Variant report

Variant	nsv945291
Chromosome Location	chr1:215717059-215737649
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:71)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:71 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:215731313-215731767	HepG2	liver:	n/a	n/a
2	BRCA1	chr1:215721111-215721310	Hela-S3	cervix:	n/a	n/a
3	CBX3	chr1:215733994-215734308	K562	blood:	n/a	n/a
4	CBX3	chr1:215728884-215729225	K562	blood:	n/a	n/a
5	CBX3	chr1:215728870-215729255	K562	blood:	n/a	n/a
6	CEBPB	chr1:215732852-215733011	K562	blood:	n/a	n/a
7	CEBPB	chr1:215725518-215725587	A549	lung:	n/a	n/a
8	CHD2	chr1:215730343-215730519	HepG2	liver:	n/a	n/a
9	CTCF	chr1:215725370-215725401	Lung_OC	lung:	n/a	n/a
10	CTCF	chr1:215725363-215725365	Lung_OC	lung:	n/a	n/a
11	EP300	chr1:215719502-215719505	K562	blood:	n/a	n/a
12	EP300	chr1:215717865-215718255	SK-N-SH_RA	brain:	n/a	n/a
13	EP300	chr1:215717950-215718275	SK-N-SH_RA	brain:	n/a	n/a
14	FOXA1	chr1:215731299-215731813	HepG2	liver:	n/a	n/a
15	FOXA2	chr1:215731350-215731709	HepG2	liver:	n/a	n/a
16	GATA3	chr1:215718170-215718876	MCF-7	breast:	n/a	chr1:215718531-215718541 chr1:215718522-215718539
17	GATA3	chr1:215718302-215718371	SH-SY5Y	brain:	n/a	n/a
18	GATA3	chr1:215718030-215718813	MCF-7	breast:	n/a	chr1:215718531-215718541 chr1:215718522-215718539
19	GATA3	chr1:215717763-215717894	SH-SY5Y	brain:	n/a	chr1:215717788-215717795
20	HDAC2	chr1:215731401-215731739	HepG2	liver:	n/a	n/a
21	HEY1	chr1:215730558-215730816	HepG2	liver:	n/a	n/a
22	IRF3	chr1:215718499-215718544	GM12878	blood:	n/a	n/a
23	JUN	chr1:215728889-215729122	K562	blood:	n/a	n/a
24	KAP1	chr1:215728636-215729380	K562	blood:	n/a	n/a
25	KAP1	chr1:215728910-215729091	U2OS	brain:	n/a	n/a
26	MAFF	chr1:215728235-215728583	K562	blood:	n/a	chr1:215728394-215728412
27	MAFF	chr1:215728234-215728584	HepG2	liver:	n/a	chr1:215728394-215728412
28	MAFK	chr1:215728229-215728587	HepG2	liver:	n/a	chr1:215728396-215728411
29	MAFK	chr1:215728237-215728553	K562	blood:	n/a	chr1:215728396-215728411
30	MAFK	chr1:215728227-215728590	HepG2	liver:	n/a	chr1:215728396-215728411
31	MAFK	chr1:215728238-215728585	IMR90	lung:	n/a	chr1:215728396-215728411
32	MAFK	chr1:215728247-215728581	Hela-S3	cervix:	n/a	chr1:215728396-215728411
33	MYC	chr1:215730463-215730520	MCF-7	breast:	n/a	n/a
34	NFIC	chr1:215731257-215731716	HepG2	liver:	n/a	n/a
35	POLR2A	chr1:215729933-215729957	MCF-7	breast:	n/a	n/a
36	POLR2A	chr1:215730411-215730456	A549	lung:	n/a	n/a
37	POLR2A	chr1:215730119-215730248	MCF-7	breast:	n/a	n/a
38	POLR2A	chr1:215729947-215729953	MCF-7	breast:	n/a	n/a
39	POLR2A	chr1:215736885-215736982	MCF-7	breast:	n/a	n/a
40	POLR2A	chr1:215730392-215730399	A549	lung:	n/a	n/a
41	POLR2A	chr1:215720123-215720146	ProgFib	skin:	n/a	n/a
42	POLR2A	chr1:215718112-215718253	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr1:215730036-215730487	MCF-7	breast:	n/a	n/a
44	POLR2A	chr1:215730064-215730081	MCF-7	breast:	n/a	n/a
45	POLR2A	chr1:215734409-215734419	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr1:215728411-215728537	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr1:215730043-215730058	MCF-7	breast:	n/a	n/a
48	POLR2A	chr1:215730534-215730591	MCF-7	breast:	n/a	n/a
49	POLR2A	chr1:215730374-215730386	A549	lung:	n/a	n/a
50	POLR2A	chr1:215730028-215730032	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	chr1:215737048-215737098	HRE	kidney:	n/a
2	chr1:215737048-215737098	SKMC	muscle:	n/a
3	chr1:215737048-215737098	SK-N-SH	brain:	n/a
4	chr1:215737048-215737098	BE2_C	brain:	n/a
5	chr1:215737048-215737098	HRCEpiC	kidney:	n/a
6	chr1:215737048-215737098	GM12891	blood:	n/a
7	chr1:215737048-215737098	NHDF-neo	bronchial:	n/a
8	chr1:215737048-215737098	RPTEC	kidney:	n/a
9	chr1:215737048-215737098	GM06990	blood:	n/a
10	chr1:215737048-215737098	SAEC	small airway:	n/a
11	chr1:215737048-215737098	Caco-2	colon:	n/a
12	chr1:215737048-215737098	PFSK-1	brain:	n/a
13	chr1:215737048-215737098	Jurkat	blood:	n/a
14	chr1:215737048-215737098	IMR90	lung:	fetal
15	chr1:215737048-215737098	BJ	skin:	n/a
16	chr1:215737048-215737098	AG10803	skin:	n/a
17	chr1:215737048-215737098	HIPEpiC	eye:	n/a
18	chr1:215737048-215737098	NT2-D1	testis:	n/a
19	chr1:215737048-215737098	HUVEC	blood vessel:	n/a
20	chr1:215737048-215737098	CMK	blood:	n/a
21	chr1:215737048-215737098	HAEpiC	amniotic membrane:	n/a
22	chr1:215737048-215737098	Hepatocyte	liver:	n/a
23	chr1:215737048-215737098	HepG2	liver:	n/a
24	chr1:215737048-215737098	GM12878	blood:	n/a
25	chr1:215737048-215737098	PANC-1	pancreas:	n/a
26	chr1:215737048-215737098	AG09309	skin:	n/a
27	chr1:215737048-215737098	PrEC	prostate:	n/a
28	chr1:215737048-215737098	H1-hESC	embryonic stem cell:	embryo
29	chr1:215737048-215737098	HRPEpiC	eye:	n/a
30	chr1:215737048-215737098	AG04450	lung:	fetal
31	chr1:215737048-215737098	ECC-1	luminal epithelium:	n/a
32	chr1:215737048-215737098	HNPCEpiC	eye:	n/a
33	chr1:215737048-215737098	ProgFib	skin:	n/a
34	chr1:215737048-215737098	GM12892	blood:	n/a
35	chr1:215737048-215737098	MCF-7	breast:	n/a
36	chr1:215737048-215737098	AG04449	skin:	fetal
37	chr1:215737048-215737098	AoSMC	blood vessel:	n/a
38	chr1:215737048-215737098	T-47D	breast:	n/a
39	chr1:215737048-215737098	NB4	blood:	n/a
40	chr1:215737048-215737098	HMEC	breast:	n/a
41	chr1:215737048-215737098	HEEpiC	esophagus:	n/a
42	chr1:215737048-215737098	SK-N-MC	brain:	n/a
43	chr1:215737048-215737098	A549	lung:	n/a
44	chr1:215737048-215737098	HCF	heart:	n/a
45	chr1:215737048-215737098	ovcar-3	ovarian:	n/a
46	chr1:215737048-215737098	SK-N-SH_RA	brain:	n/a
47	chr1:215737048-215737098	K562	blood:	n/a
48	chr1:215737048-215737098	Hela-S3	cervix:	n/a
49	chr1:215737048-215737098	HEK293	kidney:	embryo
50	chr1:215737048-215737098	HCM	heart:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:215727863..215730220-chr1:215736025..215738063,2	K562	blood:
2	chr1:215718496..215720254-chr1:215739655..215742103,3	MCF-7	breast:
3	chr1:215732968..215735499-chr1:215739364..215742165,4	MCF-7	breast:
4	chr1:215728975..215731835-chr1:215739008..215743111,5	MCF-7	breast:
5	chr1:215727863..215730220-chr1:215736025..215738063,2	K562	blood:
6	chr1:215722423..215725926-chr1:215740211..215742928,3	K562	blood:
7	chr1:215731051..215732589-chr1:215739123..215741939,2	MCF-7	breast:
8	chr1:215655508..215656065-chr1:215718108..215718963,2	MCF-7	breast:
9	chr1:215726004..215728201-chr1:215739965..215741596,2	MCF-7	breast:
10	chr1:215728115..215729776-chr1:215731286..215732796,2	MCF-7	breast:
11	chr1:215735916..215738873-chr1:215738967..215741974,4	MCF-7	breast:
12	chr1:215729059..215730729-chr1:215736109..215738919,2	MCF-7	breast:
13	chr1:215729059..215730729-chr1:215736109..215738919,2	MCF-7	breast:
14	chr1:215727802..215730014-chr1:215737556..215740283,2	K562	blood:
15	chr1:215727802..215730014-chr1:215737556..215740283,2	K562	blood:
16	chr1:215727846..215730896-chr1:215740314..215742858,4	K562	blood:
17	chr1:215728115..215729776-chr1:215731286..215732796,2	MCF-7	breast:
18	chr1:215722423..215724891-chr1:215740211..215742928,2	K562	blood:

No data

Variant related genes	Relation type
KCTD3	TF binding region
KCTD3	CpG island
ENSG00000136636	chromatin interactions

Extended variants
information (count: 629 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:629 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539285450	chr1:215717079-215717080	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116698955	chr1:215717089-215717090	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182324692	chr1:215717105-215717106	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541928491	chr1:215717111-215717112	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555293040	chr1:215717196-215717197	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572152618	chr1:215717247-215717248	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535863591	chr1:215717249-215717250	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541313125	chr1:215717267-215717268	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536256472	chr1:215717296-215717297	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139121008	chr1:215717323-215717324	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556321323	chr1:215717325-215717326	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543624225	chr1:215717343-215717344	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563920774	chr1:215717401-215717402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531388521	chr1:215717436-215717437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117865944	chr1:215717455-215717456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561659040	chr1:215717478-215717479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544978676	chr1:215717492-215717493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74573532	chr1:215717504-215717505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527318780	chr1:215717515-215717516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77670049	chr1:215717605-215717606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547650131	chr1:215717627-215717628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537777196	chr1:215717640-215717641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367815968	chr1:215717654-215717655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547756545	chr1:215717656-215717657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570628544	chr1:215717671-215717672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539737278	chr1:215717683-215717684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549667793	chr1:215717713-215717714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs79762302	chr1:215717743-215717744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143971783	chr1:215717757-215717758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555479251	chr1:215717760-215717761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572092103	chr1:215717761-215717762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150911214	chr1:215717798-215717799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372971066	chr1:215717941-215717942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558153501	chr1:215717942-215717943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139387686	chr1:215717967-215717968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544100514	chr1:215717975-215717976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs377527055	chr1:215717992-215717993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs112554451	chr1:215718023-215718024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186926667	chr1:215718088-215718089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541931674	chr1:215718101-215718102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566232944	chr1:215718150-215718151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546307146	chr1:215718240-215718241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527407049	chr1:215718241-215718242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370388624	chr1:215718294-215718295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs116614268	chr1:215718295-215718296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs376442669	chr1:215718300-215718301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533030153	chr1:215718359-215718360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550093094	chr1:215718444-215718445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190120657	chr1:215718452-215718453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535297641	chr1:215718456-215718457	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	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	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215715000-215719600	Enhancers	Colon Smooth Muscle	Colon
2	chr1:215715800-215717200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:215716000-215717400	Enhancers	Liver	Liver
4	chr1:215716200-215717200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr1:215716200-215717200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr1:215716200-215717200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr1:215716400-215717200	Enhancers	Duodenum Mucosa	Duodenum
8	chr1:215716600-215717800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr1:215716800-215717400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:215717000-215717200	Enhancers	GM12878-XiMat	blood
11	chr1:215717000-215717200	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr1:215717800-215718800	Enhancers	Rectal Smooth Muscle	rectum
13	chr1:215718800-215720200	Weak transcription	Rectal Smooth Muscle	rectum
14	chr1:215719600-215721000	Weak transcription	Colon Smooth Muscle	Colon
15	chr1:215720200-215722000	Enhancers	Rectal Smooth Muscle	rectum
16	chr1:215720800-215721200	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr1:215721000-215721400	Enhancers	Colon Smooth Muscle	Colon
18	chr1:215728600-215730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:215729000-215730400	Weak transcription	Pancreas	Pancrea
20	chr1:215729600-215729800	Enhancers	Duodenum Mucosa	Duodenum
21	chr1:215729600-215731200	ZNF genes & repeats	Fetal Intestine Small	intestine
22	chr1:215729800-215730200	ZNF genes & repeats	Spleen	Spleen
23	chr1:215729800-215730600	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr1:215729800-215730800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:215730000-215730200	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr1:215730000-215730600	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr1:215730000-215732000	Enhancers	Fetal Intestine Large	intestine
28	chr1:215730000-215732000	Enhancers	Stomach Mucosa	stomach
29	chr1:215730200-215730400	Active TSS	Spleen	Spleen
30	chr1:215730200-215730600	Enhancers	HepG2	liver
31	chr1:215730200-215731000	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr1:215730400-215730600	Flanking Active TSS	Spleen	Spleen
33	chr1:215730400-215730800	Enhancers	Pancreas	Pancrea
34	chr1:215730400-215731000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr1:215730400-215732200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:215730600-215730800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr1:215730600-215732000	Flanking Active TSS	HepG2	liver
38	chr1:215730600-215732200	Enhancers	Duodenum Mucosa	Duodenum
39	chr1:215730800-215731800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:215730800-215732000	Enhancers	Liver	Liver
41	chr1:215730800-215740200	Weak transcription	Pancreas	Pancrea
42	chr1:215731000-215731800	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr1:215731200-215731600	Weak transcription	Fetal Intestine Small	intestine
44	chr1:215731800-215732000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr1:215731800-215732000	Enhancers	Fetal Intestine Small	intestine
46	chr1:215732000-215732800	Enhancers	HepG2	liver
47	chr1:215732000-215740200	Weak transcription	Stomach Mucosa	stomach
48	chr1:215732800-215734000	Weak transcription	HepG2	liver

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