Variant report

Variant	nsv550224
Chromosome Location	chr10:25335854-25385858
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1022)
CpG islands
(count:183)
Chromatin interactive
region (count:68)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1022 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:25349028-25349245	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:25351365-25351716	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:25367422-25368533	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:25369916-25370267	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:25371398-25372030	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:25336743-25337086	K562	blood:	n/a	n/a
7	ARID3A	chr10:25349037-25349247	K562	blood:	n/a	n/a
8	ARID3A	chr10:25369889-25370231	K562	blood:	n/a	n/a
9	ARID3A	chr10:25350560-25351729	K562	blood:	n/a	n/a
10	ATF1	chr10:25365656-25366064	K562	blood:	n/a	n/a
11	ATF1	chr10:25357320-25357627	K562	blood:	n/a	n/a
12	ATF1	chr10:25350728-25351739	K562	blood:	n/a	n/a
13	ATF1	chr10:25336797-25337204	K562	blood:	n/a	n/a
14	ATF2	chr10:25357189-25357600	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr10:25348898-25349344	K562	blood:	n/a	n/a
16	ATF3	chr10:25351381-25351746	K562	blood:	n/a	n/a
17	ATF3	chr10:25351288-25351785	K562	blood:	n/a	n/a
18	ATF3	chr10:25349000-25349280	K562	blood:	n/a	n/a
19	BACH1	chr10:25370118-25370135	K562	blood:	n/a	n/a
20	BACH1	chr10:25350626-25351684	K562	blood:	n/a	n/a
21	BATF	chr10:25352365-25352714	GM12878	blood:	n/a	chr10:25352563-25352574
22	BATF	chr10:25357156-25357476	GM12878	blood:	n/a	chr10:25357432-25357445 chr10:25357318-25357327
23	BHLHE40	chr10:25369837-25370263	K562	blood:	n/a	n/a
24	BHLHE40	chr10:25369836-25370202	GM12878	blood:	n/a	n/a
25	BHLHE40	chr10:25350527-25351837	K562	blood:	n/a	n/a
26	BHLHE40	chr10:25349186-25349285	K562	blood:	n/a	n/a
27	BHLHE40	chr10:25351356-25351683	A549	lung:	n/a	n/a
28	BHLHE40	chr10:25336920-25337167	K562	blood:	n/a	n/a
29	BHLHE40	chr10:25351006-25351743	HepG2	liver:	n/a	n/a
30	BHLHE40	chr10:25365610-25366191	K562	blood:	n/a	n/a
31	BRCA1	chr10:25348995-25349471	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr10:25351123-25351936	HCT-116	colon:	n/a	n/a
33	CBX3	chr10:25383573-25383835	K562	blood:	n/a	n/a
34	CBX3	chr10:25339262-25339650	K562	blood:	n/a	n/a
35	CBX3	chr10:25369779-25370295	K562	blood:	n/a	n/a
36	CBX3	chr10:25383526-25383825	K562	blood:	n/a	n/a
37	CBX3	chr10:25350677-25351934	K562	blood:	n/a	n/a
38	CCNT2	chr10:25336793-25337253	K562	blood:	n/a	n/a
39	CCNT2	chr10:25350662-25351072	K562	blood:	n/a	n/a
40	CCNT2	chr10:25370016-25370363	K562	blood:	n/a	n/a
41	CCNT2	chr10:25351359-25351787	K562	blood:	n/a	chr10:25351586-25351606
42	CEBPB	chr10:25350723-25351872	A549	lung:	n/a	n/a
43	CEBPB	chr10:25348936-25349386	ECC-1	luminal epithelium:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
44	CEBPB	chr10:25367651-25368348	A549	lung:	n/a	n/a
45	CEBPB	chr10:25347934-25348298	K562	blood:	n/a	chr10:25348117-25348128
46	CEBPB	chr10:25367655-25368221	HepG2	liver:	n/a	n/a
47	CEBPB	chr10:25367661-25367861	K562	blood:	n/a	n/a
48	CEBPB	chr10:25349121-25349211	H1-hESC	embryonic stem cell:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
49	CEBPB	chr10:25349024-25349224	K562	blood:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
50	CEBPB	chr10:25348924-25349394	K562	blood:	n/a	chr10:25349162-25349173 chr10:25349161-25349174

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:25357368-25357418	ProgFib	skin:	n/a
2	chr10:25357368-25357418	BE2_C	brain:	n/a
3	chr10:25371488-25371538	NHDF-neo	bronchial:	n/a
4	chr10:25350802-25350852	A549	lung:	n/a
5	chr10:25371488-25371538	PrEC	prostate:	n/a
6	chr10:25357368-25357418	HCT-116	colon:	n/a
7	chr10:25371488-25371538	NHBE	bronchial:	n/a
8	chr10:25350802-25350852	RPTEC	kidney:	n/a
9	chr10:25357368-25357418	AoSMC	blood vessel:	n/a
10	chr10:25357368-25357418	HRPEpiC	eye:	n/a
11	chr10:25350802-25350852	PFSK-1	brain:	n/a
12	chr10:25350802-25350852	NT2-D1	testis:	n/a
13	chr10:25357368-25357418	NHDF-neo	bronchial:	n/a
14	chr10:25350802-25350852	HIPEpiC	eye:	n/a
15	chr10:25371488-25371538	HNPCEpiC	eye:	n/a
16	chr10:25371488-25371538	AG09309	skin:	n/a
17	chr10:25371488-25371538	MCF10A-Er-Src	breast:	n/a
18	chr10:25357368-25357418	ovcar-3	ovarian:	n/a
19	chr10:25350802-25350852	HCT-116	colon:	n/a
20	chr10:25357368-25357418	HEK293	kidney:	embryo
21	chr10:25371488-25371538	GM19239	blood:	n/a
22	chr10:25371488-25371538	SKMC	muscle:	n/a
23	chr10:25350802-25350852	AG04449	skin:	fetal
24	chr10:25350802-25350852	AG10803	skin:	n/a
25	chr10:25371488-25371538	HepG2	liver:	n/a
26	chr10:25350802-25350852	NH-A	brain:	n/a
27	chr10:25357368-25357418	NH-A	brain:	n/a
28	chr10:25350802-25350852	SK-N-MC	brain:	n/a
29	chr10:25350802-25350852	PANC-1	pancreas:	n/a
30	chr10:25371488-25371538	AoSMC	blood vessel:	n/a
31	chr10:25371488-25371538	AG04449	skin:	fetal
32	chr10:25350802-25350852	MCF10A-Er-Src	breast:	n/a
33	chr10:25357368-25357418	Caco-2	colon:	n/a
34	chr10:25357368-25357418	AG09309	skin:	n/a
35	chr10:25350802-25350852	K562	blood:	n/a
36	chr10:25350802-25350852	HRCEpiC	kidney:	n/a
37	chr10:25350802-25350852	AG09309	skin:	n/a
38	chr10:25371488-25371538	SAEC	small airway:	n/a
39	chr10:25371488-25371538	GM12891	blood:	n/a
40	chr10:25371488-25371538	SK-N-SH_RA	brain:	n/a
41	chr10:25350802-25350852	Hela-S3	cervix:	n/a
42	chr10:25357368-25357418	LNCaP	prostate:	n/a
43	chr10:25371488-25371538	U87	brain:	n/a
44	chr10:25371488-25371538	HAEpiC	amniotic membrane:	n/a
45	chr10:25357368-25357418	NT2-D1	testis:	n/a
46	chr10:25357368-25357418	ECC-1	luminal epithelium:	n/a
47	chr10:25350802-25350852	HRPEpiC	eye:	n/a
48	chr10:25371488-25371538	RPTEC	kidney:	n/a
49	chr10:25371488-25371538	SK-N-MC	brain:	n/a
50	chr10:25357368-25357418	MCF10A-Er-Src	breast:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:25307575..25310244-chr10:25349571..25352250,2	MCF-7	breast:
2	chr10:25340489..25343849-chr10:25349173..25351054,3	K562	blood:
3	chr10:25345062..25348953-chr10:25349936..25353027,4	K562	blood:
4	chr10:25350138..25352241-chr10:25355108..25357944,2	MCF-7	breast:
5	chr10:24931513..24932500-chr10:25369531..25370644,4	K562	blood:
6	chr10:25344134..25348116-chr10:25349607..25352644,3	MCF-7	breast:
7	chr10:25304278..25309002-chr10:25368191..25372754,5	K562	blood:
8	chr10:24906446..24907157-chr10:25369477..25370117,2	MCF-7	breast:
9	chr10:25350226..25351753-chr10:25385209..25386887,2	K562	blood:
10	chr10:25315371..25316092-chr10:25369588..25370596,3	K562	blood:
11	chr10:25305403..25308444-chr10:25369519..25373361,4	MCF-7	breast:
12	chr10:25239858..25242854-chr10:25350195..25352504,2	K562	blood:
13	chr10:25344528..25346562-chr10:25350767..25353027,3	K562	blood:
14	chr10:25334592..25336921-chr10:25350299..25353033,2	K562	blood:
15	chr10:25304592..25306407-chr10:25373363..25375162,2	MCF-7	breast:
16	chr10:25344134..25348116-chr10:25349607..25352644,3	MCF-7	breast:
17	chr10:25338585..25341464-chr10:25343228..25345616,2	K562	blood:
18	chr10:25362224..25363937-chr10:25363978..25365901,2	K562	blood:
19	chr10:25374556..25376666-chr10:25584263..25586779,2	K562	blood:
20	chr10:25352997..25355657-chr10:25355970..25357954,2	K562	blood:
21	chr10:25343371..25346299-chr10:25346762..25349074,2	K562	blood:
22	chr10:25356543..25358700-chr10:25359934..25363281,3	K562	blood:
23	chr10:25384858..25387044-chr10:25387748..25390557,2	K562	blood:
24	chr10:25338585..25341464-chr10:25343228..25345616,2	K562	blood:
25	chr10:25329304..25331383-chr10:25344755..25346865,2	K562	blood:
26	chr10:25079435..25081057-chr10:25368417..25370064,2	K562	blood:
27	chr10:25349510..25351855-chr10:25352161..25354821,2	MCF-7	breast:
28	chr10:25357593..25359343-chr10:25368933..25370472,2	K562	blood:
29	chr10:25304955..25307281-chr10:25348708..25354586,7	MCF-7	breast:
30	chr10:25356543..25358700-chr10:25359934..25363281,3	K562	blood:
31	chr10:25303695..25307800-chr10:25367762..25370827,4	K562	blood:
32	chr10:25239725..25241588-chr10:25374362..25376183,2	K562	blood:
33	chr10:25308766..25310925-chr10:25358161..25359867,2	K562	blood:
34	chr10:25011013..25013160-chr10:25345003..25347658,2	K562	blood:
35	chr10:25357593..25359343-chr10:25368933..25370472,2	K562	blood:
36	chr10:25372240..25374997-chr10:25377094..25379582,2	K562	blood:
37	chr10:25350138..25352241-chr10:25355108..25357944,2	MCF-7	breast:
38	chr10:25350226..25351753-chr10:25385209..25386887,2	K562	blood:
39	chr10:25331770..25334410-chr10:25337603..25339717,2	MCF-7	breast:
40	chr10:25369667..25370602-chr10:25971300..25972009,2	MCF-7	breast:
41	chr10:25016699..25017443-chr10:25369664..25370556,4	K562	blood:
42	chr10:25334592..25336921-chr10:25350299..25353033,2	K562	blood:
43	chr10:25304800..25307444-chr10:25366624..25371121,4	MCF-7	breast:
44	chr10:24854730..24857189-chr10:25359782..25362279,2	K562	blood:
45	chr10:25369500..25372471-chr10:25373482..25376338,3	MCF-7	breast:
46	chr10:25344528..25346562-chr10:25350767..25353027,3	K562	blood:
47	chr10:25303827..25307133-chr10:25349437..25354097,8	K562	blood:
48	chr10:25303827..25307969-chr10:25351029..25354599,5	K562	blood:
49	chr10:25175280..25178160-chr10:25364501..25366305,2	K562	blood:
50	chr10:25362224..25363937-chr10:25363978..25365901,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000266069	TF binding region
ENSG00000266069	CpG island
ENSG00000099256	chromatin interactions
ENSG00000151023	chromatin interactions
ENSG00000107863	chromatin interactions
ENSG00000185875	chromatin interactions
ENSG00000273107	chromatin interactions

Extended variants
information (count: 1709 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12251969	chr10:25335854-25335855	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535776673	chr10:25335935-25335936	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs557049488	chr10:25335966-25335967	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs577274974	chr10:25336031-25336032	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs373805493	chr10:25336049-25336050	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs150654993	chr10:25336086-25336087	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs565991571	chr10:25336115-25336116	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs532879623	chr10:25336135-25336136	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs577186846	chr10:25336193-25336194	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs566637631	chr10:25336201-25336202	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs535337863	chr10:25336235-25336236	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs138969907	chr10:25336236-25336237	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs549249831	chr10:25336268-25336269	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs190736179	chr10:25336273-25336274	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs4749000	chr10:25336332-25336333	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs113815802	chr10:25336348-25336349	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs115637195	chr10:25336385-25336386	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs528348021	chr10:25336389-25336390	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs142449056	chr10:25336396-25336397	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs145984297	chr10:25336413-25336414	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs59189661	chr10:25336419-25336420	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs550228081	chr10:25336445-25336446	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs74122936	chr10:25336461-25336462	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs529453530	chr10:25336467-25336468	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs549117915	chr10:25336496-25336497	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs566051461	chr10:25336544-25336545	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs534949455	chr10:25336570-25336571	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs578117059	chr10:25336598-25336599	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs534281280	chr10:25336636-25336637	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs557502788	chr10:25336690-25336691	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs571201170	chr10:25336771-25336772	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs528517472	chr10:25336773-25336774	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs183248000	chr10:25336785-25336786	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs547014198	chr10:25336805-25336806	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs57642444	chr10:25336856-25336857	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs60363457	chr10:25336907-25336908	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs114722762	chr10:25336942-25336943	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs573191515	chr10:25336956-25336957	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs144452425	chr10:25336968-25336969	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs545274815	chr10:25336973-25336974	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564355287	chr10:25336993-25336994	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs533360396	chr10:25337001-25337002	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs372688368	chr10:25337125-25337126	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs116714905	chr10:25337149-25337150	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs563442854	chr10:25337157-25337158	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs200929859	chr10:25337194-25337195	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs549179218	chr10:25337209-25337210	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs559504573	chr10:25337265-25337266	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs80169908	chr10:25337289-25337290	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs552047028	chr10:25337342-25337343	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:42)

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
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25326600-25336200	Weak transcription	Fetal Intestine Small	intestine
2	chr10:25335400-25337000	Enhancers	K562	blood
3	chr10:25335600-25336000	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr10:25335600-25336400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:25335600-25336400	Enhancers	Fetal Brain Female	brain
6	chr10:25335600-25337200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr10:25335600-25338000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr10:25336000-25336800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr10:25336000-25337800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr10:25336000-25337800	Enhancers	HMEC	breast
11	chr10:25336000-25338000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:25336000-25338000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr10:25336200-25336600	Enhancers	Brain Angular Gyrus	brain
14	chr10:25336200-25337200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr10:25336200-25337400	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr10:25336200-25337600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr10:25336200-25337600	Enhancers	Osteobl	bone
18	chr10:25336200-25337800	Enhancers	NHEK	skin
19	chr10:25336200-25338200	Enhancers	Fetal Intestine Small	intestine
20	chr10:25336400-25336800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr10:25336400-25336800	Enhancers	Ovary	ovary
22	chr10:25336400-25336800	Enhancers	NH-A	brain
23	chr10:25336400-25337000	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr10:25336400-25337200	Enhancers	Adipose Nuclei	Adipose
25	chr10:25336400-25337400	Weak transcription	Fetal Brain Female	brain
26	chr10:25336400-25337600	Enhancers	HSMM	muscle
27	chr10:25336400-25338200	Enhancers	Brain Anterior Caudate	brain
28	chr10:25336600-25337200	Enhancers	Primary hematopoietic stem cells	blood
29	chr10:25336600-25337200	Enhancers	Brain Hippocampus Middle	brain
30	chr10:25336600-25337400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr10:25336600-25338000	Enhancers	HSMMtube	muscle
32	chr10:25336800-25337200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr10:25336800-25337200	Enhancers	Muscle Satellite Cultured Cells	--
34	chr10:25336800-25337200	Weak transcription	Ovary	ovary
35	chr10:25337000-25337400	Flanking Active TSS	K562	blood
36	chr10:25337000-25337400	Enhancers	NH-A	brain
37	chr10:25337000-25338000	Enhancers	Brain Substantia Nigra	brain
38	chr10:25337000-25338200	Enhancers	Fetal Intestine Large	intestine
39	chr10:25337200-25337400	Enhancers	Placenta Amnion	Placenta Amnion
40	chr10:25337200-25337600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr10:25337200-25337600	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
42	chr10:25337200-25337800	Enhancers	Ovary	ovary
43	chr10:25337200-25338200	Enhancers	Duodenum Mucosa	Duodenum
44	chr10:25337400-25337600	Enhancers	Fetal Brain Female	brain
45	chr10:25337400-25337600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
46	chr10:25337400-25338200	Enhancers	K562	blood
47	chr10:25337400-25348200	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr10:25337600-25337800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr10:25337600-25337800	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr10:25337600-25337800	Bivalent Enhancer	Osteobl	bone

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