Variant report

Variant	esv1798897
Chromosome Location	chr4:1265740-1287474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:968)
CpG islands
(count:854)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:1284252-1284452	K562	blood:	n/a	n/a
2	ARID3A	chr4:1283360-1283638	K562	blood:	n/a	n/a
3	ARID3A	chr4:1272067-1272070	K562	blood:	n/a	n/a
4	ARID3A	chr4:1283542-1283707	HepG2	liver:	n/a	n/a
5	ATF1	chr4:1283164-1283813	K562	blood:	n/a	n/a
6	ATF2	chr4:1283376-1283779	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:1283203-1283896	GM12878	blood:	n/a	n/a
8	ATF2	chr4:1283345-1283836	GM12878	blood:	n/a	n/a
9	BCLAF1	chr4:1283222-1283951	GM12878	blood:	n/a	chr4:1283617-1283630
10	BHLHE40	chr4:1283316-1283804	K562	blood:	n/a	chr4:1283387-1283403 chr4:1283617-1283633 chr4:1283380-1283396 chr4:1283440-1283456
11	BHLHE40	chr4:1271820-1272034	HepG2	liver:	n/a	n/a
12	BHLHE40	chr4:1271718-1272018	K562	blood:	n/a	n/a
13	BHLHE40	chr4:1283271-1283879	GM12878	blood:	n/a	chr4:1283387-1283403 chr4:1283617-1283633 chr4:1283380-1283396 chr4:1283440-1283456
14	BRCA1	chr4:1283523-1283723	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr4:1283684-1283759	GM12878	blood:	n/a	n/a
16	BRCA1	chr4:1283401-1283678	HepG2	liver:	n/a	n/a
17	BRCA1	chr4:1283238-1283366	GM12878	blood:	n/a	n/a
18	BRCA1	chr4:1283314-1283769	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr4:1282998-1283828	K562	blood:	n/a	n/a
20	CBX3	chr4:1279904-1280463	K562	blood:	n/a	n/a
21	CBX3	chr4:1279973-1280373	K562	blood:	n/a	n/a
22	CCNT2	chr4:1283222-1284181	K562	blood:	n/a	chr4:1284055-1284064
23	CEBPB	chr4:1283449-1283790	Hela-S3	cervix:	n/a	chr4:1283509-1283517
24	CEBPB	chr4:1283523-1283697	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:1283491-1283769	K562	blood:	n/a	chr4:1283509-1283517
26	CEBPB	chr4:1283473-1283786	IMR90	lung:	n/a	chr4:1283509-1283517
27	CEBPB	chr4:1283501-1283731	A549	lung:	n/a	chr4:1283509-1283517
28	CEBPB	chr4:1283487-1283783	HepG2	liver:	n/a	chr4:1283509-1283517
29	CEBPB	chr4:1284240-1284361	K562	blood:	n/a	n/a
30	CEBPD	chr4:1283536-1283849	HepG2	liver:	n/a	n/a
31	CHD1	chr4:1282942-1283397	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr4:1283013-1284639	GM12878	blood:	n/a	chr4:1283413-1283423 chr4:1283602-1283612
33	CHD1	chr4:1283972-1284105	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr4:1283291-1283782	H1-hESC	embryonic stem cell:	n/a	chr4:1283413-1283423 chr4:1283602-1283612
35	CHD2	chr4:1285103-1285208	K562	blood:	n/a	n/a
36	CHD2	chr4:1283366-1283758	HepG2	liver:	n/a	chr4:1283413-1283423 chr4:1283602-1283612
37	CHD2	chr4:1283184-1283759	K562	blood:	n/a	chr4:1283413-1283423 chr4:1283602-1283612
38	CHD2	chr4:1283230-1283810	Hela-S3	cervix:	n/a	chr4:1283413-1283423 chr4:1283602-1283612
39	CHD2	chr4:1283039-1283879	GM12878	blood:	n/a	chr4:1283413-1283423 chr4:1283602-1283612
40	CHD2	chr4:1284360-1284428	K562	blood:	n/a	n/a
41	CREB1	chr4:1283143-1283896	HepG2	liver:	n/a	n/a
42	CREB1	chr4:1283170-1284132	A549	lung:	n/a	n/a
43	CREB1	chr4:1283157-1283874	GM12878	blood:	n/a	n/a
44	CREB1	chr4:1283198-1283928	K562	blood:	n/a	n/a
45	CREB1	chr4:1282975-1284036	HepG2	liver:	n/a	n/a
46	CREB1	chr4:1283329-1283893	K562	blood:	n/a	n/a
47	CREB1	chr4:1283368-1283970	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr4:1283072-1283861	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr4:1283217-1283814	ECC-1	luminal epithelium:	n/a	n/a
50	CREB1	chr4:1283308-1283775	A549	lung:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1273065-1273115	AG09309	skin:	n/a
2	chr4:1284190-1284240	Caco-2	colon:	n/a
3	chr4:1276510-1276560	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:1284574-1284624	NHBE	bronchial:	n/a
5	chr4:1284190-1284240	HNPCEpiC	eye:	n/a
6	chr4:1280066-1280116	CMK	blood:	n/a
7	chr4:1283396-1283446	AG10803	skin:	n/a
8	chr4:1284190-1284240	NHDF-neo	bronchial:	n/a
9	chr4:1284574-1284624	HEEpiC	esophagus:	n/a
10	chr4:1283667-1283717	GM12891	blood:	n/a
11	chr4:1283396-1283446	IMR90	lung:	fetal
12	chr4:1283718-1283768	AG09319	gingival:	n/a
13	chr4:1283718-1283768	HCF	heart:	n/a
14	chr4:1283667-1283717	GM06990	blood:	n/a
15	chr4:1280066-1280116	BJ	skin:	n/a
16	chr4:1284190-1284240	AG04450	lung:	fetal
17	chr4:1280066-1280116	BE2_C	brain:	n/a
18	chr4:1284330-1284380	AG04449	skin:	fetal
19	chr4:1284330-1284380	NT2-D1	testis:	n/a
20	chr4:1283667-1283717	Hela-S3	cervix:	n/a
21	chr4:1284330-1284380	SK-N-SH_RA	brain:	n/a
22	chr4:1284946-1284996	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:1273065-1273115	Hepatocyte	liver:	n/a
24	chr4:1284330-1284380	SK-N-MC	brain:	n/a
25	chr4:1284574-1284624	NH-A	brain:	n/a
26	chr4:1276510-1276560	U87	brain:	n/a
27	chr4:1283165-1283215	NHBE	bronchial:	n/a
28	chr4:1283472-1283522	NT2-D1	testis:	n/a
29	chr4:1283165-1283215	AG09309	skin:	n/a
30	chr4:1283560-1283610	HRPEpiC	eye:	n/a
31	chr4:1283667-1283717	AoSMC	blood vessel:	n/a
32	chr4:1283165-1283215	AoSMC	blood vessel:	n/a
33	chr4:1283165-1283215	HCF	heart:	n/a
34	chr4:1273065-1273115	HUVEC	blood vessel:	n/a
35	chr4:1283560-1283610	GM06990	blood:	n/a
36	chr4:1283165-1283215	SAEC	small airway:	n/a
37	chr4:1283396-1283446	AG09319	gingival:	n/a
38	chr4:1283560-1283610	MCF-7	breast:	n/a
39	chr4:1283721-1283771	NHDF-neo	bronchial:	n/a
40	chr4:1276510-1276560	IMR90	lung:	fetal
41	chr4:1276510-1276560	T-47D	breast:	n/a
42	chr4:1276510-1276560	HRCEpiC	kidney:	n/a
43	chr4:1284946-1284996	GM19239	blood:	n/a
44	chr4:1283165-1283215	MCF10A-Er-Src	breast:	n/a
45	chr4:1284574-1284624	U87	brain:	n/a
46	chr4:1283396-1283446	SK-N-SH_RA	brain:	n/a
47	chr4:1280066-1280116	HEK293	kidney:	embryo
48	chr4:1276510-1276560	HAEpiC	amniotic membrane:	n/a
49	chr4:1284574-1284624	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:1283472-1283522	SK-N-SH	brain:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:1159320..1162756-chr4:1282339..1286135,5	K562	blood:
2	chr4:1271720..1274688-chr4:1340342..1342246,2	MCF-7	breast:
3	chr4:1284419..1287813-chr4:1334118..1338051,4	MCF-7	breast:
4	chr4:1283187..1284079-chr6:26157656..26158585,2	NB4	blood:
5	chr4:1244052..1245570-chr4:1270792..1272293,2	K562	blood:
6	chr4:1249900..1253028-chr4:1267632..1270770,3	K562	blood:
7	chr4:1238004..1246805-chr4:1279798..1288475,25	K562	blood:
8	chr4:1225914..1229092-chr4:1286494..1288303,3	K562	blood:
9	chr4:1276332..1280187-chr4:1281301..1284175,8	K562	blood:
10	chr4:1242091..1248517-chr4:1279714..1285424,16	MCF-7	breast:
11	chr4:1272314..1274226-chr4:1281897..1284399,2	K562	blood:
12	chr4:1204791..1207603-chr4:1281765..1283856,2	MCF-7	breast:
13	chr4:1242715..1245196-chr4:1264185..1265808,2	MCF-7	breast:
14	chr4:1003302..1006299-chr4:1283517..1285282,2	K562	blood:
15	chr4:1280977..1287340-chr4:1335495..1344055,33	MCF-7	breast:
16	chr4:1253458..1255471-chr4:1281681..1283215,2	K562	blood:
17	chr4:1282437..1287650-chr4:1338224..1344043,13	MCF-7	breast:
18	chr4:1272489..1274226-chr4:1281012..1283397,2	K562	blood:
19	chr4:964532..968039-chr4:1281587..1285155,3	K562	blood:
20	chr4:1076538..1078176-chr4:1278229..1280499,2	MCF-7	breast:
21	chr4:1250499..1252704-chr4:1269110..1272054,2	MCF-7	breast:
22	chr4:1286127..1289218-chr4:1332032..1335159,3	K562	blood:
23	chr4:1284288..1286116-chr4:1712306..1714315,2	K562	blood:
24	chr10:112678380..112679153-chr4:1283021..1283576,2	Hela-S3	cervix:
25	chr4:1265257..1267082-chr4:1285469..1287790,2	K562	blood:
26	chr4:1266888..1269769-chr4:1282587..1285904,3	MCF-7	breast:
27	chr4:1270541..1272526-chr4:1282163..1283723,2	MCF-7	breast:
28	chr4:1078292..1079927-chr4:1283722..1285747,2	MCF-7	breast:
29	chr1:10056745..10057479-chr4:1283519..1284439,2	HCT-116	colon:
30	chr17:7387016..7389305-chr4:1283766..1286186,2	MCF-7	breast:
31	chr4:1282479..1284255-chr4:1368607..1370125,2	K562	blood:
32	chr4:1238004..1248980-chr4:1275065..1286840,30	K562	blood:
33	chr4:1283242..1284963-chr4:1794686..1797481,2	K562	blood:
34	chr4:1236833..1250005-chr4:1276188..1292579,54	MCF-7	breast:
35	chr4:1233077..1236112-chr4:1282661..1284848,3	MCF-7	breast:
36	chr4:1230672..1232310-chr4:1283727..1285762,2	K562	blood:
37	chr4:1273365..1277732-chr4:1280178..1284113,6	MCF-7	breast:
38	chr4:1280840..1286312-chr4:1338111..1343712,9	K562	blood:
39	chr4:1265257..1267082-chr4:1285469..1287790,2	K562	blood:
40	chr4:1280807..1287593-chr4:1339102..1342185,6	K562	blood:
41	chr3:195041802..195042767-chr4:1283869..1284391,2	MCF-7	breast:
42	chr4:1287434..1290416-chr4:1342936..1345119,2	K562	blood:
43	chr4:1241753..1244408-chr4:1270497..1273596,4	MCF-7	breast:
44	chr4:1266374..1269150-chr4:1278693..1281595,2	K562	blood:
45	chr4:1271525..1273880-chr4:1284535..1286045,2	K562	blood:
46	chr4:1272489..1274226-chr4:1281012..1283397,2	K562	blood:
47	chr4:1271525..1273880-chr4:1284535..1286045,2	K562	blood:
48	chr4:1279366..1281863-chr4:1281921..1284803,4	MCF-7	breast:
49	chr4:1240745..1244252-chr4:1285454..1287557,3	MCF-7	breast:
50	chr4:1005260..1007354-chr4:1282653..1285834,3	MCF-7	breast:

No data

Variant related genes	Relation type
MAEA	TF binding region
MAEA	CpG island
ENSG00000273179	chromatin interactions
ENSG00000163950	chromatin interactions
ENSG00000127418	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000163945	chromatin interactions
ENSG00000214413	chromatin interactions
ENSG00000145214	chromatin interactions
ENSG00000181222	chromatin interactions
ENSG00000182903	chromatin interactions
ENSG00000162444	chromatin interactions
ENSG00000174282	chromatin interactions
ENSG00000196810	chromatin interactions
ENSG00000068078	chromatin interactions
ENSG00000090316	chromatin interactions
ENSG00000159692	chromatin interactions

Extended variants
information (count: 1138 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1138 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147790607	chr4:1265774-1265775	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs75309133	chr4:1265860-1265861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552210231	chr4:1265866-1265867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545049881	chr4:1265867-1265868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564783640	chr4:1265868-1265869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186137912	chr4:1265881-1265882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192250926	chr4:1265913-1265914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562091945	chr4:1265940-1265941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530526555	chr4:1265953-1265954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183094110	chr4:1265967-1265968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541120107	chr4:1265990-1265991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559470016	chr4:1266022-1266023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533137825	chr4:1266033-1266034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4974577	chr4:1266046-1266047	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs4974578	chr4:1266072-1266073	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs201913719	chr4:1266077-1266078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201527500	chr4:1266110-1266111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200953004	chr4:1266114-1266115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112050460	chr4:1266159-1266160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550868163	chr4:1266160-1266161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112258258	chr4:1266169-1266170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187758992	chr4:1266202-1266203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549264098	chr4:1266206-1266207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369526095	chr4:1266220-1266221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372552690	chr4:1266254-1266255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141207744	chr4:1266264-1266265	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
27	rs190378513	chr4:1266363-1266364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534860806	chr4:1266378-1266379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181348167	chr4:1266402-1266403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138431538	chr4:1266408-1266409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184092388	chr4:1266413-1266414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs28681067	chr4:1266422-1266423	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs150647698	chr4:1266438-1266439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553081424	chr4:1266439-1266440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139474659	chr4:1266446-1266447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142158502	chr4:1266447-1266448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs28704549	chr4:1266457-1266458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs28433590	chr4:1266462-1266463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111846177	chr4:1266466-1266467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs60846617	chr4:1266477-1266478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs61715446	chr4:1266485-1266486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs58780850	chr4:1266492-1266493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs60917279	chr4:1266493-1266494	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
44	rs59132492	chr4:1266503-1266504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76096826	chr4:1266514-1266515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs61614089	chr4:1266523-1266524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs60206427	chr4:1266533-1266534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187755847	chr4:1266540-1266541	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
49	rs57357791	chr4:1266541-1266542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184735061	chr4:1266546-1266547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Type 2 diabetes	21754918	CNVD

Chromatin state (count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1245400-1282400	Weak transcription	Brain Angular Gyrus	brain
2	chr4:1245600-1266800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr4:1245800-1278600	Weak transcription	Gastric	stomach
4	chr4:1245800-1282600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr4:1245800-1282600	Weak transcription	Right Ventricle	heart
6	chr4:1246000-1282600	Weak transcription	Stomach Smooth Muscle	stomach
7	chr4:1254800-1282400	Weak transcription	Pancreas	Pancrea
8	chr4:1255000-1273000	Weak transcription	Spleen	Spleen
9	chr4:1257000-1272000	Weak transcription	Aorta	Aorta
10	chr4:1259400-1283000	Weak transcription	Ovary	ovary
11	chr4:1259800-1270600	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr4:1263400-1282600	Weak transcription	Brain Hippocampus Middle	brain
13	chr4:1263800-1282800	Weak transcription	Brain Anterior Caudate	brain
14	chr4:1264200-1271800	Weak transcription	Primary B cells from peripheral blood	blood
15	chr4:1265200-1280000	Weak transcription	Brain Cingulate Gyrus	brain
16	chr4:1267800-1282400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr4:1268400-1269400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr4:1268600-1269000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:1270400-1270600	Enhancers	Lung	lung
20	chr4:1270400-1271000	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr4:1270600-1271000	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr4:1270600-1282400	Weak transcription	Lung	lung
23	chr4:1272000-1272400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr4:1272000-1272400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr4:1272000-1279200	Weak transcription	Fetal Brain Female	brain
26	chr4:1273000-1273200	Genic enhancers	Spleen	Spleen
27	chr4:1273200-1273600	Strong transcription	Spleen	Spleen
28	chr4:1273600-1276800	Weak transcription	Spleen	Spleen
29	chr4:1274400-1275200	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr4:1276800-1277400	ZNF genes & repeats	Spleen	Spleen
31	chr4:1277400-1280000	Weak transcription	Spleen	Spleen
32	chr4:1278400-1278600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:1278600-1278800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:1278800-1281000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:1279600-1280600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
36	chr4:1279800-1280200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:1280000-1280400	ZNF genes & repeats	Brain Cingulate Gyrus	brain
38	chr4:1280000-1280400	ZNF genes & repeats	Spleen	Spleen
39	chr4:1280000-1280600	ZNF genes & repeats	Fetal Intestine Small	intestine
40	chr4:1280200-1282400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:1280400-1282400	Weak transcription	Spleen	Spleen
42	chr4:1280400-1282600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr4:1280400-1282800	Weak transcription	Brain Cingulate Gyrus	brain
44	chr4:1280600-1280800	Weak transcription	Fetal Intestine Small	intestine
45	chr4:1280600-1282400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr4:1280800-1281000	Enhancers	HepG2	liver
47	chr4:1280800-1281200	Enhancers	Fetal Intestine Large	intestine
48	chr4:1280800-1281400	Enhancers	Fetal Intestine Small	intestine
49	chr4:1281000-1281400	Flanking Active TSS	HepG2	liver
50	chr4:1281000-1283000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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