Variant report

Variant	nsv881231
Chromosome Location	chr4:187136307-187157458
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187148465-187148703	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:187137805-187137957	K562	blood:	n/a	n/a
3	CEBPB	chr4:187156190-187156343	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr4:187136984-187137184	HepG2	liver:	n/a	chr4:187137149-187137160 chr4:187136987-187137000
5	CEBPB	chr4:187152903-187153108	HepG2	liver:	n/a	chr4:187153043-187153052 chr4:187153043-187153052 chr4:187153041-187153052 chr4:187153043-187153052 chr4:187153041-187153054 chr4:187153042-187153053 chr4:187153043-187153052
6	CEBPB	chr4:187143782-187143991	H1-hESC	embryonic stem cell:	n/a	chr4:187143836-187143847
7	CEBPB	chr4:187137024-187137222	K562	blood:	n/a	chr4:187137149-187137160
8	CEBPB	chr4:187152925-187153145	K562	blood:	n/a	chr4:187153043-187153052 chr4:187153043-187153052 chr4:187153041-187153052 chr4:187153043-187153052 chr4:187153041-187153054 chr4:187153042-187153053 chr4:187153043-187153052
9	CEBPB	chr4:187152993-187153115	IMR90	lung:	n/a	chr4:187153043-187153052 chr4:187153043-187153052 chr4:187153041-187153052 chr4:187153043-187153052 chr4:187153041-187153054 chr4:187153042-187153053 chr4:187153043-187153052
10	CEBPB	chr4:187136509-187136687	K562	blood:	n/a	chr4:187136650-187136663
11	CEBPB	chr4:187153022-187153058	A549	lung:	n/a	chr4:187153043-187153052 chr4:187153043-187153052 chr4:187153041-187153052 chr4:187153043-187153052 chr4:187153041-187153054 chr4:187153042-187153053 chr4:187153043-187153052
12	CEBPB	chr4:187143700-187143985	IMR90	lung:	n/a	chr4:187143836-187143847
13	CEBPB	chr4:187157320-187157520	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:187143670-187144009	HepG2	liver:	n/a	chr4:187143836-187143847
15	CEBPB	chr4:187143815-187143937	A549	lung:	n/a	chr4:187143836-187143847
16	CTCF	chr4:187139420-187139570	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr4:187147700-187147850	GM12872	blood:	n/a	n/a
18	CTCF	chr4:187139340-187139490	HMEC	breast:	n/a	n/a
19	CTCF	chr4:187139280-187139430	HCT-116	colon:	n/a	n/a
20	CTCF	chr4:187149740-187149890	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr4:187154098-187154197	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr4:187139300-187139450	BE2_C	brain:	n/a	n/a
23	CTCF	chr4:187149440-187149590	NHLF	lung:	n/a	n/a
24	CTCF	chr4:187149809-187149896	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr4:187147840-187147990	GM12867	blood:	n/a	n/a
26	CTCF	chr4:187149760-187149910	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr4:187139280-187139430	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr4:187149820-187149970	HCFaa	heart:	n/a	n/a
29	CTCF	chr4:187154293-187154338	LNCaP	prostate:	n/a	n/a
30	CTCF	chr4:187148340-187148490	GM12869	blood:	n/a	n/a
31	CTCF	chr4:187139360-187139510	HMF	breast:	n/a	n/a
32	CTCF	chr4:187149780-187149930	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr4:187139260-187139410	NHEK	skin:	n/a	n/a
34	CTCF	chr4:187149840-187149990	RPTEC	kidney:	n/a	n/a
35	CTCF	chr4:187145200-187145350	GM12867	blood:	n/a	n/a
36	CTCF	chr4:187139400-187139550	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:187149680-187149830	HPF	lung:	n/a	n/a
38	CTCF	chr4:187139340-187139490	SK-N-SH_RA	brain:	n/a	n/a
39	E2F4	chr4:187136735-187136915	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr4:187148888-187149203	MCF10A-Er-Src	breast:	n/a	n/a
41	EP300	chr4:187137124-187138669	SK-N-SH	brain:	n/a	chr4:187137146-187137160 chr4:187138605-187138614 chr4:187138483-187138497
42	EP300	chr4:187148360-187148797	HepG2	liver:	n/a	n/a
43	EP300	chr4:187137853-187138232	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr4:187142070-187142074	K562	blood:	n/a	n/a
45	EP300	chr4:187137771-187138244	SK-N-SH_RA	brain:	n/a	n/a
46	FOXA1	chr4:187148417-187148806	HepG2	liver:	n/a	chr4:187148623-187148638
47	FOXA1	chr4:187142846-187143152	HepG2	liver:	n/a	n/a
48	FOXA1	chr4:187148354-187148928	HepG2	liver:	n/a	chr4:187148623-187148638
49	FOXA1	chr4:187148464-187148742	T-47D	breast:	n/a	chr4:187148623-187148638
50	FOXA1	chr4:187148384-187148762	HepG2	liver:	n/a	chr4:187148623-187148638

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187148009-187148059	NT2-D1	testis:	n/a
2	chr4:187148009-187148059	NT2-D1	testis:	n/a
3	chr4:187148430-187148480	A549	lung:	n/a
4	chr4:187148563-187148613	AoSMC	blood vessel:	n/a
5	chr4:187148688-187148738	AG09309	skin:	n/a
6	chr4:187148563-187148613	PrEC	prostate:	n/a
7	chr4:187148688-187148738	AG10803	skin:	n/a
8	chr4:187148316-187148366	IMR90	lung:	fetal
9	chr4:187148009-187148059	AoSMC	blood vessel:	n/a
10	chr4:187148316-187148366	SK-N-SH_RA	brain:	n/a
11	chr4:187148430-187148480	Caco-2	colon:	n/a
12	chr4:187148688-187148738	SK-N-SH_RA	brain:	n/a
13	chr4:187148563-187148613	SK-N-MC	brain:	n/a
14	chr4:187148688-187148738	PrEC	prostate:	n/a
15	chr4:187148316-187148366	ProgFib	skin:	n/a
16	chr4:187148316-187148366	PANC-1	pancreas:	n/a
17	chr4:187148430-187148480	BJ	skin:	n/a
18	chr4:187148688-187148738	HMEC	breast:	n/a
19	chr4:187148430-187148480	BE2_C	brain:	n/a
20	chr4:187148430-187148480	HCF	heart:	n/a
21	chr4:187148009-187148059	AG04450	lung:	fetal
22	chr4:187148688-187148738	NT2-D1	testis:	n/a
23	chr4:187148009-187148059	GM12878	blood:	n/a
24	chr4:187148563-187148613	AG09309	skin:	n/a
25	chr4:187148009-187148059	AG09309	skin:	n/a
26	chr4:187148688-187148738	H1-hESC	embryonic stem cell:	embryo
27	chr4:187148316-187148366	HEK293	kidney:	embryo
28	chr4:187148430-187148480	SK-N-SH	brain:	n/a
29	chr4:187148316-187148366	NHDF-neo	bronchial:	n/a
30	chr4:187148316-187148366	Caco-2	colon:	n/a
31	chr4:187148563-187148613	NB4	blood:	n/a
32	chr4:187148563-187148613	HPAEpiC	pulmonary alveolar:	n/a
33	chr4:187148009-187148059	ProgFib	skin:	n/a
34	chr4:187148430-187148480	NHDF-neo	bronchial:	n/a
35	chr4:187148688-187148738	PANC-1	pancreas:	n/a
36	chr4:187148316-187148366	GM12878	blood:	n/a
37	chr4:187148688-187148738	LNCaP	prostate:	n/a
38	chr4:187148430-187148480	ProgFib	skin:	n/a
39	chr4:187148009-187148059	PANC-1	pancreas:	n/a
40	chr4:187148316-187148366	HRPEpiC	eye:	n/a
41	chr4:187148688-187148738	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:187148316-187148366	HRCEpiC	kidney:	n/a
43	chr4:187148688-187148738	HUVEC	blood vessel:	n/a
44	chr4:187148316-187148366	NHBE	bronchial:	n/a
45	chr4:187148563-187148613	GM06990	blood:	n/a
46	chr4:187148430-187148480	GM12878	blood:	n/a
47	chr4:187148563-187148613	NHBE	bronchial:	n/a
48	chr4:187148563-187148613	CMK	blood:	n/a
49	chr4:187148316-187148366	HCPEpiC	choroid plexus:	n/a
50	chr4:187148688-187148738	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:187150164..187152191-chr4:187152887..187155596,2	K562	blood:
2	chr4:187150164..187152191-chr4:187152887..187155596,2	K562	blood:
3	chr4:187128886..187131532-chr4:187133645..187136600,2	K562	blood:
4	chr4:187143055..187145709-chr4:187150430..187152573,2	K562	blood:
5	chr4:187143055..187145709-chr4:187150430..187152573,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP4V2-1	chr4:187137130-187137268	XLOC_003821
2	lnc-CYP4V2-1	chr4:187137432-187137707	XLOC_003821

Variant related genes	Relation type
KLKB1	TF binding region
KLKB1	CpG island
ENSG00000164344	chromatin interactions

Extended variants
information (count: 830 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:830 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4862666	chr4:187136307-187136308	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs78879515	chr4:187136319-187136320	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs564751330	chr4:187136341-187136342	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546416655	chr4:187136356-187136357	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370747872	chr4:187136360-187136361	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs200208661	chr4:187136400-187136401	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532141841	chr4:187136415-187136416	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs4862667	chr4:187136416-187136417	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs4862668	chr4:187136443-187136444	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs539455157	chr4:187136454-187136455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559273362	chr4:187136463-187136464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370987330	chr4:187136503-187136504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs10533093	chr4:187136512-187136513	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113042142	chr4:187136515-187136516	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113435394	chr4:187136519-187136520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs200806549	chr4:187136531-187136532	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs62348768	chr4:187136535-187136536	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs62348769	chr4:187136553-187136554	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371609059	chr4:187136554-187136555	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113639595	chr4:187136559-187136560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs62348770	chr4:187136569-187136570	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs367562491	chr4:187136570-187136571	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs11267771	chr4:187136573-187136574	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368782274	chr4:187136598-187136599	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200963372	chr4:187136603-187136604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78778893	chr4:187136620-187136621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78334597	chr4:187136621-187136622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12642666	chr4:187136628-187136629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28398034	chr4:187136656-187136657	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs188737282	chr4:187136715-187136716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563781824	chr4:187136731-187136732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs3775297	chr4:187136735-187136736	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs539989457	chr4:187136737-187136738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs28668247	chr4:187136749-187136750	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs143023276	chr4:187136788-187136789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181675776	chr4:187136789-187136790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187076310	chr4:187136791-187136792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576978068	chr4:187136829-187136830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146062065	chr4:187136840-187136841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs28386792	chr4:187136882-187136883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs559974421	chr4:187136883-187136884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138786409	chr4:187136885-187136886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545584528	chr4:187136911-187136912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535281685	chr4:187136954-187136955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562638885	chr4:187137003-187137004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547303373	chr4:187137035-187137036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115556770	chr4:187137059-187137060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548240847	chr4:187137069-187137070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567981878	chr4:187137113-187137114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527243739	chr4:187137118-187137119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187117600-187140600	Weak transcription	Aorta	Aorta
2	chr4:187125800-187149200	Weak transcription	Colon Smooth Muscle	Colon
3	chr4:187130400-187144200	Weak transcription	Esophagus	oesophagus
4	chr4:187130600-187149400	Weak transcription	Gastric	stomach
5	chr4:187130800-187137600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:187130800-187145000	Weak transcription	Pancreas	Pancrea
7	chr4:187131000-187138200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr4:187131000-187139800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr4:187131200-187137800	Weak transcription	Fetal Lung	lung
10	chr4:187131400-187139000	Weak transcription	Small Intestine	intestine
11	chr4:187131600-187138000	Weak transcription	Brain Anterior Caudate	brain
12	chr4:187131600-187146000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr4:187131600-187148400	Weak transcription	Fetal Kidney	kidney
14	chr4:187131800-187136600	Weak transcription	Fetal Brain Female	brain
15	chr4:187131800-187137600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr4:187131800-187137800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:187131800-187137800	Weak transcription	Adipose Nuclei	Adipose
18	chr4:187131800-187138000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:187131800-187138400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr4:187131800-187138800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr4:187131800-187149000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr4:187131800-187159000	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr4:187131800-187181600	Weak transcription	Brain Hippocampus Middle	brain
24	chr4:187132400-187137200	Weak transcription	Brain Substantia Nigra	brain
25	chr4:187132600-187139200	Weak transcription	Fetal Intestine Small	intestine
26	chr4:187132800-187137200	Weak transcription	Ovary	ovary
27	chr4:187134000-187138400	Weak transcription	Fetal Intestine Large	intestine
28	chr4:187134000-187139800	Weak transcription	Liver	Liver
29	chr4:187134000-187149000	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr4:187134400-187138800	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr4:187137600-187137800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:187137600-187138000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr4:187137600-187138400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr4:187137800-187138000	Enhancers	Adipose Nuclei	Adipose
35	chr4:187137800-187138000	Enhancers	Fetal Brain Female	brain
36	chr4:187137800-187138200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr4:187137800-187138400	Enhancers	Fetal Lung	lung
38	chr4:187138000-187138200	Active TSS	Brain Anterior Caudate	brain
39	chr4:187138000-187138800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr4:187138200-187138400	Enhancers	Muscle Satellite Cultured Cells	--
41	chr4:187138200-187138600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:187138400-187138600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr4:187138400-187138800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr4:187138400-187139000	Weak transcription	Fetal Lung	lung
45	chr4:187138400-187139400	Enhancers	Fetal Intestine Large	intestine
46	chr4:187138800-187139400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:187139000-187139200	Enhancers	Fetal Lung	lung
48	chr4:187139000-187139200	Enhancers	Small Intestine	intestine
49	chr4:187139200-187139400	Enhancers	Fetal Intestine Small	intestine
50	chr4:187139800-187140200	Enhancers	Liver	Liver

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