Variant report

Variant	nsv587738
Chromosome Location	chr21:45620353-45628374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:620)
CpG islands
(count:489)
Chromatin interactive
region (count:24)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr21:45622503-45622974	K562	blood:	n/a	n/a
2	ATF1	chr21:45627754-45628197	K562	blood:	n/a	n/a
3	ATF2	chr21:45626321-45628146	GM12878	blood:	n/a	n/a
4	ATF2	chr21:45626343-45627633	GM12878	blood:	n/a	n/a
5	ATF3	chr21:45622485-45622869	K562	blood:	n/a	n/a
6	ATF3	chr21:45627837-45628247	K562	blood:	n/a	n/a
7	BATF	chr21:45623272-45623610	GM12878	blood:	n/a	n/a
8	BATF	chr21:45626310-45627816	GM12878	blood:	n/a	chr21:45627643-45627653
9	BCL11A	chr21:45626591-45627579	GM12878	blood:	n/a	chr21:45627372-45627381
10	BCL11A	chr21:45626541-45627764	GM12878	blood:	n/a	chr21:45627372-45627381
11	BCL3	chr21:45626610-45627534	GM12878	blood:	n/a	chr21:45627372-45627381
12	BCLAF1	chr21:45626329-45628360	GM12878	blood:	n/a	chr21:45627372-45627381
13	BCLAF1	chr21:45626458-45628055	GM12878	blood:	n/a	chr21:45627372-45627381
14	BHLHE40	chr21:45622180-45622754	K562	blood:	n/a	chr21:45622610-45622626
15	BHLHE40	chr21:45627566-45628378	K562	blood:	n/a	n/a
16	BHLHE40	chr21:45625372-45625609	K562	blood:	n/a	n/a
17	BHLHE40	chr21:45626173-45628119	GM12878	blood:	n/a	chr21:45626334-45626350
18	BRCA1	chr21:45626876-45627237	GM12878	blood:	n/a	n/a
19	BRCA1	chr21:45628017-45628193	Hela-S3	cervix:	n/a	n/a
20	CCNT2	chr21:45626872-45627117	K562	blood:	n/a	n/a
21	CCNT2	chr21:45622415-45622989	K562	blood:	n/a	n/a
22	CCNT2	chr21:45625404-45625479	K562	blood:	n/a	n/a
23	CCNT2	chr21:45627659-45628192	K562	blood:	n/a	n/a
24	CEBPB	chr21:45627914-45628489	IMR90	lung:	n/a	n/a
25	CEBPB	chr21:45626282-45626882	MCF-7	breast:	n/a	chr21:45626598-45626609
26	CEBPB	chr21:45626474-45626673	HepG2	liver:	n/a	chr21:45626598-45626609
27	CEBPB	chr21:45622529-45622896	H1-hESC	embryonic stem cell:	n/a	chr21:45622707-45622718
28	CEBPB	chr21:45622535-45622877	HepG2	liver:	n/a	chr21:45622707-45622718
29	CEBPB	chr21:45626550-45626764	K562	blood:	n/a	chr21:45626598-45626609
30	CEBPB	chr21:45622637-45622757	HepG2	liver:	n/a	chr21:45622707-45622718
31	CEBPB	chr21:45622576-45622838	A549	lung:	n/a	chr21:45622707-45622718
32	CEBPB	chr21:45624691-45624988	H1-hESC	embryonic stem cell:	n/a	chr21:45624810-45624821 chr21:45624807-45624824
33	CEBPB	chr21:45622518-45622870	K562	blood:	n/a	chr21:45622707-45622718
34	CEBPB	chr21:45622519-45622908	IMR90	lung:	n/a	chr21:45622707-45622718
35	CEBPB	chr21:45627260-45627583	GM12878	blood:	n/a	n/a
36	CEBPB	chr21:45626321-45628270	GM12878	blood:	n/a	chr21:45626598-45626609
37	CEBPB	chr21:45622344-45623035	MCF-7	breast:	n/a	chr21:45622707-45622718
38	CEBPB	chr21:45622544-45622829	K562	blood:	n/a	chr21:45622707-45622718
39	CEBPB	chr21:45626522-45626695	K562	blood:	n/a	chr21:45626598-45626609
40	CEBPB	chr21:45626129-45626773	IMR90	lung:	n/a	chr21:45626598-45626609
41	CEBPB	chr21:45622525-45622899	K562	blood:	n/a	chr21:45622707-45622718
42	CEBPB	chr21:45626470-45626769	Hela-S3	cervix:	n/a	chr21:45626598-45626609
43	CEBPB	chr21:45624746-45624931	HepG2	liver:	n/a	chr21:45624810-45624821 chr21:45624807-45624824
44	CEBPB	chr21:45622516-45622927	Hela-S3	cervix:	n/a	chr21:45622707-45622718
45	CEBPB	chr21:45627524-45628287	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr21:45622427-45623040	MCF-7	breast:	n/a	chr21:45622707-45622718
47	CEBPB	chr21:45624685-45624878	K562	blood:	n/a	chr21:45624810-45624821 chr21:45624807-45624824
48	CEBPB	chr21:45626140-45627182	MCF-7	breast:	n/a	chr21:45626598-45626609
49	CEBPD	chr21:45625350-45625686	K562	blood:	n/a	n/a
50	CHD1	chr21:45626187-45628235	GM12878	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45622373-45622423	ECC-1	luminal epithelium:	n/a
2	chr21:45622373-45622423	ECC-1	luminal epithelium:	n/a
3	chr21:45626491-45626541	Hepatocyte	liver:	n/a
4	chr21:45622219-45622269	HPAEpiC	pulmonary alveolar:	n/a
5	chr21:45626491-45626541	K562	blood:	n/a
6	chr21:45622122-45622172	PFSK-1	brain:	n/a
7	chr21:45622096-45622146	AG09309	skin:	n/a
8	chr21:45622373-45622423	AG09319	gingival:	n/a
9	chr21:45623005-45623055	ECC-1	luminal epithelium:	n/a
10	chr21:45626491-45626541	GM12891	blood:	n/a
11	chr21:45622096-45622146	MCF-7	breast:	n/a
12	chr21:45622373-45622423	GM12878	blood:	n/a
13	chr21:45622493-45622543	ECC-1	luminal epithelium:	n/a
14	chr21:45623005-45623055	PrEC	prostate:	n/a
15	chr21:45622373-45622423	AG10803	skin:	n/a
16	chr21:45622122-45622172	HUVEC	blood vessel:	n/a
17	chr21:45622373-45622423	Hela-S3	cervix:	n/a
18	chr21:45624178-45624228	ECC-1	luminal epithelium:	n/a
19	chr21:45622096-45622146	NT2-D1	testis:	n/a
20	chr21:45624178-45624228	NH-A	brain:	n/a
21	chr21:45623005-45623055	H1-hESC	embryonic stem cell:	embryo
22	chr21:45622096-45622146	SK-N-MC	brain:	n/a
23	chr21:45622373-45622423	Hepatocyte	liver:	n/a
24	chr21:45622219-45622269	H1-hESC	embryonic stem cell:	embryo
25	chr21:45622493-45622543	Caco-2	colon:	n/a
26	chr21:45624178-45624228	CMK	blood:	n/a
27	chr21:45624178-45624228	HAEpiC	amniotic membrane:	n/a
28	chr21:45624178-45624228	Hela-S3	cervix:	n/a
29	chr21:45622373-45622423	Jurkat	blood:	n/a
30	chr21:45622219-45622269	U87	brain:	n/a
31	chr21:45622122-45622172	GM12878	blood:	n/a
32	chr21:45623005-45623055	SAEC	small airway:	n/a
33	chr21:45626491-45626541	HCT-116	colon:	n/a
34	chr21:45622373-45622423	NHBE	bronchial:	n/a
35	chr21:45622122-45622172	Hela-S3	cervix:	n/a
36	chr21:45626491-45626541	GM12892	blood:	n/a
37	chr21:45624178-45624228	HUVEC	blood vessel:	n/a
38	chr21:45622219-45622269	HEEpiC	esophagus:	n/a
39	chr21:45622219-45622269	Hepatocyte	liver:	n/a
40	chr21:45622096-45622146	IMR90	lung:	fetal
41	chr21:45622219-45622269	AG10803	skin:	n/a
42	chr21:45622373-45622423	SKMC	muscle:	n/a
43	chr21:45622493-45622543	HCF	heart:	n/a
44	chr21:45626491-45626541	IMR90	lung:	fetal
45	chr21:45622096-45622146	HepG2	liver:	n/a
46	chr21:45626491-45626541	H1-hESC	embryonic stem cell:	embryo
47	chr21:45624178-45624228	Hepatocyte	liver:	n/a
48	chr21:45623005-45623055	CMK	blood:	n/a
49	chr21:45622219-45622269	HNPCEpiC	eye:	n/a
50	chr21:45622096-45622146	ovcar-3	ovarian:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45621014..45624737-chr21:45625090..45629806,7	K562	blood:
2	chr21:45619816..45631884-chr21:45656529..45663802,30	MCF-7	breast:
3	chr21:45552930..45554458-chr21:45622046..45624839,2	MCF-7	breast:
4	chr21:45621014..45626357-chr21:45626432..45630019,5	K562	blood:
5	chr21:45580625..45582180-chr21:45622469..45623971,2	MCF-7	breast:
6	chr21:45624595..45626687-chr21:45758161..45760406,2	MCF-7	breast:
7	chr21:45555886..45558409-chr21:45626511..45629056,2	MCF-7	breast:
8	chr21:45621014..45624737-chr21:45625090..45629806,7	K562	blood:
9	chr21:45588739..45594310-chr21:45621185..45624296,6	MCF-7	breast:
10	chr21:45620311..45631567-chr21:45651002..45670824,52	MCF-7	breast:
11	chr21:45622485..45624278-chr21:45668242..45670471,2	MCF-7	breast:
12	chr2:85664771..85665446-chr21:45627770..45628304,2	Hela-S3	cervix:
13	chr21:45620857..45623394-chr21:45709649..45711804,3	MCF-7	breast:
14	chr21:45593462..45595365-chr21:45624116..45626605,2	K562	blood:
15	chr21:45613209..45613813-chr21:45623826..45624382,2	NB4	blood:
16	chr21:45620341..45625358-chr21:45718389..45721509,5	MCF-7	breast:
17	chr21:45622629..45624491-chr21:45663848..45665509,2	MCF-7	breast:
18	chr21:45621786..45624650-chr21:45632661..45635247,3	MCF-7	breast:
19	chr21:45621014..45626357-chr21:45626432..45630019,5	K562	blood:
20	chr21:45577492..45580364-chr21:45620942..45622616,2	K562	blood:
21	chr21:45590531..45598113-chr21:45625237..45630055,9	MCF-7	breast:
22	chr21:45625593..45629065-chr21:45717787..45720760,5	MCF-7	breast:
23	chr21:45621565..45624005-chr21:45712576..45714212,3	MCF-7	breast:
24	chr21:45621411..45624934-chr21:45718058..45721352,4	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ICOSLG-2	chr21:45619132-45620582	XLOC_014114
2	lnc-ICOSLG-7	chr21:45622544-45622770	NONHSAT082495
3	lnc-ICOSLG-2	chr21:45620693-45621216	XLOC_014114
4	lnc-ICOSLG-1	chr21:45621679-45621840	NONHSAT082494
5	lnc-ICOSLG-1	chr21:45626412-45626714	NONHSAT082494
6	lnc-ICOSLG-7	chr21:45623876-45623967	NONHSAT082495
7	lnc-ICOSLG-1	chr21:45627086-45627280	NONHSAT082494
8	lnc-ICOSLG-1	chr21:45627086-45627282	XLOC_014115
9	lnc-ICOSLG-1	chr21:45626408-45626673	XLOC_014115
10	lnc-C21orf33-2	chr21:45622449-45622579	XLOC_013967
11	lnc-C21orf33-2	chr21:45621173-45621840	XLOC_013967

No data

Variant related genes	Relation type
ENSG00000232124	TF binding region
ENSG00000232698	TF binding region
ENSG00000232124	CpG island
ENSG00000232698	CpG island
ENSG00000225331	chromatin interactions
ENSG00000160223	chromatin interactions
ENSG00000232969	chromatin interactions
ENSG00000237604	chromatin interactions
ENSG00000160224	chromatin interactions
ENSG00000160221	chromatin interactions
ENSG00000267913	chromatin interactions
ENSG00000141959	chromatin interactions
ENSG00000232124	chromatin interactions
ENSG00000232698	chromatin interactions
ENSG00000232010	chromatin interactions
ENSG00000160226	chromatin interactions
PDPR	miRNA target sites
PDPK1	miRNA target sites

Extended variants
information (count: 403 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552742786	chr21:45620357-45620358	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs570996897	chr21:45620367-45620368	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs138252341	chr21:45620382-45620383	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs200211056	chr21:45620422-45620423	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs186282455	chr21:45620452-45620453	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs77437029	chr21:45620476-45620477	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs568385430	chr21:45620535-45620536	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs554249561	chr21:45620636-45620637	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs553706424	chr21:45620642-45620643	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs149620322	chr21:45620701-45620702	Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs546029672	chr21:45620706-45620707	Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs558224957	chr21:45620727-45620728	Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs577001658	chr21:45620765-45620766	Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs544376364	chr21:45620773-45620774	Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs562793073	chr21:45620792-45620793	Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs139333102	chr21:45620796-45620797	Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs569041878	chr21:45620825-45620826	Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs374397054	chr21:45620830-45620831	Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs560145133	chr21:45620833-45620834	Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs143358027	chr21:45620913-45620914	Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
21	rs552019826	chr21:45620916-45620917	Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
22	rs570505456	chr21:45620940-45620941	Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
23	rs531832037	chr21:45620955-45620956	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
24	rs147139785	chr21:45620976-45620977	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
25	rs568421794	chr21:45620979-45620980	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
26	rs371388684	chr21:45621034-45621035	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
27	rs73381313	chr21:45621035-45621036	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs191527357	chr21:45621045-45621046	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
29	rs565778721	chr21:45621054-45621055	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
30	rs148612860	chr21:45621166-45621167	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
31	rs558000883	chr21:45621169-45621170	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
32	rs555147878	chr21:45621187-45621188	Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
33	rs113526534	chr21:45621230-45621231	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
34	rs537564908	chr21:45621236-45621237	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
35	rs537660871	chr21:45621243-45621244	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
36	rs142094073	chr21:45621246-45621247	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
37	rs574788701	chr21:45621247-45621248	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
38	rs62228210	chr21:45621292-45621293	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs537493969	chr21:45621319-45621320	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
40	rs78171240	chr21:45621352-45621353	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
41	rs577221539	chr21:45621362-45621363	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
42	rs77529874	chr21:45621371-45621372	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
43	rs183405850	chr21:45621380-45621381	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
44	rs564042090	chr21:45621407-45621408	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
45	rs117039324	chr21:45621474-45621475	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
46	rs549962296	chr21:45621482-45621483	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
47	rs561990084	chr21:45621494-45621495	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
48	rs188507544	chr21:45621509-45621510	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
49	rs547720025	chr21:45621510-45621511	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
50	rs62228211	chr21:45621517-45621518	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
small cell lung cancer	17426248	CNVD
Ependymoma	20639864	CNVD
Breast cancer	21364760	CNVD
Down syndrome	21154855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45614800-45622400	Weak transcription	Pancreas	Pancrea
2	chr21:45615000-45623200	Weak transcription	Brain Hippocampus Middle	brain
3	chr21:45615400-45622200	Weak transcription	Fetal Lung	lung
4	chr21:45616600-45622000	Weak transcription	Lung	lung
5	chr21:45616600-45622200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr21:45616600-45622200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr21:45616800-45621600	Weak transcription	Esophagus	oesophagus
8	chr21:45616800-45622000	Weak transcription	Left Ventricle	heart
9	chr21:45616800-45622200	Weak transcription	Fetal Intestine Small	intestine
10	chr21:45616800-45622200	Weak transcription	Spleen	Spleen
11	chr21:45616800-45626600	Weak transcription	Thymus	Thymus
12	chr21:45617000-45622400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr21:45617000-45626000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr21:45617200-45622200	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr21:45617200-45622600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr21:45617200-45623200	Weak transcription	GM12878-XiMat	blood
17	chr21:45617200-45624000	Weak transcription	Gastric	stomach
18	chr21:45617200-45626200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr21:45617400-45622400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr21:45617400-45622400	Weak transcription	Right Atrium	heart
21	chr21:45617400-45622600	Weak transcription	Primary B cells from peripheral blood	blood
22	chr21:45617400-45622600	Weak transcription	Primary hematopoietic stem cells	blood
23	chr21:45617400-45622600	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr21:45617400-45622600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr21:45617400-45624200	Weak transcription	Brain Substantia Nigra	brain
26	chr21:45617400-45624200	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr21:45617400-45626000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr21:45617600-45622000	Weak transcription	Right Ventricle	heart
29	chr21:45617600-45622200	Weak transcription	Primary B cells from cord blood	blood
30	chr21:45617600-45622200	Weak transcription	K562	blood
31	chr21:45617600-45622400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr21:45618000-45622000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr21:45618000-45622000	Weak transcription	Fetal Muscle Leg	muscle
34	chr21:45619800-45623400	Weak transcription	Stomach Mucosa	stomach
35	chr21:45620000-45622000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr21:45620000-45623600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr21:45620200-45622000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr21:45620400-45622800	Weak transcription	Brain Anterior Caudate	brain
39	chr21:45621200-45622200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr21:45621400-45622200	Enhancers	Placenta	Placenta
41	chr21:45621600-45623000	Enhancers	Esophagus	oesophagus
42	chr21:45622000-45622200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr21:45622000-45622200	Enhancers	Left Ventricle	heart
44	chr21:45622000-45622200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
45	chr21:45622000-45622200	Enhancers	Small Intestine	intestine
46	chr21:45622000-45622200	Enhancers	Hela-S3	cervix
47	chr21:45622000-45622400	Enhancers	Right Ventricle	heart
48	chr21:45622000-45622400	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
49	chr21:45622000-45622400	Enhancers	NHEK	skin
50	chr21:45622000-45622600	Enhancers	Fetal Muscle Leg	muscle

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