Variant report

Variant	nsv559037
Chromosome Location	chr12:58027307-58028863
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:93)
CpG islands
(count:62)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:93 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr12:58026766-58027387	A549	lung:	n/a	n/a
2	BCL3	chr12:58026683-58027353	A549	lung:	n/a	chr12:58026899-58026912 chr12:58026923-58026936 chr12:58026747-58026760
3	BRCA1	chr12:58027448-58027648	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr12:58027364-58027498	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr12:58026919-58027379	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr12:58027160-58027310	Caco-2	colon:	n/a	n/a
7	CTCF	chr12:58026844-58027442	GM19240	blood:	n/a	n/a
8	CTCF	chr12:58028198-58028352	HepG2	liver:	n/a	n/a
9	CTCF	chr12:58028231-58028301	HepG2	liver:	n/a	n/a
10	CTCF	chr12:58027304-58027449	MCF-7	breast:	n/a	n/a
11	CTCF	chr12:58026798-58027589	K562	blood:	n/a	n/a
12	CTCF	chr12:58028220-58028370	AG10803	skin:	n/a	n/a
13	CTCF	chr12:58027291-58027429	GM12891	blood:	n/a	n/a
14	CTCF	chr12:58028140-58028290	HCT-116	colon:	n/a	n/a
15	CTCF	chr12:58025290-58027579	SK-N-SH	brain:	n/a	chr12:58026689-58026702 chr12:58025999-58026012
16	CTCF	chr12:58028194-58028325	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr12:58027320-58027470	HCFaa	heart:	n/a	n/a
18	CTCF	chr12:58026112-58027523	K562	blood:	n/a	chr12:58026689-58026702
19	CTCF	chr12:58026769-58027432	K562	blood:	n/a	n/a
20	CTCF	chr12:58027300-58027450	HMF	breast:	n/a	n/a
21	CTCF	chr12:58027320-58027470	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:58027272-58027400	GM19238	blood:	n/a	n/a
23	CTCF	chr12:58026515-58027461	HCT-116	colon:	n/a	chr12:58026689-58026702
24	CTCF	chr12:58027300-58027450	AG04449	skin:	n/a	n/a
25	CTCF	chr12:58027600-58027750	GM12872	blood:	n/a	n/a
26	CTCF	chr12:58026665-58027390	MCF-7	breast:	n/a	chr12:58026689-58026702
27	CTCF	chr12:58027280-58027430	GM12864	blood:	n/a	n/a
28	CTCF	chr12:58027360-58027510	HFF	foreskin:	n/a	n/a
29	CTCF	chr12:58026769-58027424	GM12878	blood:	n/a	n/a
30	CTCF	chr12:58027340-58027490	GM12871	blood:	n/a	n/a
31	CTCF	chr12:58028039-58028059	GM10266	blood:	n/a	n/a
32	CTCF	chr12:58025888-58027618	A549	lung:	n/a	chr12:58026689-58026702 chr12:58025999-58026012
33	CTCF	chr12:58027240-58027390	K562	blood:	n/a	n/a
34	CTCF	chr12:58027980-58028130	SAEC	small airway:	n/a	n/a
35	CTCF	chr12:58027270-58027426	GM12892	blood:	n/a	n/a
36	E2F4	chr12:58026807-58027433	K562	blood:	n/a	chr12:58027192-58027201 chr12:58026971-58026982
37	E2F6	chr12:58026755-58027313	A549	lung:	n/a	chr12:58027192-58027201
38	E2F6	chr12:58026621-58027521	H1-hESC	embryonic stem cell:	n/a	chr12:58027192-58027201
39	E2F6	chr12:58025890-58027512	K562	blood:	n/a	chr12:58027192-58027201
40	E2F6	chr12:58026742-58027368	H1-hESC	embryonic stem cell:	n/a	chr12:58027192-58027201
41	E2F6	chr12:58025823-58027509	A549	lung:	n/a	chr12:58027192-58027201
42	ETS1	chr12:58026855-58027318	A549	lung:	n/a	n/a
43	FOSL2	chr12:58026803-58027606	A549	lung:	n/a	chr12:58027547-58027559 chr12:58027322-58027331
44	HA-E2F1	chr12:58025936-58027531	MCF-7	breast:	n/a	chr12:58027192-58027201
45	JUN	chr12:58028737-58028962	HepG2	liver:	n/a	chr12:58028877-58028890
46	JUN	chr12:58026099-58027646	K562	blood:	n/a	chr12:58027547-58027559 chr12:58027322-58027331
47	JUND	chr12:58026779-58027494	K562	blood:	n/a	chr12:58027322-58027331
48	JUND	chr12:58028727-58029014	HepG2	liver:	n/a	n/a
49	KAP1	chr12:58026755-58027437	HEK293	kidney:	n/a	n/a
50	MAFK	chr12:58027468-58027625	Hela-S3	cervix:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:58027504-58027554	HEK293	kidney:	embryo
2	chr12:58027504-58027554	HEK293	kidney:	embryo
3	chr12:58027504-58027554	PrEC	prostate:	n/a
4	chr12:58027504-58027554	NT2-D1	testis:	n/a
5	chr12:58027504-58027554	A549	lung:	n/a
6	chr12:58027504-58027554	IMR90	lung:	fetal
7	chr12:58027504-58027554	NH-A	brain:	n/a
8	chr12:58027504-58027554	NHBE	bronchial:	n/a
9	chr12:58027504-58027554	AG04450	lung:	fetal
10	chr12:58027504-58027554	AG09319	gingival:	n/a
11	chr12:58027504-58027554	PFSK-1	brain:	n/a
12	chr12:58027504-58027554	H1-hESC	embryonic stem cell:	embryo
13	chr12:58027504-58027554	BJ	skin:	n/a
14	chr12:58027504-58027554	HNPCEpiC	eye:	n/a
15	chr12:58027504-58027554	HCT-116	colon:	n/a
16	chr12:58027504-58027554	HIPEpiC	eye:	n/a
17	chr12:58027504-58027554	MCF10A-Er-Src	breast:	n/a
18	chr12:58027504-58027554	SKMC	muscle:	n/a
19	chr12:58027504-58027554	HRE	kidney:	n/a
20	chr12:58027504-58027554	HMEC	breast:	n/a
21	chr12:58027504-58027554	AoSMC	blood vessel:	n/a
22	chr12:58027504-58027554	GM12878	blood:	n/a
23	chr12:58027504-58027554	HAEpiC	amniotic membrane:	n/a
24	chr12:58027504-58027554	HepG2	liver:	n/a
25	chr12:58027504-58027554	K562	blood:	n/a
26	chr12:58027504-58027554	GM12892	blood:	n/a
27	chr12:58027504-58027554	HEEpiC	esophagus:	n/a
28	chr12:58027504-58027554	RPTEC	kidney:	n/a
29	chr12:58027504-58027554	HCM	heart:	n/a
30	chr12:58027504-58027554	GM12891	blood:	n/a
31	chr12:58027504-58027554	Jurkat	blood:	n/a
32	chr12:58027504-58027554	HRCEpiC	kidney:	n/a
33	chr12:58027504-58027554	CMK	blood:	n/a
34	chr12:58027504-58027554	HCF	heart:	n/a
35	chr12:58027504-58027554	LNCaP	prostate:	n/a
36	chr12:58027504-58027554	SK-N-SH	brain:	n/a
37	chr12:58027504-58027554	BE2_C	brain:	n/a
38	chr12:58027504-58027554	U87	brain:	n/a
39	chr12:58027504-58027554	AG09309	skin:	n/a
40	chr12:58027504-58027554	NHDF-neo	bronchial:	n/a
41	chr12:58027504-58027554	HUVEC	blood vessel:	n/a
42	chr12:58027504-58027554	SK-N-SH_RA	brain:	n/a
43	chr12:58027504-58027554	SK-N-MC	brain:	n/a
44	chr12:58027504-58027554	Caco-2	colon:	n/a
45	chr12:58027504-58027554	MCF-7	breast:	n/a
46	chr12:58027504-58027554	AG10803	skin:	n/a
47	chr12:58027504-58027554	Hela-S3	cervix:	n/a
48	chr12:58027504-58027554	AG04449	skin:	fetal
49	chr12:58027504-58027554	SAEC	small airway:	n/a
50	chr12:58027504-58027554	GM06990	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57939451..57941325-chr12:58024374..58027583,3	K562	blood:
2	chr12:57983391..57985108-chr12:58026747..58028430,2	MCF-7	breast:
3	chr12:58017301..58018862-chr12:58026279..58027788,2	MCF-7	breast:
4	chr12:58026019..58028946-chr12:58148453..58151531,3	K562	blood:
5	chr12:57908910..57916122-chr12:58022622..58031573,17	K562	blood:
6	chr12:57935626..57940631-chr12:58026197..58030320,5	K562	blood:
7	chr12:57908910..57916403-chr12:58022622..58028885,15	K562	blood:
8	chr12:57983573..57987941-chr12:58024849..58028209,5	MCF-7	breast:
9	chr12:57915782..57916713-chr12:58026905..58027434,2	MCF-7	breast:
10	chr12:58004618..58008024-chr12:58024930..58028098,5	MCF-7	breast:
11	chr12:57940164..57942070-chr12:58025601..58028102,2	MCF-7	breast:
12	chr12:57997114..58001112-chr12:58025485..58030490,5	MCF-7	breast:
13	chr12:58026407..58027580-chr12:58087150..58087941,5	MCF-7	breast:
14	chr12:58026893..58027508-chr12:58087361..58087934,2	K562	blood:
15	chr12:58024113..58026472-chr12:58028228..58030289,2	K562	blood:
16	chr12:58026571..58028240-chr12:58118727..58121626,2	MCF-7	breast:

No data

Variant related genes	Relation type
B4GALNT1	TF binding region
B4GALNT1	CpG island
ENSG00000166986	chromatin interactions
ENSG00000255737	chromatin interactions
ENSG00000135446	chromatin interactions
ENSG00000166987	chromatin interactions
ENSG00000135506	chromatin interactions
ENSG00000166908	chromatin interactions
ENSG00000135502	chromatin interactions
ENSG00000178498	chromatin interactions
ENSG00000175203	chromatin interactions
ENSG00000175197	chromatin interactions
ENSG00000240771	chromatin interactions
ENSG00000139266	chromatin interactions
ENSG00000257499	chromatin interactions
ENSG00000135454	chromatin interactions
ENSG00000208028	chromatin interactions

Extended variants
information (count: 70 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:70 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2619468	chr12:58027307-58027308	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77195304	chr12:58027310-58027311	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
3	rs567415000	chr12:58027311-58027312	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
4	rs537897507	chr12:58027349-58027350	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
5	rs150687711	chr12:58027408-58027409	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
6	rs556093364	chr12:58027443-58027444	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
7	rs147550525	chr12:58027447-58027448	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
8	rs571618243	chr12:58027465-58027466	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
9	rs199664310	chr12:58027466-58027467	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
10	rs530867291	chr12:58027502-58027503	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
11	rs538930787	chr12:58027541-58027542	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
12	rs200569699	chr12:58027597-58027598	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
13	rs139031660	chr12:58027598-58027599	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
14	rs550890799	chr12:58027604-58027605	Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
15	rs554366537	chr12:58027645-58027646	Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
16	rs7979462	chr12:58027685-58027686	Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
17	rs7979463	chr12:58027693-58027694	Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
18	rs7953917	chr12:58027698-58027699	Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs7953934	chr12:58027730-58027731	Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
20	rs538583473	chr12:58027775-58027776	Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs139387167	chr12:58027778-58027779	Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs543196880	chr12:58027815-58027816	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
23	rs370344120	chr12:58027865-58027866	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs72377255	chr12:58027866-58027867	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs59463846	chr12:58027875-58027876	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs12296706	chr12:58027876-58027877	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs564302758	chr12:58027878-58027879	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs571170352	chr12:58027879-58027880	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs57120398	chr12:58027880-58027881	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs12811305	chr12:58027894-58027895	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs3899676	chr12:58027916-58027917	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs547092766	chr12:58027953-58027954	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs143198408	chr12:58027965-58027966	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs201486187	chr12:58027992-58027993	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
35	rs543450930	chr12:58028020-58028021	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
36	rs12296818	chr12:58028037-58028038	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs577088012	chr12:58028044-58028045	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
38	rs4397894	chr12:58028049-58028050	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
39	rs185185790	chr12:58028051-58028052	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
40	rs149575786	chr12:58028053-58028054	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
41	rs142710812	chr12:58028055-58028056	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
42	rs145038850	chr12:58028058-58028059	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
43	rs548364305	chr12:58028064-58028065	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
44	rs559664384	chr12:58028080-58028081	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
45	rs561052349	chr12:58028126-58028127	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs575572182	chr12:58028142-58028143	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs531654401	chr12:58028234-58028235	Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
48	rs544560489	chr12:58028268-58028269	Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs571279964	chr12:58028283-58028284	Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs372349757	chr12:58028304-58028305	Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Thoracic aortic aneurysm	21092924	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
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	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
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:58025000-58027600	Active TSS	Brain Angular Gyrus	brain
2	chr12:58025400-58027400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
3	chr12:58025400-58027400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:58025400-58027600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
5	chr12:58025400-58027600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
6	chr12:58025600-58027400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
7	chr12:58025600-58027400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:58025600-58027400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr12:58025600-58027400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:58025600-58027600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
11	chr12:58025600-58027600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
12	chr12:58025600-58027600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:58025600-58027600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr12:58025800-58027400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:58025800-58027400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:58025800-58027400	Active TSS	Psoas Muscle	Psoas
17	chr12:58025800-58027600	Bivalent Enhancer	Liver	Liver
18	chr12:58026000-58027400	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr12:58026000-58027400	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr12:58026000-58027400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr12:58026000-58027400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
22	chr12:58026000-58027400	Bivalent Enhancer	Stomach Mucosa	stomach
23	chr12:58026200-58027400	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr12:58026200-58027400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr12:58026200-58027400	Active TSS	NHLF	lung
26	chr12:58026200-58027600	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
27	chr12:58026600-58027400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
28	chr12:58026600-58027400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
29	chr12:58026800-58027400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
30	chr12:58026800-58027600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
31	chr12:58027000-58027400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr12:58027000-58027400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:58027000-58027400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
34	chr12:58027000-58027400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:58027000-58027400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr12:58027000-58027400	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
37	chr12:58027000-58027400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr12:58027000-58027400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr12:58027000-58027400	Flanking Active TSS	Brain Anterior Caudate	brain
40	chr12:58027000-58027400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr12:58027000-58027400	Bivalent Enhancer	Fetal Intestine Small	intestine
42	chr12:58027000-58027400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr12:58027000-58027400	Enhancers	Left Ventricle	heart
44	chr12:58027000-58027400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
45	chr12:58027000-58027400	Flanking Active TSS	GM12878-XiMat	blood
46	chr12:58027000-58027400	Flanking Active TSS	HMEC	breast
47	chr12:58027000-58027400	Flanking Active TSS	K562	blood
48	chr12:58027000-58027600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr12:58027000-58027600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
50	chr12:58027000-58027600	Bivalent Enhancer	Primary B cells from peripheral blood	blood

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