Variant report

Variant	esv3332714
Chromosome Location	chr6:150259037-150275045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:524)
CpG islands
(count:1282)
Chromatin interactive
region (count:8)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:150262888-150263243	K562	blood:	n/a	n/a
2	ATF2	chr6:150259675-150260384	GM12878	blood:	n/a	n/a
3	ATF2	chr6:150259804-150260315	GM12878	blood:	n/a	n/a
4	BACH1	chr6:150263349-150263435	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:150259845-150259973	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr6:150259890-150260217	GM12878	blood:	n/a	n/a
7	BATF	chr6:150259147-150259360	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:150259955-150260168	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:150259860-150260315	GM12878	blood:	n/a	n/a
10	BCL3	chr6:150259901-150260245	GM12878	blood:	n/a	n/a
11	BCLAF1	chr6:150259802-150260312	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:150262692-150263290	K562	blood:	n/a	n/a
13	BHLHE40	chr6:150259646-150260401	GM12878	blood:	n/a	chr6:150259658-150259674
14	CBX3	chr6:150262653-150263485	K562	blood:	n/a	n/a
15	CBX3	chr6:150275015-150275366	K562	blood:	n/a	n/a
16	CCNT2	chr6:150262706-150263315	K562	blood:	n/a	n/a
17	CEBPB	chr6:150259875-150260421	GM12878	blood:	n/a	n/a
18	CEBPB	chr6:150270020-150270068	HepG2	liver:	n/a	chr6:150270052-150270063
19	CEBPB	chr6:150269929-150270126	A549	lung:	n/a	chr6:150270052-150270063
20	CHD2	chr6:150262728-150263178	K562	blood:	n/a	n/a
21	CHD2	chr6:150262809-150263101	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr6:150259732-150260318	GM12878	blood:	n/a	n/a
23	CHD2	chr6:150262779-150263173	GM12878	blood:	n/a	n/a
24	CHD2	chr6:150259682-150259879	Hela-S3	cervix:	n/a	n/a
25	CREB1	chr6:150262830-150263246	A549	lung:	n/a	n/a
26	CREB1	chr6:150259573-150260414	GM12878	blood:	n/a	chr6:150259736-150259749
27	CREB1	chr6:150262830-150263355	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr6:150262823-150263345	GM12878	blood:	n/a	n/a
29	CREB1	chr6:150262805-150263335	ECC-1	luminal epithelium:	n/a	n/a
30	CTBP2	chr6:150262374-150263823	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr6:150259143-150259346	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr6:150268200-150268350	HEK293	kidney:	n/a	chr6:150268214-150268227
33	CTCF	chr6:150259400-150259550	HMF	breast:	n/a	n/a
34	CTCF	chr6:150259360-150259510	GM12864	blood:	n/a	n/a
35	CTCF	chr6:150261860-150262010	HepG2	liver:	n/a	n/a
36	CTCF	chr6:150274953-150275358	A549	lung:	n/a	n/a
37	CTCF	chr6:150259111-150259395	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:150258920-150259070	HAc	cerebellar:	n/a	n/a
39	CTCF	chr6:150259139-150259393	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr6:150258900-150259050	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr6:150259380-150259530	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr6:150259380-150259530	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr6:150259128-150259386	GM12878	blood:	n/a	n/a
44	CTCF	chr6:150259320-150259470	GM12871	blood:	n/a	n/a
45	CTCF	chr6:150263687-150263805	Gliobla	brain:	n/a	n/a
46	CTCF	chr6:150275004-150275386	K562	blood:	n/a	n/a
47	CTCF	chr6:150259340-150259490	HCFaa	heart:	n/a	n/a
48	CTCF	chr6:150259340-150259490	BJ	skin:	n/a	n/a
49	CTCF	chr6:150258920-150259070	AG09319	gingival:	n/a	n/a
50	CTCF	chr6:150259380-150259530	SAEC	small airway:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150263488-150263538	SKMC	muscle:	n/a
2	chr6:150263488-150263538	SKMC	muscle:	n/a
3	chr6:150260358-150260408	MCF-7	breast:	n/a
4	chr6:150263354-150263404	NHBE	bronchial:	n/a
5	chr6:150269220-150269270	SK-N-SH_RA	brain:	n/a
6	chr6:150260358-150260408	U87	brain:	n/a
7	chr6:150269220-150269270	PANC-1	pancreas:	n/a
8	chr6:150263118-150263168	AoSMC	blood vessel:	n/a
9	chr6:150263118-150263168	NT2-D1	testis:	n/a
10	chr6:150263035-150263085	GM06990	blood:	n/a
11	chr6:150263118-150263168	BE2_C	brain:	n/a
12	chr6:150262044-150262094	K562	blood:	n/a
13	chr6:150262734-150262784	Caco-2	colon:	n/a
14	chr6:150266173-150266223	HRCEpiC	kidney:	n/a
15	chr6:150260358-150260408	MCF10A-Er-Src	breast:	n/a
16	chr6:150262763-150262813	AG04449	skin:	fetal
17	chr6:150262771-150262821	HEEpiC	esophagus:	n/a
18	chr6:150263722-150263772	HRCEpiC	kidney:	n/a
19	chr6:150263070-150263120	NT2-D1	testis:	n/a
20	chr6:150262763-150262813	HEEpiC	esophagus:	n/a
21	chr6:150263722-150263772	SK-N-SH_RA	brain:	n/a
22	chr6:150274542-150274592	BE2_C	brain:	n/a
23	chr6:150262763-150262813	HCPEpiC	choroid plexus:	n/a
24	chr6:150263194-150263244	K562	blood:	n/a
25	chr6:150263722-150263772	HAEpiC	amniotic membrane:	n/a
26	chr6:150263722-150263772	GM12892	blood:	n/a
27	chr6:150260156-150260206	GM12892	blood:	n/a
28	chr6:150259930-150259980	T-47D	breast:	n/a
29	chr6:150262961-150263011	GM12878	blood:	n/a
30	chr6:150263194-150263244	LNCaP	prostate:	n/a
31	chr6:150263194-150263244	GM06990	blood:	n/a
32	chr6:150266173-150266223	GM12891	blood:	n/a
33	chr6:150266173-150266223	Jurkat	blood:	n/a
34	chr6:150263488-150263538	AG10803	skin:	n/a
35	chr6:150260156-150260206	NH-A	brain:	n/a
36	chr6:150263035-150263085	GM12892	blood:	n/a
37	chr6:150262771-150262821	AoSMC	blood vessel:	n/a
38	chr6:150262763-150262813	PFSK-1	brain:	n/a
39	chr6:150259601-150259651	HCPEpiC	choroid plexus:	n/a
40	chr6:150263488-150263538	MCF-7	breast:	n/a
41	chr6:150262965-150263015	HCT-116	colon:	n/a
42	chr6:150259860-150259910	NT2-D1	testis:	n/a
43	chr6:150263194-150263244	AG09309	skin:	n/a
44	chr6:150263722-150263772	GM12891	blood:	n/a
45	chr6:150262763-150262813	CMK	blood:	n/a
46	chr6:150262044-150262094	NT2-D1	testis:	n/a
47	chr6:150266173-150266223	Caco-2	colon:	n/a
48	chr6:150263194-150263244	AG09319	gingival:	n/a
49	chr6:150263722-150263772	AG09319	gingival:	n/a
50	chr6:150262763-150262813	BE2_C	brain:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:149846576..149848106-chr6:150258402..150260712,2	K562	blood:
2	chr6:150263150..150264777-chr6:150325600..150328449,2	MCF-7	breast:
3	chr6:150274811..150275321-chr6:150336040..150336549,2	MCF-7	breast:
4	chr6:150255165..150257260-chr6:150258635..150261924,3	MCF-7	breast:
5	chr6:150257396..150260080-chr6:150261360..150264274,3	MCF-7	breast:
6	chr6:150255655..150257664-chr6:150259479..150262477,4	K562	blood:
7	chr6:150258514..150260378-chr6:150337573..150339969,2	MCF-7	breast:
8	chr6:150254783..150257862-chr6:150259479..150262603,4	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ULBP2-4	chr6:150272969-150273375	NONHSAT115528
2	lnc-ULBP2-1	chr6:150260558-150260871	XLOC_005501
3	lnc-ULBP2-1	chr6:150260453-150260658	XLOC_005501
4	lnc-ULBP2-1	chr6:150261044-150262766	NONHSAT115525
5	lnc-ULBP2-1	chr6:150261044-150262631	XLOC_005501
6	lnc-ULBP2-1	chr6:150260117-150260140	NONHSAT115525
7	lnc-ULBP2-1	chr6:150261044-150262631	XLOC_005501

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ULBP2	hsa-miR-34a-5p	chr6:150269987-150270008
2	ULBP2	hsa-miR-34c-5p	chr6:150269988-150270008

Variant related genes	Relation type
ULBP2	TF binding region
ENSG00000215094	TF binding region
ULBP2	CpG island
ENSG00000215094	CpG island
ENSG00000218358	chromatin interactions
ENSG00000131015	chromatin interactions
ENSG00000216621	chromatin interactions
SKI	miRNA target sites
VPS36	miRNA target sites
ARID1A	miRNA target sites
ARID1B	miRNA target sites

Extended variants
information (count: 896 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:896 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369481822	chr6:150259047-150259048	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs577092999	chr6:150259050-150259051	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs181168682	chr6:150259057-150259058	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs553107046	chr6:150259064-150259065	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs377424882	chr6:150259065-150259066	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs573101369	chr6:150259074-150259075	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs542104258	chr6:150259122-150259123	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs374644941	chr6:150259164-150259165	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs530553397	chr6:150259171-150259172	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs544171264	chr6:150259176-150259177	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs371128280	chr6:150259188-150259189	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs372979912	chr6:150259201-150259202	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs564088572	chr6:150259241-150259242	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs4588700	chr6:150259249-150259250	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs371904962	chr6:150259262-150259263	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs35965288	chr6:150259263-150259264	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs150806216	chr6:150259381-150259382	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs529078679	chr6:150259415-150259416	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs138087302	chr6:150259439-150259440	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs186474809	chr6:150259455-150259456	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs189006686	chr6:150259461-150259462	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs4473866	chr6:150259479-150259480	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs4591860	chr6:150259519-150259520	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs374277652	chr6:150259523-150259524	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs115491246	chr6:150259532-150259533	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs553245843	chr6:150259537-150259538	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs533261827	chr6:150259538-150259539	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs146002859	chr6:150259539-150259540	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs555710673	chr6:150259549-150259550	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs575270775	chr6:150259551-150259552	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs4273697	chr6:150259572-150259573	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs564025412	chr6:150259583-150259584	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs542356605	chr6:150259597-150259598	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs4283897	chr6:150259598-150259599	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs181727136	chr6:150259602-150259603	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs535606364	chr6:150259641-150259642	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs540272503	chr6:150259643-150259644	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs560462554	chr6:150259659-150259660	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs529203430	chr6:150259661-150259662	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs549135420	chr6:150259665-150259666	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs558870122	chr6:150259678-150259679	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs186429173	chr6:150259701-150259702	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs550661241	chr6:150259715-150259716	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs4518509	chr6:150259727-150259728	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs190871615	chr6:150259732-150259733	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs539438082	chr6:150259757-150259758	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs575464680	chr6:150259763-150259764	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs4555924	chr6:150259790-150259791	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535794214	chr6:150259796-150259797	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs555889001	chr6:150259833-150259834	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
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
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:685 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150256800-150259400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:150258000-150259600	Bivalent Enhancer	GM12878-XiMat	blood
3	chr6:150258600-150259400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:150258800-150259400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
5	chr6:150258800-150259400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
6	chr6:150258800-150259400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
7	chr6:150258800-150259400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
8	chr6:150258800-150259400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr6:150258800-150259400	Enhancers	HMEC	breast
10	chr6:150258800-150259400	Bivalent Enhancer	Osteobl	bone
11	chr6:150258800-150259600	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
12	chr6:150258800-150259600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
13	chr6:150258800-150259600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr6:150258800-150259800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
15	chr6:150259000-150259200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
16	chr6:150259000-150259200	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
17	chr6:150259000-150259400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
18	chr6:150259000-150259400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
19	chr6:150259000-150259400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:150259000-150259400	Bivalent Enhancer	A549	lung
21	chr6:150259000-150259400	Active TSS	NHEK	skin
22	chr6:150259000-150259600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
23	chr6:150259000-150259600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr6:150259200-150259400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
25	chr6:150259200-150259400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
26	chr6:150259200-150259400	Bivalent Enhancer	Duodenum Mucosa	Duodenum
27	chr6:150259200-150259400	Bivalent/Poised TSS	HSMM	muscle
28	chr6:150259200-150259600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
29	chr6:150259200-150259600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:150259400-150259600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
31	chr6:150259400-150259600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
32	chr6:150259400-150259600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
33	chr6:150259400-150259600	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr6:150259400-150259600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
35	chr6:150259400-150259600	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr6:150259400-150259600	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:150259400-150259600	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:150259400-150259600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr6:150259400-150259600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
40	chr6:150259400-150259600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
41	chr6:150259400-150259600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
42	chr6:150259400-150259600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:150259400-150259600	Flanking Bivalent TSS/Enh	Primary T helper memory cells from peripheral blood 1	blood
44	chr6:150259400-150259600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
45	chr6:150259400-150259600	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
46	chr6:150259400-150259600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr6:150259400-150259600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:150259400-150259600	Bivalent Enhancer	Brain Cingulate Gyrus	brain
49	chr6:150259400-150259600	Bivalent Enhancer	Brain Hippocampus Middle	brain
50	chr6:150259400-150259600	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain

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