Variant report

Variant	esv1840053
Chromosome Location	chr4:165969625-166023258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:398)
CpG islands
(count:305)
Chromatin interactive
region (count:18)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:165973852-165974037	K562	blood:	n/a	n/a
2	BHLHE40	chr4:165976911-165977111	K562	blood:	n/a	n/a
3	BHLHE40	chr4:165992058-165992080	K562	blood:	n/a	n/a
4	BHLHE40	chr4:166000593-166000989	K562	blood:	n/a	n/a
5	CEBPB	chr4:166007111-166007406	A549	lung:	n/a	n/a
6	CEBPB	chr4:166007106-166007407	IMR90	lung:	n/a	n/a
7	CEBPB	chr4:165992042-165992048	K562	blood:	n/a	n/a
8	CEBPB	chr4:166007081-166007440	K562	blood:	n/a	n/a
9	CEBPB	chr4:166007082-166007441	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr4:166007105-166007438	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:166007172-166007372	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr4:166007080-166007464	ECC-1	luminal epithelium:	n/a	n/a
13	CTCF	chr4:165982160-165982310	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr4:165982160-165982310	HEEpiC	esophagus:	n/a	n/a
15	CTCF	chr4:166018100-166018250	HRPEpiC	eye:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
16	CTCF	chr4:165982140-165982290	HRE	kidney:	n/a	n/a
17	CTCF	chr4:165982100-165982250	A549	lung:	n/a	n/a
18	CTCF	chr4:166018127-166018266	Fibrobl	skin:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
19	CTCF	chr4:166018120-166018270	A549	lung:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
20	CTCF	chr4:166018145-166018248	GM19239	blood:	n/a	n/a
21	CTCF	chr4:165982120-165982270	GM12871	blood:	n/a	n/a
22	CTCF	chr4:165982187-165982351	LNCaP	prostate:	n/a	n/a
23	CTCF	chr4:166018080-166018230	BJ	skin:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
24	CTCF	chr4:165982060-165982210	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr4:166018040-166018276	LNCaP	prostate:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
26	CTCF	chr4:166018111-166018277	MCF-7	breast:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
27	CTCF	chr4:165982180-165982330	HRE	kidney:	n/a	n/a
28	CTCF	chr4:166018080-166018230	AG04449	skin:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
29	CTCF	chr4:166018080-166018230	Hela-S3	cervix:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
30	CTCF	chr4:165982177-165982300	HepG2	liver:	n/a	n/a
31	CTCF	chr4:166018060-166018210	GM06990	blood:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
32	CTCF	chr4:166018082-166018248	Kidney_OC	kidney:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
33	CTCF	chr4:166018080-166018230	HepG2	liver:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
34	CTCF	chr4:166018060-166018210	Caco-2	colon:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
35	CTCF	chr4:166018080-166018230	AG09319	gingival:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
36	CTCF	chr4:165982160-165982310	HMF	breast:	n/a	n/a
37	CTCF	chr4:166018100-166018250	HEK293	kidney:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
38	CTCF	chr4:166018060-166018210	Hela-S3	cervix:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
39	CTCF	chr4:166018140-166018290	GM06990	blood:	n/a	n/a
40	CTCF	chr4:166018100-166018250	GM12873	blood:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
41	CTCF	chr4:166018021-166018259	MCF-7	breast:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
42	CTCF	chr4:165982073-165982424	GM12878	blood:	n/a	n/a
43	CTCF	chr4:165982160-165982310	NB4	blood:	n/a	n/a
44	CTCF	chr4:165982160-165982310	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:165982680-165982830	HRE	kidney:	n/a	n/a
46	CTCF	chr4:165982140-165982290	AG04449	skin:	n/a	n/a
47	CTCF	chr4:166018100-166018250	GM12864	blood:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
48	CTCF	chr4:165982200-165982350	HCFaa	heart:	n/a	n/a
49	CTCF	chr4:166018100-166018250	GM12872	blood:	n/a	chr4:166018131-166018152 chr4:166018136-166018154
50	CTCF	chr4:165982160-165982310	HCT-116	colon:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:165980112-165980162	AG10803	skin:	n/a
2	chr4:165979202-165979252	NHBE	bronchial:	n/a
3	chr4:165979202-165979252	HCPEpiC	choroid plexus:	n/a
4	chr4:165980278-165980328	H1-hESC	embryonic stem cell:	embryo
5	chr4:165979202-165979252	GM06990	blood:	n/a
6	chr4:165980278-165980328	SKMC	muscle:	n/a
7	chr4:165980278-165980328	MCF-7	breast:	n/a
8	chr4:165979202-165979252	IMR90	lung:	fetal
9	chr4:166000605-166000655	HNPCEpiC	eye:	n/a
10	chr4:165979202-165979252	HPAEpiC	pulmonary alveolar:	n/a
11	chr4:165980278-165980328	HNPCEpiC	eye:	n/a
12	chr4:166000605-166000655	GM19239	blood:	n/a
13	chr4:165980885-165980935	HMEC	breast:	n/a
14	chr4:165980112-165980162	MCF-7	breast:	n/a
15	chr4:165980278-165980328	ECC-1	luminal epithelium:	n/a
16	chr4:165979202-165979252	HepG2	liver:	n/a
17	chr4:165980112-165980162	HL-60	blood:	n/a
18	chr4:165980278-165980328	AG09309	skin:	n/a
19	chr4:165980278-165980328	IMR90	lung:	fetal
20	chr4:165980885-165980935	SAEC	small airway:	n/a
21	chr4:165980112-165980162	T-47D	breast:	n/a
22	chr4:165980885-165980935	AG04450	lung:	fetal
23	chr4:165979202-165979252	HUVEC	blood vessel:	n/a
24	chr4:165979202-165979252	NH-A	brain:	n/a
25	chr4:165979202-165979252	ProgFib	skin:	n/a
26	chr4:165980112-165980162	Jurkat	blood:	n/a
27	chr4:165979202-165979252	MCF10A-Er-Src	breast:	n/a
28	chr4:165980112-165980162	HAEpiC	amniotic membrane:	n/a
29	chr4:165980112-165980162	NT2-D1	testis:	n/a
30	chr4:165980885-165980935	AoSMC	blood vessel:	n/a
31	chr4:165980112-165980162	SKMC	muscle:	n/a
32	chr4:165980112-165980162	ECC-1	luminal epithelium:	n/a
33	chr4:166000605-166000655	K562	blood:	n/a
34	chr4:165980112-165980162	HCPEpiC	choroid plexus:	n/a
35	chr4:165979202-165979252	HAEpiC	amniotic membrane:	n/a
36	chr4:165980278-165980328	AG04450	lung:	fetal
37	chr4:166000605-166000655	HAEpiC	amniotic membrane:	n/a
38	chr4:165980278-165980328	PrEC	prostate:	n/a
39	chr4:165980278-165980328	HepG2	liver:	n/a
40	chr4:165980885-165980935	HRE	kidney:	n/a
41	chr4:165979202-165979252	HRPEpiC	eye:	n/a
42	chr4:165980278-165980328	A549	lung:	n/a
43	chr4:165980278-165980328	Jurkat	blood:	n/a
44	chr4:165979202-165979252	HCF	heart:	n/a
45	chr4:166000605-166000655	A549	lung:	n/a
46	chr4:165980112-165980162	AG04449	skin:	fetal
47	chr4:165980278-165980328	MCF10A-Er-Src	breast:	n/a
48	chr4:165979202-165979252	PrEC	prostate:	n/a
49	chr4:165980278-165980328	HEEpiC	esophagus:	n/a
50	chr4:165980885-165980935	MCF10A-Er-Src	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:165970249..165971885-chr4:165974946..165978272,3	K562	blood:
2	chr4:165876933..165879266-chr4:165983831..165986428,2	MCF-7	breast:
3	chr4:165969592..165971444-chr4:166032460..166035429,2	MCF-7	breast:
4	chr4:166008810..166011207-chr4:166017239..166019604,2	K562	blood:
5	chr4:165974526..165976593-chr4:165977721..165979309,2	K562	blood:
6	chr4:165970250..165971885-chr4:165974946..165977597,2	K562	blood:
7	chr4:166022942..166028891-chr4:166030995..166034636,6	K562	blood:
8	chr4:166012189..166014754-chr4:166031668..166033767,2	K562	blood:
9	chr4:166023183..166024724-chr4:166027712..166029503,2	MCF-7	breast:
10	chr20:46642449..46643323-chr4:165975537..165976037,2	MCF-7	breast:
11	chr4:166008810..166011207-chr4:166017239..166019604,2	K562	blood:
12	chr4:166006157..166008971-chr4:166032182..166034962,2	MCF-7	breast:
13	chr4:165974526..165976593-chr4:165977721..165979309,2	K562	blood:
14	chr4:165970250..165971885-chr4:165974946..165977597,2	K562	blood:
15	chr4:166022079..166024029-chr4:166032477..166034231,2	K562	blood:
16	chr4:166014696..166018661-chr4:166031461..166035597,4	K562	blood:
17	chr4:165700594..165701568-chr4:166017670..166018467,3	K562	blood:
18	chr4:165970249..165971885-chr4:165974946..165978272,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM60-3	chr4:166019522-166019611	ucscGeneNc_uc003iqv_1
2	lnc-TMEM192-2	chr4:165991760-165992156	ENSG00000273097.1
3	lnc-TRIM60-3	chr4:166017786-166018009	ucscGeneNc_uc003iqv_1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TMEM192	hsa-miR-30a-5p	chr4:165998407-165998401

Variant related genes	Relation type
ENSG00000250374	TF binding region
ENSG00000273097	TF binding region
ENSG00000250374	CpG island
ENSG00000273097	CpG island
ENSG00000170088	chromatin interactions
ENSG00000250486	chromatin interactions

Extended variants
information (count: 2113 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2113 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2322014	chr4:165969625-165969626	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573110036	chr4:165969645-165969646	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs13115608	chr4:165969648-165969649	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs187206750	chr4:165969662-165969663	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs573801382	chr4:165969697-165969698	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs544291112	chr4:165969730-165969731	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs544110482	chr4:165969757-165969758	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530840598	chr4:165969761-165969762	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs192748326	chr4:165969839-165969840	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs147430209	chr4:165969840-165969841	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544581070	chr4:165969995-165969996	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139458087	chr4:165970016-165970017	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs527989561	chr4:165970032-165970033	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs549457152	chr4:165970056-165970057	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs567836459	chr4:165970061-165970062	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs538088333	chr4:165970071-165970072	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550670958	chr4:165970081-165970082	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs561244801	chr4:165970101-165970102	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375978301	chr4:165970102-165970103	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs568997978	chr4:165970115-165970116	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs184743071	chr4:165970122-165970123	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs187715980	chr4:165970172-165970173	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566604450	chr4:165970177-165970178	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534091619	chr4:165970190-165970191	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs555416849	chr4:165970196-165970197	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs573764166	chr4:165970198-165970199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546796587	chr4:165970262-165970263	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs192646606	chr4:165970271-165970272	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577725059	chr4:165970272-165970273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560353340	chr4:165970279-165970280	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560534222	chr4:165970290-165970291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs527723809	chr4:165970318-165970319	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs35589715	chr4:165970363-165970364	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543287628	chr4:165970364-165970365	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs78113130	chr4:165970387-165970388	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs75714070	chr4:165970388-165970389	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs185107748	chr4:165970446-165970447	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs189433021	chr4:165970471-165970472	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532561267	chr4:165970524-165970525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs78047305	chr4:165970532-165970533	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs9999500	chr4:165970547-165970548	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs78542816	chr4:165970694-165970695	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs551548944	chr4:165970705-165970706	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs181806251	chr4:165970755-165970756	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373721881	chr4:165970792-165970793	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533587285	chr4:165970796-165970797	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs555613972	chr4:165970836-165970837	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs78829494	chr4:165970847-165970848	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs112288018	chr4:165970851-165970852	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs34153805	chr4:165970884-165970885	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165969000-165970000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr4:165969200-165969800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr4:165969400-165969800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:165969600-165970000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr4:165969800-165974000	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr4:165973600-165974200	Enhancers	Fetal Intestine Large	intestine
7	chr4:165973600-165974200	Enhancers	K562	blood
8	chr4:165973600-165987000	Weak transcription	Right Atrium	heart
9	chr4:165973800-165974400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:165974000-165974200	Enhancers	Fetal Muscle Trunk	muscle
11	chr4:165974000-165974400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:165974000-165974400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr4:165974200-165975000	Weak transcription	Fetal Intestine Large	intestine
14	chr4:165975000-165975200	Enhancers	Fetal Intestine Large	intestine
15	chr4:165975000-165975200	Enhancers	Fetal Muscle Trunk	muscle
16	chr4:165979000-166005600	Weak transcription	Pancreas	Pancrea
17	chr4:165979200-165980800	Enhancers	Fetal Muscle Trunk	muscle
18	chr4:165979200-165982200	Enhancers	Fetal Muscle Leg	muscle
19	chr4:165979200-165995000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr4:165979400-165979800	Weak transcription	Aorta	Aorta
21	chr4:165979600-165980600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr4:165979600-165981000	Enhancers	HSMM	muscle
23	chr4:165979600-165981000	Enhancers	HSMMtube	muscle
24	chr4:165979800-165980600	ZNF genes & repeats	Aorta	Aorta
25	chr4:165979800-165981000	Enhancers	Brain Germinal Matrix	brain
26	chr4:165980000-165980400	Enhancers	Brain Angular Gyrus	brain
27	chr4:165980000-165980600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr4:165980000-165981000	Enhancers	Brain Anterior Caudate	brain
29	chr4:165980000-165981000	Enhancers	Brain Hippocampus Middle	brain
30	chr4:165980000-165981000	Enhancers	Fetal Lung	lung
31	chr4:165980000-165982200	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr4:165980200-165980600	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr4:165980400-165980800	Enhancers	Fetal Heart	heart
34	chr4:165980400-165981000	Enhancers	Brain Substantia Nigra	brain
35	chr4:165980400-165981400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:165980400-165981600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr4:165980400-165982200	Enhancers	Brain Cingulate Gyrus	brain
38	chr4:165980400-166000400	Weak transcription	Brain Angular Gyrus	brain
39	chr4:165980600-166005800	Weak transcription	Aorta	Aorta
40	chr4:165980600-166007000	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr4:165981000-165981600	Weak transcription	HSMMtube	muscle
42	chr4:165981000-165982200	Weak transcription	HSMM	muscle
43	chr4:165981000-165996800	Weak transcription	Brain Hippocampus Middle	brain
44	chr4:165981000-165997400	Weak transcription	Brain Anterior Caudate	brain
45	chr4:165981000-165999000	Weak transcription	Brain Substantia Nigra	brain
46	chr4:165981600-165982600	Enhancers	HSMMtube	muscle
47	chr4:165981800-165982000	Enhancers	Ovary	ovary
48	chr4:165981800-165982800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr4:165982000-166000400	Weak transcription	Ovary	ovary
50	chr4:165982200-165983200	Weak transcription	Fetal Muscle Leg	muscle

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