Variant report

Variant	nsv879258
Chromosome Location	chr4:69364862-69533493
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:648)
CpG islands
(count:428)
Chromatin interactive
region (count:4)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
7	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
8	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
9	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
10	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
11	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
16	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
18	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
19	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
21	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
22	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
24	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
25	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
27	CTCF	chr4:69443380-69443530	K562	blood:	n/a	n/a
28	CTCF	chr4:69443463-69443531	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:69434832-69435088	GM19238	blood:	n/a	n/a
30	CTCF	chr4:69384740-69384847	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr4:69432120-69432270	GM12875	blood:	n/a	n/a
32	CTCF	chr4:69443441-69443533	ProgFib	skin:	n/a	n/a
33	CTCF	chr4:69523173-69523177	K562	blood:	n/a	n/a
34	CTCF	chr4:69384765-69384845	NHEK	skin:	n/a	n/a
35	CTCF	chr4:69434845-69435046	GM19239	blood:	n/a	n/a
36	CTCF	chr4:69434869-69435059	GM19240	blood:	n/a	n/a
37	CTCF	chr4:69432244-69432356	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:69531989-69532010	Lung_OC	lung:	n/a	n/a
39	CTCF	chr4:69434860-69435010	GM12873	blood:	n/a	n/a
40	CTCF	chr4:69443440-69443590	GM12874	blood:	n/a	n/a
41	CTCF	chr4:69418673-69418677	HepG2	liver:	n/a	n/a
42	CTCF	chr4:69523054-69523235	NHEK	skin:	n/a	n/a
43	CTCF	chr4:69443320-69443470	RPTEC	kidney:	n/a	n/a
44	CTCF	chr4:69369303-69369304	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:69443380-69443530	GM12871	blood:	n/a	n/a
46	CTCF	chr4:69419859-69419901	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr4:69369336-69369406	GM12891	blood:	n/a	n/a
48	CTCF	chr4:69434840-69434990	HCT-116	colon:	n/a	n/a
49	CTCF	chr4:69434870-69435076	LNCaP	prostate:	n/a	n/a
50	CTCF	chr4:69443460-69443610	GM12872	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69435593-69435643	RPTEC	kidney:	n/a
2	chr4:69435593-69435643	RPTEC	kidney:	n/a
3	chr4:69522639-69522689	ProgFib	skin:	n/a
4	chr4:69435601-69435651	HCPEpiC	choroid plexus:	n/a
5	chr4:69435601-69435651	HMEC	breast:	n/a
6	chr4:69522639-69522689	GM06990	blood:	n/a
7	chr4:69381368-69381418	HMEC	breast:	n/a
8	chr4:69435593-69435643	AG04449	skin:	fetal
9	chr4:69435601-69435651	HRE	kidney:	n/a
10	chr4:69435601-69435651	HNPCEpiC	eye:	n/a
11	chr4:69522639-69522689	Jurkat	blood:	n/a
12	chr4:69435250-69435300	PANC-1	pancreas:	n/a
13	chr4:69381368-69381418	RPTEC	kidney:	n/a
14	chr4:69435601-69435651	HCT-116	colon:	n/a
15	chr4:69435250-69435300	U87	brain:	n/a
16	chr4:69381368-69381418	PFSK-1	brain:	n/a
17	chr4:69514031-69514081	RPTEC	kidney:	n/a
18	chr4:69434475-69434525	HEK293	kidney:	embryo
19	chr4:69435601-69435651	NT2-D1	testis:	n/a
20	chr4:69381368-69381418	ECC-1	luminal epithelium:	n/a
21	chr4:69522639-69522689	K562	blood:	n/a
22	chr4:69435601-69435651	Caco-2	colon:	n/a
23	chr4:69435601-69435651	CMK	blood:	n/a
24	chr4:69522639-69522689	HRCEpiC	kidney:	n/a
25	chr4:69435601-69435651	NHBE	bronchial:	n/a
26	chr4:69522639-69522689	PANC-1	pancreas:	n/a
27	chr4:69435250-69435300	MCF-7	breast:	n/a
28	chr4:69522639-69522689	HRPEpiC	eye:	n/a
29	chr4:69434475-69434525	SK-N-SH	brain:	n/a
30	chr4:69435593-69435643	HepG2	liver:	n/a
31	chr4:69435250-69435300	SK-N-MC	brain:	n/a
32	chr4:69435601-69435651	HRPEpiC	eye:	n/a
33	chr4:69434475-69434525	NHBE	bronchial:	n/a
34	chr4:69514031-69514081	NH-A	brain:	n/a
35	chr4:69514031-69514081	PrEC	prostate:	n/a
36	chr4:69522639-69522689	HCT-116	colon:	n/a
37	chr4:69434475-69434525	GM19239	blood:	n/a
38	chr4:69435601-69435651	HUVEC	blood vessel:	n/a
39	chr4:69522639-69522689	A549	lung:	n/a
40	chr4:69434475-69434525	HNPCEpiC	eye:	n/a
41	chr4:69434475-69434525	HCT-116	colon:	n/a
42	chr4:69381368-69381418	A549	lung:	n/a
43	chr4:69435250-69435300	HCM	heart:	n/a
44	chr4:69381368-69381418	SK-N-MC	brain:	n/a
45	chr4:69435593-69435643	H1-hESC	embryonic stem cell:	embryo
46	chr4:69381368-69381418	HAEpiC	amniotic membrane:	n/a
47	chr4:69522639-69522689	HepG2	liver:	n/a
48	chr4:69434475-69434525	HRPEpiC	eye:	n/a
49	chr4:69435601-69435651	SK-N-SH	brain:	n/a
50	chr4:69434475-69434525	BJ	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
2	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
3	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
4	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
2	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
3	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733
4	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
5	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
6	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735

No data

Variant related genes	Relation type
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B29P	TF binding region
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B29P	CpG island
ENSG00000272626	chromatin interactions
ENSG00000249985	chromatin interactions

Extended variants
information (count: 4629 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4629 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62317909	chr4:69364862-69364863	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527411341	chr4:69364876-69364877	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146661148	chr4:69364902-69364903	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs543982284	chr4:69364909-69364910	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs566993873	chr4:69364917-69364918	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536099231	chr4:69364926-69364927	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs555794611	chr4:69364963-69364964	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs568876773	chr4:69364990-69364991	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs2603153	chr4:69365052-69365053	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs144135064	chr4:69365070-69365071	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs529750956	chr4:69365086-69365087	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs376651959	chr4:69365135-69365136	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs146488579	chr4:69365280-69365281	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs534070317	chr4:69365291-69365292	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs35623125	chr4:69365310-69365311	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs376482058	chr4:69365319-69365320	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs553932577	chr4:69365402-69365403	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs573760358	chr4:69365403-69365404	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs149073052	chr4:69365489-69365490	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs369099888	chr4:69365503-69365504	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs562788756	chr4:69365540-69365541	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs143130009	chr4:69365569-69365570	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs62317910	chr4:69365591-69365592	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs140488875	chr4:69365612-69365613	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs527373174	chr4:69365616-69365617	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs532303636	chr4:69365618-69365619	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs191054110	chr4:69365630-69365631	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs560694420	chr4:69365650-69365651	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs147042826	chr4:69365696-69365697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138265823	chr4:69365725-69365726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548394487	chr4:69365759-69365760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569184135	chr4:69365769-69365770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144110036	chr4:69365771-69365772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551350420	chr4:69365821-69365822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146893683	chr4:69365822-69365823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374375501	chr4:69365836-69365837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368766074	chr4:69365891-69365892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534255035	chr4:69365902-69365903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553986667	chr4:69365916-69365917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573748167	chr4:69365917-69365918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138894878	chr4:69365984-69365985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149417368	chr4:69366002-69366003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62317911	chr4:69366011-69366012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs180765811	chr4:69366015-69366016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2708671	chr4:69366046-69366047	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs571954782	chr4:69366071-69366072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574844935	chr4:69366129-69366130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541086490	chr4:69366135-69366136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570837102	chr4:69366145-69366146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs62317912	chr4:69366170-69366171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:91)

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
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69363600-69365000	Enhancers	A549	lung
2	chr4:69363600-69365600	Enhancers	HepG2	liver
3	chr4:69364000-69365200	Enhancers	Liver	Liver
4	chr4:69364400-69365000	Active TSS	Fetal Intestine Large	intestine
5	chr4:69364400-69365000	Active TSS	Rectal Mucosa Donor 31	rectum
6	chr4:69364800-69365000	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr4:69365000-69365400	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr4:69365200-69370400	Weak transcription	Liver	Liver
9	chr4:69369400-69369600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:69370200-69370600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:69370400-69370800	ZNF genes & repeats	Liver	Liver
12	chr4:69370600-69371200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr4:69370600-69371200	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr4:69370800-69371200	Enhancers	Primary T cells fromperipheralblood	blood
15	chr4:69370800-69371200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr4:69370800-69371200	Enhancers	Gastric	stomach
17	chr4:69370800-69371200	Enhancers	Spleen	Spleen
18	chr4:69370800-69372000	Weak transcription	Liver	Liver
19	chr4:69371000-69371200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr4:69371200-69372200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr4:69372200-69372400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr4:69373400-69373800	Enhancers	Fetal Heart	heart
23	chr4:69373800-69374200	Weak transcription	Fetal Heart	heart
24	chr4:69374200-69375200	Enhancers	Fetal Heart	heart
25	chr4:69388400-69389000	Enhancers	NHEK	skin
26	chr4:69401800-69402200	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr4:69402000-69402400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr4:69402200-69402600	Strong transcription	Rectal Mucosa Donor 31	rectum
29	chr4:69402400-69411000	Weak transcription	Small Intestine	intestine
30	chr4:69402600-69403200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr4:69402800-69403400	ZNF genes & repeats	Liver	Liver
32	chr4:69403200-69403800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
33	chr4:69403400-69404800	Strong transcription	Liver	Liver
34	chr4:69403800-69404800	Strong transcription	Rectal Mucosa Donor 31	rectum
35	chr4:69404200-69404600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:69404200-69410000	Weak transcription	Colonic Mucosa	Colon
37	chr4:69404600-69406200	Weak transcription	Duodenum Mucosa	Duodenum
38	chr4:69404800-69405600	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr4:69404800-69406800	Weak transcription	Liver	Liver
40	chr4:69405600-69406800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
41	chr4:69406200-69407000	Strong transcription	Duodenum Mucosa	Duodenum
42	chr4:69406800-69407800	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr4:69406800-69409200	Strong transcription	Liver	Liver
44	chr4:69407000-69413800	Weak transcription	Duodenum Mucosa	Duodenum
45	chr4:69407800-69408200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
46	chr4:69408200-69408600	Enhancers	HepG2	liver
47	chr4:69408200-69409200	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr4:69409200-69413600	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr4:69409200-69418800	Weak transcription	Liver	Liver
50	chr4:69413600-69418800	Strong transcription	Rectal Mucosa Donor 31	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links