Variant report

Variant	esv3448093
Chromosome Location	chr4:142612197-142704695
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:689)
CpG islands
(count:244)
Chromatin interactive
region (count:14)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:142626031-142626694	GM12878	blood:	n/a	n/a
2	ATF2	chr4:142626170-142626819	GM12878	blood:	n/a	n/a
3	ATF2	chr4:142693264-142693852	GM12878	blood:	n/a	n/a
4	ATF2	chr4:142693144-142693871	GM12878	blood:	n/a	n/a
5	BACH1	chr4:142690136-142690456	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:142635086-142635593	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr4:142626201-142626517	GM12878	blood:	n/a	n/a
8	BATF	chr4:142693416-142693800	GM12878	blood:	n/a	n/a
9	BATF	chr4:142693361-142693795	GM12878	blood:	n/a	n/a
10	BATF	chr4:142626233-142626498	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:142693447-142693720	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:142693408-142693685	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:142626207-142626531	GM12878	blood:	n/a	n/a
14	BCLAF1	chr4:142693323-142693863	GM12878	blood:	n/a	chr4:142693790-142693797
15	BCLAF1	chr4:142627059-142627389	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:142627252-142627557	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:142693110-142693896	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:142626262-142626518	GM12878	blood:	n/a	n/a
19	BRCA1	chr4:142688586-142688665	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr4:142640292-142640302	GM12878	blood:	n/a	n/a
21	CBX3	chr4:142627650-142628029	HCT-116	colon:	n/a	n/a
22	CEBPB	chr4:142617253-142617355	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr4:142678513-142678847	HepG2	liver:	n/a	chr4:142678680-142678693 chr4:142678680-142678691 chr4:142678682-142678691
24	CEBPB	chr4:142646189-142646389	HepG2	liver:	n/a	chr4:142646281-142646292
25	CEBPB	chr4:142617151-142617458	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:142686138-142686273	HepG2	liver:	n/a	chr4:142686194-142686205
27	CEBPB	chr4:142648615-142648887	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:142678477-142678872	IMR90	lung:	n/a	chr4:142678680-142678693 chr4:142678680-142678691 chr4:142678682-142678691
29	CEBPB	chr4:142695060-142695083	A549	lung:	n/a	n/a
30	CEBPB	chr4:142626075-142626690	GM12878	blood:	n/a	n/a
31	CEBPB	chr4:142648571-142648835	A549	lung:	n/a	n/a
32	CEBPB	chr4:142678509-142678837	A549	lung:	n/a	chr4:142678680-142678693 chr4:142678680-142678691 chr4:142678682-142678691
33	CEBPB	chr4:142678535-142678739	K562	blood:	n/a	chr4:142678680-142678693 chr4:142678680-142678691 chr4:142678682-142678691
34	CEBPB	chr4:142617206-142617471	A549	lung:	n/a	n/a
35	CREB1	chr4:142693342-142693871	GM12878	blood:	n/a	n/a
36	CTCF	chr4:142632500-142632650	AG09319	gingival:	n/a	chr4:142632559-142632577
37	CTCF	chr4:142622980-142623130	BE2_C	brain:	n/a	n/a
38	CTCF	chr4:142632484-142632643	K562	blood:	n/a	chr4:142632559-142632577
39	CTCF	chr4:142623780-142623930	GM12873	blood:	n/a	n/a
40	CTCF	chr4:142632423-142632645	A549	lung:	n/a	chr4:142632559-142632577
41	CTCF	chr4:142632480-142632630	HVMF	connective:	n/a	chr4:142632559-142632577
42	CTCF	chr4:142624820-142624970	HMF	breast:	n/a	n/a
43	CTCF	chr4:142623780-142623930	SAEC	small airway:	n/a	n/a
44	CTCF	chr4:142632444-142632683	Medullo	brain:	n/a	chr4:142632559-142632577
45	CTCF	chr4:142623740-142623890	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr4:142623740-142623890	NHEK	skin:	n/a	n/a
47	CTCF	chr4:142623560-142623710	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr4:142623829-142623900	GM13976	blood:	n/a	n/a
49	CTCF	chr4:142623794-142623892	Fibrobl	skin:	n/a	n/a
50	CTCF	chr4:142623680-142623830	HCT-116	colon:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:142678613-142678663	GM06990	blood:	n/a
2	chr4:142678613-142678663	CMK	blood:	n/a
3	chr4:142652413-142652463	LNCaP	prostate:	n/a
4	chr4:142678613-142678663	H1-hESC	embryonic stem cell:	embryo
5	chr4:142652413-142652463	NHDF-neo	bronchial:	n/a
6	chr4:142678613-142678663	U87	brain:	n/a
7	chr4:142636072-142636122	HRE	kidney:	n/a
8	chr4:142636072-142636122	NT2-D1	testis:	n/a
9	chr4:142623193-142623243	HEEpiC	esophagus:	n/a
10	chr4:142623193-142623243	HRE	kidney:	n/a
11	chr4:142636072-142636122	SK-N-SH_RA	brain:	n/a
12	chr4:142623193-142623243	Hela-S3	cervix:	n/a
13	chr4:142623193-142623243	Caco-2	colon:	n/a
14	chr4:142652413-142652463	GM12891	blood:	n/a
15	chr4:142636072-142636122	K562	blood:	n/a
16	chr4:142678613-142678663	NT2-D1	testis:	n/a
17	chr4:142636072-142636122	NHDF-neo	bronchial:	n/a
18	chr4:142636072-142636122	Hela-S3	cervix:	n/a
19	chr4:142678613-142678663	AG09309	skin:	n/a
20	chr4:142652413-142652463	PrEC	prostate:	n/a
21	chr4:142623193-142623243	HRCEpiC	kidney:	n/a
22	chr4:142652413-142652463	HIPEpiC	eye:	n/a
23	chr4:142636072-142636122	AoSMC	blood vessel:	n/a
24	chr4:142623193-142623243	NB4	blood:	n/a
25	chr4:142636072-142636122	ovcar-3	ovarian:	n/a
26	chr4:142678613-142678663	K562	blood:	n/a
27	chr4:142678613-142678663	GM12878	blood:	n/a
28	chr4:142636072-142636122	SAEC	small airway:	n/a
29	chr4:142678613-142678663	HPAEpiC	pulmonary alveolar:	n/a
30	chr4:142636072-142636122	HRPEpiC	eye:	n/a
31	chr4:142623193-142623243	Hepatocyte	liver:	n/a
32	chr4:142623193-142623243	U87	brain:	n/a
33	chr4:142678613-142678663	NB4	blood:	n/a
34	chr4:142636072-142636122	GM12878	blood:	n/a
35	chr4:142636072-142636122	MCF-7	breast:	n/a
36	chr4:142623193-142623243	GM06990	blood:	n/a
37	chr4:142623193-142623243	HCPEpiC	choroid plexus:	n/a
38	chr4:142623193-142623243	GM12878	blood:	n/a
39	chr4:142678613-142678663	T-47D	breast:	n/a
40	chr4:142652413-142652463	MCF-7	breast:	n/a
41	chr4:142678613-142678663	HRCEpiC	kidney:	n/a
42	chr4:142623193-142623243	HCF	heart:	n/a
43	chr4:142652413-142652463	HepG2	liver:	n/a
44	chr4:142623193-142623243	GM12891	blood:	n/a
45	chr4:142678613-142678663	HNPCEpiC	eye:	n/a
46	chr4:142623193-142623243	HIPEpiC	eye:	n/a
47	chr4:142678613-142678663	A549	lung:	n/a
48	chr4:142636072-142636122	GM06990	blood:	n/a
49	chr4:142623193-142623243	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:142678613-142678663	SK-N-MC	brain:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:142679469..142681092-chr4:142682806..142685184,2	K562	blood:
2	chr4:142267430..142267999-chr4:142622577..142623359,2	MCF-7	breast:
3	chr4:142679469..142682376-chr4:142682806..142684496,2	K562	blood:
4	chr4:142295670..142297489-chr4:142636919..142639486,2	MCF-7	breast:
5	chr4:142679469..142682376-chr4:142682806..142684496,2	K562	blood:
6	chr19:27734776..27735283-chr4:142678250..142679232,2	MCF-7	breast:
7	chr4:142683419..142685394-chr4:142837554..142840288,2	K562	blood:
8	chr4:142679469..142681092-chr4:142682806..142685184,2	K562	blood:
9	chr4:142267058..142267811-chr4:142632121..142633106,3	MCF-7	breast:
10	chr4:142079370..142080051-chr4:142632096..142632707,2	MCF-7	breast:
11	chr4:142296713..142297323-chr4:142632141..142632805,2	MCF-7	breast:
12	chr4:142597917..142599701-chr4:142616061..142617565,2	MCF-7	breast:
13	chr4:142228030..142229421-chr4:142624406..142625337,5	MCF-7	breast:
14	chr4:142228387..142228929-chr4:142632549..142633118,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF330-6	chr4:142641622-142641920	NONHSAT098530
2	lnc-ZNF330-6	chr4:142642935-142643161	NONHSAT098532
3	lnc-ZNF330-6	chr4:142649093-142649137	NONHSAT098532
4	lnc-ZNF330-6	chr4:142640284-142640629	NONHSAT098530

No data

Variant related genes	Relation type
IL15	TF binding region
IL15	CpG island

Extended variants
information (count: 2437 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2437 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561414590	chr4:142612213-142612214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs386680238	chr4:142612253-142612254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139944956	chr4:142612259-142612260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs70949130	chr4:142612260-142612261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78997617	chr4:142612261-142612262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74608838	chr4:142612262-142612263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78639219	chr4:142612263-142612264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528978654	chr4:142612274-142612275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550116855	chr4:142612280-142612281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370616315	chr4:142612287-142612288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184331310	chr4:142612288-142612289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs72712412	chr4:142612296-142612297	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs566790068	chr4:142612303-142612304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527459162	chr4:142612338-142612339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536845581	chr4:142612341-142612342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549219670	chr4:142612360-142612361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555151573	chr4:142612422-142612423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12503010	chr4:142612492-142612493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs535962220	chr4:142612494-142612495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373652172	chr4:142612514-142612515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531419606	chr4:142612561-142612562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188242160	chr4:142612564-142612565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569155018	chr4:142612581-142612582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539849711	chr4:142612636-142612637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569885822	chr4:142612651-142612652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574044200	chr4:142612664-142612665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115637495	chr4:142612679-142612680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540401099	chr4:142612713-142612714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555547303	chr4:142612728-142612729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573364421	chr4:142612746-142612747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144931079	chr4:142612747-142612748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs72712413	chr4:142612750-142612751	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs532773645	chr4:142612753-142612754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs180907492	chr4:142612782-142612783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147975955	chr4:142612820-142612821	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs13111860	chr4:142612879-142612880	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs549158374	chr4:142612912-142612913	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567459263	chr4:142612916-142612917	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs56761520	chr4:142612948-142612949	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs72712415	chr4:142613124-142613125	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs569369370	chr4:142613146-142613147	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539417344	chr4:142613162-142613163	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375709498	chr4:142613174-142613175	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558155653	chr4:142613206-142613207	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs72946480	chr4:142613214-142613215	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11100724	chr4:142613269-142613270	Genic enhancers Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs555683067	chr4:142613302-142613303	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186288773	chr4:142613338-142613339	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs56332929	chr4:142613357-142613358	Genic enhancers Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs192383664	chr4:142613367-142613368	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Intellectual disability	22102821	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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	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
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142583400-142634600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:142601600-142613600	Weak transcription	Duodenum Mucosa	Duodenum
3	chr4:142601800-142616400	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr4:142602800-142616400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:142605800-142614600	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr4:142608400-142613200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr4:142608400-142613200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr4:142608400-142628800	Weak transcription	Aorta	Aorta
9	chr4:142608400-142629000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:142608600-142612800	Weak transcription	Left Ventricle	heart
11	chr4:142608600-142615000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr4:142608800-142613200	Weak transcription	Esophagus	oesophagus
13	chr4:142608800-142624200	Weak transcription	Spleen	Spleen
14	chr4:142608800-142655000	Weak transcription	Gastric	stomach
15	chr4:142609600-142613000	Weak transcription	Hela-S3	cervix
16	chr4:142609800-142613200	Weak transcription	A549	lung
17	chr4:142611600-142612800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:142612600-142613000	Enhancers	Liver	Liver
19	chr4:142612800-142613200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:142612800-142613400	Enhancers	Left Ventricle	heart
21	chr4:142613000-142613800	Enhancers	Hela-S3	cervix
22	chr4:142613200-142613400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:142613200-142613400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:142613200-142613400	Enhancers	Esophagus	oesophagus
25	chr4:142613200-142613400	Enhancers	Sigmoid Colon	Sigmoid Colon
26	chr4:142613200-142613600	Enhancers	A549	lung
27	chr4:142613400-142613600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr4:142613400-142628800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:142613400-142629000	Weak transcription	Left Ventricle	heart
30	chr4:142613800-142617200	Weak transcription	Hela-S3	cervix
31	chr4:142621000-142623400	Weak transcription	Stomach Smooth Muscle	stomach
32	chr4:142622800-142623000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
33	chr4:142622800-142623000	Enhancers	A549	lung
34	chr4:142622800-142624000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr4:142623000-142623200	Enhancers	Stomach Mucosa	stomach
36	chr4:142623000-142624400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:142623000-142624400	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr4:142623000-142624800	Enhancers	Fetal Muscle Leg	muscle
39	chr4:142623000-142627000	Weak transcription	A549	lung
40	chr4:142623200-142623600	Weak transcription	HSMM	muscle
41	chr4:142623200-142623800	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr4:142623200-142627000	Weak transcription	Stomach Mucosa	stomach
43	chr4:142623400-142623600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
44	chr4:142623400-142623800	Enhancers	HSMMtube	muscle
45	chr4:142623400-142624200	Enhancers	Psoas Muscle	Psoas
46	chr4:142623400-142624200	Strong transcription	Stomach Smooth Muscle	stomach
47	chr4:142623600-142623800	Enhancers	HSMM	muscle
48	chr4:142623600-142624000	Enhancers	Fetal Heart	heart
49	chr4:142623800-142624000	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr4:142623800-142624600	Enhancers	Fetal Muscle Trunk	muscle

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