Variant report

Variant	nsv1002359
Chromosome Location	chr4:69392102-69592846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:865)
CpG islands
(count:611)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:865 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

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	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
6	ATF1	chr4:69559343-69559671	K562	blood:	n/a	n/a
7	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
8	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
9	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
10	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
11	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
12	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
15	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
16	BHLHE40	chr4:69583763-69584005	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
18	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
20	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
22	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
23	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
24	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
25	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
26	CEBPB	chr4:69578074-69578242	A549	lung:	n/a	n/a
27	CEBPB	chr4:69568931-69569294	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:69580237-69580432	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr4:69574389-69574642	A549	lung:	n/a	chr4:69574511-69574522
30	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
32	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
33	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
34	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
35	CEBPB	chr4:69574361-69574618	HepG2	liver:	n/a	chr4:69574511-69574522
36	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
37	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
38	CEBPB	chr4:69574454-69574539	H1-hESC	embryonic stem cell:	n/a	chr4:69574511-69574522
39	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
41	CHD1	chr4:69583916-69583936	GM12878	blood:	n/a	n/a
42	CTCF	chr4:69434840-69434990	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:69434836-69435078	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:69434910-69435051	HepG2	liver:	n/a	n/a
45	CTCF	chr4:69523080-69523234	GM12891	blood:	n/a	n/a
46	CTCF	chr4:69419791-69419934	GM12892	blood:	n/a	n/a
47	CTCF	chr4:69419742-69419997	GM19238	blood:	n/a	n/a
48	CTCF	chr4:69539820-69539970	GM06990	blood:	n/a	n/a
49	CTCF	chr4:69539000-69539150	GM12874	blood:	n/a	n/a
50	CTCF	chr4:69443280-69443430	GM06990	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69537826-69537876	HRE	kidney:	n/a
2	chr4:69537826-69537876	HRE	kidney:	n/a
3	chr4:69537806-69537856	T-47D	breast:	n/a
4	chr4:69435601-69435651	SK-N-SH_RA	brain:	n/a
5	chr4:69537806-69537856	PrEC	prostate:	n/a
6	chr4:69435593-69435643	AG09309	skin:	n/a
7	chr4:69434475-69434525	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:69522639-69522689	AG04449	skin:	fetal
9	chr4:69537826-69537876	HCM	heart:	n/a
10	chr4:69435593-69435643	HepG2	liver:	n/a
11	chr4:69435593-69435643	RPTEC	kidney:	n/a
12	chr4:69522639-69522689	SK-N-SH_RA	brain:	n/a
13	chr4:69435250-69435300	ECC-1	luminal epithelium:	n/a
14	chr4:69537826-69537876	NB4	blood:	n/a
15	chr4:69536319-69536369	HIPEpiC	eye:	n/a
16	chr4:69536319-69536369	PFSK-1	brain:	n/a
17	chr4:69537589-69537639	HIPEpiC	eye:	n/a
18	chr4:69537826-69537876	A549	lung:	n/a
19	chr4:69435601-69435651	A549	lung:	n/a
20	chr4:69434475-69434525	HepG2	liver:	n/a
21	chr4:69536319-69536369	HAEpiC	amniotic membrane:	n/a
22	chr4:69537589-69537639	GM12892	blood:	n/a
23	chr4:69434475-69434525	MCF-7	breast:	n/a
24	chr4:69435601-69435651	NH-A	brain:	n/a
25	chr4:69435250-69435300	SK-N-SH	brain:	n/a
26	chr4:69537806-69537856	MCF10A-Er-Src	breast:	n/a
27	chr4:69434475-69434525	HCT-116	colon:	n/a
28	chr4:69435250-69435300	SKMC	muscle:	n/a
29	chr4:69537826-69537876	SAEC	small airway:	n/a
30	chr4:69434475-69434525	NT2-D1	testis:	n/a
31	chr4:69434475-69434525	HRPEpiC	eye:	n/a
32	chr4:69537826-69537876	GM19239	blood:	n/a
33	chr4:69522639-69522689	K562	blood:	n/a
34	chr4:69435250-69435300	MCF-7	breast:	n/a
35	chr4:69537806-69537856	NH-A	brain:	n/a
36	chr4:69536319-69536369	HUVEC	blood vessel:	n/a
37	chr4:69435601-69435651	HepG2	liver:	n/a
38	chr4:69522639-69522689	H1-hESC	embryonic stem cell:	embryo
39	chr4:69434475-69434525	LNCaP	prostate:	n/a
40	chr4:69536319-69536369	BE2_C	brain:	n/a
41	chr4:69514031-69514081	HIPEpiC	eye:	n/a
42	chr4:69435250-69435300	Caco-2	colon:	n/a
43	chr4:69536319-69536369	NHBE	bronchial:	n/a
44	chr4:69435593-69435643	T-47D	breast:	n/a
45	chr4:69514031-69514081	K562	blood:	n/a
46	chr4:69537589-69537639	Caco-2	colon:	n/a
47	chr4:69537589-69537639	RPTEC	kidney:	n/a
48	chr4:69434475-69434525	HAEpiC	amniotic membrane:	n/a
49	chr4:69537806-69537856	HMEC	breast:	n/a
50	chr4:69435593-69435643	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
2	chr4:69590462..69592610-chr4:69729563..69731579,3	MCF-7	breast:
3	chr3:73105975..73106777-chr4:69561197..69562068,2	MCF-7	breast:
4	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
2	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
3	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
4	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737

No data

Variant related genes	Relation type
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000248635	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B15	TF binding region
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000248635	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island

Extended variants
information (count: 5189 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:5189 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562992390	chr4:69401817-69401818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576124195	chr4:69401830-69401831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545199040	chr4:69401840-69401841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111998535	chr4:69401965-69401966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540871530	chr4:69401970-69401971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527629125	chr4:69401984-69401985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144462726	chr4:69401985-69401986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560583426	chr4:69402020-69402021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529716509	chr4:69402022-69402023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549434324	chr4:69402035-69402036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs180767332	chr4:69402060-69402061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146607478	chr4:69402093-69402094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552000010	chr4:69402208-69402209	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113217883	chr4:69402224-69402225	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112033969	chr4:69402246-69402247	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6820782	chr4:69402305-69402306	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534547148	chr4:69402328-69402329	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554189142	chr4:69402386-69402387	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567637060	chr4:69402396-69402397	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536661673	chr4:69402397-69402398	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113783376	chr4:69402477-69402478	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572924869	chr4:69402489-69402490	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544871739	chr4:69402501-69402502	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111406455	chr4:69402508-69402509	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149053318	chr4:69402574-69402575	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540954783	chr4:69402603-69402604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560867986	chr4:69402629-69402630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186016562	chr4:69402772-69402773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189282022	chr4:69402797-69402798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76588264	chr4:69402799-69402800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532276518	chr4:69402909-69402910	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564911160	chr4:69402971-69402972	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571841697	chr4:69402988-69402989	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78998153	chr4:69403026-69403027	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548076487	chr4:69403106-69403107	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181337449	chr4:69403115-69403116	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185631521	chr4:69403157-69403158	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368908134	chr4:69403185-69403186	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190327863	chr4:69403194-69403195	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536603573	chr4:69403221-69403222	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182887728	chr4:69403247-69403248	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373139562	chr4:69403248-69403249	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74658302	chr4:69403258-69403259	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570042187	chr4:69403279-69403280	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148184203	chr4:69403289-69403290	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200510363	chr4:69403310-69403311	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539157531	chr4:69403316-69403317	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375055477	chr4:69403324-69403325	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377546716	chr4:69403349-69403350	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112076153	chr4:69403356-69403357	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69401800-69402200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr4:69402000-69402400	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr4:69402200-69402600	Strong transcription	Rectal Mucosa Donor 31	rectum
4	chr4:69402400-69411000	Weak transcription	Small Intestine	intestine
5	chr4:69402600-69403200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr4:69402800-69403400	ZNF genes & repeats	Liver	Liver
7	chr4:69403200-69403800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
8	chr4:69403400-69404800	Strong transcription	Liver	Liver
9	chr4:69403800-69404800	Strong transcription	Rectal Mucosa Donor 31	rectum
10	chr4:69404200-69404600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:69404200-69410000	Weak transcription	Colonic Mucosa	Colon
12	chr4:69404600-69406200	Weak transcription	Duodenum Mucosa	Duodenum
13	chr4:69404800-69405600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr4:69404800-69406800	Weak transcription	Liver	Liver
15	chr4:69405600-69406800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
16	chr4:69406200-69407000	Strong transcription	Duodenum Mucosa	Duodenum
17	chr4:69406800-69407800	Strong transcription	Rectal Mucosa Donor 31	rectum
18	chr4:69406800-69409200	Strong transcription	Liver	Liver
19	chr4:69407000-69413800	Weak transcription	Duodenum Mucosa	Duodenum
20	chr4:69407800-69408200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
21	chr4:69408200-69408600	Enhancers	HepG2	liver
22	chr4:69408200-69409200	Strong transcription	Rectal Mucosa Donor 31	rectum
23	chr4:69409200-69413600	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr4:69409200-69418800	Weak transcription	Liver	Liver
25	chr4:69413600-69418800	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr4:69417200-69418400	Enhancers	NHEK	skin
27	chr4:69417800-69418200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:69417800-69419200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:69417800-69420600	Enhancers	HepG2	liver
30	chr4:69418600-69419200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr4:69418800-69419200	Enhancers	Liver	Liver
32	chr4:69418800-69421800	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr4:69420600-69421000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:69421000-69423400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:69421600-69423000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr4:69421800-69422200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:69421800-69422600	Strong transcription	Rectal Mucosa Donor 31	rectum
38	chr4:69422200-69430400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:69422400-69422800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:69422600-69431200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr4:69427200-69427400	Enhancers	Liver	Liver
42	chr4:69427400-69433200	Weak transcription	Liver	Liver
43	chr4:69429200-69439800	Weak transcription	Right Atrium	heart
44	chr4:69430400-69430800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:69431200-69431400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
46	chr4:69431200-69431600	Enhancers	HMEC	breast
47	chr4:69431400-69434600	Active TSS	Rectal Mucosa Donor 31	rectum
48	chr4:69432800-69434200	Active TSS	Duodenum Mucosa	Duodenum
49	chr4:69433200-69433400	Flanking Active TSS	Liver	Liver
50	chr4:69433400-69434000	Active TSS	Liver	Liver

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