Variant report

Variant	nsv1014792
Chromosome Location	chr4:54655382-54768963
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	ATF3	chr4:54706921-54707144	K562	blood:	n/a	n/a
2	BACH1	chr4:54671072-54671258	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr4:54671040-54671175	K562	blood:	n/a	n/a
4	BHLHE40	chr4:54752299-54752471	HepG2	liver:	n/a	n/a
5	CBX3	chr4:54698739-54699044	K562	blood:	n/a	n/a
6	CEBPB	chr4:54667101-54667269	K562	blood:	n/a	n/a
7	CEBPB	chr4:54707747-54707910	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:54755173-54755505	K562	blood:	n/a	chr4:54755327-54755340 chr4:54755327-54755338 chr4:54755327-54755340 chr4:54755329-54755338
9	CEBPB	chr4:54681353-54681624	K562	blood:	n/a	n/a
10	CEBPB	chr4:54684753-54685098	IMR90	lung:	n/a	chr4:54684929-54684940
11	CEBPB	chr4:54666980-54667273	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:54721290-54722522	IMR90	lung:	n/a	chr4:54721884-54721897 chr4:54721886-54721897
13	CEBPB	chr4:54684810-54685039	A549	lung:	n/a	chr4:54684929-54684940
14	CEBPB	chr4:54718423-54718773	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:54684904-54685026	H1-hESC	embryonic stem cell:	n/a	chr4:54684929-54684940
16	CEBPB	chr4:54718572-54718659	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr4:54706945-54707226	Hela-S3	cervix:	n/a	chr4:54707077-54707088
18	CEBPB	chr4:54684810-54685101	HepG2	liver:	n/a	chr4:54684929-54684940
19	CEBPB	chr4:54684827-54685027	K562	blood:	n/a	chr4:54684929-54684940
20	CEBPB	chr4:54706970-54707177	HepG2	liver:	n/a	chr4:54707077-54707088
21	CEBPB	chr4:54706920-54707256	A549	lung:	n/a	chr4:54707077-54707088
22	CEBPB	chr4:54755228-54755358	HepG2	liver:	n/a	chr4:54755327-54755340 chr4:54755327-54755338 chr4:54755327-54755340 chr4:54755329-54755338
23	CEBPB	chr4:54755163-54755502	IMR90	lung:	n/a	chr4:54755327-54755340 chr4:54755327-54755338 chr4:54755327-54755340 chr4:54755329-54755338
24	CEBPB	chr4:54728366-54728730	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:54714172-54714397	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:54706896-54707263	IMR90	lung:	n/a	chr4:54707077-54707088
27	CTCF	chr4:54755600-54755750	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr4:54671080-54671230	GM12867	blood:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
29	CTCF	chr4:54671060-54671210	GM12801	blood:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
30	CTCF	chr4:54671040-54671190	AG09319	gingival:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
31	CTCF	chr4:54699643-54699659	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr4:54671045-54671170	Lung_OC	lung:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
33	CTCF	chr4:54671020-54671170	GM12878	blood:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
34	CTCF	chr4:54671100-54671250	HA-sp	spinal cord:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
35	CTCF	chr4:54671080-54671230	GM12874	blood:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
36	CTCF	chr4:54671000-54671150	HUVEC	blood vessel:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
37	CTCF	chr4:54683020-54683170	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr4:54671018-54671227	Hela-S3	cervix:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
39	CTCF	chr4:54670984-54671253	GM12878	blood:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
40	CTCF	chr4:54670985-54671249	GM19238	blood:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
41	CTCF	chr4:54671340-54671490	WI-38	lung:	n/a	n/a
42	CTCF	chr4:54671700-54671850	GM12873	blood:	n/a	n/a
43	CTCF	chr4:54670998-54671224	Pancreas_OC	pancreas:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
44	CTCF	chr4:54671080-54671230	HFF-Myc	foreskin:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
45	CTCF	chr4:54732160-54732310	GM12864	blood:	n/a	n/a
46	CTCF	chr4:54671040-54671190	HepG2	liver:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
47	CTCF	chr4:54755540-54755690	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr4:54671031-54671225	HepG2	liver:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
49	CTCF	chr4:54671040-54671190	AG09309	skin:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120
50	CTCF	chr4:54671040-54671190	HEK293	kidney:	n/a	chr4:54671106-54671119 chr4:54671111-54671119 chr4:54671112-54671120

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:54717951-54718001	GM06990	blood:	n/a
2	chr4:54755599-54755649	AG04449	skin:	fetal
3	chr4:54729555-54729605	HCF	heart:	n/a
4	chr4:54729555-54729605	SKMC	muscle:	n/a
5	chr4:54755599-54755649	AG10803	skin:	n/a
6	chr4:54719043-54719093	HNPCEpiC	eye:	n/a
7	chr4:54765826-54765876	GM19239	blood:	n/a
8	chr4:54717951-54718001	AG10803	skin:	n/a
9	chr4:54729555-54729605	LNCaP	prostate:	n/a
10	chr4:54667491-54667541	AG04450	lung:	fetal
11	chr4:54765826-54765876	NH-A	brain:	n/a
12	chr4:54719043-54719093	GM12892	blood:	n/a
13	chr4:54765826-54765876	HRPEpiC	eye:	n/a
14	chr4:54719043-54719093	NH-A	brain:	n/a
15	chr4:54755599-54755649	PrEC	prostate:	n/a
16	chr4:54677002-54677052	NB4	blood:	n/a
17	chr4:54667491-54667541	ECC-1	luminal epithelium:	n/a
18	chr4:54706750-54706800	HRCEpiC	kidney:	n/a
19	chr4:54755599-54755649	SAEC	small airway:	n/a
20	chr4:54765826-54765876	HCM	heart:	n/a
21	chr4:54677002-54677052	T-47D	breast:	n/a
22	chr4:54667491-54667541	Jurkat	blood:	n/a
23	chr4:54667491-54667541	HL-60	blood:	n/a
24	chr4:54667491-54667541	SK-N-MC	brain:	n/a
25	chr4:54765826-54765876	HUVEC	blood vessel:	n/a
26	chr4:54719043-54719093	BJ	skin:	n/a
27	chr4:54677002-54677052	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:54719043-54719093	AoSMC	blood vessel:	n/a
29	chr4:54765826-54765876	CMK	blood:	n/a
30	chr4:54667491-54667541	HRPEpiC	eye:	n/a
31	chr4:54667491-54667541	HRCEpiC	kidney:	n/a
32	chr4:54717951-54718001	PrEC	prostate:	n/a
33	chr4:54719043-54719093	A549	lung:	n/a
34	chr4:54717951-54718001	BE2_C	brain:	n/a
35	chr4:54719043-54719093	LNCaP	prostate:	n/a
36	chr4:54667491-54667541	SK-N-SH_RA	brain:	n/a
37	chr4:54755599-54755649	HNPCEpiC	eye:	n/a
38	chr4:54765826-54765876	AG04450	lung:	fetal
39	chr4:54729555-54729605	K562	blood:	n/a
40	chr4:54667491-54667541	T-47D	breast:	n/a
41	chr4:54717951-54718001	HMEC	breast:	n/a
42	chr4:54729555-54729605	HCT-116	colon:	n/a
43	chr4:54717951-54718001	AG09319	gingival:	n/a
44	chr4:54755599-54755649	Caco-2	colon:	n/a
45	chr4:54755599-54755649	NB4	blood:	n/a
46	chr4:54755599-54755649	AG09309	skin:	n/a
47	chr4:54729555-54729605	AG04449	skin:	fetal
48	chr4:54667491-54667541	GM12892	blood:	n/a
49	chr4:54765826-54765876	NB4	blood:	n/a
50	chr4:54729555-54729605	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:54759183..54762445-chr4:54762887..54765689,4	K562	blood:
2	chr4:54761062..54763935-chr4:54765914..54768640,2	K562	blood:
3	chr4:54765055..54765944-chr4:55083853..55084724,2	K562	blood:
4	chr4:54761062..54765208-chr4:54765914..54768640,3	K562	blood:
5	chr4:54662024..54664830-chr4:54666037..54667800,2	K562	blood:
6	chr4:54064541..54065429-chr4:54671103..54671657,2	K562	blood:
7	chr4:54572400..54573190-chr4:54670618..54671680,4	MCF-7	breast:
8	chr4:54763785..54765642-chr4:54793748..54795665,2	K562	blood:
9	chr4:54678928..54681395-chr4:54684729..54686903,2	K562	blood:
10	chr4:54759183..54761604-chr4:54763153..54765045,2	K562	blood:
11	chr4:54759183..54761604-chr4:54763153..54765045,2	K562	blood:
12	chr4:54063475..54064115-chr4:54670630..54671704,5	K562	blood:
13	chr4:54678928..54681395-chr4:54684729..54686903,2	K562	blood:
14	chr4:54759183..54762445-chr4:54762887..54765689,4	K562	blood:
15	chr4:54662024..54664830-chr4:54666037..54667800,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GSX2-1	chr4:54766038-54766158	ENSG00000249706.1

Variant related genes	Relation type
ENSG00000249706	TF binding region
ENSG00000249706	CpG island
ENSG00000250815	chromatin interactions
ENSG00000249706	chromatin interactions

Extended variants
information (count: 3147 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:3147 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549064616	chr4:54655416-54655417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570599645	chr4:54655430-54655431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571859962	chr4:54655529-54655530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181333558	chr4:54655547-54655548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556482246	chr4:54655572-54655573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185804131	chr4:54655583-54655584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147254151	chr4:54655602-54655603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556054875	chr4:54655614-54655615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78743233	chr4:54655673-54655674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190174100	chr4:54655700-54655701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557691964	chr4:54655781-54655782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577721345	chr4:54655840-54655841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs6831739	chr4:54655842-54655843	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs10571345	chr4:54655860-54655861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs398063556	chr4:54655865-54655866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562555090	chr4:54655875-54655876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531565600	chr4:54655922-54655923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541635139	chr4:54655937-54655938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562060398	chr4:54655959-54655960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371783607	chr4:54655966-54655967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527573286	chr4:54655983-54655984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547424841	chr4:54655996-54655997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571836015	chr4:54655998-54655999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533081237	chr4:54656044-54656045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538914207	chr4:54656045-54656046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140674984	chr4:54656055-54656056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74988855	chr4:54656056-54656057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536094921	chr4:54656150-54656151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555674721	chr4:54656172-54656173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6842407	chr4:54656194-54656195	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs534943132	chr4:54656242-54656243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs117690308	chr4:54656279-54656280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116785254	chr4:54656295-54656296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149382802	chr4:54656369-54656370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557454583	chr4:54656435-54656436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71597855	chr4:54656437-54656438	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs542047660	chr4:54656454-54656455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6811489	chr4:54656460-54656461	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs572373250	chr4:54656467-54656468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573008660	chr4:54656563-54656564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533206204	chr4:54656615-54656616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369487717	chr4:54656668-54656669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564358028	chr4:54656709-54656710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532971881	chr4:54656719-54656720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369558814	chr4:54656750-54656751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373113811	chr4:54656759-54656760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549510226	chr4:54656767-54656768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563439274	chr4:54656779-54656780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183168934	chr4:54656780-54656781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549558699	chr4:54656789-54656790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21525872	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
Gastrointestinal stromal cancer	17527083	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17209131	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:54648600-54655600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr4:54653600-54657400	Weak transcription	Osteobl	bone
3	chr4:54653600-54659000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:54654200-54655800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:54654400-54655800	Weak transcription	Brain Hippocampus Middle	brain
6	chr4:54654400-54656200	Enhancers	Fetal Muscle Leg	muscle
7	chr4:54654400-54659000	Weak transcription	HSMMtube	muscle
8	chr4:54654600-54657200	Weak transcription	NHDF-Ad	bronchial
9	chr4:54655200-54655800	Enhancers	Fetal Kidney	kidney
10	chr4:54655200-54657400	Enhancers	Brain Cingulate Gyrus	brain
11	chr4:54655600-54657800	Enhancers	Brain Substantia Nigra	brain
12	chr4:54655800-54657600	Enhancers	Brain Hippocampus Middle	brain
13	chr4:54656200-54657000	Enhancers	Brain Anterior Caudate	brain
14	chr4:54656200-54657200	Enhancers	Brain Angular Gyrus	brain
15	chr4:54656200-54657200	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr4:54656400-54656600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr4:54656400-54656800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:54657200-54657400	Enhancers	NHDF-Ad	bronchial
19	chr4:54657200-54658200	Enhancers	Muscle Satellite Cultured Cells	--
20	chr4:54657400-54657800	Weak transcription	NHDF-Ad	bronchial
21	chr4:54657400-54658000	Enhancers	Osteobl	bone
22	chr4:54657800-54658200	Enhancers	NHDF-Ad	bronchial
23	chr4:54659000-54659400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr4:54659000-54660000	Enhancers	HSMMtube	muscle
25	chr4:54659000-54660200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:54671400-54671800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr4:54675800-54677000	Enhancers	Fetal Stomach	stomach
28	chr4:54676000-54677000	Enhancers	Stomach Smooth Muscle	stomach
29	chr4:54676400-54677000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:54676800-54677600	Enhancers	NHLF	lung
31	chr4:54677000-54681200	Weak transcription	Fetal Stomach	stomach
32	chr4:54677000-54681400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr4:54677600-54680200	Weak transcription	NHLF	lung
34	chr4:54680200-54680600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr4:54680200-54680600	Enhancers	NHDF-Ad	bronchial
36	chr4:54680200-54680800	Enhancers	NHLF	lung
37	chr4:54680200-54681000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr4:54680200-54685000	Enhancers	Fetal Lung	lung
39	chr4:54680600-54682400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr4:54680600-54682800	Weak transcription	NHDF-Ad	bronchial
41	chr4:54680800-54681200	Weak transcription	NHLF	lung
42	chr4:54681000-54681200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:54681000-54682600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr4:54681200-54681400	Enhancers	NHLF	lung
45	chr4:54681200-54681600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr4:54681200-54681600	Enhancers	Lung	lung
47	chr4:54681200-54685000	Enhancers	Fetal Stomach	stomach
48	chr4:54681400-54682400	Weak transcription	NHLF	lung
49	chr4:54681400-54684800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr4:54681600-54682600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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