Variant report

Variant	nsv469592
Chromosome Location	chr12:63486510-63679139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1171)
CpG islands
(count:856)
Chromatin interactive
region (count:43)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1171 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:63670554-63670812	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:63497272-63497631	HepG2	liver:	n/a	n/a
3	ATF1	chr12:63523763-63524061	K562	blood:	n/a	n/a
4	BACH1	chr12:63544074-63544342	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:63545234-63545470	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr12:63550104-63550132	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:63497377-63497528	HepG2	liver:	n/a	n/a
8	BRCA1	chr12:63600642-63601071	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr12:63570065-63570332	K562	blood:	n/a	n/a
10	CCNT2	chr12:63491637-63491772	K562	blood:	n/a	n/a
11	CCNT2	chr12:63523779-63524092	K562	blood:	n/a	n/a
12	CEBPB	chr12:63498228-63498531	K562	blood:	n/a	chr12:63498390-63498401
13	CEBPB	chr12:63616923-63617223	HepG2	liver:	n/a	chr12:63617048-63617059 chr12:63617110-63617121 chr12:63617048-63617061
14	CEBPB	chr12:63613489-63613787	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:63600554-63601331	MCF-7	breast:	n/a	n/a
16	CEBPB	chr12:63489181-63489556	HepG2	liver:	n/a	chr12:63489358-63489369
17	CEBPB	chr12:63577350-63577566	HepG2	liver:	n/a	chr12:63577475-63577486
18	CEBPB	chr12:63572887-63573147	A549	lung:	n/a	n/a
19	CEBPB	chr12:63489180-63489553	HepG2	liver:	n/a	chr12:63489358-63489369
20	CEBPB	chr12:63625166-63625226	HepG2	liver:	n/a	chr12:63625189-63625200
21	CEBPB	chr12:63489197-63489397	K562	blood:	n/a	chr12:63489358-63489369
22	CEBPB	chr12:63572966-63573073	K562	blood:	n/a	n/a
23	CEBPB	chr12:63600785-63601096	A549	lung:	n/a	n/a
24	CEBPB	chr12:63600261-63601236	MCF-7	breast:	n/a	n/a
25	CEBPB	chr12:63489174-63489490	HepG2	liver:	n/a	chr12:63489358-63489369
26	CEBPB	chr12:63569647-63569844	HepG2	liver:	n/a	chr12:63569707-63569718
27	CEBPB	chr12:63572869-63573101	IMR90	lung:	n/a	n/a
28	CEBPB	chr12:63573010-63573086	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:63498226-63498565	IMR90	lung:	n/a	chr12:63498390-63498401
30	CEBPB	chr12:63600679-63601182	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr12:63607177-63607379	A549	lung:	n/a	n/a
32	CEBPB	chr12:63613516-63613778	IMR90	lung:	n/a	n/a
33	CEBPB	chr12:63647886-63648072	A549	lung:	n/a	n/a
34	CEBPB	chr12:63489230-63489450	HepG2	liver:	n/a	chr12:63489358-63489369
35	CEBPB	chr12:63500753-63501013	K562	blood:	n/a	n/a
36	CEBPB	chr12:63532789-63533034	A549	lung:	n/a	n/a
37	CEBPB	chr12:63554623-63554689	A549	lung:	n/a	n/a
38	CEBPB	chr12:63489316-63489449	H1-hESC	embryonic stem cell:	n/a	chr12:63489358-63489369
39	CEBPB	chr12:63616909-63617221	IMR90	lung:	n/a	chr12:63617048-63617059 chr12:63617110-63617121 chr12:63617048-63617061
40	CEBPB	chr12:63616996-63617194	A549	lung:	n/a	chr12:63617048-63617059 chr12:63617110-63617121 chr12:63617048-63617061
41	CEBPB	chr12:63624366-63624484	HepG2	liver:	n/a	chr12:63624438-63624449
42	CEBPB	chr12:63498222-63498566	HepG2	liver:	n/a	chr12:63498390-63498401
43	CEBPB	chr12:63569654-63569734	IMR90	lung:	n/a	chr12:63569707-63569718
44	CEBPB	chr12:63577407-63577618	A549	lung:	n/a	chr12:63577475-63577486
45	CEBPB	chr12:63489246-63489392	A549	lung:	n/a	chr12:63489358-63489369
46	CEBPB	chr12:63569649-63569765	A549	lung:	n/a	chr12:63569707-63569718
47	CEBPB	chr12:63498242-63498546	A549	lung:	n/a	chr12:63498390-63498401
48	CEBPD	chr12:63523659-63524135	K562	blood:	n/a	n/a
49	CEBPD	chr12:63671661-63671966	K562	blood:	n/a	n/a
50	CEBPD	chr12:63523652-63524112	K562	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63544923-63544973	HUVEC	blood vessel:	n/a
2	chr12:63543292-63543342	SK-N-MC	brain:	n/a
3	chr12:63544923-63544973	HUVEC	blood vessel:	n/a
4	chr12:63543292-63543342	SK-N-MC	brain:	n/a
5	chr12:63544319-63544369	Hepatocyte	liver:	n/a
6	chr12:63547716-63547766	K562	blood:	n/a
7	chr12:63544923-63544973	HCPEpiC	choroid plexus:	n/a
8	chr12:63547716-63547766	PFSK-1	brain:	n/a
9	chr12:63545783-63545833	T-47D	breast:	n/a
10	chr12:63545523-63545573	HMEC	breast:	n/a
11	chr12:63543831-63543881	SK-N-SH	brain:	n/a
12	chr12:63540400-63540450	Jurkat	blood:	n/a
13	chr12:63547716-63547766	NB4	blood:	n/a
14	chr12:63543831-63543881	IMR90	lung:	fetal
15	chr12:63545288-63545338	A549	lung:	n/a
16	chr12:63544319-63544369	ovcar-3	ovarian:	n/a
17	chr12:63544319-63544369	A549	lung:	n/a
18	chr12:63544319-63544369	GM12878	blood:	n/a
19	chr12:63544430-63544480	AG04449	skin:	fetal
20	chr12:63547716-63547766	SAEC	small airway:	n/a
21	chr12:63544175-63544225	HepG2	liver:	n/a
22	chr12:63545288-63545338	HUVEC	blood vessel:	n/a
23	chr12:63545956-63546006	T-47D	breast:	n/a
24	chr12:63545523-63545573	HCM	heart:	n/a
25	chr12:63545956-63546006	SK-N-SH	brain:	n/a
26	chr12:63544857-63544907	BJ	skin:	n/a
27	chr12:63544175-63544225	HL-60	blood:	n/a
28	chr12:63545783-63545833	GM12891	blood:	n/a
29	chr12:63547716-63547766	Jurkat	blood:	n/a
30	chr12:63544430-63544480	HCPEpiC	choroid plexus:	n/a
31	chr12:63545956-63546006	HepG2	liver:	n/a
32	chr12:63544857-63544907	AG09309	skin:	n/a
33	chr12:63544175-63544225	SK-N-MC	brain:	n/a
34	chr12:63543292-63543342	HIPEpiC	eye:	n/a
35	chr12:63544319-63544369	HPAEpiC	pulmonary alveolar:	n/a
36	chr12:63544923-63544973	HIPEpiC	eye:	n/a
37	chr12:63540400-63540450	BE2_C	brain:	n/a
38	chr12:63543831-63543881	SAEC	small airway:	n/a
39	chr12:63544923-63544973	H1-hESC	embryonic stem cell:	embryo
40	chr12:63544319-63544369	NHBE	bronchial:	n/a
41	chr12:63545783-63545833	SAEC	small airway:	n/a
42	chr12:63547716-63547766	SKMC	muscle:	n/a
43	chr12:63544857-63544907	HNPCEpiC	eye:	n/a
44	chr12:63543831-63543881	HIPEpiC	eye:	n/a
45	chr12:63545783-63545833	Hepatocyte	liver:	n/a
46	chr12:63544857-63544907	HRCEpiC	kidney:	n/a
47	chr12:63545523-63545573	GM12891	blood:	n/a
48	chr12:63545956-63546006	MCF-7	breast:	n/a
49	chr12:63543292-63543342	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:63543831-63543881	PrEC	prostate:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:63503782..63505766-chr12:63506813..63509120,2	K562	blood:
2	chr12:63617360..63618250-chr8:143764719..143765546,2	MCF-7	breast:
3	chr12:63491029..63492639-chr12:64172273..64174995,2	MCF-7	breast:
4	chr12:63492473..63494372-chr12:63496119..63498429,2	K562	blood:
5	chr12:63522003..63524350-chr12:63527022..63529275,2	K562	blood:
6	chr12:63327252..63328936-chr12:63486552..63489469,2	MCF-7	breast:
7	chr12:63514993..63517783-chr12:63522556..63524545,2	MCF-7	breast:
8	chr12:63544050..63546794-chr12:63669922..63672775,2	MCF-7	breast:
9	chr12:63632053..63632963-chr5:177630919..177631572,2	Hela-S3	cervix:
10	chr12:63599815..63602634-chr12:63602685..63604731,2	MCF-7	breast:
11	chr12:63479864..63482545-chr12:63488931..63490765,2	MCF-7	breast:
12	chr12:63461645..63464045-chr12:63491435..63493739,2	MCF-7	breast:
13	chr12:63545559..63546473-chr12:63669896..63671149,5	MCF-7	breast:
14	chr12:63496969..63497998-chr12:63670271..63671167,8	MCF-7	breast:
15	chr12:63535701..63537481-chr12:63551924..63553918,2	MCF-7	breast:
16	chr12:63540258..63542828-chr12:63547028..63548966,2	K562	blood:
17	chr12:63545559..63546473-chr12:63669896..63671149,5	MCF-7	breast:
18	chr12:63497053..63498247-chr12:63670255..63671252,4	K562	blood:
19	chr12:63599815..63602634-chr12:63602685..63604731,2	MCF-7	breast:
20	chr12:63497053..63498247-chr12:63670255..63671252,4	K562	blood:
21	chr12:63545428..63546206-chr12:63674883..63675724,2	MCF-7	breast:
22	chr12:63497039..63497977-chr12:64195476..64196144,2	K562	blood:
23	chr12:63504151..63504841-chr7:82403368..82403924,2	MCF-7	breast:
24	chr12:63535701..63537481-chr12:63551924..63553918,2	MCF-7	breast:
25	chr12:63492473..63494372-chr12:63496119..63498429,2	K562	blood:
26	chr12:63327612..63330276-chr12:63491090..63493738,2	MCF-7	breast:
27	chr12:63545419..63546376-chr12:64195555..64196413,2	MCF-7	breast:
28	chr12:63503782..63505766-chr12:63506813..63509120,2	K562	blood:
29	chr12:62996207..62999162-chr12:63547684..63549229,2	MCF-7	breast:
30	chr12:63497332..63498958-chr12:63670308..63671121,8	MCF-7	breast:
31	chr12:63496969..63497998-chr12:63670271..63671167,8	MCF-7	breast:
32	chr12:63497370..63497928-chr12:64195474..64196377,2	MCF-7	breast:
33	chr12:63484569..63486639-chr12:64614558..64616326,2	MCF-7	breast:
34	chr12:63497332..63498958-chr12:63670308..63671121,8	MCF-7	breast:
35	chr12:63514993..63517783-chr12:63522556..63524545,2	MCF-7	breast:
36	chr12:63545448..63546470-chr12:63670124..63671316,6	MCF-7	breast:
37	chr12:63678879..63681620-chr17:58469964..58471603,2	MCF-7	breast:
38	chr12:63496453..63499352-chr12:64173717..64175638,2	MCF-7	breast:
39	chr12:63540258..63542828-chr12:63547028..63548966,2	K562	blood:
40	chr12:63545448..63546470-chr12:63670124..63671316,6	MCF-7	breast:
41	chr12:63522003..63524350-chr12:63527022..63529275,2	K562	blood:
42	chr12:63491617..63494128-chr12:64615499..64617059,2	K562	blood:
43	chr12:63545428..63546206-chr12:63674883..63675724,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AVPR1A-2	chr12:63504632-63504765	NONHSAT029106
2	lnc-TMEM5-5	chr12:63580624-63580735	l_664_chr12:63563604-63657550_brain
3	lnc-TMEM5-5	chr12:63563605-63563746	l_664_chr12:63563604-63657550_brain
4	lnc-MON2-3	chr12:63547640-63547786	ENSG00000257973.1
5	lnc-AVPR1A-2	chr12:63519180-63519254	NONHSAT029106
6	lnc-TMEM5-5	chr12:63563762-63563912	l_664_chr12:63563604-63657550_brain
7	lnc-TMEM5-5	chr12:63654629-63657550	l_664_chr12:63563604-63657550_brain
8	lnc-MON2-3	chr12:63546261-63546418	ENSG00000257973.1
9	lnc-MON2-3	chr12:63544845-63544872	ENSG00000257973.1

No data

Variant related genes	Relation type
AVPR1A	TF binding region
HNRNPA1P69	TF binding region
AVPR1A	CpG island
HNRNPA1P69	CpG island
ENSG00000243024	chromatin interactions
ENSG00000174206	chromatin interactions
ENSG00000199179	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000252660	chromatin interactions
ENSG00000257354	chromatin interactions
ENSG00000118600	chromatin interactions
ENSG00000166148	chromatin interactions
ENSG00000221949	chromatin interactions
ENSG00000111110	chromatin interactions

Extended variants
information (count: 2830 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2830 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190041100	chr12:63486514-63486515	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs79975686	chr12:63486529-63486530	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs562313872	chr12:63486537-63486538	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs139751016	chr12:63486544-63486545	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs112174899	chr12:63486579-63486580	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs7138569	chr12:63486584-63486585	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs181322185	chr12:63486610-63486611	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs138310485	chr12:63486636-63486637	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs369182399	chr12:63486637-63486638	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs71465186	chr12:63486639-63486640	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs546714412	chr12:63486657-63486658	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140202227	chr12:63486739-63486740	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs145406897	chr12:63486789-63486790	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs79276282	chr12:63486841-63486842	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs61920164	chr12:63486852-63486853	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs538446537	chr12:63486857-63486858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs7304533	chr12:63486875-63486876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs578217207	chr12:63486906-63486907	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113250492	chr12:63486963-63486964	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560510254	chr12:63486970-63486971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs559919584	chr12:63486971-63486972	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573323352	chr12:63486983-63486984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs148623191	chr12:63486990-63486991	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs117869956	chr12:63487032-63487033	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112260631	chr12:63487044-63487045	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs142052968	chr12:63487071-63487072	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs73132829	chr12:63487105-63487106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs78506722	chr12:63487141-63487142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs185065556	chr12:63487185-63487186	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs547694170	chr12:63487202-63487203	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs566720538	chr12:63487259-63487260	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs151176906	chr12:63487265-63487266	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs549453642	chr12:63487282-63487283	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs569421096	chr12:63487437-63487438	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs538432456	chr12:63487455-63487456	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558101944	chr12:63487460-63487461	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs376130792	chr12:63487503-63487504	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs140166850	chr12:63487538-63487539	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs144106199	chr12:63487550-63487551	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191039642	chr12:63487565-63487566	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs76885960	chr12:63487574-63487575	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs76556143	chr12:63487580-63487581	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs146472072	chr12:63487595-63487596	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs550522971	chr12:63487628-63487629	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs183663643	chr12:63487682-63487683	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545168637	chr12:63487701-63487702	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs564906291	chr12:63487765-63487766	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs189110312	chr12:63487774-63487775	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs540929807	chr12:63487776-63487777	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs60173856	chr12:63487784-63487785	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63475200-63487200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:63480400-63490600	Weak transcription	Fetal Kidney	kidney
3	chr12:63485200-63486600	Enhancers	Fetal Intestine Small	intestine
4	chr12:63485400-63487200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr12:63485800-63487000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr12:63486200-63487600	Weak transcription	Fetal Intestine Large	intestine
7	chr12:63486600-63487600	Weak transcription	Fetal Intestine Small	intestine
8	chr12:63487000-63488200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr12:63487200-63487600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr12:63487200-63488000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr12:63487600-63487800	Enhancers	H9 Cell Line	embryonic stem cell
12	chr12:63487600-63488000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:63487600-63488200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr12:63487600-63488400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr12:63487600-63490600	Enhancers	Fetal Intestine Large	intestine
16	chr12:63487600-63490600	Enhancers	Fetal Intestine Small	intestine
17	chr12:63487800-63488000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr12:63487800-63488400	Enhancers	Stomach Mucosa	stomach
19	chr12:63487800-63490000	Enhancers	HepG2	liver
20	chr12:63488000-63488200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:63488000-63488200	Enhancers	Small Intestine	intestine
22	chr12:63488200-63492600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr12:63488800-63489800	Enhancers	Liver	Liver
24	chr12:63490600-63490800	Enhancers	Fetal Kidney	kidney
25	chr12:63491200-63491800	Bivalent Enhancer	Fetal Lung	lung
26	chr12:63492400-63493400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr12:63492600-63493200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:63492600-63493400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:63492800-63493000	Enhancers	Brain Substantia Nigra	brain
30	chr12:63496600-63497400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:63496800-63497200	Enhancers	Stomach Mucosa	stomach
32	chr12:63497400-63499400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:63497600-63498200	Enhancers	Dnd41	blood
34	chr12:63499400-63499600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr12:63500800-63501200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:63500800-63501400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr12:63501000-63501400	Enhancers	HMEC	breast
38	chr12:63501400-63502000	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr12:63503800-63504200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr12:63518200-63519600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr12:63518200-63519600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr12:63518200-63519800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:63519200-63519600	Active TSS	Gastric	stomach
44	chr12:63519400-63519600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr12:63522800-63523200	Enhancers	K562	blood
46	chr12:63523200-63524200	Weak transcription	K562	blood
47	chr12:63523600-63524000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr12:63524200-63524400	Enhancers	K562	blood
49	chr12:63530000-63530600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr12:63530600-63532200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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