Variant report

Variant	nsv1044482
Chromosome Location	chr10:25889919-25977270
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	chr10:25971143-25971299	K562	blood:	n/a	n/a
2	ATF1	chr10:25927416-25927749	K562	blood:	n/a	n/a
3	ATF3	chr10:25971115-25971350	K562	blood:	n/a	n/a
4	BACH1	chr10:25971204-25971450	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr10:25971208-25971277	K562	blood:	n/a	n/a
6	BHLHE40	chr10:25927413-25927598	K562	blood:	n/a	n/a
7	BHLHE40	chr10:25950618-25950794	K562	blood:	n/a	n/a
8	CEBPB	chr10:25976286-25976552	HepG2	liver:	n/a	chr10:25976401-25976412
9	CEBPB	chr10:25972271-25972652	MCF-7	breast:	n/a	chr10:25972430-25972441 chr10:25972432-25972443 chr10:25972432-25972441 chr10:25972432-25972441 chr10:25972430-25972443 chr10:25972432-25972441 chr10:25972432-25972441
10	CEBPB	chr10:25918677-25918899	HepG2	liver:	n/a	chr10:25918834-25918845
11	CEBPB	chr10:25921186-25921318	A549	lung:	n/a	n/a
12	CEBPB	chr10:25971229-25971429	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr10:25947916-25948141	HepG2	liver:	n/a	chr10:25947999-25948010
14	CEBPB	chr10:25971079-25971381	A549	lung:	n/a	n/a
15	CEBPB	chr10:25922206-25922389	HepG2	liver:	n/a	chr10:25922262-25922273
16	CEBPB	chr10:25921236-25921282	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr10:25972313-25972537	K562	blood:	n/a	chr10:25972430-25972441 chr10:25972432-25972443 chr10:25972432-25972441 chr10:25972432-25972441 chr10:25972430-25972443 chr10:25972432-25972441 chr10:25972432-25972441
18	CEBPB	chr10:25976407-25976463	K562	blood:	n/a	n/a
19	CEBPB	chr10:25976378-25976548	H1-hESC	embryonic stem cell:	n/a	chr10:25976401-25976412
20	CEBPB	chr10:25918778-25918905	K562	blood:	n/a	chr10:25918834-25918845
21	CEBPB	chr10:25951673-25951812	K562	blood:	n/a	n/a
22	CEBPB	chr10:25922077-25922432	A549	lung:	n/a	chr10:25922262-25922273
23	CEBPB	chr10:25906942-25906995	A549	lung:	n/a	n/a
24	CEBPB	chr10:25960404-25960604	HepG2	liver:	n/a	chr10:25960498-25960509
25	CEBPB	chr10:25922118-25922397	IMR90	lung:	n/a	chr10:25922262-25922273
26	CEBPB	chr10:25972271-25972611	A549	lung:	n/a	chr10:25972430-25972441 chr10:25972432-25972443 chr10:25972432-25972441 chr10:25972432-25972441 chr10:25972430-25972443 chr10:25972432-25972441 chr10:25972432-25972441
27	CEBPB	chr10:25971109-25971300	K562	blood:	n/a	n/a
28	CEBPB	chr10:25941048-25941204	A549	lung:	n/a	chr10:25941143-25941156
29	CEBPB	chr10:25972261-25972617	HepG2	liver:	n/a	chr10:25972430-25972441 chr10:25972432-25972443 chr10:25972432-25972441 chr10:25972432-25972441 chr10:25972430-25972443 chr10:25972432-25972441 chr10:25972432-25972441
30	CEBPB	chr10:25922084-25922423	MCF-7	breast:	n/a	chr10:25922262-25922273
31	CEBPB	chr10:25922076-25922399	K562	blood:	n/a	chr10:25922262-25922273
32	CHD2	chr10:25918801-25918808	HepG2	liver:	n/a	n/a
33	CTCF	chr10:25927500-25927552	MCF-7	breast:	n/a	n/a
34	CTCF	chr10:25928680-25928830	HVMF	connective:	n/a	chr10:25928763-25928781 chr10:25928765-25928786
35	CTCF	chr10:25928760-25928910	HVMF	connective:	n/a	chr10:25928763-25928781 chr10:25928765-25928786
36	CTCF	chr10:25971160-25971361	K562	blood:	n/a	chr10:25971261-25971279 chr10:25971256-25971277
37	CTCF	chr10:25927441-25927648	A549	lung:	n/a	n/a
38	CTCF	chr10:25971127-25971398	A549	lung:	n/a	chr10:25971261-25971279 chr10:25971256-25971277
39	CTCF	chr10:25927400-25927550	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr10:25927480-25927630	GM06990	blood:	n/a	n/a
41	CTCF	chr10:25971100-25971250	MCF-7	breast:	n/a	n/a
42	CTCF	chr10:25928680-25928830	MCF-7	breast:	n/a	chr10:25928763-25928781 chr10:25928765-25928786
43	CTCF	chr10:25909186-25909238	MCF-7	breast:	n/a	n/a
44	CTCF	chr10:25971680-25971830	K562	blood:	n/a	n/a
45	CTCF	chr10:25971075-25972017	SK-N-SH	brain:	n/a	chr10:25971261-25971279 chr10:25971256-25971277
46	CTCF	chr10:25971640-25971790	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr10:25928640-25928790	HRE	kidney:	n/a	chr10:25928763-25928781 chr10:25928765-25928786
48	CTCF	chr10:25971640-25971790	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr10:25928640-25928790	HRPEpiC	eye:	n/a	chr10:25928763-25928781 chr10:25928765-25928786
50	CTCF	chr10:25971180-25971330	Hela-S3	cervix:	n/a	chr10:25971261-25971279 chr10:25971256-25971277

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:25890685-25890735	Hela-S3	cervix:	n/a
2	chr10:25890685-25890735	SKMC	muscle:	n/a
3	chr10:25890685-25890735	ECC-1	luminal epithelium:	n/a
4	chr10:25890685-25890735	ProgFib	skin:	n/a
5	chr10:25940372-25940422	SK-N-SH_RA	brain:	n/a
6	chr10:25940372-25940422	LNCaP	prostate:	n/a
7	chr10:25940372-25940422	HEK293	kidney:	embryo
8	chr10:25890685-25890735	HIPEpiC	eye:	n/a
9	chr10:25940372-25940422	Hepatocyte	liver:	n/a
10	chr10:25940372-25940422	BE2_C	brain:	n/a
11	chr10:25890685-25890735	IMR90	lung:	fetal
12	chr10:25890685-25890735	T-47D	breast:	n/a
13	chr10:25890685-25890735	HCPEpiC	choroid plexus:	n/a
14	chr10:25890685-25890735	SAEC	small airway:	n/a
15	chr10:25890685-25890735	AG04450	lung:	fetal
16	chr10:25940372-25940422	SK-N-MC	brain:	n/a
17	chr10:25890685-25890735	HRCEpiC	kidney:	n/a
18	chr10:25890685-25890735	HEEpiC	esophagus:	n/a
19	chr10:25890685-25890735	K562	blood:	n/a
20	chr10:25940372-25940422	HCPEpiC	choroid plexus:	n/a
21	chr10:25890685-25890735	GM19239	blood:	n/a
22	chr10:25940372-25940422	MCF10A-Er-Src	breast:	n/a
23	chr10:25940372-25940422	HRCEpiC	kidney:	n/a
24	chr10:25890685-25890735	HCM	heart:	n/a
25	chr10:25890685-25890735	RPTEC	kidney:	n/a
26	chr10:25940372-25940422	HUVEC	blood vessel:	n/a
27	chr10:25940372-25940422	Caco-2	colon:	n/a
28	chr10:25890685-25890735	AG04449	skin:	fetal
29	chr10:25940372-25940422	SK-N-SH	brain:	n/a
30	chr10:25890685-25890735	Caco-2	colon:	n/a
31	chr10:25890685-25890735	A549	lung:	n/a
32	chr10:25940372-25940422	ProgFib	skin:	n/a
33	chr10:25890685-25890735	HMEC	breast:	n/a
34	chr10:25940372-25940422	HEEpiC	esophagus:	n/a
35	chr10:25940372-25940422	ovcar-3	ovarian:	n/a
36	chr10:25940372-25940422	SKMC	muscle:	n/a
37	chr10:25940372-25940422	PrEC	prostate:	n/a
38	chr10:25890685-25890735	NHDF-neo	bronchial:	n/a
39	chr10:25940372-25940422	IMR90	lung:	fetal
40	chr10:25940372-25940422	HNPCEpiC	eye:	n/a
41	chr10:25890685-25890735	SK-N-SH_RA	brain:	n/a
42	chr10:25940372-25940422	Hela-S3	cervix:	n/a
43	chr10:25890685-25890735	MCF10A-Er-Src	breast:	n/a
44	chr10:25890685-25890735	HNPCEpiC	eye:	n/a
45	chr10:25940372-25940422	HL-60	blood:	n/a
46	chr10:25940372-25940422	GM12878	blood:	n/a
47	chr10:25890685-25890735	LNCaP	prostate:	n/a
48	chr10:25940372-25940422	HCM	heart:	n/a
49	chr10:25890685-25890735	PFSK-1	brain:	n/a
50	chr10:25890685-25890735	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:25369667..25370602-chr10:25971300..25972009,2	MCF-7	breast:
2	chr10:25928776..25929368-chr10:25970405..25971183,2	MCF-7	breast:
3	chr10:25892005..25894948-chr10:25981825..25984468,2	MCF-7	breast:
4	chr10:25811568..25812567-chr10:25927033..25928066,5	MCF-7	breast:
5	chr10:25968329..25970638-chr10:25971632..25973181,2	MCF-7	breast:
6	chr10:25948946..25949616-chr10:25971487..25972147,2	MCF-7	breast:
7	chr10:25928319..25929283-chr10:25971291..25972141,2	MCF-7	breast:
8	chr10:25928152..25930973-chr10:25933885..25936104,2	K562	blood:
9	chr10:25928319..25929283-chr10:25971291..25972141,2	MCF-7	breast:
10	chr10:25928110..25928805-chr10:25971297..25972199,3	MCF-7	breast:
11	chr10:25315571..25316075-chr10:25927297..25928010,2	MCF-7	breast:
12	chr10:25928776..25929368-chr10:25970405..25971183,2	MCF-7	breast:
13	chr10:25844764..25845310-chr10:25927517..25928042,2	MCF-7	breast:
14	chr10:25955331..25955925-chr10:25971196..25971887,2	MCF-7	breast:
15	chr10:25968329..25970638-chr10:25971632..25973181,2	MCF-7	breast:
16	chr10:25515615..25516464-chr10:25970963..25971954,2	MCF-7	breast:
17	chr10:25401691..25402355-chr10:25927164..25928071,3	MCF-7	breast:
18	chr10:25928110..25928805-chr10:25971297..25972199,3	MCF-7	breast:
19	chr10:25401853..25402699-chr10:25971177..25972164,3	MCF-7	breast:
20	chr10:25955331..25955925-chr10:25971196..25971887,2	MCF-7	breast:
21	chr10:25928285..25928817-chr10:26001789..26002696,2	MCF-7	breast:
22	chr10:25928152..25930973-chr10:25933885..25936104,2	K562	blood:
23	chr10:25948946..25949616-chr10:25971487..25972147,2	MCF-7	breast:
24	chr10:25811744..25812457-chr10:25926562..25927514,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR158-2	chr10:25941797-25941971	NONHSAT011809
2	lnc-GPR158-2	chr10:25957145-25957259	NR_108069
3	lnc-GPR158-2	chr10:25975301-25975337	NONHSAT011809
4	lnc-GPR158-2	chr10:25941798-25941971	NR_108067
5	lnc-GPR158-2	chr10:25971450-25972314	NR_108069
6	lnc-GPR158-2	chr10:25941798-25941971	NR_108069
7	lnc-GPR158-2	chr10:25940641-25940728	NR_108069
8	lnc-GPR158-2	chr10:25940661-25940728	NONHSAT011809
9	lnc-GPR158-2	chr10:25940662-25940728	XLOC_008416
10	lnc-GPR158-2	chr10:25975302-25975337	XLOC_008416
11	lnc-GPR158-2	chr10:25940641-25940728	NR_108067
12	lnc-GPR158-2	chr10:25974778-25974900	NONHSAT011809
13	lnc-GPR158-2	chr10:25940641-25940728	NONHSAT011808
14	lnc-GPR158-2	chr10:25941798-25941971	XLOC_008416
15	lnc-ENKUR-7	chr10:25936499-25937033	NONHSAT011807
16	lnc-GPR158-2	chr10:25974779-25974900	XLOC_008416

Variant related genes	Relation type
HIRAP1	TF binding region
GPN3P1	TF binding region
HIRAP1	CpG island
GPN3P1	CpG island
ENSG00000231422	chromatin interactions
GNAS	miRNA target sites
GNB4	miRNA target sites
GNB1	miRNA target sites

Extended variants
information (count: 1380 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:1380 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16926172	chr10:25889980-25889981	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555387541	chr10:25889991-25889992	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566535394	chr10:25890004-25890005	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193021340	chr10:25890051-25890052	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201025238	chr10:25890056-25890057	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371514966	chr10:25890084-25890085	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185362953	chr10:25890113-25890114	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571224446	chr10:25890167-25890168	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188644568	chr10:25890207-25890208	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577933061	chr10:25890221-25890222	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145766339	chr10:25890227-25890228	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181388126	chr10:25890237-25890238	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116313012	chr10:25890292-25890293	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs3802512	chr10:25890341-25890342	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs367865466	chr10:25890448-25890449	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79093790	chr10:25890455-25890456	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185228403	chr10:25890489-25890490	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146614407	chr10:25890511-25890512	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536007524	chr10:25890531-25890532	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547707757	chr10:25890561-25890562	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554682247	chr10:25890563-25890564	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533737469	chr10:25890565-25890566	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140279175	chr10:25890621-25890622	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs41279904	chr10:25890686-25890687	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547220637	chr10:25890698-25890699	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371847691	chr10:25890724-25890725	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570147614	chr10:25890761-25890762	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs137898813	chr10:25890817-25890818	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573510347	chr10:25890840-25890841	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs3758451	chr10:25890858-25890859	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369676404	chr10:25890864-25890865	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188176593	chr10:25890886-25890887	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534570957	chr10:25890921-25890922	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149445878	chr10:25890943-25890944	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540843002	chr10:25890944-25890945	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559164301	chr10:25890962-25890963	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs578024007	chr10:25890981-25890982	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543327298	chr10:25890983-25890984	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7894621	chr10:25890984-25890985	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs573716075	chr10:25890988-25890989	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542314661	chr10:25890999-25891000	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3834404	chr10:25891001-25891002	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs397817785	chr10:25891003-25891004	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143034029	chr10:25891048-25891049	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527697292	chr10:25891070-25891071	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541062879	chr10:25891073-25891074	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564118721	chr10:25891080-25891081	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533729215	chr10:25891081-25891082	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs180892724	chr10:25891100-25891101	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138895561	chr10:25891169-25891170	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:44)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Glioblastoma multiforme	21525872	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25884800-25892200	Strong transcription	Cortex derived primary cultured neurospheres	brain
2	chr10:25888200-25892800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr10:25889600-25890000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr10:25891200-25894000	Enhancers	Fetal Kidney	kidney
5	chr10:25891800-25892000	Enhancers	Brain Anterior Caudate	brain
6	chr10:25892200-25893800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr10:25893400-25893800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr10:25893800-25894200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr10:25894000-25894800	Weak transcription	Fetal Kidney	kidney
10	chr10:25894800-25895000	Enhancers	Fetal Kidney	kidney
11	chr10:25904600-25906000	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr10:25904800-25905200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr10:25904800-25905200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr10:25904800-25906200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr10:25907600-25908600	Enhancers	Adipose Nuclei	Adipose
16	chr10:25908200-25909400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr10:25908400-25908800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:25916200-25916400	Enhancers	Adipose Nuclei	Adipose
19	chr10:25916200-25916800	Enhancers	Fetal Brain Male	brain
20	chr10:25916400-25916600	Flanking Active TSS	Adipose Nuclei	Adipose
21	chr10:25916400-25917000	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr10:25916600-25916800	Enhancers	Adipose Nuclei	Adipose
23	chr10:25916800-25917000	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr10:25917000-25919600	Weak transcription	Adipose Nuclei	Adipose
25	chr10:25919600-25919800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr10:25919600-25922400	Enhancers	Adipose Nuclei	Adipose
27	chr10:25919800-25921200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr10:25921200-25922400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr10:25927600-25928000	Active TSS	K562	blood
30	chr10:25939400-25939800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr10:25940200-25940800	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr10:25950600-25950800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr10:25950600-25951000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr10:25950800-25951400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr10:25951400-25952400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr10:25952400-25952800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr10:25955000-25955400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr10:25955000-25955400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr10:25955000-25955600	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr10:25955200-25955400	Enhancers	Psoas Muscle	Psoas
41	chr10:25962800-25993600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr10:25964000-25964400	Active TSS	Brain Anterior Caudate	brain
43	chr10:25967600-25968000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr10:25968000-25970400	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr10:25968800-25969000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr10:25970000-25970200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr10:25970200-25970600	Enhancers	H9 Cell Line	embryonic stem cell
48	chr10:25970200-25970600	Enhancers	Fetal Heart	heart
49	chr10:25970400-25971200	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr10:25970400-25971200	Enhancers	Skeletal Muscle Female	skeletal muscle

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