Variant report

Variant	nsv10063
Chromosome Location	chr2:86940988-87084360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1986)
CpG islands
(count:3602)
Chromatin interactive
region (count:49)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:1986 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:87035044-87036047	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:87062188-87062388	K562	blood:	n/a	n/a
3	ARID3A	chr2:87035534-87035903	K562	blood:	n/a	n/a
4	ARID3A	chr2:86975391-86975453	K562	blood:	n/a	n/a
5	ATF1	chr2:86975197-86975467	K562	blood:	n/a	n/a
6	ATF1	chr2:87064398-87064705	K562	blood:	n/a	n/a
7	ATF1	chr2:86991865-86992162	K562	blood:	n/a	n/a
8	ATF1	chr2:87008495-87009694	K562	blood:	n/a	n/a
9	ATF1	chr2:87046445-87047301	K562	blood:	n/a	n/a
10	ATF1	chr2:87056647-87057105	K562	blood:	n/a	n/a
11	ATF2	chr2:87011024-87011666	GM12878	blood:	n/a	n/a
12	ATF2	chr2:87011061-87011568	GM12878	blood:	n/a	n/a
13	ATF3	chr2:87035386-87035875	A549	lung:	n/a	n/a
14	ATF3	chr2:87035407-87035871	A549	lung:	n/a	n/a
15	ATF3	chr2:86975156-86975457	K562	blood:	n/a	n/a
16	BACH1	chr2:87035036-87035962	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:87017296-87017709	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr2:87059079-87059327	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr2:87013427-87013719	K562	blood:	n/a	n/a
20	BATF	chr2:87011135-87011439	GM12878	blood:	n/a	n/a
21	BATF	chr2:87067239-87067491	GM12878	blood:	n/a	n/a
22	BATF	chr2:86948418-86948653	GM12878	blood:	n/a	n/a
23	BATF	chr2:86947090-86947599	GM12878	blood:	n/a	n/a
24	BATF	chr2:86946770-86947017	GM12878	blood:	n/a	n/a
25	BATF	chr2:86951503-86951728	GM12878	blood:	n/a	n/a
26	BATF	chr2:87011070-87011355	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:86946951-86947623	GM12878	blood:	n/a	chr2:86947091-86947100
28	BCL11A	chr2:87067184-87067494	GM12878	blood:	n/a	n/a
29	BCL11A	chr2:87067240-87067563	GM12878	blood:	n/a	n/a
30	BCL11A	chr2:86946482-86946653	GM12878	blood:	n/a	chr2:86946486-86946499
31	BCL11A	chr2:86947065-86947616	GM12878	blood:	n/a	chr2:86947091-86947100
32	BCLAF1	chr2:87035432-87035863	GM12878	blood:	n/a	chr2:87035834-87035847
33	BCLAF1	chr2:87011028-87011445	GM12878	blood:	n/a	n/a
34	BCLAF1	chr2:87035400-87035852	GM12878	blood:	n/a	chr2:87035834-87035847
35	BHLHE40	chr2:87012885-87013701	K562	blood:	n/a	n/a
36	BHLHE40	chr2:86946920-86947557	K562	blood:	n/a	n/a
37	BHLHE40	chr2:86947266-86947434	A549	lung:	n/a	n/a
38	BHLHE40	chr2:87035462-87036013	GM12878	blood:	n/a	n/a
39	BHLHE40	chr2:86946787-86947475	GM12878	blood:	n/a	n/a
40	BHLHE40	chr2:87005690-87005862	K562	blood:	n/a	n/a
41	BHLHE40	chr2:87064342-87064452	K562	blood:	n/a	n/a
42	BHLHE40	chr2:87034191-87035985	HepG2	liver:	n/a	n/a
43	BHLHE40	chr2:87007042-87007239	K562	blood:	n/a	n/a
44	BHLHE40	chr2:87056607-87056890	K562	blood:	n/a	n/a
45	BHLHE40	chr2:87073448-87073475	K562	blood:	n/a	n/a
46	BHLHE40	chr2:87051039-87051340	K562	blood:	n/a	n/a
47	BHLHE40	chr2:87062031-87062296	K562	blood:	n/a	n/a
48	BHLHE40	chr2:86946962-86947546	HepG2	liver:	n/a	n/a
49	BHLHE40	chr2:87035439-87036253	K562	blood:	n/a	n/a
50	BHLHE40	chr2:86946329-86946659	HepG2	liver:	n/a	n/a

(count:3602 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:87018944-87018994	SK-N-SH	brain:	n/a
2	chr2:87034200-87034250	HIPEpiC	eye:	n/a
3	chr2:87052406-87052456	GM12892	blood:	n/a
4	chr2:87018944-87018994	SK-N-SH	brain:	n/a
5	chr2:87034200-87034250	HIPEpiC	eye:	n/a
6	chr2:87052406-87052456	GM12892	blood:	n/a
7	chr2:87036948-87036998	HRPEpiC	eye:	n/a
8	chr2:86949715-86949765	NH-A	brain:	n/a
9	chr2:87069146-87069196	PFSK-1	brain:	n/a
10	chr2:87034200-87034250	HMEC	breast:	n/a
11	chr2:87021117-87021167	AG04449	skin:	fetal
12	chr2:86948118-86948168	T-47D	breast:	n/a
13	chr2:86948810-86948860	NHBE	bronchial:	n/a
14	chr2:87040878-87040928	ovcar-3	ovarian:	n/a
15	chr2:87052406-87052456	Caco-2	colon:	n/a
16	chr2:87042671-87042721	HCM	heart:	n/a
17	chr2:87035278-87035328	AoSMC	blood vessel:	n/a
18	chr2:87035698-87035748	AG09319	gingival:	n/a
19	chr2:87018585-87018635	SKMC	muscle:	n/a
20	chr2:87020377-87020427	SK-N-SH_RA	brain:	n/a
21	chr2:87018104-87018154	SAEC	small airway:	n/a
22	chr2:87020377-87020427	HepG2	liver:	n/a
23	chr2:87018054-87018104	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:87021117-87021167	HCM	heart:	n/a
25	chr2:87020937-87020987	LNCaP	prostate:	n/a
26	chr2:87035698-87035748	NT2-D1	testis:	n/a
27	chr2:87017953-87018003	HCT-116	colon:	n/a
28	chr2:87034200-87034250	NHBE	bronchial:	n/a
29	chr2:87017689-87017739	SAEC	small airway:	n/a
30	chr2:87018944-87018994	SK-N-SH_RA	brain:	n/a
31	chr2:86949715-86949765	H1-hESC	embryonic stem cell:	embryo
32	chr2:87016720-87016770	H1-hESC	embryonic stem cell:	embryo
33	chr2:87016436-87016486	HCF	heart:	n/a
34	chr2:87012810-87012860	AG09309	skin:	n/a
35	chr2:87003351-87003401	BJ	skin:	n/a
36	chr2:87016259-87016309	ovcar-3	ovarian:	n/a
37	chr2:87052406-87052456	AG10803	skin:	n/a
38	chr2:87069146-87069196	SKMC	muscle:	n/a
39	chr2:86946868-86946918	HAEpiC	amniotic membrane:	n/a
40	chr2:87017419-87017469	NHDF-neo	bronchial:	n/a
41	chr2:87018054-87018104	ovcar-3	ovarian:	n/a
42	chr2:87018104-87018154	BJ	skin:	n/a
43	chr2:86949715-86949765	GM06990	blood:	n/a
44	chr2:87020937-87020987	AG04449	skin:	fetal
45	chr2:86948118-86948168	HIPEpiC	eye:	n/a
46	chr2:87003351-87003401	ECC-1	luminal epithelium:	n/a
47	chr2:87048489-87048539	HL-60	blood:	n/a
48	chr2:87035620-87035670	HMEC	breast:	n/a
49	chr2:87035698-87035748	HRPEpiC	eye:	n/a
50	chr2:87034831-87034881	ovcar-3	ovarian:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:86932548..86934420-chr2:86983184..86985125,2	MCF-7	breast:
2	chr2:87053953..87055906-chr2:87062095..87066104,3	MCF-7	breast:
3	chr2:86849761..86852664-chr2:86946875..86949825,4	MCF-7	breast:
4	chr2:86976092..86977901-chr2:86986251..86989473,3	K562	blood:
5	chr2:87035298..87037035-chr2:87037234..87038983,2	MCF-7	breast:
6	chr2:87046936..87049292-chr2:87052783..87055158,2	K562	blood:
7	chr2:86991626..86993002-chr2:87034779..87035758,6	MCF-7	breast:
8	chr2:87009642..87012504-chr2:87015685..87018446,2	MCF-7	breast:
9	chr2:87027429..87029598-chr2:87032662..87035467,2	MCF-7	breast:
10	chr2:87010879..87013037-chr2:87016931..87018584,2	MCF-7	breast:
11	chr2:86995678..86997239-chr2:87001923..87004036,2	K562	blood:
12	chr2:87004183..87006528-chr2:87007653..87009681,2	K562	blood:
13	chr2:86940754..86943244-chr2:86946081..86948864,2	MCF-7	breast:
14	chr2:87004183..87006528-chr2:87007653..87009681,2	K562	blood:
15	chr2:86976811..86978782-chr2:86981681..86983709,3	K562	blood:
16	chr2:86972255..86973795-chr2:86976969..86979051,2	K562	blood:
17	chr2:86997290..86998210-chr2:87035221..87035730,2	MCF-7	breast:
18	chr2:86995678..86997239-chr2:87001923..87004036,2	K562	blood:
19	chr2:87002968..87006528-chr2:87006846..87010010,3	K562	blood:
20	chr2:87030047..87032736-chr2:87033123..87034744,3	MCF-7	breast:
21	chr2:86986605..86989075-chr2:86997944..86999787,2	K562	blood:
22	chr2:87002968..87006528-chr2:87006846..87010010,3	K562	blood:
23	chr17:56708571..56709224-chr2:86946909..86947842,2	Hela-S3	cervix:
24	chr2:87006827..87008386-chr2:87009565..87012245,2	K562	blood:
25	chr2:87083747..87086629-chr2:107106003..107108745,2	K562	blood:
26	chr2:86992690..86995505-chr2:86996197..86998560,2	MCF-7	breast:
27	chr2:87046936..87049292-chr2:87052783..87055158,2	K562	blood:
28	chr2:87030047..87032736-chr2:87033123..87034744,3	MCF-7	breast:
29	chr2:87037113..87040779-chr2:87041789..87043828,3	MCF-7	breast:
30	chr2:86976092..86977901-chr2:86986251..86989473,3	K562	blood:
31	chr2:87027429..87029598-chr2:87032662..87035467,2	MCF-7	breast:
32	chr2:86970428..86972701-chr2:86973505..86975478,2	MCF-7	breast:
33	chr2:86991045..86994213-chr2:86994492..86997547,4	K562	blood:
34	chr2:86623288..86624016-chr2:87035607..87036117,2	K562	blood:
35	chr2:86849445..86851190-chr2:87032691..87035125,2	MCF-7	breast:
36	chr2:86975250..86978690-chr2:86981648..86984537,4	K562	blood:
37	chr2:86850136..86852379-chr2:86973884..86976847,2	K562	blood:
38	chr2:86933727..86935990-chr2:86943530..86946218,2	MCF-7	breast:
39	chr2:87037113..87040779-chr2:87041789..87043828,3	MCF-7	breast:
40	chr2:87029729..87031828-chr2:87033631..87036000,2	K562	blood:
41	chr2:87053953..87055906-chr2:87062095..87066104,3	MCF-7	breast:
42	chr2:86666465..86668622-chr2:86979172..86981000,2	K562	blood:
43	chr2:86976811..86978782-chr2:86981681..86983709,3	K562	blood:
44	chr2:87016632..87018790-chr2:87032170..87034818,2	MCF-7	breast:
45	chr2:87006827..87008386-chr2:87009565..87012245,2	K562	blood:
46	chr2:86972255..86973795-chr2:86976969..86979051,2	K562	blood:
47	chr2:86991626..86993002-chr2:87034779..87035758,6	MCF-7	breast:
48	chr2:86850257..86852408-chr2:86970682..86973822,3	MCF-7	breast:
49	chr2:86848500..86851973-chr2:86945425..86949651,4	MCF-7	breast:

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RMND5A	hsa-miR-27a-3p	chr2:87001607-87001627
2	RMND5A	hsa-miR-125b-5p	chr2:87004984-87004990
3	RMND5A	hsa-miR-27a-3p	chr2:87001620-87001627
4	RMND5A	hsa-miR-23b-3p	chr2:87002901-87002921
5	RMND5A	hsa-miR-128-3p	chr2:87001679-87001699
6	RMND5A	hsa-miR-21-5p	chr2:87000639-87000646
7	RMND5A	hsa-miR-27a-3p	chr2:87004202-87004222
8	RMND5A	hsa-miR-27a-3p	chr2:87002320-87002339
9	RMND5A	hsa-miR-21-5p	chr2:87000626-87000646

Variant related genes	Relation type
CHMP3	TF binding region
CD8A	TF binding region
RNF103-CHMP3	TF binding region
ENSG00000229615	TF binding region
RMND5A	TF binding region
CHMP3	CpG island
CD8A	CpG island
RNF103-CHMP3	CpG island
ENSG00000229615	CpG island
RMND5A	CpG island
ENSG00000115548	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000153563	chromatin interactions
ENSG00000249884	chromatin interactions
ENSG00000239305	chromatin interactions
ENSG00000153561	chromatin interactions

Extended variants
information (count: 4523 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4523 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555348099	chr2:86941052-86941053	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs112269694	chr2:86941184-86941185	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs573649093	chr2:86941280-86941281	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs28528854	chr2:86941283-86941284	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs529636941	chr2:86941300-86941301	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs376206561	chr2:86941301-86941302	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs2090306	chr2:86941396-86941397	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs559983909	chr2:86941454-86941455	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs572291618	chr2:86941475-86941476	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs545710444	chr2:86941483-86941484	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs564303907	chr2:86941488-86941489	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs2674808	chr2:86941545-86941546	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs561670867	chr2:86941692-86941693	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs11685968	chr2:86941725-86941726	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201583392	chr2:86941782-86941783	Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs528859273	chr2:86941891-86941892	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs547398723	chr2:86941936-86941937	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs200010646	chr2:86941972-86941973	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs566403713	chr2:86942074-86942075	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs533673982	chr2:86942108-86942109	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs181072998	chr2:86942142-86942143	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs570188889	chr2:86942158-86942159	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs537150016	chr2:86942161-86942162	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs555411431	chr2:86942217-86942218	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs144220702	chr2:86942239-86942240	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs185557278	chr2:86942268-86942269	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs190316046	chr2:86942294-86942295	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs572297551	chr2:86942309-86942310	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs546069471	chr2:86942336-86942337	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs149226773	chr2:86942373-86942374	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs557678483	chr2:86942412-86942413	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs576141639	chr2:86942426-86942427	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs2674811	chr2:86942473-86942474	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs543558091	chr2:86942606-86942607	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs561799114	chr2:86942643-86942644	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs112264222	chr2:86942735-86942736	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs528974994	chr2:86942927-86942928	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs201125668	chr2:86942939-86942940	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs547122959	chr2:86943008-86943009	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs62148496	chr2:86943020-86943021	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559289041	chr2:86943102-86943103	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs533463208	chr2:86943189-86943190	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs111922091	chr2:86943193-86943194	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs552002221	chr2:86943254-86943255	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs138333408	chr2:86943367-86943368	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs532846378	chr2:86943409-86943410	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs531101332	chr2:86943466-86943467	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs373810018	chr2:86943514-86943515	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs549152609	chr2:86943580-86943581	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs567451764	chr2:86943600-86943601	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16272173	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:3407 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86933600-86941600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr2:86941400-86942400	Enhancers	Primary B cells from cord blood	blood
3	chr2:86941400-86942400	Enhancers	Fetal Heart	heart
4	chr2:86941400-86942600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr2:86941400-86942600	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr2:86941600-86941800	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr2:86941600-86942000	Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr2:86941600-86942600	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr2:86941800-86942000	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr2:86941800-86946800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr2:86942000-86942400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr2:86942000-86942400	Enhancers	Fetal Intestine Large	intestine
13	chr2:86942000-86942400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
14	chr2:86942000-86942400	Enhancers	Stomach Mucosa	stomach
15	chr2:86942000-86942400	Enhancers	HepG2	liver
16	chr2:86942000-86942400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr2:86942200-86942400	Enhancers	Fetal Intestine Small	intestine
18	chr2:86942200-86943200	Enhancers	Liver	Liver
19	chr2:86942400-86942600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr2:86942400-86942600	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr2:86942400-86943400	Weak transcription	HepG2	liver
22	chr2:86942400-86946200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr2:86942400-86946800	Weak transcription	Fetal Intestine Small	intestine
24	chr2:86942600-86943000	Weak transcription	Primary B cells from cord blood	blood
25	chr2:86942600-86944600	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr2:86942600-86946600	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr2:86942600-86946600	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr2:86942600-86946600	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr2:86942600-86946800	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr2:86943200-86946800	Weak transcription	Liver	Liver
31	chr2:86943400-86944000	Enhancers	HepG2	liver
32	chr2:86944000-86946000	Weak transcription	HepG2	liver
33	chr2:86944200-86945600	Weak transcription	Left Ventricle	heart
34	chr2:86945600-86945800	Enhancers	Primary hematopoietic stem cells	blood
35	chr2:86945600-86945800	Enhancers	Left Ventricle	heart
36	chr2:86945800-86946800	Weak transcription	Primary hematopoietic stem cells	blood
37	chr2:86945800-86946800	Weak transcription	Left Ventricle	heart
38	chr2:86945800-86946800	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr2:86946000-86946200	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr2:86946000-86946200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr2:86946000-86946200	Enhancers	A549	lung
42	chr2:86946000-86946200	Flanking Active TSS	HepG2	liver
43	chr2:86946000-86946600	Enhancers	Primary B cells from peripheral blood	blood
44	chr2:86946000-86946600	Enhancers	Primary T cells fromperipheralblood	blood
45	chr2:86946000-86948600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:86946000-86948800	Active TSS	Dnd41	blood
47	chr2:86946200-86946600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr2:86946200-86946600	Weak transcription	A549	lung
49	chr2:86946200-86948400	Active TSS	HepG2	liver
50	chr2:86946200-86948600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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