Variant report

Variant	nsv1000648
Chromosome Location	chr1:152719318-152747126
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:149)
CpG islands
(count:916)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:149 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr1:152724829-152725066	GM12878	blood:	n/a	n/a
2	CEBPB	chr1:152741613-152742048	Hela-S3	cervix:	n/a	chr1:152741819-152741830 chr1:152741818-152741829 chr1:152741818-152741831
3	CEBPB	chr1:152720808-152720838	K562	blood:	n/a	n/a
4	CEBPB	chr1:152720397-152720692	IMR90	lung:	n/a	n/a
5	CEBPB	chr1:152741735-152741946	K562	blood:	n/a	chr1:152741819-152741830 chr1:152741818-152741829 chr1:152741818-152741831
6	CEBPB	chr1:152741467-152742184	HCT-116	colon:	n/a	chr1:152741819-152741830 chr1:152741818-152741829 chr1:152741818-152741831
7	CEBPB	chr1:152736423-152736598	A549	lung:	n/a	chr1:152736523-152736534
8	CEBPB	chr1:152741694-152741984	A549	lung:	n/a	chr1:152741819-152741830 chr1:152741818-152741829 chr1:152741818-152741831
9	CEBPB	chr1:152741514-152742064	HCT-116	colon:	n/a	chr1:152741819-152741830 chr1:152741818-152741829 chr1:152741818-152741831
10	CEBPB	chr1:152720404-152720604	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:152741706-152741942	K562	blood:	n/a	chr1:152741819-152741830 chr1:152741818-152741829 chr1:152741818-152741831
12	CEBPB	chr1:152741680-152741957	IMR90	lung:	n/a	chr1:152741819-152741830 chr1:152741818-152741829 chr1:152741818-152741831
13	CEBPB	chr1:152724832-152725032	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:152741642-152741982	HepG2	liver:	n/a	chr1:152741819-152741830 chr1:152741818-152741829 chr1:152741818-152741831
15	CEBPB	chr1:152724775-152725154	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:152736359-152736676	HepG2	liver:	n/a	chr1:152736523-152736534
17	CHD1	chr1:152724614-152725396	IMR90	lung:	n/a	n/a
18	CTCF	chr1:152734600-152734750	HMF	breast:	n/a	n/a
19	CTCF	chr1:152734560-152734710	SAEC	small airway:	n/a	n/a
20	CTCF	chr1:152734559-152734823	IMR90	lung:	n/a	n/a
21	CTCF	chr1:152737680-152737830	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:152736200-152736350	GM12878	blood:	n/a	n/a
23	CTCF	chr1:152741800-152741950	HMF	breast:	n/a	n/a
24	CTCF	chr1:152734640-152734790	HMEC	breast:	n/a	n/a
25	CTCF	chr1:152734620-152734770	AG10803	skin:	n/a	n/a
26	CTCF	chr1:152741400-152741550	HMF	breast:	n/a	n/a
27	CTCF	chr1:152741800-152741950	HMEC	breast:	n/a	n/a
28	CTCF	chr1:152741820-152741970	SAEC	small airway:	n/a	n/a
29	CTCF	chr1:152741871-152741978	Medullo	brain:	n/a	n/a
30	CTCF	chr1:152734673-152734757	MCF-7	breast:	n/a	n/a
31	CTCF	chr1:152741386-152741440	MCF-7	breast:	n/a	n/a
32	CTCF	chr1:152734580-152734730	HMF	breast:	n/a	n/a
33	CTCF	chr1:152741380-152741530	HMF	breast:	n/a	n/a
34	CTCF	chr1:152741920-152742070	HMEC	breast:	n/a	n/a
35	CTCF	chr1:152741880-152742030	GM12864	blood:	n/a	n/a
36	CTCF	chr1:152741320-152741470	HPF	lung:	n/a	n/a
37	CTCF	chr1:152741400-152741550	HMEC	breast:	n/a	n/a
38	CTCF	chr1:152729526-152729569	NHEK	skin:	n/a	n/a
39	CTCF	chr1:152741380-152741530	AG10803	skin:	n/a	n/a
40	CTCF	chr1:152741880-152742030	AG10803	skin:	n/a	n/a
41	CTCF	chr1:152727968-152727987	ProgFib	skin:	n/a	n/a
42	CTCF	chr1:152741880-152742030	AG09319	gingival:	n/a	n/a
43	CTCF	chr1:152741340-152741490	HEK293	kidney:	n/a	n/a
44	CTCF	chr1:152741940-152742090	RPTEC	kidney:	n/a	n/a
45	CTCF	chr1:152727704-152727744	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr1:152741780-152741930	NHEK	skin:	n/a	n/a
47	CTCF	chr1:152741340-152741490	NHEK	skin:	n/a	n/a
48	CTCF	chr1:152741880-152742030	HMF	breast:	n/a	n/a
49	CTCF	chr1:152741360-152741510	NHEK	skin:	n/a	n/a
50	CTCF	chr1:152741800-152741950	AG09319	gingival:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152733337-152733387	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:152733337-152733387	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:152731117-152731167	U87	brain:	n/a
4	chr1:152731117-152731167	NH-A	brain:	n/a
5	chr1:152729200-152729250	PrEC	prostate:	n/a
6	chr1:152733223-152733273	HEK293	kidney:	embryo
7	chr1:152731590-152731640	HAEpiC	amniotic membrane:	n/a
8	chr1:152733223-152733273	NHDF-neo	bronchial:	n/a
9	chr1:152729200-152729250	GM12878	blood:	n/a
10	chr1:152730426-152730476	IMR90	lung:	fetal
11	chr1:152733337-152733387	IMR90	lung:	fetal
12	chr1:152729200-152729250	Hela-S3	cervix:	n/a
13	chr1:152730027-152730077	ovcar-3	ovarian:	n/a
14	chr1:152731117-152731167	HEK293	kidney:	embryo
15	chr1:152730231-152730281	HCF	heart:	n/a
16	chr1:152730718-152730768	NB4	blood:	n/a
17	chr1:152730718-152730768	T-47D	breast:	n/a
18	chr1:152733118-152733168	HNPCEpiC	eye:	n/a
19	chr1:152730027-152730077	GM06990	blood:	n/a
20	chr1:152733025-152733075	AG04450	lung:	fetal
21	chr1:152733140-152733190	NB4	blood:	n/a
22	chr1:152733223-152733273	AG09309	skin:	n/a
23	chr1:152733337-152733387	HRPEpiC	eye:	n/a
24	chr1:152729200-152729250	PFSK-1	brain:	n/a
25	chr1:152733118-152733168	BE2_C	brain:	n/a
26	chr1:152733337-152733387	LNCaP	prostate:	n/a
27	chr1:152733337-152733387	HL-60	blood:	n/a
28	chr1:152731590-152731640	H1-hESC	embryonic stem cell:	embryo
29	chr1:152731590-152731640	PrEC	prostate:	n/a
30	chr1:152733118-152733168	HRCEpiC	kidney:	n/a
31	chr1:152730361-152730411	Jurkat	blood:	n/a
32	chr1:152729200-152729250	HCPEpiC	choroid plexus:	n/a
33	chr1:152731590-152731640	NT2-D1	testis:	n/a
34	chr1:152730231-152730281	AG09319	gingival:	n/a
35	chr1:152733118-152733168	Jurkat	blood:	n/a
36	chr1:152735835-152735885	AG09319	gingival:	n/a
37	chr1:152729200-152729250	SK-N-SH_RA	brain:	n/a
38	chr1:152733025-152733075	ovcar-3	ovarian:	n/a
39	chr1:152731590-152731640	Caco-2	colon:	n/a
40	chr1:152733223-152733273	AoSMC	blood vessel:	n/a
41	chr1:152733140-152733190	HNPCEpiC	eye:	n/a
42	chr1:152729200-152729250	HEK293	kidney:	embryo
43	chr1:152733118-152733168	AG04450	lung:	fetal
44	chr1:152731117-152731167	HIPEpiC	eye:	n/a
45	chr1:152733118-152733168	H1-hESC	embryonic stem cell:	embryo
46	chr1:152733140-152733190	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:152730361-152730411	GM12878	blood:	n/a
48	chr1:152733337-152733387	U87	brain:	n/a
49	chr1:152733140-152733190	HL-60	blood:	n/a
50	chr1:152733140-152733190	T-47D	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:152733924..152735488-chr1:152736776..152739020,2	MCF-7	breast:
2	chr1:152718102..152720118-chr1:152722194..152725146,2	K562	blood:
3	chr1:152741230..152741815-chr16:81212739..81213485,2	MCF-7	breast:
4	chr1:152633504..152636346-chr1:152743964..152745780,2	K562	blood:
5	chr1:152718102..152720118-chr1:152722194..152725146,2	K562	blood:
6	chr1:152745990..152747904-chr1:152750482..152752734,2	MCF-7	breast:
7	chr1:152716869..152720481-chr1:152722647..152727810,6	MCF-7	breast:
8	chr1:152626242..152627151-chr1:152734184..152735164,3	MCF-7	breast:
9	chr1:152723383..152725427-chr1:152727579..152730521,2	K562	blood:
10	chr1:152716371..152718669-chr1:152739081..152740588,2	MCF-7	breast:
11	chr1:152711224..152713888-chr1:152737781..152739633,2	MCF-7	breast:
12	chr1:152716869..152720481-chr1:152722647..152727810,6	MCF-7	breast:
13	chr1:152728900..152731516-chr1:152732979..152735193,2	MCF-7	breast:
14	chr1:152733924..152735488-chr1:152736776..152739020,2	MCF-7	breast:
15	chr1:152715699..152717723-chr1:152736198..152738131,2	MCF-7	breast:

No data

Variant related genes	Relation type
LCE1F	TF binding region
KPRP	TF binding region
LCE1F	CpG island
KPRP	CpG island
ENSG00000187223	chromatin interactions
ENSG00000203786	chromatin interactions
ENSG00000233819	chromatin interactions

Extended variants
information (count: 1149 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:1149 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12023710	chr1:152719318-152719319	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186043522	chr1:152719320-152719321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142638473	chr1:152719356-152719357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567806311	chr1:152719448-152719449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs10888515	chr1:152719487-152719488	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs16834428	chr1:152719514-152719515	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs576488162	chr1:152719516-152719517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536136354	chr1:152719524-152719525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs66659820	chr1:152719539-152719540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59121455	chr1:152719540-152719541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545432265	chr1:152719541-152719542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs398053412	chr1:152719544-152719545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374076955	chr1:152719545-152719546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192121307	chr1:152719583-152719584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146831813	chr1:152719586-152719587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183890555	chr1:152719677-152719678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138885804	chr1:152719682-152719683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531323951	chr1:152719705-152719706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543481747	chr1:152719713-152719714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563061002	chr1:152719731-152719732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114692612	chr1:152719734-152719735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543477443	chr1:152719742-152719743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35738197	chr1:152719779-152719780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551759665	chr1:152719795-152719796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571568326	chr1:152719837-152719838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73014888	chr1:152719852-152719853	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs75215810	chr1:152719859-152719860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs79529278	chr1:152719888-152719889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567828118	chr1:152719899-152719900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143710250	chr1:152719935-152719936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148102246	chr1:152719951-152719952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187352605	chr1:152719973-152719974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548939694	chr1:152720038-152720039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559000858	chr1:152720048-152720049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572512799	chr1:152720103-152720104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190655360	chr1:152720149-152720150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554594506	chr1:152720158-152720159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371777906	chr1:152720162-152720163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75574905	chr1:152720177-152720178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142804365	chr1:152720193-152720194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146058883	chr1:152720199-152720200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562998623	chr1:152720209-152720210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532087064	chr1:152720240-152720241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138151814	chr1:152720244-152720245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558923909	chr1:152720266-152720267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528105105	chr1:152720284-152720285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548057444	chr1:152720346-152720347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561437527	chr1:152720348-152720349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527914708	chr1:152720361-152720362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530284303	chr1:152720425-152720426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152714600-152721200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:152715800-152720400	Enhancers	NHDF-Ad	bronchial
3	chr1:152717800-152719400	Enhancers	HepG2	liver
4	chr1:152718400-152724600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:152718400-152724600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr1:152718600-152720200	Weak transcription	HMEC	breast
7	chr1:152718600-152720200	Weak transcription	NHEK	skin
8	chr1:152719200-152725000	Weak transcription	NHLF	lung
9	chr1:152720200-152720600	Enhancers	HMEC	breast
10	chr1:152720200-152720800	Enhancers	NHEK	skin
11	chr1:152720400-152723400	Weak transcription	NHDF-Ad	bronchial
12	chr1:152720600-152724600	Weak transcription	HMEC	breast
13	chr1:152720800-152724400	Weak transcription	NHEK	skin
14	chr1:152721200-152723200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:152723200-152724600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:152723400-152724400	Enhancers	NHDF-Ad	bronchial
17	chr1:152724400-152724800	Weak transcription	NHDF-Ad	bronchial
18	chr1:152724400-152726200	Enhancers	NHEK	skin
19	chr1:152724600-152724800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
20	chr1:152724600-152725200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:152724600-152725400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:152724600-152725800	Enhancers	HMEC	breast
23	chr1:152724600-152726200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:152724600-152726200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:152724800-152725000	Enhancers	Muscle Satellite Cultured Cells	--
26	chr1:152724800-152725200	Enhancers	Ovary	ovary
27	chr1:152724800-152725200	Enhancers	HSMM	muscle
28	chr1:152724800-152725200	Enhancers	NH-A	brain
29	chr1:152724800-152725600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:152724800-152726800	Enhancers	NHDF-Ad	bronchial
31	chr1:152725000-152725200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
32	chr1:152725000-152726400	Enhancers	NHLF	lung
33	chr1:152725200-152725600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr1:152725200-152726800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:152725600-152729400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:152725800-152726200	Weak transcription	HMEC	breast
37	chr1:152726200-152726400	Enhancers	HMEC	breast
38	chr1:152726200-152729200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:152726200-152729400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:152726200-152729400	Weak transcription	NHEK	skin
41	chr1:152726400-152728800	Weak transcription	NHLF	lung
42	chr1:152726400-152729000	Weak transcription	HMEC	breast
43	chr1:152726800-152729400	Weak transcription	NHDF-Ad	bronchial
44	chr1:152726800-152734200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:152728800-152730600	Enhancers	NHLF	lung
46	chr1:152729000-152735000	Enhancers	HMEC	breast
47	chr1:152729200-152729400	Weak transcription	Esophagus	oesophagus
48	chr1:152729200-152735000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:152729400-152729600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr1:152729400-152729600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links