Variant report

Variant	nsv913903
Chromosome Location	chr21:45630608-45657970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:673)
CpG islands
(count:122)
Chromatin interactive
region (count:66)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:45638537-45638623	K562	blood:	n/a	n/a
2	ATF1	chr21:45638353-45638745	K562	blood:	n/a	n/a
3	ATF2	chr21:45645993-45646313	GM12878	blood:	n/a	n/a
4	ATF2	chr21:45642852-45643678	GM12878	blood:	n/a	n/a
5	ATF2	chr21:45634976-45635407	GM12878	blood:	n/a	n/a
6	ATF2	chr21:45643069-45643615	GM12878	blood:	n/a	n/a
7	ATF2	chr21:45638216-45638736	GM12878	blood:	n/a	n/a
8	ATF2	chr21:45645532-45645947	GM12878	blood:	n/a	n/a
9	ATF2	chr21:45644973-45645453	GM12878	blood:	n/a	n/a
10	ATF2	chr21:45639835-45640899	GM12878	blood:	n/a	n/a
11	ATF2	chr21:45632208-45632642	GM12878	blood:	n/a	n/a
12	ATF2	chr21:45631647-45632775	GM12878	blood:	n/a	n/a
13	BATF	chr21:45635177-45635735	GM12878	blood:	n/a	n/a
14	BATF	chr21:45635423-45635665	GM12878	blood:	n/a	n/a
15	BATF	chr21:45643665-45643873	GM12878	blood:	n/a	n/a
16	BCL11A	chr21:45640590-45640939	GM12878	blood:	n/a	n/a
17	BCL3	chr21:45631415-45632600	GM12878	blood:	n/a	n/a
18	BCL3	chr21:45643067-45643453	GM12878	blood:	n/a	n/a
19	BCL3	chr21:45644514-45644918	GM12878	blood:	n/a	n/a
20	BCL3	chr21:45642910-45643599	GM12878	blood:	n/a	n/a
21	BCL3	chr21:45631471-45632171	GM12878	blood:	n/a	n/a
22	BCLAF1	chr21:45635123-45635688	GM12878	blood:	n/a	n/a
23	BCLAF1	chr21:45638339-45638846	GM12878	blood:	n/a	n/a
24	BCLAF1	chr21:45639813-45640874	GM12878	blood:	n/a	n/a
25	BCLAF1	chr21:45644591-45644913	GM12878	blood:	n/a	n/a
26	BCLAF1	chr21:45631987-45632771	GM12878	blood:	n/a	chr21:45632621-45632630
27	BCLAF1	chr21:45642995-45643445	GM12878	blood:	n/a	n/a
28	BCLAF1	chr21:45639703-45640268	GM12878	blood:	n/a	n/a
29	BCLAF1	chr21:45640318-45640949	GM12878	blood:	n/a	n/a
30	BCLAF1	chr21:45643065-45643655	GM12878	blood:	n/a	n/a
31	BCLAF1	chr21:45631717-45632370	GM12878	blood:	n/a	n/a
32	BCLAF1	chr21:45638337-45638932	GM12878	blood:	n/a	n/a
33	BHLHE40	chr21:45643200-45643533	GM12878	blood:	n/a	n/a
34	BHLHE40	chr21:45635413-45635420	GM12878	blood:	n/a	n/a
35	BHLHE40	chr21:45638323-45638771	GM12878	blood:	n/a	n/a
36	BHLHE40	chr21:45643251-45643508	HepG2	liver:	n/a	n/a
37	BHLHE40	chr21:45632226-45632563	GM12878	blood:	n/a	n/a
38	BHLHE40	chr21:45642888-45643508	K562	blood:	n/a	n/a
39	BHLHE40	chr21:45651176-45651283	K562	blood:	n/a	n/a
40	BHLHE40	chr21:45640650-45640713	GM12878	blood:	n/a	n/a
41	BHLHE40	chr21:45638327-45638777	K562	blood:	n/a	n/a
42	BRCA1	chr21:45638147-45638309	GM12878	blood:	n/a	n/a
43	BRCA1	chr21:45631582-45632400	GM12878	blood:	n/a	n/a
44	CEBPB	chr21:45636321-45636436	HepG2	liver:	n/a	n/a
45	CEBPB	chr21:45657081-45657541	MCF-7	breast:	n/a	n/a
46	CEBPB	chr21:45644511-45644544	K562	blood:	n/a	n/a
47	CEBPB	chr21:45631340-45632716	GM12878	blood:	n/a	chr21:45632695-45632706
48	CHD1	chr21:45635312-45635511	GM12878	blood:	n/a	n/a
49	CHD2	chr21:45646141-45646157	GM12878	blood:	n/a	n/a
50	CHD2	chr21:45645857-45645881	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45656979-45657029	HAEpiC	amniotic membrane:	n/a
2	chr21:45656979-45657029	HCM	heart:	n/a
3	chr21:45648328-45648378	HRCEpiC	kidney:	n/a
4	chr21:45656979-45657029	HIPEpiC	eye:	n/a
5	chr21:45648328-45648378	NHDF-neo	bronchial:	n/a
6	chr21:45656979-45657029	HL-60	blood:	n/a
7	chr21:45648328-45648378	HIPEpiC	eye:	n/a
8	chr21:45648328-45648378	HMEC	breast:	n/a
9	chr21:45656979-45657029	A549	lung:	n/a
10	chr21:45656979-45657029	HCT-116	colon:	n/a
11	chr21:45648328-45648378	HL-60	blood:	n/a
12	chr21:45648328-45648378	SK-N-SH	brain:	n/a
13	chr21:45648328-45648378	H1-hESC	embryonic stem cell:	embryo
14	chr21:45656979-45657029	HepG2	liver:	n/a
15	chr21:45648328-45648378	Jurkat	blood:	n/a
16	chr21:45656979-45657029	HRCEpiC	kidney:	n/a
17	chr21:45648328-45648378	SK-N-MC	brain:	n/a
18	chr21:45648328-45648378	ProgFib	skin:	n/a
19	chr21:45656979-45657029	MCF10A-Er-Src	breast:	n/a
20	chr21:45656979-45657029	GM12878	blood:	n/a
21	chr21:45648328-45648378	HCM	heart:	n/a
22	chr21:45656979-45657029	NB4	blood:	n/a
23	chr21:45656979-45657029	MCF-7	breast:	n/a
24	chr21:45648328-45648378	SAEC	small airway:	n/a
25	chr21:45656979-45657029	LNCaP	prostate:	n/a
26	chr21:45656979-45657029	SAEC	small airway:	n/a
27	chr21:45648328-45648378	T-47D	breast:	n/a
28	chr21:45656979-45657029	HEEpiC	esophagus:	n/a
29	chr21:45648328-45648378	IMR90	lung:	fetal
30	chr21:45656979-45657029	RPTEC	kidney:	n/a
31	chr21:45656979-45657029	GM19239	blood:	n/a
32	chr21:45648328-45648378	AoSMC	blood vessel:	n/a
33	chr21:45648328-45648378	HRPEpiC	eye:	n/a
34	chr21:45648328-45648378	AG09319	gingival:	n/a
35	chr21:45656979-45657029	AG09309	skin:	n/a
36	chr21:45648328-45648378	HUVEC	blood vessel:	n/a
37	chr21:45656979-45657029	CMK	blood:	n/a
38	chr21:45656979-45657029	GM12891	blood:	n/a
39	chr21:45648328-45648378	HCT-116	colon:	n/a
40	chr21:45648328-45648378	PFSK-1	brain:	n/a
41	chr21:45656979-45657029	Caco-2	colon:	n/a
42	chr21:45648328-45648378	AG09309	skin:	n/a
43	chr21:45656979-45657029	HEK293	kidney:	embryo
44	chr21:45656979-45657029	BJ	skin:	n/a
45	chr21:45656979-45657029	HNPCEpiC	eye:	n/a
46	chr21:45648328-45648378	HCF	heart:	n/a
47	chr21:45648328-45648378	HNPCEpiC	eye:	n/a
48	chr21:45656979-45657029	BE2_C	brain:	n/a
49	chr21:45648328-45648378	HRE	kidney:	n/a
50	chr21:45648328-45648378	GM12891	blood:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:45637874..45640737-chr21:45652531..45655334,2	MCF-7	breast:
2	chr21:45646352..45648342-chr21:45670015..45672115,2	MCF-7	breast:
3	chr21:45626500..45630389-chr21:45636831..45640533,5	MCF-7	breast:
4	chr21:45626756..45628836-chr21:45644780..45646727,2	MCF-7	breast:
5	chr21:45571301..45575033-chr21:45652281..45654701,3	MCF-7	breast:
6	chr21:45571719..45574629-chr21:45639760..45641612,2	MCF-7	breast:
7	chr21:45621066..45623314-chr21:45644215..45646761,3	MCF-7	breast:
8	chr21:45633493..45635981-chr21:45638938..45640638,2	MCF-7	breast:
9	chr21:45644990..45647896-chr21:45648106..45650288,2	K562	blood:
10	chr21:45626963..45630289-chr21:45630866..45636096,6	MCF-7	breast:
11	chr21:45620311..45631567-chr21:45651002..45670824,52	MCF-7	breast:
12	chr21:45644108..45645781-chr21:45647217..45649363,2	MCF-7	breast:
13	chr21:45648743..45651558-chr21:45652534..45654668,2	K562	blood:
14	chr21:45657604..45660265-chr21:45683962..45685836,2	K562	blood:
15	chr21:45642545..45644733-chr21:45651214..45653220,2	K562	blood:
16	chr21:45637599..45639295-chr21:45647938..45650241,2	MCF-7	breast:
17	chr21:45631200..45631884-chr4:2306687..2307191,2	MCF-7	breast:
18	chr21:45637636..45640956-chr21:45661307..45664168,3	MCF-7	breast:
19	chr21:45655188..45657257-chr21:45719173..45720692,2	MCF-7	breast:
20	chr21:45644616..45646347-chr21:45720653..45723440,2	MCF-7	breast:
21	chr21:45591261..45594431-chr21:45640713..45642664,3	MCF-7	breast:
22	chr21:45625272..45628072-chr21:45645841..45648362,2	K562	blood:
23	chr21:45628810..45630554-chr21:45636671..45638693,2	K562	blood:
24	chr21:45638138..45641604-chr21:45643124..45645379,3	MCF-7	breast:
25	chr21:45646702..45648292-chr21:45653569..45655445,2	K562	blood:
26	chr21:45637599..45639295-chr21:45647938..45650241,2	MCF-7	breast:
27	chr21:45654371..45654896-chr21:45687445..45688145,2	K562	blood:
28	chr21:45638620..45641640-chr21:45644035..45648127,5	MCF-7	breast:
29	chr21:45620304..45623490-chr21:45641507..45643992,3	MCF-7	breast:
30	chr21:45620311..45631567-chr21:45651002..45670824,52	MCF-7	breast:
31	chr21:45655108..45658029-chr21:45775901..45777424,2	MCF-7	breast:
32	chr21:45585070..45587795-chr21:45647222..45649775,2	K562	blood:
33	chr21:45561699..45563359-chr21:45648827..45651236,2	K562	blood:
34	chr21:45561699..45563814-chr21:45648554..45651236,3	K562	blood:
35	chr21:45619816..45631884-chr21:45656529..45663802,30	MCF-7	breast:
36	chr21:45638024..45640421-chr21:45658228..45660769,4	MCF-7	breast:
37	chr21:45633493..45635981-chr21:45638938..45640638,2	MCF-7	breast:
38	chr21:45634893..45639040-chr21:45644730..45647153,4	K562	blood:
39	chr21:45634893..45639040-chr21:45644730..45647153,4	K562	blood:
40	chr21:45641049..45643518-chr21:45653800..45656237,3	MCF-7	breast:
41	chr21:45619816..45631884-chr21:45656529..45663802,30	MCF-7	breast:
42	chr21:45647000..45652679-chr21:45655526..45663684,10	MCF-7	breast:
43	chr21:45644990..45647896-chr21:45648106..45650288,2	K562	blood:
44	chr21:45638620..45641640-chr21:45644035..45648127,5	MCF-7	breast:
45	chr21:45633515..45635419-chr21:45641635..45644619,2	MCF-7	breast:
46	chr21:45633515..45635419-chr21:45641635..45644619,2	MCF-7	breast:
47	chr21:45646929..45649762-chr21:45721151..45723519,2	MCF-7	breast:
48	chr21:45642545..45644733-chr21:45651214..45653220,2	K562	blood:
49	chr21:45636499..45639520-chr21:45653196..45656118,3	K562	blood:
50	chr21:45626157..45628593-chr21:45648782..45651445,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DNMT3L-1	chr21:45649156-45649214	l_2231_chr21:45648154-45649214_adipose
2	lnc-DNMT3L-1	chr21:45648155-45648839	l_2231_chr21:45648154-45649214_adipose

No data

Variant related genes	Relation type
ENSG00000232698	TF binding region
ENSG00000232698	CpG island
ENSG00000160223	chromatin interactions
ENSG00000267913	chromatin interactions
ENSG00000232698	chromatin interactions
ENSG00000141959	chromatin interactions
ENSG00000232124	chromatin interactions
ENSG00000142182	chromatin interactions
ENSG00000232010	chromatin interactions

Extended variants
information (count: 1542 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1542 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9983407	chr21:45630608-45630609	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570772806	chr21:45630620-45630621	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs531603883	chr21:45630622-45630623	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs182995787	chr21:45630629-45630630	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs568358488	chr21:45630639-45630640	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs535983833	chr21:45630649-45630650	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs553958163	chr21:45630671-45630672	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs377051112	chr21:45630699-45630700	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs572981928	chr21:45630706-45630707	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs145345206	chr21:45630707-45630708	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs376016520	chr21:45630724-45630725	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs201318298	chr21:45630725-45630726	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs9981492	chr21:45630740-45630741	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs187373098	chr21:45630836-45630837	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577167958	chr21:45630845-45630846	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs544230956	chr21:45630848-45630849	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs559213855	chr21:45630890-45630891	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs545831037	chr21:45630905-45630906	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs564500043	chr21:45630917-45630918	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs192950224	chr21:45630998-45630999	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs150038100	chr21:45631043-45631044	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs556171514	chr21:45631078-45631079	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs386819114	chr21:45631143-45631144	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs139114020	chr21:45631146-45631147	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs111573919	chr21:45631158-45631159	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs145538742	chr21:45631169-45631170	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs574344374	chr21:45631171-45631172	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs543728377	chr21:45631188-45631189	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs529677819	chr21:45631204-45631205	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs115842939	chr21:45631236-45631237	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs113421009	chr21:45631259-45631260	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs559972774	chr21:45631275-45631276	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs527904786	chr21:45631280-45631281	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs143631520	chr21:45631292-45631293	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs374132319	chr21:45631293-45631294	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs562914726	chr21:45631300-45631301	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs533664078	chr21:45631304-45631305	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs56200755	chr21:45631307-45631308	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs144771661	chr21:45631308-45631309	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs369421852	chr21:45631309-45631310	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs201132109	chr21:45631310-45631311	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs185562219	chr21:45631318-45631319	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs564439926	chr21:45631380-45631381	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs146924805	chr21:45631440-45631441	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs373090304	chr21:45631483-45631484	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs73228987	chr21:45631511-45631512	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs569691111	chr21:45631528-45631529	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs113774388	chr21:45631529-45631530	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs550196400	chr21:45631541-45631542	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs568474800	chr21:45631566-45631567	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45627200-45631000	Enhancers	Primary B cells from cord blood	blood
2	chr21:45627600-45631600	Weak transcription	Gastric	stomach
3	chr21:45627800-45636600	Enhancers	Primary B cells from peripheral blood	blood
4	chr21:45628000-45631400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr21:45628400-45632400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr21:45628600-45631400	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr21:45628600-45631800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr21:45628600-45632000	Weak transcription	Primary T cells from cord blood	blood
9	chr21:45628600-45632000	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr21:45628600-45632200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr21:45628600-45632400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr21:45628600-45638600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr21:45628600-45639400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr21:45628600-45659600	Weak transcription	Right Atrium	heart
15	chr21:45628800-45631400	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr21:45628800-45633400	Weak transcription	NHLF	lung
17	chr21:45628800-45646800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr21:45629000-45631600	Enhancers	GM12878-XiMat	blood
19	chr21:45629000-45638200	Weak transcription	HMEC	breast
20	chr21:45629200-45635800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr21:45629200-45637600	Weak transcription	Stomach Mucosa	stomach
22	chr21:45629400-45631800	Weak transcription	K562	blood
23	chr21:45629400-45633600	Weak transcription	Esophagus	oesophagus
24	chr21:45629600-45631400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr21:45629600-45631400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr21:45629600-45632000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr21:45629600-45632000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr21:45629600-45637800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr21:45629600-45638000	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr21:45629800-45635000	Weak transcription	Placenta	Placenta
31	chr21:45629800-45635000	Weak transcription	HUVEC	blood vessel
32	chr21:45629800-45636200	Weak transcription	Fetal Muscle Leg	muscle
33	chr21:45630200-45631400	Weak transcription	Primary hematopoietic stem cells	blood
34	chr21:45630600-45631000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr21:45630600-45631200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr21:45630600-45631400	Weak transcription	Fetal Thymus	thymus
37	chr21:45630600-45631600	Weak transcription	Spleen	Spleen
38	chr21:45631000-45631400	Weak transcription	Primary B cells from cord blood	blood
39	chr21:45631200-45638000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr21:45631400-45631600	Enhancers	Primary T cells fromperipheralblood	blood
41	chr21:45631400-45632200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr21:45631400-45632600	Enhancers	Fetal Thymus	thymus
43	chr21:45631400-45632800	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr21:45631400-45632800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr21:45631400-45633200	Enhancers	Primary B cells from cord blood	blood
46	chr21:45631400-45633400	Enhancers	Primary hematopoietic stem cells	blood
47	chr21:45631400-45633400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr21:45631600-45632000	Enhancers	Spleen	Spleen
49	chr21:45631600-45632200	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr21:45631600-45632200	Enhancers	Gastric	stomach

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