Variant report

Variant	esv2760996
Chromosome Location	chr6:147229457-147269633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:649)
CpG islands
(count:125)
Chromatin interactive
region (count:52)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:147265971-147266384	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:147266254-147266309	K562	blood:	n/a	n/a
3	ARID3A	chr6:147234419-147237096	K562	blood:	n/a	n/a
4	ARID3A	chr6:147267318-147267618	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:147229968-147230305	K562	blood:	n/a	n/a
6	ATF1	chr6:147235002-147235408	K562	blood:	n/a	n/a
7	ATF1	chr6:147233135-147233228	K562	blood:	n/a	n/a
8	ATF1	chr6:147260664-147260917	K562	blood:	n/a	n/a
9	ATF1	chr6:147257445-147257513	K562	blood:	n/a	n/a
10	ATF1	chr6:147236760-147237211	K562	blood:	n/a	n/a
11	ATF1	chr6:147235628-147236245	K562	blood:	n/a	n/a
12	ATF3	chr6:147238272-147238594	K562	blood:	n/a	n/a
13	ATF3	chr6:147234822-147236272	K562	blood:	n/a	n/a
14	ATF3	chr6:147234962-147235452	K562	blood:	n/a	n/a
15	BACH1	chr6:147235049-147235767	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:147235017-147235641	K562	blood:	n/a	n/a
17	BCL3	chr6:147235496-147236532	A549	lung:	n/a	chr6:147236405-147236412
18	BHLHE40	chr6:147255643-147255644	K562	blood:	n/a	n/a
19	BHLHE40	chr6:147234056-147236200	K562	blood:	n/a	n/a
20	BHLHE40	chr6:147236766-147237247	K562	blood:	n/a	n/a
21	BRCA1	chr6:147235051-147236683	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr6:147234859-147236239	HCT-116	colon:	n/a	chr6:147236153-147236164
23	CBX3	chr6:147244411-147244927	K562	blood:	n/a	n/a
24	CBX3	chr6:147234880-147236551	K562	blood:	n/a	chr6:147236153-147236164
25	CBX3	chr6:147236611-147237346	K562	blood:	n/a	n/a
26	CBX3	chr6:147234881-147236601	HCT-116	colon:	n/a	chr6:147236153-147236164
27	CCNT2	chr6:147229840-147230416	K562	blood:	n/a	n/a
28	CCNT2	chr6:147235037-147236417	K562	blood:	n/a	n/a
29	CEBPB	chr6:147235599-147236154	A549	lung:	n/a	n/a
30	CEBPB	chr6:147234466-147235245	A549	lung:	n/a	n/a
31	CEBPB	chr6:147234361-147237038	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr6:147268357-147268644	HepG2	liver:	n/a	chr6:147268472-147268489 chr6:147268475-147268486
33	CEBPB	chr6:147234486-147236260	IMR90	lung:	n/a	n/a
34	CEBPB	chr6:147235551-147236040	A549	lung:	n/a	n/a
35	CEBPB	chr6:147268407-147268607	IMR90	lung:	n/a	chr6:147268472-147268489 chr6:147268475-147268486
36	CEBPB	chr6:147234540-147235458	A549	lung:	n/a	n/a
37	CEBPB	chr6:147229188-147229494	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr6:147235609-147236054	K562	blood:	n/a	n/a
39	CEBPB	chr6:147234521-147235252	K562	blood:	n/a	n/a
40	CEBPB	chr6:147234910-147236360	HCT-116	colon:	n/a	n/a
41	CEBPB	chr6:147264899-147265031	HepG2	liver:	n/a	n/a
42	CEBPB	chr6:147235602-147235966	K562	blood:	n/a	n/a
43	CEBPB	chr6:147234890-147235340	MCF-7	breast:	n/a	n/a
44	CEBPB	chr6:147235524-147236368	A549	lung:	n/a	n/a
45	CEBPB	chr6:147234823-147236256	K562	blood:	n/a	n/a
46	CEBPB	chr6:147234849-147235290	A549	lung:	n/a	n/a
47	CEBPB	chr6:147234816-147236561	HCT-116	colon:	n/a	n/a
48	CEBPB	chr6:147234919-147235346	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPD	chr6:147235514-147236385	K562	blood:	n/a	n/a
50	CEBPD	chr6:147235544-147236608	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:147232774-147232824	NB4	blood:	n/a
2	chr6:147235033-147235083	GM12878	blood:	n/a
3	chr6:147235033-147235083	Caco-2	colon:	n/a
4	chr6:147232774-147232824	NB4	blood:	n/a
5	chr6:147235033-147235083	GM12878	blood:	n/a
6	chr6:147235033-147235083	Caco-2	colon:	n/a
7	chr6:147235033-147235083	HAEpiC	amniotic membrane:	n/a
8	chr6:147235033-147235083	AG09309	skin:	n/a
9	chr6:147235033-147235083	HEEpiC	esophagus:	n/a
10	chr6:147235033-147235083	Jurkat	blood:	n/a
11	chr6:147235033-147235083	NT2-D1	testis:	n/a
12	chr6:147235033-147235083	CMK	blood:	n/a
13	chr6:147232774-147232824	HEK293	kidney:	embryo
14	chr6:147232774-147232824	ProgFib	skin:	n/a
15	chr6:147235033-147235083	GM12892	blood:	n/a
16	chr6:147235033-147235083	SKMC	muscle:	n/a
17	chr6:147232774-147232824	AG04450	lung:	fetal
18	chr6:147232774-147232824	HCF	heart:	n/a
19	chr6:147235033-147235083	SK-N-SH_RA	brain:	n/a
20	chr6:147235033-147235083	HRE	kidney:	n/a
21	chr6:147235033-147235083	HCT-116	colon:	n/a
22	chr6:147232774-147232824	HL-60	blood:	n/a
23	chr6:147232774-147232824	U87	brain:	n/a
24	chr6:147232774-147232824	H1-hESC	embryonic stem cell:	embryo
25	chr6:147232774-147232824	NHDF-neo	bronchial:	n/a
26	chr6:147232774-147232824	GM19239	blood:	n/a
27	chr6:147232774-147232824	GM12878	blood:	n/a
28	chr6:147232774-147232824	IMR90	lung:	fetal
29	chr6:147232774-147232824	K562	blood:	n/a
30	chr6:147235033-147235083	RPTEC	kidney:	n/a
31	chr6:147232774-147232824	Hepatocyte	liver:	n/a
32	chr6:147232774-147232824	HRE	kidney:	n/a
33	chr6:147235033-147235083	HRCEpiC	kidney:	n/a
34	chr6:147232774-147232824	PrEC	prostate:	n/a
35	chr6:147232774-147232824	GM06990	blood:	n/a
36	chr6:147235033-147235083	GM06990	blood:	n/a
37	chr6:147235033-147235083	AG04450	lung:	fetal
38	chr6:147232774-147232824	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:147232774-147232824	HRCEpiC	kidney:	n/a
40	chr6:147235033-147235083	Hela-S3	cervix:	n/a
41	chr6:147232774-147232824	HCPEpiC	choroid plexus:	n/a
42	chr6:147232774-147232824	AG09309	skin:	n/a
43	chr6:147235033-147235083	BE2_C	brain:	n/a
44	chr6:147235033-147235083	ProgFib	skin:	n/a
45	chr6:147232774-147232824	HEEpiC	esophagus:	n/a
46	chr6:147235033-147235083	K562	blood:	n/a
47	chr6:147232774-147232824	SK-N-SH_RA	brain:	n/a
48	chr6:147232774-147232824	GM12892	blood:	n/a
49	chr6:147235033-147235083	HRPEpiC	eye:	n/a
50	chr6:147235033-147235083	IMR90	lung:	fetal

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:147244432..147247370-chr6:147252827..147255501,2	K562	blood:
2	chr6:147233707..147236071-chr6:147462747..147464328,2	K562	blood:
3	chr12:62653163..62653951-chr6:147234896..147235625,2	Hela-S3	cervix:
4	chr6:147245797..147247698-chr6:147527227..147529725,2	K562	blood:
5	chr6:147255677..147257632-chr6:147259181..147261185,2	K562	blood:
6	chr6:147250308..147252005-chr6:147252419..147255385,2	K562	blood:
7	chr6:147205396..147207427-chr6:147257781..147260331,2	K562	blood:
8	chr6:147235428..147237038-chr6:147271559..147273136,2	K562	blood:
9	chr6:147230413..147232261-chr6:147234463..147236812,2	MCF-7	breast:
10	chr6:147233328..147236267-chr6:147495924..147498076,2	K562	blood:
11	chr6:147244432..147247370-chr6:147252827..147255501,2	K562	blood:
12	chr6:147240380..147243056-chr6:147250976..147252874,2	K562	blood:
13	chr6:147238517..147240324-chr6:147265571..147267356,2	K562	blood:
14	chr6:147240380..147243056-chr6:147250976..147252874,2	K562	blood:
15	chr6:147238517..147240324-chr6:147265571..147267356,2	K562	blood:
16	chr6:147222212..147229913-chr6:147522379..147526472,14	MCF-7	breast:
17	chr6:147233878..147235658-chr6:147257090..147258636,2	K562	blood:
18	chr6:147232830..147236608-chr6:147480889..147484110,6	K562	blood:
19	chr6:147233878..147235658-chr6:147257090..147258636,2	K562	blood:
20	chr6:147249918..147252907-chr6:147523590..147525925,2	K562	blood:
21	chr5:33441333..33441909-chr6:147235841..147236407,2	Hela-S3	cervix:
22	chr6:147200323..147203212-chr6:147234929..147236464,2	MCF-7	breast:
23	chr6:147232346..147237544-chr6:147521050..147527983,13	K562	blood:
24	chr6:147245165..147247960-chr6:147256037..147258072,2	K562	blood:
25	chr6:147234020..147237797-chr6:147479326..147483886,4	K562	blood:
26	chr6:147263063..147265442-chr6:147274553..147276073,2	K562	blood:
27	chr6:147255283..147257003-chr6:147267757..147269418,2	MCF-7	breast:
28	chr6:147255677..147257632-chr6:147259181..147261185,2	K562	blood:
29	chr6:147231935..147237791-chr6:147522176..147527834,11	MCF-7	breast:
30	chr6:147222683..147225262-chr6:147248637..147251442,2	K562	blood:
31	chr6:147235434..147237461-chr6:147248241..147250558,2	K562	blood:
32	chr6:147195935..147198444-chr6:147269151..147270925,2	K562	blood:
33	chr6:147235229..147236928-chr6:147271559..147273634,2	K562	blood:
34	chr6:147238598..147240366-chr6:147524082..147525890,2	MCF-7	breast:
35	chr6:147251390..147254313-chr6:147527103..147529241,2	K562	blood:
36	chr6:147250308..147252005-chr6:147252419..147255385,2	K562	blood:
37	chr6:147229321..147232231-chr6:147553682..147556359,2	K562	blood:
38	chr6:147237637..147240471-chr6:147523108..147525517,2	MCF-7	breast:
39	chr6:146134441..146136480-chr6:147234336..147236688,2	K562	blood:
40	chr6:147245165..147247960-chr6:147256037..147258072,2	K562	blood:
41	chr6:147230247..147234342-chr6:147246927..147253758,6	K562	blood:
42	chr6:147252177..147253046-chr6:147543398..147544034,2	MCF-7	breast:
43	chr6:147234520..147236599-chr6:147304755..147307670,2	MCF-7	breast:
44	chr6:147229677..147239083-chr6:147521152..147530893,22	K562	blood:
45	chr6:147254059..147256031-chr6:147270328..147273049,2	K562	blood:
46	chr6:147232975..147234547-chr6:147542627..147545100,2	K562	blood:
47	chr6:147230413..147232261-chr6:147234463..147236812,2	MCF-7	breast:
48	chr6:147247656..147249840-chr6:147522815..147524593,2	K562	blood:
49	chr6:147243166..147246060-chr6:147523234..147526138,2	MCF-7	breast:
50	chr6:147237763..147240399-chr6:147521752..147524645,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHPRH-2	chr6:147232688-147232742	ENSG00000233452
2	lnc-SHPRH-2	chr6:147232688-147232801	ENSG00000233452.2
3	lnc-SHPRH-2	chr6:147236812-147237021	NONHSAT115435
4	lnc-SHPRH-2	chr6:147232920-147233075	NONHSAT115441
5	lnc-SHPRH-2	chr6:147232688-147232801	NONHSAT115441
6	lnc-SHPRH-2	chr6:147232688-147232801	NONHSAT115435
7	lnc-SHPRH-2	chr6:147232962-147233075	ENSG00000233452
8	lnc-SHPRH-2	chr6:147236812-147237021	ENSG00000233452.2
9	lnc-C6orf103-4	chr6:147234706-147236426	NONHSAT115444

No data

Variant related genes	Relation type
STXBP5-AS1	TF binding region
STXBP5-AS1	CpG island
ENSG00000164506	chromatin interactions
ENSG00000235652	chromatin interactions
ENSG00000196634	chromatin interactions
ENSG00000198673	chromatin interactions
ENSG00000118496	chromatin interactions
ENSG00000272397	chromatin interactions
ENSG00000233452	chromatin interactions
ENSG00000113407	chromatin interactions
TBX21	miRNA target sites
SMYD2	miRNA target sites

Extended variants
information (count: 1243 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1243 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17076418	chr6:147229457-147229458	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113120112	chr6:147229468-147229469	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs549541093	chr6:147229502-147229503	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs200959585	chr6:147229515-147229516	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs141518960	chr6:147229546-147229547	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs150888437	chr6:147229560-147229561	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs558823828	chr6:147229583-147229584	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs139601410	chr6:147229645-147229646	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs555001539	chr6:147229747-147229748	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs534833887	chr6:147229827-147229828	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs144322689	chr6:147229855-147229856	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs17076421	chr6:147229879-147229880	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs187819036	chr6:147229916-147229917	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs192161283	chr6:147229932-147229933	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs373633177	chr6:147229936-147229937	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs60452853	chr6:147229942-147229943	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs577454018	chr6:147229953-147229954	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs556449648	chr6:147229991-147229992	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs373061206	chr6:147230013-147230014	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs146583756	chr6:147230026-147230027	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs528630328	chr6:147230034-147230035	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs140006761	chr6:147230069-147230070	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs377671082	chr6:147230083-147230084	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs545203135	chr6:147230099-147230100	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs560630074	chr6:147230131-147230132	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs371220545	chr6:147230137-147230138	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs4895704	chr6:147230149-147230150	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs115490785	chr6:147230217-147230218	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs532136507	chr6:147230284-147230285	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs552159007	chr6:147230305-147230306	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs540772729	chr6:147230331-147230332	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs534793256	chr6:147230333-147230334	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs554831237	chr6:147230351-147230352	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs556988301	chr6:147230356-147230357	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs537186772	chr6:147230484-147230485	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs557434113	chr6:147230578-147230579	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs184060132	chr6:147230580-147230581	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs539839257	chr6:147230638-147230639	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs560535218	chr6:147230653-147230654	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs187636864	chr6:147230695-147230696	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs369147021	chr6:147230701-147230702	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs573231024	chr6:147230711-147230712	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs542016798	chr6:147230727-147230728	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs530168560	chr6:147230799-147230800	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs561986156	chr6:147230882-147230883	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575443185	chr6:147230904-147230905	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs192152187	chr6:147230934-147230935	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs564139967	chr6:147230940-147230941	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs75730485	chr6:147230949-147230950	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs372618506	chr6:147230953-147230954	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147224000-147233600	Weak transcription	HSMM	muscle
2	chr6:147225200-147233600	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr6:147225400-147233600	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr6:147226600-147229800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr6:147226800-147231600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr6:147226800-147233200	Weak transcription	A549	lung
7	chr6:147226800-147233800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr6:147227000-147231200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr6:147227000-147231400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr6:147227000-147231800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:147227000-147231800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr6:147227000-147233000	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr6:147227000-147233000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:147227000-147235000	Weak transcription	Fetal Lung	lung
15	chr6:147227000-147235000	Weak transcription	Right Atrium	heart
16	chr6:147227200-147231400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr6:147227400-147229800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr6:147227400-147231600	Weak transcription	NHDF-Ad	bronchial
19	chr6:147227400-147231800	Weak transcription	Osteobl	bone
20	chr6:147227400-147232800	Weak transcription	Hela-S3	cervix
21	chr6:147227400-147233600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr6:147227800-147233800	Weak transcription	HMEC	breast
23	chr6:147228000-147230200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr6:147228000-147234400	Weak transcription	Fetal Kidney	kidney
25	chr6:147229200-147230400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr6:147229200-147234000	Enhancers	K562	blood
27	chr6:147229800-147231400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:147229800-147231600	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr6:147230200-147231400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:147230400-147230600	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr6:147230400-147231000	Enhancers	Fetal Intestine Small	intestine
32	chr6:147230400-147232000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr6:147231000-147234600	Weak transcription	Fetal Intestine Small	intestine
34	chr6:147231200-147232000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr6:147231400-147232000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr6:147231400-147232000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr6:147231400-147232400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr6:147231400-147232800	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:147231600-147232000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr6:147231600-147232000	Enhancers	HSMMtube	muscle
41	chr6:147231600-147232200	Enhancers	NHLF	lung
42	chr6:147231600-147232400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:147231600-147233800	Enhancers	NHDF-Ad	bronchial
44	chr6:147231600-147234600	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr6:147231600-147235000	Weak transcription	Gastric	stomach
46	chr6:147231800-147232000	Enhancers	Ovary	ovary
47	chr6:147231800-147232200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:147231800-147232200	Enhancers	Osteobl	bone
49	chr6:147231800-147232400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr6:147231800-147235000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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