Variant report

Variant	nsv947197
Chromosome Location	chr1:153006138-153017705
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:153013641-153013966	K562	blood:	n/a	n/a
2	BHLHE40	chr1:153015386-153015558	K562	blood:	n/a	n/a
3	CEBPB	chr1:153013681-153013964	K562	blood:	n/a	n/a
4	CEBPB	chr1:153012095-153012104	HepG2	liver:	n/a	n/a
5	CTCF	chr1:153010180-153010330	HPF	lung:	n/a	n/a
6	CTCF	chr1:153012380-153012530	WERI-Rb-1	eye:	n/a	n/a
7	CTCF	chr1:153012499-153012587	Fibrobl	skin:	n/a	n/a
8	CTCF	chr1:153012340-153012490	MCF-7	breast:	n/a	n/a
9	CTCF	chr1:153012360-153012510	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr1:153012280-153012430	HMEC	breast:	n/a	n/a
11	CTCF	chr1:153012300-153012450	HEEpiC	esophagus:	n/a	n/a
12	CTCF	chr1:153012340-153012490	HEK293	kidney:	n/a	n/a
13	CTCF	chr1:153012360-153012510	HCT-116	colon:	n/a	n/a
14	CUX1	chr1:153013518-153013964	K562	blood:	n/a	n/a
15	E2F4	chr1:153014551-153014726	MCF10A-Er-Src	breast:	n/a	n/a
16	EP300	chr1:153013556-153014116	K562	blood:	n/a	n/a
17	EP300	chr1:153012830-153013193	K562	blood:	n/a	n/a
18	FOS	chr1:153007855-153008054	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr1:153006511-153006647	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr1:153006415-153006713	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr1:153007859-153008034	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr1:153013545-153014108	MCF10A-Er-Src	breast:	n/a	chr1:153013923-153013930 chr1:153013922-153013930 chr1:153013548-153013556 chr1:153013922-153013930 chr1:153013785-153013794 chr1:153013784-153013795 chr1:153013918-153013929
23	FOS	chr1:153013607-153014058	MCF10A-Er-Src	breast:	n/a	chr1:153013923-153013930 chr1:153013922-153013930 chr1:153013922-153013930 chr1:153013785-153013794 chr1:153013784-153013795 chr1:153013918-153013929
24	FOS	chr1:153013607-153014112	MCF10A-Er-Src	breast:	n/a	chr1:153013923-153013930 chr1:153013922-153013930 chr1:153013922-153013930 chr1:153013785-153013794 chr1:153013784-153013795 chr1:153013918-153013929
25	FOS	chr1:153013643-153014033	MCF10A-Er-Src	breast:	n/a	chr1:153013923-153013930 chr1:153013922-153013930 chr1:153013922-153013930 chr1:153013785-153013794 chr1:153013784-153013795 chr1:153013918-153013929
26	FOS	chr1:153007729-153008053	MCF10A-Er-Src	breast:	n/a	n/a
27	GATA1	chr1:153015186-153015844	PBDE	blood:	n/a	chr1:153015503-153015520
28	HEY1	chr1:153013463-153013692	K562	blood:	n/a	n/a
29	JUN	chr1:153013532-153014063	K562	blood:	n/a	chr1:153013923-153013930 chr1:153013922-153013930 chr1:153013548-153013556 chr1:153013922-153013930 chr1:153013785-153013794 chr1:153013784-153013795 chr1:153013918-153013929
30	JUN	chr1:153013666-153013964	K562	blood:	n/a	chr1:153013923-153013930 chr1:153013922-153013930 chr1:153013922-153013930 chr1:153013785-153013794 chr1:153013784-153013795 chr1:153013918-153013929
31	JUN	chr1:153012837-153014143	K562	blood:	n/a	chr1:153013923-153013930 chr1:153013922-153013930 chr1:153013548-153013556 chr1:153013922-153013930 chr1:153013785-153013794 chr1:153013784-153013795 chr1:153013918-153013929
32	JUND	chr1:153013497-153014094	K562	blood:	n/a	chr1:153013923-153013930 chr1:153013922-153013930 chr1:153013548-153013556 chr1:153013922-153013930 chr1:153013785-153013794 chr1:153013784-153013795 chr1:153013918-153013929
33	JUND	chr1:153015451-153015699	K562	blood:	n/a	n/a
34	MAFF	chr1:153014021-153014151	HepG2	liver:	n/a	n/a
35	MAFK	chr1:153013683-153014222	K562	blood:	n/a	n/a
36	MAX	chr1:153013598-153013847	K562	blood:	n/a	chr1:153013784-153013793
37	MAZ	chr1:153013495-153013977	K562	blood:	n/a	chr1:153013921-153013930 chr1:153013784-153013793
38	MYC	chr1:153016608-153016936	K562	blood:	n/a	chr1:153016793-153016803
39	MYC	chr1:153013595-153014010	K562	blood:	n/a	chr1:153013921-153013930 chr1:153013784-153013793
40	MYC	chr1:153015672-153015802	K562	blood:	n/a	n/a
41	MYC	chr1:153013770-153013956	MCF10A-Er-Src	breast:	n/a	chr1:153013921-153013930 chr1:153013784-153013793
42	POLR2A	chr1:153015460-153015554	A549	lung:	n/a	n/a
43	POLR2A	chr1:153012812-153013764	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr1:153013431-153013628	K562	blood:	n/a	n/a
45	POLR2A	chr1:153012538-153012540	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr1:153013448-153013581	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr1:153011421-153011964	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr1:153005337-153006910	MCF10A-Er-Src	breast:	n/a	n/a
49	RCOR1	chr1:153013509-153014025	K562	blood:	n/a	n/a
50	STAT3	chr1:153007874-153007926	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153014367-153014417	ProgFib	skin:	n/a
2	chr1:153014367-153014417	ProgFib	skin:	n/a
3	chr1:153014367-153014417	BJ	skin:	n/a
4	chr1:153015281-153015331	ovcar-3	ovarian:	n/a
5	chr1:153014310-153014360	HIPEpiC	eye:	n/a
6	chr1:153014956-153015006	HCM	heart:	n/a
7	chr1:153014367-153014417	SK-N-MC	brain:	n/a
8	chr1:153013573-153013623	AG10803	skin:	n/a
9	chr1:153013830-153013880	Hela-S3	cervix:	n/a
10	chr1:153013573-153013623	A549	lung:	n/a
11	chr1:153014367-153014417	AG10803	skin:	n/a
12	chr1:153013573-153013623	NHDF-neo	bronchial:	n/a
13	chr1:153014956-153015006	H1-hESC	embryonic stem cell:	embryo
14	chr1:153013573-153013623	HEEpiC	esophagus:	n/a
15	chr1:153013573-153013623	GM12891	blood:	n/a
16	chr1:153013573-153013623	HNPCEpiC	eye:	n/a
17	chr1:153014956-153015006	A549	lung:	n/a
18	chr1:153014310-153014360	HCF	heart:	n/a
19	chr1:153014367-153014417	HCM	heart:	n/a
20	chr1:153013573-153013623	HCF	heart:	n/a
21	chr1:153015281-153015331	HEEpiC	esophagus:	n/a
22	chr1:153014956-153015006	SK-N-SH_RA	brain:	n/a
23	chr1:153013830-153013880	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:153015281-153015331	NT2-D1	testis:	n/a
25	chr1:153013573-153013623	AoSMC	blood vessel:	n/a
26	chr1:153013830-153013880	PrEC	prostate:	n/a
27	chr1:153013573-153013623	ProgFib	skin:	n/a
28	chr1:153014310-153014360	GM06990	blood:	n/a
29	chr1:153013573-153013623	HEK293	kidney:	embryo
30	chr1:153014310-153014360	AG09309	skin:	n/a
31	chr1:153013830-153013880	K562	blood:	n/a
32	chr1:153014956-153015006	GM12878	blood:	n/a
33	chr1:153013573-153013623	SK-N-SH_RA	brain:	n/a
34	chr1:153015281-153015331	Jurkat	blood:	n/a
35	chr1:153013830-153013880	HRE	kidney:	n/a
36	chr1:153014310-153014360	GM12878	blood:	n/a
37	chr1:153013830-153013880	HCM	heart:	n/a
38	chr1:153015281-153015331	SK-N-SH	brain:	n/a
39	chr1:153015281-153015331	Hela-S3	cervix:	n/a
40	chr1:153013830-153013880	HEK293	kidney:	embryo
41	chr1:153015281-153015331	AG04449	skin:	fetal
42	chr1:153015281-153015331	PANC-1	pancreas:	n/a
43	chr1:153015281-153015331	AoSMC	blood vessel:	n/a
44	chr1:153014310-153014360	HCT-116	colon:	n/a
45	chr1:153013830-153013880	NHBE	bronchial:	n/a
46	chr1:153013830-153013880	PFSK-1	brain:	n/a
47	chr1:153013830-153013880	GM12892	blood:	n/a
48	chr1:153015281-153015331	SKMC	muscle:	n/a
49	chr1:153014367-153014417	HMEC	breast:	n/a
50	chr1:153014956-153015006	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:152948835..152951226-chr1:153005121..153006755,2	MCF-7	breast:
2	chr1:152999178..153000779-chr1:153005146..153007947,2	MCF-7	breast:
3	chr1:153005373..153007183-chr1:153162991..153164575,2	MCF-7	breast:
4	chr1:152939595..152942578-chr1:153006436..153008080,2	MCF-7	breast:

Variant related genes	Relation type
SPRR2D	TF binding region
SPRR2D	CpG island

Extended variants
information (count: 530 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144314027	chr1:153006204-153006205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs684305	chr1:153006242-153006243	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs571713764	chr1:153006244-153006245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs512198	chr1:153006245-153006246	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs202030650	chr1:153006301-153006302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs202002169	chr1:153006323-153006324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376124737	chr1:153006343-153006344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184529120	chr1:153006365-153006366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560475668	chr1:153006426-153006427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1415969	chr1:153006448-153006449	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs78181157	chr1:153006451-153006452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148749804	chr1:153006456-153006457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142310723	chr1:153006458-153006459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs946095	chr1:153006470-153006471	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs558420072	chr1:153006478-153006479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572213095	chr1:153006499-153006500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs946096	chr1:153006529-153006530	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs77998899	chr1:153006568-153006569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs588449	chr1:153006627-153006628	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs145872999	chr1:153006636-153006637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373740781	chr1:153006641-153006642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567791137	chr1:153006692-153006693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562835431	chr1:153006694-153006695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs79997340	chr1:153006718-153006719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545687750	chr1:153006738-153006739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565298082	chr1:153006750-153006751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2937263	chr1:153006756-153006757	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs382653	chr1:153006761-153006762	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs561466877	chr1:153006779-153006780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs139496001	chr1:153006812-153006813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550244630	chr1:153006831-153006832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570067892	chr1:153006871-153006872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs451939	chr1:153006877-153006878	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs419721	chr1:153006902-153006903	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs552611128	chr1:153006905-153006906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565706521	chr1:153006914-153006915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143535050	chr1:153006921-153006922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554355157	chr1:153006979-153006980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10494283	chr1:153007000-153007001	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs536648051	chr1:153007038-153007039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556495149	chr1:153007097-153007098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146758526	chr1:153007103-153007104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs407103	chr1:153007106-153007107	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs34570995	chr1:153007112-153007113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565594177	chr1:153007131-153007132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78361206	chr1:153007176-153007177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188956323	chr1:153007178-153007179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561364647	chr1:153007185-153007186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530168328	chr1:153007206-153007207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550305754	chr1:153007215-153007216	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153003200-153008200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr1:153003400-153006200	Flanking Active TSS	NHEK	skin
3	chr1:153004800-153007400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:153005400-153007800	Enhancers	HMEC	breast
5	chr1:153005600-153007800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:153005800-153006200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:153006200-153008200	Enhancers	NHEK	skin
8	chr1:153007800-153008200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:153007800-153009200	Weak transcription	HMEC	breast
10	chr1:153007800-153013400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:153008200-153013200	Weak transcription	NHEK	skin
12	chr1:153012200-153013400	Weak transcription	HMEC	breast
13	chr1:153013000-153013400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:153013000-153015800	Enhancers	K562	blood
15	chr1:153013200-153014400	Enhancers	NHEK	skin
16	chr1:153013400-153013800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:153013400-153014000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:153013400-153014400	Enhancers	HMEC	breast
19	chr1:153013400-153015800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:153013600-153014600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:153013800-153014000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:153013800-153014200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:153014000-153015200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:153014400-153014800	Weak transcription	NHEK	skin
25	chr1:153014400-153015000	Weak transcription	HMEC	breast
26	chr1:153014800-153015800	Enhancers	NHEK	skin
27	chr1:153015000-153015200	Enhancers	HMEC	breast
28	chr1:153015200-153015800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:153015400-153015800	Enhancers	Placenta	Placenta
30	chr1:153015800-153016400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:153015800-153016400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:153015800-153018000	Weak transcription	NHEK	skin
33	chr1:153016400-153016600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr1:153016400-153016600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr1:153016600-153018000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links