Variant report

Variant	nsv1017623
Chromosome Location	chr4:188342873-188435238
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	BACH1	chr4:188413248-188413433	K562	blood:	n/a	chr4:188413338-188413352
2	BHLHE40	chr4:188343966-188344142	K562	blood:	n/a	n/a
3	CEBPB	chr4:188349162-188349196	H1-hESC	embryonic stem cell:	n/a	chr4:188349183-188349194
4	CEBPB	chr4:188401324-188401855	IMR90	lung:	n/a	n/a
5	CEBPB	chr4:188405573-188406437	IMR90	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
6	CEBPB	chr4:188405581-188406417	HepG2	liver:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
7	CEBPB	chr4:188406167-188406450	A549	lung:	n/a	n/a
8	CEBPB	chr4:188405582-188405932	A549	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
9	CEBPB	chr4:188405764-188405895	H1-hESC	embryonic stem cell:	n/a	chr4:188405878-188405889 chr4:188405877-188405890
10	CEBPB	chr4:188399632-188400363	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:188376676-188376735	HepG2	liver:	n/a	chr4:188376676-188376689 chr4:188376676-188376687 chr4:188376678-188376689
12	CTCF	chr4:188383305-188383331	GM19239	blood:	n/a	n/a
13	CTCF	chr4:188359021-188359098	Lung_OC	lung:	n/a	n/a
14	CTCF	chr4:188426682-188426755	LNCaP	prostate:	n/a	n/a
15	CTCF	chr4:188412728-188412816	NHEK	skin:	n/a	n/a
16	CUX1	chr4:188425013-188425025	GM12878	blood:	n/a	n/a
17	E2F4	chr4:188418016-188418170	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr4:188344570-188344645	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr4:188372133-188372215	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr4:188395046-188395246	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F6	chr4:188426476-188426590	K562	blood:	n/a	n/a
22	EP300	chr4:188413364-188413589	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chr4:188399901-188400574	T-47D	breast:	n/a	chr4:188400130-188400139
24	EP300	chr4:188413842-188413867	GM12878	blood:	n/a	n/a
25	EP300	chr4:188421092-188421565	T-47D	breast:	n/a	n/a
26	EP300	chr4:188351517-188351547	GM12878	blood:	n/a	n/a
27	EP300	chr4:188343858-188344098	K562	blood:	n/a	n/a
28	EP300	chr4:188399817-188400577	SK-N-SH	brain:	n/a	chr4:188400130-188400139
29	EP300	chr4:188401602-188401920	T-47D	breast:	n/a	n/a
30	FOS	chr4:188399962-188400312	MCF10A-Er-Src	breast:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
31	FOS	chr4:188399944-188400346	MCF10A-Er-Src	breast:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
32	FOS	chr4:188401411-188402262	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr4:188401433-188402312	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr4:188359051-188359234	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr4:188401535-188402265	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr4:188399962-188400354	MCF10A-Er-Src	breast:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
37	FOS	chr4:188401415-188402310	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr4:188399945-188400441	MCF10A-Er-Src	breast:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
39	FOS	chr4:188401061-188401145	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:188413155-188413419	MCF10A-Er-Src	breast:	n/a	chr4:188413339-188413351 chr4:188413341-188413349 chr4:188413340-188413350 chr4:188413340-188413350
41	FOSL2	chr4:188399880-188400454	SK-N-SH	brain:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
42	FOSL2	chr4:188401888-188402360	SK-N-SH	brain:	n/a	n/a
43	FOSL2	chr4:188399844-188400429	A549	lung:	n/a	chr4:188400130-188400139 chr4:188400132-188400139 chr4:188400129-188400140
44	FOXA1	chr4:188399892-188400407	T-47D	breast:	n/a	n/a
45	FOXA1	chr4:188380312-188380593	T-47D	breast:	n/a	n/a
46	FOXA1	chr4:188401582-188402085	A549	lung:	n/a	chr4:188401842-188401857
47	FOXA1	chr4:188401583-188402018	T-47D	breast:	n/a	chr4:188401842-188401857
48	FOXA1	chr4:188399903-188400446	T-47D	breast:	n/a	n/a
49	FOXA1	chr4:188414832-188415106	T-47D	breast:	n/a	n/a
50	FOXA1	chr4:188400709-188401005	T-47D	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188426506-188426556	GM06990	blood:	n/a
2	chr4:188401038-188401088	GM06990	blood:	n/a
3	chr4:188426506-188426556	GM06990	blood:	n/a
4	chr4:188401038-188401088	GM06990	blood:	n/a
5	chr4:188401038-188401088	GM12892	blood:	n/a
6	chr4:188401038-188401088	NT2-D1	testis:	n/a
7	chr4:188423066-188423116	HCM	heart:	n/a
8	chr4:188398437-188398487	AoSMC	blood vessel:	n/a
9	chr4:188391387-188391437	Hepatocyte	liver:	n/a
10	chr4:188391387-188391437	HEEpiC	esophagus:	n/a
11	chr4:188398437-188398487	BJ	skin:	n/a
12	chr4:188423066-188423116	Hepatocyte	liver:	n/a
13	chr4:188427966-188428016	HCT-116	colon:	n/a
14	chr4:188423066-188423116	PANC-1	pancreas:	n/a
15	chr4:188427966-188428016	HMEC	breast:	n/a
16	chr4:188423066-188423116	MCF10A-Er-Src	breast:	n/a
17	chr4:188426278-188426328	MCF-7	breast:	n/a
18	chr4:188398437-188398487	BE2_C	brain:	n/a
19	chr4:188426437-188426487	SK-N-SH	brain:	n/a
20	chr4:188401038-188401088	HCT-116	colon:	n/a
21	chr4:188401038-188401088	AG10803	skin:	n/a
22	chr4:188428637-188428687	AG09319	gingival:	n/a
23	chr4:188426437-188426487	HRPEpiC	eye:	n/a
24	chr4:188426278-188426328	HL-60	blood:	n/a
25	chr4:188401038-188401088	H1-hESC	embryonic stem cell:	embryo
26	chr4:188423066-188423116	HRE	kidney:	n/a
27	chr4:188401038-188401088	Jurkat	blood:	n/a
28	chr4:188427966-188428016	HCF	heart:	n/a
29	chr4:188427966-188428016	Hela-S3	cervix:	n/a
30	chr4:188423066-188423116	SK-N-SH_RA	brain:	n/a
31	chr4:188428637-188428687	HMEC	breast:	n/a
32	chr4:188391387-188391437	SK-N-MC	brain:	n/a
33	chr4:188427966-188428016	AG04450	lung:	fetal
34	chr4:188423066-188423116	AG09319	gingival:	n/a
35	chr4:188423066-188423116	AoSMC	blood vessel:	n/a
36	chr4:188423066-188423116	K562	blood:	n/a
37	chr4:188391387-188391437	ProgFib	skin:	n/a
38	chr4:188427966-188428016	CMK	blood:	n/a
39	chr4:188401038-188401088	GM12878	blood:	n/a
40	chr4:188401038-188401088	SKMC	muscle:	n/a
41	chr4:188401038-188401088	MCF10A-Er-Src	breast:	n/a
42	chr4:188428637-188428687	HEEpiC	esophagus:	n/a
43	chr4:188401038-188401088	NHDF-neo	bronchial:	n/a
44	chr4:188391387-188391437	AG09309	skin:	n/a
45	chr4:188401038-188401088	Hepatocyte	liver:	n/a
46	chr4:188426506-188426556	Caco-2	colon:	n/a
47	chr4:188426278-188426328	BJ	skin:	n/a
48	chr4:188391387-188391437	BE2_C	brain:	n/a
49	chr4:188427966-188428016	HCPEpiC	choroid plexus:	n/a
50	chr4:188398437-188398487	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:188390078..188391598-chr8:43091410..43092931,3	MCF-7	breast:
2	chr4:188426813..188429681-chrX:150150480..150152156,2	MCF-7	breast:
3	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
4	chr4:188391078..188391578-chr8:43092429..43092931,2	MCF-7	breast:
5	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
6	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
7	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
8	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
9	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
10	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
11	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
12	chr4:188360438..188363227-chr4:188363317..188366717,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML2-12	chr4:188364017-188364135	NONHSAT099697
2	lnc-ZFP42-12	chr4:188370524-188371133	l_2817_chr4:188360138-188372335_testes
3	lnc-TRIML2-12	chr4:188364965-188365452	NONHSAT099697
4	lnc-ZFP42-4	chr4:188351216-188351539	XLOC_003828
5	lnc-ZFP42-12	chr4:188360139-188360290	l_2817_chr4:188360138-188372335_testes
6	lnc-ZFP42-4	chr4:188343853-188344622	NONHSAT099695
7	lnc-ZFP42-11	chr4:188419171-188419708	NONHSAT099698
8	lnc-ZFP42-4	chr4:188351172-188352018	NONHSAT099695
9	lnc-ZFP42-11	chr4:188419753-188420210	NONHSAT099698
10	lnc-ZFP42-12	chr4:188371277-188372335	l_2817_chr4:188360138-188372335_testes
11	lnc-TRIML2-12	chr4:188362831-188363446	NONHSAT099697
12	lnc-ZFP42-4	chr4:188344049-188344151	XLOC_003828

Variant related genes	Relation type
ENSG00000251643	TF binding region
ENSG00000251643	CpG island
ENSG00000029993	chromatin interactions
ENSG00000251643	chromatin interactions

Extended variants
information (count: 2123 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2123 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553133424	chr4:188342979-188342980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181461715	chr4:188342985-188342986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76679108	chr4:188342990-188342991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544698229	chr4:188342995-188342996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558193124	chr4:188342996-188342997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575250535	chr4:188343041-188343042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78118704	chr4:188343111-188343112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560738283	chr4:188343127-188343128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186503371	chr4:188343162-188343163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11736831	chr4:188343185-188343186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs560386470	chr4:188343249-188343250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112782738	chr4:188343253-188343254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190160155	chr4:188343305-188343306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552409386	chr4:188343311-188343312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373314929	chr4:188343419-188343420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571666966	chr4:188343531-188343532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183198728	chr4:188343567-188343568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146557405	chr4:188343621-188343622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567585966	chr4:188343686-188343687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187493278	chr4:188343744-188343745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556784905	chr4:188343750-188343751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564204848	chr4:188343762-188343763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575235529	chr4:188343774-188343775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375067770	chr4:188343786-188343787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563689005	chr4:188343798-188343799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566835885	chr4:188343873-188343874	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs376449316	chr4:188343888-188343889	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs537947821	chr4:188344010-188344011	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs555955571	chr4:188344072-188344073	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs538803882	chr4:188344097-188344098	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs558750304	chr4:188344120-188344121	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs575266807	chr4:188344125-188344126	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs6839821	chr4:188344126-188344127	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs554528149	chr4:188344148-188344149	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs574396763	chr4:188344159-188344160	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs370274417	chr4:188344199-188344200	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs540523727	chr4:188344213-188344214	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs373130566	chr4:188344241-188344242	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs560447851	chr4:188344259-188344260	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs577211909	chr4:188344289-188344290	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs76349500	chr4:188344290-188344291	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs371990263	chr4:188344302-188344303	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs397880485	chr4:188344303-188344304	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs542976918	chr4:188344379-188344380	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs6553063	chr4:188344404-188344405	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs562555422	chr4:188344422-188344423	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs77414185	chr4:188344450-188344451	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs6845031	chr4:188344485-188344486	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs141077113	chr4:188344648-188344649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6553064	chr4:188344661-188344662	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:78)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cognitive impairment	21505072	CNVD

Chromatin state (count:217 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188337800-188343800	Weak transcription	Fetal Heart	heart
2	chr4:188342800-188346000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr4:188343800-188344400	Enhancers	Fetal Heart	heart
4	chr4:188345400-188346000	Enhancers	Muscle Satellite Cultured Cells	--
5	chr4:188345600-188346200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr4:188346000-188346400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:188351800-188352000	Enhancers	Aorta	Aorta
8	chr4:188352000-188357000	Weak transcription	Aorta	Aorta
9	chr4:188353400-188353800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:188353400-188355400	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr4:188353600-188355200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:188353800-188354800	Enhancers	HMEC	breast
13	chr4:188354400-188355400	Enhancers	Fetal Heart	heart
14	chr4:188354800-188355000	Flanking Active TSS	HMEC	breast
15	chr4:188355000-188355200	Active TSS	HMEC	breast
16	chr4:188355400-188357200	Weak transcription	Fetal Heart	heart
17	chr4:188357200-188357600	Enhancers	Fetal Heart	heart
18	chr4:188357200-188357600	Enhancers	Stomach Smooth Muscle	stomach
19	chr4:188357200-188357800	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr4:188357200-188357800	Enhancers	Colon Smooth Muscle	Colon
21	chr4:188357200-188358400	Enhancers	Rectal Smooth Muscle	rectum
22	chr4:188357400-188357600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr4:188357400-188358200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr4:188357800-188358400	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr4:188358400-188358600	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr4:188365000-188365400	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr4:188365400-188366200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr4:188370800-188371200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr4:188370800-188372000	Enhancers	Fetal Lung	lung
30	chr4:188374800-188375200	Enhancers	Brain Germinal Matrix	brain
31	chr4:188374800-188375200	Enhancers	Fetal Heart	heart
32	chr4:188375000-188375400	Enhancers	HSMMtube	muscle
33	chr4:188385600-188385800	Enhancers	Fetal Lung	lung
34	chr4:188385600-188386400	Enhancers	Adipose Nuclei	Adipose
35	chr4:188385600-188386400	Enhancers	Fetal Stomach	stomach
36	chr4:188385600-188386800	Enhancers	Aorta	Aorta
37	chr4:188385800-188386400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:188386400-188386600	Enhancers	Fetal Lung	lung
39	chr4:188386400-188394600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr4:188389600-188390800	Enhancers	Fetal Heart	heart
41	chr4:188389600-188391200	Enhancers	HSMMtube	muscle
42	chr4:188390400-188390600	Enhancers	Fetal Muscle Leg	muscle
43	chr4:188390400-188391000	Enhancers	Colon Smooth Muscle	Colon
44	chr4:188390400-188391600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr4:188390600-188390800	Enhancers	HSMM	muscle
46	chr4:188390600-188391200	Weak transcription	Fetal Muscle Leg	muscle
47	chr4:188390600-188391200	Enhancers	Rectal Smooth Muscle	rectum
48	chr4:188390800-188391200	Flanking Active TSS	Fetal Heart	heart
49	chr4:188391200-188391600	Enhancers	Fetal Heart	heart
50	chr4:188391200-188391600	Flanking Active TSS	HSMMtube	muscle

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