Variant report

Variant	nsv898559
Chromosome Location	chr12:282465-310334
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:298349-298388	K562	blood:	n/a	n/a
2	ATF1	chr12:308947-309267	K562	blood:	n/a	n/a
3	ATF1	chr12:285620-285967	K562	blood:	n/a	n/a
4	ATF3	chr12:289702-289924	K562	blood:	n/a	n/a
5	BACH1	chr12:308502-308715	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr12:288438-288716	H1-hESC	embryonic stem cell:	n/a	chr12:288578-288592
7	BHLHE40	chr12:302513-302839	K562	blood:	n/a	chr12:302670-302679 chr12:302671-302680 chr12:302748-302764 chr12:302671-302680 chr12:302665-302686
8	BHLHE40	chr12:298253-298607	HepG2	liver:	n/a	n/a
9	BHLHE40	chr12:289650-290110	K562	blood:	n/a	n/a
10	BHLHE40	chr12:289673-290107	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:294691-295034	K562	blood:	n/a	chr12:294869-294878 chr12:294870-294879 chr12:294867-294880 chr12:294868-294877 chr12:294869-294878
12	BHLHE40	chr12:298401-298467	K562	blood:	n/a	n/a
13	BHLHE40	chr12:294714-295081	HepG2	liver:	n/a	chr12:294869-294878 chr12:294870-294879 chr12:294867-294880 chr12:294868-294877 chr12:294869-294878
14	BRCA1	chr12:298216-298256	HepG2	liver:	n/a	n/a
15	CCNT2	chr12:284479-284668	K562	blood:	n/a	n/a
16	CCNT2	chr12:298259-298565	K562	blood:	n/a	n/a
17	CEBPB	chr12:299833-299960	K562	blood:	n/a	chr12:299932-299943
18	CEBPB	chr12:299770-300001	HepG2	liver:	n/a	chr12:299932-299943
19	CEBPB	chr12:308999-309199	IMR90	lung:	n/a	n/a
20	CEBPD	chr12:298272-298550	HepG2	liver:	n/a	n/a
21	CHD2	chr12:291781-291791	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr12:298159-298475	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr12:289744-289944	GM12878	blood:	n/a	n/a
24	CREB1	chr12:285549-286021	GM12878	blood:	n/a	n/a
25	CREB1	chr12:285466-286175	HepG2	liver:	n/a	n/a
26	CREB1	chr12:285375-286181	HepG2	liver:	n/a	n/a
27	CREB1	chr12:298202-298629	A549	lung:	n/a	n/a
28	CTCF	chr12:308500-308650	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr12:298213-298638	HepG2	liver:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
30	CTCF	chr12:298330-298547	HepG2	liver:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
31	CTCF	chr12:296060-296210	A549	lung:	n/a	chr12:296091-296112 chr12:296096-296114 chr12:296098-296111
32	CTCF	chr12:298380-298530	HAc	cerebellar:	n/a	chr12:298430-298443 chr12:298428-298446
33	CTCF	chr12:298313-298581	LNCaP	prostate:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
34	CTCF	chr12:298380-298530	SAEC	small airway:	n/a	chr12:298430-298443 chr12:298428-298446
35	CTCF	chr12:298420-298570	NHEK	skin:	n/a	chr12:298430-298443 chr12:298428-298446
36	CTCF	chr12:308460-308610	BE2_C	brain:	n/a	n/a
37	CTCF	chr12:298340-298490	HepG2	liver:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
38	CTCF	chr12:298400-298550	GM12864	blood:	n/a	chr12:298430-298443 chr12:298428-298446
39	CTCF	chr12:298420-298570	HCPEpiC	choroid plexus:	n/a	chr12:298430-298443 chr12:298428-298446
40	CTCF	chr12:298380-298530	GM12874	blood:	n/a	chr12:298430-298443 chr12:298428-298446
41	CTCF	chr12:308460-308610	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr12:285200-285350	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr12:298380-298530	HRE	kidney:	n/a	chr12:298430-298443 chr12:298428-298446
44	CTCF	chr12:298360-298510	HEEpiC	esophagus:	n/a	chr12:298430-298443 chr12:298428-298446
45	CTCF	chr12:298380-298530	Hela-S3	cervix:	n/a	chr12:298430-298443 chr12:298428-298446
46	CTCF	chr12:298360-298510	HFF-Myc	foreskin:	n/a	chr12:298430-298443 chr12:298428-298446
47	CTCF	chr12:287940-288090	WERI-Rb-1	eye:	n/a	chr12:288063-288081 chr12:288066-288075
48	CTCF	chr12:298400-298550	NHLF	lung:	n/a	chr12:298430-298443 chr12:298428-298446
49	CTCF	chr12:298340-298490	GM12865	blood:	n/a	chr12:298430-298443 chr12:298428-298446 chr12:298350-298363
50	CTCF	chr12:308520-308670	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:298378-298428	HRE	kidney:	n/a
2	chr12:298268-298318	MCF-7	breast:	n/a
3	chr12:308821-308871	HNPCEpiC	eye:	n/a
4	chr12:296540-296590	H1-hESC	embryonic stem cell:	embryo
5	chr12:296609-296659	Caco-2	colon:	n/a
6	chr12:298378-298428	HRE	kidney:	n/a
7	chr12:298268-298318	MCF-7	breast:	n/a
8	chr12:308821-308871	HNPCEpiC	eye:	n/a
9	chr12:296540-296590	H1-hESC	embryonic stem cell:	embryo
10	chr12:296609-296659	Caco-2	colon:	n/a
11	chr12:298268-298318	HepG2	liver:	n/a
12	chr12:296540-296590	Hepatocyte	liver:	n/a
13	chr12:298484-298534	AG04449	skin:	fetal
14	chr12:295951-296001	PANC-1	pancreas:	n/a
15	chr12:299649-299699	NHDF-neo	bronchial:	n/a
16	chr12:285704-285754	NT2-D1	testis:	n/a
17	chr12:298378-298428	HCF	heart:	n/a
18	chr12:297356-297406	Hepatocyte	liver:	n/a
19	chr12:308821-308871	U87	brain:	n/a
20	chr12:297831-297881	RPTEC	kidney:	n/a
21	chr12:296540-296590	CMK	blood:	n/a
22	chr12:295951-296001	GM06990	blood:	n/a
23	chr12:286620-286670	BJ	skin:	n/a
24	chr12:296609-296659	NT2-D1	testis:	n/a
25	chr12:300298-300348	NT2-D1	testis:	n/a
26	chr12:298378-298428	GM12891	blood:	n/a
27	chr12:298484-298534	NB4	blood:	n/a
28	chr12:296473-296523	Hela-S3	cervix:	n/a
29	chr12:297356-297406	PrEC	prostate:	n/a
30	chr12:296473-296523	K562	blood:	n/a
31	chr12:299649-299699	SAEC	small airway:	n/a
32	chr12:296473-296523	AG04450	lung:	fetal
33	chr12:296540-296590	HEK293	kidney:	embryo
34	chr12:296609-296659	AG10803	skin:	n/a
35	chr12:295951-296001	AG10803	skin:	n/a
36	chr12:298484-298534	PANC-1	pancreas:	n/a
37	chr12:286620-286670	AG09319	gingival:	n/a
38	chr12:308821-308871	GM12891	blood:	n/a
39	chr12:291668-291718	SAEC	small airway:	n/a
40	chr12:296609-296659	HMEC	breast:	n/a
41	chr12:300298-300348	BE2_C	brain:	n/a
42	chr12:295951-296001	SK-N-SH_RA	brain:	n/a
43	chr12:300298-300348	GM12878	blood:	n/a
44	chr12:296473-296523	AG10803	skin:	n/a
45	chr12:285704-285754	AG10803	skin:	n/a
46	chr12:300298-300348	LNCaP	prostate:	n/a
47	chr12:297356-297406	LNCaP	prostate:	n/a
48	chr12:296609-296659	MCF10A-Er-Src	breast:	n/a
49	chr12:308821-308871	NT2-D1	testis:	n/a
50	chr12:291668-291718	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:309101..311206-chr12:317148..318705,2	K562	blood:
2	chr12:297600..300406-chr12:301639..304265,3	K562	blood:
3	chr12:297965..298734-chr12:308100..308686,2	MCF-7	breast:
4	chr12:296668..298848-chr12:310032..311975,2	K562	blood:
5	chr12:284257..286850-chr12:289241..291499,2	MCF-7	breast:
6	chr12:280534..283039-chr12:284171..287283,4	K562	blood:
7	chr12:287241..288955-chr12:290597..292679,2	MCF-7	breast:
8	chr12:287922..289463-chr12:291196..293394,2	K562	blood:
9	chr12:211691..214245-chr12:294558..297175,2	K562	blood:
10	chr12:297943..299013-chr12:328724..329295,3	K562	blood:
11	chr12:298095..299012-chr12:328485..329986,6	MCF-7	breast:
12	chr12:278455..281013-chr12:283457..285093,2	K562	blood:
13	chr12:284226..286607-chr12:303579..306228,2	K562	blood:
14	chr12:272899..275602-chr12:282568..284207,2	MCF-7	breast:
15	chr12:297600..300406-chr12:301338..304265,4	K562	blood:
16	chr12:277748..279992-chr12:305232..307484,2	MCF-7	breast:
17	chr12:301002..302613-chr12:305489..307990,2	MCF-7	breast:
18	chr12:308043..310053-chr12:310352..312706,2	MCF-7	breast:
19	chr12:303209..305233-chr12:388816..390804,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IQSEC3-1	chr12:303127-303296	ENSG00000255671.1
2	lnc-SLC6A12-1	chr12:291234-291565	ENSG00000256540
3	lnc-IQSEC3-1	chr12:302202-302346	ENSG00000255671.1
4	lnc-SLC6A12-1	chr12:291234-291562	ENSG00000256540
5	lnc-CCDC77-4	chr12:285648-285729	NONHSAT025309
6	lnc-CCDC77-4	chr12:287177-287620	NONHSAT025309

Variant related genes	Relation type
ENSG00000256577	TF binding region
IQSEC3	TF binding region
ENSG00000256540	TF binding region
SLC6A12	TF binding region
ENSG00000255671	TF binding region
ENSG00000256577	CpG island
IQSEC3	CpG island
ENSG00000256540	CpG island
SLC6A12	CpG island
ENSG00000255671	CpG island
ENSG00000256540	chromatin interactions
ENSG00000120645	chromatin interactions
ENSG00000256694	chromatin interactions
ENSG00000255671	chromatin interactions
ENSG00000111181	chromatin interactions

Extended variants
information (count: 1661 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1661 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546092648	chr12:282481-282482	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs534066541	chr12:282504-282505	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs555423909	chr12:282538-282539	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573724448	chr12:282539-282540	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs117575159	chr12:282544-282545	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs532013608	chr12:282582-282583	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs563210178	chr12:282618-282619	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs184575624	chr12:282619-282620	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs370928952	chr12:282637-282638	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs560571221	chr12:282651-282652	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs77222186	chr12:282654-282655	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs549135816	chr12:282662-282663	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs560944682	chr12:282712-282713	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs187916889	chr12:282752-282753	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs140177371	chr12:282800-282801	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs571527513	chr12:282801-282802	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs76593881	chr12:282811-282812	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs572837776	chr12:282824-282825	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs374717222	chr12:282866-282867	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs192223287	chr12:282867-282868	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs76683891	chr12:282882-282883	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs555461196	chr12:282937-282938	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs573761404	chr12:282957-282958	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs537856335	chr12:282974-282975	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs556235494	chr12:282979-282980	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs554278863	chr12:282990-282991	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs545420353	chr12:283021-283022	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs35315396	chr12:283041-283042	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs372067879	chr12:283122-283123	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560826512	chr12:283177-283178	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs116210938	chr12:283194-283195	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs543216656	chr12:283245-283246	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs560981423	chr12:283260-283261	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs531394554	chr12:283279-283280	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs549844604	chr12:283282-283283	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs143805325	chr12:283283-283284	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs183565902	chr12:283290-283291	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs547402906	chr12:283344-283345	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs561501955	chr12:283385-283386	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs565608895	chr12:283400-283401	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs529852914	chr12:283415-283416	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs547938543	chr12:283416-283417	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs150921458	chr12:283469-283470	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs76223711	chr12:283481-283482	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs564076609	chr12:283511-283512	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs538003858	chr12:283517-283518	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531293922	chr12:283521-283522	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs571587810	chr12:283533-283534	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs539003760	chr12:283534-283535	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs140508242	chr12:283536-283537	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Autism	22495309	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:867 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:249000-284200	Weak transcription	Right Atrium	heart
2	chr12:253800-285600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr12:262800-284200	Weak transcription	Brain Angular Gyrus	brain
4	chr12:268800-284200	Weak transcription	Brain Anterior Caudate	brain
5	chr12:273600-284600	Weak transcription	Esophagus	oesophagus
6	chr12:276200-282800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr12:276200-284000	Enhancers	Primary hematopoietic stem cells	blood
8	chr12:276400-283000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:277200-292800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr12:277400-283200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr12:278400-283400	Weak transcription	Liver	Liver
12	chr12:278400-283600	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr12:278400-288400	Weak transcription	Fetal Kidney	kidney
14	chr12:278600-283400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr12:279000-285200	Weak transcription	Fetal Thymus	thymus
16	chr12:279800-283400	Weak transcription	Fetal Lung	lung
17	chr12:280000-283000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr12:280000-286000	Weak transcription	Fetal Brain Female	brain
19	chr12:280000-289600	Enhancers	Right Ventricle	heart
20	chr12:280400-283600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr12:280400-283800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr12:280400-286000	Bivalent Enhancer	Placenta	Placenta
23	chr12:280600-282600	Enhancers	Fetal Heart	heart
24	chr12:280600-283800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
25	chr12:280600-283800	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr12:280600-287400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:280600-288000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:281000-283000	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr12:281000-283800	Enhancers	Colonic Mucosa	Colon
30	chr12:281000-283800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
31	chr12:281000-290000	Enhancers	Left Ventricle	heart
32	chr12:281200-282800	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr12:281600-282600	Bivalent Enhancer	Stomach Mucosa	stomach
34	chr12:281600-283600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
35	chr12:281600-283800	Bivalent Enhancer	Adipose Nuclei	Adipose
36	chr12:281800-283200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr12:281800-284400	Enhancers	Spleen	Spleen
38	chr12:281800-285400	Weak transcription	Hela-S3	cervix
39	chr12:281800-289000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr12:282000-283600	Weak transcription	Fetal Intestine Small	intestine
41	chr12:282000-285400	Weak transcription	Gastric	stomach
42	chr12:282000-286600	Enhancers	Fetal Muscle Leg	muscle
43	chr12:282200-282800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr12:282200-282800	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr12:282200-283200	Weak transcription	HSMMtube	muscle
46	chr12:282200-288000	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr12:282400-282600	Enhancers	Lung	lung
48	chr12:282400-283400	Weak transcription	Duodenum Mucosa	Duodenum
49	chr12:282400-284200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr12:282600-283000	Weak transcription	Fetal Heart	heart

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