Variant report

Variant	esv3339713
Chromosome Location	chr1:93425789-93428737
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	chr1:93425910-93426345	K562	blood:	n/a	n/a
2	ARID3A	chr1:93426897-93426989	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:93425564-93426325	HepG2	liver:	n/a	n/a
4	ATF2	chr1:93427940-93428423	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:93425633-93426369	GM12878	blood:	n/a	n/a
6	ATF2	chr1:93425654-93426307	GM12878	blood:	n/a	n/a
7	ATF2	chr1:93427523-93428492	GM12878	blood:	n/a	n/a
8	ATF2	chr1:93427704-93428494	GM12878	blood:	n/a	n/a
9	BACH1	chr1:93425834-93426658	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr1:93428055-93428375	GM12878	blood:	n/a	chr1:93428209-93428220
11	BCL3	chr1:93425458-93426533	GM12878	blood:	n/a	n/a
12	BCL3	chr1:93428013-93428453	GM12878	blood:	n/a	chr1:93428187-93428196 chr1:93428188-93428197
13	BCL3	chr1:93426722-93427449	GM12878	blood:	n/a	chr1:93426870-93426883 chr1:93427198-93427211 chr1:93427329-93427342 chr1:93427203-93427212 chr1:93427002-93427015 chr1:93427327-93427340
14	BCL3	chr1:93425498-93425929	GM12878	blood:	n/a	n/a
15	BCLAF1	chr1:93425855-93426527	GM12878	blood:	n/a	n/a
16	BCLAF1	chr1:93426971-93428509	GM12878	blood:	n/a	chr1:93427198-93427211 chr1:93427329-93427342 chr1:93427203-93427212 chr1:93427002-93427015 chr1:93428187-93428196 chr1:93427327-93427340 chr1:93428188-93428197
17	BCLAF1	chr1:93425787-93426676	GM12878	blood:	n/a	chr1:93426540-93426549 chr1:93426598-93426611
18	BCLAF1	chr1:93427078-93427760	GM12878	blood:	n/a	chr1:93427198-93427211 chr1:93427329-93427342 chr1:93427203-93427212 chr1:93427327-93427340
19	BHLHE40	chr1:93425940-93427637	GM12878	blood:	n/a	chr1:93427324-93427340 chr1:93427224-93427240 chr1:93426903-93426919 chr1:93427195-93427211 chr1:93426800-93426816 chr1:93426781-93426797 chr1:93427198-93427214
20	BHLHE40	chr1:93426942-93428033	K562	blood:	n/a	chr1:93427324-93427340 chr1:93427224-93427240 chr1:93427195-93427211 chr1:93427198-93427214
21	BHLHE40	chr1:93425939-93426458	HepG2	liver:	n/a	n/a
22	BHLHE40	chr1:93425927-93426522	K562	blood:	n/a	n/a
23	BRCA1	chr1:93425956-93426469	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr1:93427240-93427441	HepG2	liver:	n/a	n/a
25	BRCA1	chr1:93427760-93427991	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr1:93427066-93427422	K562	blood:	n/a	n/a
27	CBX3	chr1:93425868-93426298	K562	blood:	n/a	n/a
28	CCNT2	chr1:93426402-93427760	K562	blood:	n/a	chr1:93426531-93426540 chr1:93426767-93426776
29	CEBPB	chr1:93428101-93428301	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:93428186-93428296	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:93425852-93426403	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:93427819-93428446	GM12878	blood:	n/a	n/a
33	CEBPB	chr1:93427429-93427732	K562	blood:	n/a	chr1:93427540-93427552
34	CEBPB	chr1:93427425-93427694	HepG2	liver:	n/a	chr1:93427540-93427552
35	CEBPB	chr1:93427380-93427702	IMR90	lung:	n/a	chr1:93427540-93427552
36	CEBPB	chr1:93427327-93427769	ECC-1	luminal epithelium:	n/a	chr1:93427540-93427552
37	CEBPB	chr1:93427184-93427741	Hela-S3	cervix:	n/a	chr1:93427540-93427552
38	CEBPB	chr1:93427490-93427639	H1-hESC	embryonic stem cell:	n/a	chr1:93427540-93427552
39	CEBPB	chr1:93425648-93426171	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:93425646-93426162	IMR90	lung:	n/a	n/a
41	CEBPD	chr1:93426778-93427378	HepG2	liver:	n/a	n/a
42	CHD1	chr1:93427154-93428515	GM12878	blood:	n/a	n/a
43	CHD1	chr1:93426047-93426482	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr1:93425733-93426480	GM12878	blood:	n/a	n/a
45	CHD1	chr1:93425664-93426809	IMR90	lung:	n/a	n/a
46	CHD1	chr1:93427493-93428063	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr1:93426823-93426827	HepG2	liver:	n/a	n/a
48	CHD2	chr1:93427148-93427348	HepG2	liver:	n/a	n/a
49	CHD2	chr1:93425974-93426307	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr1:93426540-93427354	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:93427451-93427501	Hela-S3	cervix:	n/a
2	chr1:93427451-93427501	HUVEC	blood vessel:	n/a
3	chr1:93427589-93427639	U87	brain:	n/a
4	chr1:93427468-93427518	Hela-S3	cervix:	n/a
5	chr1:93427468-93427518	T-47D	breast:	n/a
6	chr1:93427451-93427501	K562	blood:	n/a
7	chr1:93427468-93427518	GM12878	blood:	n/a
8	chr1:93427847-93427897	ECC-1	luminal epithelium:	n/a
9	chr1:93425802-93425852	HMEC	breast:	n/a
10	chr1:93425802-93425852	NT2-D1	testis:	n/a
11	chr1:93427847-93427897	SK-N-SH_RA	brain:	n/a
12	chr1:93427691-93427741	GM19239	blood:	n/a
13	chr1:93427260-93427310	A549	lung:	n/a
14	chr1:93427451-93427501	HPAEpiC	pulmonary alveolar:	n/a
15	chr1:93427451-93427501	A549	lung:	n/a
16	chr1:93427260-93427310	PANC-1	pancreas:	n/a
17	chr1:93427691-93427741	SKMC	muscle:	n/a
18	chr1:93427847-93427897	BJ	skin:	n/a
19	chr1:93427260-93427310	HNPCEpiC	eye:	n/a
20	chr1:93427451-93427501	PFSK-1	brain:	n/a
21	chr1:93427589-93427639	HL-60	blood:	n/a
22	chr1:93427847-93427897	HCT-116	colon:	n/a
23	chr1:93427260-93427310	HCT-116	colon:	n/a
24	chr1:93425802-93425852	ECC-1	luminal epithelium:	n/a
25	chr1:93427589-93427639	AG10803	skin:	n/a
26	chr1:93426922-93426972	GM12892	blood:	n/a
27	chr1:93427589-93427639	AG09309	skin:	n/a
28	chr1:93427260-93427310	HMEC	breast:	n/a
29	chr1:93426922-93426972	ECC-1	luminal epithelium:	n/a
30	chr1:93427260-93427310	AG04449	skin:	fetal
31	chr1:93427451-93427501	HEK293	kidney:	embryo
32	chr1:93427468-93427518	SK-N-SH	brain:	n/a
33	chr1:93427691-93427741	GM06990	blood:	n/a
34	chr1:93426922-93426972	AG09319	gingival:	n/a
35	chr1:93425802-93425852	HEEpiC	esophagus:	n/a
36	chr1:93427847-93427897	NT2-D1	testis:	n/a
37	chr1:93425802-93425852	NHDF-neo	bronchial:	n/a
38	chr1:93427691-93427741	NB4	blood:	n/a
39	chr1:93427847-93427897	PrEC	prostate:	n/a
40	chr1:93427260-93427310	HEEpiC	esophagus:	n/a
41	chr1:93427468-93427518	NB4	blood:	n/a
42	chr1:93425802-93425852	PANC-1	pancreas:	n/a
43	chr1:93427847-93427897	AG09309	skin:	n/a
44	chr1:93427260-93427310	IMR90	lung:	fetal
45	chr1:93427691-93427741	HUVEC	blood vessel:	n/a
46	chr1:93426981-93427031	SAEC	small airway:	n/a
47	chr1:93427691-93427741	SK-N-SH_RA	brain:	n/a
48	chr1:93427847-93427897	GM12878	blood:	n/a
49	chr1:93426922-93426972	NB4	blood:	n/a
50	chr1:93427468-93427518	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:93323615..93326108-chr1:93427081..93429012,3	K562	blood:
2	chr1:93296356..93298770-chr1:93426282..93429088,3	MCF-7	breast:
3	chr1:93378943..93379622-chr1:93425899..93426864,2	MCF-7	breast:
4	chr1:93426343..93426854-chr20:42285915..42286690,2	NB4	blood:
5	chr1:93324499..93325053-chr1:93427932..93428772,2	MCF-7	breast:
6	chr1:93418758..93421387-chr1:93428230..93431121,2	MCF-7	breast:
7	chr1:93324139..93325155-chr1:93425615..93426899,9	MCF-7	breast:
8	chr1:93409434..93411659-chr1:93423338..93426325,2	K562	blood:
9	chr1:93425058..93429733-chr1:93431759..93435608,8	K562	blood:
10	chr1:93427351..93429788-chr1:93458702..93460989,2	MCF-7	breast:
11	chr1:93296297..93299381-chr1:93425183..93428047,4	K562	blood:
12	chr1:93428117..93429773-chr1:93455192..93456852,2	K562	blood:
13	chr1:93323615..93326108-chr1:93427081..93429012,2	K562	blood:
14	chr1:28831926..28832622-chr1:93426787..93427442,3	Hela-S3	cervix:
15	chr1:93428670..93431519-chr1:93436663..93439033,2	MCF-7	breast:
16	chr1:93425993..93428373-chr1:93433568..93436256,2	MCF-7	breast:
17	chr1:93426062..93426867-chr1:93459810..93460332,2	MCF-7	breast:

Variant related genes	Relation type
FAM69A	TF binding region
FAM69A	CpG island
ENSG00000242125	chromatin interactions
ENSG00000252121	chromatin interactions
ENSG00000122406	chromatin interactions
ENSG00000180198	chromatin interactions

Extended variants
information (count: 100 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:100 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551866589	chr1:93425831-93425832	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs570401575	chr1:93425836-93425837	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534436381	chr1:93425856-93425857	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs76234228	chr1:93425857-93425858	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs566281156	chr1:93425894-93425895	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536838206	chr1:93425909-93425910	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs181544142	chr1:93425923-93425924	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576643646	chr1:93425924-93425925	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs185877826	chr1:93425971-93425972	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs75145568	chr1:93425990-93425991	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs191126414	chr1:93425993-93425994	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs183118580	chr1:93426012-93426013	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs559374256	chr1:93426029-93426030	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs112522493	chr1:93426043-93426044	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs187794015	chr1:93426044-93426045	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs190319640	chr1:93426143-93426144	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs945631	chr1:93426167-93426168	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs552414102	chr1:93426186-93426187	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs563937852	chr1:93426196-93426197	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs545735758	chr1:93426221-93426222	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs528044298	chr1:93426268-93426269	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs559216322	chr1:93426299-93426300	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568155600	chr1:93426313-93426314	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs945630	chr1:93426341-93426342	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs548061648	chr1:93426350-93426351	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs570201449	chr1:93426378-93426379	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs537357828	chr1:93426442-93426443	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs568219671	chr1:93426457-93426458	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs12747275	chr1:93426541-93426542	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs534693738	chr1:93426584-93426585	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs553090656	chr1:93426602-93426603	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs372025509	chr1:93426674-93426675	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs574571084	chr1:93426715-93426716	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs375092305	chr1:93426720-93426721	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs563354945	chr1:93426746-93426747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs369295135	chr1:93426782-93426783	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs575356770	chr1:93426817-93426818	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs945629	chr1:93426866-93426867	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs1415069	chr1:93426869-93426870	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs116489989	chr1:93426874-93426875	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs546605617	chr1:93426888-93426889	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs201322845	chr1:93426938-93426939	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs200117269	chr1:93426945-93426946	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs550613373	chr1:93426969-93426970	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs563440628	chr1:93426995-93426996	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs537604156	chr1:93427016-93427017	Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs552641276	chr1:93427021-93427022	Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs571115926	chr1:93427038-93427039	Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs534725660	chr1:93427116-93427117	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs55838613	chr1:93427162-93427163	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93409600-93426000	Weak transcription	Lung	lung
2	chr1:93410600-93425800	Weak transcription	Right Atrium	heart
3	chr1:93410600-93426000	Weak transcription	Left Ventricle	heart
4	chr1:93411000-93425800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr1:93417000-93425800	Weak transcription	Right Ventricle	heart
6	chr1:93417200-93425800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:93418200-93425800	Weak transcription	Psoas Muscle	Psoas
8	chr1:93422000-93425800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr1:93422800-93425800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:93423200-93425800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:93423200-93425800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr1:93423200-93426200	Weak transcription	Gastric	stomach
13	chr1:93423200-93426200	Weak transcription	Spleen	Spleen
14	chr1:93423800-93425800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr1:93424200-93425800	Weak transcription	Fetal Stomach	stomach
16	chr1:93424600-93425800	Weak transcription	Colon Smooth Muscle	Colon
17	chr1:93424600-93425800	Enhancers	Placenta	Placenta
18	chr1:93424800-93425800	Weak transcription	Fetal Intestine Large	intestine
19	chr1:93425200-93426000	Flanking Active TSS	Stomach Smooth Muscle	stomach
20	chr1:93425200-93428000	Active TSS	Brain Hippocampus Middle	brain
21	chr1:93425200-93428000	Active TSS	NHDF-Ad	bronchial
22	chr1:93425200-93428200	Active TSS	Liver	Liver
23	chr1:93425200-93428200	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr1:93425200-93428200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr1:93425200-93428200	Active TSS	Brain Substantia Nigra	brain
26	chr1:93425400-93425800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:93425400-93425800	Enhancers	Fetal Intestine Small	intestine
28	chr1:93425400-93425800	Flanking Active TSS	GM12878-XiMat	blood
29	chr1:93425400-93426000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:93425400-93426200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr1:93425400-93428200	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr1:93425400-93428200	Active TSS	Brain Angular Gyrus	brain
33	chr1:93425400-93428200	Active TSS	Brain Anterior Caudate	brain
34	chr1:93425600-93425800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr1:93425600-93425800	Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr1:93425600-93425800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
37	chr1:93425600-93425800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
38	chr1:93425600-93425800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
39	chr1:93425600-93425800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:93425600-93425800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr1:93425600-93425800	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:93425600-93425800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr1:93425600-93425800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr1:93425600-93425800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:93425600-93425800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr1:93425600-93425800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:93425600-93425800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
48	chr1:93425600-93425800	Enhancers	Fetal Brain Male	brain
49	chr1:93425600-93425800	Enhancers	Fetal Lung	lung
50	chr1:93425600-93425800	Flanking Active TSS	Rectal Smooth Muscle	rectum

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