Variant report

Variant	esv1829991
Chromosome Location	chr17:37869192-37876898
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	CEBPB	chr17:37873031-37873522	ECC-1	luminal epithelium:	n/a	n/a
2	CTCF	chr17:37874980-37875130	GM12878	blood:	n/a	n/a
3	CTCF	chr17:37874940-37875090	HFF-Myc	foreskin:	n/a	n/a
4	CTCF	chr17:37875080-37875230	GM12866	blood:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
5	CTCF	chr17:37875020-37875170	NHLF	lung:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
6	CTCF	chr17:37875040-37875190	GM12873	blood:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
7	CTCF	chr17:37875020-37875170	AG04449	skin:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
8	CTCF	chr17:37875020-37875170	GM12872	blood:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
9	CTCF	chr17:37875000-37875150	NHDF-neo	bronchial:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
10	CTCF	chr17:37875020-37875170	GM12864	blood:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
11	CTCF	chr17:37875060-37875210	WERI-Rb-1	eye:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
12	CTCF	chr17:37872120-37872270	NHEK	skin:	n/a	n/a
13	CTCF	chr17:37875000-37875150	HMF	breast:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
14	CTCF	chr17:37874877-37875233	MCF-7	breast:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
15	CTCF	chr17:37875080-37875230	AG09309	skin:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
16	CTCF	chr17:37875040-37875190	GM12869	blood:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
17	CTCF	chr17:37875040-37875190	HCPEpiC	choroid plexus:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
18	CTCF	chr17:37875010-37875215	K562	blood:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
19	CTCF	chr17:37875060-37875210	AG09319	gingival:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
20	CTCF	chr17:37875060-37875210	RPTEC	kidney:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
21	CTCF	chr17:37875020-37875170	MCF-7	breast:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
22	CTCF	chr17:37874980-37875130	GM12874	blood:	n/a	n/a
23	CTCF	chr17:37875020-37875170	BJ	skin:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
24	CTCF	chr17:37875360-37875510	HFF	foreskin:	n/a	n/a
25	CTCF	chr17:37875000-37875150	GM12878	blood:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
26	CTCF	chr17:37875020-37875170	K562	blood:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
27	CTCF	chr17:37874957-37875154	K562	blood:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
28	CTCF	chr17:37875020-37875170	WI-38	lung:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
29	CTCF	chr17:37874856-37875280	A549	lung:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
30	CTCF	chr17:37875020-37875170	HA-sp	spinal cord:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
31	CTCF	chr17:37875080-37875230	NB4	blood:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
32	CTCF	chr17:37875020-37875170	HL-60	blood:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
33	CTCF	chr17:37875080-37875230	HA-sp	spinal cord:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
34	CTCF	chr17:37875065-37875168	SK-N-SH_RA	brain:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
35	CTCF	chr17:37875053-37875199	MCF-7	breast:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
36	CTCF	chr17:37875040-37875190	HCFaa	heart:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
37	CTCF	chr17:37875080-37875230	HEEpiC	esophagus:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
38	CTCF	chr17:37875060-37875210	AG10803	skin:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
39	CTCF	chr17:37875024-37875210	Gliobla	brain:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
40	CTCF	chr17:37875080-37875230	SK-N-SH_RA	brain:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
41	CTCF	chr17:37875080-37875230	AG09319	gingival:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
42	CTCF	chr17:37875080-37875230	AG04450	lung:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
43	CTCF	chr17:37869924-37869996	GM20000	blood:	n/a	n/a
44	CTCF	chr17:37875080-37875230	A549	lung:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
45	CTCF	chr17:37875040-37875190	HepG2	liver:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
46	CTCF	chr17:37875100-37875250	AG04450	lung:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
47	CTCF	chr17:37875040-37875190	BE2_C	brain:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
48	CTCF	chr17:37875060-37875210	HFF	foreskin:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
49	CTCF	chr17:37874956-37875289	IMR90	lung:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138
50	CTCF	chr17:37875000-37875150	AG09309	skin:	n/a	chr17:37875128-37875137 chr17:37875123-37875139 chr17:37875122-37875140 chr17:37875117-37875138

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:37875709-37875759	HRCEpiC	kidney:	n/a
2	chr17:37875709-37875759	IMR90	lung:	fetal
3	chr17:37875709-37875759	HEEpiC	esophagus:	n/a
4	chr17:37875709-37875759	A549	lung:	n/a
5	chr17:37875709-37875759	Caco-2	colon:	n/a
6	chr17:37875709-37875759	HCT-116	colon:	n/a
7	chr17:37875709-37875759	HCF	heart:	n/a
8	chr17:37875709-37875759	HepG2	liver:	n/a
9	chr17:37875709-37875759	SK-N-SH_RA	brain:	n/a
10	chr17:37875709-37875759	Jurkat	blood:	n/a
11	chr17:37875709-37875759	ProgFib	skin:	n/a
12	chr17:37875709-37875759	GM12878	blood:	n/a
13	chr17:37875709-37875759	HIPEpiC	eye:	n/a
14	chr17:37875709-37875759	AG04450	lung:	fetal
15	chr17:37875709-37875759	HPAEpiC	pulmonary alveolar:	n/a
16	chr17:37875709-37875759	HAEpiC	amniotic membrane:	n/a
17	chr17:37875709-37875759	PANC-1	pancreas:	n/a
18	chr17:37875709-37875759	HUVEC	blood vessel:	n/a
19	chr17:37875709-37875759	HL-60	blood:	n/a
20	chr17:37875709-37875759	U87	brain:	n/a
21	chr17:37875709-37875759	PFSK-1	brain:	n/a
22	chr17:37875709-37875759	SK-N-SH	brain:	n/a
23	chr17:37875709-37875759	LNCaP	prostate:	n/a
24	chr17:37875709-37875759	HMEC	breast:	n/a
25	chr17:37875709-37875759	CMK	blood:	n/a
26	chr17:37875709-37875759	RPTEC	kidney:	n/a
27	chr17:37875709-37875759	NB4	blood:	n/a
28	chr17:37875709-37875759	MCF10A-Er-Src	breast:	n/a
29	chr17:37875709-37875759	NT2-D1	testis:	n/a
30	chr17:37875709-37875759	NHBE	bronchial:	n/a
31	chr17:37875709-37875759	GM06990	blood:	n/a
32	chr17:37875709-37875759	Hepatocyte	liver:	n/a
33	chr17:37875709-37875759	T-47D	breast:	n/a
34	chr17:37875709-37875759	H1-hESC	embryonic stem cell:	embryo
35	chr17:37875709-37875759	HRE	kidney:	n/a
36	chr17:37875709-37875759	SK-N-MC	brain:	n/a
37	chr17:37875709-37875759	MCF-7	breast:	n/a
38	chr17:37875709-37875759	Hela-S3	cervix:	n/a
39	chr17:37875709-37875759	HEK293	kidney:	embryo
40	chr17:37875709-37875759	GM12891	blood:	n/a
41	chr17:37875709-37875759	NH-A	brain:	n/a
42	chr17:37875709-37875759	SKMC	muscle:	n/a
43	chr17:37875709-37875759	BE2_C	brain:	n/a
44	chr17:37875709-37875759	HCM	heart:	n/a
45	chr17:37875709-37875759	HNPCEpiC	eye:	n/a
46	chr17:37875709-37875759	ECC-1	luminal epithelium:	n/a
47	chr17:37875709-37875759	ovcar-3	ovarian:	n/a
48	chr17:37875709-37875759	AG09319	gingival:	n/a
49	chr17:37875709-37875759	NHDF-neo	bronchial:	n/a
50	chr17:37875709-37875759	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:37843888..37846797-chr17:37874927..37876468,2	MCF-7	breast:
2	chr17:37875103..37877735-chr17:37878952..37881487,4	K562	blood:
3	chr17:37870160..37872163-chr17:37881073..37883081,3	K562	blood:
4	chr17:37867857..37869588-chr17:37870435..37872270,2	K562	blood:
5	chr17:37871119..37873027-chr17:37873590..37876087,2	K562	blood:
6	chr17:37871866..37874609-chr17:37884182..37887614,4	MCF-7	breast:
7	chr17:37875233..37878023-chr17:37910337..37912992,2	MCF-7	breast:
8	chr17:37872892..37874995-chr17:37881128..37883306,2	K562	blood:
9	chr17:37871119..37873027-chr17:37873590..37876087,2	K562	blood:
10	chr17:37873495..37876430-chr17:37881806..37884578,2	K562	blood:
11	chr17:37778246..37778910-chr17:37874656..37875550,3	MCF-7	breast:
12	chr17:37843958..37845642-chr17:37874066..37877258,3	MCF-7	breast:
13	chr17:37869068..37872163-chr17:37881073..37883703,3	K562	blood:
14	chr17:37867857..37869588-chr17:37870435..37872270,2	K562	blood:
15	chr17:37856670..37858872-chr17:37874487..37877508,3	MCF-7	breast:
16	chr17:37860257..37864274-chr17:37871854..37875164,5	MCF-7	breast:
17	chr17:37858390..37860926-chr17:37875652..37877494,2	K562	blood:
18	chr17:37842892..37845868-chr17:37868766..37870557,2	K562	blood:
19	chr17:37854757..37859429-chr17:37870382..37874180,6	K562	blood:
20	chr17:37870758..37873083-chr17:37874555..37877273,2	K562	blood:
21	chr17:37874861..37876535-chr17:37884600..37886557,2	K562	blood:

Variant related genes	Relation type
ERBB2	TF binding region
ERBB2	CpG island
ENSG00000141741	chromatin interactions
ENSG00000161395	chromatin interactions
ENSG00000265178	chromatin interactions
ENSG00000141736	chromatin interactions

Extended variants
information (count: 349 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115761749	chr17:37869222-37869223	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs530002794	chr17:37869237-37869238	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs552526803	chr17:37869281-37869282	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs570643740	chr17:37869328-37869329	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs534825855	chr17:37869443-37869444	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs547041600	chr17:37869456-37869457	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs368529349	chr17:37869489-37869490	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs535988437	chr17:37869538-37869539	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs149741928	chr17:37869716-37869717	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs575265435	chr17:37869741-37869742	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs113328199	chr17:37869769-37869770	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs184451736	chr17:37869770-37869771	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs74620197	chr17:37869782-37869783	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs76210044	chr17:37869783-37869784	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs146251853	chr17:37869878-37869879	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs540473873	chr17:37869879-37869880	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs559359298	chr17:37869890-37869891	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs574438952	chr17:37869936-37869937	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs532761555	chr17:37869962-37869963	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs113231716	chr17:37869990-37869991	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs530554273	chr17:37869997-37869998	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs189175355	chr17:37870002-37870003	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs55676939	chr17:37870007-37870008	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs71149793	chr17:37870025-37870026	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs528245283	chr17:37870063-37870064	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs528931754	chr17:37870103-37870104	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs548421318	chr17:37870167-37870168	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs146818829	chr17:37870168-37870169	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs181046534	chr17:37870182-37870183	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs55982292	chr17:37870193-37870194	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs185544969	chr17:37870302-37870303	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs79717977	chr17:37870310-37870311	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs71149794	chr17:37870311-37870312	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs535558505	chr17:37870362-37870363	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs190397060	chr17:37870363-37870364	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs568878966	chr17:37870374-37870375	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs2934967	chr17:37870378-37870379	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs75551385	chr17:37870431-37870432	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs181471382	chr17:37870442-37870443	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs534549366	chr17:37870530-37870531	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs186923239	chr17:37870531-37870532	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs148942170	chr17:37870532-37870533	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs368218140	chr17:37870588-37870589	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs541544307	chr17:37870600-37870601	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs563386448	chr17:37870666-37870667	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs575281933	chr17:37870715-37870716	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs372053351	chr17:37870736-37870737	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs35193437	chr17:37870739-37870740	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs77327588	chr17:37870751-37870752	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs564329506	chr17:37870830-37870831	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:142)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
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
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	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
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Urothelial carcinoma	21177765	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Disease	22962312	CNVD
Mental retardation	20152051	CNVD
Mental retardation	19951919	CNVD
Mental retardation	22817714	CNVD
Mental retardation	21956041	CNVD
Brain cancer	19584924	CNVD
Glioblastoma multiforme	22286061	CNVD
Schizophrenia	21399695	CNVD
Non-syndromic sensorineural hearing loss	19165922	CNVD
Prader-willi syndrome	20588305	CNVD
17q21.31 microdeletion syndrome	16940994	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
17q21.31 microdeletion syndrome	22283845	CNVD
Intellectual disability	22194194	CNVD
17q21.31 microdeletion syndrome	20606400	CNVD
17q21.31 microdeletion syndrome	18628315	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	18702822	CNVD
Breast cancer	17938205	CNVD
Breast cancer	20943603	CNVD
Pheochromocytoma	18310300	CNVD
Gastric adenocarcinoma	22014070	CNVD
Cervical cancer	17311676	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Central neurocytomas	17123091	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	19019769	CNVD
Breast cancer	19767729	CNVD
Invasive breast cancer	19060846	CNVD
Breast cancer	19123950	CNVD
Neuroblastic tumor	20581805	CNVD
Ovarian cancer	18182111	CNVD

Chromatin state (count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37857000-37872000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr17:37858000-37885200	Weak transcription	Fetal Brain Male	brain
3	chr17:37858000-37885600	Weak transcription	Hela-S3	cervix
4	chr17:37858200-37882600	Weak transcription	NHDF-Ad	bronchial
5	chr17:37858400-37879600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr17:37859400-37881000	Weak transcription	Brain Cingulate Gyrus	brain
7	chr17:37861400-37883600	Weak transcription	Brain Substantia Nigra	brain
8	chr17:37862200-37877000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
9	chr17:37862200-37885200	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr17:37862400-37876800	Strong transcription	HepG2	liver
11	chr17:37862400-37877600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr17:37862400-37878800	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr17:37862400-37885400	Strong transcription	H9 Cell Line	embryonic stem cell
14	chr17:37862400-37885600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr17:37862400-37885600	Strong transcription	Fetal Stomach	stomach
16	chr17:37862400-37885800	Weak transcription	Right Atrium	heart
17	chr17:37862600-37871400	Weak transcription	HSMM	muscle
18	chr17:37862600-37871600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr17:37862600-37885600	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr17:37862800-37872000	Weak transcription	NH-A	brain
21	chr17:37862800-37878800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr17:37862800-37883200	Weak transcription	Small Intestine	intestine
23	chr17:37862800-37885600	Strong transcription	Fetal Intestine Large	intestine
24	chr17:37863000-37869400	Strong transcription	Adipose Nuclei	Adipose
25	chr17:37863000-37870000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr17:37863000-37872400	Strong transcription	Stomach Smooth Muscle	stomach
27	chr17:37863000-37873800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr17:37863000-37876600	Strong transcription	Placenta Amnion	Placenta Amnion
29	chr17:37863000-37877000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr17:37863000-37878800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr17:37863000-37879000	Strong transcription	HSMMtube	muscle
32	chr17:37863000-37879600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr17:37863000-37885600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr17:37863200-37869200	Strong transcription	Ovary	ovary
35	chr17:37863200-37869400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr17:37863200-37876800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr17:37863200-37879400	Strong transcription	H1 Cell Line	embryonic stem cell
38	chr17:37863200-37885600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr17:37863200-37885800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr17:37863400-37869200	Strong transcription	Fetal Kidney	kidney
41	chr17:37863400-37869400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
42	chr17:37863400-37869400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr17:37863400-37869400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr17:37863400-37869400	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr17:37863400-37871800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr17:37863400-37872000	Strong transcription	Left Ventricle	heart
47	chr17:37863400-37872000	Strong transcription	Right Ventricle	heart
48	chr17:37863400-37872000	Strong transcription	Skeletal Muscle Male	skeletal muscle
49	chr17:37863400-37876200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr17:37863400-37876800	Strong transcription	Osteobl	bone

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