Variant report

Variant	nsv908210
Chromosome Location	chr17:37761202-37781849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1183)
CpG islands
(count:2323)
Chromatin interactive
region (count:80)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1183 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:37778226-37778525	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:37774705-37774830	HepG2	liver:	n/a	chr17:37774718-37774734 chr17:37774719-37774735
3	ATF2	chr17:37778264-37778711	GM12878	blood:	n/a	n/a
4	ATF2	chr17:37778126-37778563	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr17:37778210-37778523	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr17:37778719-37778910	K562	blood:	n/a	chr17:37778838-37778851
7	ATF3	chr17:37778153-37778488	HepG2	liver:	n/a	n/a
8	ATF3	chr17:37778237-37778557	K562	blood:	n/a	n/a
9	ATF3	chr17:37774014-37774192	K562	blood:	n/a	chr17:37774141-37774150 chr17:37774124-37774133
10	ATF3	chr17:37778161-37778758	GM12878	blood:	n/a	n/a
11	ATF3	chr17:37778198-37778494	K562	blood:	n/a	n/a
12	ATF3	chr17:37778158-37778583	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr17:37779702-37779946	K562	blood:	n/a	n/a
14	BACH1	chr17:37779732-37779989	K562	blood:	n/a	n/a
15	BACH1	chr17:37761753-37762227	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr17:37779646-37780011	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr17:37778574-37778862	GM12878	blood:	n/a	chr17:37778742-37778753
18	BATF	chr17:37778601-37778905	GM12878	blood:	n/a	chr17:37778742-37778753
19	BCL3	chr17:37778079-37778737	A549	lung:	n/a	n/a
20	BCL3	chr17:37779519-37780047	A549	lung:	n/a	chr17:37779578-37779587
21	BCL3	chr17:37762032-37762583	A549	lung:	n/a	n/a
22	BCLAF1	chr17:37778101-37778675	GM12878	blood:	n/a	n/a
23	BHLHE40	chr17:37773917-37774311	A549	lung:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
24	BHLHE40	chr17:37778215-37778617	GM12878	blood:	n/a	n/a
25	BHLHE40	chr17:37778241-37778585	K562	blood:	n/a	n/a
26	BHLHE40	chr17:37779676-37779994	GM12878	blood:	n/a	n/a
27	BHLHE40	chr17:37773952-37774258	HepG2	liver:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
28	BHLHE40	chr17:37779664-37779998	K562	blood:	n/a	n/a
29	BHLHE40	chr17:37773499-37774374	HepG2	liver:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
30	BHLHE40	chr17:37773888-37774303	K562	blood:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
31	BHLHE40	chr17:37773696-37774351	GM12878	blood:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
32	BRCA1	chr17:37779819-37780048	HepG2	liver:	n/a	n/a
33	BRCA1	chr17:37778276-37778612	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr17:37778264-37778528	HepG2	liver:	n/a	n/a
35	BRCA1	chr17:37774837-37774839	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr17:37779670-37780021	K562	blood:	n/a	n/a
37	CBX3	chr17:37778213-37778516	K562	blood:	n/a	n/a
38	CBX3	chr17:37778171-37778615	K562	blood:	n/a	n/a
39	CCNT2	chr17:37773930-37774203	K562	blood:	n/a	n/a
40	CEBPB	chr17:37778258-37778510	K562	blood:	n/a	n/a
41	CEBPB	chr17:37766798-37766968	K562	blood:	n/a	n/a
42	CEBPB	chr17:37775703-37776310	HepG2	liver:	n/a	n/a
43	CEBPB	chr17:37779702-37779978	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr17:37778269-37778517	HepG2	liver:	n/a	n/a
45	CEBPB	chr17:37778202-37778670	GM12878	blood:	n/a	n/a
46	CHD1	chr17:37762450-37762497	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr17:37779189-37780165	IMR90	lung:	n/a	n/a
48	CHD2	chr17:37778250-37778526	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr17:37778300-37778451	K562	blood:	n/a	n/a
50	CHD2	chr17:37769335-37769493	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2323 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:37764220-37764270	NH-A	brain:	n/a
2	chr17:37762367-37762417	A549	lung:	n/a
3	chr17:37781256-37781306	AG04450	lung:	fetal
4	chr17:37764220-37764270	PrEC	prostate:	n/a
5	chr17:37762960-37763010	Jurkat	blood:	n/a
6	chr17:37764220-37764270	NH-A	brain:	n/a
7	chr17:37762367-37762417	A549	lung:	n/a
8	chr17:37781256-37781306	AG04450	lung:	fetal
9	chr17:37764220-37764270	PrEC	prostate:	n/a
10	chr17:37762960-37763010	Jurkat	blood:	n/a
11	chr17:37764802-37764852	SK-N-SH	brain:	n/a
12	chr17:37778125-37778175	ProgFib	skin:	n/a
13	chr17:37761216-37761266	IMR90	lung:	fetal
14	chr17:37774934-37774984	HCPEpiC	choroid plexus:	n/a
15	chr17:37764158-37764208	NHBE	bronchial:	n/a
16	chr17:37764118-37764168	HPAEpiC	pulmonary alveolar:	n/a
17	chr17:37763782-37763832	K562	blood:	n/a
18	chr17:37764118-37764168	RPTEC	kidney:	n/a
19	chr17:37764220-37764270	NHBE	bronchial:	n/a
20	chr17:37779789-37779839	K562	blood:	n/a
21	chr17:37764158-37764208	AG09319	gingival:	n/a
22	chr17:37779789-37779839	AoSMC	blood vessel:	n/a
23	chr17:37764264-37764314	HCPEpiC	choroid plexus:	n/a
24	chr17:37779789-37779839	BJ	skin:	n/a
25	chr17:37779789-37779839	AG10803	skin:	n/a
26	chr17:37774058-37774108	NB4	blood:	n/a
27	chr17:37763854-37763904	HPAEpiC	pulmonary alveolar:	n/a
28	chr17:37764153-37764203	HL-60	blood:	n/a
29	chr17:37767494-37767544	AG04450	lung:	fetal
30	chr17:37762842-37762892	HCF	heart:	n/a
31	chr17:37761662-37761712	HUVEC	blood vessel:	n/a
32	chr17:37774857-37774907	BJ	skin:	n/a
33	chr17:37764706-37764756	HEEpiC	esophagus:	n/a
34	chr17:37773848-37773898	HMEC	breast:	n/a
35	chr17:37781256-37781306	BJ	skin:	n/a
36	chr17:37774457-37774507	GM12878	blood:	n/a
37	chr17:37778125-37778175	HIPEpiC	eye:	n/a
38	chr17:37774457-37774507	BE2_C	brain:	n/a
39	chr17:37764802-37764852	SAEC	small airway:	n/a
40	chr17:37762455-37762505	SKMC	muscle:	n/a
41	chr17:37763782-37763832	CMK	blood:	n/a
42	chr17:37763000-37763050	GM12892	blood:	n/a
43	chr17:37767494-37767544	HIPEpiC	eye:	n/a
44	chr17:37774893-37774943	NT2-D1	testis:	n/a
45	chr17:37762960-37763010	HIPEpiC	eye:	n/a
46	chr17:37764802-37764852	HRPEpiC	eye:	n/a
47	chr17:37761692-37761742	BJ	skin:	n/a
48	chr17:37763088-37763138	U87	brain:	n/a
49	chr17:37774934-37774984	Hepatocyte	liver:	n/a
50	chr17:37761947-37761997	BJ	skin:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:37759878..37762418-chr17:37771643..37773208,2	MCF-7	breast:
2	chr17:37772115..37773801-chr17:37825160..37827936,2	K562	blood:
3	chr17:37768363..37771309-chr17:37772118..37774468,3	K562	blood:
4	chr17:37752759..37755741-chr17:37758554..37761390,2	K562	blood:
5	chr11:119227095..119227706-chr17:37778289..37778824,2	MCF-7	breast:
6	chr17:37760982..37763537-chr17:37878611..37880800,2	K562	blood:
7	chr17:37778539..37780288-chr17:37893179..37895344,2	K562	blood:
8	chr17:37756158..37758402-chr17:37760489..37762828,2	K562	blood:
9	chr17:37758573..37760868-chr17:37767261..37768919,2	K562	blood:
10	chr17:37768363..37771309-chr17:37772118..37774468,3	K562	blood:
11	chr17:37778202..37782049-chr17:37783082..37786622,6	K562	blood:
12	chr17:37777888..37778610-chr17:37809336..37810309,3	MCF-7	breast:
13	chr17:37777900..37778761-chr17:37991112..37991981,2	K562	blood:
14	chr17:37777885..37778422-chr17:37824440..37825025,2	MCF-7	breast:
15	chr17:37763061..37765644-chr17:37767093..37771195,3	K562	blood:
16	chr17:37704025..37704767-chr17:37776994..37777805,2	MCF-7	breast:
17	chr17:37777893..37778422-chr17:37895883..37896405,2	K562	blood:
18	chr17:37780595..37782911-chr17:37786267..37787886,2	MCF-7	breast:
19	chr17:37773404..37776321-chr17:37819728..37822241,2	MCF-7	breast:
20	chr17:37732171..37732825-chr17:37779402..37780361,2	K562	blood:
21	chr17:37781012..37783798-chr17:37885303..37888164,4	K562	blood:
22	chr17:37730305..37732141-chr17:37773715..37775844,2	MCF-7	breast:
23	chr17:37779426..37780039-chr17:37828512..37829091,2	K562	blood:
24	chr17:37778895..37779929-chr17:37824753..37825581,4	K562	blood:
25	chr17:37771753..37773281-chr17:37910069..37912599,2	K562	blood:
26	chr17:37773259..37775797-chr17:37912370..37914095,2	MCF-7	breast:
27	chr17:37778256..37779018-chr17:37791676..37792248,2	K562	blood:
28	chr17:37779838..37780411-chr17:37790377..37790904,2	K562	blood:
29	chr17:37776626..37780124-chr17:37818606..37821377,4	K562	blood:
30	chr17:37704896..37707478-chr17:37777687..37780191,2	MCF-7	breast:
31	chr17:37779307..37779994-chr17:37809757..37810305,2	K562	blood:
32	chr17:37778774..37780358-chr17:37893179..37896235,3	K562	blood:
33	chr17:37778262..37779269-chr17:37908489..37909454,3	K562	blood:
34	chr17:37777901..37778833-chr17:37828093..37829149,5	MCF-7	breast:
35	chr17:37777309..37780105-chr17:37909118..37911531,3	MCF-7	breast:
36	chr17:37778310..37780085-chr17:37905969..37908685,2	K562	blood:
37	chr17:37778246..37778910-chr17:37874656..37875550,3	MCF-7	breast:
38	chr17:37779913..37781548-chr17:37921179..37923723,2	MCF-7	breast:
39	chr17:37753002..37755741-chr17:37759105..37761390,2	K562	blood:
40	chr17:37777903..37778847-chr17:37809797..37810807,7	K562	blood:
41	chr17:37777961..37778768-chr17:37910171..37911038,7	MCF-7	breast:
42	chr17:37773896..37776239-chr17:37886682..37888820,2	MCF-7	breast:
43	chr17:37769208..37773729-chr17:37777189..37781252,6	K562	blood:
44	chr17:37776436..37778537-chr17:37788682..37790894,2	MCF-7	breast:
45	chr17:37759375..37763031-chr17:37763265..37765961,4	K562	blood:
46	chr17:37777435..37780800-chr17:37803920..37808668,4	K562	blood:
47	chr17:37769144..37771005-chr17:37773634..37775729,2	MCF-7	breast:
48	chr17:37762236..37764592-chr17:37791810..37794599,2	K562	blood:
49	chr17:37777770..37778817-chr17:37910195..37911123,12	MCF-7	breast:
50	chr17:37769395..37771553-chr17:37883791..37886141,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC087491.2.1-1	chr17:37775866-37775914	ENSG00000214546.3
2	lnc-NEUROD2-2	chr17:37769986-37770227	NONHSAT053460
3	lnc-AC087491.2.1-1	chr17:37778097-37778149	ENSG00000214546.3
4	lnc-AC087491.2.1-1	chr17:37778329-37778766	ENSG00000214546.3
5	lnc-NEUROD2-3	chr17:37771818-37772115	NONHSAT053461
6	lnc-AC087491.2.1-1	chr17:37776006-37776081	ENSG00000214546.3

No data

Variant related genes	Relation type
ENSG00000214546	TF binding region
NEUROD2	TF binding region
PPP1R1B	TF binding region
ENSG00000214546	CpG island
NEUROD2	CpG island
PPP1R1B	CpG island
ENSG00000173991	chromatin interactions
ENSG00000141741	chromatin interactions
ENSG00000131771	chromatin interactions
ENSG00000141744	chromatin interactions
ENSG00000141736	chromatin interactions
ENSG00000131748	chromatin interactions
ENSG00000214546	chromatin interactions
ENSG00000141738	chromatin interactions
ENSG00000161395	chromatin interactions
ENSG00000171532	chromatin interactions
ENSG00000167258	chromatin interactions
ENSG00000108298	chromatin interactions
ENSG00000108344	chromatin interactions

Extended variants
information (count: 730 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:730 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11653421	chr17:37761202-37761203	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs563939216	chr17:37761210-37761211	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530999969	chr17:37761213-37761214	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552497007	chr17:37761323-37761324	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs12946169	chr17:37761389-37761390	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs12946177	chr17:37761394-37761395	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570821806	chr17:37761412-37761413	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144216348	chr17:37761445-37761446	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547013176	chr17:37761473-37761474	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs380373	chr17:37761482-37761483	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs449430	chr17:37761506-37761507	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs408262	chr17:37761507-37761508	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs372941240	chr17:37761511-37761512	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs536382313	chr17:37761537-37761538	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs554359530	chr17:37761544-37761545	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs576234546	chr17:37761549-37761550	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs536857164	chr17:37761564-37761565	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs558744571	chr17:37761577-37761578	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs577225942	chr17:37761586-37761587	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs11388087	chr17:37761613-37761614	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs541303698	chr17:37761637-37761638	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs114472862	chr17:37761661-37761662	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs80186804	chr17:37761723-37761724	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs574724191	chr17:37761804-37761805	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201776400	chr17:37761831-37761832	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs199955832	chr17:37761837-37761838	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563624804	chr17:37761862-37761863	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs375103270	chr17:37761863-37761864	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144499802	chr17:37761909-37761910	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs537766615	chr17:37761920-37761921	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs530996860	chr17:37761959-37761960	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552372057	chr17:37762025-37762026	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs17852041	chr17:37762037-37762038	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564313658	chr17:37762043-37762044	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs200708991	chr17:37762082-37762083	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546874342	chr17:37762121-37762122	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373856556	chr17:37762215-37762216	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs368029272	chr17:37762244-37762245	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs62077531	chr17:37762275-37762276	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs370652416	chr17:37762277-37762278	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs376940742	chr17:37762280-37762281	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs565711564	chr17:37762409-37762410	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs535868207	chr17:37762493-37762494	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs17852042	chr17:37762543-37762544	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs548121799	chr17:37762624-37762625	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs201244384	chr17:37762637-37762638	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs537108143	chr17:37762642-37762643	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs558808033	chr17:37762645-37762646	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs401641	chr17:37762652-37762653	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs112207563	chr17:37762655-37762656	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1146 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37756200-37761800	Weak transcription	Right Atrium	heart
2	chr17:37757400-37761600	Weak transcription	Pancreas	Pancrea
3	chr17:37758400-37761600	Weak transcription	Gastric	stomach
4	chr17:37759600-37761600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
5	chr17:37759600-37762400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
6	chr17:37759600-37763600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr17:37759800-37761400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
8	chr17:37759800-37761400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
9	chr17:37759800-37761800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr17:37759800-37763800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
11	chr17:37759800-37764600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
12	chr17:37760000-37761400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
13	chr17:37760000-37761600	Bivalent Enhancer	Brain Germinal Matrix	brain
14	chr17:37760000-37762000	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
15	chr17:37760000-37762400	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
16	chr17:37760000-37764000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
17	chr17:37760000-37764000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
18	chr17:37760000-37764800	Bivalent/Poised TSS	Fetal Brain Female	brain
19	chr17:37760200-37761800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
20	chr17:37760200-37762400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
21	chr17:37760200-37762400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr17:37760200-37763000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
23	chr17:37760200-37764000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
24	chr17:37760200-37764000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
25	chr17:37760200-37765000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
26	chr17:37760400-37762000	Bivalent Enhancer	Fetal Intestine Large	intestine
27	chr17:37760400-37762200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
28	chr17:37760400-37762400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr17:37760400-37765000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr17:37760600-37761400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr17:37760600-37762400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr17:37760600-37762800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
33	chr17:37760600-37763000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr17:37760800-37761400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
35	chr17:37760800-37761400	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
36	chr17:37760800-37761600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr17:37761000-37761400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr17:37761000-37761400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr17:37761000-37761400	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr17:37761000-37761400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
41	chr17:37761000-37761400	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
42	chr17:37761000-37761600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
43	chr17:37761000-37761800	Bivalent Enhancer	Primary B cells from cord blood	blood
44	chr17:37761000-37761800	Bivalent Enhancer	A549	lung
45	chr17:37761000-37763000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
46	chr17:37761000-37763600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr17:37761000-37764600	Bivalent Enhancer	Fetal Muscle Leg	muscle
48	chr17:37761200-37761400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr17:37761200-37761400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr17:37761200-37761400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell

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