Variant report

Variant	esv2754254
Chromosome Location	chr4:86979147-87108510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:422)
CpG islands
(count:367)
Chromatin interactive
region (count:21)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:87029865-87030369	HepG2	liver:	n/a	n/a
2	BACH1	chr4:86997741-86997912	K562	blood:	n/a	n/a
3	BHLHE40	chr4:87030030-87030251	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:87020633-87020671	K562	blood:	n/a	n/a
5	CBX3	chr4:87003832-87004143	K562	blood:	n/a	n/a
6	CEBPB	chr4:87039044-87039507	A549	lung:	n/a	n/a
7	CEBPB	chr4:87108365-87108678	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:87013848-87014567	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr4:87013839-87014568	A549	lung:	n/a	n/a
10	CEBPB	chr4:87011114-87011427	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:87063552-87063827	HepG2	liver:	n/a	chr4:87063684-87063695
12	CEBPB	chr4:87039260-87039438	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:87011188-87011394	K562	blood:	n/a	n/a
14	CEBPB	chr4:87014294-87014539	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:87014247-87014568	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:87055574-87055650	K562	blood:	n/a	chr4:87055591-87055602 chr4:87055593-87055606 chr4:87055591-87055602 chr4:87055595-87055606
17	CEBPB	chr4:87022205-87022405	A549	lung:	n/a	n/a
18	CEBPB	chr4:87108462-87108618	A549	lung:	n/a	n/a
19	CEBPB	chr4:87080544-87080605	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:87108494-87108549	K562	blood:	n/a	n/a
21	CEBPB	chr4:87080285-87080666	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:87013911-87014575	K562	blood:	n/a	n/a
23	CEBPB	chr4:87011160-87011360	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:87105460-87105731	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr4:87011200-87011377	K562	blood:	n/a	n/a
26	CEBPB	chr4:87063544-87063833	A549	lung:	n/a	chr4:87063684-87063695
27	CEBPB	chr4:87013871-87014555	A549	lung:	n/a	n/a
28	CEBPB	chr4:87011178-87011337	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:87013806-87014579	A549	lung:	n/a	n/a
30	CEBPB	chr4:87013868-87014577	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:87063517-87063828	IMR90	lung:	n/a	chr4:87063684-87063695
32	CEBPB	chr4:87063561-87063863	K562	blood:	n/a	chr4:87063684-87063695
33	CTCF	chr4:87099280-87099430	WI-38	lung:	n/a	chr4:87099308-87099329 chr4:87099313-87099331
34	CTCF	chr4:86979800-86979950	HCT-116	colon:	n/a	n/a
35	CTCF	chr4:87089364-87089407	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:87081504-87081582	Fibrobl	skin:	n/a	n/a
37	CTCF	chr4:87074931-87074990	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr4:87069577-87069592	GM13976	blood:	n/a	n/a
39	CTCF	chr4:86979640-86979790	HepG2	liver:	n/a	n/a
40	CTCF	chr4:87069562-87069571	GM13976	blood:	n/a	n/a
41	CTCF	chr4:87036612-87036649	LNCaP	prostate:	n/a	n/a
42	CTCF	chr4:87036507-87036542	GM10266	blood:	n/a	n/a
43	CTCF	chr4:87044740-87044890	AG10803	skin:	n/a	n/a
44	CTCF	chr4:87099160-87099310	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr4:87035094-87035127	Lung_OC	lung:	n/a	n/a
46	CTCF	chr4:87094959-87095028	GM20000	blood:	n/a	n/a
47	CTCF	chr4:86979560-86979710	HCT-116	colon:	n/a	n/a
48	CTCF	chr4:87099180-87099330	HPAF	blood vessel:	n/a	chr4:87099308-87099329
49	CTCF	chr4:87038180-87038330	AG04449	skin:	n/a	n/a
50	CTCF	chr4:87099220-87099370	HPAF	blood vessel:	n/a	chr4:87099308-87099329 chr4:87099313-87099331

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:87028501-87028551	NB4	blood:	n/a
2	chr4:87028501-87028551	NB4	blood:	n/a
3	chr4:86997288-86997338	MCF10A-Er-Src	breast:	n/a
4	chr4:87028602-87028652	A549	lung:	n/a
5	chr4:87028602-87028652	ECC-1	luminal epithelium:	n/a
6	chr4:87056153-87056203	HRPEpiC	eye:	n/a
7	chr4:87028501-87028551	Jurkat	blood:	n/a
8	chr4:87030123-87030173	H1-hESC	embryonic stem cell:	embryo
9	chr4:87056153-87056203	T-47D	breast:	n/a
10	chr4:87028501-87028551	SK-N-MC	brain:	n/a
11	chr4:87028602-87028652	HCT-116	colon:	n/a
12	chr4:86997288-86997338	Jurkat	blood:	n/a
13	chr4:87028501-87028551	A549	lung:	n/a
14	chr4:87030123-87030173	SAEC	small airway:	n/a
15	chr4:87056153-87056203	AG04449	skin:	fetal
16	chr4:87028602-87028652	PFSK-1	brain:	n/a
17	chr4:87028602-87028652	GM12891	blood:	n/a
18	chr4:86997288-86997338	PrEC	prostate:	n/a
19	chr4:87028602-87028652	GM06990	blood:	n/a
20	chr4:87028602-87028652	GM12878	blood:	n/a
21	chr4:86997288-86997338	PFSK-1	brain:	n/a
22	chr4:86997288-86997338	IMR90	lung:	fetal
23	chr4:87056153-87056203	BE2_C	brain:	n/a
24	chr4:87030123-87030173	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:87028501-87028551	GM12892	blood:	n/a
26	chr4:87056153-87056203	SK-N-SH_RA	brain:	n/a
27	chr4:87056153-87056203	NB4	blood:	n/a
28	chr4:87040423-87040473	SK-N-SH_RA	brain:	n/a
29	chr4:87028501-87028551	HUVEC	blood vessel:	n/a
30	chr4:87028501-87028551	SKMC	muscle:	n/a
31	chr4:87056153-87056203	IMR90	lung:	fetal
32	chr4:87028501-87028551	HepG2	liver:	n/a
33	chr4:87030123-87030173	HMEC	breast:	n/a
34	chr4:87056153-87056203	HUVEC	blood vessel:	n/a
35	chr4:86997288-86997338	NB4	blood:	n/a
36	chr4:87030123-87030173	A549	lung:	n/a
37	chr4:87028602-87028652	H1-hESC	embryonic stem cell:	embryo
38	chr4:86997288-86997338	Hela-S3	cervix:	n/a
39	chr4:86997288-86997338	AoSMC	blood vessel:	n/a
40	chr4:87028602-87028652	ProgFib	skin:	n/a
41	chr4:87040423-87040473	ovcar-3	ovarian:	n/a
42	chr4:87030123-87030173	ECC-1	luminal epithelium:	n/a
43	chr4:87040423-87040473	NH-A	brain:	n/a
44	chr4:87028501-87028551	ProgFib	skin:	n/a
45	chr4:87040423-87040473	GM12892	blood:	n/a
46	chr4:86997288-86997338	HEEpiC	esophagus:	n/a
47	chr4:87028501-87028551	HCT-116	colon:	n/a
48	chr4:86997288-86997338	GM12892	blood:	n/a
49	chr4:87028602-87028652	HRCEpiC	kidney:	n/a
50	chr4:87028602-87028652	HRPEpiC	eye:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:87070864..87073086-chr4:87075454..87077437,2	K562	blood:
2	chr4:87074554..87076995-chr4:87081060..87082909,2	MCF-7	breast:
3	chr4:87024355..87027343-chr4:87027765..87029282,2	MCF-7	breast:
4	chr4:86996065..86997848-chr4:87003738..87005825,2	K562	blood:
5	chr4:86996065..86997848-chr4:87003738..87005825,2	K562	blood:
6	chr4:87079015..87081853-chr4:87083542..87085468,2	K562	blood:
7	chr4:87024355..87027343-chr4:87027765..87029282,2	MCF-7	breast:
8	chr4:87048655..87051037-chr4:87083679..87085994,2	MCF-7	breast:
9	chr4:86996153..86999257-chr4:86999314..87002749,3	K562	blood:
10	chr4:86974348..86976679-chr4:86978244..86980026,2	MCF-7	breast:
11	chr4:87079015..87081853-chr4:87083542..87085468,2	K562	blood:
12	chr4:87048655..87051037-chr4:87083679..87085994,2	MCF-7	breast:
13	chr4:87068101..87070840-chr4:87077987..87079819,2	MCF-7	breast:
14	chr4:87074554..87076995-chr4:87081060..87082909,2	MCF-7	breast:
15	chr17:67196658..67197255-chr4:86998915..86999454,2	HCT-116	colon:
16	chr4:87070864..87073086-chr4:87075454..87077437,2	K562	blood:
17	chr4:87070864..87072590-chr4:87074186..87076954,2	K562	blood:
18	chr4:86996153..86999257-chr4:86999314..87002749,3	K562	blood:
19	chr4:87070864..87072590-chr4:87074186..87076954,2	K562	blood:
20	chr4:87018345..87020243-chr4:87021552..87023121,2	MCF-7	breast:
21	chr4:87068101..87070840-chr4:87077987..87079819,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP24-1	chr4:87041137-87041754	ENSG00000250062.1
2	lnc-SLC10A6-4	chr4:87085599-87085718	NONHSAT097276
3	lnc-SLC10A6-4	chr4:87097140-87097232	NONHSAT097276
4	lnc-ARHGAP24-1	chr4:87039065-87039115	ENSG00000250062.1
5	lnc-ARHGAP24-1	chr4:87048745-87048853	ENSG00000250062.1
6	lnc-ARHGAP24-1	chr4:87041137-87041754	NONHSAT097275
7	lnc-ARHGAP24-1	chr4:87040867-87041036	ENSG00000250062.1
8	lnc-ARHGAP24-1	chr4:87041137-87041754	ENSG00000250062.1
9	lnc-ARHGAP24-1	chr4:87048745-87048940	NONHSAT097275
10	lnc-ARHGAP24-1	chr4:87048745-87048841	ENSG00000250062.1
11	lnc-ARHGAP24-1	chr4:87040879-87041036	NONHSAT097275

No data

Variant related genes	Relation type
MAPK10	TF binding region
ENSG00000250062	TF binding region
MAPK10	CpG island
ENSG00000250062	CpG island
ENSG00000109339	chromatin interactions

Extended variants
information (count: 4347 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:4347 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3775180	chr4:86979147-86979148	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530234913	chr4:86979165-86979166	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540093755	chr4:86979199-86979200	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145563601	chr4:86979213-86979214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184929775	chr4:86979246-86979247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530967747	chr4:86979249-86979250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs3775181	chr4:86979253-86979254	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs35485855	chr4:86979280-86979281	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571478630	chr4:86979378-86979379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538896401	chr4:86979387-86979388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115079539	chr4:86979390-86979391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550245985	chr4:86979391-86979392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138085752	chr4:86979428-86979429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535942880	chr4:86979453-86979454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191060916	chr4:86979493-86979494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529617229	chr4:86979494-86979495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183872135	chr4:86979558-86979559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs3775182	chr4:86979583-86979584	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
19	rs577489453	chr4:86979604-86979605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541677005	chr4:86979605-86979606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559997809	chr4:86979653-86979654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556849049	chr4:86979661-86979662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141988231	chr4:86979722-86979723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143645449	chr4:86979768-86979769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531003470	chr4:86979823-86979824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552310155	chr4:86979824-86979825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114645395	chr4:86979876-86979877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532312820	chr4:86979896-86979897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535321204	chr4:86979899-86979900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs3775183	chr4:86979927-86979928	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs565632852	chr4:86979936-86979937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536085495	chr4:86979959-86979960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115732700	chr4:86979997-86979998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569442484	chr4:86980030-86980031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188781695	chr4:86980056-86980057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs3775184	chr4:86980059-86980060	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs191508340	chr4:86980087-86980088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535011158	chr4:86980100-86980101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148123458	chr4:86980143-86980144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs746438	chr4:86980256-86980257	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs542470747	chr4:86980422-86980423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556032688	chr4:86980424-86980425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183508300	chr4:86980458-86980459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs62305521	chr4:86980481-86980482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150634234	chr4:86980482-86980483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564324855	chr4:86980573-86980574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187244252	chr4:86980588-86980589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555475338	chr4:86980638-86980639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564437188	chr4:86980738-86980739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191622603	chr4:86980753-86980754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	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
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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	20459617	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD

Chromatin state (count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86916800-86985400	Weak transcription	Ovary	ovary
2	chr4:86936400-86990600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:86949200-86988600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr4:86955000-86985000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr4:86955200-87003800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr4:86958400-86992600	Weak transcription	Fetal Kidney	kidney
7	chr4:86961200-86979400	Weak transcription	Fetal Stomach	stomach
8	chr4:86961200-86981000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr4:86963600-86988800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:86965200-86985800	Weak transcription	Adipose Nuclei	Adipose
11	chr4:86965200-86987000	Weak transcription	Brain Substantia Nigra	brain
12	chr4:86970000-86988400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:86971800-87003800	Weak transcription	Brain Hippocampus Middle	brain
14	chr4:86975200-87003600	Weak transcription	Stomach Smooth Muscle	stomach
15	chr4:86976000-86984200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr4:86976200-86987800	Weak transcription	Brain Germinal Matrix	brain
17	chr4:86976400-87000200	Weak transcription	Fetal Brain Female	brain
18	chr4:86976800-86986400	Weak transcription	Fetal Brain Male	brain
19	chr4:86977400-87003800	Weak transcription	Brain Anterior Caudate	brain
20	chr4:86978800-86988800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr4:86979000-86979200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:86979400-86980000	Strong transcription	Fetal Stomach	stomach
23	chr4:86979600-86985400	Weak transcription	Aorta	Aorta
24	chr4:86980000-87004000	Weak transcription	Fetal Stomach	stomach
25	chr4:86980800-86981200	Enhancers	Fetal Muscle Leg	muscle
26	chr4:86981000-86981600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr4:86981600-86987000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr4:86982200-86983000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr4:86983200-86983400	Enhancers	Fetal Lung	lung
30	chr4:86983400-86986200	Weak transcription	Fetal Lung	lung
31	chr4:86984200-86985800	Strong transcription	Brain Cingulate Gyrus	brain
32	chr4:86985000-86985800	Strong transcription	Brain Inferior Temporal Lobe	brain
33	chr4:86985000-86989000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:86985400-86985600	ZNF genes & repeats	Aorta	Aorta
35	chr4:86985400-86985800	Strong transcription	Ovary	ovary
36	chr4:86985800-86988400	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr4:86985800-87003600	Weak transcription	Brain Cingulate Gyrus	brain
38	chr4:86985800-87004000	Weak transcription	Ovary	ovary
39	chr4:86988400-86988600	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr4:86988400-86990000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:86988600-86989200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr4:86988800-86989200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:86988800-86989200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:86989200-86996600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr4:86989200-86998800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr4:86989200-87004000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:86990000-86990400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:86990400-86997400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr4:86996600-86997000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr4:86996600-86997800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived

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