Variant report

Variant	esv2760882
Chromosome Location	chr4:99460485-99521345
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:320)
CpG islands
(count:488)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:320 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:99505407-99505929	HepG2	liver:	n/a	n/a
2	BACH1	chr4:99490369-99490371	K562	blood:	n/a	n/a
3	BCL3	chr4:99505403-99505680	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:99477121-99477203	K562	blood:	n/a	n/a
5	BRCA1	chr4:99465734-99465781	GM12878	blood:	n/a	n/a
6	BRCA1	chr4:99478792-99478889	Hela-S3	cervix:	n/a	n/a
7	CCNT2	chr4:99501383-99501552	K562	blood:	n/a	n/a
8	CEBPB	chr4:99478611-99479054	IMR90	lung:	n/a	n/a
9	CEBPB	chr4:99505479-99505698	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:99487887-99487953	K562	blood:	n/a	n/a
11	CEBPB	chr4:99487766-99488102	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:99506481-99506598	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:99494898-99495408	MCF-7	breast:	n/a	chr4:99495110-99495121
14	CEBPB	chr4:99479718-99479914	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:99460654-99460953	HepG2	liver:	n/a	chr4:99460805-99460816
16	CEBPB	chr4:99493920-99494170	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:99478517-99479070	HCT-116	colon:	n/a	n/a
18	CEBPB	chr4:99505387-99505745	A549	lung:	n/a	n/a
19	CEBPB	chr4:99460657-99460969	IMR90	lung:	n/a	chr4:99460805-99460816
20	CEBPB	chr4:99487742-99488080	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:99478719-99478988	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:99505416-99505755	IMR90	lung:	n/a	n/a
23	CEBPB	chr4:99493797-99494232	MCF-7	breast:	n/a	n/a
24	CEBPB	chr4:99468061-99468265	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:99487683-99488114	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:99505360-99505867	MCF-7	breast:	n/a	n/a
27	CEBPB	chr4:99494928-99495326	MCF-7	breast:	n/a	chr4:99495110-99495121
28	CEBPB	chr4:99505341-99505913	A549	lung:	n/a	n/a
29	CEBPB	chr4:99487795-99488072	A549	lung:	n/a	n/a
30	CEBPB	chr4:99460761-99460842	K562	blood:	n/a	chr4:99460805-99460816
31	CEBPB	chr4:99505345-99505825	MCF-7	breast:	n/a	n/a
32	CEBPB	chr4:99505384-99505922	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:99478677-99479014	A549	lung:	n/a	n/a
34	CEBPB	chr4:99478740-99479026	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr4:99460679-99460934	A549	lung:	n/a	chr4:99460805-99460816
36	CEBPB	chr4:99478739-99478984	A549	lung:	n/a	n/a
37	CEBPB	chr4:99505410-99505745	A549	lung:	n/a	n/a
38	CHD2	chr4:99466131-99466149	K562	blood:	n/a	n/a
39	CTCF	chr4:99468200-99468350	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr4:99461637-99461668	GM10248	blood:	n/a	n/a
41	CTCF	chr4:99468180-99468330	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr4:99477240-99477390	HCFaa	heart:	n/a	n/a
43	CTCF	chr4:99468160-99468310	BJ	skin:	n/a	n/a
44	CTCF	chr4:99468277-99468317	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr4:99468160-99468310	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr4:99468140-99468290	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr4:99468200-99468350	HCM	heart:	n/a	n/a
48	CTCF	chr4:99481670-99481709	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr4:99468160-99468310	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr4:99468169-99468353	Fibrobl	skin:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99480257-99480307	PFSK-1	brain:	n/a
2	chr4:99487497-99487547	ECC-1	luminal epithelium:	n/a
3	chr4:99504122-99504172	MCF10A-Er-Src	breast:	n/a
4	chr4:99477634-99477684	SK-N-SH	brain:	n/a
5	chr4:99467377-99467427	HNPCEpiC	eye:	n/a
6	chr4:99467377-99467427	Hepatocyte	liver:	n/a
7	chr4:99501119-99501169	SKMC	muscle:	n/a
8	chr4:99501119-99501169	PrEC	prostate:	n/a
9	chr4:99477634-99477684	ECC-1	luminal epithelium:	n/a
10	chr4:99504122-99504172	HCT-116	colon:	n/a
11	chr4:99467377-99467427	BE2_C	brain:	n/a
12	chr4:99477634-99477684	AG04450	lung:	fetal
13	chr4:99477634-99477684	AG04449	skin:	fetal
14	chr4:99479630-99479680	IMR90	lung:	fetal
15	chr4:99501119-99501169	HUVEC	blood vessel:	n/a
16	chr4:99480257-99480307	U87	brain:	n/a
17	chr4:99467377-99467427	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:99480257-99480307	MCF10A-Er-Src	breast:	n/a
19	chr4:99487497-99487547	AG09319	gingival:	n/a
20	chr4:99501119-99501169	GM19239	blood:	n/a
21	chr4:99477634-99477684	SK-N-SH_RA	brain:	n/a
22	chr4:99477634-99477684	RPTEC	kidney:	n/a
23	chr4:99504122-99504172	Caco-2	colon:	n/a
24	chr4:99477634-99477684	BE2_C	brain:	n/a
25	chr4:99502614-99502664	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:99502614-99502664	MCF-7	breast:	n/a
27	chr4:99480257-99480307	GM12878	blood:	n/a
28	chr4:99477634-99477684	Hela-S3	cervix:	n/a
29	chr4:99479630-99479680	BJ	skin:	n/a
30	chr4:99479630-99479680	AG09319	gingival:	n/a
31	chr4:99487497-99487547	PrEC	prostate:	n/a
32	chr4:99480257-99480307	ovcar-3	ovarian:	n/a
33	chr4:99487497-99487547	ovcar-3	ovarian:	n/a
34	chr4:99467377-99467427	AG09319	gingival:	n/a
35	chr4:99502614-99502664	Caco-2	colon:	n/a
36	chr4:99479630-99479680	PrEC	prostate:	n/a
37	chr4:99477634-99477684	HCT-116	colon:	n/a
38	chr4:99502614-99502664	HAEpiC	amniotic membrane:	n/a
39	chr4:99487497-99487547	T-47D	breast:	n/a
40	chr4:99467377-99467427	H1-hESC	embryonic stem cell:	embryo
41	chr4:99487497-99487547	NT2-D1	testis:	n/a
42	chr4:99480257-99480307	HCPEpiC	choroid plexus:	n/a
43	chr4:99504122-99504172	SKMC	muscle:	n/a
44	chr4:99480257-99480307	ECC-1	luminal epithelium:	n/a
45	chr4:99487497-99487547	HCPEpiC	choroid plexus:	n/a
46	chr4:99477634-99477684	HCM	heart:	n/a
47	chr4:99467377-99467427	HRPEpiC	eye:	n/a
48	chr4:99502614-99502664	IMR90	lung:	fetal
49	chr4:99504122-99504172	HUVEC	blood vessel:	n/a
50	chr4:99467377-99467427	PFSK-1	brain:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:99496585..99499120-chr4:99503712..99505800,2	MCF-7	breast:
2	chr4:99463140..99464695-chr4:99465921..99468144,2	K562	blood:
3	chr4:99495926..99497504-chr4:99501942..99504413,2	MCF-7	breast:
4	chr4:99479404..99481203-chr4:99500448..99502208,2	MCF-7	breast:
5	chr4:99495926..99497504-chr4:99501942..99504413,2	MCF-7	breast:
6	chr4:99435319..99436156-chr4:99495025..99495627,2	MCF-7	breast:
7	chr4:99483863..99486365-chr4:99487741..99490347,3	K562	blood:
8	chr4:99488456..99490510-chr4:99608692..99610309,2	K562	blood:
9	chr4:99499694..99502354-chr4:99504624..99508480,3	K562	blood:
10	chr4:99460334..99463092-chr4:99464059..99466192,2	MCF-7	breast:
11	chr4:99494775..99495594-chr4:99505088..99505683,2	MCF-7	breast:
12	chr4:99494205..99497159-chr4:99499484..99501729,2	MCF-7	breast:
13	chr4:99520635..99523456-chr4:99526451..99529728,3	K562	blood:
14	chr4:99458682..99461399-chr4:99848606..99851117,2	MCF-7	breast:
15	chr4:99499694..99502354-chr4:99504624..99508480,3	K562	blood:
16	chr4:99483863..99486365-chr4:99487741..99490347,3	K562	blood:
17	chr4:99500568..99502223-chr4:99504228..99505932,2	MCF-7	breast:
18	chr4:99460334..99463092-chr4:99464059..99466192,2	MCF-7	breast:
19	chr4:99496585..99499120-chr4:99503712..99505800,2	MCF-7	breast:
20	chr4:99502636..99505543-chr4:99509229..99510735,2	K562	blood:
21	chr4:99485403..99488335-chr4:99490236..99493906,4	MCF-7	breast:
22	chr4:99494205..99497159-chr4:99499484..99501729,2	MCF-7	breast:
23	chr4:99459317..99461488-chr4:99464335..99467316,2	K562	blood:
24	chr4:99479404..99481203-chr4:99500448..99502208,2	MCF-7	breast:
25	chr4:99426574..99427400-chr4:99494800..99495327,2	MCF-7	breast:
26	chr4:99465722..99468319-chr4:99566226..99568875,2	MCF-7	breast:
27	chr4:99463140..99464695-chr4:99465921..99468144,2	K562	blood:
28	chr4:99494775..99495594-chr4:99505088..99505683,2	MCF-7	breast:
29	chr4:99502636..99505543-chr4:99509229..99510735,2	K562	blood:
30	chr4:99485403..99488335-chr4:99490236..99493906,4	MCF-7	breast:
31	chr4:99494665..99495526-chr4:99539142..99539720,2	MCF-7	breast:
32	chr4:99500568..99502223-chr4:99504228..99505932,2	MCF-7	breast:
33	chr4:99459317..99461488-chr4:99464335..99467316,2	K562	blood:
34	chr4:96237471..96240020-chr4:99477884..99480366,2	K562	blood:

No data

Variant related genes	Relation type
TSPAN5	TF binding region
TSPAN5	CpG island
ENSG00000263923	chromatin interactions
ENSG00000151247	chromatin interactions

Extended variants
information (count: 2089 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2089 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555215588	chr4:99460514-99460515	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs117163070	chr4:99460540-99460541	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs142077287	chr4:99460557-99460558	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532643615	chr4:99460558-99460559	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs551158866	chr4:99460577-99460578	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs181674373	chr4:99460603-99460604	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs77214212	chr4:99460618-99460619	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs374482252	chr4:99460659-99460660	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs548574706	chr4:99460724-99460725	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs79071816	chr4:99460730-99460731	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs76446106	chr4:99460751-99460752	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs534270311	chr4:99460788-99460789	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs150849218	chr4:99460839-99460840	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs571414986	chr4:99460850-99460851	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs530114900	chr4:99460887-99460888	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs538407270	chr4:99460961-99460962	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs377269736	chr4:99460968-99460969	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs71828643	chr4:99460970-99460971	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs202111260	chr4:99460972-99460973	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs80157916	chr4:99460985-99460986	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs542544825	chr4:99460995-99460996	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs554130920	chr4:99461004-99461005	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs572547089	chr4:99461017-99461018	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs201071598	chr4:99461030-99461031	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs114636330	chr4:99461050-99461051	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs139280736	chr4:99461070-99461071	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs532243921	chr4:99461091-99461092	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs544445419	chr4:99461097-99461098	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs537232427	chr4:99461109-99461110	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs563118608	chr4:99461122-99461123	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs114619963	chr4:99461150-99461151	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs530395941	chr4:99461155-99461156	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs548933439	chr4:99461181-99461182	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs35099611	chr4:99461194-99461195	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs397879609	chr4:99461196-99461197	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs566861101	chr4:99461349-99461350	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs187073126	chr4:99461379-99461380	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs552543212	chr4:99461506-99461507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570814897	chr4:99461520-99461521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4699648	chr4:99461552-99461553	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs541167103	chr4:99461562-99461563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113346329	chr4:99461575-99461576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4699649	chr4:99461649-99461650	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs536134153	chr4:99461662-99461663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554492557	chr4:99461679-99461680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191012813	chr4:99461686-99461687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182046910	chr4:99461696-99461697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558539026	chr4:99461745-99461746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576835836	chr4:99461776-99461777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544322296	chr4:99461778-99461779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99445200-99461800	Weak transcription	HMEC	breast
2	chr4:99445400-99465400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr4:99446000-99467400	Weak transcription	Fetal Stomach	stomach
4	chr4:99446800-99461600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:99448200-99461000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:99449400-99461200	Weak transcription	NHEK	skin
7	chr4:99449400-99464200	Weak transcription	Fetal Brain Female	brain
8	chr4:99449800-99467400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:99450200-99467400	Weak transcription	Osteobl	bone
10	chr4:99450400-99461800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr4:99450400-99465200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr4:99450800-99468000	Weak transcription	HSMM	muscle
13	chr4:99458200-99465400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr4:99458800-99461200	Enhancers	Brain Substantia Nigra	brain
15	chr4:99458800-99464400	Enhancers	Ovary	ovary
16	chr4:99459000-99468000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:99459200-99460600	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr4:99459200-99462000	Weak transcription	Fetal Intestine Small	intestine
19	chr4:99459200-99465000	Weak transcription	Fetal Brain Male	brain
20	chr4:99459200-99468000	Weak transcription	Esophagus	oesophagus
21	chr4:99459200-99479600	Weak transcription	Spleen	Spleen
22	chr4:99459400-99461800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:99459600-99465000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr4:99459600-99465400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr4:99459600-99465400	Weak transcription	Brain Cingulate Gyrus	brain
26	chr4:99459600-99466000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr4:99459600-99467800	Weak transcription	NHLF	lung
28	chr4:99459800-99461800	Weak transcription	Brain Hippocampus Middle	brain
29	chr4:99459800-99462000	Weak transcription	Brain Angular Gyrus	brain
30	chr4:99459800-99465400	Weak transcription	Brain Anterior Caudate	brain
31	chr4:99460200-99463400	Weak transcription	Fetal Heart	heart
32	chr4:99460400-99461000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:99460400-99461200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr4:99460600-99463400	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr4:99460800-99461200	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr4:99461000-99461200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr4:99461000-99467400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:99461200-99461600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:99461200-99461600	Weak transcription	Brain Substantia Nigra	brain
40	chr4:99461200-99464200	Enhancers	NHEK	skin
41	chr4:99461200-99465400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr4:99461600-99462600	Enhancers	Brain Substantia Nigra	brain
43	chr4:99461600-99464000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:99461800-99463000	Enhancers	Brain Hippocampus Middle	brain
45	chr4:99461800-99463200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr4:99461800-99463400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:99461800-99463600	Enhancers	HMEC	breast
48	chr4:99461800-99463800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr4:99462000-99462400	Enhancers	Brain Angular Gyrus	brain
50	chr4:99462400-99465400	Weak transcription	Brain Angular Gyrus	brain

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