Variant report

Variant	nsv882539
Chromosome Location	chr5:104051192-104133164
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	BATF	chr5:104087774-104088008	GM12878	blood:	n/a	chr5:104087867-104087878
2	BATF	chr5:104087746-104087944	GM12878	blood:	n/a	chr5:104087867-104087878
3	CEBPB	chr5:104102566-104102783	HepG2	liver:	n/a	chr5:104102656-104102667
4	CEBPB	chr5:104090393-104090670	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr5:104068408-104068610	HepG2	liver:	n/a	chr5:104068507-104068518
6	CEBPB	chr5:104102501-104102787	A549	lung:	n/a	chr5:104102656-104102667
7	CTCF	chr5:104083629-104083642	Kidney_OC	kidney:	n/a	n/a
8	CTCF	chr5:104069920-104070070	BE2_C	brain:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
9	CTCF	chr5:104067389-104067440	GM20000	blood:	n/a	n/a
10	CTCF	chr5:104062865-104062887	GM13976	blood:	n/a	n/a
11	CTCF	chr5:104069780-104070070	RPTEC	kidney:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
12	CTCF	chr5:104069900-104070050	WERI-Rb-1	eye:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
13	CTCF	chr5:104069858-104070019	MCF-7	breast:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
14	CTCF	chr5:104072300-104072385	LNCaP	prostate:	n/a	n/a
15	CTCF	chr5:104069880-104070030	Hela-S3	cervix:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
16	CTCF	chr5:104083160-104083310	GM12868	blood:	n/a	n/a
17	CTCF	chr5:104102206-104102345	Medullo	brain:	n/a	n/a
18	CTCF	chr5:104069903-104069973	HepG2	liver:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
19	CTCF	chr5:104069894-104069990	MCF-7	breast:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
20	CTCF	chr5:104069900-104070050	HBMEC	blood vessel:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
21	CTCF	chr5:104069820-104069970	HCT-116	colon:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
22	CTCF	chr5:104063840-104063990	GM12864	blood:	n/a	n/a
23	CTCF	chr5:104069906-104070004	Hela-S3	cervix:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
24	CTCF	chr5:104069880-104070030	HCT-116	colon:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
25	CTCF	chr5:104083547-104083599	LNCaP	prostate:	n/a	n/a
26	CTCF	chr5:104118782-104118821	Medullo	brain:	n/a	n/a
27	CTCF	chr5:104056762-104056779	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr5:104069860-104070010	HRPEpiC	eye:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
29	CTCF	chr5:104069845-104070041	H1-hESC	embryonic stem cell:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
30	CTCF	chr5:104069920-104070070	HPF	lung:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
31	CTCF	chr5:104069890-104069999	HUVEC	blood vessel:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
32	CTCF	chr5:104056791-104056829	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr5:104069860-104070010	HBMEC	blood vessel:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
34	CTCF	chr5:104072280-104072430	BE2_C	brain:	n/a	n/a
35	CTCF	chr5:104072240-104072390	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr5:104069980-104070130	MCF-7	breast:	n/a	n/a
37	CTCF	chr5:104088500-104088650	Caco-2	colon:	n/a	n/a
38	CTCF	chr5:104069820-104069970	HRE	kidney:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
39	CTCF	chr5:104072300-104072450	BE2_C	brain:	n/a	n/a
40	CTCF	chr5:104069820-104069970	MCF-7	breast:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
41	CTCF	chr5:104069820-104069970	HEK293	kidney:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
42	CTCF	chr5:104069920-104070070	HCPEpiC	choroid plexus:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
43	CTCF	chr5:104056841-104056858	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr5:104070060-104070210	GM12866	blood:	n/a	n/a
45	CTCF	chr5:104069900-104070050	HRE	kidney:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
46	CTCF	chr5:104069880-104070030	HepG2	liver:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
47	CTCF	chr5:104069860-104070010	BE2_C	brain:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
48	E2F4	chr5:104064975-104065151	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr5:104067032-104067247	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr5:104101042-104101511	MCF10A-Er-Src	breast:	n/a	chr5:104101361-104101378 chr5:104101364-104101375 chr5:104101361-104101378

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104090236-104090286	AG04450	lung:	fetal
2	chr5:104090236-104090286	AG10803	skin:	n/a
3	chr5:104090236-104090286	ovcar-3	ovarian:	n/a
4	chr5:104090236-104090286	PrEC	prostate:	n/a
5	chr5:104090236-104090286	GM12878	blood:	n/a
6	chr5:104090236-104090286	HMEC	breast:	n/a
7	chr5:104090236-104090286	ProgFib	skin:	n/a
8	chr5:104090236-104090286	RPTEC	kidney:	n/a
9	chr5:104090236-104090286	AG04449	skin:	fetal
10	chr5:104090236-104090286	HCT-116	colon:	n/a
11	chr5:104090236-104090286	SK-N-MC	brain:	n/a
12	chr5:104090236-104090286	HCM	heart:	n/a
13	chr5:104090236-104090286	GM19239	blood:	n/a
14	chr5:104090236-104090286	SAEC	small airway:	n/a
15	chr5:104090236-104090286	NH-A	brain:	n/a
16	chr5:104090236-104090286	HCPEpiC	choroid plexus:	n/a
17	chr5:104090236-104090286	NT2-D1	testis:	n/a
18	chr5:104090236-104090286	MCF10A-Er-Src	breast:	n/a
19	chr5:104090236-104090286	CMK	blood:	n/a
20	chr5:104090236-104090286	K562	blood:	n/a
21	chr5:104090236-104090286	SKMC	muscle:	n/a
22	chr5:104090236-104090286	SK-N-SH	brain:	n/a
23	chr5:104090236-104090286	NB4	blood:	n/a
24	chr5:104090236-104090286	HEK293	kidney:	embryo
25	chr5:104090236-104090286	NHBE	bronchial:	n/a
26	chr5:104090236-104090286	AG09309	skin:	n/a
27	chr5:104090236-104090286	HUVEC	blood vessel:	n/a
28	chr5:104090236-104090286	Hela-S3	cervix:	n/a
29	chr5:104090236-104090286	U87	brain:	n/a
30	chr5:104090236-104090286	HL-60	blood:	n/a
31	chr5:104090236-104090286	LNCaP	prostate:	n/a
32	chr5:104090236-104090286	PFSK-1	brain:	n/a
33	chr5:104090236-104090286	HCF	heart:	n/a
34	chr5:104090236-104090286	T-47D	breast:	n/a
35	chr5:104090236-104090286	HRCEpiC	kidney:	n/a
36	chr5:104090236-104090286	BJ	skin:	n/a
37	chr5:104090236-104090286	SK-N-SH_RA	brain:	n/a
38	chr5:104090236-104090286	Caco-2	colon:	n/a
39	chr5:104090236-104090286	HepG2	liver:	n/a
40	chr5:104090236-104090286	PANC-1	pancreas:	n/a
41	chr5:104090236-104090286	MCF-7	breast:	n/a
42	chr5:104090236-104090286	HRPEpiC	eye:	n/a
43	chr5:104090236-104090286	HAEpiC	amniotic membrane:	n/a
44	chr5:104090236-104090286	HEEpiC	esophagus:	n/a
45	chr5:104090236-104090286	GM12892	blood:	n/a
46	chr5:104090236-104090286	HNPCEpiC	eye:	n/a
47	chr5:104090236-104090286	GM06990	blood:	n/a
48	chr5:104090236-104090286	AoSMC	blood vessel:	n/a
49	chr5:104090236-104090286	HIPEpiC	eye:	n/a
50	chr5:104090236-104090286	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:104086946..104088891-chr5:104090048..104092847,2	MCF-7	breast:
2	chr5:104086946..104088891-chr5:104090048..104092847,2	MCF-7	breast:
3	chr5:103812785..103815361-chr5:104049597..104051659,2	K562	blood:
4	chr5:104091669..104093962-chr5:104097846..104099466,2	MCF-7	breast:
5	chr5:104080992..104082950-chr5:104084605..104086219,2	K562	blood:
6	chr5:104091669..104093962-chr5:104097846..104099466,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-5	chr5:104052350-104052364	NONHSAT103082
2	lnc-NUDT12-5	chr5:104109314-104109524	NONHSAT103088
3	lnc-NUDT12-5	chr5:104052350-104052364	NONHSAT103081
4	lnc-NUDT12-5	chr5:104098932-104099084	ENSG00000251574
5	lnc-NUDT12-5	chr5:104075198-104075242	ENSG00000251574
6	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
7	lnc-NUDT12-5	chr5:104075198-104075336	ENSG00000251574
8	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
9	lnc-NUDT12-5	chr5:104074955-104075113	ENSG00000251574
10	lnc-NUDT12-5	chr5:104109314-104109524	NONHSAT103082
11	lnc-NUDT12-5	chr5:104079393-104079555	ENSG00000251574
12	lnc-NUDT12-5	chr5:104109434-104109523	ENSG00000251574
13	lnc-NUDT12-5	chr5:104075198-104075336	ENSG00000251574
14	lnc-NUDT12-5	chr5:104080291-104080310	NONHSAT103088
15	lnc-NUDT12-5	chr5:104082242-104082310	ENSG00000251574
16	lnc-NUDT12-13	chr5:104103132-104103235	l_2988_chr5:104103131-104137422_testes
17	lnc-NUDT12-5	chr5:104074998-104075113	ENSG00000251574
18	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
19	lnc-NUDT12-5	chr5:104109314-104109492	ENSG00000251574
20	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
21	lnc-NUDT12-5	chr5:104072462-104072616	ENSG00000251574
22	lnc-C5orf30-2	chr5:104079736-104079888	XLOC_004497
23	lnc-C5orf30-3	chr5:104109342-104109441	ENSG00000253776
24	lnc-NUDT12-5	chr5:104098981-104099084	NONHSAT103081
25	lnc-NUDT12-5	chr5:104074962-104075113	ENSG00000251574
26	lnc-NUDT12-5	chr5:104081064-104081147	NONHSAT103088
27	lnc-NUDT12-5	chr5:104079736-104079892	ENSG00000251574
28	lnc-NUDT12-5	chr5:104109314-104109397	ENSG00000251574
29	lnc-NUDT12-5	chr5:104109314-104109361	ENSG00000251574
30	lnc-NUDT12-13	chr5:104118423-104118445	l_2988_chr5:104103131-104137422_testes
31	lnc-NUDT12-5	chr5:104109434-104109524	NONHSAT103081
32	lnc-NUDT12-5	chr5:104098981-104099084	NONHSAT103082
33	lnc-C5orf30-2	chr5:104098977-104099084	XLOC_004497
34	lnc-NUDT12-5	chr5:104109314-104109485	ENSG00000251574

Variant related genes	Relation type
ENSG00000253776	TF binding region
RNU6-334P	TF binding region
ENSG00000251574	TF binding region
ENSG00000253776	CpG island
RNU6-334P	CpG island
ENSG00000251574	CpG island
ENSG00000251574	chromatin interactions
CREB3L2	miRNA target sites

Extended variants
information (count: 1097 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1097 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12719533	chr5:104051192-104051193	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537356241	chr5:104051219-104051220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557023334	chr5:104051229-104051230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574023514	chr5:104051238-104051239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542742596	chr5:104051285-104051286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559827666	chr5:104051313-104051314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558810983	chr5:104051315-104051316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs118168004	chr5:104051323-104051324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372983683	chr5:104051344-104051345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114007599	chr5:104051388-104051389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564284380	chr5:104051410-104051411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559716606	chr5:104051418-104051419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533216481	chr5:104051438-104051439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs193114264	chr5:104051443-104051444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563127215	chr5:104051474-104051475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528917949	chr5:104051493-104051494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548781566	chr5:104051501-104051502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562566629	chr5:104051503-104051504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534424884	chr5:104051512-104051513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs62363614	chr5:104051518-104051519	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs571507826	chr5:104051522-104051523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537339291	chr5:104051531-104051532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs79041808	chr5:104051545-104051546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542547977	chr5:104051552-104051553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142428104	chr5:104051553-104051554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141664881	chr5:104051560-104051561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536622995	chr5:104051575-104051576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553420326	chr5:104051579-104051580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376239805	chr5:104051587-104051588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545523546	chr5:104051622-104051623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185573610	chr5:104051632-104051633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563960077	chr5:104051635-104051636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370345698	chr5:104051707-104051708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531159431	chr5:104051717-104051718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190102312	chr5:104051758-104051759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577953256	chr5:104051767-104051768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138556286	chr5:104051771-104051772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs57088551	chr5:104051776-104051777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543335682	chr5:104051820-104051821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs13186456	chr5:104051895-104051896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192031543	chr5:104051908-104051909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147029560	chr5:104051912-104051913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147669012	chr5:104051926-104051927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552790889	chr5:104051947-104051948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140360140	chr5:104051969-104051970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558930402	chr5:104051974-104051975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528126722	chr5:104051978-104051979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184137040	chr5:104052041-104052042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs564976739	chr5:104052052-104052053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188541152	chr5:104052069-104052070	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Obesity	20622171	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104049800-104051200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:104051200-104053000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:104052000-104052600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:104065400-104065800	Enhancers	Rectal Smooth Muscle	rectum
5	chr5:104065800-104066200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr5:104065800-104067800	Enhancers	Fetal Lung	lung
7	chr5:104066200-104066400	Enhancers	Rectal Smooth Muscle	rectum
8	chr5:104066400-104067600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr5:104067200-104067600	Enhancers	Colon Smooth Muscle	Colon
10	chr5:104067600-104068200	Enhancers	Rectal Smooth Muscle	rectum
11	chr5:104067600-104069200	Weak transcription	Colon Smooth Muscle	Colon
12	chr5:104068200-104068600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr5:104068600-104070200	Enhancers	Rectal Smooth Muscle	rectum
14	chr5:104069200-104070200	Enhancers	Colon Smooth Muscle	Colon
15	chr5:104089600-104090800	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr5:104089800-104090000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr5:104089800-104090200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr5:104089800-104091200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr5:104089800-104091200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:104089800-104091200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr5:104089800-104091200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr5:104089800-104091400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr5:104090000-104090600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr5:104090000-104090600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr5:104090200-104090400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr5:104090200-104090600	Enhancers	Brain Germinal Matrix	brain
27	chr5:104090200-104091000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:104090400-104090800	Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr5:104090600-104090800	Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr5:104090800-104091000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr5:104091200-104092600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr5:104091400-104095000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr5:104095000-104095800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr5:104112400-104113000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr5:104112600-104113000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:104124800-104125400	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr5:104124800-104125400	Enhancers	Rectal Smooth Muscle	rectum
38	chr5:104124800-104125600	Enhancers	Fetal Lung	lung
39	chr5:104124800-104126400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr5:104126400-104130000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:104127800-104129000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:104128400-104129800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr5:104128600-104129000	Enhancers	Fetal Intestine Small	intestine
44	chr5:104128600-104129000	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr5:104128600-104129200	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr5:104128600-104129400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr5:104128600-104129400	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr5:104128600-104130000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
49	chr5:104128600-104130200	Enhancers	Fetal Intestine Large	intestine
50	chr5:104128800-104129200	Enhancers	NH-A	brain

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