Variant report

Variant	esv2760911
Chromosome Location	chr4:69334141-69592846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1235)
CpG islands
(count:796)
Chromatin interactive
region (count:12)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1235 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

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	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
8	ATF1	chr4:69559343-69559671	K562	blood:	n/a	n/a
9	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
10	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
11	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
12	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
13	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
14	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
15	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
18	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
19	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
21	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
23	BHLHE40	chr4:69583763-69584005	GM12878	blood:	n/a	n/a
24	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
25	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
26	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
27	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
29	CEBPB	chr4:69574389-69574642	A549	lung:	n/a	chr4:69574511-69574522
30	CEBPB	chr4:69580237-69580432	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
32	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:69574361-69574618	HepG2	liver:	n/a	chr4:69574511-69574522
34	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
35	CEBPB	chr4:69574454-69574539	H1-hESC	embryonic stem cell:	n/a	chr4:69574511-69574522
36	CEBPB	chr4:69568931-69569294	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
38	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
39	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
42	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
43	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
44	CEBPB	chr4:69578074-69578242	A549	lung:	n/a	n/a
45	CHD1	chr4:69583916-69583936	GM12878	blood:	n/a	n/a
46	CTCF	chr4:69443380-69443530	HCT-116	colon:	n/a	n/a
47	CTCF	chr4:69443380-69443530	GM12873	blood:	n/a	n/a
48	CTCF	chr4:69434820-69434970	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr4:69537040-69537190	GM12864	blood:	n/a	n/a
50	CTCF	chr4:69427324-69427392	GM20000	blood:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69340916-69340966	HAEpiC	amniotic membrane:	n/a
2	chr4:69537589-69537639	AG10803	skin:	n/a
3	chr4:69537589-69537639	T-47D	breast:	n/a
4	chr4:69340916-69340966	HAEpiC	amniotic membrane:	n/a
5	chr4:69537589-69537639	AG10803	skin:	n/a
6	chr4:69537589-69537639	T-47D	breast:	n/a
7	chr4:69381368-69381418	HEK293	kidney:	embryo
8	chr4:69340916-69340966	ProgFib	skin:	n/a
9	chr4:69381368-69381418	NHBE	bronchial:	n/a
10	chr4:69514031-69514081	AoSMC	blood vessel:	n/a
11	chr4:69340916-69340966	GM12891	blood:	n/a
12	chr4:69537826-69537876	SKMC	muscle:	n/a
13	chr4:69514031-69514081	U87	brain:	n/a
14	chr4:69514031-69514081	HCF	heart:	n/a
15	chr4:69434475-69434525	H1-hESC	embryonic stem cell:	embryo
16	chr4:69435250-69435300	BJ	skin:	n/a
17	chr4:69537589-69537639	HEEpiC	esophagus:	n/a
18	chr4:69340916-69340966	H1-hESC	embryonic stem cell:	embryo
19	chr4:69434475-69434525	AG04450	lung:	fetal
20	chr4:69434475-69434525	IMR90	lung:	fetal
21	chr4:69355121-69355171	H1-hESC	embryonic stem cell:	embryo
22	chr4:69435601-69435651	Hela-S3	cervix:	n/a
23	chr4:69537589-69537639	SK-N-SH	brain:	n/a
24	chr4:69514031-69514081	GM12878	blood:	n/a
25	chr4:69355121-69355171	BE2_C	brain:	n/a
26	chr4:69522639-69522689	T-47D	breast:	n/a
27	chr4:69537806-69537856	AG04450	lung:	fetal
28	chr4:69537806-69537856	HCF	heart:	n/a
29	chr4:69522639-69522689	AG10803	skin:	n/a
30	chr4:69355121-69355171	MCF-7	breast:	n/a
31	chr4:69340916-69340966	HRPEpiC	eye:	n/a
32	chr4:69435250-69435300	Caco-2	colon:	n/a
33	chr4:69355121-69355171	HL-60	blood:	n/a
34	chr4:69381368-69381418	HRPEpiC	eye:	n/a
35	chr4:69435250-69435300	RPTEC	kidney:	n/a
36	chr4:69435593-69435643	K562	blood:	n/a
37	chr4:69537826-69537876	NB4	blood:	n/a
38	chr4:69435250-69435300	NHBE	bronchial:	n/a
39	chr4:69522639-69522689	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:69537589-69537639	SKMC	muscle:	n/a
41	chr4:69355121-69355171	ovcar-3	ovarian:	n/a
42	chr4:69381368-69381418	GM06990	blood:	n/a
43	chr4:69537806-69537856	Hepatocyte	liver:	n/a
44	chr4:69537589-69537639	Hepatocyte	liver:	n/a
45	chr4:69340916-69340966	U87	brain:	n/a
46	chr4:69536319-69536369	HCPEpiC	choroid plexus:	n/a
47	chr4:69514031-69514081	BJ	skin:	n/a
48	chr4:69434475-69434525	AG09309	skin:	n/a
49	chr4:69536319-69536369	HUVEC	blood vessel:	n/a
50	chr4:69355121-69355171	AG10803	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:73105975..73106777-chr4:69561197..69562068,2	MCF-7	breast:
2	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
3	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
4	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
5	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:
6	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
7	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
8	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
9	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:
10	chr4:69590462..69592610-chr4:69729563..69731579,3	MCF-7	breast:
11	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
12	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-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
2	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
3	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
4	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
5	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733
6	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736

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
UGT2B29P	TF binding region
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000248635	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island
UGT2B29P	CpG island
ENSG00000083896	chromatin interactions
ENSG00000272626	chromatin interactions
ENSG00000087128	chromatin interactions
ENSG00000249985	chromatin interactions

Extended variants
information (count: 6925 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6925 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562396177	chr4:69334161-69334162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140404882	chr4:69334222-69334223	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544443146	chr4:69334268-69334269	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564686208	chr4:69334357-69334358	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566936643	chr4:69334366-69334367	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533593965	chr4:69334384-69334385	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143573318	chr4:69334395-69334396	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs71269064	chr4:69334413-69334414	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35225655	chr4:69334414-69334415	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs373493115	chr4:69334527-69334528	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549362504	chr4:69334552-69334553	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569225299	chr4:69334561-69334562	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375185351	chr4:69334605-69334606	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369420585	chr4:69334662-69334663	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150211392	chr4:69334697-69334698	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567834778	chr4:69334741-69334742	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188461034	chr4:69334805-69334806	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs139049632	chr4:69334809-69334810	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551677398	chr4:69334820-69334821	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192068326	chr4:69334823-69334824	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs142955099	chr4:69334873-69334874	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545822960	chr4:69334878-69334879	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs376396916	chr4:69334880-69334881	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs147536775	chr4:69334892-69334893	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs536602867	chr4:69334924-69334925	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs35126132	chr4:69335111-69335112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs2045099	chr4:69335120-69335121	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs182906927	chr4:69335129-69335130	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542229163	chr4:69335165-69335166	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs187539960	chr4:69335179-69335180	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs575985736	chr4:69335186-69335187	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149637831	chr4:69335187-69335188	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192581292	chr4:69335188-69335189	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs183502590	chr4:69335215-69335216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs574028569	chr4:69335240-69335241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187543426	chr4:69335255-69335256	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs560721427	chr4:69335268-69335269	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs529635667	chr4:69335278-69335279	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs34072207	chr4:69335293-69335294	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs559619937	chr4:69335311-69335312	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113357900	chr4:69335336-69335337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs569222368	chr4:69335344-69335345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531638345	chr4:69335381-69335382	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551852385	chr4:69335387-69335388	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571450678	chr4:69335398-69335399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533690564	chr4:69335436-69335437	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547208430	chr4:69335444-69335445	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs148762946	chr4:69335466-69335467	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs371000004	chr4:69335481-69335482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs561723416	chr4:69335507-69335508	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:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69319600-69335800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:69326200-69334200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:69326200-69348800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:69326600-69334200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:69333200-69349400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:69334200-69334800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:69334200-69335000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
8	chr4:69335000-69339000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:69339000-69339200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
10	chr4:69339600-69355000	Weak transcription	Esophagus	oesophagus
11	chr4:69341400-69342600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:69341600-69342000	Enhancers	NHDF-Ad	bronchial
13	chr4:69342000-69342200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:69345600-69346000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:69345600-69346000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr4:69345600-69346200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:69345600-69346400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:69348800-69349000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:69350400-69358000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr4:69355000-69355400	ZNF genes & repeats	Esophagus	oesophagus
21	chr4:69355200-69355400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:69355200-69355400	ZNF genes & repeats	Pancreas	Pancrea
23	chr4:69355200-69355800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:69355400-69362000	Weak transcription	Esophagus	oesophagus
25	chr4:69357600-69358400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr4:69359400-69360800	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr4:69359800-69360600	Enhancers	Duodenum Mucosa	Duodenum
28	chr4:69359800-69360800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr4:69360000-69360400	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr4:69360000-69360800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr4:69360000-69360800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr4:69360200-69360600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr4:69360200-69360600	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr4:69360200-69360600	Enhancers	GM12878-XiMat	blood
35	chr4:69360200-69360800	Enhancers	Primary B cells from peripheral blood	blood
36	chr4:69360200-69360800	Enhancers	Primary hematopoietic stem cells	blood
37	chr4:69360200-69360800	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr4:69360400-69360800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr4:69360400-69360800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr4:69360400-69360800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:69360400-69361000	Enhancers	Primary T cells from cord blood	blood
42	chr4:69360800-69364400	Weak transcription	Primary hematopoietic stem cells	blood
43	chr4:69361800-69362000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr4:69363600-69364000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr4:69363600-69364000	Enhancers	Fetal Kidney	kidney
46	chr4:69363600-69364200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr4:69363600-69365000	Enhancers	A549	lung
48	chr4:69363600-69365600	Enhancers	HepG2	liver
49	chr4:69364000-69364400	Enhancers	Fetal Intestine Large	intestine
50	chr4:69364000-69364600	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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