Variant report

Variant	esv3393504
Chromosome Location	chr1:155190128-155194426
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	chr1:155192881-155193170	K562	blood:	n/a	n/a
2	ATF3	chr1:155194392-155194847	K562	blood:	n/a	n/a
3	BDP1	chr1:155193690-155194244	Hela-S3	cervix:	n/a	chr1:155193724-155193737
4	BHLHE40	chr1:155193025-155193187	K562	blood:	n/a	n/a
5	BRCA1	chr1:155193712-155193748	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:155194010-155195055	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:155188676-155190182	Hela-S3	cervix:	n/a	chr1:155189137-155189148
8	CTCF	chr1:155192380-155192530	GM12864	blood:	n/a	n/a
9	CTCF	chr1:155192340-155192490	GM12874	blood:	n/a	n/a
10	CTCF	chr1:155192340-155192490	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr1:155192260-155192410	GM06990	blood:	n/a	n/a
12	CTCF	chr1:155192320-155192470	GM12872	blood:	n/a	n/a
13	CTCF	chr1:155192360-155192510	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr1:155192320-155192470	GM12869	blood:	n/a	n/a
15	CTCF	chr1:155192340-155192490	GM12873	blood:	n/a	n/a
16	CUX1	chr1:155193142-155193167	K562	blood:	n/a	n/a
17	ELK1	chr1:155193108-155193170	GM12878	blood:	n/a	n/a
18	ELK1	chr1:155193809-155193830	GM12878	blood:	n/a	n/a
19	ELK1	chr1:155193614-155193626	Hela-S3	cervix:	n/a	n/a
20	EP300	chr1:155194160-155194872	K562	blood:	n/a	chr1:155194634-155194643
21	FOS	chr1:155192245-155192258	MCF10A-Er-Src	breast:	n/a	n/a
22	FOSL1	chr1:155194392-155194756	K562	blood:	n/a	chr1:155194634-155194644 chr1:155194635-155194643 chr1:155194635-155194643 chr1:155194633-155194644 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194636-155194643
23	FOSL2	chr1:155194349-155194920	MCF-7	breast:	n/a	chr1:155194634-155194644 chr1:155194635-155194643 chr1:155194635-155194643 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194636-155194643
24	FOSL2	chr1:155194375-155195077	A549	lung:	n/a	chr1:155195055-155195065 chr1:155194634-155194644 chr1:155194635-155194643 chr1:155194635-155194643 chr1:155195055-155195065 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194636-155194643
25	GATA2	chr1:155194371-155194927	HUVEC	blood vessel:	n/a	n/a
26	GATA3	chr1:155194242-155195058	A549	lung:	n/a	n/a
27	GATA3	chr1:155194317-155194946	MCF-7	breast:	n/a	n/a
28	GATA3	chr1:155194178-155195058	MCF-7	breast:	n/a	chr1:155194228-155194235 chr1:155194223-155194239 chr1:155194223-155194239 chr1:155194228-155194235 chr1:155194226-155194235 chr1:155194221-155194242 chr1:155194228-155194235 chr1:155194226-155194236
29	GATA3	chr1:155194393-155194885	T-47D	breast:	n/a	n/a
30	GATA3	chr1:155194240-155195096	SK-N-SH	brain:	n/a	n/a
31	GATA3	chr1:155194394-155194876	T-47D	breast:	n/a	n/a
32	GATA3	chr1:155194296-155195097	SK-N-SH	brain:	n/a	n/a
33	GTF2F1	chr1:155193918-155195066	Hela-S3	cervix:	n/a	n/a
34	HCFC1	chr1:155188551-155190331	Hela-S3	cervix:	n/a	n/a
35	IRF1	chr1:155192930-155193196	K562	blood:	n/a	n/a
36	JUN	chr1:155194420-155195062	Hela-S3	cervix:	n/a	chr1:155194634-155194644 chr1:155194635-155194643 chr1:155194635-155194643 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194636-155194643
37	JUN	chr1:155193365-155195785	K562	blood:	n/a	chr1:155195055-155195065 chr1:155194634-155194644 chr1:155194635-155194643 chr1:155194635-155194643 chr1:155195055-155195065 chr1:155194634-155194644 chr1:155195420-155195432 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194636-155194643
38	JUND	chr1:155194307-155195014	SK-N-SH	brain:	n/a	chr1:155194634-155194644 chr1:155194635-155194643 chr1:155194635-155194643 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194633-155194644 chr1:155194634-155194644 chr1:155194636-155194643
39	JUND	chr1:155194335-155195240	SK-N-SH	brain:	n/a	chr1:155195055-155195065 chr1:155194634-155194644 chr1:155194635-155194643 chr1:155194635-155194643 chr1:155195055-155195065 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194633-155194644 chr1:155194634-155194644 chr1:155194636-155194643
40	JUND	chr1:155194375-155194963	SK-N-SH	brain:	n/a	chr1:155194634-155194644 chr1:155194635-155194643 chr1:155194635-155194643 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194633-155194644 chr1:155194634-155194644 chr1:155194636-155194643
41	JUND	chr1:155192857-155193241	K562	blood:	n/a	n/a
42	JUND	chr1:155194382-155194911	T-47D	breast:	n/a	chr1:155194634-155194644 chr1:155194635-155194643 chr1:155194635-155194643 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194633-155194644 chr1:155194634-155194644 chr1:155194636-155194643
43	JUND	chr1:155194151-155194951	K562	blood:	n/a	chr1:155194634-155194644 chr1:155194635-155194643 chr1:155194635-155194643 chr1:155194634-155194644 chr1:155194634-155194644 chr1:155194633-155194644 chr1:155194634-155194644 chr1:155194636-155194643
44	MAFF	chr1:155193011-155193248	K562	blood:	n/a	n/a
45	MAFK	chr1:155192978-155193178	K562	blood:	n/a	n/a
46	MAX	chr1:155194390-155195004	MCF-7	breast:	n/a	n/a
47	MAX	chr1:155194368-155194942	A549	lung:	n/a	n/a
48	MAX	chr1:155194388-155194827	SK-N-SH	brain:	n/a	n/a
49	MAZ	chr1:155193036-155193075	K562	blood:	n/a	n/a
50	MEF2A	chr1:155192840-155193198	K562	blood:	n/a	chr1:155193022-155193037 chr1:155193023-155193037

No.	Distal block	Cell Line	Cell type
1	chr1:155192189..155193749-chr1:155195303..155196996,2	MCF-7	breast:
2	chr1:155190873..155193241-chr1:155231143..155233279,2	MCF-7	breast:
3	chr1:155170199..155172108-chr1:155187853..155191276,3	MCF-7	breast:
4	chr1:155187443..155190276-chr1:155193102..155195669,3	K562	blood:
5	chr1:155162028..155164533-chr1:155190701..155192344,2	MCF-7	breast:
6	chr1:155189654..155191436-chr1:155193964..155195496,2	K562	blood:
7	chr1:155186661..155189522-chr1:155194169..155197986,6	K562	blood:
8	chr1:155187302..155192095-chr1:155195846..155198767,7	MCF-7	breast:
9	chr1:155194186..155196114-chr1:155247004..155249508,2	MCF-7	breast:
10	chr1:155188805..155190957-chr1:155195706..155197646,3	K562	blood:
11	chr1:155193544..155197336-chr1:155293049..155296583,5	MCF-7	breast:
12	chr1:155187157..155191331-chr1:155209670..155212928,5	MCF-7	breast:
13	chr1:155162153..155164913-chr1:155193095..155194598,2	MCF-7	breast:
14	chr1:155143901..155153030-chr1:155191166..155199183,23	MCF-7	breast:
15	chr1:155186477..155191173-chr1:155191711..155194571,4	MCF-7	breast:
16	chr1:155143241..155145865-chr1:155194153..155197077,2	MCF-7	breast:
17	chr1:155175944..155179285-chr1:155187472..155192193,6	MCF-7	breast:
18	chr1:155155866..155157645-chr1:155191595..155193213,2	MCF-7	breast:
19	chr1:155145152..155147163-chr1:155193032..155194544,2	K562	blood:
20	chr1:155160177..155166575-chr1:155191666..155199927,14	MCF-7	breast:
21	chr1:155189654..155191436-chr1:155193964..155195496,2	K562	blood:
22	chr1:155192655..155194574-chr1:155230487..155232931,2	MCF-7	breast:
23	chr1:155174590..155181850-chr1:155192419..155201858,28	K562	blood:
24	chr1:155175739..155181576-chr1:155185947..155190429,10	K562	blood:
25	chr1:155191881..155194028-chr1:155195597..155197149,2	MCF-7	breast:
26	chr1:155174605..155182734-chr1:155187211..155200915,43	MCF-7	breast:
27	chr1:155193150..155195582-chr1:155212833..155215072,2	MCF-7	breast:
28	chr1:155193188..155195403-chr1:155211959..155214156,2	K562	blood:

Variant related genes	Relation type
GBAP1	TF binding region
ENSG00000271748	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000231064	chromatin interactions
ENSG00000173171	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000116521	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000143630	chromatin interactions
ENSG00000169231	chromatin interactions
ENSG00000163462	chromatin interactions
ENSG00000163463	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000185499	chromatin interactions

Extended variants
information (count: 150 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:150 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181369369	chr1:155190139-155190140	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs374423676	chr1:155190156-155190157	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs551007795	chr1:155190169-155190170	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs369272653	chr1:155190230-155190231	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs2990220	chr1:155190254-155190255	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs113690547	chr1:155190282-155190283	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs554985890	chr1:155190290-155190291	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs566802992	chr1:155190291-155190292	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs185646701	chr1:155190292-155190293	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs565889116	chr1:155190306-155190307	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs558723528	chr1:155190390-155190391	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs576976194	chr1:155190409-155190410	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs574466171	chr1:155190470-155190471	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs190013098	chr1:155190480-155190481	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs533503106	chr1:155190493-155190494	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs575152227	chr1:155190523-155190524	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs542583037	chr1:155190593-155190594	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs561060387	chr1:155190611-155190612	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs528388681	chr1:155190627-155190628	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs540482604	chr1:155190644-155190645	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs534886077	chr1:155190660-155190661	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs182610327	chr1:155190686-155190687	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs532307268	chr1:155190758-155190759	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs375946963	chr1:155190821-155190822	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs550812120	chr1:155190822-155190823	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs199812111	chr1:155190825-155190826	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs569308454	chr1:155190866-155190867	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs530068050	chr1:155190879-155190880	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs372903192	chr1:155190891-155190892	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs548547408	chr1:155190897-155190898	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs187211825	chr1:155190913-155190914	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs534223044	chr1:155190988-155190989	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs558784971	chr1:155191040-155191041	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs540161538	chr1:155191052-155191053	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs538404929	chr1:155191125-155191126	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs556804571	chr1:155191139-155191140	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs575280654	chr1:155191164-155191165	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs542300932	chr1:155191173-155191174	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs554604305	chr1:155191189-155191190	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs572831849	chr1:155191210-155191211	Weak transcription Enhancers Strong transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs540545757	chr1:155191221-155191222	Weak transcription Enhancers Strong transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs558469028	chr1:155191245-155191246	Weak transcription Enhancers Strong transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs578175733	chr1:155191292-155191293	Weak transcription Enhancers Strong transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs375829879	chr1:155191364-155191365	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs532370146	chr1:155191372-155191373	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs147743808	chr1:155191377-155191378	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs369676960	chr1:155191462-155191463	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs562875866	chr1:155191504-155191505	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs530207486	chr1:155191509-155191510	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs61811946	chr1:155191519-155191520	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	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
Non-syndromic sensorineural hearing loss	15273396	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
Ewing''s sarcoma	21437220	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
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
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
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
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155179600-155195400	Weak transcription	Aorta	Aorta
2	chr1:155179600-155195800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:155179600-155196200	Weak transcription	Pancreas	Pancrea
4	chr1:155179600-155196600	Weak transcription	Gastric	stomach
5	chr1:155179600-155196600	Weak transcription	Small Intestine	intestine
6	chr1:155179800-155193800	Weak transcription	HSMMtube	muscle
7	chr1:155180000-155194000	Weak transcription	HUVEC	blood vessel
8	chr1:155180000-155195600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr1:155180200-155194000	Weak transcription	HSMM	muscle
10	chr1:155180600-155195600	Weak transcription	HepG2	liver
11	chr1:155182200-155195800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr1:155182200-155196400	Weak transcription	Esophagus	oesophagus
13	chr1:155182200-155196600	Weak transcription	Lung	lung
14	chr1:155182600-155196200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr1:155182800-155194800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr1:155182800-155194800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:155182800-155196400	Weak transcription	Left Ventricle	heart
18	chr1:155186000-155195200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr1:155186600-155193000	Weak transcription	A549	lung
20	chr1:155186800-155193600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:155186800-155193600	Weak transcription	Fetal Muscle Leg	muscle
22	chr1:155186800-155193600	Weak transcription	Thymus	Thymus
23	chr1:155187800-155190800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr1:155187800-155196000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr1:155188000-155193800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:155188400-155191000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:155188600-155196600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr1:155188800-155190600	Enhancers	Duodenum Mucosa	Duodenum
29	chr1:155188800-155190800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr1:155188800-155190800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr1:155188800-155191000	Enhancers	Primary hematopoietic stem cells	blood
32	chr1:155189000-155190400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr1:155189000-155190600	Enhancers	Primary T cells fromperipheralblood	blood
34	chr1:155189000-155190800	Enhancers	Stomach Mucosa	stomach
35	chr1:155189000-155191000	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr1:155189200-155190800	Enhancers	Primary T cells from cord blood	blood
37	chr1:155189200-155192000	Weak transcription	Primary B cells from peripheral blood	blood
38	chr1:155189200-155196000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:155189200-155196200	Enhancers	Primary B cells from cord blood	blood
40	chr1:155189400-155190600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:155189400-155190600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr1:155189400-155192800	Weak transcription	Fetal Stomach	stomach
43	chr1:155189400-155193600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr1:155189400-155193600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr1:155189400-155194000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr1:155189400-155194000	Weak transcription	NH-A	brain
47	chr1:155189400-155195400	Weak transcription	Liver	Liver
48	chr1:155189400-155195400	Weak transcription	Fetal Muscle Trunk	muscle
49	chr1:155189400-155195800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr1:155189400-155196000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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