Variant report

Variant	esv3416394
Chromosome Location	chr17:45259161-45266566
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:522)
CpG islands
(count:245)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:522 , 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	ARID3A	chr17:45266342-45267543	K562	blood:	n/a	n/a
2	ARID3A	chr17:45266247-45267162	HepG2	liver:	n/a	n/a
3	ATF1	chr17:45266344-45267086	K562	blood:	n/a	n/a
4	ATF3	chr17:45266379-45266689	HepG2	liver:	n/a	n/a
5	ATF3	chr17:45266405-45266609	K562	blood:	n/a	n/a
6	BACH1	chr17:45266355-45267146	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr17:45266347-45267173	K562	blood:	n/a	n/a
8	BCL3	chr17:45265592-45266765	A549	lung:	n/a	chr17:45265804-45265813
9	BCL3	chr17:45265817-45267101	A549	lung:	n/a	n/a
10	BHLHE40	chr17:45266276-45267161	K562	blood:	n/a	n/a
11	BHLHE40	chr17:45266270-45267108	GM12878	blood:	n/a	n/a
12	BRCA1	chr17:45266340-45266833	GM12878	blood:	n/a	n/a
13	BRCA1	chr17:45266290-45267028	HepG2	liver:	n/a	n/a
14	BRCA1	chr17:45265538-45267148	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr17:45266167-45267200	K562	blood:	n/a	n/a
16	CBX3	chr17:45266166-45266692	K562	blood:	n/a	n/a
17	CCNT2	chr17:45266227-45267088	K562	blood:	n/a	n/a
18	CEBPB	chr17:45266154-45267265	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr17:45261602-45261890	A549	lung:	n/a	chr17:45261754-45261765 chr17:45261714-45261725 chr17:45261754-45261767 chr17:45261755-45261766 chr17:45261754-45261767 chr17:45261753-45261770 chr17:45261754-45261765
20	CEBPB	chr17:45261575-45261867	Hela-S3	cervix:	n/a	chr17:45261754-45261765 chr17:45261714-45261725 chr17:45261754-45261767 chr17:45261755-45261766 chr17:45261754-45261767 chr17:45261753-45261770 chr17:45261754-45261765
21	CEBPB	chr17:45266161-45267214	K562	blood:	n/a	n/a
22	CEBPB	chr17:45258766-45259309	K562	blood:	n/a	n/a
23	CEBPB	chr17:45261583-45261912	HepG2	liver:	n/a	chr17:45261754-45261765 chr17:45261714-45261725 chr17:45261754-45261767 chr17:45261755-45261766 chr17:45261754-45261767 chr17:45261753-45261770 chr17:45261754-45261765
24	CEBPB	chr17:45261577-45261872	K562	blood:	n/a	chr17:45261754-45261765 chr17:45261714-45261725 chr17:45261754-45261767 chr17:45261755-45261766 chr17:45261754-45261767 chr17:45261753-45261770 chr17:45261754-45261765
25	CEBPB	chr17:45265951-45266802	GM12878	blood:	n/a	n/a
26	CEBPB	chr17:45266152-45267016	HepG2	liver:	n/a	n/a
27	CEBPD	chr17:45266334-45267230	K562	blood:	n/a	n/a
28	CEBPD	chr17:45266285-45266708	HepG2	liver:	n/a	n/a
29	CHD1	chr17:45265833-45267106	GM12878	blood:	n/a	n/a
30	CHD2	chr17:45265998-45267059	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr17:45266111-45267114	GM12878	blood:	n/a	n/a
32	CHD2	chr17:45266289-45267035	K562	blood:	n/a	n/a
33	CHD2	chr17:45266356-45267003	HepG2	liver:	n/a	n/a
34	CREB1	chr17:45266158-45267165	A549	lung:	n/a	n/a
35	CREB1	chr17:45265429-45265971	GM12878	blood:	n/a	n/a
36	CREB1	chr17:45266088-45267109	GM12878	blood:	n/a	n/a
37	CREB1	chr17:45266101-45267227	K562	blood:	n/a	n/a
38	CTBP2	chr17:45266100-45266990	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr17:45266422-45266630	MCF-7	breast:	n/a	n/a
40	CTCF	chr17:45266480-45266630	GM12869	blood:	n/a	n/a
41	CTCF	chr17:45266449-45266640	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr17:45266440-45266590	GM12868	blood:	n/a	n/a
43	CTCF	chr17:45266473-45266581	GM19240	blood:	n/a	n/a
44	CTCF	chr17:45266400-45266550	HMF	breast:	n/a	n/a
45	CTCF	chr17:45266400-45266550	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr17:45266440-45266590	NHLF	lung:	n/a	n/a
47	CTCF	chr17:45266463-45266606	GM10248	blood:	n/a	n/a
48	CTCF	chr17:45266453-45266563	Gliobla	brain:	n/a	n/a
49	CTCF	chr17:45266440-45266634	GM12892	blood:	n/a	n/a
50	CTCF	chr17:45266460-45266610	AoAF	blood vessel:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45266302-45266352	HRPEpiC	eye:	n/a
2	chr17:45266302-45266352	HRPEpiC	eye:	n/a
3	chr17:45262260-45262310	AG09319	gingival:	n/a
4	chr17:45266302-45266352	HNPCEpiC	eye:	n/a
5	chr17:45266192-45266242	ProgFib	skin:	n/a
6	chr17:45266192-45266242	HIPEpiC	eye:	n/a
7	chr17:45266302-45266352	SK-N-SH_RA	brain:	n/a
8	chr17:45266192-45266242	AG10803	skin:	n/a
9	chr17:45266192-45266242	HPAEpiC	pulmonary alveolar:	n/a
10	chr17:45262260-45262310	HEK293	kidney:	embryo
11	chr17:45266517-45266567	HCT-116	colon:	n/a
12	chr17:45266302-45266352	AG10803	skin:	n/a
13	chr17:45266192-45266242	BE2_C	brain:	n/a
14	chr17:45266517-45266567	HCF	heart:	n/a
15	chr17:45262260-45262310	HEEpiC	esophagus:	n/a
16	chr17:45266517-45266567	HPAEpiC	pulmonary alveolar:	n/a
17	chr17:45266517-45266567	Jurkat	blood:	n/a
18	chr17:45266517-45266567	MCF10A-Er-Src	breast:	n/a
19	chr17:45262260-45262310	CMK	blood:	n/a
20	chr17:45266192-45266242	SKMC	muscle:	n/a
21	chr17:45266192-45266242	GM06990	blood:	n/a
22	chr17:45266192-45266242	T-47D	breast:	n/a
23	chr17:45266302-45266352	T-47D	breast:	n/a
24	chr17:45266192-45266242	HCF	heart:	n/a
25	chr17:45266302-45266352	HCM	heart:	n/a
26	chr17:45266517-45266567	HEEpiC	esophagus:	n/a
27	chr17:45266517-45266567	AoSMC	blood vessel:	n/a
28	chr17:45266517-45266567	HCPEpiC	choroid plexus:	n/a
29	chr17:45266192-45266242	Jurkat	blood:	n/a
30	chr17:45262260-45262310	GM19239	blood:	n/a
31	chr17:45266302-45266352	RPTEC	kidney:	n/a
32	chr17:45262260-45262310	HL-60	blood:	n/a
33	chr17:45262260-45262310	Hela-S3	cervix:	n/a
34	chr17:45262260-45262310	GM12892	blood:	n/a
35	chr17:45266192-45266242	HRCEpiC	kidney:	n/a
36	chr17:45266517-45266567	U87	brain:	n/a
37	chr17:45266517-45266567	LNCaP	prostate:	n/a
38	chr17:45266517-45266567	HUVEC	blood vessel:	n/a
39	chr17:45266517-45266567	HAEpiC	amniotic membrane:	n/a
40	chr17:45266192-45266242	HEK293	kidney:	embryo
41	chr17:45266302-45266352	BE2_C	brain:	n/a
42	chr17:45266192-45266242	GM12891	blood:	n/a
43	chr17:45266517-45266567	NHBE	bronchial:	n/a
44	chr17:45266192-45266242	SK-N-SH	brain:	n/a
45	chr17:45266517-45266567	SK-N-SH_RA	brain:	n/a
46	chr17:45266517-45266567	GM12891	blood:	n/a
47	chr17:45266192-45266242	AG04450	lung:	fetal
48	chr17:45266192-45266242	GM12878	blood:	n/a
49	chr17:45262260-45262310	NB4	blood:	n/a
50	chr17:45262260-45262310	NHDF-neo	bronchial:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45259720..45263817-chr17:45399412..45402337,5	K562	blood:
2	chr17:45264174..45269379-chr17:45283146..45288200,6	K562	blood:
3	chr17:45260373..45262889-chr17:45263866..45266203,2	MCF-7	breast:
4	chr17:45260373..45262889-chr17:45263866..45266203,2	MCF-7	breast:
5	chr17:45253169..45255870-chr17:45262068..45264746,2	MCF-7	breast:
6	chr17:45261453..45263452-chr17:45285830..45288227,2	K562	blood:
7	chr17:45257479..45260473-chr2:133018355..133021074,2	MCF-7	breast:
8	chr17:45247336..45250133-chr17:45265157..45267526,3	MCF-7	breast:
9	chr17:45257003..45258810-chr17:45262193..45263942,2	MCF-7	breast:
10	chr17:45264009..45265710-chr17:45352857..45355559,2	K562	blood:
11	chr17:45249552..45252803-chr17:45263494..45265675,3	MCF-7	breast:
12	chr17:45262874..45265503-chr17:45367086..45368739,2	K562	blood:
13	chr17:45256968..45259015-chr17:45265544..45267226,2	MCF-7	breast:
14	chr17:45230648..45232405-chr17:45259040..45262576,3	K562	blood:
15	chr1:155278256..155278852-chr17:45266250..45266967,2	Hela-S3	cervix:
16	chr17:45264972..45267284-chr17:45403808..45405423,2	K562	blood:
17	chr17:45264884..45268790-chr17:45285196..45288860,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPRML-6	chr17:45262555-45264268	l_1461_chr17:45262554-45265845_brain
2	lnc-RPRML-6	chr17:45264566-45265845	l_1461_chr17:45262554-45265845_brain
3	lnc-RPRML-7	chr17:45266512-45266618	NONHSAT054290

No data

Variant related genes	Relation type
CDC27	TF binding region
CDC27	CpG island
ENSG00000178852	chromatin interactions
ENSG00000004897	chromatin interactions
ENSG00000233786	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000263293	chromatin interactions
ENSG00000259207	chromatin interactions
ENSG00000198336	chromatin interactions

Extended variants
information (count: 209 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:209 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144155421	chr17:45259305-45259306	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs539936474	chr17:45259317-45259318	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs572484642	chr17:45259326-45259327	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs11570460	chr17:45259336-45259337	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs527415980	chr17:45259362-45259363	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112607142	chr17:45259405-45259406	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs11570459	chr17:45259411-45259412	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575458787	chr17:45259469-45259470	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs139980206	chr17:45259479-45259480	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs149864837	chr17:45259513-45259514	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs11570458	chr17:45259580-45259581	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs193008947	chr17:45259592-45259593	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs560541542	chr17:45259605-45259606	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs112931476	chr17:45259635-45259636	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs570839271	chr17:45259643-45259644	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs11570457	chr17:45259647-45259648	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs11570456	chr17:45259693-45259694	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs372149135	chr17:45259761-45259762	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs111634577	chr17:45259781-45259782	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs562742361	chr17:45259801-45259802	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs532026413	chr17:45259825-45259826	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs551826058	chr17:45259865-45259866	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs187721374	chr17:45259906-45259907	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs370898217	chr17:45259925-45259926	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs367624910	chr17:45259939-45259940	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs534149499	chr17:45260021-45260022	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs145802800	chr17:45260079-45260080	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs540104533	chr17:45260083-45260084	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs563979572	chr17:45260106-45260107	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs558486668	chr17:45260145-45260146	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs191442983	chr17:45260223-45260224	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs555297362	chr17:45260227-45260228	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs575199479	chr17:45260254-45260255	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs79048040	chr17:45260255-45260256	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs562611358	chr17:45260296-45260297	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs140682760	chr17:45260310-45260311	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs540392408	chr17:45260365-45260366	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs373798464	chr17:45260385-45260386	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs533241852	chr17:45260402-45260403	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs577052923	chr17:45260445-45260446	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs535068427	chr17:45260510-45260511	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs541106439	chr17:45260520-45260521	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs560702838	chr17:45260545-45260546	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs8081278	chr17:45260610-45260611	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs551527416	chr17:45260650-45260651	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs78578806	chr17:45260671-45260672	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs77309811	chr17:45260674-45260675	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs62077278	chr17:45260702-45260703	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs201199955	chr17:45260746-45260747	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs542797985	chr17:45260765-45260766	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	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
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	17142309	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45251200-45259200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr17:45251200-45260600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr17:45252600-45259200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr17:45253200-45265200	Weak transcription	Brain Germinal Matrix	brain
5	chr17:45254200-45259200	Strong transcription	Osteobl	bone
6	chr17:45255200-45263200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr17:45257000-45265600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr17:45257600-45259400	Genic enhancers	HepG2	liver
9	chr17:45258600-45259400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr17:45258800-45259200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr17:45258800-45259200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr17:45258800-45259200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr17:45258800-45259200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr17:45258800-45259200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr17:45258800-45259200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
16	chr17:45258800-45259200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr17:45258800-45259200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr17:45258800-45259200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr17:45258800-45259200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr17:45258800-45259200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr17:45258800-45259200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr17:45258800-45259200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
23	chr17:45258800-45259200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr17:45258800-45259200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
25	chr17:45258800-45259200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
26	chr17:45258800-45259200	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr17:45258800-45259200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr17:45258800-45259200	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr17:45258800-45259200	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr17:45258800-45259200	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr17:45258800-45259200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
32	chr17:45258800-45259200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr17:45258800-45259200	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
34	chr17:45258800-45259200	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
35	chr17:45258800-45259200	ZNF genes & repeats	Primary B cells from cord blood	blood
36	chr17:45258800-45259200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
37	chr17:45258800-45259200	ZNF genes & repeats	Primary T cells from cord blood	blood
38	chr17:45258800-45259200	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
39	chr17:45258800-45259200	Enhancers	Primary hematopoietic stem cells	blood
40	chr17:45258800-45259200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
41	chr17:45258800-45259200	Flanking Bivalent TSS/Enh	Primary T helper memory cells from peripheral blood 2	blood
42	chr17:45258800-45259200	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
43	chr17:45258800-45259200	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
44	chr17:45258800-45259200	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
45	chr17:45258800-45259200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
46	chr17:45258800-45259200	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
47	chr17:45258800-45259200	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
48	chr17:45258800-45259200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
49	chr17:45258800-45259200	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr17:45258800-45259200	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood

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