Variant report

Variant	esv1845994
Chromosome Location	chr5:88736275-88847756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:232)
CpG islands
(count:122)
Chromatin interactive
region (count:28)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:232 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:88817310-88817324	K562	blood:	n/a	n/a
2	BACH1	chr5:88795775-88795852	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr5:88741099-88741470	K562	blood:	n/a	n/a
4	BRCA1	chr5:88753787-88754226	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr5:88809302-88809304	GM12878	blood:	n/a	n/a
6	CBX3	chr5:88753637-88754397	HCT-116	colon:	n/a	n/a
7	CEBPB	chr5:88739941-88740225	HepG2	liver:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
8	CEBPB	chr5:88829954-88830488	Hela-S3	cervix:	n/a	chr5:88829989-88830000
9	CEBPB	chr5:88740045-88740222	K562	blood:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
10	CEBPB	chr5:88824948-88825243	IMR90	lung:	n/a	chr5:88825114-88825125
11	CEBPB	chr5:88739908-88740272	K562	blood:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
12	CEBPB	chr5:88842597-88842674	K562	blood:	n/a	chr5:88842610-88842623 chr5:88842610-88842623
13	CEBPB	chr5:88835734-88836007	HepG2	liver:	n/a	chr5:88835925-88835938
14	CEBPB	chr5:88824980-88825267	HepG2	liver:	n/a	chr5:88825114-88825125
15	CEBPB	chr5:88753839-88754164	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:88788231-88788292	IMR90	lung:	n/a	n/a
17	CEBPB	chr5:88736883-88737045	K562	blood:	n/a	n/a
18	CEBPB	chr5:88739924-88740310	K562	blood:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
19	CEBPB	chr5:88842596-88842791	H1-hESC	embryonic stem cell:	n/a	chr5:88842610-88842623 chr5:88842610-88842623
20	CEBPB	chr5:88739974-88740255	A549	lung:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
21	CEBPB	chr5:88829927-88830135	A549	lung:	n/a	chr5:88829989-88830000
22	CEBPB	chr5:88781938-88782238	HepG2	liver:	n/a	n/a
23	CEBPB	chr5:88825008-88825224	A549	lung:	n/a	chr5:88825114-88825125
24	CEBPB	chr5:88749511-88749746	HepG2	liver:	n/a	chr5:88749608-88749619
25	CEBPB	chr5:88749568-88749650	A549	lung:	n/a	chr5:88749608-88749619
26	CEBPB	chr5:88829907-88830147	HepG2	liver:	n/a	chr5:88829989-88830000
27	CEBPB	chr5:88739924-88740262	IMR90	lung:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
28	CHD2	chr5:88753889-88754125	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr5:88741050-88741122	K562	blood:	n/a	n/a
30	CTCF	chr5:88819834-88819895	GM20000	blood:	n/a	n/a
31	CTCF	chr5:88806478-88806779	GM12878	blood:	n/a	n/a
32	CTCF	chr5:88737080-88737230	HCM	heart:	n/a	n/a
33	CTCF	chr5:88772909-88772979	Lung_OC	lung:	n/a	n/a
34	CTCF	chr5:88742875-88742876	K562	blood:	n/a	n/a
35	CTCF	chr5:88785217-88785237	GM20000	blood:	n/a	n/a
36	CTCF	chr5:88800543-88800593	LNCaP	prostate:	n/a	n/a
37	CTCF	chr5:88795520-88795670	HPF	lung:	n/a	n/a
38	CTCF	chr5:88741048-88741117	GM19240	blood:	n/a	n/a
39	CTCF	chr5:88759540-88759690	WI-38	lung:	n/a	n/a
40	CTCF	chr5:88841342-88841394	Lung_OC	lung:	n/a	n/a
41	CTCF	chr5:88742840-88742990	BJ	skin:	n/a	n/a
42	CTCF	chr5:88806606-88806676	HUVEC	blood vessel:	n/a	n/a
43	CUX1	chr5:88752868-88752919	GM12878	blood:	n/a	n/a
44	E2F6	chr5:88749586-88750084	H1-hESC	embryonic stem cell:	n/a	chr5:88749850-88749858 chr5:88749854-88749861 chr5:88749850-88749858 chr5:88749854-88749861 chr5:88749850-88749862 chr5:88749847-88749864 chr5:88749851-88749865 chr5:88749854-88749861 chr5:88749850-88749857 chr5:88749849-88749859 chr5:88749849-88749860 chr5:88749850-88749861 chr5:88749853-88749862
45	EBF1	chr5:88836105-88836151	GM12878	blood:	n/a	n/a
46	EGR1	chr5:88746137-88746291	GM12878	blood:	n/a	chr5:88746214-88746228
47	ELK1	chr5:88835270-88835330	Hela-S3	cervix:	n/a	n/a
48	ELK1	chr5:88753963-88754135	Hela-S3	cervix:	n/a	n/a
49	EP300	chr5:88753645-88754391	SK-N-SH	brain:	n/a	n/a
50	EP300	chr5:88753812-88754150	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:88841819-88841869	U87	brain:	n/a
2	chr5:88743831-88743881	HCT-116	colon:	n/a
3	chr5:88743831-88743881	NB4	blood:	n/a
4	chr5:88841819-88841869	HMEC	breast:	n/a
5	chr5:88841819-88841869	GM12891	blood:	n/a
6	chr5:88743831-88743881	Hepatocyte	liver:	n/a
7	chr5:88743831-88743881	K562	blood:	n/a
8	chr5:88841819-88841869	ovcar-3	ovarian:	n/a
9	chr5:88743831-88743881	HIPEpiC	eye:	n/a
10	chr5:88743831-88743881	LNCaP	prostate:	n/a
11	chr5:88743831-88743881	HNPCEpiC	eye:	n/a
12	chr5:88841819-88841869	NH-A	brain:	n/a
13	chr5:88841819-88841869	CMK	blood:	n/a
14	chr5:88841819-88841869	Hepatocyte	liver:	n/a
15	chr5:88743831-88743881	GM12891	blood:	n/a
16	chr5:88743831-88743881	SKMC	muscle:	n/a
17	chr5:88841819-88841869	HCM	heart:	n/a
18	chr5:88841819-88841869	GM19239	blood:	n/a
19	chr5:88841819-88841869	HL-60	blood:	n/a
20	chr5:88743831-88743881	HCF	heart:	n/a
21	chr5:88743831-88743881	NH-A	brain:	n/a
22	chr5:88743831-88743881	HCM	heart:	n/a
23	chr5:88841819-88841869	GM12878	blood:	n/a
24	chr5:88743831-88743881	BJ	skin:	n/a
25	chr5:88743831-88743881	Hela-S3	cervix:	n/a
26	chr5:88841819-88841869	NHDF-neo	bronchial:	n/a
27	chr5:88743831-88743881	T-47D	breast:	n/a
28	chr5:88841819-88841869	Jurkat	blood:	n/a
29	chr5:88841819-88841869	HRCEpiC	kidney:	n/a
30	chr5:88743831-88743881	PANC-1	pancreas:	n/a
31	chr5:88841819-88841869	SK-N-MC	brain:	n/a
32	chr5:88743831-88743881	HCPEpiC	choroid plexus:	n/a
33	chr5:88841819-88841869	ECC-1	luminal epithelium:	n/a
34	chr5:88743831-88743881	AG04449	skin:	fetal
35	chr5:88841819-88841869	HepG2	liver:	n/a
36	chr5:88743831-88743881	PFSK-1	brain:	n/a
37	chr5:88841819-88841869	HUVEC	blood vessel:	n/a
38	chr5:88841819-88841869	SKMC	muscle:	n/a
39	chr5:88743831-88743881	AoSMC	blood vessel:	n/a
40	chr5:88841819-88841869	HCPEpiC	choroid plexus:	n/a
41	chr5:88743831-88743881	SK-N-SH_RA	brain:	n/a
42	chr5:88743831-88743881	GM12878	blood:	n/a
43	chr5:88743831-88743881	A549	lung:	n/a
44	chr5:88841819-88841869	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:88743831-88743881	HMEC	breast:	n/a
46	chr5:88841819-88841869	AG04449	skin:	fetal
47	chr5:88841819-88841869	A549	lung:	n/a
48	chr5:88743831-88743881	AG09319	gingival:	n/a
49	chr5:88841819-88841869	AG09309	skin:	n/a
50	chr5:88841819-88841869	AoSMC	blood vessel:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:88787804..88789965-chr5:88795171..88796808,2	K562	blood:
2	chr5:88804889..88807788-chr5:88808205..88810352,2	MCF-7	breast:
3	chr5:88745543..88747237-chr5:88748817..88750936,2	K562	blood:
4	chr5:88737623..88740179-chr5:88745152..88747035,3	K562	blood:
5	chr5:88745543..88747237-chr5:88748817..88750936,2	K562	blood:
6	chr5:88626274..88628932-chr5:88808961..88810687,2	K562	blood:
7	chr5:88767316..88769071-chr5:88771619..88773249,2	K562	blood:
8	chr5:88735614..88737189-chr5:88739533..88741408,2	K562	blood:
9	chr5:88735614..88738275-chr5:88739232..88742098,4	K562	blood:
10	chr5:88787804..88789965-chr5:88795171..88796808,2	K562	blood:
11	chr5:88154042..88155720-chr5:88829784..88831835,2	K562	blood:
12	chr5:88735614..88737189-chr5:88739533..88741408,2	K562	blood:
13	chr5:88756505..88760313-chr5:88761840..88765543,4	K562	blood:
14	chr5:88824860..88827557-chr5:88839879..88842454,2	MCF-7	breast:
15	chr5:88742180..88743903-chr5:88752684..88754964,2	K562	blood:
16	chr5:88796469..88798538-chr5:88815057..88816852,2	K562	blood:
17	chr5:88737623..88740179-chr5:88745152..88747035,3	K562	blood:
18	chr5:88812007..88813585-chr5:88815371..88817871,2	K562	blood:
19	chr5:88735614..88738275-chr5:88739232..88742098,4	K562	blood:
20	chr5:88756505..88760313-chr5:88761840..88765543,4	K562	blood:
21	chr5:88796469..88798538-chr5:88815057..88816852,2	K562	blood:
22	chr5:88781201..88784356-chr5:88786376..88788302,3	K562	blood:
23	chr5:88767316..88769071-chr5:88771619..88773249,2	K562	blood:
24	chr5:88781201..88784356-chr5:88786376..88788302,3	K562	blood:
25	chr5:88812007..88813585-chr5:88815371..88817871,2	K562	blood:
26	chr5:88742180..88743903-chr5:88752684..88754964,2	K562	blood:
27	chr5:88804889..88807788-chr5:88808205..88810352,2	MCF-7	breast:
28	chr5:88824860..88827557-chr5:88839879..88842454,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASA1-7	chr5:88751921-88751947	NONHSAT102714
2	lnc-RASA1-7	chr5:88761733-88761799	ENSG00000248309
3	lnc-RASA1-7	chr5:88761483-88761592	ENSG00000248309
4	lnc-MEF2C-4	chr5:88762354-88762488	XLOC_004920
5	lnc-RASA1-7	chr5:88761483-88761592	ENSG00000248309
6	lnc-POLR3G-6	chr5:88798050-88798601	l_2967_chr5:88797271-88798601_brain
7	lnc-RASA1-7	chr5:88797239-88797268	l_2966_chr5:88236262-88274788_thyroid
8	lnc-RASA1-7	chr5:88761483-88761592	NONHSAT102714
9	lnc-MEF2C-4	chr5:88765739-88765856	XLOC_004920
10	lnc-POLR3G-6	chr5:88797272-88797348	l_2967_chr5:88797271-88798601_brain
11	lnc-RASA1-7	chr5:88761733-88761925	NONHSAT102714
12	lnc-POLR3G-6	chr5:88797489-88798034	l_2967_chr5:88797271-88798601_brain
13	lnc-RASA1-7	chr5:88761733-88762215	ENSG00000248309

No data

Variant related genes	Relation type
ENSG00000250831	TF binding region
ENSG00000250831	CpG island
MAPK1	miRNA target sites
TRPC3	miRNA target sites
CD276	miRNA target sites
CDKN1C	miRNA target sites

Extended variants
information (count: 2176 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2176 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9293514	chr5:88736275-88736276	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs9293515	chr5:88736293-88736294	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs538642310	chr5:88736311-88736312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559039403	chr5:88736322-88736323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572471233	chr5:88736396-88736397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541480451	chr5:88736406-88736407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561155413	chr5:88736434-88736435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190276742	chr5:88736474-88736475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138135959	chr5:88736477-88736478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563628219	chr5:88736553-88736554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531368601	chr5:88736559-88736560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73772160	chr5:88736576-88736577	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs564868486	chr5:88736578-88736579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs202087667	chr5:88736669-88736670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527406220	chr5:88736721-88736722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7724981	chr5:88736827-88736828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181482226	chr5:88736867-88736868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567516941	chr5:88736935-88736936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144248429	chr5:88736941-88736942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550134215	chr5:88736947-88736948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187566927	chr5:88736974-88736975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373018951	chr5:88737033-88737034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558698486	chr5:88737058-88737059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566023297	chr5:88737085-88737086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534794380	chr5:88737114-88737115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535500973	chr5:88737204-88737205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554639871	chr5:88737215-88737216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574731542	chr5:88737223-88737224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148320684	chr5:88737231-88737232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540991416	chr5:88737232-88737233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141449604	chr5:88737246-88737247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564331071	chr5:88737265-88737266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577487644	chr5:88737340-88737341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375769755	chr5:88737399-88737400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143507878	chr5:88737458-88737459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546440824	chr5:88737558-88737559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369597328	chr5:88737567-88737568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140033006	chr5:88737574-88737575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527277466	chr5:88737593-88737594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541171732	chr5:88737663-88737664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560950503	chr5:88737681-88737682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529943814	chr5:88737682-88737683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556767792	chr5:88737718-88737719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554794093	chr5:88737790-88737791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569800069	chr5:88737824-88737825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191852022	chr5:88737851-88737852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs117855797	chr5:88737862-88737863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs180941509	chr5:88737904-88737905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534688033	chr5:88737926-88737927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79121955	chr5:88737934-88737935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	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
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Colorectal cancer	16774939	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:88731800-88738200	Enhancers	Primary B cells from peripheral blood	blood
2	chr5:88732000-88738600	Enhancers	Primary B cells from cord blood	blood
3	chr5:88732400-88737000	Enhancers	HSMM	muscle
4	chr5:88732800-88739200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:88734800-88736600	Weak transcription	Fetal Heart	heart
6	chr5:88735000-88736800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr5:88735000-88740400	Weak transcription	K562	blood
8	chr5:88735600-88739400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:88735800-88739000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr5:88736600-88736800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr5:88736600-88736800	Enhancers	HSMMtube	muscle
12	chr5:88736600-88737000	Enhancers	Fetal Heart	heart
13	chr5:88736800-88737000	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr5:88736800-88742600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr5:88737400-88738400	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr5:88737600-88738200	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr5:88737600-88741400	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr5:88738200-88739200	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr5:88738200-88739400	Weak transcription	Primary B cells from peripheral blood	blood
20	chr5:88738400-88738800	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr5:88738600-88738800	Flanking Active TSS	Primary B cells from cord blood	blood
22	chr5:88738600-88741000	Enhancers	Fetal Brain Male	brain
23	chr5:88738800-88739200	Enhancers	Primary B cells from cord blood	blood
24	chr5:88738800-88739600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr5:88739000-88741400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr5:88739200-88739800	Enhancers	Fetal Brain Female	brain
27	chr5:88739200-88740400	Flanking Active TSS	Primary B cells from cord blood	blood
28	chr5:88739200-88741400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr5:88739200-88742200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:88739400-88739800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr5:88739400-88741000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr5:88739400-88741000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr5:88739400-88752000	Enhancers	Primary B cells from peripheral blood	blood
34	chr5:88739600-88740800	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr5:88739600-88740800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr5:88739600-88741000	Enhancers	Primary hematopoietic stem cells	blood
37	chr5:88739800-88740000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr5:88739800-88740600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:88739800-88743200	Weak transcription	Fetal Brain Female	brain
40	chr5:88740000-88741200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr5:88740000-88741600	Enhancers	GM12878-XiMat	blood
42	chr5:88740200-88743000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr5:88740400-88741200	Enhancers	Primary T cells from cord blood	blood
44	chr5:88740400-88742000	Enhancers	K562	blood
45	chr5:88740400-88744800	Enhancers	Primary B cells from cord blood	blood
46	chr5:88740800-88741200	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr5:88740800-88752400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr5:88741000-88741200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:88741000-88743000	Weak transcription	Fetal Brain Male	brain
50	chr5:88741200-88741600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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