Variant report

Variant	esv3528915
Chromosome Location	chr4:100025155-100096234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:555)
CpG islands
(count:366)
Chromatin interactive
region (count:10)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:100080697-100081156	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:100089099-100089294	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:100078087-100079360	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:100087752-100088164	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:100039424-100039514	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:100063004-100063010	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:100065108-100065911	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:100051750-100051887	K562	blood:	n/a	n/a
9	BHLHE40	chr4:100078565-100079055	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:100075842-100076106	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:100065301-100065731	HepG2	liver:	n/a	chr4:100065485-100065498 chr4:100065485-100065498 chr4:100065485-100065496
12	CEBPB	chr4:100075833-100076394	A549	lung:	n/a	n/a
13	CEBPB	chr4:100078634-100078996	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:100078267-100078975	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:100065319-100065653	HepG2	liver:	n/a	chr4:100065485-100065498 chr4:100065485-100065498 chr4:100065485-100065496
16	CEBPB	chr4:100065340-100065623	HepG2	liver:	n/a	chr4:100065485-100065498 chr4:100065485-100065498 chr4:100065485-100065496
17	CEBPB	chr4:100065337-100065723	HepG2	liver:	n/a	chr4:100065485-100065498 chr4:100065485-100065498 chr4:100065485-100065496
18	CEBPB	chr4:100065361-100065625	IMR90	lung:	n/a	chr4:100065485-100065498 chr4:100065485-100065498 chr4:100065485-100065496
19	CEBPB	chr4:100078582-100078960	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:100075857-100076449	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:100082376-100082606	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:100078242-100079073	HepG2	liver:	n/a	n/a
23	CEBPD	chr4:100078593-100078969	HepG2	liver:	n/a	n/a
24	CHD2	chr4:100078646-100078941	HepG2	liver:	n/a	n/a
25	CREB1	chr4:100078248-100079074	HepG2	liver:	n/a	n/a
26	CTCF	chr4:100039120-100039270	GM12866	blood:	n/a	n/a
27	CTCF	chr4:100080892-100081217	HepG2	liver:	n/a	chr4:100080985-100080993 chr4:100081042-100081063
28	CTCF	chr4:100081060-100081210	HCT-116	colon:	n/a	n/a
29	CTCF	chr4:100081020-100081138	MCF-7	breast:	n/a	chr4:100081042-100081063
30	CTCF	chr4:100080940-100081090	HepG2	liver:	n/a	chr4:100080985-100080993 chr4:100081042-100081063
31	CTCF	chr4:100039020-100039170	GM12868	blood:	n/a	n/a
32	CTCF	chr4:100039040-100039190	GM12874	blood:	n/a	n/a
33	CTCF	chr4:100080980-100081130	HPAF	blood vessel:	n/a	chr4:100080985-100080993 chr4:100081042-100081063
34	CTCF	chr4:100039400-100039550	AG10803	skin:	n/a	n/a
35	CTCF	chr4:100039360-100039510	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr4:100039118-100039174	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr4:100039237-100039647	GM12878	blood:	n/a	n/a
38	CTCF	chr4:100039539-100039540	GM13977	blood:	n/a	n/a
39	CTCF	chr4:100039349-100039553	LNCaP	prostate:	n/a	n/a
40	CTCF	chr4:100039372-100039551	GM12878	blood:	n/a	n/a
41	CTCF	chr4:100039340-100039490	GM12874	blood:	n/a	n/a
42	CTCF	chr4:100039400-100039550	GM12872	blood:	n/a	n/a
43	CTCF	chr4:100039394-100039397	GM10266	blood:	n/a	n/a
44	CTCF	chr4:100081000-100081150	WERI-Rb-1	eye:	n/a	chr4:100081042-100081063
45	CTCF	chr4:100039340-100039490	GM12871	blood:	n/a	n/a
46	CTCF	chr4:100080900-100081173	K562	blood:	n/a	chr4:100080985-100080993 chr4:100081042-100081063
47	CTCF	chr4:100039420-100039570	GM12864	blood:	n/a	n/a
48	CTCF	chr4:100039360-100039510	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr4:100039420-100039570	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:100039380-100039530	HepG2	liver:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:100041888-100041938	HNPCEpiC	eye:	n/a
2	chr4:100082970-100083020	Caco-2	colon:	n/a
3	chr4:100041888-100041938	AG09319	gingival:	n/a
4	chr4:100038717-100038767	HCT-116	colon:	n/a
5	chr4:100065546-100065596	PrEC	prostate:	n/a
6	chr4:100083331-100083381	K562	blood:	n/a
7	chr4:100083121-100083171	GM12891	blood:	n/a
8	chr4:100082970-100083020	SKMC	muscle:	n/a
9	chr4:100083121-100083171	GM12878	blood:	n/a
10	chr4:100065546-100065596	SK-N-MC	brain:	n/a
11	chr4:100083121-100083171	PrEC	prostate:	n/a
12	chr4:100082970-100083020	T-47D	breast:	n/a
13	chr4:100041888-100041938	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:100038717-100038767	NT2-D1	testis:	n/a
15	chr4:100038717-100038767	HNPCEpiC	eye:	n/a
16	chr4:100083331-100083381	AG09309	skin:	n/a
17	chr4:100083331-100083381	LNCaP	prostate:	n/a
18	chr4:100065546-100065596	AG09319	gingival:	n/a
19	chr4:100038717-100038767	HMEC	breast:	n/a
20	chr4:100083121-100083171	HRCEpiC	kidney:	n/a
21	chr4:100065546-100065596	SK-N-SH_RA	brain:	n/a
22	chr4:100082970-100083020	H1-hESC	embryonic stem cell:	embryo
23	chr4:100083331-100083381	GM12891	blood:	n/a
24	chr4:100082970-100083020	NT2-D1	testis:	n/a
25	chr4:100083121-100083171	HepG2	liver:	n/a
26	chr4:100082970-100083020	HIPEpiC	eye:	n/a
27	chr4:100083121-100083171	HEEpiC	esophagus:	n/a
28	chr4:100038717-100038767	MCF10A-Er-Src	breast:	n/a
29	chr4:100083121-100083171	T-47D	breast:	n/a
30	chr4:100082970-100083020	HepG2	liver:	n/a
31	chr4:100082970-100083020	SAEC	small airway:	n/a
32	chr4:100082970-100083020	HL-60	blood:	n/a
33	chr4:100038717-100038767	NHBE	bronchial:	n/a
34	chr4:100065546-100065596	HUVEC	blood vessel:	n/a
35	chr4:100038717-100038767	SK-N-MC	brain:	n/a
36	chr4:100082970-100083020	CMK	blood:	n/a
37	chr4:100082970-100083020	Hela-S3	cervix:	n/a
38	chr4:100065546-100065596	AG10803	skin:	n/a
39	chr4:100082970-100083020	U87	brain:	n/a
40	chr4:100041888-100041938	A549	lung:	n/a
41	chr4:100041888-100041938	SK-N-SH_RA	brain:	n/a
42	chr4:100083331-100083381	AG04450	lung:	fetal
43	chr4:100083331-100083381	ovcar-3	ovarian:	n/a
44	chr4:100083121-100083171	PANC-1	pancreas:	n/a
45	chr4:100083331-100083381	HRCEpiC	kidney:	n/a
46	chr4:100082970-100083020	AG10803	skin:	n/a
47	chr4:100083121-100083171	GM19239	blood:	n/a
48	chr4:100083121-100083171	Hela-S3	cervix:	n/a
49	chr4:100041888-100041938	GM12878	blood:	n/a
50	chr4:100083331-100083381	Caco-2	colon:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:100069725..100072421-chr4:100081070..100082749,2	K562	blood:
2	chr4:100039119..100039756-chr4:100378505..100379028,2	MCF-7	breast:
3	chr4:100062982..100065976-chr4:100067343..100070151,2	K562	blood:
4	chr4:100009811..100011847-chr4:100024562..100026344,2	MCF-7	breast:
5	chr4:100008381..100011330-chr4:100056699..100058939,2	MCF-7	breast:
6	chr4:100039143..100039863-chr4:100383697..100384671,5	MCF-7	breast:
7	chr4:99914784..99916943-chr4:100045840..100048250,2	K562	blood:
8	chr4:99916019..99918646-chr4:100083097..100084598,2	K562	blood:
9	chr4:100039211..100039845-chr4:100326145..100326879,2	MCF-7	breast:
10	chr4:100038972..100039679-chr4:100326321..100327345,4	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADH4-1	chr4:100081671-100082422	NONHSAT097522
2	lnc-METAP1-3	chr4:100054706-100054956	ENSG00000246090
3	lnc-METAP1-3	chr4:100075702-100078736	ENSG00000246090
4	lnc-ADH4-1	chr4:100082094-100082802	NONHSAT097524
5	lnc-METAP1-3	chr4:100082941-100083061	ENSG00000246090
6	lnc-ADH4-1	chr4:100081751-100082804	NONHSAT097523
7	lnc-METAP1-3	chr4:100082967-100083061	ENSG00000246090

No data

Variant related genes	Relation type
PCNAP1	TF binding region
ADH4	TF binding region
ENSG00000246090	TF binding region
PCNAP1	CpG island
ADH4	CpG island
ENSG00000246090	CpG island
ENSG00000265213	chromatin interactions
ENSG00000198099	chromatin interactions
ENSG00000164024	chromatin interactions
ENSG00000246090	chromatin interactions
ENSG00000249065	chromatin interactions
ENSG00000197894	chromatin interactions

Extended variants
information (count: 2602 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2602 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545571312	chr4:100025170-100025171	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs189609165	chr4:100025200-100025201	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs138629108	chr4:100025201-100025202	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs531011118	chr4:100025295-100025296	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs114562449	chr4:100025329-100025330	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs148903524	chr4:100025408-100025409	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs528476019	chr4:100025427-100025428	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs547242901	chr4:100025465-100025466	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs562219207	chr4:100025485-100025486	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs533117014	chr4:100025486-100025487	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs7689911	chr4:100025508-100025509	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs569781169	chr4:100025542-100025543	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs375000555	chr4:100025545-100025546	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs116045977	chr4:100025585-100025586	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs555520081	chr4:100025586-100025587	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs7690613	chr4:100025633-100025634	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs181095446	chr4:100025719-100025720	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs553042393	chr4:100025758-100025759	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs61431883	chr4:100025783-100025784	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs545403980	chr4:100025806-100025807	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185455193	chr4:100025823-100025824	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs554308529	chr4:100025855-100025856	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575751483	chr4:100025862-100025863	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs2851274	chr4:100025866-100025867	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs142940810	chr4:100025868-100025869	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs369036931	chr4:100025869-100025870	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs576811425	chr4:100025880-100025881	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs58811889	chr4:100025888-100025889	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs2602847	chr4:100025963-100025964	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs569127392	chr4:100025984-100025985	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs560025494	chr4:100025989-100025990	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs530314773	chr4:100026012-100026013	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs542460566	chr4:100026022-100026023	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561050206	chr4:100026031-100026032	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs537851545	chr4:100026039-100026040	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs563845567	chr4:100026042-100026043	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs540224858	chr4:100026043-100026044	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs565170861	chr4:100026057-100026058	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs533235432	chr4:100026081-100026082	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs1840228	chr4:100026098-100026099	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs1840229	chr4:100026109-100026110	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs182814848	chr4:100026153-100026154	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs549056049	chr4:100026164-100026165	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs145861813	chr4:100026230-100026231	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs142593205	chr4:100026244-100026245	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs72677574	chr4:100026273-100026274	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs186358022	chr4:100026283-100026284	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536112232	chr4:100026293-100026294	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs571174925	chr4:100026299-100026300	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs1840230	chr4:100026332-100026333	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:86)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100011400-100025800	Weak transcription	Esophagus	oesophagus
2	chr4:100011600-100025600	Weak transcription	Primary T cells from cord blood	blood
3	chr4:100012800-100063800	Weak transcription	Aorta	Aorta
4	chr4:100020600-100034800	Weak transcription	Stomach Smooth Muscle	stomach
5	chr4:100020800-100032800	Weak transcription	Fetal Intestine Small	intestine
6	chr4:100020800-100038600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr4:100021000-100032200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:100021000-100041200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:100021400-100025200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr4:100022200-100025400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr4:100023000-100055600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:100023800-100025800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr4:100024000-100025800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:100024000-100025800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr4:100024600-100025200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:100024800-100025600	Enhancers	Adipose Nuclei	Adipose
17	chr4:100025000-100025800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr4:100025400-100025800	Enhancers	Placenta Amnion	Placenta Amnion
19	chr4:100025600-100025800	Enhancers	Placenta	Placenta
20	chr4:100025600-100025800	Enhancers	Osteobl	bone
21	chr4:100025800-100038400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr4:100026200-100026400	Enhancers	Lung	lung
23	chr4:100028600-100029200	Enhancers	H9 Cell Line	embryonic stem cell
24	chr4:100028800-100029400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr4:100029000-100029200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr4:100029000-100029400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr4:100029800-100030600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr4:100031200-100031800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:100034800-100035000	Enhancers	Ovary	ovary
30	chr4:100034800-100035000	Enhancers	Stomach Smooth Muscle	stomach
31	chr4:100035000-100098200	Weak transcription	Ovary	ovary
32	chr4:100038200-100040000	Enhancers	Liver	Liver
33	chr4:100038400-100038800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
34	chr4:100038800-100040400	Enhancers	HepG2	liver
35	chr4:100038800-100055200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr4:100039000-100039200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:100039000-100039400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
38	chr4:100039000-100039800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr4:100039200-100040000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr4:100039400-100042000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr4:100039600-100040000	Enhancers	Fetal Intestine Large	intestine
42	chr4:100039600-100040000	Enhancers	Fetal Lung	lung
43	chr4:100039600-100041200	Enhancers	Duodenum Mucosa	Duodenum
44	chr4:100039800-100064800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr4:100040000-100043800	Weak transcription	Fetal Lung	lung
46	chr4:100040000-100045000	Weak transcription	Liver	Liver
47	chr4:100040000-100050800	Weak transcription	Fetal Intestine Large	intestine
48	chr4:100040400-100040800	Weak transcription	HepG2	liver
49	chr4:100040800-100041000	Enhancers	HepG2	liver
50	chr4:100041000-100046400	Weak transcription	HepG2	liver

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