Variant report

Variant	nsv966315
Chromosome Location	chr4:120323446-120375667
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:623)
CpG islands
(count:428)
Chromatin interactive
region (count:4)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:623 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr4:120375640-120376007	HepG2	liver:	n/a	n/a
3	ATF1	chr4:120324198-120324405	K562	blood:	n/a	n/a
4	ATF1	chr4:120375410-120376174	K562	blood:	n/a	n/a
5	ATF2	chr4:120375574-120376077	H1-hESC	embryonic stem cell:	n/a	chr4:120375758-120375769
6	ATF2	chr4:120375554-120376118	H1-hESC	embryonic stem cell:	n/a	chr4:120375758-120375769
7	ATF2	chr4:120375508-120376132	GM12878	blood:	n/a	chr4:120375758-120375769
8	ATF2	chr4:120375555-120376037	GM12878	blood:	n/a	chr4:120375758-120375769
9	ATF3	chr4:120375534-120376115	HepG2	liver:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
10	ATF3	chr4:120375667-120376101	K562	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
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	chr4:120375591-120376108	K562	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
14	ATF3	chr4:120375643-120376128	GM12878	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
15	BATF	chr4:120336031-120336269	GM12878	blood:	n/a	n/a
16	BATF	chr4:120375371-120376260	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:120375469-120376323	GM12878	blood:	n/a	n/a
18	BCL3	chr4:120375586-120376104	A549	lung:	n/a	n/a
19	BCLAF1	chr4:120375555-120376089	GM12878	blood:	n/a	n/a
20	BCLAF1	chr4:120375644-120376123	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:120375666-120376228	K562	blood:	n/a	n/a
22	BRCA1	chr4:120375657-120376065	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr4:120375591-120376075	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr4:120375579-120376037	K562	blood:	n/a	n/a
25	CBX3	chr4:120374867-120376298	K562	blood:	n/a	n/a
26	CEBPB	chr4:120375413-120375949	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:120375455-120375925	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:120375396-120375977	K562	blood:	n/a	n/a
29	CEBPB	chr4:120338250-120338527	K562	blood:	n/a	n/a
30	CEBPB	chr4:120331779-120331807	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:120375400-120376070	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:120375366-120375954	K562	blood:	n/a	n/a
33	CEBPB	chr4:120341188-120341402	IMR90	lung:	n/a	chr4:120341261-120341272
34	CEBPB	chr4:120375425-120375563	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:120375413-120375995	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:120375439-120376084	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:120375417-120375936	A549	lung:	n/a	n/a
38	CEBPD	chr4:120375316-120375938	K562	blood:	n/a	n/a
39	CEBPD	chr4:120375633-120376140	HepG2	liver:	n/a	n/a
40	CHD2	chr4:120375631-120376139	GM12878	blood:	n/a	n/a
41	CHD2	chr4:120375606-120376150	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr4:120375644-120376161	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr4:120375382-120376154	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr4:120375358-120376212	A549	lung:	n/a	n/a
45	CREB1	chr4:120375487-120376118	GM12878	blood:	n/a	n/a
46	CREB1	chr4:120375572-120376066	A549	lung:	n/a	n/a
47	CREB1	chr4:120375651-120376225	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr4:120375370-120376141	K562	blood:	n/a	n/a
49	CREB1	chr4:120375581-120376083	ECC-1	luminal epithelium:	n/a	n/a
50	CREB1	chr4:120375371-120376117	HepG2	liver:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120332083-120332133	GM12878	blood:	n/a
2	chr4:120332083-120332133	GM12878	blood:	n/a
3	chr4:120327182-120327232	HCF	heart:	n/a
4	chr4:120332083-120332133	AG09309	skin:	n/a
5	chr4:120328025-120328075	SKMC	muscle:	n/a
6	chr4:120327182-120327232	HepG2	liver:	n/a
7	chr4:120327182-120327232	RPTEC	kidney:	n/a
8	chr4:120375409-120375459	AG04449	skin:	fetal
9	chr4:120329925-120329975	MCF-7	breast:	n/a
10	chr4:120373434-120373484	HRE	kidney:	n/a
11	chr4:120327182-120327232	GM19239	blood:	n/a
12	chr4:120332083-120332133	NHBE	bronchial:	n/a
13	chr4:120327624-120327674	SK-N-MC	brain:	n/a
14	chr4:120332083-120332133	NT2-D1	testis:	n/a
15	chr4:120373434-120373484	IMR90	lung:	fetal
16	chr4:120327624-120327674	Jurkat	blood:	n/a
17	chr4:120328025-120328075	PFSK-1	brain:	n/a
18	chr4:120327624-120327674	BE2_C	brain:	n/a
19	chr4:120375409-120375459	HEEpiC	esophagus:	n/a
20	chr4:120373434-120373484	HCPEpiC	choroid plexus:	n/a
21	chr4:120327182-120327232	SAEC	small airway:	n/a
22	chr4:120373434-120373484	GM12891	blood:	n/a
23	chr4:120329925-120329975	HEK293	kidney:	embryo
24	chr4:120327182-120327232	PFSK-1	brain:	n/a
25	chr4:120327182-120327232	AG04450	lung:	fetal
26	chr4:120327182-120327232	NB4	blood:	n/a
27	chr4:120327182-120327232	NHDF-neo	bronchial:	n/a
28	chr4:120327624-120327674	SK-N-SH	brain:	n/a
29	chr4:120327182-120327232	GM06990	blood:	n/a
30	chr4:120373434-120373484	Hela-S3	cervix:	n/a
31	chr4:120375409-120375459	NHDF-neo	bronchial:	n/a
32	chr4:120373434-120373484	MCF10A-Er-Src	breast:	n/a
33	chr4:120328025-120328075	A549	lung:	n/a
34	chr4:120329925-120329975	HMEC	breast:	n/a
35	chr4:120327624-120327674	NHDF-neo	bronchial:	n/a
36	chr4:120332083-120332133	AG04450	lung:	fetal
37	chr4:120327624-120327674	BJ	skin:	n/a
38	chr4:120327624-120327674	ProgFib	skin:	n/a
39	chr4:120327182-120327232	ovcar-3	ovarian:	n/a
40	chr4:120327624-120327674	HRE	kidney:	n/a
41	chr4:120373434-120373484	HRPEpiC	eye:	n/a
42	chr4:120327624-120327674	GM19239	blood:	n/a
43	chr4:120329925-120329975	GM12892	blood:	n/a
44	chr4:120327182-120327232	SK-N-SH_RA	brain:	n/a
45	chr4:120373434-120373484	NT2-D1	testis:	n/a
46	chr4:120327624-120327674	HNPCEpiC	eye:	n/a
47	chr4:120327182-120327232	AG09309	skin:	n/a
48	chr4:120327624-120327674	GM12892	blood:	n/a
49	chr4:120375409-120375459	Hepatocyte	liver:	n/a
50	chr4:120329925-120329975	HUVEC	blood vessel:	n/a

(count:4 , 50 per page) page: 1

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

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDE5A-3	chr4:120361716-120361790	NONHSAT098064
2	lnc-PDE5A-3	chr4:120370725-120371280	NONHSAT098065
3	lnc-PDE5A-3	chr4:120365524-120365586	NONHSAT098064
4	lnc-AC110373.1-2	chr4:120330488-120331388	ENSG00000260091.1
5	lnc-PDE5A-3	chr4:120371197-120371312	NONHSAT098064
6	lnc-PDE5A-3	chr4:120362106-120362207	NONHSAT098064
7	lnc-AC110373.1-2	chr4:120330489-120331408	NONHSAT098058
8	lnc-PDE5A-3	chr4:120375401-120375783	NONHSAT098065

No data

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

Extended variants
information (count: 1934 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1934 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535725454	chr4:120323474-120323475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs55853707	chr4:120323479-120323480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115312503	chr4:120323502-120323503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544316345	chr4:120323528-120323529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs151054926	chr4:120323569-120323570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10518331	chr4:120323595-120323596	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs191164931	chr4:120323604-120323605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs60583767	chr4:120323631-120323632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140706157	chr4:120323724-120323725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528229777	chr4:120323745-120323746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150122183	chr4:120323767-120323768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371726861	chr4:120323778-120323779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534799925	chr4:120323798-120323799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562913946	chr4:120323835-120323836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183998572	chr4:120323855-120323856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551865076	chr4:120323890-120323891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565279840	chr4:120323898-120323899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199654415	chr4:120323983-120323984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527784467	chr4:120324025-120324026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554591011	chr4:120324054-120324055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78577255	chr4:120324070-120324071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566656590	chr4:120324092-120324093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs28709577	chr4:120324121-120324122	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs114995868	chr4:120324137-120324138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142162856	chr4:120324147-120324148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537402376	chr4:120324173-120324174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557723983	chr4:120324186-120324187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145766728	chr4:120324200-120324201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533618783	chr4:120324244-120324245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553978101	chr4:120324256-120324257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138482315	chr4:120324260-120324261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377355939	chr4:120324282-120324283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61269662	chr4:120324317-120324318	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs563001991	chr4:120324364-120324365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576668348	chr4:120324374-120324375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188393497	chr4:120324380-120324381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565260254	chr4:120324390-120324391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527821687	chr4:120324391-120324392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144385754	chr4:120324402-120324403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs386678953	chr4:120324417-120324418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13133522	chr4:120324424-120324425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs6846131	chr4:120324454-120324455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112446035	chr4:120324459-120324460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549268332	chr4:120324464-120324465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577098995	chr4:120324466-120324467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6820376	chr4:120324476-120324477	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs538138723	chr4:120324499-120324500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149861164	chr4:120324547-120324548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59446710	chr4:120324549-120324550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551116721	chr4:120324556-120324557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
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

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120317600-120325600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:120318000-120333400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:120324200-120342200	Weak transcription	Pancreas	Pancrea
4	chr4:120324400-120326000	Weak transcription	Fetal Intestine Small	intestine
5	chr4:120324600-120328000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr4:120324600-120330400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr4:120324800-120325000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:120325000-120325600	Weak transcription	Fetal Stomach	stomach
9	chr4:120325000-120329800	Weak transcription	Liver	Liver
10	chr4:120325000-120331400	Weak transcription	Fetal Muscle Trunk	muscle
11	chr4:120325000-120331800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr4:120325000-120341200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:120325200-120334200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr4:120325600-120326600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:120325600-120326600	Strong transcription	Fetal Stomach	stomach
16	chr4:120326000-120327200	Strong transcription	Fetal Intestine Small	intestine
17	chr4:120326600-120329000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr4:120326600-120329800	Weak transcription	Fetal Stomach	stomach
19	chr4:120326600-120331600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:120326600-120334400	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr4:120326600-120360800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:120326800-120331600	Weak transcription	Fetal Muscle Leg	muscle
23	chr4:120327000-120327200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr4:120327000-120328600	Weak transcription	Lung	lung
25	chr4:120327000-120329800	Weak transcription	Gastric	stomach
26	chr4:120327200-120335200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr4:120327200-120339200	Weak transcription	Esophagus	oesophagus
28	chr4:120327200-120361400	Weak transcription	Fetal Intestine Small	intestine
29	chr4:120327800-120332000	Weak transcription	Stomach Smooth Muscle	stomach
30	chr4:120328000-120329600	Enhancers	Placenta	Placenta
31	chr4:120328000-120330200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr4:120328200-120329800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr4:120328200-120329800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr4:120328600-120329000	Strong transcription	Lung	lung
35	chr4:120328800-120331400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:120328800-120375200	Weak transcription	Ovary	ovary
37	chr4:120329000-120329800	Weak transcription	Lung	lung
38	chr4:120329200-120331400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr4:120329600-120330600	Genic enhancers	Placenta	Placenta
40	chr4:120329800-120330200	Strong transcription	Lung	lung
41	chr4:120329800-120330400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr4:120329800-120330400	Strong transcription	Gastric	stomach
43	chr4:120329800-120330600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr4:120329800-120330600	Strong transcription	Liver	Liver
45	chr4:120329800-120330600	Strong transcription	Fetal Stomach	stomach
46	chr4:120330000-120330600	Enhancers	Adipose Nuclei	Adipose
47	chr4:120330200-120332600	Weak transcription	Lung	lung
48	chr4:120330200-120367600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr4:120330400-120332000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr4:120330400-120333200	Weak transcription	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links