Variant report

Variant	nsv829962
Chromosome Location	chr4:69786869-69910283
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	chr4:69898611-69898899	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69819154-69819171	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69885882-69886539	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69884842-69885191	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69813520-69815344	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69888831-69889086	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69885444-69885630	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:69816858-69818218	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:69819937-69820253	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:69815737-69816071	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:69890715-69891247	HepG2	liver:	n/a	n/a
12	ATF1	chr4:69819917-69820207	K562	blood:	n/a	n/a
13	ATF2	chr4:69816810-69817127	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr4:69900085-69900485	A549	lung:	n/a	n/a
15	BATF	chr4:69817167-69817565	GM12878	blood:	n/a	chr4:69817539-69817548
16	BATF	chr4:69904359-69904628	GM12878	blood:	n/a	chr4:69904462-69904472 chr4:69904458-69904468 chr4:69904461-69904472
17	BCL11A	chr4:69817186-69817521	GM12878	blood:	n/a	n/a
18	BCL3	chr4:69899981-69900657	A549	lung:	n/a	n/a
19	BCL3	chr4:69900041-69900545	A549	lung:	n/a	n/a
20	BCL3	chr4:69885805-69886533	A549	lung:	n/a	n/a
21	BCL3	chr4:69898499-69898958	A549	lung:	n/a	n/a
22	BHLHE40	chr4:69852928-69852991	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:69817141-69817585	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:69898527-69898916	A549	lung:	n/a	n/a
25	CEBPB	chr4:69808523-69808836	IMR90	lung:	n/a	chr4:69808687-69808698
26	CEBPB	chr4:69882088-69882303	IMR90	lung:	n/a	chr4:69882226-69882239 chr4:69882226-69882239 chr4:69882226-69882239 chr4:69882226-69882237 chr4:69882228-69882239
27	CEBPB	chr4:69882055-69882382	HepG2	liver:	n/a	chr4:69882226-69882239 chr4:69882226-69882239 chr4:69882226-69882239 chr4:69882226-69882237 chr4:69882228-69882239
28	CEBPB	chr4:69898624-69898950	MCF-7	breast:	n/a	n/a
29	CEBPB	chr4:69910170-69910524	IMR90	lung:	n/a	chr4:69910371-69910382
30	CEBPB	chr4:69898670-69898946	MCF-7	breast:	n/a	n/a
31	CEBPB	chr4:69900095-69900462	A549	lung:	n/a	n/a
32	CEBPB	chr4:69883582-69883882	HepG2	liver:	n/a	chr4:69883701-69883712 chr4:69883703-69883714 chr4:69883701-69883714 chr4:69883701-69883714
33	CEBPB	chr4:69813781-69814379	HepG2	liver:	n/a	chr4:69813934-69813945
34	CEBPB	chr4:69894252-69894628	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr4:69817993-69818138	HepG2	liver:	n/a	chr4:69818070-69818081
36	CEBPB	chr4:69793025-69793234	A549	lung:	n/a	chr4:69793134-69793145 chr4:69793136-69793145
37	CEBPB	chr4:69895793-69896419	HepG2	liver:	n/a	chr4:69896249-69896260 chr4:69896406-69896417 chr4:69896248-69896259 chr4:69896406-69896417
38	CEBPB	chr4:69813749-69814386	HepG2	liver:	n/a	chr4:69813934-69813945
39	CEBPB	chr4:69829647-69829949	HepG2	liver:	n/a	chr4:69829802-69829813
40	CEBPB	chr4:69899904-69900396	A549	lung:	n/a	n/a
41	CEBPB	chr4:69888809-69888934	HepG2	liver:	n/a	chr4:69888891-69888904 chr4:69888893-69888904 chr4:69888891-69888902
42	CEBPB	chr4:69888701-69889087	HepG2	liver:	n/a	chr4:69888891-69888904 chr4:69888893-69888904 chr4:69888891-69888902
43	CEBPB	chr4:69886177-69886484	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:69813842-69814114	A549	lung:	n/a	chr4:69813934-69813945
45	CEBPB	chr4:69882137-69882260	K562	blood:	n/a	chr4:69882226-69882239 chr4:69882226-69882239 chr4:69882226-69882239 chr4:69882226-69882237 chr4:69882228-69882239
46	CEBPB	chr4:69831597-69831751	HepG2	liver:	n/a	chr4:69831648-69831659
47	CEBPB	chr4:69886176-69886490	A549	lung:	n/a	n/a
48	CEBPB	chr4:69898612-69899241	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:69896090-69896374	A549	lung:	n/a	chr4:69896249-69896260 chr4:69896248-69896259
50	CEBPB	chr4:69898630-69898927	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69859705-69859755	NB4	blood:	n/a
2	chr4:69859705-69859755	NB4	blood:	n/a
3	chr4:69859705-69859755	IMR90	lung:	fetal
4	chr4:69818856-69818906	MCF10A-Er-Src	breast:	n/a
5	chr4:69819820-69819870	IMR90	lung:	fetal
6	chr4:69819820-69819870	T-47D	breast:	n/a
7	chr4:69810056-69810106	ProgFib	skin:	n/a
8	chr4:69829409-69829459	H1-hESC	embryonic stem cell:	embryo
9	chr4:69817080-69817130	SKMC	muscle:	n/a
10	chr4:69829409-69829459	ECC-1	luminal epithelium:	n/a
11	chr4:69859705-69859755	AG09309	skin:	n/a
12	chr4:69818856-69818906	NB4	blood:	n/a
13	chr4:69829409-69829459	HRPEpiC	eye:	n/a
14	chr4:69829409-69829459	RPTEC	kidney:	n/a
15	chr4:69810056-69810106	NHDF-neo	bronchial:	n/a
16	chr4:69810056-69810106	BE2_C	brain:	n/a
17	chr4:69819820-69819870	HCT-116	colon:	n/a
18	chr4:69859705-69859755	HMEC	breast:	n/a
19	chr4:69829409-69829459	Caco-2	colon:	n/a
20	chr4:69819820-69819870	HL-60	blood:	n/a
21	chr4:69819820-69819870	HMEC	breast:	n/a
22	chr4:69810056-69810106	SK-N-SH	brain:	n/a
23	chr4:69817080-69817130	AG04449	skin:	fetal
24	chr4:69829409-69829459	AG04449	skin:	fetal
25	chr4:69817080-69817130	IMR90	lung:	fetal
26	chr4:69829409-69829459	PFSK-1	brain:	n/a
27	chr4:69829409-69829459	HIPEpiC	eye:	n/a
28	chr4:69829409-69829459	AG09319	gingival:	n/a
29	chr4:69810056-69810106	ovcar-3	ovarian:	n/a
30	chr4:69829409-69829459	GM12891	blood:	n/a
31	chr4:69810056-69810106	NHBE	bronchial:	n/a
32	chr4:69817080-69817130	MCF10A-Er-Src	breast:	n/a
33	chr4:69810056-69810106	T-47D	breast:	n/a
34	chr4:69819820-69819870	GM12878	blood:	n/a
35	chr4:69859705-69859755	PANC-1	pancreas:	n/a
36	chr4:69810056-69810106	AG10803	skin:	n/a
37	chr4:69859705-69859755	SK-N-SH	brain:	n/a
38	chr4:69818856-69818906	HCF	heart:	n/a
39	chr4:69819820-69819870	NH-A	brain:	n/a
40	chr4:69817080-69817130	HRE	kidney:	n/a
41	chr4:69859705-69859755	HCT-116	colon:	n/a
42	chr4:69859705-69859755	PrEC	prostate:	n/a
43	chr4:69818856-69818906	SAEC	small airway:	n/a
44	chr4:69829409-69829459	BE2_C	brain:	n/a
45	chr4:69817080-69817130	NT2-D1	testis:	n/a
46	chr4:69859705-69859755	HNPCEpiC	eye:	n/a
47	chr4:69859705-69859755	MCF10A-Er-Src	breast:	n/a
48	chr4:69810056-69810106	CMK	blood:	n/a
49	chr4:69810056-69810106	GM12892	blood:	n/a
50	chr4:69810056-69810106	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:69894916..69897017-chr4:69914362..69916605,2	MCF-7	breast:
2	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2A3-7	chr4:69862653-69863427	NONHSAT096749
2	lnc-UGT2A3-3	chr4:69841579-69841711	NONHSAT096748
3	lnc-UGT2A3-3	chr4:69838717-69838993	NONHSAT096748
4	lnc-UGT2A3-9	chr4:69887374-69888058	NONHSAT096750
5	lnc-UGT2A3-3	chr4:69840118-69840199	NONHSAT096748
6	lnc-UGT2A3-3	chr4:69839506-69839719	NONHSAT096748

Variant related genes	Relation type
ENSG00000249890	TF binding region
ENSG00000251685	TF binding region
ENSG00000251498	TF binding region
ENSG00000249735	TF binding region
UGT2A3	TF binding region
ENSG00000198277	TF binding region
ENSG00000250919	TF binding region
ENSG00000250277	TF binding region
ENSG00000249890	CpG island
ENSG00000251685	CpG island
ENSG00000251498	CpG island
ENSG00000249735	CpG island
UGT2A3	CpG island
ENSG00000198277	CpG island
ENSG00000250919	CpG island
ENSG00000250277	CpG island

Extended variants
information (count: 5311 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5311 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7688541	chr4:69789680-69789681	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs55647928	chr4:69789705-69789706	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs546574106	chr4:69789717-69789718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182440667	chr4:69789842-69789843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13128843	chr4:69789855-69789856	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs549169671	chr4:69789856-69789857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143969494	chr4:69789890-69789891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115141425	chr4:69789920-69789921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185634341	chr4:69789926-69789927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533794837	chr4:69789928-69789929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115420194	chr4:69789956-69789957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559959189	chr4:69789965-69789966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536353818	chr4:69789974-69789975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555937447	chr4:69790026-69790027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs55795005	chr4:69790028-69790029	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs190346585	chr4:69790049-69790050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182742569	chr4:69790058-69790059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540537229	chr4:69790062-69790063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573445908	chr4:69790064-69790065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529226991	chr4:69790117-69790118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188237494	chr4:69790122-69790123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191910302	chr4:69790204-69790205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570015474	chr4:69790243-69790244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372305440	chr4:69790255-69790256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs367921149	chr4:69790280-69790281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531572992	chr4:69790282-69790283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551583120	chr4:69790317-69790318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551924250	chr4:69790320-69790321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558973742	chr4:69790333-69790334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs17147006	chr4:69790343-69790344	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs11736796	chr4:69790366-69790367	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs547332523	chr4:69790373-69790374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567255785	chr4:69790394-69790395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533096052	chr4:69790420-69790421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535866289	chr4:69790431-69790432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556263849	chr4:69790480-69790481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11946857	chr4:69790483-69790484	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs192607927	chr4:69790499-69790500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538076525	chr4:69790530-69790531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557945897	chr4:69790568-69790569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375731670	chr4:69790582-69790583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs34220506	chr4:69790594-69790595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373788854	chr4:69790596-69790597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569714635	chr4:69790625-69790626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116446381	chr4:69790656-69790657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540925330	chr4:69790694-69790695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554167424	chr4:69790695-69790696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12650284	chr4:69790761-69790762	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs114267108	chr4:69790779-69790780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563002265	chr4:69790811-69790812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69789600-69789800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr4:69789800-69790400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr4:69790000-69790600	Enhancers	HepG2	liver
4	chr4:69790400-69790600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:69790600-69792800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:69790600-69793800	Weak transcription	HepG2	liver
7	chr4:69791800-69794800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr4:69792000-69795000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr4:69792400-69812600	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr4:69792800-69793000	ZNF genes & repeats	Fetal Intestine Large	intestine
11	chr4:69792800-69793200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:69792800-69793400	Enhancers	Liver	Liver
13	chr4:69793000-69797200	Strong transcription	Fetal Intestine Large	intestine
14	chr4:69793400-69794800	Weak transcription	Liver	Liver
15	chr4:69793800-69794200	ZNF genes & repeats	Fetal Intestine Small	intestine
16	chr4:69793800-69797200	Strong transcription	HepG2	liver
17	chr4:69794200-69806200	Weak transcription	Fetal Intestine Small	intestine
18	chr4:69794600-69809400	Weak transcription	Pancreas	Pancrea
19	chr4:69794800-69796400	Strong transcription	Rectal Mucosa Donor 31	rectum
20	chr4:69794800-69796600	Strong transcription	Liver	Liver
21	chr4:69795000-69798000	Strong transcription	Duodenum Mucosa	Duodenum
22	chr4:69796400-69814400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr4:69796600-69813800	Weak transcription	Liver	Liver
24	chr4:69797200-69802400	Weak transcription	HepG2	liver
25	chr4:69797200-69806000	Weak transcription	Fetal Intestine Large	intestine
26	chr4:69798000-69806200	Weak transcription	Duodenum Mucosa	Duodenum
27	chr4:69802400-69803000	Enhancers	HepG2	liver
28	chr4:69803000-69804000	Weak transcription	HepG2	liver
29	chr4:69804000-69804400	Enhancers	HepG2	liver
30	chr4:69804400-69809400	Weak transcription	HepG2	liver
31	chr4:69805800-69806000	Active TSS	Sigmoid Colon	Sigmoid Colon
32	chr4:69806000-69807400	Strong transcription	Fetal Intestine Large	intestine
33	chr4:69806000-69809400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr4:69806200-69807000	ZNF genes & repeats	Fetal Intestine Small	intestine
35	chr4:69806200-69807400	Strong transcription	Duodenum Mucosa	Duodenum
36	chr4:69807000-69812600	Weak transcription	Fetal Intestine Small	intestine
37	chr4:69807400-69809200	Weak transcription	Fetal Intestine Large	intestine
38	chr4:69807400-69812200	Weak transcription	Duodenum Mucosa	Duodenum
39	chr4:69808600-69819600	Weak transcription	Small Intestine	intestine
40	chr4:69809200-69810000	Strong transcription	Fetal Intestine Large	intestine
41	chr4:69809400-69809600	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
42	chr4:69809400-69809800	Genic enhancers	Pancreas	Pancrea
43	chr4:69809400-69809800	Genic enhancers	HepG2	liver
44	chr4:69809600-69814600	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr4:69809800-69812400	Enhancers	HepG2	liver
46	chr4:69809800-69814600	Weak transcription	Pancreas	Pancrea
47	chr4:69810000-69811000	Weak transcription	Fetal Intestine Large	intestine
48	chr4:69811000-69811600	ZNF genes & repeats	Fetal Intestine Large	intestine
49	chr4:69811600-69817600	Active TSS	Fetal Intestine Large	intestine
50	chr4:69812200-69817800	Active TSS	Duodenum Mucosa	Duodenum

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