Variant report

Variant	esv1839947
Chromosome Location	chr12:106622186-106642064
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:519)
CpG islands
(count:1099)
Chromatin interactive
region (count:42)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:519 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr12:106642047-106642646	A549	lung:	n/a	chr12:106642156-106642169 chr12:106642135-106642144
2	BHLHE40	chr12:106641572-106641918	GM12878	blood:	n/a	chr12:106641740-106641756
3	BHLHE40	chr12:106641655-106641899	HepG2	liver:	n/a	chr12:106641740-106641756
4	BHLHE40	chr12:106641123-106641230	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:106641682-106641768	K562	blood:	n/a	chr12:106641740-106641756
6	CCNT2	chr12:106641692-106641893	K562	blood:	n/a	n/a
7	CEBPB	chr12:106639649-106640022	A549	lung:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
8	CEBPB	chr12:106631521-106631712	A549	lung:	n/a	chr12:106631622-106631631 chr12:106631622-106631631
9	CEBPB	chr12:106639596-106640084	A549	lung:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
10	CEBPB	chr12:106639646-106640005	Hela-S3	cervix:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
11	CEBPB	chr12:106639695-106639963	HepG2	liver:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
12	CEBPB	chr12:106639807-106639998	H1-hESC	embryonic stem cell:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
13	CEBPB	chr12:106639683-106640014	IMR90	lung:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
14	CEBPB	chr12:106631505-106631721	HepG2	liver:	n/a	chr12:106631622-106631631 chr12:106631622-106631631
15	CEBPD	chr12:106641712-106642110	HepG2	liver:	n/a	n/a
16	CEBPD	chr12:106641748-106642031	HepG2	liver:	n/a	n/a
17	CHD1	chr12:106639633-106643296	IMR90	lung:	n/a	chr12:106641025-106641035
18	CHD2	chr12:106641823-106641890	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr12:106639604-106640069	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr12:106640657-106641082	Hela-S3	cervix:	n/a	chr12:106641025-106641035
21	CHD2	chr12:106641149-106641203	GM12878	blood:	n/a	n/a
22	CHD2	chr12:106627437-106627602	K562	blood:	n/a	n/a
23	CHD2	chr12:106641803-106641805	HepG2	liver:	n/a	n/a
24	CREB1	chr12:106641338-106642036	A549	lung:	n/a	n/a
25	CTCF	chr12:106641140-106641290	GM12878	blood:	n/a	n/a
26	CTCF	chr12:106640935-106641008	GM13976	blood:	n/a	n/a
27	CTCF	chr12:106641220-106641370	GM12865	blood:	n/a	n/a
28	CTCF	chr12:106625380-106625530	A549	lung:	n/a	chr12:106625433-106625446 chr12:106625408-106625426
29	CTCF	chr12:106641200-106641350	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr12:106641160-106641310	RPTEC	kidney:	n/a	n/a
31	CTCF	chr12:106625385-106625450	MCF-7	breast:	n/a	chr12:106625433-106625446 chr12:106625408-106625426
32	CTCF	chr12:106641160-106641310	HAc	cerebellar:	n/a	n/a
33	CTCF	chr12:106640560-106640710	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr12:106641188-106641345	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr12:106641140-106641290	HMEC	breast:	n/a	n/a
36	CTCF	chr12:106641140-106641290	SAEC	small airway:	n/a	n/a
37	CTCF	chr12:106641180-106641330	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr12:106625383-106625432	HepG2	liver:	n/a	chr12:106625408-106625426
39	CTCF	chr12:106641250-106641280	LNCaP	prostate:	n/a	n/a
40	CTCF	chr12:106640980-106641130	GM12873	blood:	n/a	chr12:106641027-106641040
41	CTCF	chr12:106641120-106641270	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr12:106641140-106641290	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr12:106630560-106630710	K562	blood:	n/a	n/a
44	CTCF	chr12:106641140-106641290	GM12864	blood:	n/a	n/a
45	CTCF	chr12:106641200-106641350	BJ	skin:	n/a	n/a
46	CTCF	chr12:106641000-106641150	WI-38	lung:	n/a	chr12:106641027-106641040
47	CTCF	chr12:106641180-106641330	AG09309	skin:	n/a	n/a
48	CTCF	chr12:106641120-106641270	GM12872	blood:	n/a	n/a
49	CTCF	chr12:106625333-106625503	HepG2	liver:	n/a	chr12:106625433-106625446 chr12:106625408-106625426
50	CTCF	chr12:106630557-106630756	K562	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:106633641-106633691	HCF	heart:	n/a
2	chr12:106633641-106633691	HCF	heart:	n/a
3	chr12:106641008-106641058	AG10803	skin:	n/a
4	chr12:106638076-106638126	A549	lung:	n/a
5	chr12:106633938-106633988	BJ	skin:	n/a
6	chr12:106642001-106642051	BJ	skin:	n/a
7	chr12:106626993-106627043	Jurkat	blood:	n/a
8	chr12:106642001-106642051	NH-A	brain:	n/a
9	chr12:106636634-106636684	U87	brain:	n/a
10	chr12:106631875-106631925	HRE	kidney:	n/a
11	chr12:106641486-106641536	HEEpiC	esophagus:	n/a
12	chr12:106630712-106630762	AG09319	gingival:	n/a
13	chr12:106641134-106641184	NH-A	brain:	n/a
14	chr12:106639919-106639969	IMR90	lung:	fetal
15	chr12:106633047-106633097	PFSK-1	brain:	n/a
16	chr12:106641486-106641536	BJ	skin:	n/a
17	chr12:106642001-106642051	H1-hESC	embryonic stem cell:	embryo
18	chr12:106639919-106639969	SK-N-SH_RA	brain:	n/a
19	chr12:106636634-106636684	SAEC	small airway:	n/a
20	chr12:106639919-106639969	AG09319	gingival:	n/a
21	chr12:106639919-106639969	PrEC	prostate:	n/a
22	chr12:106633047-106633097	HCM	heart:	n/a
23	chr12:106642001-106642051	SAEC	small airway:	n/a
24	chr12:106632050-106632100	Caco-2	colon:	n/a
25	chr12:106641008-106641058	SK-N-MC	brain:	n/a
26	chr12:106633641-106633691	HRE	kidney:	n/a
27	chr12:106641994-106642044	GM06990	blood:	n/a
28	chr12:106642001-106642051	AG09319	gingival:	n/a
29	chr12:106632050-106632100	ProgFib	skin:	n/a
30	chr12:106639919-106639969	SK-N-SH	brain:	n/a
31	chr12:106626686-106626736	T-47D	breast:	n/a
32	chr12:106632050-106632100	T-47D	breast:	n/a
33	chr12:106633047-106633097	HRE	kidney:	n/a
34	chr12:106641486-106641536	GM19239	blood:	n/a
35	chr12:106636634-106636684	AG09309	skin:	n/a
36	chr12:106641994-106642044	HCPEpiC	choroid plexus:	n/a
37	chr12:106641486-106641536	GM12891	blood:	n/a
38	chr12:106632050-106632100	HCF	heart:	n/a
39	chr12:106633440-106633490	HRE	kidney:	n/a
40	chr12:106642001-106642051	AG04449	skin:	fetal
41	chr12:106633641-106633691	AG09309	skin:	n/a
42	chr12:106633440-106633490	Jurkat	blood:	n/a
43	chr12:106641134-106641184	PFSK-1	brain:	n/a
44	chr12:106636634-106636684	NHDF-neo	bronchial:	n/a
45	chr12:106633440-106633490	BJ	skin:	n/a
46	chr12:106642001-106642051	ECC-1	luminal epithelium:	n/a
47	chr12:106631875-106631925	MCF10A-Er-Src	breast:	n/a
48	chr12:106639919-106639969	HL-60	blood:	n/a
49	chr12:106641134-106641184	NT2-D1	testis:	n/a
50	chr12:106630712-106630762	T-47D	breast:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:106627724..106631160-chr12:106750781..106752959,4	MCF-7	breast:
2	chr12:106641570..106642137-chr12:106697112..106697741,2	MCF-7	breast:
3	chr12:106617980..106623111-chr12:106673260..106676714,5	MCF-7	breast:
4	chr12:106629030..106630922-chr12:106737245..106739641,2	MCF-7	breast:
5	chr12:106618176..106623447-chr12:106639085..106644031,7	MCF-7	breast:
6	chr12:106637683..106639757-chr12:106691523..106693781,3	MCF-7	breast:
7	chr12:106625081..106625716-chr12:106675920..106676462,2	MCF-7	breast:
8	chr12:106640063..106644049-chr12:106694395..106698756,11	MCF-7	breast:
9	chr12:106639673..106643649-chr12:106748400..106753718,9	MCF-7	breast:
10	chr12:106627619..106631130-chr12:106633186..106636182,4	MCF-7	breast:
11	chr12:106633129..106634918-chr12:106751021..106753631,2	MCF-7	breast:
12	chr12:106630484..106633329-chr12:106636143..106637779,2	K562	blood:
13	chr12:105500524..105503114-chr12:106640734..106642263,2	MCF-7	breast:
14	chr12:106639346..106644112-chr12:106694122..106698214,13	MCF-7	breast:
15	chr12:106616826..106619612-chr12:106623488..106625547,2	K562	blood:
16	chr12:106639693..106641308-chr12:106715072..106718036,2	MCF-7	breast:
17	chr12:106636406..106639904-chr12:106695865..106698141,3	MCF-7	breast:
18	chr12:106640021..106643402-chr12:106749618..106753030,5	MCF-7	breast:
19	chr12:106622589..106625717-chr12:106638331..106640361,3	MCF-7	breast:
20	chr12:106640861..106643735-chr12:106674267..106678317,3	MCF-7	breast:
21	chr12:106634944..106646449-chr12:106667585..106679535,27	MCF-7	breast:
22	chr12:106626663..106628634-chr12:106673414..106675622,2	MCF-7	breast:
23	chr12:106620940..106625050-chr12:106630217..106634289,4	MCF-7	breast:
24	chr12:106622227..106624483-chr12:107349565..107351095,2	K562	blood:
25	chr12:106630802..106633610-chr12:106666760..106669656,2	MCF-7	breast:
26	chr12:106619967..106622887-chr12:106695577..106697877,2	MCF-7	breast:
27	chr12:106622014..106624785-chr12:106736683..106738357,2	MCF-7	breast:
28	chr12:106624850..106627248-chr12:106695973..106698694,2	MCF-7	breast:
29	chr12:106640559..106643459-chr12:107485293..107487296,2	K562	blood:
30	chr12:106622589..106625717-chr12:106638331..106640361,3	MCF-7	breast:
31	chr12:106641882..106643930-chr12:106685440..106687264,2	MCF-7	breast:
32	chr12:106628053..106629764-chr12:106751194..106753543,2	K562	blood:
33	chr12:106621785..106624266-chr12:106738678..106741420,2	MCF-7	breast:
34	chr12:106620792..106623041-chr12:106734428..106736723,2	MCF-7	breast:
35	chr12:106620786..106622962-chr12:106640518..106642749,2	MCF-7	breast:
36	chr12:106626541..106632087-chr12:106638755..106642966,8	MCF-7	breast:
37	chr12:106531582..106534564-chr12:106638638..106642825,4	MCF-7	breast:
38	chr12:106616785..106619757-chr12:106628880..106631149,2	MCF-7	breast:
39	chr12:106630484..106633329-chr12:106636143..106637779,2	K562	blood:
40	chr12:106622344..106624016-chr12:106673655..106676594,2	MCF-7	breast:
41	chr12:106620940..106625050-chr12:106630217..106634289,4	MCF-7	breast:
42	chr12:106627619..106631130-chr12:106633186..106636182,4	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUAK1-5	chr12:106631814-106632649	NONHSAT030470
2	lnc-NUAK1-2	chr12:106640493-106640734	ENSG00000258355.1
3	lnc-NUAK1-2	chr12:106639391-106639460	ENSG00000258355.1

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CKAP4	hsa-miR-7-5p	chr12:106632337-106632330
2	CKAP4	hsa-miR-7-5p	chr12:106632331-106632353
3	CKAP4	hsa-miR-30c-5p	chr12:106631732-106631754

Variant related genes	Relation type
CKAP4	TF binding region
ENSG00000258355	TF binding region
CKAP4	CpG island
ENSG00000258355	CpG island
ENSG00000257548	chromatin interactions
ENSG00000074590	chromatin interactions
ENSG00000258355	chromatin interactions
ENSG00000238609	chromatin interactions
ENSG00000136051	chromatin interactions
ENSG00000257999	chromatin interactions
ENSG00000008405	chromatin interactions
ENSG00000136026	chromatin interactions
ENSG00000166046	chromatin interactions
ENSG00000013503	chromatin interactions
ENSG00000151135	chromatin interactions

Extended variants
information (count: 947 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:947 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1215763	chr12:106622186-106622187	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535886906	chr12:106622189-106622190	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs140582119	chr12:106622208-106622209	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs566226536	chr12:106622240-106622241	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs191510260	chr12:106622249-106622250	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs145353092	chr12:106622253-106622254	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs557631139	chr12:106622256-106622257	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs577787792	chr12:106622257-106622258	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs7297603	chr12:106622270-106622271	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs557256173	chr12:106622285-106622286	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs183023703	chr12:106622290-106622291	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs187005639	chr12:106622293-106622294	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs147657196	chr12:106622312-106622313	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs35921884	chr12:106622343-106622344	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs7297510	chr12:106622349-106622350	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs191692673	chr12:106622371-106622372	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs548579097	chr12:106622379-106622380	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs568782586	chr12:106622384-106622385	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs182071734	chr12:106622396-106622397	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs1215762	chr12:106622448-106622449	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs116363578	chr12:106622450-106622451	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs187650661	chr12:106622451-106622452	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs142478588	chr12:106622515-106622516	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs193226552	chr12:106622535-106622536	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs113697480	chr12:106622538-106622539	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs370983402	chr12:106622549-106622550	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs551877290	chr12:106622584-106622585	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs571338092	chr12:106622591-106622592	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs115422090	chr12:106622600-106622601	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs548274900	chr12:106622645-106622646	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs556972107	chr12:106622659-106622660	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs371570586	chr12:106622679-106622680	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs536150595	chr12:106622706-106622707	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs151307641	chr12:106622733-106622734	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs572529377	chr12:106622734-106622735	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs548309990	chr12:106622798-106622799	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs140542544	chr12:106622844-106622845	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs565028110	chr12:106622845-106622846	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs578105081	chr12:106622881-106622882	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs11833736	chr12:106622895-106622896	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs150446767	chr12:106622923-106622924	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs558574125	chr12:106622930-106622931	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs138490322	chr12:106622936-106622937	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs185474409	chr12:106622943-106622944	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs559760462	chr12:106622949-106622950	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs528527383	chr12:106622962-106622963	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs551573577	chr12:106622966-106622967	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs190779717	chr12:106622971-106622972	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs192128752	chr12:106622972-106622973	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs537152011	chr12:106622974-106622975	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106606600-106626400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:106618000-106632000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr12:106618000-106632200	Weak transcription	Psoas Muscle	Psoas
4	chr12:106618600-106630600	Weak transcription	Ovary	ovary
5	chr12:106618600-106632200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr12:106620800-106622200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:106620800-106622200	Enhancers	Primary T cells from cord blood	blood
8	chr12:106620800-106622200	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr12:106620800-106622200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr12:106620800-106622200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr12:106620800-106622200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr12:106620800-106622200	Enhancers	HMEC	breast
13	chr12:106620800-106622400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr12:106620800-106622400	Enhancers	Primary T cells fromperipheralblood	blood
15	chr12:106620800-106622400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr12:106620800-106622400	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr12:106620800-106622400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr12:106620800-106623000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr12:106620800-106623200	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr12:106620800-106630400	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr12:106621000-106625000	Weak transcription	Left Ventricle	heart
22	chr12:106621200-106632000	Weak transcription	Brain Hippocampus Middle	brain
23	chr12:106621200-106632600	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr12:106621400-106630200	Weak transcription	NHLF	lung
25	chr12:106621400-106632600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr12:106621400-106638200	Weak transcription	Primary hematopoietic stem cells	blood
27	chr12:106621600-106622200	Bivalent Enhancer	Primary B cells from cord blood	blood
28	chr12:106621600-106624800	Weak transcription	Right Atrium	heart
29	chr12:106621600-106626600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:106621600-106630400	Weak transcription	HSMM	muscle
31	chr12:106621600-106630600	Weak transcription	Liver	Liver
32	chr12:106621600-106630600	Weak transcription	A549	lung
33	chr12:106621600-106631400	Weak transcription	Adipose Nuclei	Adipose
34	chr12:106621600-106631800	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr12:106621600-106632600	Weak transcription	Colonic Mucosa	Colon
36	chr12:106621600-106632800	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr12:106621800-106622400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr12:106621800-106627600	Weak transcription	Esophagus	oesophagus
39	chr12:106621800-106628000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr12:106621800-106628600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr12:106621800-106629200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr12:106621800-106629600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr12:106621800-106629800	Weak transcription	Stomach Mucosa	stomach
44	chr12:106621800-106630400	Weak transcription	Fetal Lung	lung
45	chr12:106621800-106630600	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr12:106621800-106630600	Weak transcription	Spleen	Spleen
47	chr12:106621800-106631800	Weak transcription	Gastric	stomach
48	chr12:106621800-106631800	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr12:106621800-106632800	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr12:106622000-106623200	Enhancers	Monocytes-CD14+_RO01746	blood

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