Variant report

Variant	esv2755544
Chromosome Location	chr5:107614101-107748101
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	chr5:107717239-107717244	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:107717768-107718442	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:107715842-107716195	K562	blood:	n/a	n/a
4	ARID3A	chr5:107674937-107675137	K562	blood:	n/a	n/a
5	ARID3A	chr5:107620107-107620141	K562	blood:	n/a	n/a
6	ARID3A	chr5:107681343-107681626	K562	blood:	n/a	n/a
7	ARID3A	chr5:107717923-107718429	K562	blood:	n/a	n/a
8	ARID3A	chr5:107715451-107716224	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:107722046-107722745	HepG2	liver:	n/a	n/a
10	ATF1	chr5:107696104-107696307	K562	blood:	n/a	n/a
11	ATF1	chr5:107624684-107624909	K562	blood:	n/a	n/a
12	ATF1	chr5:107717901-107718554	K562	blood:	n/a	n/a
13	ATF2	chr5:107717847-107718362	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr5:107717546-107718945	GM12878	blood:	n/a	n/a
15	ATF2	chr5:107717907-107718336	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr5:107717812-107718688	GM12878	blood:	n/a	n/a
17	ATF2	chr5:107716180-107716691	GM12878	blood:	n/a	n/a
18	ATF3	chr5:107717647-107718420	A549	lung:	n/a	chr5:107718092-107718105 chr5:107717778-107717787 chr5:107718093-107718103
19	BACH1	chr5:107717727-107718392	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr5:107718011-107718378	GM12878	blood:	n/a	n/a
21	BCL11A	chr5:107717867-107718444	GM12878	blood:	n/a	chr5:107718134-107718147 chr5:107717884-107717897
22	BCL11A	chr5:107718074-107718297	GM12878	blood:	n/a	chr5:107718134-107718147
23	BCL3	chr5:107716191-107716684	GM12878	blood:	n/a	chr5:107716623-107716636
24	BCL3	chr5:107717470-107718506	GM12878	blood:	n/a	chr5:107717772-107717785 chr5:107717718-107717731 chr5:107717832-107717845 chr5:107718134-107718147 chr5:107717837-107717846 chr5:107717697-107717710 chr5:107717884-107717897
25	BCL3	chr5:107717823-107718853	A549	lung:	n/a	chr5:107717832-107717845 chr5:107718134-107718147 chr5:107717837-107717846 chr5:107717884-107717897
26	BCL3	chr5:107666346-107666596	GM12878	blood:	n/a	n/a
27	BCL3	chr5:107717590-107718627	A549	lung:	n/a	chr5:107717772-107717785 chr5:107717718-107717731 chr5:107717832-107717845 chr5:107718134-107718147 chr5:107717837-107717846 chr5:107717697-107717710 chr5:107717884-107717897
28	BCLAF1	chr5:107717319-107718870	GM12878	blood:	n/a	chr5:107717453-107717466 chr5:107717772-107717785 chr5:107717718-107717731 chr5:107717832-107717845 chr5:107718134-107718147 chr5:107717837-107717846 chr5:107717697-107717710 chr5:107717884-107717897
29	BCLAF1	chr5:107716161-107716675	GM12878	blood:	n/a	chr5:107716623-107716636
30	BCLAF1	chr5:107717545-107719214	GM12878	blood:	n/a	chr5:107717772-107717785 chr5:107717718-107717731 chr5:107717832-107717845 chr5:107718134-107718147 chr5:107717837-107717846 chr5:107717697-107717710 chr5:107717884-107717897
31	BCLAF1	chr5:107716928-107717520	GM12878	blood:	n/a	chr5:107717453-107717466 chr5:107717132-107717145 chr5:107717280-107717293 chr5:107717044-107717057 chr5:107716940-107716953 chr5:107717307-107717320 chr5:107716942-107716955 chr5:107717134-107717143
32	BHLHE40	chr5:107716207-107716584	GM12878	blood:	n/a	n/a
33	BHLHE40	chr5:107717380-107718531	HepG2	liver:	n/a	chr5:107717552-107717568 chr5:107717447-107717463 chr5:107717831-107717847 chr5:107717771-107717787 chr5:107717560-107717576
34	BHLHE40	chr5:107717037-107718942	K562	blood:	n/a	chr5:107717552-107717568 chr5:107717247-107717263 chr5:107717308-107717324 chr5:107717447-107717463 chr5:107717831-107717847 chr5:107717085-107717101 chr5:107717771-107717787 chr5:107717560-107717576 chr5:107717039-107717055
35	BHLHE40	chr5:107717305-107718951	GM12878	blood:	n/a	chr5:107717552-107717568 chr5:107717308-107717324 chr5:107717447-107717463 chr5:107717831-107717847 chr5:107717771-107717787 chr5:107717560-107717576
36	BHLHE40	chr5:107666323-107666558	K562	blood:	n/a	n/a
37	BRCA1	chr5:107717635-107718253	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr5:107717878-107718250	HepG2	liver:	n/a	n/a
39	CBX3	chr5:107709172-107709413	K562	blood:	n/a	n/a
40	CBX3	chr5:107709123-107709557	HCT-116	colon:	n/a	n/a
41	CBX3	chr5:107709123-107709498	K562	blood:	n/a	n/a
42	CBX3	chr5:107718013-107718358	K562	blood:	n/a	n/a
43	CBX3	chr5:107711457-107711756	K562	blood:	n/a	n/a
44	CBX3	chr5:107717413-107718704	K562	blood:	n/a	chr5:107718536-107718547
45	CBX3	chr5:107708074-107708501	K562	blood:	n/a	n/a
46	CBX3	chr5:107708110-107708382	K562	blood:	n/a	n/a
47	CBX3	chr5:107711447-107711797	K562	blood:	n/a	n/a
48	CCNT2	chr5:107716315-107718569	K562	blood:	n/a	chr5:107716347-107716356 chr5:107716353-107716362 chr5:107716783-107716792 chr5:107716666-107716675
49	CCNT2	chr5:107645829-107646060	K562	blood:	n/a	n/a
50	CEBPB	chr5:107631605-107632100	Hela-S3	cervix:	n/a	chr5:107631760-107631771 chr5:107631760-107631769

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:107717965-107718015	PFSK-1	brain:	n/a
2	chr5:107713125-107713175	BJ	skin:	n/a
3	chr5:107746626-107746676	HCPEpiC	choroid plexus:	n/a
4	chr5:107717975-107718025	HNPCEpiC	eye:	n/a
5	chr5:107713125-107713175	HIPEpiC	eye:	n/a
6	chr5:107715830-107715880	HEEpiC	esophagus:	n/a
7	chr5:107614099-107614149	AG10803	skin:	n/a
8	chr5:107718043-107718093	ECC-1	luminal epithelium:	n/a
9	chr5:107614099-107614149	GM12878	blood:	n/a
10	chr5:107717965-107718015	GM12892	blood:	n/a
11	chr5:107716468-107716518	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:107746626-107746676	GM12892	blood:	n/a
13	chr5:107717972-107718022	Hela-S3	cervix:	n/a
14	chr5:107716468-107716518	AG04450	lung:	fetal
15	chr5:107717975-107718025	HUVEC	blood vessel:	n/a
16	chr5:107717310-107717360	NT2-D1	testis:	n/a
17	chr5:107718043-107718093	LNCaP	prostate:	n/a
18	chr5:107746626-107746676	Jurkat	blood:	n/a
19	chr5:107717310-107717360	PrEC	prostate:	n/a
20	chr5:107717310-107717360	HPAEpiC	pulmonary alveolar:	n/a
21	chr5:107717630-107717680	H1-hESC	embryonic stem cell:	embryo
22	chr5:107702185-107702235	NT2-D1	testis:	n/a
23	chr5:107717975-107718025	HEEpiC	esophagus:	n/a
24	chr5:107717630-107717680	HNPCEpiC	eye:	n/a
25	chr5:107702185-107702235	HAEpiC	amniotic membrane:	n/a
26	chr5:107614099-107614149	U87	brain:	n/a
27	chr5:107717310-107717360	AG04450	lung:	fetal
28	chr5:107717630-107717680	RPTEC	kidney:	n/a
29	chr5:107614099-107614149	ECC-1	luminal epithelium:	n/a
30	chr5:107717630-107717680	PANC-1	pancreas:	n/a
31	chr5:107717310-107717360	HCF	heart:	n/a
32	chr5:107614099-107614149	PANC-1	pancreas:	n/a
33	chr5:107722229-107722279	PFSK-1	brain:	n/a
34	chr5:107717630-107717680	HRPEpiC	eye:	n/a
35	chr5:107717972-107718022	HEK293	kidney:	embryo
36	chr5:107717310-107717360	NHBE	bronchial:	n/a
37	chr5:107718300-107718350	RPTEC	kidney:	n/a
38	chr5:107717972-107718022	HEEpiC	esophagus:	n/a
39	chr5:107614099-107614149	AG04450	lung:	fetal
40	chr5:107718043-107718093	NT2-D1	testis:	n/a
41	chr5:107717630-107717680	SKMC	muscle:	n/a
42	chr5:107718300-107718350	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:107702185-107702235	AG04449	skin:	fetal
44	chr5:107718043-107718093	HCF	heart:	n/a
45	chr5:107718043-107718093	PFSK-1	brain:	n/a
46	chr5:107717310-107717360	H1-hESC	embryonic stem cell:	embryo
47	chr5:107718300-107718350	Hepatocyte	liver:	n/a
48	chr5:107718043-107718093	AG09319	gingival:	n/a
49	chr5:107702185-107702235	A549	lung:	n/a
50	chr5:107746626-107746676	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr17:8076579..8077271-chr5:107717045..107717954,2	Hela-S3	cervix:
2	chr20:15213744..15214594-chr5:107680986..107681674,2	MCF-7	breast:
3	chr5:107703047..107709148-chr5:107715421..107721287,10	K562	blood:
4	chr5:107703017..107709518-chr5:107714821..107720551,7	MCF-7	breast:
5	chr5:107717757..107719316-chr5:108082854..108085189,2	MCF-7	breast:
6	chr5:107721991..107723529-chr5:107734221..107736637,2	MCF-7	breast:
7	chr5:107662350..107665061-chr5:107666147..107667939,2	MCF-7	breast:
8	chr5:107704058..107705992-chr5:107711279..107713882,3	MCF-7	breast:
9	chr5:107690532..107692643-chr5:107717200..107720124,2	K562	blood:
10	chr5:107596085..107596926-chr5:107614295..107614996,3	MCF-7	breast:
11	chr5:107629129..107630886-chr5:107639365..107641581,2	K562	blood:
12	chr5:107673625..107675150-chr5:107717919..107720038,2	K562	blood:
13	chr12:49524532..49525108-chr5:107717478..107718091,2	Hela-S3	cervix:
14	chr5:104726534..104729492-chr5:107716153..107718681,2	K562	blood:
15	chr5:107674221..107676262-chr5:107681301..107685297,3	K562	blood:
16	chr5:102896315..102898883-chr5:107715677..107718329,2	K562	blood:
17	chr5:107695811..107698012-chr5:107701922..107703734,2	K562	blood:
18	chr5:107725102..107727598-chr5:107729614..107733735,4	MCF-7	breast:
19	chr5:107702113..107704886-chr5:107707019..107708765,2	K562	blood:
20	chr17:56707838..56709408-chr5:107717077..107719444,2	MCF-7	breast:
21	chr5:107720815..107723363-chr5:107732371..107733940,2	MCF-7	breast:
22	chr5:107720815..107723363-chr5:107732371..107733940,2	MCF-7	breast:
23	chr5:107629129..107630886-chr5:107639365..107641581,2	K562	blood:
24	chr5:107687278..107689541-chr5:107694592..107696182,2	K562	blood:
25	chr5:107704058..107705992-chr5:107711279..107713882,3	MCF-7	breast:
26	chr5:107693754..107695689-chr5:107714400..107716161,2	K562	blood:
27	chr5:107721991..107723529-chr5:107734221..107736637,2	MCF-7	breast:
28	chr5:107717195..107717792-chr6:27098236..27098991,2	Hela-S3	cervix:
29	chr5:107687021..107688771-chr5:107717411..107719935,2	MCF-7	breast:
30	chr5:107696918..107699388-chr5:107716914..107718993,2	K562	blood:
31	chr5:107693754..107695689-chr5:107714400..107716161,2	K562	blood:
32	chr12:120729283..120730124-chr5:107716642..107717534,2	Hela-S3	cervix:
33	chr5:107662350..107665061-chr5:107666147..107667939,2	MCF-7	breast:
34	chr5:107705561..107708007-chr5:107713920..107718411,4	MCF-7	breast:
35	chr5:107703017..107709518-chr5:107714821..107720551,7	MCF-7	breast:
36	chr5:107700359..107701872-chr5:107716648..107719223,2	MCF-7	breast:
37	chr11:393917..395827-chr5:107707504..107710114,2	MCF-7	breast:
38	chr5:107700578..107705838-chr5:107715421..107718628,5	K562	blood:
39	chr5:107596357..107597019-chr5:107678266..107678805,2	MCF-7	breast:
40	chr5:107700359..107701872-chr5:107716648..107719223,2	MCF-7	breast:
41	chr5:107705544..107707049-chr5:107712715..107714654,2	K562	blood:
42	chr5:107715395..107721337-chr5:107744476..107755519,20	MCF-7	breast:
43	chr5:107673625..107675150-chr5:107717919..107720038,2	K562	blood:
44	chr1:11968697..11971206-chr5:107717145..107718846,2	MCF-7	breast:
45	chr5:107652768..107655007-chr5:107665345..107667956,2	K562	blood:
46	chr19:18496936..18497493-chr5:107717910..107718500,2	HCT-116	colon:
47	chr5:107705977..107708184-chr5:107711910..107713807,2	MCF-7	breast:
48	chr5:107725102..107727598-chr5:107729614..107733735,4	MCF-7	breast:
49	chr5:107696924..107698880-chr5:107700620..107702301,2	MCF-7	breast:
50	chr5:107715063..107717038-chr5:110074735..110077588,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FER-2	chr5:107728769-107728778	XLOC_004500
2	lnc-FER-2	chr5:107747429-107747552	NONHSAT103122
3	lnc-FER-2	chr5:107747430-107747552	XLOC_004500
4	lnc-FER-2	chr5:107747430-107747552	NONHSAT103121
5	lnc-FER-2	chr5:107717871-107718109	NONHSAT103121
6	lnc-FER-2	chr5:107728768-107728778	NONHSAT103122
7	lnc-FER-2	chr5:107717801-107724211	NONHSAT103120

Variant related genes	Relation type
FBXL17	TF binding region
FBXL17	CpG island
ENSG00000197111	chromatin interactions
ENSG00000121022	chromatin interactions
ENSG00000197043	chromatin interactions
ENSG00000168906	chromatin interactions
ENSG00000201801	chromatin interactions
ENSG00000130513	chromatin interactions
ENSG00000198961	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000168040	chromatin interactions
ENSG00000011028	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000251574	chromatin interactions
ENSG00000112874	chromatin interactions
ENSG00000080503	chromatin interactions
ENSG00000164209	chromatin interactions
ENSG00000264175	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000145743	chromatin interactions
ENSG00000184363	chromatin interactions
ENSG00000151422	chromatin interactions
ENSG00000104218	chromatin interactions

Extended variants
information (count: 5037 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5037 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374661046	chr5:107614106-107614107	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs539237606	chr5:107614129-107614130	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142905266	chr5:107614132-107614133	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566397822	chr5:107614136-107614137	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6883115	chr5:107614140-107614141	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs551799024	chr5:107614190-107614191	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571620737	chr5:107614198-107614199	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141270275	chr5:107614208-107614209	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557463362	chr5:107614295-107614296	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143637506	chr5:107614324-107614325	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116468976	chr5:107614360-107614361	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552886443	chr5:107614384-107614385	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1849011	chr5:107614397-107614398	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs544929998	chr5:107614427-107614428	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564551046	chr5:107614444-107614445	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146783811	chr5:107614448-107614449	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140900237	chr5:107614468-107614469	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560675327	chr5:107614521-107614522	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529735284	chr5:107614523-107614524	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549593473	chr5:107614526-107614527	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150160445	chr5:107614537-107614538	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528785076	chr5:107614544-107614545	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs76780455	chr5:107614580-107614581	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561362856	chr5:107614599-107614600	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571692228	chr5:107614605-107614606	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537470480	chr5:107614635-107614636	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550978568	chr5:107614763-107614764	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567804563	chr5:107614827-107614828	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148879842	chr5:107614847-107614848	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181842189	chr5:107614856-107614857	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557283141	chr5:107614862-107614863	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572912641	chr5:107614870-107614871	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538938232	chr5:107614886-107614887	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187057653	chr5:107614909-107614910	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576342122	chr5:107614935-107614936	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543556962	chr5:107614971-107614972	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191447908	chr5:107615007-107615008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565041013	chr5:107615040-107615041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143527148	chr5:107615060-107615061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574522214	chr5:107615083-107615084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375956554	chr5:107615128-107615129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184096745	chr5:107615136-107615137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186081156	chr5:107615157-107615158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189909737	chr5:107615178-107615179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528651395	chr5:107615218-107615219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551982865	chr5:107615239-107615240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs62359543	chr5:107615253-107615254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs78202943	chr5:107615255-107615256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565612237	chr5:107615269-107615270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534300895	chr5:107615316-107615317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
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
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107575400-107617600	Weak transcription	Primary B cells from cord blood	blood
2	chr5:107577000-107616000	Weak transcription	Primary T cells from cord blood	blood
3	chr5:107585000-107617800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:107596600-107616000	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr5:107602200-107615800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:107604800-107644400	Weak transcription	Fetal Intestine Small	intestine
7	chr5:107607400-107617600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr5:107607600-107614400	Weak transcription	Lung	lung
9	chr5:107611600-107617800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr5:107612400-107624600	Weak transcription	Aorta	Aorta
11	chr5:107612800-107614600	Enhancers	Fetal Heart	heart
12	chr5:107613400-107614200	Enhancers	Colon Smooth Muscle	Colon
13	chr5:107613400-107615000	Enhancers	Liver	Liver
14	chr5:107613400-107616400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:107613600-107614200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:107613600-107614200	Enhancers	Brain Anterior Caudate	brain
17	chr5:107613600-107614800	Enhancers	Right Ventricle	heart
18	chr5:107613600-107615000	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr5:107613800-107614200	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr5:107613800-107615000	Enhancers	Left Ventricle	heart
21	chr5:107613800-107616000	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr5:107614000-107614800	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr5:107614000-107614800	Enhancers	Gastric	stomach
24	chr5:107614000-107615000	Enhancers	Psoas Muscle	Psoas
25	chr5:107614000-107615000	Enhancers	Right Atrium	heart
26	chr5:107614000-107615000	Genic enhancers	Sigmoid Colon	Sigmoid Colon
27	chr5:107614000-107617200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr5:107614200-107614600	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:107614200-107614600	Enhancers	Primary T cells fromperipheralblood	blood
30	chr5:107614200-107615800	Weak transcription	Colon Smooth Muscle	Colon
31	chr5:107614400-107614600	Enhancers	Adipose Nuclei	Adipose
32	chr5:107614400-107614800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr5:107614400-107614800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:107614400-107614800	Enhancers	Spleen	Spleen
35	chr5:107614400-107615000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr5:107614400-107615200	Enhancers	Lung	lung
37	chr5:107614400-107615200	Enhancers	Pancreas	Pancrea
38	chr5:107614600-107615000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr5:107614600-107615200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr5:107614600-107615200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr5:107614600-107627000	Weak transcription	Fetal Heart	heart
42	chr5:107614800-107615000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr5:107614800-107615000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr5:107614800-107616000	Weak transcription	Adipose Nuclei	Adipose
45	chr5:107615000-107615400	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr5:107615000-107615800	Weak transcription	Liver	Liver
47	chr5:107615000-107617800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr5:107615000-107619200	Weak transcription	Psoas Muscle	Psoas
49	chr5:107615000-107705600	Weak transcription	Left Ventricle	heart
50	chr5:107615200-107660400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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