Variant report

Variant	esv3424702
Chromosome Location	chr1:153015726-153032343
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:183)
CpG islands
(count:366)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:183 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:153031308-153032283	K562	blood:	n/a	n/a
2	ARID3A	chr1:153030693-153030952	K562	blood:	n/a	n/a
3	ATF1	chr1:153031406-153032192	K562	blood:	n/a	n/a
4	ATF3	chr1:153031669-153032213	K562	blood:	n/a	n/a
5	ATF3	chr1:153031812-153032059	K562	blood:	n/a	n/a
6	BHLHE40	chr1:153031557-153032209	K562	blood:	n/a	n/a
7	CBX3	chr1:153031761-153032266	K562	blood:	n/a	n/a
8	CCNT2	chr1:153031399-153032490	K562	blood:	n/a	chr1:153031986-153032006
9	CEBPB	chr1:153031752-153032198	K562	blood:	n/a	n/a
10	CEBPB	chr1:153031640-153032161	K562	blood:	n/a	n/a
11	CEBPD	chr1:153031258-153032304	K562	blood:	n/a	n/a
12	CEBPD	chr1:153031328-153032328	K562	blood:	n/a	n/a
13	CHD2	chr1:153031845-153032048	K562	blood:	n/a	n/a
14	CTCF	chr1:153028820-153028970	HEEpiC	esophagus:	n/a	n/a
15	CTCF	chr1:153030720-153030870	K562	blood:	n/a	n/a
16	CTCF	chr1:153030640-153030790	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr1:153030520-153030670	GM12872	blood:	n/a	n/a
18	CTCF	chr1:153030720-153030870	GM12864	blood:	n/a	n/a
19	CTCF	chr1:153028800-153028950	HMEC	breast:	n/a	n/a
20	CTCF	chr1:153021595-153021606	K562	blood:	n/a	n/a
21	CTCF	chr1:153030740-153030890	HEK293	kidney:	n/a	n/a
22	CTCF	chr1:153030715-153030887	LNCaP	prostate:	n/a	n/a
23	CTCF	chr1:153030680-153030830	NHEK	skin:	n/a	n/a
24	CTCF	chr1:153030700-153030850	GM06990	blood:	n/a	n/a
25	CTCF	chr1:153030640-153030790	A549	lung:	n/a	n/a
26	CTCF	chr1:153030480-153030630	SAEC	small airway:	n/a	n/a
27	CTCF	chr1:153028840-153028990	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr1:153030680-153030830	HCT-116	colon:	n/a	n/a
29	CTCF	chr1:153028747-153028824	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:153030680-153030830	BJ	skin:	n/a	n/a
31	CTCF	chr1:153030760-153030910	GM12872	blood:	n/a	n/a
32	CTCF	chr1:153028820-153028970	HEK293	kidney:	n/a	n/a
33	CTCF	chr1:153027024-153027130	GM20000	blood:	n/a	n/a
34	CTCF	chr1:153030512-153030963	MCF-7	breast:	n/a	n/a
35	CTCF	chr1:153030700-153030850	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr1:153030760-153030910	HMEC	breast:	n/a	n/a
37	CTCF	chr1:153021543-153021615	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr1:153030723-153030896	A549	lung:	n/a	n/a
39	CTCF	chr1:153030720-153030870	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr1:153030720-153030870	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr1:153030740-153030890	HL-60	blood:	n/a	n/a
42	CTCF	chr1:153028820-153028970	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:153030720-153030870	GM12878	blood:	n/a	n/a
44	CTCF	chr1:153030691-153030978	K562	blood:	n/a	n/a
45	CTCF	chr1:153021559-153021593	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:153030822-153030869	GM12878	blood:	n/a	n/a
47	CTCF	chr1:153030795-153030896	IMR90	lung:	n/a	n/a
48	CTCF	chr1:153028760-153028910	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr1:153030784-153030875	Medullo	brain:	n/a	n/a
50	CTCF	chr1:153030760-153030910	AG04449	skin:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153029939-153029989	CMK	blood:	n/a
2	chr1:153030751-153030801	HL-60	blood:	n/a
3	chr1:153030567-153030617	AoSMC	blood vessel:	n/a
4	chr1:153030514-153030564	H1-hESC	embryonic stem cell:	embryo
5	chr1:153030567-153030617	Hepatocyte	liver:	n/a
6	chr1:153030751-153030801	AG09319	gingival:	n/a
7	chr1:153030567-153030617	HRE	kidney:	n/a
8	chr1:153030514-153030564	Caco-2	colon:	n/a
9	chr1:153030594-153030644	HMEC	breast:	n/a
10	chr1:153029005-153029055	HNPCEpiC	eye:	n/a
11	chr1:153030751-153030801	GM06990	blood:	n/a
12	chr1:153030567-153030617	LNCaP	prostate:	n/a
13	chr1:153030751-153030801	LNCaP	prostate:	n/a
14	chr1:153029005-153029055	GM06990	blood:	n/a
15	chr1:153030751-153030801	GM12891	blood:	n/a
16	chr1:153030594-153030644	MCF10A-Er-Src	breast:	n/a
17	chr1:153029005-153029055	PrEC	prostate:	n/a
18	chr1:153029939-153029989	Jurkat	blood:	n/a
19	chr1:153030514-153030564	PANC-1	pancreas:	n/a
20	chr1:153030594-153030644	Hepatocyte	liver:	n/a
21	chr1:153030751-153030801	AG04450	lung:	fetal
22	chr1:153029939-153029989	HNPCEpiC	eye:	n/a
23	chr1:153030514-153030564	HCM	heart:	n/a
24	chr1:153030567-153030617	HEK293	kidney:	embryo
25	chr1:153029005-153029055	HepG2	liver:	n/a
26	chr1:153030751-153030801	NHDF-neo	bronchial:	n/a
27	chr1:153030567-153030617	T-47D	breast:	n/a
28	chr1:153030567-153030617	BJ	skin:	n/a
29	chr1:153030514-153030564	HCF	heart:	n/a
30	chr1:153030751-153030801	Caco-2	colon:	n/a
31	chr1:153030594-153030644	Caco-2	colon:	n/a
32	chr1:153030751-153030801	CMK	blood:	n/a
33	chr1:153030594-153030644	HIPEpiC	eye:	n/a
34	chr1:153029005-153029055	HL-60	blood:	n/a
35	chr1:153029005-153029055	HUVEC	blood vessel:	n/a
36	chr1:153030594-153030644	HL-60	blood:	n/a
37	chr1:153029005-153029055	RPTEC	kidney:	n/a
38	chr1:153030751-153030801	HMEC	breast:	n/a
39	chr1:153030567-153030617	HCF	heart:	n/a
40	chr1:153030751-153030801	SAEC	small airway:	n/a
41	chr1:153030594-153030644	A549	lung:	n/a
42	chr1:153030751-153030801	AG10803	skin:	n/a
43	chr1:153029939-153029989	H1-hESC	embryonic stem cell:	embryo
44	chr1:153030514-153030564	K562	blood:	n/a
45	chr1:153030514-153030564	AG04449	skin:	fetal
46	chr1:153030514-153030564	HRE	kidney:	n/a
47	chr1:153030751-153030801	MCF10A-Er-Src	breast:	n/a
48	chr1:153030514-153030564	GM12892	blood:	n/a
49	chr1:153029939-153029989	HL-60	blood:	n/a
50	chr1:153029939-153029989	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:152946838..152947509-chr1:153030402..153031164,2	MCF-7	breast:
2	chr1:153031331..153032975-chr1:153077540..153080303,2	K562	blood:
3	chr1:152890031..152890981-chr1:153030436..153031260,2	MCF-7	breast:
4	chr1:153020357..153022432-chr1:153024274..153025794,2	K562	blood:
5	chr1:153030355..153031203-chr1:153153146..153153758,2	MCF-7	breast:
6	chr1:153020357..153022432-chr1:153024274..153025794,2	K562	blood:
7	chr1:153023664..153025787-chr1:153028264..153031002,2	K562	blood:

No data

Variant related genes	Relation type
SPRR2D	TF binding region
SPRR2A	TF binding region
SPRR2D	CpG island
SPRR2A	CpG island
ENSG00000203785	chromatin interactions
ENSG00000241794	chromatin interactions

Extended variants
information (count: 672 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1284903	chr1:153015743-153015744	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs371292818	chr1:153015760-153015761	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs1697428	chr1:153015761-153015762	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs1284902	chr1:153015787-153015788	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs1284901	chr1:153015801-153015802	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs1284900	chr1:153015812-153015813	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs186322167	chr1:153015833-153015834	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs1284899	chr1:153015839-153015840	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs143287543	chr1:153015842-153015843	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs560321964	chr1:153015844-153015845	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs1284898	chr1:153015849-153015850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79582188	chr1:153015874-153015875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549474845	chr1:153015877-153015878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1284897	chr1:153015895-153015896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1284896	chr1:153015902-153015903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541317628	chr1:153015946-153015947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191623164	chr1:153015952-153015953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148309320	chr1:153015955-153015956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs180789421	chr1:153016053-153016054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185213952	chr1:153016062-153016063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559920759	chr1:153016104-153016105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11588011	chr1:153016123-153016124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs61811883	chr1:153016124-153016125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551375989	chr1:153016195-153016196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368912	chr1:153016204-153016205	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs115015034	chr1:153016219-153016220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553969052	chr1:153016221-153016222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573896856	chr1:153016251-153016252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377125828	chr1:153016273-153016274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535941660	chr1:153016316-153016317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76966042	chr1:153016327-153016328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189775923	chr1:153016379-153016380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76533368	chr1:153016411-153016412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564540822	chr1:153016451-153016452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577874828	chr1:153016492-153016493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534036992	chr1:153016502-153016503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540538125	chr1:153016557-153016558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72704884	chr1:153016588-153016589	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs377768	chr1:153016594-153016595	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549193998	chr1:153016608-153016609	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs74132527	chr1:153016629-153016630	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs376613458	chr1:153016643-153016644	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs531604476	chr1:153016664-153016665	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs551708012	chr1:153016708-153016709	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs571679930	chr1:153016716-153016717	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs527549578	chr1:153016721-153016722	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs547735958	chr1:153016764-153016765	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs78044295	chr1:153016767-153016768	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs536483591	chr1:153016794-153016795	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs555978139	chr1:153016799-153016800	Weak transcription	TF binding region	1 gene(s)	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
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
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153013000-153015800	Enhancers	K562	blood
2	chr1:153013400-153015800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr1:153014800-153015800	Enhancers	NHEK	skin
4	chr1:153015200-153015800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:153015400-153015800	Enhancers	Placenta	Placenta
6	chr1:153015800-153016400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:153015800-153016400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:153015800-153018000	Weak transcription	NHEK	skin
9	chr1:153016400-153016600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:153016400-153016600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:153016600-153018000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr1:153018000-153019800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:153018000-153019800	Enhancers	NHEK	skin
14	chr1:153019400-153030000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:153021800-153022600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:153021800-153022600	Enhancers	Esophagus	oesophagus
17	chr1:153028200-153028400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:153028400-153030000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr1:153028600-153030000	Active TSS	Esophagus	oesophagus
20	chr1:153028800-153029000	Enhancers	K562	blood
21	chr1:153029000-153030400	Weak transcription	K562	blood
22	chr1:153029800-153030200	Enhancers	GM12878-XiMat	blood
23	chr1:153029800-153030600	Enhancers	HMEC	breast
24	chr1:153029800-153032400	Enhancers	NHEK	skin
25	chr1:153030000-153030200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr1:153030000-153030400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:153030000-153030400	Weak transcription	Esophagus	oesophagus
28	chr1:153030000-153032400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:153030200-153030800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:153030400-153030600	Enhancers	Esophagus	oesophagus
31	chr1:153030400-153031400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr1:153030400-153031600	Enhancers	K562	blood
33	chr1:153030600-153031400	Weak transcription	HMEC	breast
34	chr1:153030600-153032000	Weak transcription	Esophagus	oesophagus
35	chr1:153030800-153032200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:153031200-153032000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:153031400-153032000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:153031400-153032000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:153031400-153032200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:153031400-153032200	Enhancers	HMEC	breast
41	chr1:153031600-153032200	Enhancers	Placenta	Placenta
42	chr1:153031600-153032200	Enhancers	Pancreas	Pancrea
43	chr1:153031600-153032200	Enhancers	Placenta Amnion	Placenta Amnion
44	chr1:153031600-153032400	Flanking Active TSS	K562	blood
45	chr1:153031800-153032200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr1:153031800-153032400	Enhancers	Gastric	stomach
47	chr1:153032000-153032200	Enhancers	Esophagus	oesophagus
48	chr1:153032200-153053400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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