Variant report

Variant	esv1850497
Chromosome Location	chr1:78596312-78645701
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	chr1:78596459-78596769	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:78609381-78609670	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:78596442-78596745	K562	blood:	n/a	n/a
4	BRCA1	chr1:78596634-78596748	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr1:78596678-78596683	GM12878	blood:	n/a	n/a
6	BRCA1	chr1:78610806-78611063	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr1:78637506-78638212	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:78622961-78623232	K562	blood:	n/a	chr1:78623063-78623074
9	CEBPB	chr1:78610741-78611013	K562	blood:	n/a	n/a
10	CEBPB	chr1:78616525-78616776	IMR90	lung:	n/a	chr1:78616636-78616647
11	CEBPB	chr1:78622879-78623080	A549	lung:	n/a	chr1:78623063-78623074 chr1:78622943-78622954
12	CEBPB	chr1:78622805-78623314	IMR90	lung:	n/a	chr1:78623063-78623074 chr1:78622943-78622954
13	CEBPB	chr1:78623033-78623206	H1-hESC	embryonic stem cell:	n/a	chr1:78623063-78623074
14	CEBPB	chr1:78636467-78636728	HepG2	liver:	n/a	chr1:78636592-78636603
15	CEBPB	chr1:78616517-78616790	HepG2	liver:	n/a	chr1:78616636-78616647
16	CEBPB	chr1:78622853-78623221	HepG2	liver:	n/a	chr1:78623063-78623074 chr1:78622943-78622954
17	CEBPB	chr1:78622817-78623280	HCT-116	colon:	n/a	chr1:78623063-78623074 chr1:78622943-78622954
18	CEBPB	chr1:78610798-78611030	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:78616527-78616777	A549	lung:	n/a	chr1:78616636-78616647
20	CEBPB	chr1:78622703-78623316	Hela-S3	cervix:	n/a	chr1:78623063-78623074 chr1:78622943-78622954
21	CEBPB	chr1:78610797-78611039	HepG2	liver:	n/a	n/a
22	CHD1	chr1:78610647-78611847	IMR90	lung:	n/a	n/a
23	CHD2	chr1:78610790-78611041	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr1:78608959-78608977	GM12891	blood:	n/a	n/a
25	CTCF	chr1:78610760-78610910	HAc	cerebellar:	n/a	n/a
26	CTCF	chr1:78596516-78596740	H1-hESC	embryonic stem cell:	n/a	chr1:78596631-78596652 chr1:78596629-78596647
27	CTCF	chr1:78610860-78611010	HVMF	connective:	n/a	chr1:78610911-78610927 chr1:78610910-78610928 chr1:78610912-78610933
28	CTCF	chr1:78631820-78631970	NHEK	skin:	n/a	n/a
29	CTCF	chr1:78596540-78596690	AG09319	gingival:	n/a	chr1:78596631-78596652 chr1:78596629-78596647
30	CTCF	chr1:78608800-78608950	GM12872	blood:	n/a	n/a
31	CTCF	chr1:78596500-78596650	HFF-Myc	foreskin:	n/a	chr1:78596629-78596647
32	CTCF	chr1:78610860-78611010	AG04450	lung:	n/a	chr1:78610911-78610927 chr1:78610910-78610928 chr1:78610912-78610933
33	CTCF	chr1:78596580-78596730	GM12868	blood:	n/a	chr1:78596631-78596652 chr1:78596629-78596647
34	CTCF	chr1:78610768-78611076	HepG2	liver:	n/a	chr1:78610911-78610927 chr1:78610910-78610928 chr1:78610912-78610933
35	CTCF	chr1:78596493-78596764	HUVEC	blood vessel:	n/a	chr1:78596631-78596652 chr1:78596629-78596647
36	CTCF	chr1:78596560-78596710	BE2_C	brain:	n/a	chr1:78596631-78596652 chr1:78596629-78596647
37	CTCF	chr1:78596540-78596690	HMEC	breast:	n/a	chr1:78596631-78596652 chr1:78596629-78596647
38	CTCF	chr1:78610840-78610990	A549	lung:	n/a	chr1:78610911-78610927 chr1:78610910-78610928 chr1:78610912-78610933
39	CTCF	chr1:78596500-78596650	GM06990	blood:	n/a	chr1:78596629-78596647
40	CTCF	chr1:78596438-78596834	GM12878	blood:	n/a	chr1:78596631-78596652 chr1:78596629-78596647
41	CTCF	chr1:78610860-78611010	GM12874	blood:	n/a	chr1:78610911-78610927 chr1:78610910-78610928 chr1:78610912-78610933
42	CTCF	chr1:78610860-78611010	AG10803	skin:	n/a	chr1:78610911-78610927 chr1:78610910-78610928 chr1:78610912-78610933
43	CTCF	chr1:78610860-78611010	HCT-116	colon:	n/a	chr1:78610911-78610927 chr1:78610910-78610928 chr1:78610912-78610933
44	CTCF	chr1:78610880-78611030	HVMF	connective:	n/a	chr1:78610911-78610927 chr1:78610910-78610928 chr1:78610912-78610933
45	CTCF	chr1:78608700-78608850	GM12873	blood:	n/a	chr1:78608785-78608794
46	CTCF	chr1:78596500-78596650	NHEK	skin:	n/a	chr1:78596629-78596647
47	CTCF	chr1:78596600-78596750	HepG2	liver:	n/a	chr1:78596631-78596652 chr1:78596629-78596647
48	CTCF	chr1:78610772-78611054	K562	blood:	n/a	chr1:78610911-78610927 chr1:78610910-78610928 chr1:78610912-78610933
49	CTCF	chr1:78596560-78596710	GM06990	blood:	n/a	chr1:78596631-78596652 chr1:78596629-78596647
50	CTCF	chr1:78596500-78596650	Caco-2	colon:	n/a	chr1:78596629-78596647

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:78621066-78621116	HEEpiC	esophagus:	n/a
2	chr1:78637036-78637086	SK-N-SH	brain:	n/a
3	chr1:78602941-78602991	AoSMC	blood vessel:	n/a
4	chr1:78637036-78637086	PANC-1	pancreas:	n/a
5	chr1:78602941-78602991	SK-N-SH	brain:	n/a
6	chr1:78602941-78602991	BE2_C	brain:	n/a
7	chr1:78621066-78621116	ovcar-3	ovarian:	n/a
8	chr1:78637036-78637086	Hela-S3	cervix:	n/a
9	chr1:78621066-78621116	Hela-S3	cervix:	n/a
10	chr1:78621066-78621116	T-47D	breast:	n/a
11	chr1:78602941-78602991	HCF	heart:	n/a
12	chr1:78602941-78602991	Hepatocyte	liver:	n/a
13	chr1:78602941-78602991	Caco-2	colon:	n/a
14	chr1:78621066-78621116	HepG2	liver:	n/a
15	chr1:78637036-78637086	SAEC	small airway:	n/a
16	chr1:78621066-78621116	BE2_C	brain:	n/a
17	chr1:78637036-78637086	SK-N-MC	brain:	n/a
18	chr1:78637036-78637086	NHBE	bronchial:	n/a
19	chr1:78621066-78621116	ECC-1	luminal epithelium:	n/a
20	chr1:78637036-78637086	AG09319	gingival:	n/a
21	chr1:78602941-78602991	NHBE	bronchial:	n/a
22	chr1:78621066-78621116	ProgFib	skin:	n/a
23	chr1:78637036-78637086	AG10803	skin:	n/a
24	chr1:78621066-78621116	MCF-7	breast:	n/a
25	chr1:78637036-78637086	T-47D	breast:	n/a
26	chr1:78621066-78621116	CMK	blood:	n/a
27	chr1:78637036-78637086	HMEC	breast:	n/a
28	chr1:78602941-78602991	PANC-1	pancreas:	n/a
29	chr1:78637036-78637086	HIPEpiC	eye:	n/a
30	chr1:78602941-78602991	NB4	blood:	n/a
31	chr1:78602941-78602991	AG09319	gingival:	n/a
32	chr1:78637036-78637086	SK-N-SH_RA	brain:	n/a
33	chr1:78637036-78637086	HCT-116	colon:	n/a
34	chr1:78602941-78602991	SK-N-SH_RA	brain:	n/a
35	chr1:78637036-78637086	H1-hESC	embryonic stem cell:	embryo
36	chr1:78621066-78621116	AG09309	skin:	n/a
37	chr1:78602941-78602991	Hela-S3	cervix:	n/a
38	chr1:78602941-78602991	BJ	skin:	n/a
39	chr1:78621066-78621116	NB4	blood:	n/a
40	chr1:78621066-78621116	HL-60	blood:	n/a
41	chr1:78637036-78637086	NB4	blood:	n/a
42	chr1:78602941-78602991	GM06990	blood:	n/a
43	chr1:78602941-78602991	ECC-1	luminal epithelium:	n/a
44	chr1:78637036-78637086	HNPCEpiC	eye:	n/a
45	chr1:78621066-78621116	NT2-D1	testis:	n/a
46	chr1:78637036-78637086	NHDF-neo	bronchial:	n/a
47	chr1:78637036-78637086	HepG2	liver:	n/a
48	chr1:78621066-78621116	U87	brain:	n/a
49	chr1:78621066-78621116	HCM	heart:	n/a
50	chr1:78602941-78602991	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:78598713..78601395-chr1:78602545..78604596,2	K562	blood:
2	chr1:78595990..78596703-chr1:79072748..79073691,2	MCF-7	breast:
3	chr1:78598713..78601395-chr1:78602545..78604596,2	K562	blood:
4	chr1:78593850..78595901-chr1:78596317..78598534,2	K562	blood:
5	chr1:78610479..78611396-chr1:79072751..79074031,3	MCF-7	breast:
6	chr1:78590091..78592317-chr1:78595079..78598058,2	K562	blood:
7	chr1:78610589..78611378-chr1:79072767..79073322,3	MCF-7	breast:
8	chr1:78594062..78596652-chr1:78598664..78601035,2	K562	blood:
9	chr1:78610377..78611338-chr1:79072756..79073636,3	K562	blood:
10	chr1:78598713..78600693-chr1:78601161..78604045,2	K562	blood:
11	chr1:78605308..78608170-chr1:78609160..78611288,2	MCF-7	breast:
12	chr1:78598713..78600693-chr1:78601161..78604045,2	K562	blood:
13	chr1:78469789..78471628-chr1:78598179..78600096,2	K562	blood:
14	chr1:78589424..78592317-chr1:78594735..78598058,3	K562	blood:
15	chr1:78594062..78596652-chr1:78598664..78601035,2	K562	blood:
16	chr1:78596135..78597095-chr1:79035945..79036466,2	MCF-7	breast:
17	chr1:78605308..78608170-chr1:78609160..78611288,2	MCF-7	breast:
18	chr1:78610308..78611200-chr1:78741448..78742370,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FUBP1-4	chr1:78636165-78636921	NONHSAT004068

Variant related genes	Relation type
RNFT1P2	TF binding region
RNFT1P2	CpG island
ENSG00000162616	chromatin interactions
ENSG00000273338	chromatin interactions

Extended variants
information (count: 1792 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1792 , 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	rs609390	chr1:78596312-78596313	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs599987	chr1:78596328-78596329	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs561402935	chr1:78596342-78596343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190104537	chr1:78596372-78596373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563661825	chr1:78596417-78596418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565562042	chr1:78596425-78596426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565248948	chr1:78596428-78596429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532703596	chr1:78596443-78596444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553302935	chr1:78596452-78596453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551208984	chr1:78596480-78596481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562837482	chr1:78596481-78596482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530269456	chr1:78596496-78596497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548355744	chr1:78596497-78596498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34800531	chr1:78596524-78596525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143000321	chr1:78596567-78596568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533853593	chr1:78596577-78596578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551899322	chr1:78596628-78596629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147472655	chr1:78596631-78596632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148531708	chr1:78596641-78596642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556464019	chr1:78596661-78596662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568348175	chr1:78596666-78596667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200828497	chr1:78596667-78596668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12752029	chr1:78596705-78596706	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs369760994	chr1:78596709-78596710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192511456	chr1:78596737-78596738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200092430	chr1:78596826-78596827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201043605	chr1:78596830-78596831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143150594	chr1:78596831-78596832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548565769	chr1:78596834-78596835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191259739	chr1:78596842-78596843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540682815	chr1:78596847-78596848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558682994	chr1:78596877-78596878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577214741	chr1:78596930-78596931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576316450	chr1:78596985-78596986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112859168	chr1:78596997-78596998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562875197	chr1:78597086-78597087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1299237	chr1:78597091-78597092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530306090	chr1:78597130-78597131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542037176	chr1:78597164-78597165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544861370	chr1:78597284-78597285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560276624	chr1:78597447-78597448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185083178	chr1:78597448-78597449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552299432	chr1:78597502-78597503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs593652	chr1:78597512-78597513	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs577153436	chr1:78597530-78597531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572421107	chr1:78597560-78597561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541540984	chr1:78597565-78597566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531374294	chr1:78597585-78597586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200250581	chr1:78597623-78597624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74407585	chr1:78597625-78597626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Ewing''s sarcoma	17952124	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
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78555400-78608600	Weak transcription	Pancreas	Pancrea
2	chr1:78567600-78607200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr1:78580200-78598000	Weak transcription	Aorta	Aorta
4	chr1:78580200-78608600	Weak transcription	HepG2	liver
5	chr1:78584200-78630600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr1:78584400-78597200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:78586400-78608600	Weak transcription	Colonic Mucosa	Colon
8	chr1:78587400-78607200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr1:78588200-78597600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:78594400-78598600	Weak transcription	Duodenum Mucosa	Duodenum
11	chr1:78594600-78600000	Weak transcription	Fetal Intestine Small	intestine
12	chr1:78594600-78600400	Weak transcription	Fetal Intestine Large	intestine
13	chr1:78594600-78604600	Weak transcription	Liver	Liver
14	chr1:78597600-78597800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:78598000-78598200	Enhancers	Aorta	Aorta
16	chr1:78598600-78600000	Strong transcription	Duodenum Mucosa	Duodenum
17	chr1:78600000-78601000	Strong transcription	Fetal Intestine Small	intestine
18	chr1:78600000-78607200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr1:78600400-78601600	Strong transcription	Fetal Intestine Large	intestine
20	chr1:78601000-78606200	Weak transcription	Fetal Intestine Small	intestine
21	chr1:78601600-78607200	Weak transcription	Fetal Intestine Large	intestine
22	chr1:78601800-78603000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:78601800-78603400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:78602200-78602800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:78603000-78608400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr1:78603200-78609000	Weak transcription	Fetal Stomach	stomach
27	chr1:78603400-78608400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:78604600-78605200	Enhancers	Liver	Liver
29	chr1:78605200-78605600	Weak transcription	Liver	Liver
30	chr1:78605600-78607400	Enhancers	Liver	Liver
31	chr1:78606200-78608000	Enhancers	Fetal Intestine Small	intestine
32	chr1:78607200-78607400	Enhancers	GM12878-XiMat	blood
33	chr1:78607200-78607800	Active TSS	Rectal Mucosa Donor 29	rectum
34	chr1:78607200-78608000	Enhancers	Duodenum Mucosa	Duodenum
35	chr1:78607200-78609600	Enhancers	Fetal Intestine Large	intestine
36	chr1:78607200-78609600	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr1:78607200-78609800	Enhancers	Small Intestine	intestine
38	chr1:78607400-78608000	Flanking Active TSS	Liver	Liver
39	chr1:78607400-78608000	Flanking Active TSS	GM12878-XiMat	blood
40	chr1:78607600-78608000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr1:78607600-78608600	Enhancers	Primary B cells from peripheral blood	blood
42	chr1:78607600-78608600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr1:78607600-78609200	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr1:78607800-78608600	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr1:78608000-78608400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr1:78608000-78608400	Weak transcription	Duodenum Mucosa	Duodenum
47	chr1:78608000-78608400	Weak transcription	Fetal Intestine Small	intestine
48	chr1:78608000-78608400	Enhancers	GM12878-XiMat	blood
49	chr1:78608000-78608600	Active TSS	Liver	Liver
50	chr1:78608400-78608600	Enhancers	Primary B cells from cord blood	blood

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