Variant report

Variant	nsv885914
Chromosome Location	chr6:57224854-57364314
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1046)
CpG islands
(count:672)
Chromatin interactive
region (count:37)
LncRNA
region (count:5)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:57236576-57237274	HepG2	liver:	n/a	n/a
2	ATF1	chr6:57329848-57330048	K562	blood:	n/a	n/a
3	ATF1	chr6:57296724-57296768	K562	blood:	n/a	n/a
4	ATF2	chr6:57288321-57288802	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:57288167-57288786	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:57334050-57334159	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:57350106-57350125	K562	blood:	n/a	n/a
8	BACH1	chr6:57337567-57337643	K562	blood:	n/a	n/a
9	BACH1	chr6:57364094-57364109	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:57228847-57228853	K562	blood:	n/a	n/a
11	BACH1	chr6:57269047-57269216	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:57305657-57305828	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:57363671-57363854	K562	blood:	n/a	n/a
14	BACH1	chr6:57288493-57288790	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr6:57254076-57254287	GM12878	blood:	n/a	chr6:57254189-57254200
16	BCL11A	chr6:57288290-57288688	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr6:57288294-57288755	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL11A	chr6:57284786-57285093	GM12878	blood:	n/a	n/a
19	BCL11A	chr6:57284708-57285068	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:57298227-57298377	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:57268781-57268800	K562	blood:	n/a	n/a
22	BHLHE40	chr6:57284768-57285156	GM12878	blood:	n/a	n/a
23	BRCA1	chr6:57249520-57249524	GM12878	blood:	n/a	n/a
24	BRCA1	chr6:57229139-57229210	GM12878	blood:	n/a	n/a
25	CBX3	chr6:57253942-57254357	HCT-116	colon:	n/a	n/a
26	CCNT2	chr6:57354598-57355019	K562	blood:	n/a	n/a
27	CCNT2	chr6:57249858-57249985	K562	blood:	n/a	n/a
28	CCNT2	chr6:57337935-57338250	K562	blood:	n/a	n/a
29	CEBPB	chr6:57282596-57282698	A549	lung:	n/a	n/a
30	CEBPB	chr6:57265576-57265803	HepG2	liver:	n/a	chr6:57265718-57265729
31	CEBPB	chr6:57342505-57343002	A549	lung:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
32	CEBPB	chr6:57342545-57342922	K562	blood:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
33	CEBPB	chr6:57232651-57232929	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:57351364-57351927	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:57351508-57351781	K562	blood:	n/a	n/a
36	CEBPB	chr6:57339225-57340861	IMR90	lung:	n/a	chr6:57340669-57340680 chr6:57340072-57340083
37	CEBPB	chr6:57236682-57236968	HepG2	liver:	n/a	chr6:57236826-57236839 chr6:57236826-57236837
38	CEBPB	chr6:57345012-57345358	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:57351453-57351791	A549	lung:	n/a	n/a
40	CEBPB	chr6:57289988-57290014	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr6:57340502-57340798	A549	lung:	n/a	chr6:57340669-57340680
42	CEBPB	chr6:57342547-57342921	IMR90	lung:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
43	CEBPB	chr6:57309469-57309669	IMR90	lung:	n/a	chr6:57309567-57309578 chr6:57309569-57309580 chr6:57309567-57309580
44	CEBPB	chr6:57342549-57342911	A549	lung:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
45	CEBPB	chr6:57280403-57280644	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:57300355-57300642	MCF-7	breast:	n/a	n/a
47	CEBPB	chr6:57288420-57288760	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr6:57296931-57297294	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:57339921-57340252	Hela-S3	cervix:	n/a	chr6:57340072-57340083
50	CEBPB	chr6:57342573-57342758	K562	blood:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:57335405-57335455	IMR90	lung:	fetal
2	chr6:57335405-57335455	IMR90	lung:	fetal
3	chr6:57235407-57235457	HL-60	blood:	n/a
4	chr6:57272398-57272448	AG04449	skin:	fetal
5	chr6:57272398-57272448	MCF-7	breast:	n/a
6	chr6:57253598-57253648	H1-hESC	embryonic stem cell:	embryo
7	chr6:57335405-57335455	HRE	kidney:	n/a
8	chr6:57359134-57359184	BJ	skin:	n/a
9	chr6:57305889-57305939	AG04449	skin:	fetal
10	chr6:57350270-57350320	IMR90	lung:	fetal
11	chr6:57350270-57350320	HEEpiC	esophagus:	n/a
12	chr6:57235407-57235457	IMR90	lung:	fetal
13	chr6:57272398-57272448	IMR90	lung:	fetal
14	chr6:57235407-57235457	U87	brain:	n/a
15	chr6:57288411-57288461	HNPCEpiC	eye:	n/a
16	chr6:57235407-57235457	HCM	heart:	n/a
17	chr6:57339858-57339908	IMR90	lung:	fetal
18	chr6:57235407-57235457	HPAEpiC	pulmonary alveolar:	n/a
19	chr6:57335405-57335455	HL-60	blood:	n/a
20	chr6:57245939-57245989	GM12892	blood:	n/a
21	chr6:57350270-57350320	HEK293	kidney:	embryo
22	chr6:57235407-57235457	PANC-1	pancreas:	n/a
23	chr6:57272398-57272448	AG09319	gingival:	n/a
24	chr6:57350270-57350320	SK-N-MC	brain:	n/a
25	chr6:57245939-57245989	HRCEpiC	kidney:	n/a
26	chr6:57359134-57359184	Hela-S3	cervix:	n/a
27	chr6:57335405-57335455	HAEpiC	amniotic membrane:	n/a
28	chr6:57272398-57272448	HEK293	kidney:	embryo
29	chr6:57272398-57272448	HAEpiC	amniotic membrane:	n/a
30	chr6:57306409-57306459	HCF	heart:	n/a
31	chr6:57350270-57350320	AG09319	gingival:	n/a
32	chr6:57350270-57350320	U87	brain:	n/a
33	chr6:57235407-57235457	ECC-1	luminal epithelium:	n/a
34	chr6:57253598-57253648	PANC-1	pancreas:	n/a
35	chr6:57350270-57350320	PANC-1	pancreas:	n/a
36	chr6:57350270-57350320	H1-hESC	embryonic stem cell:	embryo
37	chr6:57235407-57235457	PrEC	prostate:	n/a
38	chr6:57359134-57359184	HCT-116	colon:	n/a
39	chr6:57339858-57339908	SK-N-SH	brain:	n/a
40	chr6:57235407-57235457	RPTEC	kidney:	n/a
41	chr6:57305889-57305939	NT2-D1	testis:	n/a
42	chr6:57288411-57288461	AoSMC	blood vessel:	n/a
43	chr6:57339858-57339908	HAEpiC	amniotic membrane:	n/a
44	chr6:57306409-57306459	PANC-1	pancreas:	n/a
45	chr6:57335405-57335455	NHBE	bronchial:	n/a
46	chr6:57253598-57253648	NHBE	bronchial:	n/a
47	chr6:57288411-57288461	Caco-2	colon:	n/a
48	chr6:57335405-57335455	MCF-7	breast:	n/a
49	chr6:57339858-57339908	BJ	skin:	n/a
50	chr6:57245939-57245989	T-47D	breast:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:57225893..57228835-chr6:57230897..57233508,2	K562	blood:
2	chr6:57297690..57300107-chr6:57303137..57305465,2	MCF-7	breast:
3	chr6:57225893..57228835-chr6:57230897..57233508,2	K562	blood:
4	chr6:57349293..57351634-chr6:57356907..57359151,3	MCF-7	breast:
5	chr6:57344628..57347602-chr6:57348060..57349813,2	K562	blood:
6	chr6:57297598..57300578-chr6:57301764..57305557,4	K562	blood:
7	chr6:57337415..57340116-chr6:57349926..57352459,2	K562	blood:
8	chr6:57232895..57235001-chr6:57373838..57375777,2	K562	blood:
9	chr6:57198328..57200503-chr6:57228180..57229836,2	K562	blood:
10	chr6:57229138..57231697-chr6:57233407..57236328,3	K562	blood:
11	chr6:57337415..57340116-chr6:57349926..57352459,2	K562	blood:
12	chr6:57285506..57287843-chr6:57289585..57292088,2	MCF-7	breast:
13	chr6:57287892..57290689-chr6:57302857..57304913,2	K562	blood:
14	chr6:57302195..57303819-chr6:57305158..57307849,2	MCF-7	breast:
15	chr6:57344628..57347602-chr6:57348060..57349813,2	K562	blood:
16	chr6:57302195..57303819-chr6:57305158..57307849,2	MCF-7	breast:
17	chr6:57226391..57228337-chr6:57232279..57234513,2	K562	blood:
18	chr6:57296504..57298287-chr6:57300033..57301535,2	K562	blood:
19	chr6:57296504..57298287-chr6:57300033..57301535,2	K562	blood:
20	chr6:57244329..57246093-chr6:57248866..57250667,2	K562	blood:
21	chr6:57230388..57232358-chr6:57233911..57236761,3	MCF-7	breast:
22	chr6:57297690..57300107-chr6:57303137..57305465,2	MCF-7	breast:
23	chr6:57187827..57190385-chr6:57223942..57226286,2	MCF-7	breast:
24	chr6:57214841..57217586-chr6:57224303..57226247,2	K562	blood:
25	chr6:57293162..57295571-chr6:57300739..57302981,3	K562	blood:
26	chr6:57230388..57232358-chr6:57233911..57236761,3	MCF-7	breast:
27	chr6:57358740..57361214-chr6:57362213..57364300,2	K562	blood:
28	chr6:57229138..57231697-chr6:57233407..57236328,3	K562	blood:
29	chr6:57287892..57290689-chr6:57302857..57304913,2	K562	blood:
30	chr6:57297598..57300578-chr6:57301764..57305557,4	K562	blood:
31	chr6:57346719..57348670-chr6:57349128..57351994,2	MCF-7	breast:
32	chr6:57361390..57363831-chr6:57368584..57370615,2	MCF-7	breast:
33	chr6:57293162..57295571-chr6:57300739..57302981,3	K562	blood:
34	chr6:57285506..57287843-chr6:57289585..57292088,2	MCF-7	breast:
35	chr6:57358740..57361214-chr6:57362213..57364300,2	K562	blood:
36	chr6:57226391..57228337-chr6:57232279..57234513,2	K562	blood:
37	chr6:57346719..57348670-chr6:57349128..57351994,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAG2-1	chr6:57362331-57362565	ENSG00000266579.1
2	lnc-RAB23-9	chr6:57236060-57236103	ucscGeneNc_uc003pdu_1
3	lnc-RAB23-9	chr6:57235203-57235424	ucscGeneNc_uc003pdu_1
4	lnc-RAB23-9	chr6:57233281-57234474	ucscGeneNc_uc003pdu_1
5	lnc-BAG2-1	chr6:57358736-57358845	ENSG00000266579.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548u	chr6:57254978-57255000	MIMAT0015013

No data

Variant related genes	Relation type
MIR548U	TF binding region
PRIM2	TF binding region
ENSG00000266579	TF binding region
MIR548U	CpG island
PRIM2	CpG island
ENSG00000266579	CpG island
ENSG00000146143	chromatin interactions
ENSG00000266579	chromatin interactions

Extended variants
information (count: 7931 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7931 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs994272	chr6:57224854-57224855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566190546	chr6:57224891-57224892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533877392	chr6:57224894-57224895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548840795	chr6:57224918-57224919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567251434	chr6:57224925-57224926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537865681	chr6:57224939-57224940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556465005	chr6:57224944-57224945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs994271	chr6:57224955-57224956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs9475870	chr6:57224966-57224967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376597033	chr6:57224968-57224969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112172279	chr6:57224979-57224980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9475871	chr6:57224984-57224985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553927726	chr6:57225012-57225013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572184927	chr6:57225042-57225043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543089661	chr6:57225044-57225045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9475872	chr6:57225059-57225060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9475873	chr6:57225069-57225070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72870491	chr6:57225079-57225080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9475874	chr6:57225095-57225096	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs554792354	chr6:57225112-57225113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375813455	chr6:57225114-57225115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543426002	chr6:57225174-57225175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9396283	chr6:57225190-57225191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9370587	chr6:57225229-57225230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71299585	chr6:57225301-57225302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9370588	chr6:57225307-57225308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10535484	chr6:57225332-57225333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72544283	chr6:57225336-57225337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs66794212	chr6:57225337-57225338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565197055	chr6:57225397-57225398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532664475	chr6:57225404-57225405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12200910	chr6:57225412-57225413	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs541403309	chr6:57225435-57225436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs9357952	chr6:57225454-57225455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559881831	chr6:57225473-57225474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561532275	chr6:57225512-57225513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530260430	chr6:57225553-57225554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368342981	chr6:57225603-57225604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs887557	chr6:57225605-57225606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113260769	chr6:57225631-57225632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs887556	chr6:57225706-57225707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567387782	chr6:57225732-57225733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs5876539	chr6:57225741-57225742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs5876540	chr6:57225742-57225743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531293778	chr6:57225749-57225750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368667501	chr6:57225762-57225763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547129795	chr6:57225766-57225767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs887555	chr6:57225767-57225768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs887554	chr6:57225865-57225866	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs376315233	chr6:57225875-57225876	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1842 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57194600-57226200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:57194600-57244800	Weak transcription	Spleen	Spleen
3	chr6:57195600-57238400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:57199600-57229000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:57199800-57251000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:57208800-57231200	Weak transcription	Aorta	Aorta
7	chr6:57209000-57244800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:57212000-57226000	Weak transcription	Primary B cells from cord blood	blood
9	chr6:57214200-57226000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr6:57215400-57229600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr6:57216000-57226000	Weak transcription	NHLF	lung
12	chr6:57216600-57225800	Weak transcription	GM12878-XiMat	blood
13	chr6:57219800-57225000	Weak transcription	Primary T cells from cord blood	blood
14	chr6:57220000-57229400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:57220000-57230400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr6:57221000-57226000	Weak transcription	Pancreas	Pancrea
17	chr6:57221000-57238400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:57221000-57245000	Weak transcription	K562	blood
19	chr6:57222400-57248200	Weak transcription	A549	lung
20	chr6:57223800-57227000	Weak transcription	Osteobl	bone
21	chr6:57224000-57241000	Weak transcription	Dnd41	blood
22	chr6:57224400-57226000	Weak transcription	Thymus	Thymus
23	chr6:57224400-57229200	Weak transcription	NHDF-Ad	bronchial
24	chr6:57224400-57230200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr6:57225800-57226600	ZNF genes & repeats	GM12878-XiMat	blood
26	chr6:57226000-57226200	Enhancers	H9 Cell Line	embryonic stem cell
27	chr6:57226000-57226200	ZNF genes & repeats	Pancreas	Pancrea
28	chr6:57226000-57226400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr6:57226000-57226400	ZNF genes & repeats	Thymus	Thymus
30	chr6:57226000-57226400	ZNF genes & repeats	NHLF	lung
31	chr6:57226000-57227000	ZNF genes & repeats	Primary B cells from cord blood	blood
32	chr6:57226200-57231200	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr6:57226200-57231200	Weak transcription	Pancreas	Pancrea
34	chr6:57226400-57227600	Weak transcription	Thymus	Thymus
35	chr6:57226400-57229000	Weak transcription	NHLF	lung
36	chr6:57226400-57236000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr6:57226600-57236600	Weak transcription	GM12878-XiMat	blood
38	chr6:57227000-57227600	Enhancers	Osteobl	bone
39	chr6:57227000-57234000	Weak transcription	Primary B cells from cord blood	blood
40	chr6:57227600-57229200	Weak transcription	Osteobl	bone
41	chr6:57229000-57229200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr6:57229000-57229600	Enhancers	NHLF	lung
43	chr6:57229000-57245000	Weak transcription	Left Ventricle	heart
44	chr6:57229200-57229800	Enhancers	Osteobl	bone
45	chr6:57229200-57230200	Enhancers	NHDF-Ad	bronchial
46	chr6:57229200-57231200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:57229400-57230000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:57229400-57230200	Enhancers	Fetal Lung	lung
49	chr6:57229600-57230000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr6:57229600-57230200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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