Variant report

Variant	nsv2072
Chromosome Location	chr17:45998637-46019626
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:855)
CpG islands
(count:671)
Chromatin interactive
region (count:61)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:46018740-46019665	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:46013389-46013642	K562	blood:	n/a	n/a
3	ARID3A	chr17:46012798-46012823	HepG2	liver:	n/a	n/a
4	ATF1	chr17:46018588-46019073	K562	blood:	n/a	n/a
5	ATF2	chr17:46018330-46019136	GM12878	blood:	n/a	n/a
6	ATF2	chr17:46018362-46019363	GM12878	blood:	n/a	n/a
7	ATF3	chr17:46018644-46019200	A549	lung:	n/a	chr17:46019009-46019029 chr17:46019020-46019040
8	ATF3	chr17:46018877-46019079	GM12878	blood:	n/a	chr17:46019009-46019029 chr17:46019020-46019040
9	ATF3	chr17:46018854-46019219	HepG2	liver:	n/a	chr17:46019009-46019029 chr17:46019020-46019040
10	ATF3	chr17:46018883-46019289	K562	blood:	n/a	chr17:46019009-46019029 chr17:46019020-46019040
11	ATF3	chr17:46013443-46013733	K562	blood:	n/a	n/a
12	BATF	chr17:46015317-46015627	GM12878	blood:	n/a	n/a
13	BATF	chr17:46004874-46005020	GM12878	blood:	n/a	n/a
14	BCL11A	chr17:46015409-46015573	GM12878	blood:	n/a	n/a
15	BCL3	chr17:46018135-46019136	A549	lung:	n/a	chr17:46018664-46018673
16	BCL3	chr17:46018204-46019611	A549	lung:	n/a	chr17:46019209-46019218 chr17:46018664-46018673
17	BHLHE40	chr17:46010297-46010648	HepG2	liver:	n/a	n/a
18	BHLHE40	chr17:46018391-46019553	HepG2	liver:	n/a	n/a
19	BHLHE40	chr17:46018370-46019254	K562	blood:	n/a	n/a
20	BHLHE40	chr17:46018311-46019208	GM12878	blood:	n/a	n/a
21	BHLHE40	chr17:46013284-46013718	K562	blood:	n/a	n/a
22	BRCA1	chr17:46018697-46018705	GM12878	blood:	n/a	n/a
23	BRCA1	chr17:46019345-46019349	GM12878	blood:	n/a	n/a
24	BRCA1	chr17:46018611-46019142	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr17:46010339-46010480	HepG2	liver:	n/a	n/a
26	BRCA1	chr17:46018522-46019071	HepG2	liver:	n/a	n/a
27	CBX3	chr17:46013187-46013719	K562	blood:	n/a	n/a
28	CBX3	chr17:46018211-46019081	K562	blood:	n/a	n/a
29	CBX3	chr17:46018135-46019722	K562	blood:	n/a	n/a
30	CCNT2	chr17:46018938-46019228	K562	blood:	n/a	chr17:46019208-46019217
31	CEBPB	chr17:46018414-46019017	K562	blood:	n/a	chr17:46018888-46018896
32	CEBPB	chr17:46010360-46010584	HepG2	liver:	n/a	chr17:46010506-46010517
33	CEBPB	chr17:46013424-46013767	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr17:46018651-46019609	HepG2	liver:	n/a	chr17:46018888-46018896
35	CEBPB	chr17:46016720-46016822	K562	blood:	n/a	n/a
36	CEBPB	chr17:46019261-46019494	HepG2	liver:	n/a	n/a
37	CEBPB	chr17:46018542-46019590	HepG2	liver:	n/a	chr17:46018888-46018896
38	CEBPB	chr17:46018613-46019551	Hela-S3	cervix:	n/a	chr17:46018888-46018896
39	CEBPB	chr17:46019085-46019653	HepG2	liver:	n/a	n/a
40	CEBPB	chr17:46010327-46010705	HepG2	liver:	n/a	chr17:46010506-46010517
41	CEBPB	chr17:46010336-46010692	HepG2	liver:	n/a	chr17:46010506-46010517
42	CEBPB	chr17:46010490-46010520	H1-hESC	embryonic stem cell:	n/a	chr17:46010506-46010517
43	CEBPB	chr17:46010322-46010656	HepG2	liver:	n/a	chr17:46010506-46010517
44	CEBPB	chr17:46010428-46010646	IMR90	lung:	n/a	chr17:46010506-46010517
45	CEBPB	chr17:46010431-46010685	K562	blood:	n/a	chr17:46010506-46010517
46	CEBPD	chr17:46018790-46019498	HepG2	liver:	n/a	n/a
47	CEBPD	chr17:46010362-46010613	HepG2	liver:	n/a	n/a
48	CEBPD	chr17:46010253-46010662	HepG2	liver:	n/a	n/a
49	CEBPZ	chr17:46018589-46018993	HepG2	liver:	n/a	n/a
50	CHD1	chr17:46018988-46019355	GM12878	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:46019174-46019224	GM12878	blood:	n/a
2	chr17:46019006-46019056	LNCaP	prostate:	n/a
3	chr17:46019017-46019067	HIPEpiC	eye:	n/a
4	chr17:46005612-46005662	AG09309	skin:	n/a
5	chr17:46019165-46019215	HNPCEpiC	eye:	n/a
6	chr17:46019174-46019224	GM12892	blood:	n/a
7	chr17:46018654-46018704	MCF10A-Er-Src	breast:	n/a
8	chr17:46018875-46018925	HCF	heart:	n/a
9	chr17:46019174-46019224	MCF10A-Er-Src	breast:	n/a
10	chr17:46018654-46018704	T-47D	breast:	n/a
11	chr17:46018209-46018259	HCPEpiC	choroid plexus:	n/a
12	chr17:46018809-46018859	HRPEpiC	eye:	n/a
13	chr17:46018809-46018859	AG09319	gingival:	n/a
14	chr17:46019174-46019224	PFSK-1	brain:	n/a
15	chr17:46019006-46019056	HIPEpiC	eye:	n/a
16	chr17:46005612-46005662	HRE	kidney:	n/a
17	chr17:46017593-46017643	HCT-116	colon:	n/a
18	chr17:46019017-46019067	HRPEpiC	eye:	n/a
19	chr17:46018209-46018259	HIPEpiC	eye:	n/a
20	chr17:46019165-46019215	SK-N-MC	brain:	n/a
21	chr17:46019006-46019056	NHDF-neo	bronchial:	n/a
22	chr17:46019017-46019067	HCPEpiC	choroid plexus:	n/a
23	chr17:46019174-46019224	ECC-1	luminal epithelium:	n/a
24	chr17:46019017-46019067	GM06990	blood:	n/a
25	chr17:46005612-46005662	HCPEpiC	choroid plexus:	n/a
26	chr17:46019017-46019067	AoSMC	blood vessel:	n/a
27	chr17:46019006-46019056	NHBE	bronchial:	n/a
28	chr17:46019165-46019215	ECC-1	luminal epithelium:	n/a
29	chr17:46019165-46019215	HUVEC	blood vessel:	n/a
30	chr17:46019174-46019224	HPAEpiC	pulmonary alveolar:	n/a
31	chr17:46019017-46019067	BJ	skin:	n/a
32	chr17:46018209-46018259	Caco-2	colon:	n/a
33	chr17:46019184-46019234	HRPEpiC	eye:	n/a
34	chr17:46017593-46017643	PrEC	prostate:	n/a
35	chr17:46018875-46018925	MCF10A-Er-Src	breast:	n/a
36	chr17:46019165-46019215	LNCaP	prostate:	n/a
37	chr17:46018654-46018704	AG09319	gingival:	n/a
38	chr17:46017593-46017643	AG04450	lung:	fetal
39	chr17:46017593-46017643	AG10803	skin:	n/a
40	chr17:46017593-46017643	Hela-S3	cervix:	n/a
41	chr17:46018209-46018259	HEEpiC	esophagus:	n/a
42	chr17:46019184-46019234	GM19239	blood:	n/a
43	chr17:46019165-46019215	GM06990	blood:	n/a
44	chr17:46018809-46018859	IMR90	lung:	fetal
45	chr17:46019184-46019234	NHDF-neo	bronchial:	n/a
46	chr17:46018654-46018704	HRCEpiC	kidney:	n/a
47	chr17:46019184-46019234	HEK293	kidney:	embryo
48	chr17:46019174-46019224	K562	blood:	n/a
49	chr17:46005612-46005662	SKMC	muscle:	n/a
50	chr17:46018209-46018259	ProgFib	skin:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:46005896..46008732-chr17:46011956..46013614,2	K562	blood:
2	chr17:45970912..45974701-chr17:46018890..46021752,3	K562	blood:
3	chr17:46018061..46020719-chr17:46045036..46046879,2	K562	blood:
4	chr17:45993643..45995953-chr17:46019014..46020704,3	MCF-7	breast:
5	chr17:46005701..46007603-chr17:46012685..46014665,2	K562	blood:
6	chr17:46010778..46013733-chr5:72250921..72253254,2	MCF-7	breast:
7	chr17:46003485..46006244-chr17:46007523..46010248,2	K562	blood:
8	chr17:45998420..46000052-chr17:46002158..46004611,2	K562	blood:
9	chr17:45989573..45991691-chr17:45999240..46001944,2	K562	blood:
10	chr17:45906214..45908869-chr17:46017254..46019863,3	MCF-7	breast:
11	chr17:45886985..45889138-chr17:46015655..46018408,2	K562	blood:
12	chr17:45973963..45975508-chr17:45999326..46001270,2	MCF-7	breast:
13	chr17:46007857..46010307-chr17:46016278..46019958,3	K562	blood:
14	chr17:46007432..46009811-chr17:46047388..46051059,3	K562	blood:
15	chr17:46000022..46002269-chr17:46003613..46007289,3	MCF-7	breast:
16	chr17:45968434..45977260-chr17:46017847..46029594,27	MCF-7	breast:
17	chr17:45927242..45929769-chr17:46017796..46019388,2	MCF-7	breast:
18	chr17:45997083..45999024-chr17:46022042..46024143,2	MCF-7	breast:
19	chr17:45971510..45977679-chr17:46016123..46021422,20	MCF-7	breast:
20	chr17:45992709..45994396-chr17:45996856..45998957,2	MCF-7	breast:
21	chr17:45993823..45996426-chr17:45998099..46000336,2	K562	blood:
22	chr17:45973265..45977043-chr17:45998491..46003792,7	MCF-7	breast:
23	chr17:45974878..45977034-chr17:46001885..46004238,2	K562	blood:
24	chr17:46015450..46017408-chr17:46022063..46023841,2	K562	blood:
25	chr17:45991270..45994231-chr17:46005074..46007219,2	K562	blood:
26	chr17:45999369..46002049-chr17:46009098..46012075,3	MCF-7	breast:
27	chr17:46014365..46016390-chr17:46047533..46049102,2	MCF-7	breast:
28	chr17:45977677..45979429-chr17:46010688..46013383,2	MCF-7	breast:
29	chr17:45915810..45917332-chr17:46018370..46020809,2	K562	blood:
30	chr17:45978341..45980674-chr17:46019226..46022209,2	MCF-7	breast:
31	chr17:45897782..45899976-chr17:46017642..46019403,2	MCF-7	breast:
32	chr17:46017765..46021634-chr17:46045854..46051133,6	MCF-7	breast:
33	chr17:46014622..46017443-chr17:46017878..46019872,2	MCF-7	breast:
34	chr17:45974031..45975859-chr17:46008200..46010414,2	MCF-7	breast:
35	chr17:45972432..45975243-chr17:46004442..46007242,3	MCF-7	breast:
36	chr17:45991986..45994660-chr17:45998582..46001397,3	K562	blood:
37	chr17:45978248..45980745-chr17:46013180..46016044,2	K562	blood:
38	chr17:46005701..46007603-chr17:46012685..46014665,2	K562	blood:
39	chr17:46005896..46008732-chr17:46011956..46013614,2	K562	blood:
40	chr17:45920681..45922665-chr17:46015895..46018695,2	K562	blood:
41	chr17:45992911..45994770-chr17:46006904..46009157,2	K562	blood:
42	chr17:45998420..46000052-chr17:46002158..46004611,2	K562	blood:
43	chr17:46012053..46013747-chr17:46016298..46020138,4	MCF-7	breast:
44	chr17:46004717..46007682-chr17:46032533..46035119,2	K562	blood:
45	chr17:45973395..45975502-chr17:46008931..46011121,2	MCF-7	breast:
46	chr17:46003485..46006244-chr17:46007523..46010248,2	K562	blood:
47	chr17:46018628..46019574-chr3:44379424..44380123,2	Hela-S3	cervix:
48	chr17:45915913..45917925-chr17:46018896..46020443,2	MCF-7	breast:
49	chr17:46005203..46007396-chr17:46018097..46019833,3	MCF-7	breast:
50	chr17:45973201..45977546-chr17:46016018..46021091,7	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR15L-5	chr17:46018702-46018770	NONHSAT054343
2	lnc-PRR15L-5	chr17:46018702-46018725	ENSG00000234494.2
3	lnc-PRR15L-3	chr17:46010338-46010362	ENSG00000266601.1
4	lnc-PRR15L-5	chr17:46018702-46018776	ENSG00000234494.3
5	lnc-PRR15L-3	chr17:46007048-46007338	ENSG00000266601.1
6	lnc-PRR15L-5	chr17:46018702-46018755	ENSG00000234494.2
7	lnc-PRR15L-5	chr17:46018713-46018770	NONHSAT054344
8	lnc-PRR15L-5	chr17:46018713-46018756	ENSG00000234494.2
9	lnc-PRR15L-3	chr17:46010454-46010472	ENSG00000266601.1
10	lnc-PRR15L-5	chr17:46018702-46018776	ENSG00000234494.2

No data

Variant related genes	Relation type
ENSG00000263798	TF binding region
PNPO	TF binding region
ENSG00000266601	TF binding region
ENSG00000234494	TF binding region
ENSG00000263798	CpG island
PNPO	CpG island
ENSG00000266601	CpG island
ENSG00000234494	CpG island
ENSG00000157107	chromatin interactions
ENSG00000264019	chromatin interactions
ENSG00000159111	chromatin interactions
ENSG00000167182	chromatin interactions
ENSG00000108465	chromatin interactions
ENSG00000189120	chromatin interactions
ENSG00000167183	chromatin interactions
ENSG00000266601	chromatin interactions
ENSG00000141295	chromatin interactions
ENSG00000234494	chromatin interactions
ENSG00000006025	chromatin interactions
ENSG00000179152	chromatin interactions
ENSG00000108439	chromatin interactions
ENSG00000264920	chromatin interactions
ENSG00000272081	chromatin interactions
ENSG00000263798	chromatin interactions
ENSG00000271937	chromatin interactions

Extended variants
information (count: 710 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:710 , 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	rs374983538	chr17:45998639-45998640	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs542330035	chr17:45998645-45998646	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs200996583	chr17:45998657-45998658	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs183952826	chr17:45998679-45998680	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs188015050	chr17:45998685-45998686	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs149404525	chr17:45998688-45998689	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs573316889	chr17:45998714-45998715	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs143789223	chr17:45998722-45998723	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs532425428	chr17:45998728-45998729	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs552232672	chr17:45998764-45998765	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs114431647	chr17:45998767-45998768	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs377244976	chr17:45998776-45998777	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs547844842	chr17:45998830-45998831	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs567835978	chr17:45998877-45998878	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs537208708	chr17:45998941-45998942	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs557523739	chr17:45998948-45998949	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs192110736	chr17:45998951-45998952	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs113657940	chr17:45998962-45998963	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs376116517	chr17:45999001-45999002	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs553426659	chr17:45999040-45999041	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573242598	chr17:45999069-45999070	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs148137250	chr17:45999111-45999112	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs73323310	chr17:45999120-45999121	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs575815533	chr17:45999134-45999135	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544757035	chr17:45999150-45999151	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs184703102	chr17:45999158-45999159	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563277312	chr17:45999177-45999178	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs187520712	chr17:45999209-45999210	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs142887003	chr17:45999282-45999283	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559403067	chr17:45999288-45999289	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs528049740	chr17:45999351-45999352	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547792577	chr17:45999434-45999435	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs75424283	chr17:45999439-45999440	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs530518808	chr17:45999456-45999457	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs550432778	chr17:45999498-45999499	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs571012248	chr17:45999533-45999534	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs192829544	chr17:45999551-45999552	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs199619735	chr17:45999552-45999553	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs553605218	chr17:45999597-45999598	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs375455305	chr17:45999616-45999617	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs530547098	chr17:45999622-45999623	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs535805145	chr17:45999623-45999624	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs58174625	chr17:45999634-45999635	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs552243978	chr17:45999673-45999674	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs184834526	chr17:45999724-45999725	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575754159	chr17:45999729-45999730	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs72268130	chr17:45999891-45999892	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs544668809	chr17:45999927-45999928	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs117940541	chr17:46000079-46000080	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs571721046	chr17:46000095-46000096	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
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
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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	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
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	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
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1065 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45975200-45999400	Weak transcription	Fetal Kidney	kidney
2	chr17:45975200-46000400	Weak transcription	Small Intestine	intestine
3	chr17:45975800-46000600	Weak transcription	Hela-S3	cervix
4	chr17:45979800-46000400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr17:45980200-46001800	Weak transcription	K562	blood
6	chr17:45980200-46002400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr17:45980200-46006400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr17:45982400-46000600	Weak transcription	Stomach Mucosa	stomach
9	chr17:45983000-46001000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr17:45983000-46004000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr17:45983200-46000400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr17:45983200-46001200	Weak transcription	A549	lung
13	chr17:45983200-46018200	Weak transcription	Fetal Brain Male	brain
14	chr17:45983400-46000600	Weak transcription	NHDF-Ad	bronchial
15	chr17:45984200-46000600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr17:45985600-46000600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr17:45986000-46000400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr17:45987000-46000200	Weak transcription	Aorta	Aorta
19	chr17:45988400-46000400	Weak transcription	Brain Substantia Nigra	brain
20	chr17:45988400-46000600	Weak transcription	HSMM	muscle
21	chr17:45991800-46000400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr17:45991800-46006400	Strong transcription	Fetal Stomach	stomach
23	chr17:45992400-46008400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr17:45992600-46000400	Weak transcription	HSMMtube	muscle
25	chr17:45993400-46000400	Weak transcription	NH-A	brain
26	chr17:45993600-46000600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr17:45993800-46017400	Weak transcription	Psoas Muscle	Psoas
28	chr17:45994000-46000600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr17:45994000-46013200	Weak transcription	Fetal Heart	heart
30	chr17:45994200-46000400	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr17:45994200-46000400	Weak transcription	Left Ventricle	heart
32	chr17:45994200-46006000	Strong transcription	Fetal Muscle Trunk	muscle
33	chr17:45994400-46000200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr17:45994400-46000400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr17:45994400-46000400	Weak transcription	Gastric	stomach
36	chr17:45994400-46002400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr17:45994400-46006000	Strong transcription	Fetal Muscle Leg	muscle
38	chr17:45994600-45999000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr17:45994600-45999000	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr17:45994600-46000000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr17:45994600-46000000	Weak transcription	Lung	lung
42	chr17:45994600-46000000	Weak transcription	NHLF	lung
43	chr17:45994600-46000200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr17:45994600-46000200	Weak transcription	Colonic Mucosa	Colon
45	chr17:45994600-46000200	Weak transcription	Right Ventricle	heart
46	chr17:45994600-46000400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr17:45994600-46000400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr17:45994600-46000400	Weak transcription	Colon Smooth Muscle	Colon
49	chr17:45994600-46000400	Weak transcription	Esophagus	oesophagus
50	chr17:45994600-46000400	Weak transcription	Pancreas	Pancrea

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