Variant report

Variant	nsv830226
Chromosome Location	chr1:73950139-74125303
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:294)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:294 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:74038887-74039318	GM12878	blood:	n/a	n/a
2	BACH1	chr1:74049699-74049801	K562	blood:	n/a	n/a
3	BATF	chr1:74039056-74039372	GM12878	blood:	n/a	n/a
4	BATF	chr1:74039079-74039364	GM12878	blood:	n/a	n/a
5	CCNT2	chr1:73979521-73979667	K562	blood:	n/a	n/a
6	CEBPB	chr1:73964652-73964675	K562	blood:	n/a	n/a
7	CEBPB	chr1:74018019-74018219	IMR90	lung:	n/a	chr1:74018057-74018068
8	CEBPB	chr1:74069924-74070190	HepG2	liver:	n/a	chr1:74070041-74070052 chr1:74070083-74070094
9	CEBPB	chr1:73979116-73979322	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:74084978-74085201	HepG2	liver:	n/a	chr1:74085043-74085054
11	CEBPB	chr1:74063684-74063854	A549	lung:	n/a	chr1:74063764-74063775
12	CEBPB	chr1:74017984-74018203	HepG2	liver:	n/a	chr1:74018057-74018068
13	CEBPB	chr1:74037672-74037929	HepG2	liver:	n/a	chr1:74037774-74037785
14	CEBPB	chr1:74119436-74119658	HepG2	liver:	n/a	chr1:74119539-74119548
15	CEBPB	chr1:73986843-73987368	HepG2	liver:	n/a	chr1:73986939-73986950
16	CEBPB	chr1:74063622-74063888	HepG2	liver:	n/a	chr1:74063764-74063775
17	CEBPB	chr1:74037640-74037932	A549	lung:	n/a	chr1:74037774-74037785
18	CHD2	chr1:74073025-74073235	HepG2	liver:	n/a	n/a
19	CTCF	chr1:73989937-73989991	ProgFib	skin:	n/a	n/a
20	CTCF	chr1:74093540-74093690	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr1:74100820-74100970	SAEC	small airway:	n/a	n/a
22	CTCF	chr1:74054091-74054127	Fibrobl	skin:	n/a	n/a
23	CTCF	chr1:73992920-73993070	HAc	cerebellar:	n/a	n/a
24	CTCF	chr1:74100788-74101007	NHEK	skin:	n/a	n/a
25	CTCF	chr1:74100962-74100970	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr1:74006031-74006105	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr1:74093600-74093750	RPTEC	kidney:	n/a	n/a
28	CTCF	chr1:74093504-74093746	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr1:74007250-74007288	GM13976	blood:	n/a	n/a
30	CTCF	chr1:74100808-74100993	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr1:74100760-74100910	HMEC	breast:	n/a	n/a
32	CTCF	chr1:74100726-74101069	GM12878	blood:	n/a	n/a
33	CTCF	chr1:74093540-74093690	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr1:74100648-74100996	MCF-7	breast:	n/a	n/a
35	CTCF	chr1:74100960-74101110	GM12865	blood:	n/a	n/a
36	CTCF	chr1:74100809-74100989	LNCaP	prostate:	n/a	n/a
37	CTCF	chr1:74100880-74101030	Caco-2	colon:	n/a	n/a
38	CTCF	chr1:74100800-74100950	RPTEC	kidney:	n/a	n/a
39	CTCF	chr1:74093520-74093670	HAc	cerebellar:	n/a	n/a
40	CTCF	chr1:74095356-74095404	GM13976	blood:	n/a	n/a
41	CTCF	chr1:74100873-74100958	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr1:74093549-74093702	GM13977	blood:	n/a	n/a
43	CTCF	chr1:74093462-74093780	GM12878	blood:	n/a	n/a
44	CTCF	chr1:74100883-74100915	GM10248	blood:	n/a	n/a
45	CTCF	chr1:74084825-74084885	Fibrobl	skin:	n/a	n/a
46	CTCF	chr1:74065716-74065763	HepG2	liver:	n/a	n/a
47	CTCF	chr1:74100808-74100998	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr1:74093589-74093709	Medullo	brain:	n/a	n/a
49	CTCF	chr1:74100780-74100930	HRE	kidney:	n/a	n/a
50	CTCF	chr1:74100815-74100991	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74059019-74059069	BE2_C	brain:	n/a
2	chr1:74059019-74059069	NT2-D1	testis:	n/a
3	chr1:74059019-74059069	GM12878	blood:	n/a
4	chr1:74059019-74059069	AG09319	gingival:	n/a
5	chr1:74059019-74059069	NHDF-neo	bronchial:	n/a
6	chr1:74059019-74059069	SK-N-SH_RA	brain:	n/a
7	chr1:74059019-74059069	GM12891	blood:	n/a
8	chr1:74059019-74059069	LNCaP	prostate:	n/a
9	chr1:74059019-74059069	HUVEC	blood vessel:	n/a
10	chr1:74059019-74059069	HCPEpiC	choroid plexus:	n/a
11	chr1:74059019-74059069	SK-N-SH	brain:	n/a
12	chr1:74059019-74059069	ovcar-3	ovarian:	n/a
13	chr1:74059019-74059069	AG04449	skin:	fetal
14	chr1:74059019-74059069	HRCEpiC	kidney:	n/a
15	chr1:74059019-74059069	Caco-2	colon:	n/a
16	chr1:74059019-74059069	Jurkat	blood:	n/a
17	chr1:74059019-74059069	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:74059019-74059069	SKMC	muscle:	n/a
19	chr1:74059019-74059069	HRE	kidney:	n/a
20	chr1:74059019-74059069	HCF	heart:	n/a
21	chr1:74059019-74059069	Hela-S3	cervix:	n/a
22	chr1:74059019-74059069	GM06990	blood:	n/a
23	chr1:74059019-74059069	BJ	skin:	n/a
24	chr1:74059019-74059069	AoSMC	blood vessel:	n/a
25	chr1:74059019-74059069	HCT-116	colon:	n/a
26	chr1:74059019-74059069	GM12892	blood:	n/a
27	chr1:74059019-74059069	HepG2	liver:	n/a
28	chr1:74059019-74059069	AG10803	skin:	n/a
29	chr1:74059019-74059069	SAEC	small airway:	n/a
30	chr1:74059019-74059069	NB4	blood:	n/a
31	chr1:74059019-74059069	ProgFib	skin:	n/a
32	chr1:74059019-74059069	PrEC	prostate:	n/a
33	chr1:74059019-74059069	HAEpiC	amniotic membrane:	n/a
34	chr1:74059019-74059069	HEK293	kidney:	embryo
35	chr1:74059019-74059069	HEEpiC	esophagus:	n/a
36	chr1:74059019-74059069	AG04450	lung:	fetal
37	chr1:74059019-74059069	HMEC	breast:	n/a
38	chr1:74059019-74059069	GM19239	blood:	n/a
39	chr1:74059019-74059069	A549	lung:	n/a
40	chr1:74059019-74059069	AG09309	skin:	n/a
41	chr1:74059019-74059069	IMR90	lung:	fetal
42	chr1:74059019-74059069	U87	brain:	n/a
43	chr1:74059019-74059069	CMK	blood:	n/a
44	chr1:74059019-74059069	MCF-7	breast:	n/a
45	chr1:74059019-74059069	PFSK-1	brain:	n/a
46	chr1:74059019-74059069	NH-A	brain:	n/a
47	chr1:74059019-74059069	MCF10A-Er-Src	breast:	n/a
48	chr1:74059019-74059069	H1-hESC	embryonic stem cell:	embryo
49	chr1:74059019-74059069	T-47D	breast:	n/a
50	chr1:74059019-74059069	HRPEpiC	eye:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:74107568..74110277-chr1:74120867..74122777,2	K562	blood:
2	chr1:74039840..74042073-chr1:74070289..74072234,2	K562	blood:
3	chr1:74039840..74042073-chr1:74070289..74072234,2	K562	blood:
4	chr1:74055680..74057811-chr1:74058708..74060253,2	K562	blood:
5	chr1:74107568..74110277-chr1:74120867..74122777,2	K562	blood:
6	chr1:74055680..74057811-chr1:74058708..74060253,2	K562	blood:
7	chr1:74098550..74101436-chr1:74121744..74123511,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FPGT-8	chr1:73953224-73953485	NONHSAT003948
2	lnc-FPGT-2	chr1:74100899-74100924	ENSG00000223479

No data

Variant related genes	Relation type
ENSG00000223479	TF binding region
ENSG00000223479	CpG island
ENSG00000223479	chromatin interactions

Extended variants
information (count: 1959 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1959 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554087510	chr1:73953226-73953227	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs572632985	chr1:73953246-73953247	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs546154952	chr1:73953270-73953271	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs559623415	chr1:73953340-73953341	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs6673962	chr1:73953361-73953362	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs564815678	chr1:73953394-73953395	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs532133100	chr1:73953395-73953396	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs544238218	chr1:73953417-73953418	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs562523606	chr1:73953447-73953448	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs529838641	chr1:73953473-73953474	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs561649454	chr1:73957206-73957207	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs138543985	chr1:73957231-73957232	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs186975180	chr1:73957245-73957246	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs550898175	chr1:73957268-73957269	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs377690454	chr1:73957288-73957289	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs149277629	chr1:73957303-73957304	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs536695035	chr1:73957304-73957305	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs115626076	chr1:73957310-73957311	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs567260799	chr1:73957391-73957392	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs185582776	chr1:73965425-73965426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143398303	chr1:73965451-73965452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571584551	chr1:73965486-73965487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538987181	chr1:73965495-73965496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557061372	chr1:73965500-73965501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575620088	chr1:73965512-73965513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542750938	chr1:73965544-73965545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555084911	chr1:73965567-73965568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112281115	chr1:73965581-73965582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573060380	chr1:73965596-73965597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112042504	chr1:73965656-73965657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78797601	chr1:73965702-73965703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532681690	chr1:73965743-73965744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148195813	chr1:73965775-73965776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141298720	chr1:73965824-73965825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531022236	chr1:73965858-73965859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558692211	chr1:73965865-73965866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530577214	chr1:73965866-73965867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10789373	chr1:73965869-73965870	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs35363533	chr1:73965870-73965871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34861613	chr1:73965910-73965911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115968267	chr1:73965938-73965939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112029153	chr1:73965948-73965949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546829809	chr1:73965995-73965996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12124740	chr1:73966076-73966077	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs191234790	chr1:73966086-73966087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17094002	chr1:73966109-73966110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569146858	chr1:73966114-73966115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139141154	chr1:73966124-73966125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554596923	chr1:73966188-73966189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112815938	chr1:73966233-73966234	Enhancers	n/a	n/a	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
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:73957200-73957400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr1:73965400-73966000	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr1:73965600-73966400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr1:73965800-73966200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr1:73976400-73977400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:73976400-73978400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:73976600-73977000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr1:73981200-73982200	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr1:73981600-73981800	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr1:73981800-73982400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr1:73982000-73982200	Enhancers	Brain Germinal Matrix	brain
12	chr1:73982200-73987000	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr1:73982400-73983000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr1:73982400-73983400	Weak transcription	Brain Germinal Matrix	brain
15	chr1:73983000-73984400	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr1:73983000-73987000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr1:73983400-73983600	Enhancers	Fetal Brain Female	brain
18	chr1:73983400-73983800	Enhancers	Fetal Brain Male	brain
19	chr1:73983400-73984000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr1:73983400-73984000	Enhancers	Brain Germinal Matrix	brain
21	chr1:73986800-73987200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:73987000-73987400	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr1:73987000-73987600	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr1:73992400-73992600	Enhancers	Pancreas	Pancrea
25	chr1:73992400-73993000	Active TSS	Brain Substantia Nigra	brain
26	chr1:73993200-73993600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr1:74002800-74003400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr1:74002800-74003400	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr1:74003200-74003400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr1:74008600-74010000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr1:74008800-74009400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr1:74008800-74009600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:74009000-74009600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr1:74009000-74009800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:74009600-74010600	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr1:74010600-74010800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr1:74015400-74016000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr1:74024600-74025200	Enhancers	Stomach Mucosa	stomach
39	chr1:74027000-74027200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
40	chr1:74027200-74027600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr1:74027200-74029000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr1:74029800-74030400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr1:74029800-74030400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr1:74029800-74030800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr1:74030000-74030600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:74030000-74030800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:74030000-74031000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr1:74030200-74030800	Enhancers	H9 Cell Line	embryonic stem cell
49	chr1:74038800-74039000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr1:74039000-74039400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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