Variant report

Variant	nsv970966
Chromosome Location	chr7:149961366-150002640
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:676)
CpG islands
(count:734)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:149983307-149983448	HepG2	liver:	n/a	n/a
2	ATF1	chr7:150002546-150002653	K562	blood:	n/a	n/a
3	ATF1	chr7:150000092-150000441	K562	blood:	n/a	n/a
4	BATF	chr7:149969030-149969355	GM12878	blood:	n/a	chr7:149969272-149969281
5	BATF	chr7:149987527-149987750	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:149973520-149973524	K562	blood:	n/a	n/a
7	BHLHE40	chr7:150002428-150002740	K562	blood:	n/a	n/a
8	BHLHE40	chr7:150000217-150000290	K562	blood:	n/a	n/a
9	BRCA1	chr7:149973340-149973525	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr7:149999775-150000569	K562	blood:	n/a	n/a
11	CBX3	chr7:150002345-150002822	K562	blood:	n/a	n/a
12	CEBPB	chr7:149964429-149964633	HepG2	liver:	n/a	chr7:149964457-149964468
13	CEBPB	chr7:150001694-150002331	K562	blood:	n/a	n/a
14	CEBPB	chr7:149995177-149995311	K562	blood:	n/a	n/a
15	CEBPB	chr7:150002021-150002217	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:149983312-149983640	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr7:149999938-150000284	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr7:149999947-150000138	K562	blood:	n/a	n/a
19	CEBPB	chr7:149964447-149964475	K562	blood:	n/a	chr7:149964457-149964468
20	CEBPB	chr7:150002008-150002213	K562	blood:	n/a	n/a
21	CEBPB	chr7:150001988-150002268	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:149983378-149983618	K562	blood:	n/a	n/a
23	CEBPD	chr7:149983266-149983622	K562	blood:	n/a	n/a
24	CHD1	chr7:149973430-149973530	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:149964040-149964190	HRE	kidney:	n/a	n/a
26	CTCF	chr7:149983290-149983490	HepG2	liver:	n/a	n/a
27	CTCF	chr7:149983300-149983450	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr7:149992825-149992930	NHEK	skin:	n/a	chr7:149992885-149992906
29	CTCF	chr7:149983420-149983570	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:149992803-149992934	Kidney_OC	kidney:	n/a	chr7:149992885-149992906
31	CTCF	chr7:149973340-149973490	HL-60	blood:	n/a	chr7:149973397-149973405
32	CTCF	chr7:149983234-149983518	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr7:149973168-149973542	IMR90	lung:	n/a	chr7:149973397-149973405
34	CTCF	chr7:149973310-149973496	SK-N-SH_RA	brain:	n/a	chr7:149973397-149973405
35	CTCF	chr7:149973320-149973470	RPTEC	kidney:	n/a	chr7:149973397-149973405
36	CTCF	chr7:149983238-149983503	Fibrobl	skin:	n/a	n/a
37	CTCF	chr7:149973600-149973750	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr7:149983249-149983533	Lung_OC	lung:	n/a	n/a
39	CTCF	chr7:149983223-149983564	A549	lung:	n/a	n/a
40	CTCF	chr7:149983236-149983533	GM12878	blood:	n/a	n/a
41	CTCF	chr7:149973320-149973470	GM12868	blood:	n/a	chr7:149973397-149973405
42	CTCF	chr7:149973309-149973504	HepG2	liver:	n/a	chr7:149973397-149973405
43	CTCF	chr7:149973340-149973490	GM12872	blood:	n/a	chr7:149973397-149973405
44	CTCF	chr7:149983251-149983536	HepG2	liver:	n/a	n/a
45	CTCF	chr7:149973360-149973510	HEK293	kidney:	n/a	chr7:149973397-149973405
46	CTCF	chr7:149983180-149983330	AG10803	skin:	n/a	n/a
47	CTCF	chr7:149964055-149964244	K562	blood:	n/a	n/a
48	CTCF	chr7:149983440-149983590	WI-38	lung:	n/a	n/a
49	CTCF	chr7:149983320-149983470	HEK293	kidney:	n/a	n/a
50	CTCF	chr7:149973420-149973570	NHEK	skin:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:149971707-149971757	Caco-2	colon:	n/a
2	chr7:149964288-149964338	NHDF-neo	bronchial:	n/a
3	chr7:149971707-149971757	Caco-2	colon:	n/a
4	chr7:149964288-149964338	NHDF-neo	bronchial:	n/a
5	chr7:149999961-150000011	IMR90	lung:	fetal
6	chr7:149971780-149971830	AoSMC	blood vessel:	n/a
7	chr7:149971780-149971830	AG10803	skin:	n/a
8	chr7:149966466-149966516	U87	brain:	n/a
9	chr7:149978533-149978583	H1-hESC	embryonic stem cell:	embryo
10	chr7:149964288-149964338	AG09309	skin:	n/a
11	chr7:149979234-149979284	ProgFib	skin:	n/a
12	chr7:149966466-149966516	Caco-2	colon:	n/a
13	chr7:149971780-149971830	AG04450	lung:	fetal
14	chr7:149978533-149978583	HRCEpiC	kidney:	n/a
15	chr7:149978533-149978583	NHDF-neo	bronchial:	n/a
16	chr7:149964341-149964391	MCF10A-Er-Src	breast:	n/a
17	chr7:149978595-149978645	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:149978533-149978583	BJ	skin:	n/a
19	chr7:149971780-149971830	H1-hESC	embryonic stem cell:	embryo
20	chr7:150001179-150001229	GM12892	blood:	n/a
21	chr7:149979234-149979284	A549	lung:	n/a
22	chr7:149979234-149979284	MCF-7	breast:	n/a
23	chr7:149964341-149964391	PFSK-1	brain:	n/a
24	chr7:149978595-149978645	HIPEpiC	eye:	n/a
25	chr7:149964341-149964391	HepG2	liver:	n/a
26	chr7:149971780-149971830	GM12878	blood:	n/a
27	chr7:149978533-149978583	HRE	kidney:	n/a
28	chr7:149978533-149978583	GM12892	blood:	n/a
29	chr7:149999961-150000011	HAEpiC	amniotic membrane:	n/a
30	chr7:149971707-149971757	HCPEpiC	choroid plexus:	n/a
31	chr7:149978595-149978645	NHBE	bronchial:	n/a
32	chr7:149964341-149964391	HMEC	breast:	n/a
33	chr7:149964341-149964391	HCM	heart:	n/a
34	chr7:149978595-149978645	GM12891	blood:	n/a
35	chr7:149973088-149973138	NHBE	bronchial:	n/a
36	chr7:149999961-150000011	NT2-D1	testis:	n/a
37	chr7:149979234-149979284	GM12892	blood:	n/a
38	chr7:149978533-149978583	MCF-7	breast:	n/a
39	chr7:149994668-149994718	PANC-1	pancreas:	n/a
40	chr7:149964341-149964391	HAEpiC	amniotic membrane:	n/a
41	chr7:149994668-149994718	ovcar-3	ovarian:	n/a
42	chr7:149994668-149994718	U87	brain:	n/a
43	chr7:149966466-149966516	SKMC	muscle:	n/a
44	chr7:149978595-149978645	AG09309	skin:	n/a
45	chr7:149999961-150000011	RPTEC	kidney:	n/a
46	chr7:149971707-149971757	RPTEC	kidney:	n/a
47	chr7:149994668-149994718	HUVEC	blood vessel:	n/a
48	chr7:149964288-149964338	NB4	blood:	n/a
49	chr7:149971780-149971830	PrEC	prostate:	n/a
50	chr7:149978533-149978583	Hela-S3	cervix:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150000959..150002639-chr7:150065876..150067550,2	MCF-7	breast:
2	chr7:150000379..150002496-chr7:150064234..150066632,2	K562	blood:
3	chr7:149981999..149984542-chr7:150453171..150454808,2	K562	blood:
4	chr7:149972216..149975169-chr7:150445403..150447436,2	K562	blood:
5	chr7:149983204..149983759-chr7:150454066..150454591,2	MCF-7	breast:
6	chr7:149982878..149983831-chr7:150117963..150118748,4	MCF-7	breast:
7	chr7:150002516..150004738-chr7:150017976..150020518,2	K562	blood:
8	chr7:149982871..149983953-chr7:150117906..150118807,5	K562	blood:
9	chr7:150002193..150004738-chr7:150017976..150020637,3	K562	blood:

No data

Variant related genes	Relation type
ACTR3C	TF binding region
ACTR3C	CpG island
ENSG00000106526	chromatin interactions
ENSG00000214022	chromatin interactions
ENSG00000196456	chromatin interactions
ENSG00000241134	chromatin interactions
ENSG00000127399	chromatin interactions

Extended variants
information (count: 1621 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1621 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541064965	chr7:149961389-149961390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112751213	chr7:149961390-149961391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs578206415	chr7:149961408-149961409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543978064	chr7:149961421-149961422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145338745	chr7:149961429-149961430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528968199	chr7:149961430-149961431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562486595	chr7:149961452-149961453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577471820	chr7:149961487-149961488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528090683	chr7:149961531-149961532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551118631	chr7:149961578-149961579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571504733	chr7:149961590-149961591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141889015	chr7:149961638-149961639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181396895	chr7:149961646-149961647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567354202	chr7:149961649-149961650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115027183	chr7:149961657-149961658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375809174	chr7:149961659-149961660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150206801	chr7:149961668-149961669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186590372	chr7:149961685-149961686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534679489	chr7:149961708-149961709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190325085	chr7:149961743-149961744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs578172227	chr7:149961748-149961749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543782276	chr7:149961781-149961782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557483222	chr7:149961815-149961816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574294808	chr7:149961824-149961825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376111218	chr7:149961843-149961844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559468783	chr7:149961853-149961854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573008684	chr7:149961859-149961860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544954654	chr7:149961865-149961866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564748055	chr7:149961872-149961873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530785179	chr7:149961958-149961959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560798530	chr7:149961964-149961965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550608442	chr7:149961989-149961990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144812631	chr7:149962005-149962006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138746122	chr7:149962022-149962023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111244711	chr7:149962027-149962028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143439112	chr7:149962044-149962045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375874159	chr7:149962045-149962046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141632146	chr7:149962067-149962068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150529248	chr7:149962096-149962097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140420271	chr7:149962104-149962105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551725525	chr7:149962108-149962109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571554640	chr7:149962146-149962147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181840547	chr7:149962189-149962190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186387497	chr7:149962211-149962212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574413953	chr7:149962212-149962213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536824929	chr7:149962224-149962225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199946958	chr7:149962250-149962251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548026616	chr7:149962270-149962271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140187901	chr7:149962287-149962288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113105853	chr7:149962313-149962314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
early-passage human iPS cells	21368824	CNVD
Congenital long qt syndrome	19214780	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149940200-149962200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr7:149950800-149961800	Weak transcription	Fetal Intestine Large	intestine
3	chr7:149953400-149965800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr7:149953600-149983600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr7:149956000-149961400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:149959200-149980800	Weak transcription	Fetal Intestine Small	intestine
7	chr7:149959200-149986200	Weak transcription	Lung	lung
8	chr7:149961000-149961600	Strong transcription	Pancreas	Pancrea
9	chr7:149961000-149962000	Strong transcription	Liver	Liver
10	chr7:149961200-149965600	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr7:149961600-149978200	Weak transcription	Pancreas	Pancrea
12	chr7:149962000-149983600	Weak transcription	Liver	Liver
13	chr7:149969200-149969800	Enhancers	Primary T cells from cord blood	blood
14	chr7:149969200-149970000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr7:149969200-149970000	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr7:149973400-149973600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:149973600-149973800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr7:149973600-149974200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr7:149973600-149974400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:149973800-149974200	Enhancers	H1 Cell Line	embryonic stem cell
21	chr7:149974200-149989000	Weak transcription	Esophagus	oesophagus
22	chr7:149974400-149976600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr7:149975000-149975200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
24	chr7:149975200-149975400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:149975400-149977400	Enhancers	Brain Germinal Matrix	brain
26	chr7:149976400-149977000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr7:149976400-149977200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr7:149976400-149993200	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr7:149976600-149976800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
30	chr7:149976600-149977400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:149976600-149977600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr7:149976800-149977800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr7:149977000-149977400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr7:149977000-149977600	Enhancers	Fetal Brain Male	brain
35	chr7:149977400-149978000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:149977400-149983800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:149977600-149977800	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr7:149977800-149978200	Enhancers	H1 Cell Line	embryonic stem cell
39	chr7:149978000-149978200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:149978200-149978800	Enhancers	Pancreas	Pancrea
41	chr7:149978200-149983200	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr7:149978200-149985000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:149978800-150000000	Weak transcription	Pancreas	Pancrea
44	chr7:149979200-149979400	Enhancers	Fetal Brain Male	brain
45	chr7:149979400-149987800	Weak transcription	Right Atrium	heart
46	chr7:149980800-149981600	Strong transcription	Fetal Intestine Small	intestine
47	chr7:149981600-149990800	Weak transcription	Fetal Intestine Small	intestine
48	chr7:149983000-149983400	Enhancers	HepG2	liver
49	chr7:149983000-149995600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr7:149983200-149983400	Enhancers	H1 Cell Line	embryonic stem cell

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