Variant report

Variant	esv1828562
Chromosome Location	chr4:69360476-69551732
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1122)
CpG islands
(count:672)
Chromatin interactive
region (count:6)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1122 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
8	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
9	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
10	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
11	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
12	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
13	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
14	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
17	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
18	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
19	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
21	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
23	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
24	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
25	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
27	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
28	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
29	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
30	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
32	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
33	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
35	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
36	CTCF	chr4:69443440-69443590	GM12864	blood:	n/a	n/a
37	CTCF	chr4:69538977-69539098	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:69538960-69539110	A549	lung:	n/a	n/a
39	CTCF	chr4:69537037-69537264	MCF-7	breast:	n/a	n/a
40	CTCF	chr4:69537020-69537170	GM12874	blood:	n/a	n/a
41	CTCF	chr4:69538974-69539100	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr4:69432160-69432310	GM12872	blood:	n/a	n/a
43	CTCF	chr4:69432180-69432330	HepG2	liver:	n/a	n/a
44	CTCF	chr4:69537040-69537190	GM12869	blood:	n/a	n/a
45	CTCF	chr4:69384740-69384847	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr4:69537040-69537190	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:69419814-69419975	GM10248	blood:	n/a	n/a
48	CTCF	chr4:69364240-69364390	Caco-2	colon:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
49	CTCF	chr4:69432307-69432348	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr4:69364100-69364470	ECC-1	luminal epithelium:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69537826-69537876	SAEC	small airway:	n/a
2	chr4:69537826-69537876	SAEC	small airway:	n/a
3	chr4:69537826-69537876	NB4	blood:	n/a
4	chr4:69435601-69435651	NB4	blood:	n/a
5	chr4:69435601-69435651	HAEpiC	amniotic membrane:	n/a
6	chr4:69435601-69435651	T-47D	breast:	n/a
7	chr4:69514031-69514081	T-47D	breast:	n/a
8	chr4:69537589-69537639	AoSMC	blood vessel:	n/a
9	chr4:69537589-69537639	HL-60	blood:	n/a
10	chr4:69537806-69537856	NH-A	brain:	n/a
11	chr4:69537806-69537856	H1-hESC	embryonic stem cell:	embryo
12	chr4:69435593-69435643	RPTEC	kidney:	n/a
13	chr4:69435593-69435643	GM06990	blood:	n/a
14	chr4:69536319-69536369	GM12892	blood:	n/a
15	chr4:69435250-69435300	HAEpiC	amniotic membrane:	n/a
16	chr4:69537806-69537856	BE2_C	brain:	n/a
17	chr4:69536319-69536369	HRPEpiC	eye:	n/a
18	chr4:69536319-69536369	RPTEC	kidney:	n/a
19	chr4:69435601-69435651	ProgFib	skin:	n/a
20	chr4:69435593-69435643	AG09319	gingival:	n/a
21	chr4:69536319-69536369	HEK293	kidney:	embryo
22	chr4:69435601-69435651	RPTEC	kidney:	n/a
23	chr4:69435601-69435651	GM12891	blood:	n/a
24	chr4:69435601-69435651	SK-N-SH	brain:	n/a
25	chr4:69522639-69522689	HUVEC	blood vessel:	n/a
26	chr4:69536319-69536369	NB4	blood:	n/a
27	chr4:69522639-69522689	IMR90	lung:	fetal
28	chr4:69435250-69435300	NH-A	brain:	n/a
29	chr4:69435601-69435651	HMEC	breast:	n/a
30	chr4:69435250-69435300	PrEC	prostate:	n/a
31	chr4:69434475-69434525	H1-hESC	embryonic stem cell:	embryo
32	chr4:69434475-69434525	HMEC	breast:	n/a
33	chr4:69435593-69435643	ProgFib	skin:	n/a
34	chr4:69435593-69435643	NHDF-neo	bronchial:	n/a
35	chr4:69537826-69537876	Jurkat	blood:	n/a
36	chr4:69514031-69514081	U87	brain:	n/a
37	chr4:69381368-69381418	AoSMC	blood vessel:	n/a
38	chr4:69435250-69435300	CMK	blood:	n/a
39	chr4:69514031-69514081	MCF10A-Er-Src	breast:	n/a
40	chr4:69434475-69434525	NT2-D1	testis:	n/a
41	chr4:69434475-69434525	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:69435593-69435643	Hepatocyte	liver:	n/a
43	chr4:69514031-69514081	CMK	blood:	n/a
44	chr4:69434475-69434525	NHBE	bronchial:	n/a
45	chr4:69537806-69537856	ProgFib	skin:	n/a
46	chr4:69522639-69522689	NHDF-neo	bronchial:	n/a
47	chr4:69522639-69522689	HRPEpiC	eye:	n/a
48	chr4:69514031-69514081	PANC-1	pancreas:	n/a
49	chr4:69522639-69522689	A549	lung:	n/a
50	chr4:69514031-69514081	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
2	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
3	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
4	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
5	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
6	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B15	TF binding region
UGT2B29P	TF binding region
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island
UGT2B29P	CpG island
ENSG00000249985	chromatin interactions
ENSG00000272626	chromatin interactions
ENSG00000083896	chromatin interactions

Extended variants
information (count: 5061 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5061 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2708673	chr4:69360483-69360484	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192032102	chr4:69360517-69360518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183795505	chr4:69360540-69360541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550213666	chr4:69360578-69360579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186595337	chr4:69360660-69360661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539170346	chr4:69360668-69360669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189818043	chr4:69360698-69360699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558777236	chr4:69360721-69360722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572318880	chr4:69360733-69360734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34594059	chr4:69360760-69360761	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs554580013	chr4:69360771-69360772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553198381	chr4:69360832-69360833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144307775	chr4:69360951-69360952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566559814	chr4:69360962-69360963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543069883	chr4:69361004-69361005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147809633	chr4:69361030-69361031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141217628	chr4:69361037-69361038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545531538	chr4:69361112-69361113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3805207	chr4:69361118-69361119	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs527882137	chr4:69361204-69361205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs558330190	chr4:69361219-69361220	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150924913	chr4:69361223-69361224	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182336027	chr4:69361242-69361243	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs575947900	chr4:69361250-69361251	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2603156	chr4:69361326-69361327	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs35307342	chr4:69361389-69361390	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs71269068	chr4:69361441-69361442	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs35777071	chr4:69361445-69361446	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs370277100	chr4:69361455-69361456	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs552709406	chr4:69361462-69361463	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs186995861	chr4:69361463-69361464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs145450963	chr4:69361474-69361475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs554822536	chr4:69361595-69361596	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs191854621	chr4:69361605-69361606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138363247	chr4:69361885-69361886	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs560795911	chr4:69362016-69362017	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs576475337	chr4:69362051-69362052	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs3792631	chr4:69362088-69362089	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs374594159	chr4:69362165-69362166	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs530974640	chr4:69362200-69362201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552659057	chr4:69362203-69362204	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572271747	chr4:69362216-69362217	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs183538538	chr4:69362242-69362243	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs561563872	chr4:69362243-69362244	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530319006	chr4:69362251-69362252	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs544142994	chr4:69362258-69362259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs563629696	chr4:69362275-69362276	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs372210263	chr4:69362291-69362292	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2278921	chr4:69362301-69362302	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs148289963	chr4:69362305-69362306	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69355400-69362000	Weak transcription	Esophagus	oesophagus
2	chr4:69359400-69360800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr4:69359800-69360600	Enhancers	Duodenum Mucosa	Duodenum
4	chr4:69359800-69360800	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr4:69360000-69360800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr4:69360000-69360800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:69360200-69360600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr4:69360200-69360600	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr4:69360200-69360600	Enhancers	GM12878-XiMat	blood
10	chr4:69360200-69360800	Enhancers	Primary B cells from peripheral blood	blood
11	chr4:69360200-69360800	Enhancers	Primary hematopoietic stem cells	blood
12	chr4:69360200-69360800	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr4:69360400-69360800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr4:69360400-69360800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr4:69360400-69360800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:69360400-69361000	Enhancers	Primary T cells from cord blood	blood
17	chr4:69360800-69364400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr4:69361800-69362000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr4:69363600-69364000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:69363600-69364000	Enhancers	Fetal Kidney	kidney
21	chr4:69363600-69364200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr4:69363600-69365000	Enhancers	A549	lung
23	chr4:69363600-69365600	Enhancers	HepG2	liver
24	chr4:69364000-69364400	Enhancers	Fetal Intestine Large	intestine
25	chr4:69364000-69364600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr4:69364000-69365200	Enhancers	Liver	Liver
27	chr4:69364200-69364600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr4:69364400-69364600	Active TSS	Pancreatic Islets	Pancreatic Islet
29	chr4:69364400-69364800	Enhancers	Primary hematopoietic stem cells	blood
30	chr4:69364400-69364800	Active TSS	Rectal Mucosa Donor 29	rectum
31	chr4:69364400-69365000	Active TSS	Fetal Intestine Large	intestine
32	chr4:69364400-69365000	Active TSS	Rectal Mucosa Donor 31	rectum
33	chr4:69364600-69364800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr4:69364800-69365000	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr4:69365000-69365400	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr4:69365200-69370400	Weak transcription	Liver	Liver
37	chr4:69369400-69369600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr4:69370200-69370600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:69370400-69370800	ZNF genes & repeats	Liver	Liver
40	chr4:69370600-69371200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:69370600-69371200	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr4:69370800-69371200	Enhancers	Primary T cells fromperipheralblood	blood
43	chr4:69370800-69371200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr4:69370800-69371200	Enhancers	Gastric	stomach
45	chr4:69370800-69371200	Enhancers	Spleen	Spleen
46	chr4:69370800-69372000	Weak transcription	Liver	Liver
47	chr4:69371000-69371200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr4:69371200-69372200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr4:69372200-69372400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr4:69373400-69373800	Enhancers	Fetal Heart	heart

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