Variant report

Variant	nsv971388
Chromosome Location	chr7:65291064-65316035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:65301736-65302051	K562	blood:	n/a	n/a
2	ARID3A	chr7:65301784-65302028	HepG2	liver:	n/a	n/a
3	ATF1	chr7:65302462-65302647	K562	blood:	n/a	n/a
4	BHLHE40	chr7:65302528-65302815	K562	blood:	n/a	n/a
5	BRCA1	chr7:65305283-65305337	GM12878	blood:	n/a	n/a
6	CBX3	chr7:65302488-65302854	K562	blood:	n/a	n/a
7	CBX3	chr7:65313184-65313538	K562	blood:	n/a	n/a
8	CBX3	chr7:65305453-65305819	K562	blood:	n/a	n/a
9	CCNT2	chr7:65300352-65300552	K562	blood:	n/a	n/a
10	CEBPB	chr7:65313890-65313913	HepG2	liver:	n/a	chr7:65313890-65313901
11	CEBPB	chr7:65302559-65302726	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:65302541-65302720	K562	blood:	n/a	n/a
13	CEBPB	chr7:65305553-65305716	K562	blood:	n/a	n/a
14	CEBPB	chr7:65308651-65308852	HepG2	liver:	n/a	chr7:65308694-65308705 chr7:65308693-65308706
15	CEBPB	chr7:65313883-65313907	IMR90	lung:	n/a	chr7:65313890-65313901
16	CEBPB	chr7:65302514-65302800	A549	lung:	n/a	n/a
17	CEBPB	chr7:65302565-65302719	K562	blood:	n/a	n/a
18	CEBPB	chr7:65302461-65302809	IMR90	lung:	n/a	n/a
19	CTCF	chr7:65305600-65305750	HCM	heart:	n/a	chr7:65305621-65305639
20	CTCF	chr7:65305496-65305787	GM12892	blood:	n/a	chr7:65305621-65305639
21	CTCF	chr7:65305560-65305710	HCT-116	colon:	n/a	chr7:65305621-65305639
22	CTCF	chr7:65304320-65304470	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr7:65305580-65305730	GM12878	blood:	n/a	chr7:65305621-65305639
24	CTCF	chr7:65305520-65305670	GM12878	blood:	n/a	chr7:65305621-65305639
25	CTCF	chr7:65305420-65305570	GM12873	blood:	n/a	n/a
26	CTCF	chr7:65305480-65305630	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr7:65305571-65305721	K562	blood:	n/a	chr7:65305621-65305639
28	CTCF	chr7:65304260-65304410	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr7:65305880-65306030	GM06990	blood:	n/a	n/a
30	CTCF	chr7:65303180-65303330	HEK293	kidney:	n/a	n/a
31	CTCF	chr7:65305540-65305690	BE2_C	brain:	n/a	chr7:65305621-65305639
32	CTCF	chr7:65305460-65305610	HMEC	breast:	n/a	n/a
33	CTCF	chr7:65303180-65303330	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr7:65305543-65305736	GM20000	blood:	n/a	chr7:65305621-65305639
35	CTCF	chr7:65305986-65306035	GM19239	blood:	n/a	n/a
36	CTCF	chr7:65305540-65305690	WERI-Rb-1	eye:	n/a	chr7:65305621-65305639
37	CTCF	chr7:65305574-65305696	GM19239	blood:	n/a	chr7:65305621-65305639
38	CTCF	chr7:65305690-65305704	GM13976	blood:	n/a	n/a
39	CTCF	chr7:65303140-65303290	GM12873	blood:	n/a	n/a
40	CTCF	chr7:65305480-65305630	HCM	heart:	n/a	n/a
41	CTCF	chr7:65305456-65305726	K562	blood:	n/a	chr7:65305621-65305639
42	CTCF	chr7:65305531-65305749	GM10248	blood:	n/a	chr7:65305621-65305639
43	CTCF	chr7:65305520-65305670	GM12865	blood:	n/a	chr7:65305621-65305639
44	CTCF	chr7:65305603-65305650	HepG2	liver:	n/a	chr7:65305621-65305639
45	CTCF	chr7:65306160-65306310	GM12878	blood:	n/a	n/a
46	CTCF	chr7:65305540-65305690	HMF	breast:	n/a	chr7:65305621-65305639
47	CTCF	chr7:65305560-65305710	BE2_C	brain:	n/a	chr7:65305621-65305639
48	CTCF	chr7:65305560-65305710	GM12869	blood:	n/a	chr7:65305621-65305639
49	CTCF	chr7:65305540-65305690	HEEpiC	esophagus:	n/a	chr7:65305621-65305639
50	CTCF	chr7:65305540-65305690	GM12874	blood:	n/a	chr7:65305621-65305639

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65315216-65315266	HAEpiC	amniotic membrane:	n/a
2	chr7:65303149-65303199	SAEC	small airway:	n/a
3	chr7:65303149-65303199	LNCaP	prostate:	n/a
4	chr7:65302258-65302308	HPAEpiC	pulmonary alveolar:	n/a
5	chr7:65303149-65303199	HEK293	kidney:	embryo
6	chr7:65302258-65302308	U87	brain:	n/a
7	chr7:65315216-65315266	NHBE	bronchial:	n/a
8	chr7:65302258-65302308	GM12892	blood:	n/a
9	chr7:65303149-65303199	GM06990	blood:	n/a
10	chr7:65315216-65315266	CMK	blood:	n/a
11	chr7:65315216-65315266	LNCaP	prostate:	n/a
12	chr7:65315216-65315266	GM12892	blood:	n/a
13	chr7:65302258-65302308	K562	blood:	n/a
14	chr7:65315216-65315266	HRE	kidney:	n/a
15	chr7:65315216-65315266	MCF10A-Er-Src	breast:	n/a
16	chr7:65303149-65303199	HEEpiC	esophagus:	n/a
17	chr7:65315216-65315266	Hela-S3	cervix:	n/a
18	chr7:65315216-65315266	HNPCEpiC	eye:	n/a
19	chr7:65303149-65303199	SK-N-SH	brain:	n/a
20	chr7:65315216-65315266	HEK293	kidney:	embryo
21	chr7:65315216-65315266	HEEpiC	esophagus:	n/a
22	chr7:65315216-65315266	MCF-7	breast:	n/a
23	chr7:65302258-65302308	HRCEpiC	kidney:	n/a
24	chr7:65315216-65315266	HUVEC	blood vessel:	n/a
25	chr7:65302258-65302308	ECC-1	luminal epithelium:	n/a
26	chr7:65315216-65315266	T-47D	breast:	n/a
27	chr7:65302258-65302308	Jurkat	blood:	n/a
28	chr7:65303149-65303199	Hela-S3	cervix:	n/a
29	chr7:65302258-65302308	Caco-2	colon:	n/a
30	chr7:65302258-65302308	HCM	heart:	n/a
31	chr7:65303149-65303199	IMR90	lung:	fetal
32	chr7:65315216-65315266	PFSK-1	brain:	n/a
33	chr7:65303149-65303199	HL-60	blood:	n/a
34	chr7:65315216-65315266	GM06990	blood:	n/a
35	chr7:65315216-65315266	HRCEpiC	kidney:	n/a
36	chr7:65302258-65302308	HCPEpiC	choroid plexus:	n/a
37	chr7:65302258-65302308	AG04449	skin:	fetal
38	chr7:65315216-65315266	Caco-2	colon:	n/a
39	chr7:65302258-65302308	HUVEC	blood vessel:	n/a
40	chr7:65303149-65303199	SKMC	muscle:	n/a
41	chr7:65303149-65303199	U87	brain:	n/a
42	chr7:65315216-65315266	AoSMC	blood vessel:	n/a
43	chr7:65315216-65315266	HCM	heart:	n/a
44	chr7:65303149-65303199	AG09319	gingival:	n/a
45	chr7:65302258-65302308	NHDF-neo	bronchial:	n/a
46	chr7:65303149-65303199	ProgFib	skin:	n/a
47	chr7:65303149-65303199	GM12892	blood:	n/a
48	chr7:65303149-65303199	HRCEpiC	kidney:	n/a
49	chr7:65302258-65302308	GM19239	blood:	n/a
50	chr7:65315216-65315266	GM19239	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:65290518..65293145-chr7:65296020..65298724,2	MCF-7	breast:
2	chr7:65296135..65298930-chr7:65301259..65302803,2	K562	blood:
3	chr7:65303936..65305643-chr7:65310020..65312064,2	MCF-7	breast:
4	chr7:65290518..65293145-chr7:65296020..65298724,2	MCF-7	breast:
5	chr7:65296135..65298930-chr7:65301259..65302803,2	K562	blood:
6	chr7:65287691..65289965-chr7:65292443..65295054,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VKORC1L1-4	chr7:65303020-65303077	NONHSAT121122
2	lnc-VKORC1L1-1	chr7:65293604-65293652	XLOC_006132
3	lnc-VKORC1L1-4	chr7:65300762-65300945	NONHSAT121122
4	lnc-VKORC1L1-1	chr7:65292534-65292729	XLOC_006132
5	lnc-VKORC1L1-3	chr7:65305199-65305583	NONHSAT121123

No data

Variant related genes	Relation type
ENSG00000236529	TF binding region
ENSG00000236529	CpG island
ENSG00000236529	chromatin interactions

Extended variants
information (count: 883 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:883 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376449762	chr7:65291084-65291085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs139350079	chr7:65291090-65291091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537226339	chr7:65291096-65291097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557317422	chr7:65291103-65291104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574068722	chr7:65291107-65291108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542765243	chr7:65291161-65291162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553286297	chr7:65291195-65291196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573296041	chr7:65291227-65291228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs60608110	chr7:65291229-65291230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35950721	chr7:65291230-65291231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs397738434	chr7:65291231-65291232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186944216	chr7:65291244-65291245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529182175	chr7:65291245-65291246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73368778	chr7:65291248-65291249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150072077	chr7:65291288-65291289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543602212	chr7:65291305-65291306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147744316	chr7:65291308-65291309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536468282	chr7:65291332-65291333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562665153	chr7:65291349-65291350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369888120	chr7:65291356-65291357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548824806	chr7:65291373-65291374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35779737	chr7:65291379-65291380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189780344	chr7:65291427-65291428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201545108	chr7:65291432-65291433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184160940	chr7:65291513-65291514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372447221	chr7:65291526-65291527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528058407	chr7:65291534-65291535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550990151	chr7:65291574-65291575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571604593	chr7:65291612-65291613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537388802	chr7:65291658-65291659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142343208	chr7:65291684-65291685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567767999	chr7:65291708-65291709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373710248	chr7:65291718-65291719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536723955	chr7:65291731-65291732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79891278	chr7:65291732-65291733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553207549	chr7:65291792-65291793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112652938	chr7:65291801-65291802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539015236	chr7:65291818-65291819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559040781	chr7:65291864-65291865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577993519	chr7:65291866-65291867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188862256	chr7:65291875-65291876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543353692	chr7:65291902-65291903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563467931	chr7:65291904-65291905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573766668	chr7:65291913-65291914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542838536	chr7:65291995-65291996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4718285	chr7:65292005-65292006	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs528218965	chr7:65292006-65292007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs193219498	chr7:65292040-65292041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34815098	chr7:65292254-65292255	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs571607158	chr7:65292255-65292256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Hodgkin''s lymphoma	18641027	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
Glioblastoma	21080181	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	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
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65247800-65303400	Weak transcription	Duodenum Mucosa	Duodenum
2	chr7:65260800-65302600	Weak transcription	Gastric	stomach
3	chr7:65264000-65302600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:65264000-65302800	Weak transcription	Esophagus	oesophagus
5	chr7:65264000-65310800	Weak transcription	Fetal Intestine Small	intestine
6	chr7:65264200-65292400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:65264600-65292800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr7:65265600-65304400	Weak transcription	Left Ventricle	heart
9	chr7:65266800-65311000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:65267600-65304000	Weak transcription	Placenta	Placenta
11	chr7:65270200-65302800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:65273400-65305400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr7:65273800-65303200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:65274600-65303000	Weak transcription	Stomach Smooth Muscle	stomach
15	chr7:65275200-65304000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr7:65285600-65294200	Weak transcription	Spleen	Spleen
17	chr7:65288200-65292200	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr7:65288800-65306000	Weak transcription	Aorta	Aorta
19	chr7:65290400-65305800	Weak transcription	GM12878-XiMat	blood
20	chr7:65290600-65294600	Weak transcription	HepG2	liver
21	chr7:65290800-65292000	Strong transcription	Pancreas	Pancrea
22	chr7:65291000-65295600	Weak transcription	Adipose Nuclei	Adipose
23	chr7:65291200-65302200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:65292000-65292400	Weak transcription	Pancreas	Pancrea
25	chr7:65292200-65292800	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr7:65292400-65292800	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:65292400-65292800	Strong transcription	Pancreas	Pancrea
28	chr7:65292400-65293000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:65292800-65301200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:65292800-65302600	Weak transcription	Pancreas	Pancrea
31	chr7:65292800-65303800	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr7:65294200-65298400	Weak transcription	Psoas Muscle	Psoas
33	chr7:65297200-65305000	Weak transcription	Small Intestine	intestine
34	chr7:65297400-65311000	Weak transcription	Liver	Liver
35	chr7:65300200-65300400	Enhancers	K562	blood
36	chr7:65300200-65300600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:65300200-65300600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:65300400-65302600	Weak transcription	K562	blood
39	chr7:65301200-65301400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:65301200-65303000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:65301200-65303000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr7:65301200-65303800	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr7:65301400-65302600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:65302200-65311000	Weak transcription	Right Ventricle	heart
45	chr7:65302400-65302800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr7:65302400-65302800	Enhancers	HUVEC	blood vessel
47	chr7:65302400-65302800	Enhancers	NHEK	skin
48	chr7:65302400-65303000	Enhancers	Hela-S3	cervix
49	chr7:65302600-65302800	Enhancers	HMEC	breast
50	chr7:65302600-65303000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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