Variant report

Variant	nsv887816
Chromosome Location	chr7:18935310-18959138
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr7:18934946-18935470	HCT-116	colon:	n/a	n/a
2	CEBPB	chr7:18934830-18935687	HCT-116	colon:	n/a	chr7:18935614-18935626
3	CEBPB	chr7:18940561-18940789	IMR90	lung:	n/a	chr7:18940689-18940702 chr7:18940622-18940635
4	CEBPB	chr7:18945099-18945329	A549	lung:	n/a	n/a
5	CTCF	chr7:18946560-18946710	HFF-Myc	foreskin:	n/a	n/a
6	CTCF	chr7:18946720-18946870	HFF-Myc	foreskin:	n/a	n/a
7	CTCF	chr7:18946640-18946790	HPAF	blood vessel:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
8	CTCF	chr7:18946595-18946814	Gliobla	brain:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
9	CTCF	chr7:18946640-18946790	SK-N-SH_RA	brain:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
10	CTCF	chr7:18946660-18946810	HPAF	blood vessel:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
11	CTCF	chr7:18946440-18946590	HMEC	breast:	n/a	n/a
12	CTCF	chr7:18946580-18946730	HPF	lung:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
13	CTCF	chr7:18946489-18946821	H1-hESC	embryonic stem cell:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
14	CTCF	chr7:18946420-18946570	A549	lung:	n/a	n/a
15	CTCF	chr7:18946642-18946767	ProgFib	skin:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
16	CTCF	chr7:18946560-18946710	GM12875	blood:	n/a	n/a
17	CTCF	chr7:18946680-18946830	A549	lung:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
18	CTCF	chr7:18946654-18946790	HUVEC	blood vessel:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
19	CTCF	chr7:18946694-18946725	MCF-7	breast:	n/a	chr7:18946706-18946724 chr7:18946707-18946723 chr7:18946709-18946722
20	CTCF	chr7:18946660-18946810	WI-38	lung:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
21	CTCF	chr7:18946700-18946850	HMEC	breast:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
22	CTCF	chr7:18946660-18946810	HRPEpiC	eye:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
23	CTCF	chr7:18946510-18946986	HCT-116	colon:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722 chr7:18946970-18946978
24	CTCF	chr7:18946580-18946730	BE2_C	brain:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
25	CTCF	chr7:18946708-18946756	Hela-S3	cervix:	n/a	chr7:18946708-18946729 chr7:18946709-18946722
26	CTCF	chr7:18946595-18946807	H1-hESC	embryonic stem cell:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
27	CTCF	chr7:18946647-18946777	LNCaP	prostate:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
28	CTCF	chr7:18946540-18946690	HAc	cerebellar:	n/a	n/a
29	CTCF	chr7:18946680-18946830	MCF-7	breast:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
30	CTCF	chr7:18946616-18946783	SK-N-SH_RA	brain:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
31	CTCF	chr7:18946540-18946690	GM12873	blood:	n/a	n/a
32	CTCF	chr7:18946660-18946810	HBMEC	blood vessel:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
33	CTCF	chr7:18946600-18946750	AoAF	blood vessel:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
34	CTCF	chr7:18946640-18946790	BE2_C	brain:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
35	CTCF	chr7:18946640-18946790	HAc	cerebellar:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
36	CTCF	chr7:18946710-18946738	HepG2	liver:	n/a	n/a
37	CTCF	chr7:18946660-18946810	HMF	breast:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
38	CTCF	chr7:18946660-18946810	HA-sp	spinal cord:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
39	CTCF	chr7:18946520-18946670	Caco-2	colon:	n/a	n/a
40	CTCF	chr7:18946580-18946730	HMEC	breast:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
41	CTCF	chr7:18952820-18952970	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr7:18946695-18946756	NHEK	skin:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
43	CTCF	chr7:18946640-18946790	NHEK	skin:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
44	CTCF	chr7:18946620-18946770	HBMEC	blood vessel:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
45	CTCF	chr7:18946660-18946810	HCT-116	colon:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
46	CTCF	chr7:18946620-18946770	SAEC	small airway:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
47	CTCF	chr7:18946560-18946710	NHEK	skin:	n/a	n/a
48	CTCF	chr7:18956960-18957110	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr7:18946620-18946770	HEK293	kidney:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
50	CTCF	chr7:18946600-18946750	HRPEpiC	eye:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TWIST1-2	chr7:18938932-18939056	ENSG00000226522.1

Variant related genes	Relation type
ENSG00000226522	TF binding region

Extended variants
information (count: 1058 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1058 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11764843	chr7:18935310-18935311	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540089261	chr7:18935331-18935332	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs185960222	chr7:18935348-18935349	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs149358588	chr7:18935377-18935378	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs144692198	chr7:18935389-18935390	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs563461645	chr7:18935400-18935401	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs530623349	chr7:18935426-18935427	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs545641741	chr7:18935456-18935457	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs201717791	chr7:18935459-18935460	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs11765532	chr7:18935464-18935465	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs140157148	chr7:18935470-18935471	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs376231102	chr7:18935477-18935478	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs370624935	chr7:18935505-18935506	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs530386289	chr7:18935514-18935515	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs548612457	chr7:18935551-18935552	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs191195886	chr7:18935560-18935561	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs537639183	chr7:18935608-18935609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552844143	chr7:18935610-18935611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181919816	chr7:18935611-18935612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534733327	chr7:18935639-18935640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552903894	chr7:18935646-18935647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574363288	chr7:18935647-18935648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186532159	chr7:18935650-18935651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114607859	chr7:18935652-18935653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145661278	chr7:18935653-18935654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545580428	chr7:18935658-18935659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371255391	chr7:18935670-18935671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563967870	chr7:18935687-18935688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576899021	chr7:18935726-18935727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10486317	chr7:18935733-18935734	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs190585296	chr7:18935742-18935743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183088941	chr7:18935751-18935752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10486318	chr7:18935767-18935768	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs116683619	chr7:18935768-18935769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531266088	chr7:18935785-18935786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113064426	chr7:18935794-18935795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571074788	chr7:18935803-18935804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534669422	chr7:18935950-18935951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568014557	chr7:18935953-18935954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546385126	chr7:18935957-18935958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188153094	chr7:18935994-18935995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112195593	chr7:18936032-18936033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191196602	chr7:18936033-18936034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556954656	chr7:18936067-18936068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533776260	chr7:18936095-18936096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62448101	chr7:18936127-18936128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547827051	chr7:18936164-18936165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539370766	chr7:18936200-18936201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557496255	chr7:18936210-18936211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572711527	chr7:18936225-18936226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Melanoma	18172304	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
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18903000-18940000	Weak transcription	Aorta	Aorta
2	chr7:18931200-18943400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:18931400-18940000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:18934400-18935600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:18934400-18936600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:18934400-18936800	Enhancers	NHLF	lung
7	chr7:18934800-18935400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:18934800-18936200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:18934800-18936200	Enhancers	A549	lung
10	chr7:18934800-18936200	Enhancers	Hela-S3	cervix
11	chr7:18934800-18936600	Enhancers	HSMM	muscle
12	chr7:18934800-18936600	Enhancers	HUVEC	blood vessel
13	chr7:18935000-18935600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:18935000-18935600	Enhancers	HSMMtube	muscle
15	chr7:18935200-18935600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr7:18935200-18935600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:18935200-18935600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr7:18935200-18935600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr7:18935200-18935600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr7:18935200-18935600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr7:18935200-18935600	Flanking Active TSS	HMEC	breast
22	chr7:18935200-18935600	Flanking Active TSS	NH-A	brain
23	chr7:18935200-18935600	Flanking Active TSS	NHDF-Ad	bronchial
24	chr7:18935200-18935600	Flanking Active TSS	NHEK	skin
25	chr7:18935200-18935600	Flanking Active TSS	Osteobl	bone
26	chr7:18935200-18936400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr7:18935200-18936600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:18935200-18936600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr7:18935200-18936800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr7:18935400-18936400	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:18935400-18936600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr7:18935400-18936600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr7:18935400-18937400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:18935600-18935800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr7:18935600-18936200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr7:18935600-18936200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr7:18935600-18936200	Enhancers	Fetal Kidney	kidney
38	chr7:18935600-18936200	Enhancers	Osteobl	bone
39	chr7:18935600-18936400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:18935600-18936600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr7:18935600-18936600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:18935600-18936600	Enhancers	HMEC	breast
43	chr7:18935600-18936600	Enhancers	NH-A	brain
44	chr7:18935600-18936600	Enhancers	NHDF-Ad	bronchial
45	chr7:18935600-18936600	Enhancers	NHEK	skin
46	chr7:18935600-18940000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr7:18935800-18936200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:18935800-18936200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr7:18936000-18936600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:18936200-18936600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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