Variant report

Variant	nsv1001751
Chromosome Location	chr4:124693346-124733305
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	ARID3A	chr4:124694167-124694301	K562	blood:	n/a	n/a
2	ARID3A	chr4:124694121-124694321	HepG2	liver:	n/a	n/a
3	ATF2	chr4:124706623-124707026	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:124697378-124697846	GM12878	blood:	n/a	n/a
5	ATF2	chr4:124697321-124697887	GM12878	blood:	n/a	n/a
6	ATF2	chr4:124706614-124707078	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:124708623-124708915	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr4:124697431-124697787	GM12878	blood:	n/a	n/a
9	BATF	chr4:124697418-124697814	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:124697364-124697785	GM12878	blood:	n/a	n/a
11	BCLAF1	chr4:124697348-124697815	GM12878	blood:	n/a	n/a
12	BCLAF1	chr4:124697428-124697845	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:124694048-124694337	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:124694029-124694272	K562	blood:	n/a	n/a
15	BRCA1	chr4:124694138-124694260	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:124694097-124694261	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:124709864-124710017	HepG2	liver:	n/a	chr4:124709941-124709952
18	CEBPB	chr4:124704280-124704614	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:124706608-124707065	IMR90	lung:	n/a	chr4:124706800-124706813 chr4:124706800-124706811
20	CEBPB	chr4:124693988-124694350	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr4:124706624-124707006	H1-hESC	embryonic stem cell:	n/a	chr4:124706800-124706813 chr4:124706800-124706811
22	CEBPB	chr4:124709759-124710122	IMR90	lung:	n/a	chr4:124710090-124710101 chr4:124710088-124710100 chr4:124709941-124709952
23	CEBPB	chr4:124694052-124694327	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:124706683-124707047	ECC-1	luminal epithelium:	n/a	chr4:124706800-124706813 chr4:124706800-124706811
25	CEBPB	chr4:124706563-124706954	ECC-1	luminal epithelium:	n/a	chr4:124706800-124706813 chr4:124706800-124706811
26	CEBPB	chr4:124706746-124706826	HepG2	liver:	n/a	chr4:124706800-124706813 chr4:124706800-124706811
27	CEBPB	chr4:124694038-124694304	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:124728374-124728672	K562	blood:	n/a	chr4:124728523-124728534
29	CEBPB	chr4:124725797-124726064	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:124728366-124728684	H1-hESC	embryonic stem cell:	n/a	chr4:124728523-124728534
31	CEBPB	chr4:124728367-124728700	IMR90	lung:	n/a	chr4:124728523-124728534
32	CEBPB	chr4:124728401-124728672	Hela-S3	cervix:	n/a	chr4:124728523-124728534
33	CEBPB	chr4:124694065-124694323	K562	blood:	n/a	n/a
34	CEBPB	chr4:124728386-124728710	HepG2	liver:	n/a	chr4:124728523-124728534
35	CHD2	chr4:124697512-124697721	GM12878	blood:	n/a	n/a
36	CHD2	chr4:124694120-124694211	HepG2	liver:	n/a	n/a
37	CHD2	chr4:124694016-124694337	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr4:124706605-124707148	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr4:124693925-124694290	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTBP2	chr4:124706640-124707096	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr4:124693994-124694323	Gliobla	brain:	n/a	chr4:124694166-124694187 chr4:124694165-124694181 chr4:124694164-124694182 chr4:124694169-124694177
42	CTCF	chr4:124697480-124697630	GM12872	blood:	n/a	n/a
43	CTCF	chr4:124694060-124694210	A549	lung:	n/a	chr4:124694166-124694187 chr4:124694165-124694181 chr4:124694164-124694182 chr4:124694169-124694177
44	CTCF	chr4:124693975-124694371	K562	blood:	n/a	chr4:124694166-124694187 chr4:124694165-124694181 chr4:124694164-124694182 chr4:124694169-124694177
45	CTCF	chr4:124694062-124694273	H1-hESC	embryonic stem cell:	n/a	chr4:124694166-124694187 chr4:124694165-124694181 chr4:124694164-124694182 chr4:124694169-124694177
46	CTCF	chr4:124694120-124694270	HCT-116	colon:	n/a	chr4:124694166-124694187 chr4:124694165-124694181 chr4:124694164-124694182 chr4:124694169-124694177
47	CTCF	chr4:124694100-124694250	SAEC	small airway:	n/a	chr4:124694166-124694187 chr4:124694165-124694181 chr4:124694164-124694182 chr4:124694169-124694177
48	CTCF	chr4:124693853-124693903	GM10266	blood:	n/a	n/a
49	CTCF	chr4:124694019-124694331	K562	blood:	n/a	chr4:124694166-124694187 chr4:124694165-124694181 chr4:124694164-124694182 chr4:124694169-124694177
50	CTCF	chr4:124694080-124694230	HMF	breast:	n/a	chr4:124694166-124694187 chr4:124694165-124694181 chr4:124694164-124694182 chr4:124694169-124694177

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:124694137-124694187	PFSK-1	brain:	n/a
2	chr4:124694661-124694711	AoSMC	blood vessel:	n/a
3	chr4:124695251-124695301	HMEC	breast:	n/a
4	chr4:124694178-124694228	RPTEC	kidney:	n/a
5	chr4:124694661-124694711	NHBE	bronchial:	n/a
6	chr4:124695251-124695301	H1-hESC	embryonic stem cell:	embryo
7	chr4:124707571-124707621	AG10803	skin:	n/a
8	chr4:124694178-124694228	GM12878	blood:	n/a
9	chr4:124694137-124694187	IMR90	lung:	fetal
10	chr4:124694661-124694711	GM19239	blood:	n/a
11	chr4:124698165-124698215	SK-N-MC	brain:	n/a
12	chr4:124707571-124707621	HEK293	kidney:	embryo
13	chr4:124695251-124695301	HCF	heart:	n/a
14	chr4:124694661-124694711	AG04450	lung:	fetal
15	chr4:124694137-124694187	AoSMC	blood vessel:	n/a
16	chr4:124698165-124698215	SK-N-SH_RA	brain:	n/a
17	chr4:124694178-124694228	BE2_C	brain:	n/a
18	chr4:124698165-124698215	GM12878	blood:	n/a
19	chr4:124695251-124695301	HCT-116	colon:	n/a
20	chr4:124694661-124694711	AG10803	skin:	n/a
21	chr4:124694661-124694711	K562	blood:	n/a
22	chr4:124694137-124694187	HRE	kidney:	n/a
23	chr4:124694137-124694187	AG09309	skin:	n/a
24	chr4:124695251-124695301	HL-60	blood:	n/a
25	chr4:124707571-124707621	HL-60	blood:	n/a
26	chr4:124694661-124694711	U87	brain:	n/a
27	chr4:124698165-124698215	NB4	blood:	n/a
28	chr4:124694661-124694711	HNPCEpiC	eye:	n/a
29	chr4:124694178-124694228	SK-N-SH_RA	brain:	n/a
30	chr4:124694178-124694228	AG09309	skin:	n/a
31	chr4:124707571-124707621	Hela-S3	cervix:	n/a
32	chr4:124694137-124694187	HCPEpiC	choroid plexus:	n/a
33	chr4:124694661-124694711	HL-60	blood:	n/a
34	chr4:124698165-124698215	BJ	skin:	n/a
35	chr4:124694137-124694187	Hela-S3	cervix:	n/a
36	chr4:124707571-124707621	BE2_C	brain:	n/a
37	chr4:124707571-124707621	RPTEC	kidney:	n/a
38	chr4:124694178-124694228	SKMC	muscle:	n/a
39	chr4:124694178-124694228	HEK293	kidney:	embryo
40	chr4:124695251-124695301	HIPEpiC	eye:	n/a
41	chr4:124707571-124707621	HCM	heart:	n/a
42	chr4:124695251-124695301	SAEC	small airway:	n/a
43	chr4:124694137-124694187	H1-hESC	embryonic stem cell:	embryo
44	chr4:124694178-124694228	HNPCEpiC	eye:	n/a
45	chr4:124695251-124695301	BJ	skin:	n/a
46	chr4:124694137-124694187	HIPEpiC	eye:	n/a
47	chr4:124694661-124694711	HIPEpiC	eye:	n/a
48	chr4:124698165-124698215	CMK	blood:	n/a
49	chr4:124694137-124694187	HEK293	kidney:	embryo
50	chr4:124707571-124707621	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:124693285..124694245-chr4:124911389..124911929,2	MCF-7	breast:
2	chr4:124699081..124701132-chr4:124702124..124704664,2	K562	blood:
3	chr4:124693744..124694615-chr4:125242649..125243563,2	MCF-7	breast:
4	chr4:124688857..124690611-chr4:124692312..124695187,2	K562	blood:
5	chr4:124724821..124726500-chr4:124729716..124731857,2	MCF-7	breast:
6	chr4:124702920..124705025-chr4:124707186..124709646,2	K562	blood:
7	chr4:124702920..124705025-chr4:124707186..124709646,2	K562	blood:
8	chr4:124724821..124726500-chr4:124729716..124731857,2	MCF-7	breast:
9	chr4:124693711..124694660-chr4:124911167..124912152,7	MCF-7	breast:
10	chr4:124693814..124694331-chr4:125183401..125183907,2	MCF-7	breast:
11	chr4:124693787..124694688-chr4:125032781..125033558,3	MCF-7	breast:
12	chr4:124699081..124701132-chr4:124702124..124704664,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT6-5	chr4:124707520-124707893	NONHSAT098202
2	lnc-SPRY1-2	chr4:124695419-124695530	ENSG00000249464
3	lnc-NUDT6-5	chr4:124708066-124708291	NONHSAT098202
4	lnc-SPRY1-2	chr4:124695419-124695530	NONHSAT098201

Variant related genes	Relation type
LINC01091	TF binding region
LINC01091	CpG island
BIVM	miRNA target sites

Extended variants
information (count: 1199 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1199 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16997770	chr4:124693346-124693347	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527839126	chr4:124693377-124693378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547870376	chr4:124693383-124693384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79563804	chr4:124693450-124693451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs62321800	chr4:124693516-124693517	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs550230391	chr4:124693549-124693550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570065758	chr4:124693555-124693556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188898132	chr4:124693570-124693571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556347526	chr4:124693619-124693620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78408176	chr4:124693623-124693624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111236012	chr4:124693645-124693646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6840618	chr4:124693650-124693651	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs547423160	chr4:124693709-124693710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs17424031	chr4:124693724-124693725	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs72913221	chr4:124693868-124693869	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs556585429	chr4:124693993-124693994	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs576420657	chr4:124694062-124694063	Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs2162095	chr4:124694077-124694078	Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs114765215	chr4:124694118-124694119	Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs34096127	chr4:124694209-124694210	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs193114744	chr4:124694255-124694256	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs541230075	chr4:124694268-124694269	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561515157	chr4:124694453-124694454	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs6847105	chr4:124694461-124694462	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs183558980	chr4:124694508-124694509	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs563684465	chr4:124694533-124694534	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs532503052	chr4:124694591-124694592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188499786	chr4:124694609-124694610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6846982	chr4:124694616-124694617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs919015	chr4:124694678-124694679	Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs144419850	chr4:124694684-124694685	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs568242286	chr4:124694704-124694705	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs114311583	chr4:124694822-124694823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs207465034	chr4:124694834-124694835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530419166	chr4:124694848-124694849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556597462	chr4:124694849-124694850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570115374	chr4:124694927-124694928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191735713	chr4:124694990-124694991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs13129313	chr4:124694994-124694995	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572681761	chr4:124695001-124695002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541686179	chr4:124695058-124695059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554908538	chr4:124695060-124695061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565634678	chr4:124695080-124695081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563922656	chr4:124695114-124695115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543938637	chr4:124695116-124695117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199791541	chr4:124695120-124695121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150215592	chr4:124695127-124695128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116370256	chr4:124695232-124695233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533718147	chr4:124695252-124695253	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs371467478	chr4:124695307-124695308	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Hodgkin''s lymphoma	17606441	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124687000-124704600	Weak transcription	Fetal Muscle Leg	muscle
2	chr4:124689600-124698200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr4:124689600-124698200	Weak transcription	Aorta	Aorta
4	chr4:124694000-124694200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:124694000-124694200	ZNF genes & repeats	Fetal Muscle Trunk	muscle
6	chr4:124694000-124694200	Enhancers	Pancreas	Pancrea
7	chr4:124694200-124697600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr4:124694200-124707800	Weak transcription	Pancreas	Pancrea
9	chr4:124694800-124696000	Enhancers	HUVEC	blood vessel
10	chr4:124696000-124698400	Weak transcription	HUVEC	blood vessel
11	chr4:124697000-124697200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:124697000-124697200	Enhancers	Psoas Muscle	Psoas
13	chr4:124697000-124698200	Enhancers	GM12878-XiMat	blood
14	chr4:124697800-124698200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr4:124697800-124698600	Enhancers	Fetal Stomach	stomach
16	chr4:124697800-124699800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:124698000-124699200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:124698200-124698400	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr4:124698200-124698800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr4:124698200-124699000	Enhancers	Brain Anterior Caudate	brain
21	chr4:124698200-124699000	Enhancers	Brain Hippocampus Middle	brain
22	chr4:124698400-124698800	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr4:124698400-124698800	Enhancers	Psoas Muscle	Psoas
24	chr4:124698400-124698800	Enhancers	HUVEC	blood vessel
25	chr4:124698400-124699000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:124698400-124699000	Enhancers	Adipose Nuclei	Adipose
27	chr4:124698400-124699000	Enhancers	NHDF-Ad	bronchial
28	chr4:124698600-124698800	Enhancers	Right Atrium	heart
29	chr4:124698600-124699000	Enhancers	Brain Angular Gyrus	brain
30	chr4:124698600-124699000	Enhancers	Brain Cingulate Gyrus	brain
31	chr4:124698600-124699000	Enhancers	Ovary	ovary
32	chr4:124698600-124704800	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr4:124698800-124703600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr4:124698800-124708000	Weak transcription	Right Atrium	heart
35	chr4:124699000-124703800	Weak transcription	NHDF-Ad	bronchial
36	chr4:124699200-124699800	Weak transcription	Ovary	ovary
37	chr4:124699200-124703800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:124699800-124703600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:124703600-124703800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr4:124703600-124703800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr4:124703600-124706400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr4:124703600-124708600	Enhancers	Osteobl	bone
43	chr4:124703600-124710000	Enhancers	NHLF	lung
44	chr4:124703800-124704000	Enhancers	Stomach Mucosa	stomach
45	chr4:124703800-124704600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:124703800-124704600	Weak transcription	Ovary	ovary
47	chr4:124703800-124704800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr4:124703800-124706200	Enhancers	NHDF-Ad	bronchial
49	chr4:124703800-124710200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:124704000-124708200	Weak transcription	Stomach Mucosa	stomach

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