Variant report

Variant	nsv1029755
Chromosome Location	chr5:104249927-104707358
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104599139-104599705	K562	blood:	n/a	n/a
2	ARID3A	chr5:104255114-104255149	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:104369169-104369636	K562	blood:	n/a	n/a
4	ARID3A	chr5:104565880-104566023	K562	blood:	n/a	n/a
5	ARID3A	chr5:104574137-104574841	K562	blood:	n/a	n/a
6	ATF1	chr5:104566225-104566645	K562	blood:	n/a	n/a
7	ATF1	chr5:104475478-104475496	K562	blood:	n/a	n/a
8	ATF1	chr5:104370024-104370214	K562	blood:	n/a	n/a
9	ATF1	chr5:104599299-104599581	K562	blood:	n/a	n/a
10	ATF1	chr5:104373680-104373755	K562	blood:	n/a	n/a
11	BACH1	chr5:104541248-104541265	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr5:104502865-104503067	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr5:104369418-104369675	K562	blood:	n/a	n/a
14	BRCA1	chr5:104393511-104393580	GM12878	blood:	n/a	n/a
15	BRCA1	chr5:104325896-104325918	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr5:104317800-104317805	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr5:104488401-104488414	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr5:104370642-104370939	K562	blood:	n/a	n/a
19	CBX3	chr5:104428357-104428592	K562	blood:	n/a	n/a
20	CBX3	chr5:104393083-104393385	K562	blood:	n/a	n/a
21	CBX3	chr5:104686453-104686733	K562	blood:	n/a	n/a
22	CBX3	chr5:104699005-104699210	K562	blood:	n/a	n/a
23	CBX3	chr5:104393078-104393434	K562	blood:	n/a	n/a
24	CCNT2	chr5:104599218-104599525	K562	blood:	n/a	n/a
25	CCNT2	chr5:104370115-104370461	K562	blood:	n/a	n/a
26	CCNT2	chr5:104369421-104369754	K562	blood:	n/a	chr5:104369561-104369581
27	CCNT2	chr5:104306891-104307038	K562	blood:	n/a	n/a
28	CCNT2	chr5:104566220-104566624	K562	blood:	n/a	n/a
29	CEBPB	chr5:104665939-104666271	K562	blood:	n/a	chr5:104666084-104666093 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666082-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666083-104666094
30	CEBPB	chr5:104665178-104665382	HepG2	liver:	n/a	chr5:104665268-104665280 chr5:104665263-104665274
31	CEBPB	chr5:104321962-104322422	MCF-7	breast:	n/a	n/a
32	CEBPB	chr5:104437346-104437647	K562	blood:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
33	CEBPB	chr5:104484312-104484512	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr5:104437342-104437688	Hela-S3	cervix:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
35	CEBPB	chr5:104475600-104475772	HepG2	liver:	n/a	n/a
36	CEBPB	chr5:104516185-104516507	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:104370011-104370528	HepG2	liver:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
38	CEBPB	chr5:104593448-104593544	K562	blood:	n/a	chr5:104593456-104593469 chr5:104593456-104593469 chr5:104593458-104593469 chr5:104593456-104593469 chr5:104593458-104593469
39	CEBPB	chr5:104391872-104392206	HepG2	liver:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
40	CEBPB	chr5:104534357-104534498	HepG2	liver:	n/a	chr5:104534396-104534407
41	CEBPB	chr5:104373830-104373968	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:104510149-104510395	H1-hESC	embryonic stem cell:	n/a	chr5:104510228-104510239
43	CEBPB	chr5:104665950-104666211	Hela-S3	cervix:	n/a	chr5:104666084-104666093 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666082-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666083-104666094
44	CEBPB	chr5:104423410-104423746	IMR90	lung:	n/a	chr5:104423566-104423577
45	CEBPB	chr5:104423406-104423707	A549	lung:	n/a	chr5:104423566-104423577
46	CEBPB	chr5:104288117-104288374	HepG2	liver:	n/a	chr5:104288258-104288271 chr5:104288258-104288269
47	CEBPB	chr5:104526203-104526286	K562	blood:	n/a	n/a
48	CEBPB	chr5:104437340-104437708	ECC-1	luminal epithelium:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
49	CEBPB	chr5:104665908-104666270	HepG2	liver:	n/a	chr5:104666084-104666093 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666082-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666083-104666094
50	CEBPB	chr5:104437342-104437690	HepG2	liver:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104434827-104434877	Jurkat	blood:	n/a
2	chr5:104265747-104265797	HNPCEpiC	eye:	n/a
3	chr5:104434827-104434877	Jurkat	blood:	n/a
4	chr5:104265747-104265797	HNPCEpiC	eye:	n/a
5	chr5:104435608-104435658	GM12878	blood:	n/a
6	chr5:104434864-104434914	HEK293	kidney:	embryo
7	chr5:104435608-104435658	HEK293	kidney:	embryo
8	chr5:104433849-104433899	HEEpiC	esophagus:	n/a
9	chr5:104345171-104345221	ECC-1	luminal epithelium:	n/a
10	chr5:104434827-104434877	HMEC	breast:	n/a
11	chr5:104435062-104435112	HRPEpiC	eye:	n/a
12	chr5:104265747-104265797	PFSK-1	brain:	n/a
13	chr5:104345171-104345221	IMR90	lung:	fetal
14	chr5:104434827-104434877	HRPEpiC	eye:	n/a
15	chr5:104434827-104434877	MCF-7	breast:	n/a
16	chr5:104345171-104345221	GM12891	blood:	n/a
17	chr5:104433849-104433899	Caco-2	colon:	n/a
18	chr5:104435608-104435658	AoSMC	blood vessel:	n/a
19	chr5:104435608-104435658	HCT-116	colon:	n/a
20	chr5:104345171-104345221	SK-N-SH	brain:	n/a
21	chr5:104265747-104265797	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:104345171-104345221	HRCEpiC	kidney:	n/a
23	chr5:104435608-104435658	HAEpiC	amniotic membrane:	n/a
24	chr5:104434827-104434877	AG10803	skin:	n/a
25	chr5:104345171-104345221	NB4	blood:	n/a
26	chr5:104265747-104265797	HCT-116	colon:	n/a
27	chr5:104435062-104435112	HCPEpiC	choroid plexus:	n/a
28	chr5:104433849-104433899	NT2-D1	testis:	n/a
29	chr5:104345171-104345221	HMEC	breast:	n/a
30	chr5:104265747-104265797	NHBE	bronchial:	n/a
31	chr5:104435608-104435658	ECC-1	luminal epithelium:	n/a
32	chr5:104434827-104434877	GM06990	blood:	n/a
33	chr5:104433849-104433899	AoSMC	blood vessel:	n/a
34	chr5:104435062-104435112	HepG2	liver:	n/a
35	chr5:104345171-104345221	NT2-D1	testis:	n/a
36	chr5:104435608-104435658	GM12891	blood:	n/a
37	chr5:104435062-104435112	NHDF-neo	bronchial:	n/a
38	chr5:104435062-104435112	Hepatocyte	liver:	n/a
39	chr5:104265747-104265797	BJ	skin:	n/a
40	chr5:104434827-104434877	SKMC	muscle:	n/a
41	chr5:104433849-104433899	MCF10A-Er-Src	breast:	n/a
42	chr5:104434864-104434914	Hepatocyte	liver:	n/a
43	chr5:104435608-104435658	AG04450	lung:	fetal
44	chr5:104265747-104265797	HUVEC	blood vessel:	n/a
45	chr5:104435608-104435658	AG04449	skin:	fetal
46	chr5:104434827-104434877	BJ	skin:	n/a
47	chr5:104433849-104433899	GM12892	blood:	n/a
48	chr5:104435608-104435658	HIPEpiC	eye:	n/a
49	chr5:104435062-104435112	HCM	heart:	n/a
50	chr5:104434864-104434914	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:104686842..104688917-chr5:104691899..104693400,2	K562	blood:
2	chr5:104645770..104648035-chr5:104661663..104663662,2	MCF-7	breast:
3	chr5:104296966..104298915-chr5:104301513..104303519,2	K562	blood:
4	chr5:104649160..104650852-chr5:104651591..104654211,3	K562	blood:
5	chr17:57921408..57924296-chr5:104291652..104294224,2	MCF-7	breast:
6	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
7	chr5:104565194..104566957-chr5:104571048..104573999,2	K562	blood:
8	chr5:104604624..104606834-chr5:104613480..104615859,2	K562	blood:
9	chr5:104296966..104298915-chr5:104301513..104303519,2	K562	blood:
10	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
11	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
12	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:
13	chr5:104682524..104684533-chr5:104692732..104695457,2	MCF-7	breast:
14	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
15	chr5:104567163..104569932-chr5:104572220..104574679,2	MCF-7	breast:
16	chr5:104369671..104371200-chr5:104727235..104729208,2	K562	blood:
17	chr5:104679097..104680828-chr5:104708980..104711591,2	K562	blood:
18	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
19	chr5:104542507..104545042-chr5:104552566..104554250,2	K562	blood:
20	chr5:104270441..104272983-chr5:104273696..104275223,2	K562	blood:
21	chr5:104248370..104250240-chr5:104261197..104262793,2	MCF-7	breast:
22	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
23	chr5:104271936..104274851-chr5:104276428..104278480,3	MCF-7	breast:
24	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:
25	chr5:104584886..104590168-chr5:104590478..104594256,4	K562	blood:
26	chr5:104542507..104545042-chr5:104552566..104554250,2	K562	blood:
27	chr5:104576197..104577737-chr5:104582724..104585208,2	K562	blood:
28	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
29	chr12:23105697..23106553-chr5:104539343..104540254,2	MCF-7	breast:
30	chr5:104302225..104304920-chr5:104306783..104309637,2	MCF-7	breast:
31	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
32	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:
33	chr5:104524711..104526370-chr5:104889242..104892104,2	K562	blood:
34	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
35	chr5:104308244..104309781-chr5:104310392..104313289,2	K562	blood:
36	chr5:104649160..104650852-chr5:104651591..104654211,3	K562	blood:
37	chr5:103843512..103846064-chr5:104654970..104657716,2	K562	blood:
38	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
39	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
40	chr5:104294786..104295742-chr9:99125283..99126098,2	MCF-7	breast:
41	chr5:104248370..104250240-chr5:104261197..104262793,2	MCF-7	breast:
42	chr5:104245189..104247786-chr5:104277262..104279951,2	MCF-7	breast:
43	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
44	chr5:104256936..104259316-chr5:104275958..104278631,2	K562	blood:
45	chr5:104582906..104584797-chr5:104601356..104603170,2	K562	blood:
46	chr5:104369743..104372595-chr5:104912590..104914639,2	K562	blood:
47	chr5:104660610..104663385-chr5:104663843..104665843,2	K562	blood:
48	chr5:104682989..104685447-chr5:104726579..104728705,2	K562	blood:
49	chr5:104277822..104279427-chr5:104300449..104302157,2	MCF-7	breast:
50	chr5:104567163..104569932-chr5:104572220..104574679,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104581998-104582065	ENSG00000253584
2	lnc-NUDT12-7	chr5:104344562-104344618	ENSG00000253584
3	lnc-NUDT12-7	chr5:104308988-104309359	ENSG00000253584
4	lnc-NUDT12-7	chr5:104253193-104253599	ENSG00000253584
5	lnc-C5orf30-8	chr5:104435174-104435799	NONHSAT103096
6	lnc-NUDT12-7	chr5:104344562-104344612	ENSG00000253584
7	lnc-C5orf30-8	chr5:104435175-104435799	NR_000039
8	lnc-NUDT12-7	chr5:104311375-104311586	ENSG00000253584
9	lnc-NUDT12-7	chr5:104315392-104315477	ENSG00000253584
10	lnc-NUDT12-7	chr5:104582013-104582067	NONHSAT103097

Variant related genes	Relation type
ENSG00000253584	TF binding region
ENSG00000251574	TF binding region
RAB9BP1	TF binding region
ENSG00000253584	CpG island
ENSG00000251574	CpG island
RAB9BP1	CpG island
ENSG00000251574	chromatin interactions

Extended variants
information (count: 4386 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:4386 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs118191061	chr5:104249929-104249930	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs551270088	chr5:104249933-104249934	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs567820496	chr5:104249935-104249936	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs112139464	chr5:104249937-104249938	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs115655264	chr5:104249958-104249959	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs144033870	chr5:104249959-104249960	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs180909395	chr5:104250068-104250069	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs559067282	chr5:104250069-104250070	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs146459088	chr5:104250103-104250104	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs185312018	chr5:104250111-104250112	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs563604149	chr5:104250136-104250137	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs559950479	chr5:104250158-104250159	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs12187327	chr5:104250159-104250160	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs558959086	chr5:104250164-104250165	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs528057985	chr5:104250168-104250169	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs115296157	chr5:104250229-104250230	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs564601759	chr5:104250235-104250236	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs550920762	chr5:104250244-104250245	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs201371543	chr5:104250250-104250251	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs531141446	chr5:104250301-104250302	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs189825631	chr5:104250305-104250306	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs567844536	chr5:104250321-104250322	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs201882979	chr5:104250350-104250351	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs114169316	chr5:104250361-104250362	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs560524743	chr5:104250371-104250372	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs547255855	chr5:104250517-104250518	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs566899704	chr5:104250528-104250529	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs539000883	chr5:104250534-104250535	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs181430560	chr5:104250566-104250567	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs78693617	chr5:104250588-104250589	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs186899005	chr5:104250647-104250648	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs538334064	chr5:104250674-104250675	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs556919148	chr5:104250680-104250681	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs573767886	chr5:104250774-104250775	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs542585421	chr5:104250792-104250793	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs191700389	chr5:104250825-104250826	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs527709294	chr5:104250851-104250852	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs73777355	chr5:104250860-104250861	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs544561267	chr5:104250862-104250863	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs553771188	chr5:104250863-104250864	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs150089027	chr5:104250887-104250888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530565846	chr5:104250915-104250916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550641639	chr5:104250958-104250959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561355965	chr5:104250988-104250989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183941068	chr5:104251037-104251038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543016557	chr5:104251082-104251083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs138923795	chr5:104251090-104251091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567129917	chr5:104251113-104251114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532553955	chr5:104251116-104251117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552650281	chr5:104251153-104251154	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Obesity	20622171	CNVD
Schizophrenia	21346763	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD

Chromatin state (count:154 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104247800-104250400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr5:104249400-104251600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:104249600-104250000	Enhancers	Fetal Brain Male	brain
4	chr5:104249600-104251000	Enhancers	Brain Germinal Matrix	brain
5	chr5:104250400-104251000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:104250800-104251400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:104255800-104256200	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr5:104260000-104260800	Enhancers	Fetal Intestine Large	intestine
9	chr5:104264600-104265200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:104265200-104268200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:104268200-104268400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr5:104268200-104268400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:104268400-104268600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr5:104277200-104277400	Enhancers	Fetal Intestine Large	intestine
15	chr5:104277200-104277400	Enhancers	Fetal Intestine Small	intestine
16	chr5:104277400-104278400	Weak transcription	Fetal Intestine Large	intestine
17	chr5:104277600-104283000	Weak transcription	Fetal Intestine Small	intestine
18	chr5:104277800-104278600	Enhancers	Hela-S3	cervix
19	chr5:104278200-104278800	Enhancers	Colon Smooth Muscle	Colon
20	chr5:104278400-104279200	Enhancers	Fetal Intestine Large	intestine
21	chr5:104279200-104283000	Weak transcription	Fetal Intestine Large	intestine
22	chr5:104283000-104283800	Enhancers	Fetal Intestine Large	intestine
23	chr5:104283000-104283800	Enhancers	Fetal Intestine Small	intestine
24	chr5:104283800-104287800	Weak transcription	Fetal Intestine Small	intestine
25	chr5:104287400-104288000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr5:104287600-104287800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:104287600-104288000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr5:104288000-104290600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:104307400-104307600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:104310000-104310200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:104310000-104310600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:104310200-104310600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:104310600-104312800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:104310600-104312800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr5:104312800-104313200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:104312800-104313400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:104312800-104313600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr5:104313000-104313600	Enhancers	Aorta	Aorta
39	chr5:104321200-104321400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr5:104322000-104322200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr5:104322000-104323400	Enhancers	Fetal Intestine Small	intestine
42	chr5:104322000-104323600	Enhancers	Fetal Intestine Large	intestine
43	chr5:104322600-104324600	Enhancers	K562	blood
44	chr5:104324800-104326000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr5:104325200-104326400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr5:104369400-104369800	Enhancers	K562	blood
47	chr5:104369400-104370000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr5:104369400-104370200	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr5:104369800-104370200	Flanking Active TSS	K562	blood
50	chr5:104370200-104370400	Enhancers	K562	blood

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