Variant report

Variant	nsv5945
Chromosome Location	chr7:127852004-127880768
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:456)
CpG islands
(count:244)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:127855096-127855126	K562	blood:	n/a	n/a
2	ATF1	chr7:127876915-127877457	K562	blood:	n/a	n/a
3	ATF1	chr7:127857114-127857386	K562	blood:	n/a	n/a
4	ATF2	chr7:127857014-127857515	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr7:127862045-127862344	K562	blood:	n/a	n/a
6	BACH1	chr7:127862036-127862281	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:127862104-127862273	K562	blood:	n/a	n/a
8	BACH1	chr7:127869506-127869599	K562	blood:	n/a	n/a
9	BACH1	chr7:127877271-127877311	K562	blood:	n/a	n/a
10	BHLHE40	chr7:127876976-127877461	K562	blood:	n/a	n/a
11	BHLHE40	chr7:127858489-127858893	K562	blood:	n/a	n/a
12	BHLHE40	chr7:127862100-127862409	K562	blood:	n/a	n/a
13	BRCA1	chr7:127861828-127862245	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr7:127878910-127879546	K562	blood:	n/a	n/a
15	CBX3	chr7:127876814-127877569	K562	blood:	n/a	n/a
16	CBX3	chr7:127879018-127879517	K562	blood:	n/a	n/a
17	CBX3	chr7:127879164-127879492	HCT-116	colon:	n/a	n/a
18	CCNT2	chr7:127877155-127877436	K562	blood:	n/a	n/a
19	CEBPB	chr7:127869706-127869935	K562	blood:	n/a	chr7:127869798-127869809
20	CEBPB	chr7:127869646-127869933	HepG2	liver:	n/a	chr7:127869798-127869809
21	CEBPB	chr7:127876965-127877363	K562	blood:	n/a	chr7:127877088-127877096
22	CEBPB	chr7:127876977-127877338	Hela-S3	cervix:	n/a	chr7:127877088-127877096
23	CEBPB	chr7:127857206-127857625	IMR90	lung:	n/a	chr7:127857398-127857409
24	CEBPB	chr7:127877064-127877208	HepG2	liver:	n/a	chr7:127877088-127877096
25	CEBPB	chr7:127861732-127862327	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr7:127857232-127857583	A549	lung:	n/a	chr7:127857398-127857409
27	CEBPB	chr7:127874590-127874917	HepG2	liver:	n/a	chr7:127874727-127874740 chr7:127874728-127874739
28	CEBPB	chr7:127874725-127874744	IMR90	lung:	n/a	chr7:127874727-127874740 chr7:127874728-127874739
29	CEBPB	chr7:127877024-127877338	HepG2	liver:	n/a	chr7:127877088-127877096
30	CEBPB	chr7:127876932-127877339	K562	blood:	n/a	chr7:127877088-127877096
31	CEBPB	chr7:127877001-127877275	K562	blood:	n/a	chr7:127877088-127877096
32	CEBPB	chr7:127857204-127857455	K562	blood:	n/a	chr7:127857398-127857409
33	CEBPB	chr7:127857358-127857456	HepG2	liver:	n/a	chr7:127857398-127857409
34	CEBPB	chr7:127857195-127857631	A549	lung:	n/a	chr7:127857398-127857409
35	CEBPB	chr7:127877007-127877405	A549	lung:	n/a	chr7:127877088-127877096
36	CEBPB	chr7:127876977-127877339	A549	lung:	n/a	chr7:127877088-127877096
37	CEBPB	chr7:127876954-127877461	IMR90	lung:	n/a	chr7:127877088-127877096
38	CEBPB	chr7:127876946-127877437	MCF-7	breast:	n/a	chr7:127877088-127877096
39	CEBPB	chr7:127874612-127874914	MCF-7	breast:	n/a	chr7:127874727-127874740 chr7:127874728-127874739
40	CEBPB	chr7:127857172-127857637	Hela-S3	cervix:	n/a	chr7:127857398-127857409
41	CHD2	chr7:127861986-127862394	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr7:127857105-127857488	K562	blood:	n/a	chr7:127857246-127857259
43	CREB1	chr7:127857058-127857439	H1-hESC	embryonic stem cell:	n/a	chr7:127857246-127857259
44	CTCF	chr7:127858620-127858770	GM06990	blood:	n/a	n/a
45	CTCF	chr7:127858480-127858630	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr7:127858425-127858618	A549	lung:	n/a	n/a
47	CTCF	chr7:127857040-127857190	HCFaa	heart:	n/a	n/a
48	CTCF	chr7:127858380-127858530	AG09309	skin:	n/a	n/a
49	CTCF	chr7:127875720-127875870	BE2_C	brain:	n/a	n/a
50	CTCF	chr7:127875700-127875850	HEK293	kidney:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:127861992-127862042	PANC-1	pancreas:	n/a
2	chr7:127876829-127876879	PrEC	prostate:	n/a
3	chr7:127879920-127879970	HRE	kidney:	n/a
4	chr7:127880619-127880669	HIPEpiC	eye:	n/a
5	chr7:127876829-127876879	Caco-2	colon:	n/a
6	chr7:127876829-127876879	Hela-S3	cervix:	n/a
7	chr7:127880619-127880669	HUVEC	blood vessel:	n/a
8	chr7:127879920-127879970	GM19239	blood:	n/a
9	chr7:127876829-127876879	GM12892	blood:	n/a
10	chr7:127861992-127862042	HRCEpiC	kidney:	n/a
11	chr7:127880619-127880669	HCM	heart:	n/a
12	chr7:127861992-127862042	CMK	blood:	n/a
13	chr7:127861992-127862042	HCPEpiC	choroid plexus:	n/a
14	chr7:127876829-127876879	HIPEpiC	eye:	n/a
15	chr7:127861992-127862042	HRE	kidney:	n/a
16	chr7:127880619-127880669	ProgFib	skin:	n/a
17	chr7:127879920-127879970	GM12891	blood:	n/a
18	chr7:127876829-127876879	PFSK-1	brain:	n/a
19	chr7:127861992-127862042	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:127861992-127862042	GM12878	blood:	n/a
21	chr7:127876829-127876879	HCF	heart:	n/a
22	chr7:127861992-127862042	HCT-116	colon:	n/a
23	chr7:127876829-127876879	HL-60	blood:	n/a
24	chr7:127876829-127876879	SKMC	muscle:	n/a
25	chr7:127879920-127879970	HMEC	breast:	n/a
26	chr7:127880619-127880669	AG10803	skin:	n/a
27	chr7:127880619-127880669	A549	lung:	n/a
28	chr7:127879920-127879970	HCM	heart:	n/a
29	chr7:127876829-127876879	HRE	kidney:	n/a
30	chr7:127861992-127862042	HIPEpiC	eye:	n/a
31	chr7:127879920-127879970	IMR90	lung:	fetal
32	chr7:127879920-127879970	U87	brain:	n/a
33	chr7:127879920-127879970	HRCEpiC	kidney:	n/a
34	chr7:127861992-127862042	AG09319	gingival:	n/a
35	chr7:127861992-127862042	Caco-2	colon:	n/a
36	chr7:127879920-127879970	A549	lung:	n/a
37	chr7:127861992-127862042	HepG2	liver:	n/a
38	chr7:127880619-127880669	NT2-D1	testis:	n/a
39	chr7:127861992-127862042	SK-N-MC	brain:	n/a
40	chr7:127876829-127876879	ECC-1	luminal epithelium:	n/a
41	chr7:127876829-127876879	SK-N-SH_RA	brain:	n/a
42	chr7:127880619-127880669	HAEpiC	amniotic membrane:	n/a
43	chr7:127880619-127880669	Hela-S3	cervix:	n/a
44	chr7:127876829-127876879	BE2_C	brain:	n/a
45	chr7:127879920-127879970	GM12878	blood:	n/a
46	chr7:127876829-127876879	Hepatocyte	liver:	n/a
47	chr7:127880619-127880669	HPAEpiC	pulmonary alveolar:	n/a
48	chr7:127876829-127876879	HCM	heart:	n/a
49	chr7:127879920-127879970	PFSK-1	brain:	n/a
50	chr7:127861992-127862042	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:127862647..127864792-chr7:127867370..127870104,2	K562	blood:
2	chr7:127854529..127856623-chr7:127857622..127859528,2	MCF-7	breast:
3	chr7:127862647..127864792-chr7:127867370..127870104,2	K562	blood:
4	chr7:127867634..127869490-chr7:127873026..127875409,2	MCF-7	breast:
5	chr7:127869772..127871626-chr7:127914672..127917131,2	K562	blood:
6	chr7:127874763..127879327-chr7:127896549..127902097,6	MCF-7	breast:
7	chr7:127873554..127876347-chr7:127879499..127882292,2	MCF-7	breast:
8	chr7:127870227..127873605-chr7:127875454..127877245,3	K562	blood:
9	chr7:127875949..127878533-chr7:127881337..127883773,2	K562	blood:
10	chr7:127865874..127867760-chr7:127871525..127873172,2	K562	blood:
11	chr7:127857539..127859442-chr7:127980846..127983357,2	K562	blood:
12	chr7:127867634..127869490-chr7:127873026..127875409,2	MCF-7	breast:
13	chr7:127854529..127856623-chr7:127857622..127859528,2	MCF-7	breast:
14	chr7:127874560..127877136-chr7:127887540..127890542,3	K562	blood:
15	chr7:127865874..127867760-chr7:127871525..127873172,2	K562	blood:
16	chr7:127032256..127035129-chr7:127876340..127878786,2	K562	blood:
17	chr7:127861984..127865041-chr7:127865310..127867337,3	K562	blood:
18	chr7:127874560..127877136-chr7:127888514..127890542,2	K562	blood:
19	chr7:127870227..127873605-chr7:127875454..127877245,3	K562	blood:
20	chr7:127848604..127851949-chr7:127853770..127856964,3	K562	blood:
21	chr7:127861984..127865041-chr7:127865310..127867337,3	K562	blood:
22	chr7:127863182..127865481-chr7:127873510..127875848,2	K562	blood:
23	chr7:127707231..127709152-chr7:127855482..127857395,2	K562	blood:
24	chr7:127858029..127859044-chr7:127962044..127962840,5	MCF-7	breast:
25	chr7:127872543..127874497-chr7:127956158..127958595,2	K562	blood:
26	chr7:127849594..127850163-chr7:127861948..127862627,2	K562	blood:
27	chr7:127804591..127807479-chr7:127875712..127877601,2	K562	blood:
28	chr7:127863182..127865481-chr7:127873510..127875848,2	K562	blood:
29	chr7:127654215..127656574-chr7:127869545..127871812,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM28-2	chr7:127861457-127861593	XLOC_006597
2	lnc-RBM28-2	chr7:127876311-127876469	XLOC_006597
3	lnc-LEP-2	chr7:127846774-127858291	NONHSAT123172
4	lnc-LEP-2	chr7:127864086-127864945	NONHSAT123172

No data

Variant related genes	Relation type
LEP	TF binding region
LEP	CpG island
ENSG00000048405	chromatin interactions
ENSG00000174697	chromatin interactions

Extended variants
information (count: 1188 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1188 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545095055	chr7:127852047-127852048	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs564327191	chr7:127852055-127852056	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs11981584	chr7:127852065-127852066	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	mRNA abundance
4	rs540572721	chr7:127852206-127852207	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs183397372	chr7:127852211-127852212	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs546924298	chr7:127852258-127852259	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs529102842	chr7:127852294-127852295	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs550633474	chr7:127852310-127852311	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs568871958	chr7:127852329-127852330	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs115287108	chr7:127852336-127852337	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs563417222	chr7:127852348-127852349	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs78336513	chr7:127852365-127852366	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs574310105	chr7:127852450-127852451	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs562049664	chr7:127852461-127852462	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs540336548	chr7:127852521-127852522	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs187689165	chr7:127852606-127852607	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs567507349	chr7:127852607-127852608	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs529430340	chr7:127852610-127852611	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs556592955	chr7:127852627-127852628	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs559962557	chr7:127852629-127852630	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs372137940	chr7:127852630-127852631	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs77388478	chr7:127852656-127852657	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs578035771	chr7:127852700-127852701	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs193174216	chr7:127852706-127852707	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs554199144	chr7:127852731-127852732	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs185025408	chr7:127852743-127852744	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs576990799	chr7:127852814-127852815	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs375350397	chr7:127852846-127852847	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs189971646	chr7:127852892-127852893	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs369992340	chr7:127852900-127852901	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs34494123	chr7:127852908-127852909	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs573744066	chr7:127852909-127852910	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs544095359	chr7:127852960-127852961	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs11982473	chr7:127852982-127852983	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs73226660	chr7:127852988-127852989	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs201111726	chr7:127852989-127852990	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs534435081	chr7:127852991-127852992	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs559698905	chr7:127852992-127852993	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs10244926	chr7:127853118-127853119	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs146333003	chr7:127853134-127853135	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs549232519	chr7:127853209-127853210	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs567641383	chr7:127853229-127853230	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs562663170	chr7:127853312-127853313	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs538389202	chr7:127853363-127853364	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs192645028	chr7:127853374-127853375	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs183802783	chr7:127853390-127853391	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs112020889	chr7:127853396-127853397	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs571851680	chr7:127853466-127853467	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs538753784	chr7:127853471-127853472	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs554334413	chr7:127853498-127853499	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Endometrioid adenocarcinoma	16974079	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
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127844000-127875600	Weak transcription	Right Atrium	heart
2	chr7:127849400-127852800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:127849800-127852400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr7:127850000-127852200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:127850000-127867400	Weak transcription	Spleen	Spleen
6	chr7:127850200-127855000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr7:127850400-127854600	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr7:127850400-127854600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr7:127850400-127856000	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr7:127850800-127852400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr7:127850800-127852400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:127851000-127852200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr7:127851200-127852400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr7:127851200-127852400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:127851200-127852400	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr7:127851200-127852600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
17	chr7:127851200-127852800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr7:127851200-127852800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
19	chr7:127851200-127853400	Weak transcription	Osteobl	bone
20	chr7:127851400-127852400	Enhancers	HMEC	breast
21	chr7:127851400-127852600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:127851400-127852600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:127851400-127852800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr7:127851400-127852800	Enhancers	HSMM	muscle
25	chr7:127851400-127854800	Weak transcription	HSMMtube	muscle
26	chr7:127851600-127852200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:127851800-127852200	Enhancers	H9 Cell Line	embryonic stem cell
28	chr7:127851800-127852600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:127852200-127852400	Bivalent Enhancer	HepG2	liver
30	chr7:127852200-127855000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr7:127852200-127855200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr7:127852400-127855000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr7:127852400-127855200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr7:127852400-127855200	Weak transcription	HMEC	breast
35	chr7:127852400-127855400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr7:127852400-127857000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:127852800-127853400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr7:127852800-127853400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr7:127852800-127853400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:127852800-127854600	Weak transcription	HSMM	muscle
41	chr7:127853200-127853600	Enhancers	Adipose Nuclei	Adipose
42	chr7:127853200-127855600	Weak transcription	Brain Cingulate Gyrus	brain
43	chr7:127853400-127853600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr7:127853400-127853600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:127853400-127853600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:127853400-127853600	Enhancers	Placenta	Placenta
47	chr7:127853600-127855000	Weak transcription	Adipose Nuclei	Adipose
48	chr7:127853800-127855200	Weak transcription	Placenta	Placenta
49	chr7:127854600-127857000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr7:127854600-127857000	Enhancers	Monocytes-CD14+_RO01746	blood

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