Variant report

Variant	nsv574992
Chromosome Location	chr17:37818561-37822311
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:325)
CpG islands
(count:612)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:37820347-37820555	HepG2	liver:	n/a	n/a
2	BACH1	chr17:37820027-37820211	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr17:37819921-37821125	A549	lung:	n/a	n/a
4	BCL3	chr17:37821874-37822887	A549	lung:	n/a	chr17:37821930-37821938
5	BCL3	chr17:37819865-37821233	A549	lung:	n/a	n/a
6	BHLHE40	chr17:37820000-37820364	K562	blood:	n/a	chr17:37820029-37820045
7	CBX3	chr17:37819912-37820391	K562	blood:	n/a	n/a
8	CCNT2	chr17:37820045-37820596	K562	blood:	n/a	n/a
9	CHD2	chr17:37820120-37820281	Hela-S3	cervix:	n/a	n/a
10	CTBP2	chr17:37819972-37820384	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr17:37821900-37822050	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr17:37821920-37822070	AG04449	skin:	n/a	n/a
13	CTCF	chr17:37821940-37822090	NHEK	skin:	n/a	n/a
14	CTCF	chr17:37820160-37820310	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr17:37822010-37822033	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr17:37822140-37822290	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr17:37822020-37822170	NHEK	skin:	n/a	n/a
18	CTCF	chr17:37821940-37822090	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr17:37821956-37822104	Gliobla	brain:	n/a	n/a
20	CTCF	chr17:37821920-37822070	GM12872	blood:	n/a	n/a
21	CTCF	chr17:37822160-37822310	AG04449	skin:	n/a	n/a
22	CTCF	chr17:37821840-37821990	GM12866	blood:	n/a	n/a
23	CTCF	chr17:37821931-37822134	Fibrobl	skin:	n/a	n/a
24	CTCF	chr17:37821880-37822030	GM12874	blood:	n/a	n/a
25	CTCF	chr17:37821940-37822090	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr17:37822100-37822250	HPF	lung:	n/a	n/a
27	CTCF	chr17:37821960-37822110	GM12873	blood:	n/a	n/a
28	CTCF	chr17:37821920-37822070	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr17:37821820-37821970	GM12865	blood:	n/a	n/a
30	CTCF	chr17:37821940-37822090	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr17:37821880-37822030	A549	lung:	n/a	n/a
32	CTCF	chr17:37821900-37822050	GM12864	blood:	n/a	n/a
33	CTCF	chr17:37821943-37822105	MCF-7	breast:	n/a	n/a
34	CTCF	chr17:37821940-37822090	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr17:37821960-37822110	GM12872	blood:	n/a	n/a
36	CTCF	chr17:37821900-37822050	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr17:37821933-37822127	NHEK	skin:	n/a	n/a
38	CTCF	chr17:37821900-37822050	SAEC	small airway:	n/a	n/a
39	CTCF	chr17:37822000-37822150	GM12866	blood:	n/a	n/a
40	CTCF	chr17:37820000-37820150	HEK293	kidney:	n/a	n/a
41	CTCF	chr17:37822240-37822390	GM12873	blood:	n/a	n/a
42	CTCF	chr17:37822260-37822410	AG09309	skin:	n/a	n/a
43	CTCF	chr17:37821920-37822070	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr17:37822112-37822436	K562	blood:	n/a	n/a
45	CTCF	chr17:37822160-37822310	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr17:37821900-37822050	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr17:37821920-37822070	GM12871	blood:	n/a	n/a
48	CTCF	chr17:37821980-37822130	HRE	kidney:	n/a	n/a
49	CTCF	chr17:37820140-37820290	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr17:37820135-37820327	K562	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:37821536-37821586	NH-A	brain:	n/a
2	chr17:37821481-37821531	K562	blood:	n/a
3	chr17:37821536-37821586	NH-A	brain:	n/a
4	chr17:37821481-37821531	K562	blood:	n/a
5	chr17:37821481-37821531	MCF-7	breast:	n/a
6	chr17:37820135-37820185	IMR90	lung:	fetal
7	chr17:37821661-37821711	MCF-7	breast:	n/a
8	chr17:37822045-37822095	ProgFib	skin:	n/a
9	chr17:37821478-37821528	AG04449	skin:	fetal
10	chr17:37822045-37822095	HL-60	blood:	n/a
11	chr17:37822045-37822095	IMR90	lung:	fetal
12	chr17:37821478-37821528	PrEC	prostate:	n/a
13	chr17:37820515-37820565	HNPCEpiC	eye:	n/a
14	chr17:37821536-37821586	A549	lung:	n/a
15	chr17:37821447-37821497	PrEC	prostate:	n/a
16	chr17:37821661-37821711	U87	brain:	n/a
17	chr17:37821481-37821531	SK-N-SH	brain:	n/a
18	chr17:37821447-37821497	PFSK-1	brain:	n/a
19	chr17:37821481-37821531	GM12878	blood:	n/a
20	chr17:37820495-37820545	GM06990	blood:	n/a
21	chr17:37821447-37821497	IMR90	lung:	fetal
22	chr17:37821478-37821528	AG09309	skin:	n/a
23	chr17:37820515-37820565	HL-60	blood:	n/a
24	chr17:37820495-37820545	HCM	heart:	n/a
25	chr17:37821447-37821497	HEK293	kidney:	embryo
26	chr17:37820361-37820411	BJ	skin:	n/a
27	chr17:37822045-37822095	T-47D	breast:	n/a
28	chr17:37821661-37821711	AG04450	lung:	fetal
29	chr17:37820135-37820185	HRCEpiC	kidney:	n/a
30	chr17:37821447-37821497	Hepatocyte	liver:	n/a
31	chr17:37821661-37821711	GM12892	blood:	n/a
32	chr17:37820515-37820565	AG10803	skin:	n/a
33	chr17:37821536-37821586	HCF	heart:	n/a
34	chr17:37820361-37820411	SK-N-MC	brain:	n/a
35	chr17:37821661-37821711	HMEC	breast:	n/a
36	chr17:37821536-37821586	GM06990	blood:	n/a
37	chr17:37821661-37821711	HUVEC	blood vessel:	n/a
38	chr17:37821661-37821711	HCPEpiC	choroid plexus:	n/a
39	chr17:37820361-37820411	HCM	heart:	n/a
40	chr17:37820495-37820545	AG04450	lung:	fetal
41	chr17:37821447-37821497	A549	lung:	n/a
42	chr17:37820135-37820185	NHBE	bronchial:	n/a
43	chr17:37820361-37820411	GM12892	blood:	n/a
44	chr17:37821478-37821528	HIPEpiC	eye:	n/a
45	chr17:37821447-37821497	Caco-2	colon:	n/a
46	chr17:37821661-37821711	AG09319	gingival:	n/a
47	chr17:37820495-37820545	HCF	heart:	n/a
48	chr17:37822045-37822095	HNPCEpiC	eye:	n/a
49	chr17:37822045-37822095	AG09309	skin:	n/a
50	chr17:37820515-37820565	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr17:37814865..37817539-chr17:37818088..37820916,2	MCF-7	breast:
2	chr17:37792116..37794246-chr17:37816401..37819185,2	MCF-7	breast:
3	chr17:37796408..37798750-chr17:37816714..37819349,2	MCF-7	breast:
4	chr17:37773404..37776321-chr17:37819728..37822241,2	MCF-7	breast:
5	chr17:37820269..37822636-chr17:37824547..37827418,2	MCF-7	breast:
6	chr17:37777756..37783081-chr17:37819129..37825010,9	K562	blood:
7	chr17:37820151..37821695-chr17:37885037..37886831,2	K562	blood:
8	chr12:7052950..7053652-chr17:37821467..37822209,2	Hela-S3	cervix:
9	chr17:37791520..37796368-chr17:37822308..37826994,8	K562	blood:
10	chr17:37790905..37794856-chr17:37820000..37822270,4	K562	blood:
11	chr17:37806279..37807957-chr17:37817089..37818610,2	K562	blood:
12	chr17:37820097..37822634-chr17:37895456..37897611,2	K562	blood:
13	chr17:37818282..37821110-chr17:37882752..37884709,2	K562	blood:
14	chr17:37821804..37826261-chr17:37885454..37888153,4	K562	blood:
15	chr17:37806164..37807865-chr17:37817828..37819682,2	MCF-7	breast:
16	chr17:37822303..37824126-chr17:37856298..37859081,2	K562	blood:
17	chr17:37820932..37826284-chr17:37838504..37843351,7	K562	blood:

No data

Variant related genes	Relation type
TCAP	TF binding region
PNMT	TF binding region
TCAP	CpG island
PNMT	CpG island
ENSG00000161395	chromatin interactions
ENSG00000141738	chromatin interactions
ENSG00000141736	chromatin interactions
ENSG00000141744	chromatin interactions
ENSG00000214546	chromatin interactions
ENSG00000131771	chromatin interactions
ENSG00000141741	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000131748	chromatin interactions

Extended variants
information (count: 220 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:220 , 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	rs2941513	chr17:37818561-37818562	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139432375	chr17:37818570-37818571	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs562962022	chr17:37818589-37818590	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs377433763	chr17:37818615-37818616	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs530678699	chr17:37818661-37818662	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs552059590	chr17:37818676-37818677	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs78374585	chr17:37818694-37818695	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs534509871	chr17:37818792-37818793	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs546809652	chr17:37818794-37818795	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs144131619	chr17:37818809-37818810	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs34352266	chr17:37818833-37818834	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs78619027	chr17:37818836-37818837	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs557357185	chr17:37818847-37818848	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs2941512	chr17:37818871-37818872	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs540091977	chr17:37818930-37818931	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs558484143	chr17:37818931-37818932	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs2952150	chr17:37818932-37818933	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs540453257	chr17:37818958-37818959	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs562331781	chr17:37819017-37819018	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs368213268	chr17:37819021-37819022	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs368676307	chr17:37819034-37819035	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs34282352	chr17:37819056-37819057	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs373816766	chr17:37819060-37819061	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs574417032	chr17:37819062-37819063	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs78029334	chr17:37819092-37819093	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs562900538	chr17:37819127-37819128	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs151032154	chr17:37819132-37819133	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs35874339	chr17:37819134-37819135	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs368839197	chr17:37819141-37819142	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs146010122	chr17:37819145-37819146	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs139221372	chr17:37819150-37819151	Weak transcription Enhancers Strong transcription 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	rs188080925	chr17:37819153-37819154	Weak transcription Enhancers Strong transcription 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	rs371137052	chr17:37819182-37819183	Weak transcription Enhancers Strong transcription 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	rs111294298	chr17:37819183-37819184	Weak transcription Enhancers Strong transcription 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	rs192495661	chr17:37819205-37819206	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs371191084	chr17:37819211-37819212	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs528415391	chr17:37819221-37819222	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs546448589	chr17:37819230-37819231	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs558297016	chr17:37819239-37819240	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs2934961	chr17:37819241-37819242	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs551097184	chr17:37819263-37819264	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs569418909	chr17:37819299-37819300	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs375575018	chr17:37819324-37819325	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs15968	chr17:37819335-37819336	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs558215495	chr17:37819344-37819345	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs573434877	chr17:37819395-37819396	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs534525076	chr17:37819397-37819398	Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs531705954	chr17:37819415-37819416	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs139905785	chr17:37819423-37819424	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs544453062	chr17:37819448-37819449	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:128)

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
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37795000-37823800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr17:37799800-37819600	Weak transcription	Osteobl	bone
3	chr17:37800000-37818600	Weak transcription	Hela-S3	cervix
4	chr17:37800000-37820000	Weak transcription	NH-A	brain
5	chr17:37803800-37821800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr17:37808400-37819200	Weak transcription	Small Intestine	intestine
7	chr17:37809800-37819400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr17:37810000-37819400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr17:37810000-37819600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr17:37810000-37820000	Weak transcription	HSMMtube	muscle
11	chr17:37810000-37820400	Strong transcription	Brain Germinal Matrix	brain
12	chr17:37810200-37819800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr17:37810600-37818600	Strong transcription	Fetal Intestine Small	intestine
14	chr17:37810600-37819200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr17:37810600-37819200	Strong transcription	Fetal Intestine Large	intestine
16	chr17:37810600-37820000	Weak transcription	K562	blood
17	chr17:37810600-37821000	Weak transcription	Fetal Brain Male	brain
18	chr17:37810800-37819400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr17:37810800-37819600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr17:37810800-37820600	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr17:37811000-37818600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr17:37811000-37818600	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr17:37811400-37818600	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr17:37811800-37819400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr17:37811800-37820800	Strong transcription	Fetal Brain Female	brain
26	chr17:37812000-37819400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr17:37812000-37819600	Genic enhancers	Lung	lung
28	chr17:37812400-37819200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr17:37812400-37819600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr17:37812600-37819400	Strong transcription	Placenta Amnion	Placenta Amnion
31	chr17:37812600-37819600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr17:37813000-37820800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr17:37813400-37819400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr17:37814000-37819200	Strong transcription	Muscle Satellite Cultured Cells	--
35	chr17:37814000-37819800	Strong transcription	Dnd41	blood
36	chr17:37814000-37820400	Genic enhancers	Fetal Muscle Trunk	muscle
37	chr17:37814200-37819400	Genic enhancers	Primary B cells from peripheral blood	blood
38	chr17:37814600-37819000	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr17:37814800-37819800	Genic enhancers	Fetal Muscle Leg	muscle
40	chr17:37815000-37819400	Genic enhancers	Placenta	Placenta
41	chr17:37815600-37818600	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr17:37816200-37818600	Strong transcription	Rectal Smooth Muscle	rectum
43	chr17:37816200-37819200	Genic enhancers	Liver	Liver
44	chr17:37816200-37819400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr17:37816200-37819400	Genic enhancers	Brain Anterior Caudate	brain
46	chr17:37816400-37819200	Genic enhancers	Stomach Smooth Muscle	stomach
47	chr17:37816400-37819400	Strong transcription	NHLF	lung
48	chr17:37816400-37819600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr17:37816400-37819600	Genic enhancers	Right Ventricle	heart
50	chr17:37816400-37819600	Strong transcription	Monocytes-CD14+_RO01746	blood

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