Variant report

Variant	nsv1021630
Chromosome Location	chr9:10336415-10881683
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	chr9:10434055-10434089	HepG2	liver:	n/a	n/a
2	ATF1	chr9:10397745-10397834	K562	blood:	n/a	n/a
3	BACH1	chr9:10612811-10613185	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:10731396-10731463	K562	blood:	n/a	n/a
5	CCNT2	chr9:10612838-10613346	K562	blood:	n/a	n/a
6	CEBPB	chr9:10425961-10426226	A549	lung:	n/a	chr9:10426091-10426102 chr9:10426090-10426103
7	CEBPB	chr9:10512234-10512477	K562	blood:	n/a	chr9:10512340-10512351 chr9:10512339-10512352 chr9:10512339-10512352
8	CEBPB	chr9:10605774-10606014	HepG2	liver:	n/a	chr9:10605898-10605911 chr9:10605898-10605911 chr9:10605895-10605912 chr9:10605898-10605909 chr9:10605900-10605911 chr9:10605898-10605911
9	CEBPB	chr9:10387659-10387714	HepG2	liver:	n/a	n/a
10	CEBPB	chr9:10789715-10790204	HepG2	liver:	n/a	chr9:10790076-10790087
11	CEBPB	chr9:10448014-10448202	K562	blood:	n/a	chr9:10448100-10448111
12	CEBPB	chr9:10599485-10599703	HepG2	liver:	n/a	chr9:10599614-10599625 chr9:10599614-10599627
13	CEBPB	chr9:10366571-10366826	A549	lung:	n/a	chr9:10366647-10366658 chr9:10366646-10366657
14	CEBPB	chr9:10425961-10426264	HepG2	liver:	n/a	chr9:10426091-10426102 chr9:10426090-10426103
15	CEBPB	chr9:10340764-10340950	A549	lung:	n/a	chr9:10340898-10340915 chr9:10340899-10340912 chr9:10340899-10340912 chr9:10340899-10340910
16	CEBPB	chr9:10447965-10448279	HepG2	liver:	n/a	chr9:10448100-10448111
17	CEBPB	chr9:10838394-10838591	HepG2	liver:	n/a	chr9:10838508-10838519
18	CEBPB	chr9:10864356-10864613	Hela-S3	cervix:	n/a	chr9:10864432-10864449 chr9:10864433-10864444 chr9:10864433-10864446 chr9:10864434-10864445 chr9:10864480-10864491
19	CEBPB	chr9:10635667-10636017	HepG2	liver:	n/a	chr9:10635839-10635852 chr9:10635840-10635851 chr9:10635841-10635850
20	CEBPB	chr9:10512172-10512513	A549	lung:	n/a	chr9:10512340-10512351 chr9:10512339-10512352 chr9:10512339-10512352
21	CEBPB	chr9:10523193-10523241	HepG2	liver:	n/a	chr9:10523228-10523239 chr9:10523226-10523237 chr9:10523226-10523239 chr9:10523228-10523239 chr9:10523226-10523239
22	CEBPB	chr9:10870850-10871102	H1-hESC	embryonic stem cell:	n/a	chr9:10870983-10870994
23	CEBPB	chr9:10597856-10598158	HepG2	liver:	n/a	chr9:10597988-10598005
24	CEBPB	chr9:10831699-10831969	HepG2	liver:	n/a	n/a
25	CEBPB	chr9:10635685-10636024	IMR90	lung:	n/a	chr9:10635839-10635852 chr9:10635840-10635851 chr9:10635841-10635850
26	CEBPB	chr9:10678846-10679125	IMR90	lung:	n/a	n/a
27	CEBPB	chr9:10555251-10555579	HepG2	liver:	n/a	chr9:10555408-10555417 chr9:10555406-10555417
28	CEBPB	chr9:10584890-10585155	A549	lung:	n/a	chr9:10585075-10585088 chr9:10585076-10585087 chr9:10585075-10585086
29	CEBPB	chr9:10612917-10612934	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr9:10870900-10871067	K562	blood:	n/a	chr9:10870983-10870994
31	CEBPB	chr9:10555246-10555567	IMR90	lung:	n/a	chr9:10555408-10555417 chr9:10555406-10555417
32	CEBPB	chr9:10597948-10598030	H1-hESC	embryonic stem cell:	n/a	chr9:10597988-10598005
33	CEBPB	chr9:10597859-10598088	A549	lung:	n/a	chr9:10597988-10598005
34	CEBPB	chr9:10864332-10864582	A549	lung:	n/a	chr9:10864432-10864449 chr9:10864433-10864444 chr9:10864433-10864446 chr9:10864434-10864445 chr9:10864480-10864491
35	CEBPB	chr9:10366538-10366836	HepG2	liver:	n/a	chr9:10366647-10366658 chr9:10366646-10366657
36	CEBPB	chr9:10512167-10512523	HepG2	liver:	n/a	chr9:10512340-10512351 chr9:10512339-10512352 chr9:10512339-10512352
37	CEBPB	chr9:10447962-10448204	H1-hESC	embryonic stem cell:	n/a	chr9:10448100-10448111
38	CEBPB	chr9:10663860-10664105	A549	lung:	n/a	chr9:10663898-10663909
39	CEBPB	chr9:10870813-10871159	IMR90	lung:	n/a	chr9:10870983-10870994
40	CEBPB	chr9:10605774-10606046	IMR90	lung:	n/a	chr9:10605898-10605911 chr9:10605898-10605911 chr9:10605895-10605912 chr9:10605898-10605909 chr9:10605900-10605911 chr9:10605898-10605911
41	CEBPB	chr9:10433949-10434113	HepG2	liver:	n/a	chr9:10434019-10434032 chr9:10434019-10434032 chr9:10434020-10434031
42	CEBPB	chr9:10599520-10599740	IMR90	lung:	n/a	chr9:10599614-10599625 chr9:10599614-10599627
43	CEBPB	chr9:10864349-10864630	HepG2	liver:	n/a	chr9:10864432-10864449 chr9:10864433-10864444 chr9:10864433-10864446 chr9:10864434-10864445 chr9:10864480-10864491
44	CEBPB	chr9:10563387-10563417	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr9:10455088-10455277	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr9:10870845-10871173	Hela-S3	cervix:	n/a	chr9:10870983-10870994
47	CEBPB	chr9:10800986-10801148	HepG2	liver:	n/a	chr9:10801096-10801107
48	CEBPB	chr9:10584953-10585136	HepG2	liver:	n/a	chr9:10585075-10585088 chr9:10585076-10585087 chr9:10585075-10585086
49	CEBPB	chr9:10631704-10631897	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr9:10512160-10512530	IMR90	lung:	n/a	chr9:10512340-10512351 chr9:10512339-10512352 chr9:10512339-10512352

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:10613332-10613382	RPTEC	kidney:	n/a
2	chr9:10613328-10613378	NB4	blood:	n/a
3	chr9:10612700-10612750	ovcar-3	ovarian:	n/a
4	chr9:10613328-10613378	BJ	skin:	n/a
5	chr9:10371306-10371356	A549	lung:	n/a
6	chr9:10613328-10613378	GM12878	blood:	n/a
7	chr9:10615205-10615255	AG04449	skin:	fetal
8	chr9:10613328-10613378	A549	lung:	n/a
9	chr9:10615205-10615255	NH-A	brain:	n/a
10	chr9:10613328-10613378	Caco-2	colon:	n/a
11	chr9:10615205-10615255	GM12878	blood:	n/a
12	chr9:10615205-10615255	SK-N-SH_RA	brain:	n/a
13	chr9:10612700-10612750	HL-60	blood:	n/a
14	chr9:10371306-10371356	SK-N-MC	brain:	n/a
15	chr9:10613332-10613382	HCT-116	colon:	n/a
16	chr9:10613332-10613382	U87	brain:	n/a
17	chr9:10371306-10371356	PANC-1	pancreas:	n/a
18	chr9:10612700-10612750	GM12891	blood:	n/a
19	chr9:10613328-10613378	Hela-S3	cervix:	n/a
20	chr9:10371306-10371356	HRCEpiC	kidney:	n/a
21	chr9:10612700-10612750	BE2_C	brain:	n/a
22	chr9:10613328-10613378	AG04449	skin:	fetal
23	chr9:10612700-10612750	HPAEpiC	pulmonary alveolar:	n/a
24	chr9:10612700-10612750	A549	lung:	n/a
25	chr9:10371306-10371356	BJ	skin:	n/a
26	chr9:10613328-10613378	HCT-116	colon:	n/a
27	chr9:10615205-10615255	RPTEC	kidney:	n/a
28	chr9:10612700-10612750	HIPEpiC	eye:	n/a
29	chr9:10371306-10371356	HPAEpiC	pulmonary alveolar:	n/a
30	chr9:10613332-10613382	HCF	heart:	n/a
31	chr9:10613332-10613382	IMR90	lung:	fetal
32	chr9:10615205-10615255	HRCEpiC	kidney:	n/a
33	chr9:10612700-10612750	HAEpiC	amniotic membrane:	n/a
34	chr9:10613332-10613382	HEK293	kidney:	embryo
35	chr9:10371306-10371356	IMR90	lung:	fetal
36	chr9:10613328-10613378	PrEC	prostate:	n/a
37	chr9:10613328-10613378	HIPEpiC	eye:	n/a
38	chr9:10613332-10613382	AG04450	lung:	fetal
39	chr9:10371306-10371356	NHBE	bronchial:	n/a
40	chr9:10371306-10371356	ProgFib	skin:	n/a
41	chr9:10615205-10615255	LNCaP	prostate:	n/a
42	chr9:10613328-10613378	AG04450	lung:	fetal
43	chr9:10613332-10613382	SKMC	muscle:	n/a
44	chr9:10613332-10613382	K562	blood:	n/a
45	chr9:10612700-10612750	ECC-1	luminal epithelium:	n/a
46	chr9:10615205-10615255	MCF10A-Er-Src	breast:	n/a
47	chr9:10615205-10615255	HRE	kidney:	n/a
48	chr9:10612700-10612750	T-47D	breast:	n/a
49	chr9:10613332-10613382	GM12878	blood:	n/a
50	chr9:10613332-10613382	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:10855828..10856443-chr9:12329128..12329639,2	MCF-7	breast:
2	chr9:10365979..10366914-chr9:12329143..12329893,2	MCF-7	breast:
3	chr9:10455080..10457059-chr9:10458329..10460552,2	MCF-7	breast:
4	chr9:10800011..10802927-chr9:10803312..10805681,2	K562	blood:
5	chr9:10593948..10596046-chr9:10596166..10598402,2	MCF-7	breast:
6	chr17:59389836..59390496-chr9:10867919..10868419,2	MCF-7	breast:
7	chr9:10855589..10857004-chr9:11319142..11320476,6	MCF-7	breast:
8	chr9:10855837..10856356-chr9:11319207..11319905,2	MCF-7	breast:
9	chr2:145089819..145090468-chr9:10441934..10442434,2	NB4	blood:
10	chr9:10656522..10658673-chr9:10675612..10678102,2	K562	blood:
11	chr9:10366359..10367238-chr9:11319480..11320059,2	MCF-7	breast:
12	chr9:10455080..10457059-chr9:10458329..10460552,2	MCF-7	breast:
13	chr9:10855600..10856394-chr9:12425953..12426703,2	MCF-7	breast:
14	chr9:10799917..10802612-chr9:10809081..10811192,2	K562	blood:
15	chr9:10656522..10658673-chr9:10675612..10678102,2	K562	blood:
16	chr9:10593948..10596046-chr9:10596166..10598402,2	MCF-7	breast:
17	chr9:10697506..10699235-chr9:10701323..10703741,2	K562	blood:
18	chr9:10800011..10802927-chr9:10803312..10805681,2	K562	blood:
19	chr9:10799917..10802612-chr9:10809081..10811192,2	K562	blood:
20	chr9:10697506..10699235-chr9:10701323..10703741,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TYRP1-3	chr9:10616617-10616669	ENSG00000226717
2	lnc-TYRP1-3	chr9:10617861-10620420	ENSG00000226717.2
3	lnc-TYRP1-3	chr9:10613202-10613426	ENSG00000226717
4	lnc-TYRP1-5	chr9:10532145-10532411	NONHSAT130199
5	lnc-PTPRD-1	chr9:10631750-10631785	ENSG00000232035
6	lnc-TYRP1-3	chr9:10613186-10613426	NONHSAT130200
7	lnc-TYRP1-3	chr9:10617861-10618218	ENSG00000226717
8	lnc-TYRP1-3	chr9:10613202-10613426	ENSG00000226717.2
9	lnc-TYRP1-3	chr9:10616617-10616669	ENSG00000226717.2
10	lnc-TYRP1-3	chr9:10616617-10616671	NONHSAT130200
11	lnc-PTPRD-1	chr9:10632083-10632203	ENSG00000232035
12	lnc-TYRP1-3	chr9:10613237-10613443	NONHSAT130202
13	lnc-TYRP1-3	chr9:10616617-10616663	NONHSAT130202

Variant related genes	Relation type
ENSG00000226717	TF binding region
ENSG00000234360	TF binding region
PTPRD	TF binding region
ENSG00000232035	TF binding region
ENSG00000227138	TF binding region
IMP3P1	TF binding region
ENSG00000226717	CpG island
ENSG00000234360	CpG island
PTPRD	CpG island
ENSG00000232035	CpG island
ENSG00000227138	CpG island
IMP3P1	CpG island
ENSG00000121964	chromatin interactions
RPAP2	miRNA target sites
KIF5B	miRNA target sites

Extended variants
information (count: 6376 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:6376 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181200113	chr9:10336461-10336462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572482266	chr9:10336466-10336467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553980952	chr9:10336500-10336501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577236877	chr9:10336622-10336623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538660034	chr9:10336651-10336652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546065107	chr9:10336659-10336660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12001268	chr9:10336685-10336686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186746413	chr9:10336698-10336699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550232918	chr9:10336712-10336713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531729186	chr9:10336716-10336717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10123985	chr9:10336717-10336718	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs529309107	chr9:10336718-10336719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527748858	chr9:10336729-10336730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10123946	chr9:10336730-10336731	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs570691451	chr9:10336745-10336746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368363285	chr9:10336746-10336747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550443624	chr9:10336767-10336768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570204029	chr9:10336803-10336804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537854070	chr9:10336847-10336848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554232784	chr9:10336882-10336883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140423564	chr9:10336889-10336890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533849731	chr9:10336892-10336893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544184025	chr9:10336917-10336918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539949094	chr9:10336939-10336940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191539127	chr9:10336943-10336944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554042512	chr9:10336955-10336956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577103984	chr9:10336977-10336978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148845152	chr9:10337010-10337011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545827045	chr9:10337013-10337014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556426688	chr9:10337023-10337024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576216561	chr9:10337072-10337073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114296490	chr9:10337079-10337080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561720916	chr9:10337093-10337094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111684867	chr9:10337096-10337097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527809980	chr9:10337126-10337127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12380295	chr9:10337141-10337142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs564384554	chr9:10337181-10337182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574727924	chr9:10337196-10337197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533572490	chr9:10337213-10337214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73644418	chr9:10337250-10337251	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs117696286	chr9:10337286-10337287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144090088	chr9:10337287-10337288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548235833	chr9:10337299-10337300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568045952	chr9:10337331-10337332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182736262	chr9:10337345-10337346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185872776	chr9:10337400-10337401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570516104	chr9:10337404-10337405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145019362	chr9:10337442-10337443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148953852	chr9:10337465-10337466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143731073	chr9:10337482-10337483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

Disease	PMID	Source
abnormal development	18461090	CNVD
Disorders of sex development	21048976	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Lung cancer	20668451	CNVD
Schizophrenia	20838587	CNVD
Glioblastoma	18772890	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Barrett''s syndrome	19417022	CNVD
Breast cancer	22522925	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:10331600-10338200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr9:10331600-10338200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr9:10333400-10338000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr9:10333600-10339400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr9:10336200-10338000	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr9:10338000-10338200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr9:10338000-10339000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr9:10338200-10338400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr9:10338200-10338400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr9:10338200-10339000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr9:10338200-10339000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chr9:10338200-10339000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr9:10338200-10339000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr9:10338200-10339200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
15	chr9:10338200-10340400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
16	chr9:10338400-10338600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
17	chr9:10338600-10340400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:10339000-10339600	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr9:10339000-10339600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
20	chr9:10339000-10339600	Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr9:10339000-10339600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr9:10339000-10339800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr9:10339000-10339800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr9:10339200-10339400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr9:10339400-10340200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr9:10339600-10339800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr9:10339600-10340200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr9:10339600-10340200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr9:10339600-10340400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr9:10339800-10340000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
31	chr9:10339800-10340400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr9:10340000-10340400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
33	chr9:10340200-10340600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
34	chr9:10340200-10341400	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr9:10341400-10341600	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr9:10349200-10349600	Enhancers	Fetal Brain Male	brain
37	chr9:10351800-10352600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr9:10356600-10357800	Enhancers	Brain Germinal Matrix	brain
39	chr9:10357200-10357600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr9:10357200-10358000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr9:10357400-10357800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr9:10357400-10358200	Enhancers	Fetal Brain Female	brain
43	chr9:10357600-10358000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr9:10357800-10360200	Weak transcription	Brain Germinal Matrix	brain
45	chr9:10360200-10360600	Enhancers	Brain Germinal Matrix	brain
46	chr9:10360600-10364800	Weak transcription	Brain Germinal Matrix	brain
47	chr9:10364800-10365200	Enhancers	Brain Germinal Matrix	brain
48	chr9:10365200-10369600	Weak transcription	Brain Germinal Matrix	brain
49	chr9:10366000-10366400	Enhancers	Fetal Brain Male	brain
50	chr9:10369600-10370200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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