Variant report

Variant	nsv879925
Chromosome Location	chr4:128586241-128665981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:574)
CpG islands
(count:977)
Chromatin interactive
region (count:20)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:574 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:128653832-128654129	K562	blood:	n/a	n/a
2	ARID3A	chr4:128658272-128658704	K562	blood:	n/a	n/a
3	ATF1	chr4:128653837-128654173	K562	blood:	n/a	n/a
4	ATF2	chr4:128619738-128620345	GM12878	blood:	n/a	n/a
5	ATF2	chr4:128619722-128620294	GM12878	blood:	n/a	n/a
6	ATF3	chr4:128651355-128651575	K562	blood:	n/a	chr4:128651557-128651566
7	ATF3	chr4:128619938-128620425	HCT-116	colon:	n/a	n/a
8	BATF	chr4:128619897-128620328	GM12878	blood:	n/a	n/a
9	BATF	chr4:128619916-128620358	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:128619778-128620281	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:128619905-128620297	GM12878	blood:	n/a	n/a
12	BCL3	chr4:128619800-128620319	GM12878	blood:	n/a	n/a
13	BCLAF1	chr4:128619855-128620353	GM12878	blood:	n/a	n/a
14	BCLAF1	chr4:128619765-128620391	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:128608804-128608829	K562	blood:	n/a	n/a
16	BHLHE40	chr4:128619830-128620287	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:128651381-128651572	K562	blood:	n/a	n/a
18	CBX3	chr4:128619927-128620413	HCT-116	colon:	n/a	n/a
19	CBX3	chr4:128663246-128663643	K562	blood:	n/a	n/a
20	CBX3	chr4:128619911-128620372	HCT-116	colon:	n/a	n/a
21	CBX3	chr4:128629996-128630593	HCT-116	colon:	n/a	n/a
22	CBX3	chr4:128629998-128630740	HCT-116	colon:	n/a	n/a
23	CEBPB	chr4:128619959-128620538	A549	lung:	n/a	chr4:128620151-128620164
24	CEBPB	chr4:128620076-128620434	A549	lung:	n/a	chr4:128620151-128620164
25	CEBPB	chr4:128656194-128656400	A549	lung:	n/a	n/a
26	CEBPB	chr4:128619883-128620426	GM12878	blood:	n/a	chr4:128620151-128620164
27	CEBPB	chr4:128620047-128620457	ECC-1	luminal epithelium:	n/a	chr4:128620151-128620164
28	CEBPB	chr4:128619919-128620521	ECC-1	luminal epithelium:	n/a	chr4:128620151-128620164
29	CEBPB	chr4:128630125-128630810	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:128620014-128620810	IMR90	lung:	n/a	chr4:128620151-128620164
31	CEBPB	chr4:128607797-128608186	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr4:128620165-128620873	K562	blood:	n/a	n/a
33	CEBPB	chr4:128606458-128606811	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:128594282-128594498	K562	blood:	n/a	n/a
35	CEBPB	chr4:128658476-128658755	K562	blood:	n/a	n/a
36	CEBPB	chr4:128619793-128620638	HCT-116	colon:	n/a	chr4:128620151-128620164
37	CEBPB	chr4:128620161-128620418	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr4:128619947-128620777	Hela-S3	cervix:	n/a	chr4:128620151-128620164
39	CEBPB	chr4:128620085-128620432	A549	lung:	n/a	chr4:128620151-128620164
40	CEBPB	chr4:128606467-128606803	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:128619803-128620583	HCT-116	colon:	n/a	chr4:128620151-128620164
42	CHD2	chr4:128630159-128630416	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr4:128619925-128620334	GM12878	blood:	n/a	n/a
44	CREB1	chr4:128619889-128620450	GM12878	blood:	n/a	n/a
45	CREB1	chr4:128619888-128620393	GM12878	blood:	n/a	n/a
46	CTCF	chr4:128653794-128654148	ECC-1	luminal epithelium:	n/a	n/a
47	CTCF	chr4:128653920-128654070	AG09319	gingival:	n/a	n/a
48	CTCF	chr4:128653860-128654010	GM12872	blood:	n/a	n/a
49	CTCF	chr4:128606440-128606590	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr4:128606690-128606721	GM10266	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:128651500-128651550	SAEC	small airway:	n/a
2	chr4:128651500-128651550	SAEC	small airway:	n/a
3	chr4:128651526-128651576	PANC-1	pancreas:	n/a
4	chr4:128647957-128648007	HCPEpiC	choroid plexus:	n/a
5	chr4:128647957-128648007	GM06990	blood:	n/a
6	chr4:128651532-128651582	AG04449	skin:	fetal
7	chr4:128651543-128651593	HRE	kidney:	n/a
8	chr4:128651564-128651614	IMR90	lung:	fetal
9	chr4:128651707-128651757	SK-N-SH_RA	brain:	n/a
10	chr4:128637608-128637658	HRCEpiC	kidney:	n/a
11	chr4:128651206-128651256	PrEC	prostate:	n/a
12	chr4:128651221-128651271	IMR90	lung:	fetal
13	chr4:128650393-128650443	Jurkat	blood:	n/a
14	chr4:128651221-128651271	BE2_C	brain:	n/a
15	chr4:128647957-128648007	NHDF-neo	bronchial:	n/a
16	chr4:128637608-128637658	HCF	heart:	n/a
17	chr4:128651206-128651256	H1-hESC	embryonic stem cell:	embryo
18	chr4:128651543-128651593	NH-A	brain:	n/a
19	chr4:128651500-128651550	NT2-D1	testis:	n/a
20	chr4:128651543-128651593	HCF	heart:	n/a
21	chr4:128651526-128651576	T-47D	breast:	n/a
22	chr4:128651518-128651568	NHBE	bronchial:	n/a
23	chr4:128651564-128651614	GM12891	blood:	n/a
24	chr4:128650828-128650878	NH-A	brain:	n/a
25	chr4:128651936-128651986	SK-N-SH_RA	brain:	n/a
26	chr4:128650393-128650443	ovcar-3	ovarian:	n/a
27	chr4:128637608-128637658	HIPEpiC	eye:	n/a
28	chr4:128651564-128651614	GM12878	blood:	n/a
29	chr4:128651500-128651550	RPTEC	kidney:	n/a
30	chr4:128651936-128651986	GM12891	blood:	n/a
31	chr4:128630266-128630316	LNCaP	prostate:	n/a
32	chr4:128651543-128651593	K562	blood:	n/a
33	chr4:128654094-128654144	NH-A	brain:	n/a
34	chr4:128651206-128651256	U87	brain:	n/a
35	chr4:128651518-128651568	GM12891	blood:	n/a
36	chr4:128651206-128651256	SK-N-MC	brain:	n/a
37	chr4:128654094-128654144	CMK	blood:	n/a
38	chr4:128651206-128651256	GM12878	blood:	n/a
39	chr4:128637608-128637658	GM06990	blood:	n/a
40	chr4:128651526-128651576	HIPEpiC	eye:	n/a
41	chr4:128651564-128651614	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:128651936-128651986	BJ	skin:	n/a
43	chr4:128651221-128651271	ECC-1	luminal epithelium:	n/a
44	chr4:128651221-128651271	AoSMC	blood vessel:	n/a
45	chr4:128654094-128654144	AG04450	lung:	fetal
46	chr4:128651532-128651582	HCF	heart:	n/a
47	chr4:128651532-128651582	GM12891	blood:	n/a
48	chr4:128651936-128651986	HepG2	liver:	n/a
49	chr4:128651221-128651271	H1-hESC	embryonic stem cell:	embryo
50	chr4:128650393-128650443	SKMC	muscle:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:128526494..128527032-chr4:128651880..128652572,2	MCF-7	breast:
2	chr4:128552432..128554682-chr4:128586410..128589274,2	K562	blood:
3	chr4:128651856..128654321-chr4:128662379..128665043,2	K562	blood:
4	chr4:128657662..128659612-chr4:128665725..128667631,2	K562	blood:
5	chr4:128590271..128592310-chr4:128594273..128597099,2	K562	blood:
6	chr4:128609167..128611494-chr4:128612179..128614803,2	K562	blood:
7	chr4:128657662..128659612-chr4:128665725..128667631,2	K562	blood:
8	chr4:128587279..128589400-chr4:128808635..128811454,2	K562	blood:
9	chr4:128525423..128527600-chr4:128653005..128654534,14	MCF-7	breast:
10	chr4:128530677..128531222-chr4:128653500..128654487,2	K562	blood:
11	chr4:128620470..128623327-chr4:128629151..128632115,2	K562	blood:
12	chr4:128581030..128583943-chr4:128656313..128658380,2	K562	blood:
13	chr4:128620470..128623327-chr4:128629151..128632115,2	K562	blood:
14	chr4:128651856..128654321-chr4:128662379..128665043,2	K562	blood:
15	chr4:128609167..128611494-chr4:128612179..128614803,2	K562	blood:
16	chr4:128653835..128656903-chr4:128701461..128704105,3	K562	blood:
17	chr4:128593863..128595593-chr4:128981619..128984198,2	K562	blood:
18	chr4:128580018..128583364-chr4:128583861..128587537,3	K562	blood:
19	chr4:128525866..128527137-chr4:128653218..128654151,10	K562	blood:
20	chr4:128552219..128554682-chr4:128585825..128589274,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC25A31-3	chr4:128605564-128605641	NONHSAT098240
2	lnc-SLC25A31-3	chr4:128595309-128595368	NONHSAT098240
3	lnc-SLC25A31-3	chr4:128606597-128607105	NONHSAT098240

No data

Variant related genes	Relation type
SLC25A31	TF binding region
INTU	TF binding region
SLC25A31	CpG island
INTU	CpG island
ENSG00000164066	chromatin interactions
ENSG00000138709	chromatin interactions
ENSG00000164070	chromatin interactions

Extended variants
information (count: 2602 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2602 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13126673	chr4:128586241-128586242	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374524407	chr4:128586271-128586272	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551729215	chr4:128586298-128586299	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181527773	chr4:128586300-128586301	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs544927903	chr4:128586397-128586398	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs187058052	chr4:128586485-128586486	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs576473792	chr4:128586519-128586520	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs571141426	chr4:128586536-128586537	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538141825	chr4:128586542-128586543	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562095512	chr4:128586551-128586552	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs529393417	chr4:128586569-128586570	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541551830	chr4:128586597-128586598	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs190758668	chr4:128586619-128586620	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs149572882	chr4:128586622-128586623	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10034548	chr4:128586653-128586654	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs564024265	chr4:128586664-128586665	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs530395539	chr4:128586710-128586711	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548548183	chr4:128586717-128586718	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567444305	chr4:128586794-128586795	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs146087076	chr4:128586834-128586835	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs546678052	chr4:128586852-128586853	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs536198699	chr4:128586957-128586958	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs140092321	chr4:128586984-128586985	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs183325631	chr4:128587007-128587008	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs376641430	chr4:128587040-128587041	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs142111718	chr4:128587079-128587080	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs60803593	chr4:128587127-128587128	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs372018781	chr4:128587128-128587129	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs570600390	chr4:128587134-128587135	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs555791622	chr4:128587159-128587160	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558164324	chr4:128587215-128587216	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs146368663	chr4:128587231-128587232	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs559804971	chr4:128587293-128587294	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs148574808	chr4:128587350-128587351	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs61039595	chr4:128587359-128587360	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs73847035	chr4:128587362-128587363	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs115457791	chr4:128587363-128587364	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs151129492	chr4:128587398-128587399	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs560501213	chr4:128587414-128587415	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs139458837	chr4:128587416-128587417	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs13106965	chr4:128587436-128587437	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs13134485	chr4:128587456-128587457	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs571343063	chr4:128587462-128587463	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs73847036	chr4:128587479-128587480	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs13106988	chr4:128587506-128587507	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs186566120	chr4:128587517-128587518	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs13134704	chr4:128587524-128587525	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567286355	chr4:128587538-128587539	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs189836400	chr4:128587578-128587579	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs376947974	chr4:128587638-128587639	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
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
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
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
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128554600-128627400	Weak transcription	Pancreas	Pancrea
2	chr4:128554600-128644800	Weak transcription	Lung	lung
3	chr4:128554800-128596600	Weak transcription	Fetal Muscle Leg	muscle
4	chr4:128554800-128604400	Weak transcription	Right Ventricle	heart
5	chr4:128555000-128608800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr4:128555200-128587400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr4:128555600-128627600	Weak transcription	Brain Angular Gyrus	brain
8	chr4:128556200-128590200	Weak transcription	NH-A	brain
9	chr4:128556200-128615600	Weak transcription	Fetal Brain Male	brain
10	chr4:128562800-128597400	Weak transcription	Esophagus	oesophagus
11	chr4:128562800-128616400	Weak transcription	Aorta	Aorta
12	chr4:128563600-128614000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr4:128563600-128627400	Weak transcription	Brain Substantia Nigra	brain
14	chr4:128565400-128587600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr4:128565400-128592800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr4:128565400-128615400	Weak transcription	Colon Smooth Muscle	Colon
17	chr4:128566600-128589200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr4:128566600-128590000	Weak transcription	Fetal Kidney	kidney
19	chr4:128566600-128590000	Weak transcription	HSMM	muscle
20	chr4:128566600-128596600	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr4:128566600-128644600	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr4:128567000-128597400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr4:128567200-128614000	Weak transcription	Psoas Muscle	Psoas
24	chr4:128567400-128596800	Weak transcription	Fetal Intestine Small	intestine
25	chr4:128568400-128609600	Weak transcription	Brain Anterior Caudate	brain
26	chr4:128568600-128586800	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr4:128568600-128587600	Weak transcription	Brain Germinal Matrix	brain
28	chr4:128568600-128592000	Weak transcription	Fetal Intestine Large	intestine
29	chr4:128568600-128596000	Weak transcription	Fetal Brain Female	brain
30	chr4:128568800-128613400	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr4:128568800-128614600	Weak transcription	Brain Hippocampus Middle	brain
32	chr4:128571400-128596000	Weak transcription	Fetal Lung	lung
33	chr4:128577400-128590000	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr4:128577800-128592200	Weak transcription	A549	lung
35	chr4:128577800-128592600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr4:128578400-128589600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:128579800-128596800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:128579800-128596800	Weak transcription	Primary hematopoietic stem cells	blood
39	chr4:128580200-128586800	Weak transcription	Adipose Nuclei	Adipose
40	chr4:128580400-128587000	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr4:128580400-128607400	Weak transcription	Left Ventricle	heart
42	chr4:128581000-128586800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr4:128581000-128597000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:128581800-128586800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:128581800-128588200	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr4:128581800-128588800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr4:128581800-128594200	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr4:128581800-128608600	Weak transcription	Ovary	ovary
49	chr4:128582000-128596600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr4:128582000-128597400	Weak transcription	Fetal Stomach	stomach

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