Variant report

Variant	nsv522255
Chromosome Location	chr1:175827683-175849898
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:117)
CpG islands
(count:123)
Chromatin interactive
region (count:10)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:117 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:175844611-175844616	K562	blood:	n/a	n/a
2	ATF2	chr1:175834360-175834859	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr1:175834476-175834918	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:175829768-175829786	K562	blood:	n/a	n/a
5	BHLHE40	chr1:175847950-175848303	HepG2	liver:	n/a	n/a
6	BHLHE40	chr1:175847509-175847534	K562	blood:	n/a	n/a
7	BHLHE40	chr1:175842584-175842692	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:175847940-175848287	K562	blood:	n/a	n/a
9	BRCA1	chr1:175834428-175835071	H1-hESC	embryonic stem cell:	n/a	chr1:175834556-175834563
10	CEBPB	chr1:175835485-175835732	A549	lung:	n/a	n/a
11	CEBPB	chr1:175847953-175848175	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:175834045-175834921	H1-hESC	embryonic stem cell:	n/a	chr1:175834462-175834479 chr1:175834257-175834269
13	CHD2	chr1:175834292-175834892	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr1:175834308-175834885	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr1:175833486-175833566	MCF-7	breast:	n/a	n/a
16	CTCF	chr1:175834640-175834790	WERI-Rb-1	eye:	n/a	chr1:175834711-175834719
17	CTCF	chr1:175834712-175834735	MCF-7	breast:	n/a	n/a
18	CTCF	chr1:175848977-175849030	Lung_OC	lung:	n/a	n/a
19	CTCF	chr1:175833460-175833610	GM12865	blood:	n/a	n/a
20	CTCF	chr1:175834622-175834806	H1-hESC	embryonic stem cell:	n/a	chr1:175834711-175834719
21	CTCF	chr1:175846317-175846378	MCF-7	breast:	n/a	chr1:175846326-175846334
22	CTCF	chr1:175833513-175833577	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr1:175833496-175833560	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr1:175833486-175833568	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:175834580-175834864	H1-hESC	embryonic stem cell:	n/a	chr1:175834711-175834719
26	CTCF	chr1:175834736-175834738	MCF-7	breast:	n/a	n/a
27	CTCF	chr1:175834640-175834790	MCF-7	breast:	n/a	chr1:175834711-175834719
28	CTCF	chr1:175833487-175833596	GM19238	blood:	n/a	n/a
29	CTCF	chr1:175828890-175828965	LNCaP	prostate:	n/a	n/a
30	CTCF	chr1:175833532-175833550	MCF-7	breast:	n/a	n/a
31	CTCF	chr1:175833380-175833530	HEK293	kidney:	n/a	n/a
32	CTCF	chr1:175833511-175833559	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:175827754-175827816	GM10266	blood:	n/a	n/a
34	CTCF	chr1:175834503-175834816	H1-hESC	embryonic stem cell:	n/a	chr1:175834711-175834719
35	CTCF	chr1:175846334-175846359	GM19239	blood:	n/a	n/a
36	CUX1	chr1:175842476-175842819	GM12878	blood:	n/a	n/a
37	E2F4	chr1:175843242-175843640	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F6	chr1:175834249-175834967	H1-hESC	embryonic stem cell:	n/a	n/a
39	EBF1	chr1:175842353-175842840	GM12878	blood:	n/a	chr1:175842628-175842641 chr1:175842630-175842639
40	EBF1	chr1:175842404-175842874	GM12878	blood:	n/a	chr1:175842628-175842641 chr1:175842630-175842639
41	EBF1	chr1:175842301-175842943	GM12878	blood:	n/a	chr1:175842628-175842641 chr1:175842630-175842639
42	EP300	chr1:175834347-175834845	H1-hESC	embryonic stem cell:	n/a	chr1:175834466-175834480
43	EP300	chr1:175842376-175842721	GM12878	blood:	n/a	n/a
44	EP300	chr1:175849816-175851904	SK-N-SH	brain:	n/a	chr1:175850646-175850653 chr1:175850600-175850610
45	FAM48A	chr1:175835444-175835579	GM12878	blood:	n/a	n/a
46	FOS	chr1:175847682-175847773	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr1:175843272-175843627	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr1:175843219-175843705	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:175847639-175848202	MCF10A-Er-Src	breast:	n/a	chr1:175847862-175847872 chr1:175847859-175847870
50	FOS	chr1:175843340-175843540	MCF10A-Er-Src	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:175834835-175834885	HMEC	breast:	n/a
2	chr1:175834835-175834885	HMEC	breast:	n/a
3	chr1:175834835-175834885	T-47D	breast:	n/a
4	chr1:175834835-175834885	SK-N-SH	brain:	n/a
5	chr1:175832735-175832785	NHDF-neo	bronchial:	n/a
6	chr1:175832735-175832785	IMR90	lung:	fetal
7	chr1:175834835-175834885	GM12878	blood:	n/a
8	chr1:175834835-175834885	HCPEpiC	choroid plexus:	n/a
9	chr1:175832735-175832785	Hela-S3	cervix:	n/a
10	chr1:175832735-175832785	SKMC	muscle:	n/a
11	chr1:175832735-175832785	ovcar-3	ovarian:	n/a
12	chr1:175832735-175832785	Hepatocyte	liver:	n/a
13	chr1:175832735-175832785	GM12891	blood:	n/a
14	chr1:175834835-175834885	GM06990	blood:	n/a
15	chr1:175834835-175834885	HEEpiC	esophagus:	n/a
16	chr1:175834835-175834885	RPTEC	kidney:	n/a
17	chr1:175834835-175834885	Caco-2	colon:	n/a
18	chr1:175832735-175832785	SK-N-SH	brain:	n/a
19	chr1:175834835-175834885	AG04449	skin:	fetal
20	chr1:175832735-175832785	AG04450	lung:	fetal
21	chr1:175832735-175832785	K562	blood:	n/a
22	chr1:175834835-175834885	U87	brain:	n/a
23	chr1:175832735-175832785	SAEC	small airway:	n/a
24	chr1:175834835-175834885	AG09319	gingival:	n/a
25	chr1:175834835-175834885	CMK	blood:	n/a
26	chr1:175834835-175834885	IMR90	lung:	fetal
27	chr1:175832735-175832785	HEK293	kidney:	embryo
28	chr1:175834835-175834885	MCF-7	breast:	n/a
29	chr1:175832735-175832785	GM19239	blood:	n/a
30	chr1:175832735-175832785	AoSMC	blood vessel:	n/a
31	chr1:175834835-175834885	HCF	heart:	n/a
32	chr1:175832735-175832785	HIPEpiC	eye:	n/a
33	chr1:175832735-175832785	AG10803	skin:	n/a
34	chr1:175832735-175832785	HCF	heart:	n/a
35	chr1:175832735-175832785	RPTEC	kidney:	n/a
36	chr1:175834835-175834885	Jurkat	blood:	n/a
37	chr1:175832735-175832785	GM06990	blood:	n/a
38	chr1:175834835-175834885	AG10803	skin:	n/a
39	chr1:175832735-175832785	NT2-D1	testis:	n/a
40	chr1:175832735-175832785	A549	lung:	n/a
41	chr1:175834835-175834885	PFSK-1	brain:	n/a
42	chr1:175832735-175832785	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:175832735-175832785	Caco-2	colon:	n/a
44	chr1:175832735-175832785	HRPEpiC	eye:	n/a
45	chr1:175834835-175834885	PANC-1	pancreas:	n/a
46	chr1:175834835-175834885	H1-hESC	embryonic stem cell:	embryo
47	chr1:175832735-175832785	GM12878	blood:	n/a
48	chr1:175832735-175832785	H1-hESC	embryonic stem cell:	embryo
49	chr1:175834835-175834885	HCT-116	colon:	n/a
50	chr1:175832735-175832785	HNPCEpiC	eye:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:175840723..175842476-chr1:175845280..175846892,2	K562	blood:
2	chr1:175830385..175834328-chr1:175834992..175839373,5	K562	blood:
3	chr1:175822157..175824950-chr1:175834242..175836093,2	MCF-7	breast:
4	chr1:175834477..175835136-chr1:175856790..175857390,2	MCF-7	breast:
5	chr1:175843437..175845524-chr1:175846686..175849178,2	MCF-7	breast:
6	chr1:175836721..175839174-chr1:175839948..175842188,2	K562	blood:
7	chr1:175836721..175839174-chr1:175839948..175842188,2	K562	blood:
8	chr1:175830385..175834328-chr1:175834992..175839373,5	K562	blood:
9	chr1:175843437..175845524-chr1:175846686..175849178,2	MCF-7	breast:
10	chr1:175842526..175844262-chr1:175844858..175846890,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAPPA2-3	chr1:175847951-175849237	XLOC_000470
2	lnc-TNR-5	chr1:175833329-175833467	NONHSAT007760
3	lnc-PAPPA2-3	chr1:175846479-175846730	XLOC_000470
4	lnc-PAPPA2-3	chr1:175849335-175849604	XLOC_000470

No data

Variant related genes	Relation type
ENSG00000224718	TF binding region
ENSG00000224718	CpG island
ENSG00000224718	chromatin interactions
IRF4	miRNA target sites
ARID3B	miRNA target sites

Extended variants
information (count: 847 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:847 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11810084	chr1:175827683-175827684	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536869686	chr1:175827715-175827716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532650453	chr1:175827758-175827759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545927554	chr1:175827813-175827814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187063821	chr1:175827829-175827830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150170130	chr1:175827852-175827853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116217260	chr1:175827858-175827859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567593668	chr1:175827870-175827871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578041915	chr1:175827872-175827873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs36063113	chr1:175827874-175827875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529919010	chr1:175827884-175827885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4652132	chr1:175827920-175827921	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs569509355	chr1:175827962-175827963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190374384	chr1:175828019-175828020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375870361	chr1:175828023-175828024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558273023	chr1:175828025-175828026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565421922	chr1:175828036-175828037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11802080	chr1:175828039-175828040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs472862	chr1:175828106-175828107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182839613	chr1:175828117-175828118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11802096	chr1:175828141-175828142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs535551623	chr1:175828150-175828151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs473002	chr1:175828161-175828162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs138691441	chr1:175828170-175828171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546167280	chr1:175828195-175828196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148934761	chr1:175828278-175828279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10913087	chr1:175828386-175828387	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs147043758	chr1:175828400-175828401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138379633	chr1:175828451-175828452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143935938	chr1:175828469-175828470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549854533	chr1:175828474-175828475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112385239	chr1:175828510-175828511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532046289	chr1:175828523-175828524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369486534	chr1:175828700-175828701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187136361	chr1:175828712-175828713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565461544	chr1:175828731-175828732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs58613222	chr1:175828776-175828777	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs548384862	chr1:175828781-175828782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11589791	chr1:175828785-175828786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190096542	chr1:175828824-175828825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537646983	chr1:175828875-175828876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560270	chr1:175828877-175828878	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs577447840	chr1:175828889-175828890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12094484	chr1:175828899-175828900	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs141557262	chr1:175828976-175828977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573390813	chr1:175829033-175829034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542301314	chr1:175829038-175829039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72711119	chr1:175829080-175829081	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs11810955	chr1:175829097-175829098	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs543589866	chr1:175829284-175829285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	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
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
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175815800-175830400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:175822600-175829800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:175825400-175827800	Enhancers	Fetal Brain Male	brain
4	chr1:175825600-175827800	Enhancers	Brain Cingulate Gyrus	brain
5	chr1:175825600-175827800	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr1:175825800-175827800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:175826600-175831800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr1:175827200-175830000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr1:175827400-175827800	Enhancers	Brain Anterior Caudate	brain
10	chr1:175827400-175830400	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr1:175827400-175830400	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr1:175827400-175831000	Weak transcription	Brain Germinal Matrix	brain
13	chr1:175827400-175831600	Weak transcription	Brain Angular Gyrus	brain
14	chr1:175827400-175831600	Weak transcription	Brain Hippocampus Middle	brain
15	chr1:175827400-175831600	Weak transcription	Brain Substantia Nigra	brain
16	chr1:175827400-175832800	Weak transcription	Fetal Brain Female	brain
17	chr1:175827600-175832000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr1:175827800-175831400	Weak transcription	Brain Anterior Caudate	brain
19	chr1:175827800-175831600	Weak transcription	Brain Cingulate Gyrus	brain
20	chr1:175827800-175831600	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr1:175827800-175831800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:175827800-175831800	Weak transcription	Fetal Brain Male	brain
23	chr1:175828400-175831000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr1:175828800-175829000	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr1:175828800-175830600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:175829200-175830400	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr1:175829800-175830800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:175829800-175830800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:175829800-175835000	Enhancers	Fetal Intestine Large	intestine
30	chr1:175830000-175830600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:175830200-175830600	Enhancers	H9 Cell Line	embryonic stem cell
32	chr1:175830400-175830600	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr1:175830400-175830800	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr1:175830400-175831000	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr1:175830400-175831000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:175830400-175831600	Enhancers	H1 Cell Line	embryonic stem cell
37	chr1:175830400-175832600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr1:175830400-175834800	Enhancers	Fetal Intestine Small	intestine
39	chr1:175830600-175830800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:175830600-175831400	Enhancers	GM12878-XiMat	blood
41	chr1:175830600-175831600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr1:175830600-175831600	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr1:175830600-175831600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr1:175830600-175832600	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr1:175830800-175831600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr1:175830800-175831800	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr1:175830800-175832000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:175830800-175832200	Enhancers	Duodenum Mucosa	Duodenum
49	chr1:175830800-175833000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr1:175830800-175834000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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