Variant report

Variant	nsv1455
Chromosome Location	chr1:75812377-75864182
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:247)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:247 , 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	ARID3A	chr1:75819638-75820397	K562	blood:	n/a	n/a
2	ATF1	chr1:75820019-75820285	K562	blood:	n/a	n/a
3	BACH1	chr1:75860456-75860736	K562	blood:	n/a	chr1:75860631-75860645
4	BHLHE40	chr1:75840049-75840076	K562	blood:	n/a	n/a
5	BHLHE40	chr1:75839714-75839746	K562	blood:	n/a	n/a
6	BHLHE40	chr1:75839104-75839347	K562	blood:	n/a	n/a
7	CBX3	chr1:75832305-75832631	K562	blood:	n/a	n/a
8	CBX3	chr1:75819901-75820405	K562	blood:	n/a	n/a
9	CBX3	chr1:75832317-75832654	K562	blood:	n/a	n/a
10	CCNT2	chr1:75819899-75820649	K562	blood:	n/a	n/a
11	CEBPB	chr1:75812342-75812598	HepG2	liver:	n/a	chr1:75812521-75812532 chr1:75812432-75812443
12	CEBPB	chr1:75824165-75824225	HepG2	liver:	n/a	chr1:75824192-75824203
13	CEBPB	chr1:75820528-75820772	K562	blood:	n/a	chr1:75820647-75820660
14	CEBPB	chr1:75812372-75812604	K562	blood:	n/a	chr1:75812521-75812532 chr1:75812432-75812443
15	CEBPB	chr1:75815230-75815367	HepG2	liver:	n/a	n/a
16	CTCF	chr1:75832560-75832615	K562	blood:	n/a	n/a
17	CTCF	chr1:75844620-75844707	Medullo	brain:	n/a	n/a
18	CTCF	chr1:75844550-75844731	GM10266	blood:	n/a	n/a
19	CTCF	chr1:75844587-75844716	LNCaP	prostate:	n/a	n/a
20	CTCF	chr1:75844680-75844830	HepG2	liver:	n/a	n/a
21	CTCF	chr1:75844625-75844686	GM13977	blood:	n/a	n/a
22	CTCF	chr1:75820217-75820305	K562	blood:	n/a	n/a
23	CTCF	chr1:75844623-75844712	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr1:75844578-75844734	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr1:75844320-75844804	K562	blood:	n/a	n/a
26	CTCF	chr1:75844545-75844645	MCF-7	breast:	n/a	n/a
27	CTCF	chr1:75820339-75820376	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr1:75844543-75844652	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr1:75839960-75839982	ProgFib	skin:	n/a	n/a
30	CTCF	chr1:75821785-75821810	Lung_OC	lung:	n/a	n/a
31	CTCF	chr1:75844464-75844763	K562	blood:	n/a	n/a
32	CTCF	chr1:75844493-75844695	A549	lung:	n/a	n/a
33	CTCF	chr1:75844555-75844763	LNCaP	prostate:	n/a	n/a
34	CTCF	chr1:75844467-75844706	A549	lung:	n/a	n/a
35	CTCF	chr1:75844368-75844732	A549	lung:	n/a	n/a
36	CTCF	chr1:75844618-75844663	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr1:75844605-75844746	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr1:75825174-75825215	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr1:75844617-75844734	GM12878	blood:	n/a	n/a
40	CTCF	chr1:75844450-75844850	K562	blood:	n/a	n/a
41	CTCF	chr1:75844626-75844707	MCF-7	breast:	n/a	n/a
42	E2F4	chr1:75861106-75861641	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr1:75862397-75862626	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F6	chr1:75820189-75820336	K562	blood:	n/a	n/a
45	EGR1	chr1:75819987-75820367	K562	blood:	n/a	n/a
46	EGR1	chr1:75820005-75820349	K562	blood:	n/a	n/a
47	ELF1	chr1:75822743-75823087	K562	blood:	n/a	chr1:75822927-75822940
48	EP300	chr1:75840790-75840906	GM12878	blood:	n/a	n/a
49	EP300	chr1:75860883-75860905	GM12878	blood:	n/a	n/a
50	EP300	chr1:75840946-75841331	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:75841810-75841860	CMK	blood:	n/a
2	chr1:75841810-75841860	NT2-D1	testis:	n/a
3	chr1:75841810-75841860	IMR90	lung:	fetal
4	chr1:75841810-75841860	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:75841810-75841860	AG04449	skin:	fetal
6	chr1:75841810-75841860	SK-N-SH	brain:	n/a
7	chr1:75841810-75841860	HRCEpiC	kidney:	n/a
8	chr1:75841810-75841860	AG09309	skin:	n/a
9	chr1:75841810-75841860	HL-60	blood:	n/a
10	chr1:75841810-75841860	T-47D	breast:	n/a
11	chr1:75841810-75841860	HCM	heart:	n/a
12	chr1:75841810-75841860	SAEC	small airway:	n/a
13	chr1:75841810-75841860	GM12892	blood:	n/a
14	chr1:75841810-75841860	AG04450	lung:	fetal
15	chr1:75841810-75841860	GM12878	blood:	n/a
16	chr1:75841810-75841860	SK-N-SH_RA	brain:	n/a
17	chr1:75841810-75841860	HRE	kidney:	n/a
18	chr1:75841810-75841860	GM19239	blood:	n/a
19	chr1:75841810-75841860	MCF-7	breast:	n/a
20	chr1:75841810-75841860	H1-hESC	embryonic stem cell:	embryo
21	chr1:75841810-75841860	K562	blood:	n/a
22	chr1:75841810-75841860	HAEpiC	amniotic membrane:	n/a
23	chr1:75841810-75841860	HEEpiC	esophagus:	n/a
24	chr1:75841810-75841860	HUVEC	blood vessel:	n/a
25	chr1:75841810-75841860	HMEC	breast:	n/a
26	chr1:75841810-75841860	BJ	skin:	n/a
27	chr1:75841810-75841860	ovcar-3	ovarian:	n/a
28	chr1:75841810-75841860	HepG2	liver:	n/a
29	chr1:75841810-75841860	A549	lung:	n/a
30	chr1:75841810-75841860	NH-A	brain:	n/a
31	chr1:75841810-75841860	HCPEpiC	choroid plexus:	n/a
32	chr1:75841810-75841860	AoSMC	blood vessel:	n/a
33	chr1:75841810-75841860	AG10803	skin:	n/a
34	chr1:75841810-75841860	NHBE	bronchial:	n/a
35	chr1:75841810-75841860	HCT-116	colon:	n/a
36	chr1:75841810-75841860	GM06990	blood:	n/a
37	chr1:75841810-75841860	PFSK-1	brain:	n/a
38	chr1:75841810-75841860	PrEC	prostate:	n/a
39	chr1:75841810-75841860	ECC-1	luminal epithelium:	n/a
40	chr1:75841810-75841860	LNCaP	prostate:	n/a
41	chr1:75841810-75841860	AG09319	gingival:	n/a
42	chr1:75841810-75841860	GM12891	blood:	n/a
43	chr1:75841810-75841860	Jurkat	blood:	n/a
44	chr1:75841810-75841860	HNPCEpiC	eye:	n/a
45	chr1:75841810-75841860	Hepatocyte	liver:	n/a
46	chr1:75841810-75841860	HEK293	kidney:	embryo
47	chr1:75841810-75841860	RPTEC	kidney:	n/a
48	chr1:75841810-75841860	HRPEpiC	eye:	n/a
49	chr1:75841810-75841860	SK-N-MC	brain:	n/a
50	chr1:75841810-75841860	ProgFib	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:75830302..75833170-chr1:75834752..75836342,2	K562	blood:
2	chr1:75819174..75821466-chr1:76259462..76262137,2	K562	blood:
3	chr1:75837137..75838827-chr1:75839642..75842194,2	K562	blood:
4	chr1:75820905..75823291-chr1:75839784..75841753,2	K562	blood:
5	chr1:75821210..75823123-chr1:75827154..75829590,2	K562	blood:
6	chr1:75826578..75828663-chr1:75838109..75841105,2	K562	blood:
7	chr1:75837137..75838827-chr1:75839642..75842194,2	K562	blood:
8	chr1:75832449..75834069-chr1:76250552..76252423,2	K562	blood:
9	chr1:75826578..75828663-chr1:75838109..75841105,2	K562	blood:
10	chr1:75830302..75833170-chr1:75834752..75836342,2	K562	blood:
11	chr1:75821210..75823123-chr1:75827154..75829590,2	K562	blood:
12	chr1:75820905..75823291-chr1:75839784..75841753,2	K562	blood:

No data

Variant related genes	Relation type
SLC44A5	TF binding region
SLC44A5	CpG island
ENSG00000137955	chromatin interactions

Extended variants
information (count: 1041 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188903435	chr1:75812396-75812397	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs145032310	chr1:75812423-75812424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570927490	chr1:75812454-75812455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200144808	chr1:75812455-75812456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146812701	chr1:75812509-75812510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541870559	chr1:75812522-75812523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560244222	chr1:75812529-75812530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530393402	chr1:75812615-75812616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181372924	chr1:75812621-75812622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546413134	chr1:75812622-75812623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186229180	chr1:75812666-75812667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552311092	chr1:75812681-75812682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78795823	chr1:75812696-75812697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189505755	chr1:75812714-75812715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181012204	chr1:75812788-75812789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529203567	chr1:75812817-75812818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185993525	chr1:75812824-75812825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs60212160	chr1:75812840-75812841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565825819	chr1:75812851-75812852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74915221	chr1:75812865-75812866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539591375	chr1:75812874-75812875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191069678	chr1:75812892-75812893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552065055	chr1:75812924-75812925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570661064	chr1:75812938-75812939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537662673	chr1:75812993-75812994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140559564	chr1:75812997-75812998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574790512	chr1:75813040-75813041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77206273	chr1:75813088-75813089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183200684	chr1:75813121-75813122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185883096	chr1:75813141-75813142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs17096785	chr1:75813146-75813147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566548021	chr1:75813194-75813195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564039973	chr1:75813301-75813302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190394493	chr1:75813305-75813306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72682092	chr1:75813313-75813314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561510377	chr1:75813326-75813327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562364707	chr1:75813336-75813337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10677527	chr1:75813370-75813371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35319800	chr1:75813372-75813373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs67290523	chr1:75813393-75813394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs397769234	chr1:75813394-75813395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4949666	chr1:75818830-75818831	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs566622071	chr1:75818986-75818987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374370672	chr1:75819038-75819039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533083647	chr1:75819064-75819065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549911205	chr1:75819091-75819092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1249837	chr1:75819102-75819103	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs558788326	chr1:75819123-75819124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183561966	chr1:75819155-75819156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374219984	chr1:75819188-75819189	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:139 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75807000-75812400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:75808800-75813000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:75811600-75812600	Enhancers	NH-A	brain
4	chr1:75812000-75812400	Flanking Active TSS	HUVEC	blood vessel
5	chr1:75812400-75813400	Enhancers	HUVEC	blood vessel
6	chr1:75813000-75813200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr1:75818800-75819400	Enhancers	K562	blood
8	chr1:75819400-75819600	Flanking Active TSS	K562	blood
9	chr1:75819600-75819800	Enhancers	K562	blood
10	chr1:75819800-75820000	Flanking Active TSS	K562	blood
11	chr1:75820000-75821000	Enhancers	K562	blood
12	chr1:75821000-75822600	Weak transcription	K562	blood
13	chr1:75822600-75822800	Enhancers	K562	blood
14	chr1:75822800-75823200	Active TSS	K562	blood
15	chr1:75823200-75823400	Enhancers	K562	blood
16	chr1:75823400-75824600	Weak transcription	K562	blood
17	chr1:75824600-75824800	Enhancers	K562	blood
18	chr1:75824800-75830000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr1:75827400-75832800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:75828600-75831600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr1:75829600-75832600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:75831200-75841000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr1:75831400-75841400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr1:75832200-75833000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr1:75832800-75833600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:75832800-75833600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr1:75832800-75833600	ZNF genes & repeats	Primary B cells from cord blood	blood
28	chr1:75832800-75833600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:75832800-75833600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:75832800-75833600	ZNF genes & repeats	Adipose Nuclei	Adipose
31	chr1:75832800-75833600	ZNF genes & repeats	Brain Germinal Matrix	brain
32	chr1:75833000-75833400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr1:75833000-75833400	ZNF genes & repeats	Pancreas	Pancrea
34	chr1:75833000-75833400	ZNF genes & repeats	K562	blood
35	chr1:75833000-75834400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:75833200-75833400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
37	chr1:75833200-75833400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
38	chr1:75833200-75833400	ZNF genes & repeats	Gastric	stomach
39	chr1:75833200-75836200	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr1:75833400-75833600	Enhancers	Gastric	stomach
41	chr1:75833400-75837000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr1:75833400-75839200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr1:75833400-75839200	Weak transcription	K562	blood
44	chr1:75833400-75841000	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr1:75833600-75834000	Weak transcription	Primary B cells from cord blood	blood
46	chr1:75833600-75837600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr1:75833600-75839200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:75833600-75841200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr1:75834400-75838200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:75836200-75838400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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