Variant report

Variant	nsv880329
Chromosome Location	chr4:188432233-188492766
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	CEBPB	chr4:188440459-188440698	IMR90	lung:	n/a	n/a
2	CEBPB	chr4:188492567-188492769	HepG2	liver:	n/a	chr4:188492666-188492677
3	CEBPB	chr4:188492564-188492757	K562	blood:	n/a	chr4:188492666-188492677
4	CEBPB	chr4:188474103-188474183	K562	blood:	n/a	n/a
5	CEBPB	chr4:188440289-188440620	HepG2	liver:	n/a	n/a
6	CEBPB	chr4:188479534-188479869	IMR90	lung:	n/a	n/a
7	CTCF	chr4:188442915-188443011	Kidney_OC	kidney:	n/a	n/a
8	CTCF	chr4:188451774-188451781	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr4:188475140-188475290	AG04450	lung:	n/a	n/a
10	CTCF	chr4:188443124-188443168	Medullo	brain:	n/a	n/a
11	CTCF	chr4:188458895-188458970	Fibrobl	skin:	n/a	n/a
12	CTCF	chr4:188441212-188441256	LNCaP	prostate:	n/a	n/a
13	CTCF	chr4:188451786-188451820	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr4:188476228-188476262	GM20000	blood:	n/a	n/a
15	CTCF	chr4:188458880-188459030	HVMF	connective:	n/a	n/a
16	CTCF	chr4:188458860-188459010	BJ	skin:	n/a	n/a
17	E2F4	chr4:188438067-188438123	MCF10A-Er-Src	breast:	n/a	n/a
18	EP300	chr4:188437667-188437686	GM12878	blood:	n/a	n/a
19	FOS	chr4:188476455-188476656	MCF10A-Er-Src	breast:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554
20	FOS	chr4:188479536-188479871	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
21	FOS	chr4:188479537-188479903	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
22	FOS	chr4:188476506-188476656	MCF10A-Er-Src	breast:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554
23	FOS	chr4:188479576-188479879	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
24	FOS	chr4:188479536-188479878	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
25	FOSL2	chr4:188476250-188476756	A549	lung:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554
26	FOXA1	chr4:188482506-188482661	T-47D	breast:	n/a	n/a
27	FOXA2	chr4:188476383-188476791	A549	lung:	n/a	n/a
28	GATA3	chr4:188476912-188477168	SH-SY5Y	brain:	n/a	n/a
29	JUN	chr4:188432774-188433012	K562	blood:	n/a	n/a
30	JUN	chr4:188475494-188475577	K562	blood:	n/a	n/a
31	JUN	chr4:188484429-188484629	K562	blood:	n/a	n/a
32	JUND	chr4:188452451-188452524	H1-hESC	embryonic stem cell:	n/a	n/a
33	JUND	chr4:188476398-188476661	HepG2	liver:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554 chr4:188476544-188476555
34	MAFF	chr4:188456784-188456861	HepG2	liver:	n/a	n/a
35	MAFK	chr4:188456684-188456898	HepG2	liver:	n/a	chr4:188456792-188456812 chr4:188456792-188456803
36	MAX	chr4:188479935-188480096	NB4	blood:	n/a	n/a
37	MAZ	chr4:188471769-188471776	HepG2	liver:	n/a	n/a
38	POLR2A	chr4:188472127-188472271	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr4:188437385-188437763	H1-neurons	neurons:	n/a	n/a
40	POLR2A	chr4:188483463-188483897	H1-neurons	neurons:	n/a	n/a
41	POLR2A	chr4:188447063-188447242	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr4:188437404-188437793	H1-neurons	neurons:	n/a	n/a
43	POLR2A	chr4:188479216-188479242	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr4:188487997-188488170	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr4:188475437-188475513	A549	lung:	n/a	n/a
46	POLR2A	chr4:188438742-188438880	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr4:188464133-188464254	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr4:188487205-188487339	ProgFib	skin:	n/a	n/a
49	POLR2A	chr4:188476959-188477058	ProgFib	skin:	n/a	n/a
50	POLR2A	chr4:188483430-188483871	H1-neurons	neurons:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188462685-188462735	HL-60	blood:	n/a
2	chr4:188462685-188462735	HRCEpiC	kidney:	n/a
3	chr4:188462685-188462735	AoSMC	blood vessel:	n/a
4	chr4:188462685-188462735	BE2_C	brain:	n/a
5	chr4:188462685-188462735	HAEpiC	amniotic membrane:	n/a
6	chr4:188462685-188462735	K562	blood:	n/a
7	chr4:188462685-188462735	HIPEpiC	eye:	n/a
8	chr4:188462685-188462735	BJ	skin:	n/a
9	chr4:188462685-188462735	SK-N-MC	brain:	n/a
10	chr4:188462685-188462735	IMR90	lung:	fetal
11	chr4:188462685-188462735	SK-N-SH_RA	brain:	n/a
12	chr4:188462685-188462735	ECC-1	luminal epithelium:	n/a
13	chr4:188462685-188462735	AG04449	skin:	fetal
14	chr4:188462685-188462735	HMEC	breast:	n/a
15	chr4:188462685-188462735	HPAEpiC	pulmonary alveolar:	n/a
16	chr4:188462685-188462735	A549	lung:	n/a
17	chr4:188462685-188462735	HepG2	liver:	n/a
18	chr4:188462685-188462735	MCF10A-Er-Src	breast:	n/a
19	chr4:188462685-188462735	GM12878	blood:	n/a
20	chr4:188462685-188462735	H1-hESC	embryonic stem cell:	embryo
21	chr4:188462685-188462735	CMK	blood:	n/a
22	chr4:188462685-188462735	GM06990	blood:	n/a
23	chr4:188462685-188462735	HEK293	kidney:	embryo
24	chr4:188462685-188462735	SK-N-SH	brain:	n/a
25	chr4:188462685-188462735	PrEC	prostate:	n/a
26	chr4:188462685-188462735	PFSK-1	brain:	n/a
27	chr4:188462685-188462735	Jurkat	blood:	n/a
28	chr4:188462685-188462735	NHDF-neo	bronchial:	n/a
29	chr4:188462685-188462735	HEEpiC	esophagus:	n/a
30	chr4:188462685-188462735	NT2-D1	testis:	n/a
31	chr4:188462685-188462735	GM12891	blood:	n/a
32	chr4:188462685-188462735	GM12892	blood:	n/a
33	chr4:188462685-188462735	RPTEC	kidney:	n/a
34	chr4:188462685-188462735	SKMC	muscle:	n/a
35	chr4:188462685-188462735	HNPCEpiC	eye:	n/a
36	chr4:188462685-188462735	HUVEC	blood vessel:	n/a
37	chr4:188462685-188462735	HCPEpiC	choroid plexus:	n/a
38	chr4:188462685-188462735	GM19239	blood:	n/a
39	chr4:188462685-188462735	NH-A	brain:	n/a
40	chr4:188462685-188462735	HCF	heart:	n/a
41	chr4:188462685-188462735	Hela-S3	cervix:	n/a
42	chr4:188462685-188462735	AG10803	skin:	n/a
43	chr4:188462685-188462735	HCT-116	colon:	n/a
44	chr4:188462685-188462735	PANC-1	pancreas:	n/a
45	chr4:188462685-188462735	ovcar-3	ovarian:	n/a
46	chr4:188462685-188462735	ProgFib	skin:	n/a
47	chr4:188462685-188462735	T-47D	breast:	n/a
48	chr4:188462685-188462735	U87	brain:	n/a
49	chr4:188462685-188462735	AG09319	gingival:	n/a
50	chr4:188462685-188462735	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML2-4	chr4:188476930-188477103	ENSG00000250590
2	lnc-TRIML2-4	chr4:188454036-188454357	ENSG00000250590
3	lnc-TRIML2-4	chr4:188476930-188477058	ENSG00000250590
4	lnc-TRIML2-4	chr4:188476215-188476298	ENSG00000250590
5	lnc-TRIML2-4	chr4:188454033-188454357	NR_110436
6	lnc-TRIML2-4	chr4:188479231-188479418	ENSG00000250590
7	lnc-TRIML2-4	chr4:188478901-188479074	ENSG00000250590
8	lnc-TRIML2-4	chr4:188454032-188454357	ENSG00000250590
9	lnc-TRIML2-4	chr4:188454032-188454357	ENSG00000250590
10	lnc-TRIML2-5	chr4:188437307-188437878	XLOC_004219
11	lnc-TRIML2-5	chr4:188438236-188438362	XLOC_004219
12	lnc-TRIML2-4	chr4:188477065-188477112	ENSG00000250590
13	lnc-TRIML2-4	chr4:188479391-188479418	NONHSAT099704

Variant related genes	Relation type
ENSG00000251490	TF binding region
ENSG00000250590	TF binding region
ENSG00000251490	CpG island
ENSG00000250590	CpG island
ANP32E	miRNA target sites
ANTXR1	miRNA target sites

Extended variants
information (count: 913 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:913 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11929993	chr4:188432233-188432234	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186677192	chr4:188432293-188432294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569789233	chr4:188432325-188432326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149186076	chr4:188432357-188432358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556668235	chr4:188432394-188432395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115209004	chr4:188432403-188432404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572392695	chr4:188432425-188432426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11930080	chr4:188432452-188432453	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs558451359	chr4:188432453-188432454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs578253829	chr4:188432496-188432497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35595460	chr4:188432649-188432650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540265519	chr4:188432724-188432725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544002963	chr4:188432753-188432754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191143729	chr4:188432794-188432795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573666027	chr4:188432862-188432863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542399039	chr4:188432863-188432864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559299008	chr4:188432876-188432877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528029320	chr4:188432884-188432885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374174010	chr4:188433003-188433004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183710183	chr4:188433018-188433019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371446041	chr4:188433020-188433021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373491833	chr4:188433092-188433093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368344778	chr4:188433107-188433108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564806543	chr4:188433192-188433193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs530737344	chr4:188433203-188433204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550343830	chr4:188433210-188433211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567386960	chr4:188433334-188433335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535938024	chr4:188433343-188433344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549159355	chr4:188433366-188433367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531770650	chr4:188437364-188437365	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs75073594	chr4:188437371-188437372	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs556385521	chr4:188437385-188437386	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs1966607	chr4:188437431-188437432	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs986375	chr4:188437462-188437463	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs555010716	chr4:188437466-188437467	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs574855511	chr4:188437467-188437468	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs540211313	chr4:188437468-188437469	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs185789118	chr4:188437556-188437557	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs532656223	chr4:188437590-188437591	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs111944461	chr4:188437649-188437650	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs79709208	chr4:188437670-188437671	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs538722329	chr4:188437671-188437672	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs79915610	chr4:188437685-188437686	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs531893952	chr4:188437780-188437781	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs548513117	chr4:188437789-188437790	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs568120910	chr4:188437801-188437802	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs57654912	chr4:188437850-188437851	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs78443773	chr4:188438251-188438252	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs545803267	chr4:188438317-188438318	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs74760893	chr4:188438339-188438340	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
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
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
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Autism	20808228	CNVD
Cognitive impairment	21505072	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188432000-188433000	Enhancers	Adipose Nuclei	Adipose
2	chr4:188433000-188433400	Enhancers	A549	lung
3	chr4:188451200-188451800	Enhancers	Fetal Muscle Trunk	muscle
4	chr4:188454000-188454200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr4:188454200-188455200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr4:188454600-188456200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr4:188455000-188455800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:188455000-188455800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr4:188455000-188456200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr4:188455200-188456000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr4:188462000-188462600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr4:188462000-188462800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr4:188462200-188462600	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr4:188462200-188462600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:188462200-188463600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr4:188462400-188462600	Enhancers	HSMM	muscle
17	chr4:188462400-188462600	Enhancers	NHDF-Ad	bronchial
18	chr4:188462400-188462800	Enhancers	HSMMtube	muscle
19	chr4:188462600-188463000	Flanking Active TSS	HSMM	muscle
20	chr4:188462600-188463000	Flanking Active TSS	NHDF-Ad	bronchial
21	chr4:188462600-188463600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:188462800-188463000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:188462800-188463200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:188462800-188463200	Flanking Active TSS	HSMMtube	muscle
25	chr4:188462800-188463600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr4:188463000-188463600	Enhancers	HSMM	muscle
27	chr4:188463000-188463600	Enhancers	NHDF-Ad	bronchial
28	chr4:188463200-188463600	Enhancers	HSMMtube	muscle
29	chr4:188463200-188468600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr4:188463600-188465600	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr4:188463600-188465600	Weak transcription	HSMM	muscle
32	chr4:188463600-188465600	Weak transcription	HSMMtube	muscle
33	chr4:188463600-188465800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:188463600-188470600	Weak transcription	NHDF-Ad	bronchial
35	chr4:188465400-188465600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:188465600-188465800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr4:188465600-188465800	Enhancers	HSMM	muscle
38	chr4:188465600-188466000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:188465600-188466000	Enhancers	HSMMtube	muscle
40	chr4:188465600-188466200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr4:188465600-188466200	Enhancers	HMEC	breast
42	chr4:188465600-188466200	Enhancers	NHEK	skin
43	chr4:188465800-188466200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr4:188465800-188466200	Weak transcription	HSMM	muscle
45	chr4:188465800-188468600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:188466000-188466200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:188466000-188468400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr4:188466200-188466400	Enhancers	HSMM	muscle
49	chr4:188466200-188468200	Weak transcription	HMEC	breast
50	chr4:188466200-188468400	Weak transcription	Muscle Satellite Cultured Cells	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links