Variant report

Variant	esv1819960
Chromosome Location	chr4:107216320-107246136
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:712)
CpG islands
(count:1039)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:107240223-107240253	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:107224851-107225233	K562	blood:	n/a	n/a
3	ARID3A	chr4:107234380-107234799	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:107236935-107238209	HepG2	liver:	n/a	n/a
5	ATF1	chr4:107236740-107238091	K562	blood:	n/a	n/a
6	ATF2	chr4:107237102-107237989	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:107237195-107237980	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:107237261-107238038	GM12878	blood:	n/a	n/a
9	ATF2	chr4:107237040-107238074	GM12878	blood:	n/a	n/a
10	ATF3	chr4:107237169-107237603	A549	lung:	n/a	chr4:107237306-107237314
11	ATF3	chr4:107237198-107237880	GM12878	blood:	n/a	chr4:107237306-107237314
12	ATF3	chr4:107237243-107237804	K562	blood:	n/a	chr4:107237306-107237314
13	ATF3	chr4:107237200-107237728	H1-hESC	embryonic stem cell:	n/a	chr4:107237306-107237314
14	BACH1	chr4:107236325-107236349	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:107236955-107237132	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:107236816-107237016	K562	blood:	n/a	n/a
17	BCL3	chr4:107237245-107237821	A549	lung:	n/a	n/a
18	BCL3	chr4:107237087-107237869	A549	lung:	n/a	n/a
19	BCLAF1	chr4:107236774-107237953	GM12878	blood:	n/a	n/a
20	BCLAF1	chr4:107236610-107238013	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:107234293-107234627	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:107234291-107234938	K562	blood:	n/a	n/a
23	BHLHE40	chr4:107234336-107234585	HepG2	liver:	n/a	n/a
24	BHLHE40	chr4:107243118-107243318	K562	blood:	n/a	n/a
25	BHLHE40	chr4:107236945-107238657	GM12878	blood:	n/a	chr4:107237160-107237176
26	BHLHE40	chr4:107236263-107238635	K562	blood:	n/a	chr4:107237160-107237176
27	BHLHE40	chr4:107237099-107238030	HepG2	liver:	n/a	chr4:107237160-107237176
28	BRCA1	chr4:107237177-107237878	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr4:107236757-107236957	HepG2	liver:	n/a	n/a
30	BRCA1	chr4:107237136-107238059	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr4:107237242-107237930	HepG2	liver:	n/a	n/a
32	CBX3	chr4:107236972-107238087	K562	blood:	n/a	n/a
33	CCNT2	chr4:107237073-107237833	K562	blood:	n/a	n/a
34	CCNT2	chr4:107234261-107234508	K562	blood:	n/a	n/a
35	CEBPB	chr4:107237319-107238005	K562	blood:	n/a	n/a
36	CEBPB	chr4:107238512-107238864	K562	blood:	n/a	chr4:107238684-107238695
37	CEBPB	chr4:107237016-107238447	GM12878	blood:	n/a	n/a
38	CEBPB	chr4:107238537-107238802	HepG2	liver:	n/a	chr4:107238684-107238695
39	CEBPB	chr4:107243700-107243836	HepG2	liver:	n/a	chr4:107243767-107243780
40	CEBPB	chr4:107236995-107237923	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:107238532-107238826	IMR90	lung:	n/a	chr4:107238684-107238695
42	CEBPB	chr4:107222912-107223212	IMR90	lung:	n/a	n/a
43	CEBPD	chr4:107237028-107237593	HepG2	liver:	n/a	n/a
44	CEBPD	chr4:107224664-107225112	K562	blood:	n/a	n/a
45	CEBPD	chr4:107237052-107238119	K562	blood:	n/a	n/a
46	CHD1	chr4:107237073-107238602	GM12878	blood:	n/a	n/a
47	CHD1	chr4:107237674-107238049	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr4:107239960-107240142	GM12878	blood:	n/a	n/a
49	CHD1	chr4:107236630-107237059	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr4:107236785-107237858	K562	blood:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:107236485-107236535	ProgFib	skin:	n/a
2	chr4:107237473-107237523	NHDF-neo	bronchial:	n/a
3	chr4:107236485-107236535	ProgFib	skin:	n/a
4	chr4:107237473-107237523	NHDF-neo	bronchial:	n/a
5	chr4:107237688-107237738	NHBE	bronchial:	n/a
6	chr4:107237870-107237920	ovcar-3	ovarian:	n/a
7	chr4:107238125-107238175	T-47D	breast:	n/a
8	chr4:107238125-107238175	HMEC	breast:	n/a
9	chr4:107237183-107237233	HepG2	liver:	n/a
10	chr4:107237940-107237990	ovcar-3	ovarian:	n/a
11	chr4:107237727-107237777	U87	brain:	n/a
12	chr4:107224533-107224583	ProgFib	skin:	n/a
13	chr4:107223505-107223555	AG09309	skin:	n/a
14	chr4:107223505-107223555	NHBE	bronchial:	n/a
15	chr4:107237488-107237538	AG04449	skin:	fetal
16	chr4:107238104-107238154	Hepatocyte	liver:	n/a
17	chr4:107237688-107237738	Caco-2	colon:	n/a
18	chr4:107237870-107237920	NT2-D1	testis:	n/a
19	chr4:107242537-107242587	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:107237991-107238041	NH-A	brain:	n/a
21	chr4:107237870-107237920	SK-N-SH_RA	brain:	n/a
22	chr4:107237870-107237920	AG04450	lung:	fetal
23	chr4:107224533-107224583	Hepatocyte	liver:	n/a
24	chr4:107237488-107237538	HepG2	liver:	n/a
25	chr4:107237473-107237523	HL-60	blood:	n/a
26	chr4:107242537-107242587	PANC-1	pancreas:	n/a
27	chr4:107237940-107237990	GM19239	blood:	n/a
28	chr4:107236485-107236535	BJ	skin:	n/a
29	chr4:107242537-107242587	RPTEC	kidney:	n/a
30	chr4:107237686-107237736	MCF-7	breast:	n/a
31	chr4:107223505-107223555	HCPEpiC	choroid plexus:	n/a
32	chr4:107237991-107238041	HCT-116	colon:	n/a
33	chr4:107238125-107238175	Caco-2	colon:	n/a
34	chr4:107237688-107237738	AG09309	skin:	n/a
35	chr4:107237991-107238041	A549	lung:	n/a
36	chr4:107237727-107237777	ovcar-3	ovarian:	n/a
37	chr4:107236753-107236803	RPTEC	kidney:	n/a
38	chr4:107223505-107223555	NH-A	brain:	n/a
39	chr4:107237183-107237233	HAEpiC	amniotic membrane:	n/a
40	chr4:107237183-107237233	H1-hESC	embryonic stem cell:	embryo
41	chr4:107224533-107224583	PrEC	prostate:	n/a
42	chr4:107237688-107237738	HRE	kidney:	n/a
43	chr4:107224533-107224583	RPTEC	kidney:	n/a
44	chr4:107238125-107238175	A549	lung:	n/a
45	chr4:107223505-107223555	HMEC	breast:	n/a
46	chr4:107238125-107238175	H1-hESC	embryonic stem cell:	embryo
47	chr4:107238125-107238175	NHDF-neo	bronchial:	n/a
48	chr4:107236753-107236803	GM19239	blood:	n/a
49	chr4:107237688-107237738	NT2-D1	testis:	n/a
50	chr4:107237686-107237736	SK-N-SH	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:107243946..107245943-chr4:107262663..107264283,2	K562	blood:
2	chr4:100869528..100871186-chr4:107235611..107237116,2	K562	blood:
3	chr4:107226289..107231817-chr4:107234990..107238909,9	MCF-7	breast:
4	chr4:107237104..107239222-chr4:107242946..107245918,2	MCF-7	breast:
5	chr4:107238766..107241197-chr4:107243663..107246436,3	MCF-7	breast:
6	chr4:107215261..107218209-chr4:107235780..107238587,4	MCF-7	breast:
7	chr4:107237734..107238393-chr9:33167089..33167643,2	NB4	blood:
8	chr4:107217698..107220197-chr4:107235297..107237150,2	MCF-7	breast:
9	chr4:107226289..107231817-chr4:107234990..107238909,9	MCF-7	breast:
10	chr4:107243504..107246800-chr4:107249107..107253056,3	MCF-7	breast:
11	chr4:107217698..107220197-chr4:107235297..107237150,2	MCF-7	breast:
12	chr4:107216359..107217869-chr4:107220445..107222881,2	K562	blood:
13	chr4:107238766..107241197-chr4:107243663..107246436,3	MCF-7	breast:
14	chr4:107158622..107160496-chr4:107233252..107235582,2	MCF-7	breast:
15	chr4:107237524..107239037-chr4:107241153..107242940,2	MCF-7	breast:
16	chr4:107237524..107239037-chr4:107241153..107242940,2	MCF-7	breast:
17	chr4:107218591..107221173-chr4:107222816..107224928,3	K562	blood:
18	chr20:57463851..57464376-chr4:107236670..107237605,2	Hela-S3	cervix:
19	chr4:107224095..107225735-chr4:107236744..107238775,2	MCF-7	breast:
20	chr11:62608849..62609649-chr4:107237489..107238158,2	Hela-S3	cervix:
21	chr4:107217078..107218792-chr4:107237509..107239809,2	K562	blood:
22	chr4:107222542..107224748-chr4:107236218..107238932,2	MCF-7	breast:
23	chr4:107216359..107217869-chr4:107220445..107222881,2	K562	blood:
24	chr4:107218105..107220091-chr4:107221627..107224316,2	K562	blood:

No data

Variant related genes	Relation type
AIMP1	TF binding region
TBCK	TF binding region
AIMP1	CpG island
TBCK	CpG island
ENSG00000164022	chromatin interactions
ENSG00000225806	chromatin interactions
ENSG00000145348	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000245322	chromatin interactions
ENSG00000086062	chromatin interactions
ENSG00000087460	chromatin interactions

Extended variants
information (count: 1030 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1030 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35784409	chr4:107216320-107216321	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs530629690	chr4:107216343-107216344	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs550689189	chr4:107216348-107216349	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567418310	chr4:107216370-107216371	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs112727666	chr4:107216372-107216373	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs148350284	chr4:107216401-107216402	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs574854880	chr4:107216405-107216406	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs56313516	chr4:107216416-107216417	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs13102159	chr4:107216463-107216464	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs13102333	chr4:107216504-107216505	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs189073130	chr4:107216515-107216516	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs13130214	chr4:107216524-107216525	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs370287074	chr4:107216560-107216561	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs558161468	chr4:107216573-107216574	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs373938712	chr4:107216596-107216597	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs558987339	chr4:107216610-107216611	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs573145359	chr4:107216637-107216638	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs115470984	chr4:107216681-107216682	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs182512549	chr4:107216696-107216697	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs141536659	chr4:107216833-107216834	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs554639805	chr4:107216837-107216838	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs574619423	chr4:107216841-107216842	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs28440815	chr4:107216867-107216868	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs7688008	chr4:107216896-107216897	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs375658879	chr4:107217070-107217071	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562921847	chr4:107217124-107217125	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs72878531	chr4:107217163-107217164	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs78127074	chr4:107217164-107217165	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs545248209	chr4:107217178-107217179	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs565077824	chr4:107217201-107217202	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs530731880	chr4:107217209-107217210	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs113684158	chr4:107217265-107217266	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs150479588	chr4:107217286-107217287	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs138310525	chr4:107217368-107217369	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs529778552	chr4:107217383-107217384	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs17036654	chr4:107217398-107217399	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs566414109	chr4:107217429-107217430	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs144121156	chr4:107217453-107217454	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs552824869	chr4:107217464-107217465	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs116432218	chr4:107217493-107217494	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs72660520	chr4:107217521-107217522	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs554709461	chr4:107217543-107217544	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs574715556	chr4:107217558-107217559	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs58172100	chr4:107217575-107217576	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186228643	chr4:107217614-107217615	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577162634	chr4:107217620-107217621	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs189131400	chr4:107217658-107217659	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs181565954	chr4:107217659-107217660	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs185714824	chr4:107217660-107217661	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544532089	chr4:107217744-107217745	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	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
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
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	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
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cognitive impairment	21505072	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Cancer	21215367	CNVD

Chromatin state (count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107114600-107236000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr4:107155600-107236000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr4:107178000-107236200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:107178000-107236200	Weak transcription	Right Ventricle	heart
5	chr4:107178000-107236600	Weak transcription	Esophagus	oesophagus
6	chr4:107178000-107236600	Weak transcription	Pancreas	Pancrea
7	chr4:107178200-107236000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr4:107194400-107221200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:107194800-107227600	Weak transcription	Brain Angular Gyrus	brain
10	chr4:107198800-107235600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr4:107201400-107227800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr4:107202200-107219400	Weak transcription	Fetal Brain Male	brain
13	chr4:107202800-107236000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr4:107204000-107235800	Weak transcription	Psoas Muscle	Psoas
15	chr4:107204000-107236200	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr4:107204200-107220400	Weak transcription	Fetal Heart	heart
17	chr4:107205600-107236000	Weak transcription	Brain Anterior Caudate	brain
18	chr4:107205800-107227600	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr4:107207000-107227600	Weak transcription	Brain Substantia Nigra	brain
20	chr4:107207400-107217200	Weak transcription	Spleen	Spleen
21	chr4:107207800-107217600	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr4:107208000-107217600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr4:107208000-107218200	Strong transcription	Primary B cells from cord blood	blood
24	chr4:107208000-107223000	Weak transcription	Colonic Mucosa	Colon
25	chr4:107208000-107229600	Weak transcription	Aorta	Aorta
26	chr4:107208200-107223200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr4:107208800-107217200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr4:107208800-107222600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr4:107208800-107226000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr4:107209000-107223400	Weak transcription	NHLF	lung
31	chr4:107209000-107226800	Weak transcription	NHEK	skin
32	chr4:107209000-107229400	Weak transcription	GM12878-XiMat	blood
33	chr4:107209000-107231200	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr4:107209200-107217200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr4:107209200-107224600	Weak transcription	K562	blood
36	chr4:107209200-107236000	Weak transcription	HMEC	breast
37	chr4:107209600-107217800	Strong transcription	Primary T helper cells PMA-I stimulated	--
38	chr4:107211000-107217800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr4:107211000-107219000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:107211000-107226200	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr4:107211400-107218000	Strong transcription	Liver	Liver
42	chr4:107211600-107216400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr4:107211600-107216400	Strong transcription	Adipose Nuclei	Adipose
44	chr4:107211600-107217400	Strong transcription	Placenta	Placenta
45	chr4:107211600-107221400	Strong transcription	Primary T cells fromperipheralblood	blood
46	chr4:107211800-107216400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:107211800-107216400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr4:107211800-107216400	Strong transcription	Duodenum Mucosa	Duodenum
49	chr4:107211800-107216400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr4:107211800-107216400	Strong transcription	Fetal Intestine Large	intestine

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