Variant report

Variant	nsv523474
Chromosome Location	chr1:74699099-74794119
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:215)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:215 , 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	ATF2	chr1:74710842-74711284	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr1:74710792-74711328	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:74721725-74721860	K562	blood:	n/a	n/a
4	BACH1	chr1:74721367-74721402	K562	blood:	n/a	n/a
5	BCL11A	chr1:74710899-74711179	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr1:74710883-74711156	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr1:74746472-74746612	K562	blood:	n/a	n/a
8	CEBPB	chr1:74780146-74780463	IMR90	lung:	n/a	n/a
9	CEBPB	chr1:74729369-74729404	H1-hESC	embryonic stem cell:	n/a	chr1:74729392-74729403
10	CEBPB	chr1:74777395-74777659	HepG2	liver:	n/a	chr1:74777540-74777553 chr1:74777541-74777552
11	CEBPB	chr1:74714756-74714989	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:74768320-74768669	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:74783464-74783590	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:74764987-74765324	HepG2	liver:	n/a	chr1:74765155-74765166 chr1:74765142-74765150
15	CEBPB	chr1:74771504-74771688	HepG2	liver:	n/a	chr1:74771612-74771623
16	CEBPB	chr1:74783362-74783693	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:74710897-74711276	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr1:74780245-74780491	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:74728463-74728579	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:74764993-74765325	A549	lung:	n/a	chr1:74765155-74765166 chr1:74765142-74765150
21	CEBPZ	chr1:74790846-74791124	HepG2	liver:	n/a	n/a
22	CTCF	chr1:74779180-74779330	HAc	cerebellar:	n/a	n/a
23	CTCF	chr1:74737355-74737403	HepG2	liver:	n/a	n/a
24	CTCF	chr1:74724669-74724758	K562	blood:	n/a	n/a
25	CTCF	chr1:74737280-74737430	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr1:74737260-74737410	HEK293	kidney:	n/a	n/a
27	CTCF	chr1:74737340-74737490	HepG2	liver:	n/a	n/a
28	CTCF	chr1:74737378-74737427	LNCaP	prostate:	n/a	n/a
29	CTCF	chr1:74737140-74737290	HCT-116	colon:	n/a	n/a
30	CTCF	chr1:74761842-74761913	Fibrobl	skin:	n/a	n/a
31	CTCF	chr1:74737347-74737405	GM19239	blood:	n/a	n/a
32	CTCF	chr1:74737300-74737450	HRE	kidney:	n/a	n/a
33	CTCF	chr1:74737280-74737430	HepG2	liver:	n/a	n/a
34	CTCF	chr1:74737320-74737470	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr1:74737320-74737470	GM12864	blood:	n/a	n/a
36	CTCF	chr1:74737400-74737550	HMEC	breast:	n/a	n/a
37	CTCF	chr1:74737280-74737430	GM12873	blood:	n/a	n/a
38	CTCF	chr1:74737346-74737388	GM12892	blood:	n/a	n/a
39	CTCF	chr1:74737355-74737375	GM20000	blood:	n/a	n/a
40	CTCF	chr1:74790800-74790950	HepG2	liver:	n/a	n/a
41	CTCF	chr1:74737240-74737390	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr1:74737315-74737416	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr1:74737293-74737455	LNCaP	prostate:	n/a	n/a
44	E2F4	chr1:74791612-74791689	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr1:74701224-74701434	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr1:74759287-74759597	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr1:74776700-74776900	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F6	chr1:74781759-74782401	H1-hESC	embryonic stem cell:	n/a	n/a
49	E2F6	chr1:74782034-74782339	H1-hESC	embryonic stem cell:	n/a	n/a
50	EBF1	chr1:74762695-74763155	GM12878	blood:	n/a	chr1:74763014-74763025

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74719316-74719366	BJ	skin:	n/a
2	chr1:74719316-74719366	IMR90	lung:	fetal
3	chr1:74719316-74719366	AG10803	skin:	n/a
4	chr1:74719316-74719366	HAEpiC	amniotic membrane:	n/a
5	chr1:74719316-74719366	Caco-2	colon:	n/a
6	chr1:74719316-74719366	HEK293	kidney:	embryo
7	chr1:74719316-74719366	MCF-7	breast:	n/a
8	chr1:74719316-74719366	Jurkat	blood:	n/a
9	chr1:74719316-74719366	GM06990	blood:	n/a
10	chr1:74719316-74719366	HCPEpiC	choroid plexus:	n/a
11	chr1:74719316-74719366	NT2-D1	testis:	n/a
12	chr1:74719316-74719366	AoSMC	blood vessel:	n/a
13	chr1:74719316-74719366	NHDF-neo	bronchial:	n/a
14	chr1:74719316-74719366	HRPEpiC	eye:	n/a
15	chr1:74719316-74719366	PFSK-1	brain:	n/a
16	chr1:74719316-74719366	NH-A	brain:	n/a
17	chr1:74719316-74719366	H1-hESC	embryonic stem cell:	embryo
18	chr1:74719316-74719366	HepG2	liver:	n/a
19	chr1:74719316-74719366	AG04450	lung:	fetal
20	chr1:74719316-74719366	SK-N-SH_RA	brain:	n/a
21	chr1:74719316-74719366	Hepatocyte	liver:	n/a
22	chr1:74719316-74719366	NB4	blood:	n/a
23	chr1:74719316-74719366	SAEC	small airway:	n/a
24	chr1:74719316-74719366	GM12892	blood:	n/a
25	chr1:74719316-74719366	ProgFib	skin:	n/a
26	chr1:74719316-74719366	HUVEC	blood vessel:	n/a
27	chr1:74719316-74719366	AG04449	skin:	fetal
28	chr1:74719316-74719366	SKMC	muscle:	n/a
29	chr1:74719316-74719366	HL-60	blood:	n/a
30	chr1:74719316-74719366	K562	blood:	n/a
31	chr1:74719316-74719366	SK-N-MC	brain:	n/a
32	chr1:74719316-74719366	A549	lung:	n/a
33	chr1:74719316-74719366	HCT-116	colon:	n/a
34	chr1:74719316-74719366	PrEC	prostate:	n/a
35	chr1:74719316-74719366	HNPCEpiC	eye:	n/a
36	chr1:74719316-74719366	SK-N-SH	brain:	n/a
37	chr1:74719316-74719366	U87	brain:	n/a
38	chr1:74719316-74719366	Hela-S3	cervix:	n/a
39	chr1:74719316-74719366	NHBE	bronchial:	n/a
40	chr1:74719316-74719366	HIPEpiC	eye:	n/a
41	chr1:74719316-74719366	HMEC	breast:	n/a
42	chr1:74719316-74719366	ECC-1	luminal epithelium:	n/a
43	chr1:74719316-74719366	ovcar-3	ovarian:	n/a
44	chr1:74719316-74719366	MCF10A-Er-Src	breast:	n/a
45	chr1:74719316-74719366	GM19239	blood:	n/a
46	chr1:74719316-74719366	GM12891	blood:	n/a
47	chr1:74719316-74719366	LNCaP	prostate:	n/a
48	chr1:74719316-74719366	HCM	heart:	n/a
49	chr1:74719316-74719366	BE2_C	brain:	n/a
50	chr1:74719316-74719366	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:74622416..74625063-chr1:74764779..74767346,2	K562	blood:
2	chr1:74692052..74694076-chr1:74701127..74702957,2	K562	blood:
3	chr1:74701198..74703916-chr1:74780316..74782785,2	K562	blood:
4	chr1:74701198..74703916-chr1:74780316..74782785,2	K562	blood:
5	chr1:74725032..74727117-chr1:74729630..74732086,2	K562	blood:
6	chr1:74725032..74727117-chr1:74729630..74732086,2	K562	blood:
7	chr1:74789903..74792042-chr1:74796412..74799113,2	MCF-7	breast:
8	chr1:74725032..74727513-chr1:74728453..74731130,2	K562	blood:
9	chr1:74725032..74727513-chr1:74728453..74731130,2	K562	blood:

No data

Variant related genes	Relation type
TNNI3K	TF binding region
TNNI3K	CpG island

Extended variants
information (count: 3505 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:3505 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3753183	chr1:74699099-74699100	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374987001	chr1:74699102-74699103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549513908	chr1:74699110-74699111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562064686	chr1:74699130-74699131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529034061	chr1:74699160-74699161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367642576	chr1:74699209-74699210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182263962	chr1:74699271-74699272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539569214	chr1:74699273-74699274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145242401	chr1:74699297-74699298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187232654	chr1:74699307-74699308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201589568	chr1:74699318-74699319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs492302	chr1:74699331-74699332	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs547391681	chr1:74699351-74699352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376213333	chr1:74699388-74699389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576134558	chr1:74699495-74699496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147680719	chr1:74699522-74699523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191766055	chr1:74699536-74699537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565913897	chr1:74699591-74699592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs45613243	chr1:74699642-74699643	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs553618333	chr1:74699648-74699649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572140904	chr1:74699650-74699651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557894756	chr1:74699728-74699729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs578001487	chr1:74699743-74699744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181830130	chr1:74699749-74699750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557878352	chr1:74699756-74699757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575947539	chr1:74699758-74699759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543435190	chr1:74699834-74699835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs80216689	chr1:74699849-74699850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529167525	chr1:74699855-74699856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540801391	chr1:74699859-74699860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559125960	chr1:74699910-74699911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs518769	chr1:74699912-74699913	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs144582312	chr1:74699919-74699920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs3753186	chr1:74699923-74699924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530788471	chr1:74700024-74700025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34049093	chr1:74700046-74700047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs45511100	chr1:74700070-74700071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534542593	chr1:74700083-74700084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs45565731	chr1:74700102-74700103	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs567826663	chr1:74700113-74700114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535359385	chr1:74700170-74700171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190275048	chr1:74700177-74700178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549676352	chr1:74700230-74700231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116060702	chr1:74700233-74700234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539288514	chr1:74700236-74700237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542041646	chr1:74700240-74700241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs474215	chr1:74700251-74700252	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs376309868	chr1:74700262-74700263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs149001203	chr1:74700279-74700280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs17527164	chr1:74700284-74700285	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74671400-74719400	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr1:74671400-74751800	Weak transcription	Ovary	ovary
3	chr1:74675800-74724000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr1:74697800-74710600	Weak transcription	Psoas Muscle	Psoas
5	chr1:74699000-74700800	Enhancers	Fetal Heart	heart
6	chr1:74699200-74699600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:74700600-74713800	Weak transcription	Adipose Nuclei	Adipose
8	chr1:74700800-74701000	Flanking Active TSS	Fetal Heart	heart
9	chr1:74701000-74703400	Active TSS	Fetal Heart	heart
10	chr1:74701600-74704200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr1:74701600-74704200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr1:74701800-74705000	Active TSS	Right Atrium	heart
13	chr1:74702000-74702400	Active TSS	Right Ventricle	heart
14	chr1:74702200-74702600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:74702200-74703800	Active TSS	Left Ventricle	heart
16	chr1:74702400-74703200	Weak transcription	Right Ventricle	heart
17	chr1:74703200-74703800	Active TSS	Right Ventricle	heart
18	chr1:74703400-74703600	Transcr. at gene 5' and 3'	Fetal Heart	heart
19	chr1:74703600-74704200	Flanking Active TSS	Fetal Heart	heart
20	chr1:74703800-74716600	Weak transcription	Left Ventricle	heart
21	chr1:74704200-74704600	Enhancers	Fetal Heart	heart
22	chr1:74704600-74705600	Flanking Active TSS	Fetal Heart	heart
23	chr1:74705600-74706000	Enhancers	Fetal Heart	heart
24	chr1:74706000-74706200	Flanking Active TSS	Fetal Heart	heart
25	chr1:74706200-74708000	Weak transcription	Fetal Heart	heart
26	chr1:74708000-74711000	Enhancers	Fetal Heart	heart
27	chr1:74709200-74709600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:74709600-74710000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:74709800-74710400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:74709800-74710600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr1:74709800-74710600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
32	chr1:74710000-74712200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
33	chr1:74710000-74712400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
34	chr1:74710000-74713000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:74710200-74710400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:74710200-74712200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
37	chr1:74710400-74711000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:74710400-74711400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:74710400-74711800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr1:74710400-74713000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr1:74710600-74710800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
42	chr1:74710600-74711000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
43	chr1:74710800-74711200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
44	chr1:74710800-74711200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr1:74710800-74711600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr1:74710800-74712400	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr1:74710800-74713200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr1:74711000-74711200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
49	chr1:74711000-74711200	Flanking Active TSS	Fetal Heart	heart
50	chr1:74711000-74711200	Enhancers	Right Ventricle	heart

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