Variant report

Variant	nsv870909
Chromosome Location	chr1:77104773-77195164
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:435)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:77139682-77140065	HepG2	liver:	n/a	n/a
2	ATF1	chr1:77119453-77119559	K562	blood:	n/a	n/a
3	ATF3	chr1:77156408-77156900	HCT-116	colon:	n/a	n/a
4	BATF	chr1:77143528-77143773	GM12878	blood:	n/a	chr1:77143665-77143676
5	BATF	chr1:77179188-77179435	GM12878	blood:	n/a	n/a
6	BCL11A	chr1:77179313-77179521	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:77179232-77179520	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:77133723-77134000	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:77112842-77112874	K562	blood:	n/a	n/a
10	CBX3	chr1:77156384-77156905	HCT-116	colon:	n/a	n/a
11	CCNT2	chr1:77153768-77154264	K562	blood:	n/a	n/a
12	CEBPB	chr1:77105633-77106254	HCT-116	colon:	n/a	n/a
13	CEBPB	chr1:77181185-77181456	IMR90	lung:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
14	CEBPB	chr1:77181111-77181550	HCT-116	colon:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
15	CEBPB	chr1:77182007-77182282	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:77167086-77167347	HepG2	liver:	n/a	chr1:77167220-77167231
17	CEBPB	chr1:77181235-77181390	K562	blood:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
18	CEBPB	chr1:77164266-77164461	HepG2	liver:	n/a	chr1:77164405-77164416
19	CEBPB	chr1:77167065-77167392	IMR90	lung:	n/a	chr1:77167220-77167231
20	CEBPB	chr1:77181200-77181483	A549	lung:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
21	CEBPB	chr1:77167167-77167294	H1-hESC	embryonic stem cell:	n/a	chr1:77167220-77167231
22	CEBPB	chr1:77105851-77106102	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:77181160-77181514	HepG2	liver:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
24	CEBPB	chr1:77105688-77106193	HCT-116	colon:	n/a	n/a
25	CEBPB	chr1:77181194-77181509	Hela-S3	cervix:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
26	CTCF	chr1:77144800-77144950	GM12866	blood:	n/a	n/a
27	CTCF	chr1:77147900-77148050	HEK293	kidney:	n/a	n/a
28	CTCF	chr1:77165519-77165698	GM12878	blood:	n/a	n/a
29	CTCF	chr1:77165539-77165689	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:77165817-77165944	GM12892	blood:	n/a	n/a
31	CTCF	chr1:77147920-77148070	RPTEC	kidney:	n/a	n/a
32	CTCF	chr1:77148000-77148150	HMEC	breast:	n/a	n/a
33	CTCF	chr1:77148012-77148123	GM12878	blood:	n/a	n/a
34	CTCF	chr1:77154760-77154910	GM12870	blood:	n/a	n/a
35	CTCF	chr1:77165537-77165693	GM12892	blood:	n/a	n/a
36	CTCF	chr1:77147984-77148132	LNCaP	prostate:	n/a	n/a
37	CTCF	chr1:77147960-77148110	MCF-7	breast:	n/a	n/a
38	CTCF	chr1:77123600-77123750	GM12868	blood:	n/a	n/a
39	CTCF	chr1:77165603-77165650	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:77165557-77165665	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:77165556-77165674	HepG2	liver:	n/a	n/a
42	CTCF	chr1:77162120-77162270	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr1:77165872-77165909	GM19239	blood:	n/a	n/a
44	CTCF	chr1:77165855-77165948	GM19240	blood:	n/a	n/a
45	CTCF	chr1:77165580-77165730	GM12864	blood:	n/a	n/a
46	CTCF	chr1:77179258-77179397	GM12878	blood:	n/a	n/a
47	CTCF	chr1:77165619-77165707	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr1:77165539-77165709	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:77165544-77165696	GM12891	blood:	n/a	n/a
50	CTCF	chr1:77165584-77165663	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77165604-77165654	NHDF-neo	bronchial:	n/a
2	chr1:77165565-77165615	U87	brain:	n/a
3	chr1:77165604-77165654	AG09319	gingival:	n/a
4	chr1:77165604-77165654	HAEpiC	amniotic membrane:	n/a
5	chr1:77165565-77165615	GM12891	blood:	n/a
6	chr1:77165604-77165654	ProgFib	skin:	n/a
7	chr1:77165604-77165654	NHBE	bronchial:	n/a
8	chr1:77165565-77165615	Jurkat	blood:	n/a
9	chr1:77165604-77165654	RPTEC	kidney:	n/a
10	chr1:77165604-77165654	HRPEpiC	eye:	n/a
11	chr1:77165461-77165511	SK-N-SH_RA	brain:	n/a
12	chr1:77165461-77165511	LNCaP	prostate:	n/a
13	chr1:77165461-77165511	IMR90	lung:	fetal
14	chr1:77165565-77165615	HUVEC	blood vessel:	n/a
15	chr1:77165461-77165511	GM12878	blood:	n/a
16	chr1:77165565-77165615	T-47D	breast:	n/a
17	chr1:77165461-77165511	AG10803	skin:	n/a
18	chr1:77165461-77165511	HAEpiC	amniotic membrane:	n/a
19	chr1:77165565-77165615	Caco-2	colon:	n/a
20	chr1:77165604-77165654	SK-N-MC	brain:	n/a
21	chr1:77165604-77165654	HRE	kidney:	n/a
22	chr1:77165461-77165511	CMK	blood:	n/a
23	chr1:77165461-77165511	HEEpiC	esophagus:	n/a
24	chr1:77165461-77165511	Hela-S3	cervix:	n/a
25	chr1:77165604-77165654	NT2-D1	testis:	n/a
26	chr1:77165604-77165654	HIPEpiC	eye:	n/a
27	chr1:77165604-77165654	SKMC	muscle:	n/a
28	chr1:77165461-77165511	HCM	heart:	n/a
29	chr1:77165604-77165654	Jurkat	blood:	n/a
30	chr1:77165565-77165615	NH-A	brain:	n/a
31	chr1:77165604-77165654	IMR90	lung:	fetal
32	chr1:77165565-77165615	HepG2	liver:	n/a
33	chr1:77165461-77165511	H1-hESC	embryonic stem cell:	embryo
34	chr1:77165604-77165654	AG04450	lung:	fetal
35	chr1:77165604-77165654	AG10803	skin:	n/a
36	chr1:77165461-77165511	GM12892	blood:	n/a
37	chr1:77165461-77165511	AG04450	lung:	fetal
38	chr1:77165604-77165654	U87	brain:	n/a
39	chr1:77165461-77165511	NHBE	bronchial:	n/a
40	chr1:77165604-77165654	HCF	heart:	n/a
41	chr1:77165461-77165511	SAEC	small airway:	n/a
42	chr1:77165565-77165615	AoSMC	blood vessel:	n/a
43	chr1:77165604-77165654	CMK	blood:	n/a
44	chr1:77165565-77165615	HCT-116	colon:	n/a
45	chr1:77165565-77165615	SAEC	small airway:	n/a
46	chr1:77165461-77165511	MCF10A-Er-Src	breast:	n/a
47	chr1:77165565-77165615	HL-60	blood:	n/a
48	chr1:77165461-77165511	HEK293	kidney:	embryo
49	chr1:77165461-77165511	AoSMC	blood vessel:	n/a
50	chr1:77165565-77165615	HEEpiC	esophagus:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:77180012..77182664-chr1:77186329..77188985,2	MCF-7	breast:
2	chr1:77160313..77162146-chr1:77164141..77166438,2	K562	blood:
3	chr1:77147990..77150135-chr1:77152468..77154920,2	MCF-7	breast:
4	chr1:77180012..77182664-chr1:77186329..77188985,2	MCF-7	breast:
5	chr1:77147990..77150135-chr1:77152468..77154920,2	MCF-7	breast:
6	chr1:77076114..77078249-chr1:77109036..77110684,2	MCF-7	breast:
7	chr1:77169289..77170251-chr1:77243231..77243897,2	MCF-7	breast:
8	chr1:77152003..77153806-chr1:77226748..77229399,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000264686	TF binding region
TPI1P1	TF binding region
ENSG00000264686	CpG island
TPI1P1	CpG island
ENSG00000226415	chromatin interactions

Extended variants
information (count: 1778 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1778 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2349044	chr1:77104773-77104774	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570563495	chr1:77104814-77104815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116388531	chr1:77104822-77104823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11369796	chr1:77104862-77104863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs397721293	chr1:77104869-77104870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554363918	chr1:77104920-77104921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186294382	chr1:77104943-77104944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575540473	chr1:77104958-77104959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542535744	chr1:77104965-77104966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554782088	chr1:77104969-77104970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572967090	chr1:77105017-77105018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569521314	chr1:77105020-77105021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368599266	chr1:77105021-77105022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78773155	chr1:77105023-77105024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190726196	chr1:77105046-77105047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576972564	chr1:77105155-77105156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs72680019	chr1:77105191-77105192	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs562467240	chr1:77105202-77105203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536828322	chr1:77105254-77105255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557247929	chr1:77105268-77105269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530455639	chr1:77105316-77105317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181665691	chr1:77105386-77105387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35591108	chr1:77105395-77105396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370456791	chr1:77105457-77105458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186497018	chr1:77105485-77105486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560806144	chr1:77105547-77105548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577057787	chr1:77105579-77105580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527880984	chr1:77105611-77105612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552310726	chr1:77105618-77105619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146065681	chr1:77105637-77105638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374289900	chr1:77105695-77105696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139999918	chr1:77105696-77105697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549790517	chr1:77105752-77105753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569905574	chr1:77105778-77105779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35866038	chr1:77105815-77105816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111901195	chr1:77105821-77105822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs687569	chr1:77105841-77105842	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs143910336	chr1:77105874-77105875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191338563	chr1:77105901-77105902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555850925	chr1:77105953-77105954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111518680	chr1:77105967-77105968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573380619	chr1:77106070-77106071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533986876	chr1:77106076-77106077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566049172	chr1:77106079-77106080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542317532	chr1:77106146-77106147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114603188	chr1:77106156-77106157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139729632	chr1:77106177-77106178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564853	chr1:77106202-77106203	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs601818	chr1:77106223-77106224	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs562540084	chr1:77106225-77106226	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77098600-77106200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:77102000-77105600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr1:77105600-77106400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr1:77105800-77106200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:77106200-77106800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:77107800-77108200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr1:77119200-77119600	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr1:77123000-77123400	Enhancers	Fetal Intestine Small	intestine
9	chr1:77123200-77123800	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr1:77126600-77127200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr1:77131800-77132600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:77131800-77132600	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr1:77131800-77133000	Enhancers	Liver	Liver
14	chr1:77132200-77132600	Enhancers	Fetal Intestine Large	intestine
15	chr1:77132200-77132600	Enhancers	Fetal Muscle Leg	muscle
16	chr1:77132200-77132600	Enhancers	Stomach Mucosa	stomach
17	chr1:77132200-77133200	Enhancers	Psoas Muscle	Psoas
18	chr1:77132400-77132600	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr1:77132400-77132600	Enhancers	Aorta	Aorta
20	chr1:77132400-77132600	Enhancers	Brain Germinal Matrix	brain
21	chr1:77132400-77132600	Enhancers	Gastric	stomach
22	chr1:77132400-77133200	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr1:77132400-77133800	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr1:77132600-77133600	Weak transcription	Stomach Mucosa	stomach
25	chr1:77132600-77137200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:77132600-77138800	Weak transcription	Fetal Intestine Large	intestine
27	chr1:77132800-77134600	Weak transcription	Brain Germinal Matrix	brain
28	chr1:77133000-77133400	Active TSS	Liver	Liver
29	chr1:77133000-77134200	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr1:77133400-77134400	Weak transcription	Liver	Liver
31	chr1:77133400-77136200	Enhancers	Fetal Brain Male	brain
32	chr1:77133600-77133800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr1:77133600-77133800	Enhancers	Aorta	Aorta
34	chr1:77133600-77133800	Enhancers	Fetal Lung	lung
35	chr1:77133600-77133800	Enhancers	Stomach Mucosa	stomach
36	chr1:77133600-77134000	Enhancers	Fetal Kidney	kidney
37	chr1:77133600-77134000	Active TSS	HUVEC	blood vessel
38	chr1:77133600-77135200	Enhancers	Fetal Intestine Small	intestine
39	chr1:77133800-77134400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:77134000-77134400	Weak transcription	Aorta	Aorta
41	chr1:77134200-77136200	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr1:77134400-77135200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:77134400-77135200	Enhancers	Liver	Liver
44	chr1:77134600-77136200	Enhancers	Brain Germinal Matrix	brain
45	chr1:77134800-77135000	Enhancers	Aorta	Aorta
46	chr1:77135000-77136200	Enhancers	Fetal Brain Female	brain
47	chr1:77135200-77137600	Weak transcription	Liver	Liver
48	chr1:77135200-77138800	Weak transcription	Fetal Intestine Small	intestine
49	chr1:77136200-77139400	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr1:77136200-77140600	Weak transcription	Fetal Brain Female	brain

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