Variant report

Variant	nsv876299
Chromosome Location	chr3:644290-892951
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	BACH1	chr3:888492-888519	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr3:892848-893082	GM12878	blood:	n/a	chr3:892988-892999
3	BATF	chr3:892892-893121	GM12878	blood:	n/a	chr3:892988-892999
4	BHLHE40	chr3:846853-846863	GM12878	blood:	n/a	n/a
5	BRCA1	chr3:817416-817453	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr3:649451-649478	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr3:674381-674581	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr3:815996-816027	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr3:754720-755580	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:795219-795424	K562	blood:	n/a	n/a
11	CEBPB	chr3:775096-775429	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:700965-701296	IMR90	lung:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
13	CEBPB	chr3:816945-817493	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:780130-780267	K562	blood:	n/a	chr3:780198-780209
15	CEBPB	chr3:754295-754516	HepG2	liver:	n/a	chr3:754384-754393 chr3:754382-754393
16	CEBPB	chr3:879534-879816	A549	lung:	n/a	n/a
17	CEBPB	chr3:780178-780270	H1-hESC	embryonic stem cell:	n/a	chr3:780198-780209
18	CEBPB	chr3:746911-747209	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:672472-672697	A549	lung:	n/a	chr3:672554-672567 chr3:672555-672566
20	CEBPB	chr3:780119-780347	HepG2	liver:	n/a	chr3:780198-780209
21	CEBPB	chr3:766071-766268	HepG2	liver:	n/a	chr3:766173-766184
22	CEBPB	chr3:649955-650248	IMR90	lung:	n/a	chr3:650073-650084 chr3:650075-650084
23	CEBPB	chr3:674328-674574	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr3:700997-701241	H1-hESC	embryonic stem cell:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
25	CEBPB	chr3:766028-766169	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr3:697395-697928	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr3:650039-650244	HepG2	liver:	n/a	chr3:650073-650084 chr3:650075-650084
28	CEBPB	chr3:649124-649464	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr3:672488-672700	HepG2	liver:	n/a	chr3:672554-672567 chr3:672555-672566
30	CEBPB	chr3:834255-834315	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr3:701078-701278	A549	lung:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
32	CEBPB	chr3:650024-650224	A549	lung:	n/a	chr3:650073-650084 chr3:650075-650084
33	CEBPB	chr3:700961-701300	Hela-S3	cervix:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
34	CEBPB	chr3:754275-756263	Hela-S3	cervix:	n/a	chr3:754384-754393 chr3:754382-754393 chr3:755103-755114
35	CEBPB	chr3:700968-701307	HepG2	liver:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
36	CEBPB	chr3:872412-872499	A549	lung:	n/a	n/a
37	CHD1	chr3:660628-660658	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr3:834356-834507	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr3:754899-755419	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr3:674231-674676	GM12878	blood:	n/a	chr3:674455-674465 chr3:674451-674467 chr3:674453-674466 chr3:674453-674462 chr3:674453-674466 chr3:674450-674468 chr3:674452-674473
41	CTCF	chr3:674420-674570	WI-38	lung:	n/a	chr3:674455-674465 chr3:674451-674467 chr3:674453-674466 chr3:674453-674462 chr3:674453-674466 chr3:674450-674468 chr3:674452-674473
42	CTCF	chr3:823700-823823	GM13977	blood:	n/a	n/a
43	CTCF	chr3:771984-771991	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr3:674360-674510	HPF	lung:	n/a	chr3:674455-674465 chr3:674451-674467 chr3:674453-674466 chr3:674453-674462 chr3:674453-674466 chr3:674450-674468 chr3:674452-674473
45	CTCF	chr3:662427-662492	GM20000	blood:	n/a	n/a
46	CTCF	chr3:674340-674490	GM12867	blood:	n/a	chr3:674455-674465 chr3:674451-674467 chr3:674453-674466 chr3:674453-674462 chr3:674453-674466 chr3:674450-674468 chr3:674452-674473
47	CTCF	chr3:674279-674626	MCF-7	breast:	n/a	chr3:674455-674465 chr3:674451-674467 chr3:674453-674466 chr3:674453-674462 chr3:674453-674466 chr3:674450-674468 chr3:674452-674473
48	CTCF	chr3:892820-892970	GM12870	blood:	n/a	n/a
49	CTCF	chr3:674330-674577	Spleen_OC	spleen:	n/a	chr3:674455-674465 chr3:674451-674467 chr3:674453-674466 chr3:674453-674462 chr3:674453-674466 chr3:674450-674468 chr3:674452-674473
50	CTCF	chr3:676240-676390	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:782757-782807	CMK	blood:	n/a
2	chr3:782757-782807	Hela-S3	cervix:	n/a
3	chr3:782757-782807	HPAEpiC	pulmonary alveolar:	n/a
4	chr3:782757-782807	H1-hESC	embryonic stem cell:	embryo
5	chr3:782757-782807	AG09309	skin:	n/a
6	chr3:782757-782807	ECC-1	luminal epithelium:	n/a
7	chr3:782757-782807	HNPCEpiC	eye:	n/a
8	chr3:782757-782807	MCF10A-Er-Src	breast:	n/a
9	chr3:782757-782807	SAEC	small airway:	n/a
10	chr3:782757-782807	A549	lung:	n/a
11	chr3:782757-782807	AG04450	lung:	fetal
12	chr3:782757-782807	AG04449	skin:	fetal
13	chr3:782757-782807	K562	blood:	n/a
14	chr3:782757-782807	HEEpiC	esophagus:	n/a
15	chr3:782757-782807	BE2_C	brain:	n/a
16	chr3:782757-782807	GM12892	blood:	n/a
17	chr3:782757-782807	HCT-116	colon:	n/a
18	chr3:782757-782807	PFSK-1	brain:	n/a
19	chr3:782757-782807	NH-A	brain:	n/a
20	chr3:782757-782807	HAEpiC	amniotic membrane:	n/a
21	chr3:782757-782807	Jurkat	blood:	n/a
22	chr3:782757-782807	SK-N-SH_RA	brain:	n/a
23	chr3:782757-782807	PrEC	prostate:	n/a
24	chr3:782757-782807	SK-N-SH	brain:	n/a
25	chr3:782757-782807	HCM	heart:	n/a
26	chr3:782757-782807	ProgFib	skin:	n/a
27	chr3:782757-782807	RPTEC	kidney:	n/a
28	chr3:782757-782807	NHDF-neo	bronchial:	n/a
29	chr3:782757-782807	AoSMC	blood vessel:	n/a
30	chr3:782757-782807	HRE	kidney:	n/a
31	chr3:782757-782807	LNCaP	prostate:	n/a
32	chr3:782757-782807	HepG2	liver:	n/a
33	chr3:782757-782807	AG10803	skin:	n/a
34	chr3:782757-782807	HIPEpiC	eye:	n/a
35	chr3:782757-782807	GM12891	blood:	n/a
36	chr3:782757-782807	BJ	skin:	n/a
37	chr3:782757-782807	HRPEpiC	eye:	n/a
38	chr3:782757-782807	NHBE	bronchial:	n/a
39	chr3:782757-782807	ovcar-3	ovarian:	n/a
40	chr3:782757-782807	U87	brain:	n/a
41	chr3:782757-782807	HMEC	breast:	n/a
42	chr3:782757-782807	HCPEpiC	choroid plexus:	n/a
43	chr3:782757-782807	SK-N-MC	brain:	n/a
44	chr3:782757-782807	GM06990	blood:	n/a
45	chr3:782757-782807	T-47D	breast:	n/a
46	chr3:782757-782807	HCF	heart:	n/a
47	chr3:782757-782807	PANC-1	pancreas:	n/a
48	chr3:782757-782807	SKMC	muscle:	n/a
49	chr3:782757-782807	AG09319	gingival:	n/a
50	chr3:782757-782807	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr3:844122..846364-chr3:847958..849773,2	K562	blood:
2	chr3:709932..711493-chr3:712317..715172,2	K562	blood:
3	chr3:746367..749271-chr3:749542..752426,2	K562	blood:
4	chr3:674217..674800-chr3:1123463..1123990,2	MCF-7	breast:
5	chr3:829999..831597-chr3:832456..834541,2	MCF-7	breast:
6	chr3:731301..733205-chr3:733252..736265,3	K562	blood:
7	chr3:726576..727076-chr3:11025934..11026463,2	MCF-7	breast:
8	chr3:751166..753010-chr3:765105..767568,2	K562	blood:
9	chr3:731301..733205-chr3:733252..736265,3	K562	blood:
10	chr3:746367..749271-chr3:749542..752426,2	K562	blood:
11	chr3:829999..831597-chr3:832456..834541,2	MCF-7	breast:
12	chr3:762317..764340-chr3:779905..782757,2	K562	blood:
13	chr3:844122..846364-chr3:847958..849773,2	K562	blood:
14	chr3:709932..711493-chr3:712317..715172,2	K562	blood:
15	chr1:229050784..229051693-chr3:758018..758663,2	MCF-7	breast:
16	chr20:12921782..12922300-chr3:762237..762760,2	MCF-7	breast:
17	chr3:751166..753010-chr3:765105..767568,2	K562	blood:
18	chr3:805612..808013-chr3:811141..813375,2	K562	blood:
19	chr3:805612..808013-chr3:811141..813375,2	K562	blood:
20	chr3:762317..764340-chr3:779905..782757,2	K562	blood:
21	chr12:101154422..101155178-chr3:753774..754622,2	MCF-7	breast:
22	chr20:14175439..14177996-chr3:730394..733241,2	MCF-7	breast:
23	chr3:703062..705164-chr3:828470..830008,2	K562	blood:
24	chr3:674203..674975-chr3:2197712..2198482,2	MCF-7	breast:
25	chr3:703062..705164-chr3:828470..830008,2	K562	blood:
26	chr3:522873..523625-chr3:674344..674995,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHL1-3	chr3:884059-884327	ENSG00000224957
2	lnc-CHL1-3	chr3:882398-882493	NR_110118
3	lnc-CHL1-3	chr3:868690-868816	ENSG00000224957
4	lnc-IL5RA-14	chr3:659472-659997	NONHSAT087571
5	lnc-CHL1-3	chr3:884059-887698	NR_110118
6	lnc-CHL1-3	chr3:791898-791933	ENSG00000224957
7	lnc-CHL1-6	chr3:766898-766933	ucscGeneNc_uc003boy_1
8	lnc-CHL1-6	chr3:857398-857493	ucscGeneNc_uc003boy_1
9	lnc-CHL1-3	chr3:791898-791933	NR_110118
10	lnc-CHL1-6	chr3:859059-862698	ucscGeneNc_uc003boy_1

Variant related genes	Relation type
ENSG00000238075	TF binding region
ENSG00000238075	CpG island
HIF1A	miRNA target sites
IL10	miRNA target sites
COPS7A	miRNA target sites

Extended variants
information (count: 2666 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2666 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28374140	chr3:649007-649008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563487915	chr3:649013-649014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs66723717	chr3:649036-649037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs202178236	chr3:649057-649058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530755226	chr3:649065-649066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2627924	chr3:649068-649069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552399100	chr3:649083-649084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2387541	chr3:649128-649129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs9824590	chr3:649137-649138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528334292	chr3:649145-649146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2387542	chr3:649150-649151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2627923	chr3:649158-649159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546581723	chr3:649185-649186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs57077865	chr3:649192-649193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139570606	chr3:649193-649194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2674523	chr3:649206-649207	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528972409	chr3:649242-649243	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550297100	chr3:649245-649246	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568587738	chr3:649255-649256	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537292544	chr3:649256-649257	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558713767	chr3:649273-649274	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10433628	chr3:649275-649276	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59831647	chr3:649296-649297	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs57071196	chr3:649306-649307	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2946138	chr3:649353-649354	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2944109	chr3:649358-649359	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs56114234	chr3:649367-649368	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142714247	chr3:649370-649371	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs28584693	chr3:649378-649379	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534959250	chr3:649389-649390	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553353795	chr3:649391-649392	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs199816078	chr3:649419-649420	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574706066	chr3:649420-649421	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs28655941	chr3:649431-649432	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4267630	chr3:649441-649442	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542223545	chr3:649451-649452	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77692588	chr3:649464-649465	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs55958218	chr3:649469-649470	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs9631480	chr3:649479-649480	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557538649	chr3:649491-649492	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575799352	chr3:649494-649495	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs80069418	chr3:649508-649509	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs55936096	chr3:649521-649522	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74817980	chr3:649564-649565	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113012492	chr3:649567-649568	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs59714276	chr3:649570-649571	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546030168	chr3:649614-649615	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs7623646	chr3:649617-649618	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs564081287	chr3:649630-649631	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2627922	chr3:649641-649642	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:649000-650000	Enhancers	Hela-S3	cervix
2	chr3:649200-650200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:659600-660000	Active TSS	Spleen	Spleen
4	chr3:663600-664000	Enhancers	Fetal Brain Male	brain
5	chr3:674200-674800	Enhancers	Brain Substantia Nigra	brain
6	chr3:674200-675000	Enhancers	Hela-S3	cervix
7	chr3:675800-676400	Enhancers	Fetal Thymus	thymus
8	chr3:682800-683200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:684800-685200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr3:697200-697600	Enhancers	Hela-S3	cervix
11	chr3:703200-703400	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr3:703400-703800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr3:706200-708000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:715600-716600	Enhancers	Fetal Brain Male	brain
15	chr3:716600-717800	Weak transcription	Fetal Brain Male	brain
16	chr3:718000-718200	Enhancers	Fetal Brain Male	brain
17	chr3:722800-723800	Enhancers	Hela-S3	cervix
18	chr3:723800-724400	Weak transcription	Hela-S3	cervix
19	chr3:724400-724600	Enhancers	Hela-S3	cervix
20	chr3:727000-727200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:729000-729400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr3:730600-732600	Weak transcription	Fetal Muscle Trunk	muscle
23	chr3:732000-732800	ZNF genes & repeats	Aorta	Aorta
24	chr3:732200-732400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr3:732200-732400	Weak transcription	Fetal Muscle Leg	muscle
26	chr3:732400-732800	ZNF genes & repeats	Lung	lung
27	chr3:732600-732800	Enhancers	Fetal Muscle Trunk	muscle
28	chr3:732800-734000	Weak transcription	Aorta	Aorta
29	chr3:742000-742400	Enhancers	Hela-S3	cervix
30	chr3:742200-742800	Enhancers	Fetal Muscle Leg	muscle
31	chr3:742400-743600	Flanking Active TSS	Hela-S3	cervix
32	chr3:743600-744000	Enhancers	Hela-S3	cervix
33	chr3:744200-756600	Weak transcription	Aorta	Aorta
34	chr3:746000-746200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr3:746400-747800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr3:747400-747600	Enhancers	Brain Hippocampus Middle	brain
37	chr3:747600-748200	Weak transcription	Brain Hippocampus Middle	brain
38	chr3:747800-750000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr3:748200-749600	Enhancers	Brain Hippocampus Middle	brain
40	chr3:748400-748800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr3:748400-748800	Enhancers	Brain Cingulate Gyrus	brain
42	chr3:748600-749000	Active TSS	Brain Substantia Nigra	brain
43	chr3:748600-749200	Enhancers	Brain Anterior Caudate	brain
44	chr3:749200-749600	Weak transcription	Brain Anterior Caudate	brain
45	chr3:749600-750000	Enhancers	Brain Anterior Caudate	brain
46	chr3:750000-753000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr3:753000-757600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr3:753600-755200	Enhancers	Hela-S3	cervix
49	chr3:754400-755800	Enhancers	Fetal Brain Male	brain
50	chr3:754600-755200	Enhancers	Fetal Brain Female	brain

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