Variant report

Variant	esv1847721
Chromosome Location	chr1:76269439-76383565
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	ARID3A	chr1:76320748-76320934	K562	blood:	n/a	n/a
2	ARID3A	chr1:76273737-76273897	K562	blood:	n/a	n/a
3	ARID3A	chr1:76277740-76278046	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:76320652-76320915	HepG2	liver:	n/a	n/a
5	ATF1	chr1:76337837-76338185	K562	blood:	n/a	n/a
6	ATF1	chr1:76320739-76320991	K562	blood:	n/a	n/a
7	BHLHE40	chr1:76320708-76320981	K562	blood:	n/a	n/a
8	CEBPB	chr1:76273130-76273423	IMR90	lung:	n/a	chr1:76273277-76273288 chr1:76273302-76273313
9	CEBPB	chr1:76275339-76275405	A549	lung:	n/a	n/a
10	CEBPB	chr1:76273236-76273361	H1-hESC	embryonic stem cell:	n/a	chr1:76273277-76273288 chr1:76273302-76273313
11	CEBPB	chr1:76320619-76321020	K562	blood:	n/a	chr1:76320818-76320829
12	CEBPB	chr1:76320731-76320940	K562	blood:	n/a	chr1:76320818-76320829
13	CEBPB	chr1:76302317-76302563	IMR90	lung:	n/a	chr1:76302408-76302419
14	CEBPB	chr1:76357194-76357223	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:76320533-76321186	HCT-116	colon:	n/a	chr1:76320818-76320829
16	CEBPB	chr1:76343805-76344014	HepG2	liver:	n/a	chr1:76343874-76343885
17	CEBPB	chr1:76277802-76278090	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:76321460-76321852	K562	blood:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
19	CEBPB	chr1:76321572-76321747	H1-hESC	embryonic stem cell:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
20	CEBPB	chr1:76320689-76320951	HepG2	liver:	n/a	chr1:76320818-76320829
21	CEBPB	chr1:76320619-76321015	K562	blood:	n/a	chr1:76320818-76320829
22	CEBPB	chr1:76302322-76302430	HepG2	liver:	n/a	chr1:76302408-76302419
23	CEBPB	chr1:76343758-76343986	K562	blood:	n/a	chr1:76343874-76343885
24	CEBPB	chr1:76320629-76321005	IMR90	lung:	n/a	chr1:76320818-76320829
25	CEBPB	chr1:76340798-76341108	HepG2	liver:	n/a	chr1:76340931-76340942
26	CEBPB	chr1:76320631-76321012	HepG2	liver:	n/a	chr1:76320818-76320829
27	CEBPB	chr1:76269277-76269540	K562	blood:	n/a	chr1:76269364-76269377 chr1:76269366-76269377 chr1:76269364-76269377 chr1:76269366-76269377 chr1:76269364-76269377
28	CEBPB	chr1:76277845-76278041	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:76320701-76321133	HCT-116	colon:	n/a	chr1:76320818-76320829
30	CEBPB	chr1:76321326-76321765	A549	lung:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
31	CEBPB	chr1:76321244-76321816	IMR90	lung:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
32	CEBPB	chr1:76320633-76321019	HepG2	liver:	n/a	chr1:76320818-76320829
33	CEBPB	chr1:76320673-76320990	HepG2	liver:	n/a	chr1:76320818-76320829
34	CEBPB	chr1:76340779-76341116	IMR90	lung:	n/a	chr1:76340931-76340942
35	CEBPB	chr1:76340847-76341003	K562	blood:	n/a	chr1:76340931-76340942
36	CEBPB	chr1:76273151-76273448	HepG2	liver:	n/a	chr1:76273277-76273288 chr1:76273302-76273313
37	CEBPB	chr1:76340832-76341109	A549	lung:	n/a	chr1:76340931-76340942
38	CEBPB	chr1:76320629-76321043	MCF-7	breast:	n/a	chr1:76320818-76320829
39	CEBPB	chr1:76321321-76321799	HepG2	liver:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
40	CEBPB	chr1:76273177-76273447	Hela-S3	cervix:	n/a	chr1:76273277-76273288 chr1:76273302-76273313
41	CEBPB	chr1:76320641-76321823	Hela-S3	cervix:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76320818-76320829 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
42	CEBPB	chr1:76317452-76317652	K562	blood:	n/a	n/a
43	CEBPB	chr1:76273150-76273442	A549	lung:	n/a	chr1:76273277-76273288 chr1:76273302-76273313
44	CEBPD	chr1:76320743-76320886	HepG2	liver:	n/a	n/a
45	CEBPD	chr1:76320651-76320976	K562	blood:	n/a	n/a
46	CEBPD	chr1:76320728-76321019	K562	blood:	n/a	n/a
47	CEBPD	chr1:76320695-76320891	HepG2	liver:	n/a	n/a
48	CTCF	chr1:76308320-76308470	GM12866	blood:	n/a	n/a
49	CTCF	chr1:76374480-76374630	HFF	foreskin:	n/a	n/a
50	CTCF	chr1:76308300-76308450	AG04449	skin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:76327097..76328864-chr1:76332786..76334905,2	K562	blood:
2	chr1:76383436..76384363-chr16:27389146..27390073,2	MCF-7	breast:
3	chr1:76259303..76263920-chr1:76276444..76279468,6	K562	blood:
4	chr1:76277873..76279387-chr1:76283733..76285650,2	K562	blood:
5	chr1:76349813..76351661-chr1:76356485..76359051,2	K562	blood:
6	chr1:76374124..76374771-chr1:76619576..76620091,2	MCF-7	breast:
7	chr1:76277185..76279387-chr1:76282606..76285233,2	K562	blood:
8	chr1:76327097..76328864-chr1:76332786..76334905,2	K562	blood:
9	chr1:76275487..76277176-chr1:76281868..76284838,2	K562	blood:
10	chr1:76280713..76282619-chr1:76284272..76285904,2	K562	blood:
11	chr1:76332563..76334955-chr1:76337624..76339658,2	K562	blood:
12	chr1:76380506..76383484-chr1:76388793..76390855,2	K562	blood:
13	chr1:76187328..76189918-chr1:76280301..76282636,2	K562	blood:
14	chr1:76277185..76279387-chr1:76282606..76285233,2	K562	blood:
15	chr1:76263795..76266043-chr1:76279563..76282282,3	K562	blood:
16	chr1:76275487..76277176-chr1:76281868..76284838,2	K562	blood:
17	chr1:76262942..76264627-chr1:76319779..76321493,2	K562	blood:
18	chr1:76261350..76264622-chr1:76266576..76269506,4	MCF-7	breast:
19	chr1:76252066..76254293-chr1:76270264..76272290,2	MCF-7	breast:
20	chr1:76256252..76258786-chr1:76340738..76342721,2	K562	blood:
21	chr1:76252079..76256078-chr1:76276265..76280067,4	K562	blood:
22	chr1:76277873..76279387-chr1:76283733..76285650,2	K562	blood:
23	chr1:76280713..76282619-chr1:76284272..76285904,2	K562	blood:
24	chr1:76332563..76334955-chr1:76337624..76339658,2	K562	blood:
25	chr1:76373718..76374271-chr1:76796370..76797302,2	MCF-7	breast:
26	chr1:76349813..76351661-chr1:76356485..76359051,2	K562	blood:
27	chr1:76257881..76260713-chr1:76287046..76289517,2	K562	blood:
28	chr1:76333672..76334172-chr20:20341161..20341713,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RABGGTB-2	chr1:76279964-76280171	NONHSAT004005
2	lnc-RABGGTB-2	chr1:76279983-76280171	l_74_chr1:76279982-76304643_kidney
3	lnc-RABGGTB-2	chr1:76304311-76304643	l_74_chr1:76279982-76304643_kidney
4	lnc-RABGGTB-2	chr1:76304311-76304501	NONHSAT004005

Variant related genes	Relation type
ENSG00000266832	TF binding region
ENSG00000207241	chromatin interactions
ENSG00000137955	chromatin interactions
ENSG00000201487	chromatin interactions
ENSG00000178193	chromatin interactions
ENSG00000057468	chromatin interactions
ENSG00000206620	chromatin interactions

Extended variants
information (count: 2470 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2470 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5745324	chr1:76269439-76269440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs17853143	chr1:76269450-76269451	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs150878521	chr1:76269451-76269452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs5745325	chr1:76269460-76269461	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs140743278	chr1:76269462-76269463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369865402	chr1:76269514-76269515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545551255	chr1:76269522-76269523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572731487	chr1:76269561-76269562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200513557	chr1:76269574-76269575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576543230	chr1:76269616-76269617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552635266	chr1:76269621-76269622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376634545	chr1:76269624-76269625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370839813	chr1:76269645-76269646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139750304	chr1:76269694-76269695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188394022	chr1:76269703-76269704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs193031030	chr1:76269733-76269734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184063878	chr1:76269739-76269740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559277841	chr1:76269770-76269771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539823966	chr1:76269814-76269815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533490770	chr1:76269853-76269854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374492043	chr1:76269862-76269863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551551464	chr1:76269884-76269885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188650466	chr1:76269946-76269947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368850462	chr1:76269999-76270000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs5745326	chr1:76270021-76270022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs5745327	chr1:76270040-76270041	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs34616994	chr1:76270045-76270046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374301299	chr1:76270047-76270048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550146599	chr1:76270061-76270062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191615988	chr1:76270101-76270102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183761345	chr1:76270137-76270138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs5775308	chr1:76270194-76270195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12057365	chr1:76270205-76270206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199793792	chr1:76270206-76270207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200494445	chr1:76270207-76270208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553823832	chr1:76270293-76270294	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs559504112	chr1:76270313-76270314	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs111661299	chr1:76270318-76270319	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs150666458	chr1:76270352-76270353	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs549056239	chr1:76270356-76270357	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs12126956	chr1:76270359-76270360	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs557544092	chr1:76270362-76270363	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs12119259	chr1:76270416-76270417	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs189433699	chr1:76270418-76270419	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs555502177	chr1:76270424-76270425	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs4422958	chr1:76270437-76270438	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs573999820	chr1:76270462-76270463	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs541300567	chr1:76270475-76270476	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs559714627	chr1:76270483-76270484	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs533159041	chr1:76270524-76270525	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
abnormal development	18461090	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76262400-76273200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:76262400-76282800	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr1:76262600-76288800	Weak transcription	Brain Substantia Nigra	brain
4	chr1:76262600-76294600	Weak transcription	Primary B cells from cord blood	blood
5	chr1:76263000-76276600	Weak transcription	Gastric	stomach
6	chr1:76263000-76287400	Weak transcription	Aorta	Aorta
7	chr1:76263000-76289000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:76263000-76296200	Weak transcription	Ovary	ovary
9	chr1:76263200-76277000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr1:76263400-76289000	Weak transcription	Brain Hippocampus Middle	brain
11	chr1:76263600-76284000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr1:76264000-76270600	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr1:76264000-76274200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:76264000-76277000	Weak transcription	HUVEC	blood vessel
15	chr1:76264200-76274800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:76264200-76279800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:76264200-76291400	Weak transcription	Psoas Muscle	Psoas
18	chr1:76264600-76273600	Weak transcription	Primary B cells from peripheral blood	blood
19	chr1:76264600-76278000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:76264600-76288600	Weak transcription	Left Ventricle	heart
21	chr1:76264800-76277000	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr1:76264800-76288600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr1:76264800-76288600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr1:76265600-76270200	Weak transcription	Adipose Nuclei	Adipose
25	chr1:76266000-76272800	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr1:76269400-76269600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:76269400-76269600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:76269400-76269600	Enhancers	NHDF-Ad	bronchial
29	chr1:76272800-76273800	Strong transcription	Skeletal Muscle Female	skeletal muscle
30	chr1:76273800-76276600	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr1:76275000-76275400	Enhancers	Stomach Mucosa	stomach
32	chr1:76275400-76277000	Weak transcription	Stomach Mucosa	stomach
33	chr1:76276600-76276800	Enhancers	Gastric	stomach
34	chr1:76276600-76277400	Strong transcription	Skeletal Muscle Female	skeletal muscle
35	chr1:76277000-76277800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:76277000-76278000	Enhancers	Muscle Satellite Cultured Cells	--
37	chr1:76277000-76278000	Enhancers	Stomach Mucosa	stomach
38	chr1:76277000-76278000	Enhancers	HUVEC	blood vessel
39	chr1:76277200-76277400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr1:76277200-76277600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:76277200-76277600	Enhancers	NH-A	brain
42	chr1:76277200-76278000	Enhancers	Osteobl	bone
43	chr1:76277400-76278200	Enhancers	HepG2	liver
44	chr1:76277400-76278800	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr1:76278800-76279600	Strong transcription	Skeletal Muscle Female	skeletal muscle
46	chr1:76279600-76288600	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr1:76279800-76280000	Active TSS	Sigmoid Colon	Sigmoid Colon
48	chr1:76282200-76295200	Weak transcription	Right Ventricle	heart
49	chr1:76287200-76289000	Weak transcription	Stomach Smooth Muscle	stomach
50	chr1:76287400-76287600	ZNF genes & repeats	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links