Variant report

Variant	nsv872517
Chromosome Location	chr1:166539001-166590046
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:265)
CpG islands
(count:122)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:166549726-166549735	K562	blood:	n/a	n/a
2	ARID3A	chr1:166555984-166555985	K562	blood:	n/a	n/a
3	ARID3A	chr1:166554164-166554757	K562	blood:	n/a	n/a
4	ARID3A	chr1:166567973-166568032	K562	blood:	n/a	n/a
5	ATF1	chr1:166554199-166554710	K562	blood:	n/a	n/a
6	ATF1	chr1:166549456-166549773	K562	blood:	n/a	n/a
7	BACH1	chr1:166583164-166583219	K562	blood:	n/a	n/a
8	BACH1	chr1:166585471-166585771	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:166554084-166554626	K562	blood:	n/a	n/a
10	BACH1	chr1:166585472-166585825	K562	blood:	n/a	n/a
11	BHLHE40	chr1:166548205-166548329	K562	blood:	n/a	n/a
12	BHLHE40	chr1:166554131-166554801	K562	blood:	n/a	n/a
13	CBX3	chr1:166554160-166554714	K562	blood:	n/a	n/a
14	CBX3	chr1:166554065-166554902	K562	blood:	n/a	n/a
15	CCNT2	chr1:166554158-166554688	K562	blood:	n/a	n/a
16	CEBPB	chr1:166572326-166572939	MCF-7	breast:	n/a	chr1:166572450-166572463 chr1:166572452-166572463 chr1:166572452-166572463
17	CEBPB	chr1:166554389-166554670	K562	blood:	n/a	n/a
18	CEBPB	chr1:166584502-166584549	K562	blood:	n/a	n/a
19	CEBPB	chr1:166554114-166554825	K562	blood:	n/a	n/a
20	CEBPB	chr1:166570981-166571218	K562	blood:	n/a	n/a
21	CEBPB	chr1:166551307-166551346	K562	blood:	n/a	n/a
22	CEBPB	chr1:166589724-166589993	K562	blood:	n/a	n/a
23	CEBPB	chr1:166572416-166572866	MCF-7	breast:	n/a	chr1:166572450-166572463 chr1:166572452-166572463 chr1:166572452-166572463
24	CEBPB	chr1:166587229-166587284	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:166554118-166554758	K562	blood:	n/a	n/a
26	CEBPD	chr1:166554144-166554854	K562	blood:	n/a	n/a
27	CEBPD	chr1:166554203-166554831	K562	blood:	n/a	n/a
28	CTCF	chr1:166565980-166566130	GM12878	blood:	n/a	n/a
29	CTCF	chr1:166554142-166554793	K562	blood:	n/a	n/a
30	CTCF	chr1:166587278-166587336	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr1:166552280-166552430	GM12873	blood:	n/a	n/a
32	CTCF	chr1:166554240-166554390	K562	blood:	n/a	n/a
33	CTCF	chr1:166554265-166554352	K562	blood:	n/a	n/a
34	CTCF	chr1:166554168-166554459	K562	blood:	n/a	n/a
35	CUX1	chr1:166582185-166582312	K562	blood:	n/a	n/a
36	CUX1	chr1:166549357-166549673	K562	blood:	n/a	n/a
37	CUX1	chr1:166554102-166554899	K562	blood:	n/a	n/a
38	CUX1	chr1:166574478-166574564	K562	blood:	n/a	n/a
39	E2F4	chr1:166558120-166558538	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr1:166555629-166556082	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr1:166572547-166572893	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F6	chr1:166579805-166579979	K562	blood:	n/a	n/a
43	EGR1	chr1:166572326-166572860	MCF-7	breast:	n/a	n/a
44	EGR1	chr1:166572440-166572910	MCF-7	breast:	n/a	n/a
45	ELF1	chr1:166572385-166572898	MCF-7	breast:	n/a	n/a
46	EP300	chr1:166549355-166549689	K562	blood:	n/a	chr1:166549440-166549447
47	EP300	chr1:166554101-166554822	K562	blood:	n/a	n/a
48	EP300	chr1:166572432-166572956	MCF-7	breast:	n/a	n/a
49	EP300	chr1:166582244-166582413	K562	blood:	n/a	n/a
50	EP300	chr1:166550321-166550409	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:166572716-166572766	AoSMC	blood vessel:	n/a
2	chr1:166572716-166572766	U87	brain:	n/a
3	chr1:166571691-166571741	HCM	heart:	n/a
4	chr1:166571691-166571741	HL-60	blood:	n/a
5	chr1:166572716-166572766	NH-A	brain:	n/a
6	chr1:166572716-166572766	HUVEC	blood vessel:	n/a
7	chr1:166572716-166572766	LNCaP	prostate:	n/a
8	chr1:166572716-166572766	HMEC	breast:	n/a
9	chr1:166571691-166571741	SK-N-MC	brain:	n/a
10	chr1:166571691-166571741	AG09319	gingival:	n/a
11	chr1:166572716-166572766	HepG2	liver:	n/a
12	chr1:166571691-166571741	HEK293	kidney:	embryo
13	chr1:166572716-166572766	A549	lung:	n/a
14	chr1:166571691-166571741	H1-hESC	embryonic stem cell:	embryo
15	chr1:166572716-166572766	IMR90	lung:	fetal
16	chr1:166571691-166571741	HNPCEpiC	eye:	n/a
17	chr1:166571691-166571741	U87	brain:	n/a
18	chr1:166571691-166571741	GM12892	blood:	n/a
19	chr1:166572716-166572766	ProgFib	skin:	n/a
20	chr1:166572716-166572766	GM12892	blood:	n/a
21	chr1:166571691-166571741	A549	lung:	n/a
22	chr1:166572716-166572766	H1-hESC	embryonic stem cell:	embryo
23	chr1:166571691-166571741	HRE	kidney:	n/a
24	chr1:166571691-166571741	AG04450	lung:	fetal
25	chr1:166572716-166572766	AG09309	skin:	n/a
26	chr1:166572716-166572766	GM12878	blood:	n/a
27	chr1:166572716-166572766	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:166571691-166571741	IMR90	lung:	fetal
29	chr1:166572716-166572766	AG04449	skin:	fetal
30	chr1:166572716-166572766	PFSK-1	brain:	n/a
31	chr1:166572716-166572766	Hepatocyte	liver:	n/a
32	chr1:166571691-166571741	ECC-1	luminal epithelium:	n/a
33	chr1:166572716-166572766	NT2-D1	testis:	n/a
34	chr1:166571691-166571741	NHDF-neo	bronchial:	n/a
35	chr1:166571691-166571741	GM12891	blood:	n/a
36	chr1:166572716-166572766	ovcar-3	ovarian:	n/a
37	chr1:166572716-166572766	PrEC	prostate:	n/a
38	chr1:166571691-166571741	AG10803	skin:	n/a
39	chr1:166572716-166572766	Hela-S3	cervix:	n/a
40	chr1:166571691-166571741	NT2-D1	testis:	n/a
41	chr1:166571691-166571741	PrEC	prostate:	n/a
42	chr1:166571691-166571741	Hepatocyte	liver:	n/a
43	chr1:166572716-166572766	HCM	heart:	n/a
44	chr1:166572716-166572766	HCPEpiC	choroid plexus:	n/a
45	chr1:166572716-166572766	NB4	blood:	n/a
46	chr1:166571691-166571741	AoSMC	blood vessel:	n/a
47	chr1:166571691-166571741	T-47D	breast:	n/a
48	chr1:166571691-166571741	BE2_C	brain:	n/a
49	chr1:166571691-166571741	HCPEpiC	choroid plexus:	n/a
50	chr1:166572716-166572766	HEK293	kidney:	embryo

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:166553441..166555941-chr1:166692722..166694602,2	K562	blood:
2	chr1:166559872..166561580-chr1:166564185..166567051,2	K562	blood:
3	chr1:166552002..166554385-chr1:166564291..166566907,2	K562	blood:
4	chr1:166552621..166555359-chr1:166806304..166809167,2	K562	blood:
5	chr1:166526359..166528969-chr1:166551076..166553291,2	K562	blood:
6	chr1:166559872..166561580-chr1:166564185..166567051,2	K562	blood:
7	chr1:166584740..166586661-chr1:166593653..166596420,2	K562	blood:
8	chr1:166541145..166543068-chr1:166552578..166555523,2	K562	blood:
9	chr1:166541145..166543068-chr1:166552578..166555523,2	K562	blood:
10	chr1:166433876..166435453-chr1:166541076..166543354,2	K562	blood:
11	chr1:166545251..166548120-chr6:140575352..140577699,2	MCF-7	breast:
12	chr1:166563481..166565697-chr1:166594929..166597318,2	K562	blood:
13	chr1:166538818..166541010-chr1:166552416..166555173,2	K562	blood:
14	chr1:166566883..166568406-chr1:166568618..166571458,2	MCF-7	breast:
15	chr1:166548285..166550394-chr1:166561795..166564014,2	K562	blood:
16	chr1:166557976..166561372-chr1:166563125..166565685,3	K562	blood:
17	chr1:166557976..166561372-chr1:166563125..166565685,3	K562	blood:
18	chr1:166546817..166549594-chr1:166554279..166555815,3	K562	blood:
19	chr1:166534937..166537659-chr1:166540902..166543509,2	K562	blood:
20	chr1:166538818..166541010-chr1:166552416..166555173,2	K562	blood:
21	chr1:166555656..166557626-chr1:166807250..166809697,2	K562	blood:
22	chr1:166582556..166584274-chr1:166807960..166809715,2	MCF-7	breast:
23	chr1:166566883..166568406-chr1:166568618..166571458,2	MCF-7	breast:
24	chr1:166552002..166554385-chr1:166564291..166566907,2	K562	blood:
25	chr1:166546817..166549594-chr1:166554279..166555815,3	K562	blood:
26	chr1:166548285..166550394-chr1:166561795..166564014,2	K562	blood:
27	chr1:166589682..166592157-chr1:166593940..166597259,3	K562	blood:

No data

Variant related genes	Relation type
FMO9P	TF binding region
FMO9P	CpG island
ENSG00000143157	chromatin interactions
ENSG00000238087	chromatin interactions

Extended variants
information (count: 1691 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1691 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544342931	chr1:166540923-166540924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs372548529	chr1:166540940-166540941	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs145165236	chr1:166540960-166540961	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs199690811	chr1:166540964-166540965	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs386636431	chr1:166540965-166540966	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369225295	chr1:166541001-166541002	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192737079	chr1:166541035-166541036	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs74119781	chr1:166541068-166541069	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs555391237	chr1:166541069-166541070	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs76168127	chr1:166541112-166541113	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs183218954	chr1:166541113-166541114	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs150228812	chr1:166541115-166541116	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564369399	chr1:166541136-166541137	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533000643	chr1:166541164-166541165	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543668437	chr1:166541170-166541171	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs187694886	chr1:166541179-166541180	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529039191	chr1:166541183-166541184	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs269694	chr1:166541194-166541195	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs565689623	chr1:166541218-166541219	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs528056412	chr1:166541225-166541226	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551386463	chr1:166541227-166541228	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs571153363	chr1:166541248-166541249	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs114787755	chr1:166541255-166541256	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539731395	chr1:166541274-166541275	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200867922	chr1:166541289-166541290	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs556382055	chr1:166541295-166541296	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs569916008	chr1:166541296-166541297	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs373468952	chr1:166541306-166541307	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs191424186	chr1:166541310-166541311	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs572362425	chr1:166541315-166541316	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116396672	chr1:166541337-166541338	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs117395401	chr1:166541347-166541348	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs149310774	chr1:166541361-166541362	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs80178892	chr1:166541557-166541558	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs374017055	chr1:166541592-166541593	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185081482	chr1:166541626-166541627	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs145460018	chr1:166541631-166541632	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs529058254	chr1:166541644-166541645	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542759492	chr1:166541648-166541649	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555523092	chr1:166541655-166541656	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs138091436	chr1:166541686-166541687	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs189514300	chr1:166541693-166541694	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs77044917	chr1:166541733-166541734	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142683384	chr1:166541736-166541737	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs269695	chr1:166541755-166541756	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs565309602	chr1:166541771-166541772	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs145932468	chr1:166541779-166541780	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs35356875	chr1:166541791-166541792	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs71301018	chr1:166541795-166541796	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs569928284	chr1:166541801-166541802	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	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
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
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
Breast cancer	21509527	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
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	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	chr1:166542000-166543200	Enhancers	K562	blood
2	chr1:166543200-166544600	Weak transcription	K562	blood
3	chr1:166547200-166549400	Weak transcription	K562	blood
4	chr1:166549400-166550200	Enhancers	K562	blood
5	chr1:166550200-166552400	Weak transcription	K562	blood
6	chr1:166552400-166554600	Enhancers	K562	blood
7	chr1:166553800-166554800	Enhancers	Fetal Heart	heart
8	chr1:166554200-166554400	Enhancers	Left Ventricle	heart
9	chr1:166554200-166554800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:166554400-166555000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr1:166554600-166555400	Flanking Active TSS	K562	blood
12	chr1:166555400-166556000	Enhancers	K562	blood
13	chr1:166556000-166559400	Weak transcription	K562	blood
14	chr1:166557400-166559000	Enhancers	Hela-S3	cervix
15	chr1:166559400-166559800	Enhancers	K562	blood
16	chr1:166559800-166569800	Weak transcription	K562	blood
17	chr1:166569800-166571400	Enhancers	K562	blood
18	chr1:166571000-166571200	Enhancers	HMEC	breast
19	chr1:166571400-166572400	Weak transcription	HMEC	breast
20	chr1:166571400-166574400	Weak transcription	K562	blood
21	chr1:166572400-166572800	Enhancers	HMEC	breast
22	chr1:166572800-166573000	Enhancers	Left Ventricle	heart
23	chr1:166574400-166575200	Enhancers	Fetal Heart	heart
24	chr1:166574400-166575400	Enhancers	K562	blood
25	chr1:166575000-166575400	Enhancers	Left Ventricle	heart
26	chr1:166575200-166578400	Weak transcription	Fetal Heart	heart
27	chr1:166575400-166579600	Weak transcription	Left Ventricle	heart
28	chr1:166575400-166579600	Weak transcription	K562	blood
29	chr1:166578400-166580000	Enhancers	Fetal Heart	heart
30	chr1:166579600-166580000	Enhancers	Left Ventricle	heart
31	chr1:166579600-166580400	Enhancers	K562	blood
32	chr1:166580400-166582400	Weak transcription	K562	blood
33	chr1:166582400-166582800	Enhancers	K562	blood
34	chr1:166587200-166587400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr1:166587400-166587800	Enhancers	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links