Variant report

Variant	esv2538163
Chromosome Location	chr4:120252854-120388678
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1318)
CpG islands
(count:734)
Chromatin interactive
region (count:5)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1318 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:120375657-120375939	K562	blood:	n/a	n/a
2	ARID3A	chr4:120292324-120292770	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:120375640-120376007	HepG2	liver:	n/a	n/a
4	ATF1	chr4:120324198-120324405	K562	blood:	n/a	n/a
5	ATF1	chr4:120375410-120376174	K562	blood:	n/a	n/a
6	ATF2	chr4:120375554-120376118	H1-hESC	embryonic stem cell:	n/a	chr4:120375758-120375769
7	ATF2	chr4:120291443-120291898	GM12878	blood:	n/a	n/a
8	ATF2	chr4:120375508-120376132	GM12878	blood:	n/a	chr4:120375758-120375769
9	ATF2	chr4:120375574-120376077	H1-hESC	embryonic stem cell:	n/a	chr4:120375758-120375769
10	ATF2	chr4:120375555-120376037	GM12878	blood:	n/a	chr4:120375758-120375769
11	ATF3	chr4:120375585-120375981	A549	lung:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
12	ATF3	chr4:120375570-120376147	H1-hESC	embryonic stem cell:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
13	ATF3	chr4:120375697-120376130	H1-hESC	embryonic stem cell:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
14	ATF3	chr4:120375689-120376103	HepG2	liver:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
15	ATF3	chr4:120375591-120376108	K562	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
16	ATF3	chr4:120375643-120376128	GM12878	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
17	ATF3	chr4:120375748-120376028	GM12878	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
18	ATF3	chr4:120376142-120376354	K562	blood:	n/a	n/a
19	ATF3	chr4:120375534-120376115	HepG2	liver:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
20	ATF3	chr4:120375667-120376101	K562	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
21	BACH1	chr4:120375824-120376166	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr4:120288050-120288247	GM12878	blood:	n/a	n/a
23	BATF	chr4:120383409-120383814	GM12878	blood:	n/a	n/a
24	BATF	chr4:120377931-120378220	GM12878	blood:	n/a	n/a
25	BATF	chr4:120375371-120376260	GM12878	blood:	n/a	n/a
26	BATF	chr4:120336031-120336269	GM12878	blood:	n/a	n/a
27	BATF	chr4:120383430-120383818	GM12878	blood:	n/a	n/a
28	BATF	chr4:120291572-120291901	GM12878	blood:	n/a	n/a
29	BATF	chr4:120377964-120378201	GM12878	blood:	n/a	n/a
30	BATF	chr4:120291551-120292008	GM12878	blood:	n/a	n/a
31	BATF	chr4:120295932-120296203	GM12878	blood:	n/a	chr4:120296096-120296107
32	BCL11A	chr4:120375997-120376209	GM12878	blood:	n/a	n/a
33	BCL11A	chr4:120383416-120384004	GM12878	blood:	n/a	chr4:120383850-120383859
34	BCL11A	chr4:120375469-120376323	GM12878	blood:	n/a	n/a
35	BCL11A	chr4:120378027-120378298	GM12878	blood:	n/a	n/a
36	BCL11A	chr4:120291635-120291957	GM12878	blood:	n/a	n/a
37	BCL3	chr4:120375586-120376104	A549	lung:	n/a	n/a
38	BCLAF1	chr4:120375555-120376089	GM12878	blood:	n/a	n/a
39	BCLAF1	chr4:120375644-120376123	GM12878	blood:	n/a	n/a
40	BHLHE40	chr4:120375666-120376228	K562	blood:	n/a	n/a
41	BHLHE40	chr4:120292531-120292706	HepG2	liver:	n/a	n/a
42	BHLHE40	chr4:120375682-120376067	GM12878	blood:	n/a	n/a
43	BRCA1	chr4:120375591-120376075	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr4:120375657-120376065	H1-hESC	embryonic stem cell:	n/a	n/a
45	BRCA1	chr4:120375670-120376051	GM12878	blood:	n/a	n/a
46	BRCA1	chr4:120375681-120376092	HepG2	liver:	n/a	n/a
47	CBX3	chr4:120375579-120376037	K562	blood:	n/a	n/a
48	CBX3	chr4:120375690-120376086	HCT-116	colon:	n/a	n/a
49	CBX3	chr4:120309985-120310304	K562	blood:	n/a	n/a
50	CBX3	chr4:120374867-120376298	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120376055-120376105	Jurkat	blood:	n/a
2	chr4:120375997-120376047	HUVEC	blood vessel:	n/a
3	chr4:120376055-120376105	Jurkat	blood:	n/a
4	chr4:120375997-120376047	HUVEC	blood vessel:	n/a
5	chr4:120378622-120378672	PrEC	prostate:	n/a
6	chr4:120329925-120329975	MCF-7	breast:	n/a
7	chr4:120327624-120327674	H1-hESC	embryonic stem cell:	embryo
8	chr4:120375409-120375459	GM12891	blood:	n/a
9	chr4:120375747-120375797	SK-N-MC	brain:	n/a
10	chr4:120375409-120375459	U87	brain:	n/a
11	chr4:120373434-120373484	AG04450	lung:	fetal
12	chr4:120329925-120329975	HCF	heart:	n/a
13	chr4:120375409-120375459	HEEpiC	esophagus:	n/a
14	chr4:120378622-120378672	ovcar-3	ovarian:	n/a
15	chr4:120375747-120375797	NT2-D1	testis:	n/a
16	chr4:120376055-120376105	PANC-1	pancreas:	n/a
17	chr4:120375997-120376047	SK-N-SH_RA	brain:	n/a
18	chr4:120376055-120376105	GM12891	blood:	n/a
19	chr4:120376055-120376105	HEK293	kidney:	embryo
20	chr4:120375997-120376047	HEEpiC	esophagus:	n/a
21	chr4:120375747-120375797	Hepatocyte	liver:	n/a
22	chr4:120378622-120378672	NH-A	brain:	n/a
23	chr4:120376055-120376105	HNPCEpiC	eye:	n/a
24	chr4:120328025-120328075	NH-A	brain:	n/a
25	chr4:120328025-120328075	A549	lung:	n/a
26	chr4:120328025-120328075	Caco-2	colon:	n/a
27	chr4:120329925-120329975	HRCEpiC	kidney:	n/a
28	chr4:120373434-120373484	BJ	skin:	n/a
29	chr4:120376271-120376321	RPTEC	kidney:	n/a
30	chr4:120329925-120329975	PFSK-1	brain:	n/a
31	chr4:120376055-120376105	HCT-116	colon:	n/a
32	chr4:120327182-120327232	BE2_C	brain:	n/a
33	chr4:120375747-120375797	GM06990	blood:	n/a
34	chr4:120375409-120375459	PrEC	prostate:	n/a
35	chr4:120375747-120375797	AG09309	skin:	n/a
36	chr4:120375409-120375459	ovcar-3	ovarian:	n/a
37	chr4:120332083-120332133	NB4	blood:	n/a
38	chr4:120375409-120375459	SKMC	muscle:	n/a
39	chr4:120375997-120376047	HIPEpiC	eye:	n/a
40	chr4:120378622-120378672	AG04449	skin:	fetal
41	chr4:120376271-120376321	AG04449	skin:	fetal
42	chr4:120373434-120373484	SK-N-MC	brain:	n/a
43	chr4:120373434-120373484	ECC-1	luminal epithelium:	n/a
44	chr4:120376271-120376321	MCF10A-Er-Src	breast:	n/a
45	chr4:120327182-120327232	PrEC	prostate:	n/a
46	chr4:120376055-120376105	GM06990	blood:	n/a
47	chr4:120327182-120327232	AoSMC	blood vessel:	n/a
48	chr4:120375747-120375797	Caco-2	colon:	n/a
49	chr4:120375997-120376047	GM12891	blood:	n/a
50	chr4:120375409-120375459	AG04449	skin:	fetal

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:120132920..120134685-chr4:120374052..120375829,2	K562	blood:
2	chr4:119679216..119681142-chr4:120375525..120377542,2	MCF-7	breast:
3	chr4:120372429..120374699-chr4:120400382..120402462,2	K562	blood:
4	chr4:120388467..120390905-chr4:120393709..120395328,2	K562	blood:
5	chr4:120132920..120134685-chr4:120374052..120375829,3	K562	blood:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC110373.1-2	chr4:120330488-120331388	ENSG00000260091.1
2	lnc-AC110373.1-8	chr4:120381886-120381982	NONHSAT098079
3	lnc-AC110373.1-2	chr4:120330489-120331408	NONHSAT098058
4	lnc-AC110373.1-8	chr4:120384051-120384134	NONHSAT098081
5	lnc-AC110373.1-8	chr4:120381592-120381982	NONHSAT098080
6	lnc-PDE5A-3	chr4:120362106-120362207	NONHSAT098064
7	lnc-AC110373.1-3	chr4:120377505-120377592	ENSG00000250950.1
8	lnc-AC110373.1-8	chr4:120382872-120383065	NONHSAT098080
9	lnc-AC110373.1-8	chr4:120382872-120383006	NONHSAT098079
10	lnc-PDE5A-3	chr4:120365524-120365586	NONHSAT098064
11	lnc-PDE5A-3	chr4:120370725-120371280	NONHSAT098065
12	lnc-AC110373.1-8	chr4:120381811-120381982	NONHSAT098081
13	lnc-PDE5A-3	chr4:120375401-120375783	NONHSAT098065
14	lnc-AC110373.1-8	chr4:120384051-120384134	NONHSAT098082
15	lnc-PDE5A-3	chr4:120361716-120361790	NONHSAT098064
16	lnc-AC110373.1-8	chr4:120382872-120383006	NONHSAT098082
17	lnc-AC110373.1-8	chr4:120381834-120381982	NONHSAT098082
18	lnc-AC110373.1-3	chr4:120377948-120378432	ENSG00000250950.1
19	lnc-AC110373.1-8	chr4:120379123-120379232	NONHSAT098078
20	lnc-AC110373.1-8	chr4:120382872-120383006	NONHSAT098081
21	lnc-AC110373.1-8	chr4:120381367-120381397	NONHSAT098079
22	lnc-PDE5A-3	chr4:120371197-120371312	NONHSAT098064
23	lnc-AC110373.1-8	chr4:120384051-120384134	NONHSAT098079
24	lnc-AC110373.1-8	chr4:120382872-120383019	NONHSAT098078
25	lnc-AC110373.1-8	chr4:120381898-120381975	NONHSAT098078

No data

Variant related genes	Relation type
ENSG00000260091	TF binding region
RNU6-1217P	TF binding region
ENSG00000250950	TF binding region
RNU4-33P	TF binding region
ENSG00000248280	TF binding region
ENSG00000249244	TF binding region
ENSG00000245958	TF binding region
KLHL2P1	TF binding region
ENSG00000260091	CpG island
RNU6-1217P	CpG island
ENSG00000250950	CpG island
RNU4-33P	CpG island
ENSG00000248280	CpG island
ENSG00000249244	CpG island
ENSG00000245958	CpG island
KLHL2P1	CpG island
ENSG00000145390	chromatin interactions
ENSG00000150961	chromatin interactions
ENSG00000178636	chromatin interactions

Extended variants
information (count: 4513 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4513 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371014435	chr4:120252884-120252885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531420258	chr4:120252894-120252895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79251454	chr4:120252929-120252930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183331752	chr4:120252961-120252962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143613217	chr4:120253001-120253002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527390006	chr4:120253003-120253004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549920469	chr4:120253010-120253011	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs146773062	chr4:120253039-120253040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1980024	chr4:120253047-120253048	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs538924917	chr4:120253068-120253069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185488469	chr4:120253083-120253084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189770016	chr4:120253132-120253133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558856193	chr4:120253167-120253168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34425882	chr4:120253177-120253178	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs554281566	chr4:120253207-120253208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574444102	chr4:120253267-120253268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183418805	chr4:120253291-120253292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73844762	chr4:120253345-120253346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs28373117	chr4:120253465-120253466	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs143733047	chr4:120253470-120253471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111977211	chr4:120253492-120253493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528772488	chr4:120253507-120253508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11725719	chr4:120253575-120253576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10024933	chr4:120253582-120253583	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs561964887	chr4:120253633-120253634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111733572	chr4:120253673-120253674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531013500	chr4:120253722-120253723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191975958	chr4:120253723-120253724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs9991959	chr4:120253773-120253774	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs532296322	chr4:120253850-120253851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552407229	chr4:120253892-120253893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4107728	chr4:120253910-120253911	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs146980231	chr4:120253965-120253966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183242981	chr4:120254008-120254009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567996525	chr4:120254016-120254017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537142116	chr4:120254075-120254076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187798276	chr4:120254077-120254078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557154401	chr4:120254151-120254152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143700375	chr4:120254198-120254199	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs545951039	chr4:120254204-120254205	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs553168398	chr4:120254254-120254255	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs573175632	chr4:120254258-120254259	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs200277746	chr4:120254273-120254274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78466167	chr4:120254297-120254298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10212714	chr4:120254302-120254303	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs534306817	chr4:120254307-120254308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558359189	chr4:120254338-120254339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10212956	chr4:120254343-120254344	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs1849457	chr4:120254355-120254356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs558078481	chr4:120254365-120254366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	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
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:841 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120251200-120257600	Weak transcription	Left Ventricle	heart
2	chr4:120251800-120258000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr4:120253800-120254000	Enhancers	Esophagus	oesophagus
4	chr4:120254000-120254200	Weak transcription	Esophagus	oesophagus
5	chr4:120256800-120258000	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr4:120256800-120259000	Enhancers	Spleen	Spleen
7	chr4:120257000-120257200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr4:120257000-120258400	Enhancers	HMEC	breast
9	chr4:120257600-120257800	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr4:120257600-120258400	Enhancers	NHEK	skin
11	chr4:120257600-120259000	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr4:120257800-120258400	Weak transcription	Left Ventricle	heart
13	chr4:120257800-120258600	Enhancers	HUVEC	blood vessel
14	chr4:120257800-120258600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr4:120258000-120258200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr4:120258000-120258400	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr4:120258000-120259000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr4:120258200-120258600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:120258200-120259000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:120258200-120259200	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr4:120258600-120259000	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr4:120258800-120259000	Enhancers	Left Ventricle	heart
23	chr4:120259000-120259400	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr4:120262200-120264600	Weak transcription	HepG2	liver
25	chr4:120263200-120264000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr4:120264000-120264400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr4:120264400-120266400	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr4:120264600-120264800	Enhancers	HepG2	liver
29	chr4:120266400-120275000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr4:120269000-120269200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:120269000-120269400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr4:120269200-120277600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr4:120269600-120293000	Weak transcription	Fetal Heart	heart
34	chr4:120273800-120274000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:120273800-120275200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr4:120274400-120275200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr4:120274400-120275400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:120274400-120275400	Enhancers	NHEK	skin
39	chr4:120274600-120274800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr4:120274800-120275200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:120274800-120275400	Enhancers	HMEC	breast
42	chr4:120275000-120275200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr4:120275400-120276600	Weak transcription	HMEC	breast
44	chr4:120276800-120277000	Enhancers	HMEC	breast
45	chr4:120276800-120277600	Enhancers	HSMM	muscle
46	chr4:120276800-120278000	Enhancers	Muscle Satellite Cultured Cells	--
47	chr4:120277000-120277200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:120277600-120278000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr4:120277600-120278000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr4:120277800-120278000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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