon:	n/a
3	chr7:135938950-135939000	GM12891	blood:	n/a
4	chr7:135938950-135939000	HEEpiC	esophagus:	n/a
5	chr7:135938950-135939000	NH-A	brain:	n/a
6	chr7:135938950-135939000	RPTEC	kidney:	n/a
7	chr7:135938950-135939000	HCM	heart:	n/a
8	chr7:135938950-135939000	ovcar-3	ovarian:	n/a
9	chr7:135938950-135939000	HMEC	breast:	n/a
10	chr7:135938950-135939000	MCF10A-Er-Src	breast:	n/a
11	chr7:135938950-135939000	PANC-1	pancreas:	n/a
12	chr7:135938950-135939000	MCF-7	breast:	n/a
13	chr7:135938950-135939000	BJ	skin:	n/a
14	chr7:135938950-135939000	CMK	blood:	n/a
15	chr7:135938950-135939000	SK-N-SH_RA	brain:	n/a
16	chr7:135938950-135939000	AG10803	skin:	n/a
17	chr7:135938950-135939000	GM19239	blood:	n/a
18	chr7:135938950-135939000	SK-N-SH	brain:	n/a
19	chr7:135938950-135939000	HIPEpiC	eye:	n/a
20	chr7:135938950-135939000	HepG2	liver:	n/a
21	chr7:135938950-135939000	AG09309	skin:	n/a
22	chr7:135938950-135939000	PFSK-1	brain:	n/a
23	chr7:135938950-135939000	AG09319	gingival:	n/a
24	chr7:135938950-135939000	HL-60	blood:	n/a
25	chr7:135938950-135939000	U87	brain:	n/a
26	chr7:135938950-135939000	HCPEpiC	choroid plexus:	n/a
27	chr7:135938950-135939000	HRCEpiC	kidney:	n/a
28	chr7:135938950-135939000	HCF	heart:	n/a
29	chr7:135938950-135939000	Jurkat	blood:	n/a
30	chr7:135938950-135939000	HRE	kidney:	n/a
31	chr7:135938950-135939000	SKMC	muscle:	n/a
32	chr7:135938950-135939000	SK-N-MC	brain:	n/a
33	chr7:135938950-135939000	NB4	blood:	n/a
34	chr7:135938950-135939000	BE2_C	brain:	n/a
35	chr7:135938950-135939000	Hepatocyte	liver:	n/a
36	chr7:135938950-135939000	NHBE	bronchial:	n/a
37	chr7:135938950-135939000	GM12878	blood:	n/a
38	chr7:135938950-135939000	GM06990	blood:	n/a
39	chr7:135938950-135939000	NHDF-neo	bronchial:	n/a
40	chr7:135938950-135939000	AoSMC	blood vessel:	n/a
41	chr7:135938950-135939000	H1-hESC	embryonic stem cell:	embryo
42	chr7:135938950-135939000	HCT-116	colon:	n/a
43	chr7:135938950-135939000	HRPEpiC	eye:	n/a
44	chr7:135938950-135939000	ECC-1	luminal epithelium:	n/a
45	chr7:135938950-135939000	HAEpiC	amniotic membrane:	n/a
46	chr7:135938950-135939000	K562	blood:	n/a
47	chr7:135938950-135939000	HPAEpiC	pulmonary alveolar:	n/a
48	chr7:135938950-135939000	T-47D	breast:	n/a
49	chr7:135938950-135939000	PrEC	prostate:	n/a
50	chr7:135938950-135939000	GM12892	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:135969459..135971484-chr7:135972716..135974904,2	K562	blood:
2	chr7:135925867..135928083-chr7:135931669..135933724,2	K562	blood:
3	chr7:135896650..135898487-chr7:135926765..135928429,2	K562	blood:
4	chr7:135901171..135902875-chr7:135904714..135906876,2	K562	blood:
5	chr7:135871453..135873315-chr7:135899511..135901972,2	K562	blood:
6	chr7:135925867..135928083-chr7:135931669..135933724,2	K562	blood:
7	chr7:135913397..135914921-chr7:135917469..135919011,2	K562	blood:
8	chr7:135894378..135896833-chr7:135914235..135916684,2	K562	blood:
9	chr7:135887570..135889713-chr7:135900025..135901819,2	K562	blood:
10	chr7:135922145..135923762-chr7:135932917..135934651,2	K562	blood:
11	chr7:135904376..135906256-chr7:135913327..135915875,2	K562	blood:
12	chr7:135969459..135971484-chr7:135972716..135974904,2	K562	blood:
13	chr7:135971453..135973945-chr7:135974750..135976881,2	K562	blood:
14	chr7:135923364..135924230-chr8:93753197..93753880,2	MCF-7	breast:
15	chr7:135917405..135919301-chr7:135920842..135922833,2	K562	blood:
16	chr7:135914976..135916896-chr7:135930254..135932259,2	K562	blood:
17	chr7:135917405..135919301-chr7:135920842..135922833,2	K562	blood:
18	chr7:135979464..135980429-chr7:136090686..136091523,2	MCF-7	breast:
19	chr7:135901171..135902875-chr7:135904714..135906876,2	K562	blood:
20	chr7:135959287..135961683-chr7:136109473..136111426,2	K562	blood:
21	chr7:135914976..135916896-chr7:135930254..135932259,2	K562	blood:
22	chr7:135348191..135350354-chr7:135915037..135917617,2	K562	blood:
23	chr7:135979400..135982923-chr7:135987230..135990822,3	K562	blood:
24	chr7:135904376..135906256-chr7:135913327..135915875,2	K562	blood:
25	chr7:135913397..135914921-chr7:135917469..135919011,2	K562	blood:
26	chr7:135922145..135923762-chr7:135932917..135934651,2	K562	blood:
27	chr7:135971453..135973945-chr7:135974750..135976881,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHRM2-2	chr7:135926898-135927119	ENSG00000232053.2
2	lnc-CHRM2-2	chr7:135926898-135927106	ENSG00000232053

No data

Variant related genes	Relation type
ENSG00000236503	TF binding region
ENSG00000220982	TF binding region
ENSG00000236503	CpG island
ENSG00000220982	CpG island

Extended variants
information (count: 1726 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1726 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201105345	chr7:135902630-135902631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536299734	chr7:135902635-135902636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs11765865	chr7:135902636-135902637	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs144584169	chr7:135902769-135902770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538898883	chr7:135902795-135902796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559184688	chr7:135902803-135902804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376773477	chr7:135902806-135902807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112289889	chr7:135902807-135902808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181854672	chr7:135902838-135902839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576221225	chr7:135902867-135902868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78212943	chr7:135902889-135902890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574530023	chr7:135902893-135902894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs59449011	chr7:135902968-135902969	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs563272121	chr7:135903064-135903065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4728383	chr7:135903087-135903088	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs552058592	chr7:135903113-135903114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559516143	chr7:135903126-135903127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186576723	chr7:135903141-135903142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190587085	chr7:135903142-135903143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182878940	chr7:135903147-135903148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550234258	chr7:135903152-135903153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10252049	chr7:135903178-135903179	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs34323518	chr7:135903195-135903196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78932752	chr7:135903213-135903214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs6944953	chr7:135903242-135903243	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs367924746	chr7:135903247-135903248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564481745	chr7:135903329-135903330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536567791	chr7:135907226-135907227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184996793	chr7:135907230-135907231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575555532	chr7:135907239-135907240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544693084	chr7:135907270-135907271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs71174580	chr7:135907279-135907280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111574811	chr7:135907280-135907281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs367691252	chr7:135907281-135907282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142981116	chr7:135907282-135907283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs367738917	chr7:135907284-135907285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577790920	chr7:135907313-135907314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540396923	chr7:135907319-135907320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537324790	chr7:135907323-135907324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539433942	chr7:135907324-135907325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377011890	chr7:135907325-135907326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201003297	chr7:135907328-135907329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs71174581	chr7:135907335-135907336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6946487	chr7:135907340-135907341	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs529503175	chr7:135907386-135907387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577679737	chr7:135908012-135908013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181007843	chr7:135908018-135908019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553900105	chr7:135908077-135908078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573943218	chr7:135908083-135908084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543295891	chr7:135908116-135908117	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	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
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:135902600-135903400	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr7:135907200-135907400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:135908000-135908200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr7:135913000-135913200	Enhancers	Duodenum Smooth Muscle	Duodenum
5	chr7:135913000-135913200	Flanking Bivalent TSS/Enh	Esophagus	oesophagus
6	chr7:135914000-135914600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr7:135914400-135914800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr7:135914600-135915000	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr7:135914800-135917000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr7:135918600-135919600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:135919200-135919600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:135919600-135919800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:135920400-135921400	ZNF genes & repeats	K562	blood
14	chr7:135921400-135921800	Weak transcription	K562	blood
15	chr7:135921800-135922400	Enhancers	K562	blood
16	chr7:135922200-135923000	Enhancers	Fetal Heart	heart
17	chr7:135922400-135925800	Weak transcription	K562	blood
18	chr7:135925200-135925600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:135925800-135927200	Enhancers	K562	blood
20	chr7:135927200-135929600	Weak transcription	K562	blood
21	chr7:135929600-135930000	Enhancers	K562	blood
22	chr7:135930000-135930800	Flanking Active TSS	K562	blood
23	chr7:135930800-135933800	Enhancers	K562	blood
24	chr7:135933400-135933800	Enhancers	Placenta	Placenta
25	chr7:135944400-135950800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:135944800-135945200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr7:135951400-135951800	Enhancers	Colon Smooth Muscle	Colon
28	chr7:135951400-135951800	Enhancers	Rectal Smooth Muscle	rectum
29	chr7:135957400-135957800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:135957800-135960800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr7:135958200-135958800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:135960800-135961000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr7:135961000-135961400	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr7:135961400-135962800	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr7:135962200-135964000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr7:135962400-135963800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:135962800-135963000	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr7:135963000-135963800	Enhancers	Colon Smooth Muscle	Colon
39	chr7:135963000-135963800	Enhancers	Rectal Smooth Muscle	rectum
40	chr7:135969800-135970200	Enhancers	Colon Smooth Muscle	Colon
41	chr7:135970200-135972400	Weak transcription	Colon Smooth Muscle	Colon
42	chr7:135972000-135972600	Enhancers	Rectal Smooth Muscle	rectum
43	chr7:135972400-135973200	Enhancers	Colon Smooth Muscle	Colon
44	chr7:135972600-135976600	Weak transcription	Rectal Smooth Muscle	rectum
45	chr7:135973200-135977200	Weak transcription	Colon Smooth Muscle	Colon
46	chr7:135975600-135975800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr7:135975800-135977200	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr7:135976600-135979000	Enhancers	Rectal Smooth Muscle	rectum
49	chr7:135977200-135978000	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr7:135977200-135979200	Enhancers	Colon Smooth Muscle	Colon

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