Variant report

Variant	nsv1062386
Chromosome Location	chr21:47314890-47343364
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:349)
CpG islands
(count:793)
Chromatin interactive
region (count:57)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:349 , 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	chr21:47343277-47343282	HepG2	liver:	n/a	n/a
2	CEBPB	chr21:47337363-47337796	MCF-7	breast:	n/a	chr21:47337632-47337643 chr21:47337634-47337643 chr21:47337634-47337645
3	CEBPB	chr21:47343103-47343371	IMR90	lung:	n/a	n/a
4	CEBPB	chr21:47337515-47337786	HepG2	liver:	n/a	chr21:47337632-47337643 chr21:47337634-47337643 chr21:47337634-47337645
5	CEBPB	chr21:47337545-47337774	A549	lung:	n/a	chr21:47337632-47337643 chr21:47337634-47337643 chr21:47337634-47337645
6	CEBPB	chr21:47337481-47337802	IMR90	lung:	n/a	chr21:47337632-47337643 chr21:47337634-47337643 chr21:47337634-47337645
7	CHD1	chr21:47342483-47343479	IMR90	lung:	n/a	n/a
8	CHD2	chr21:47343132-47343376	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr21:47343180-47343330	GM06990	blood:	n/a	chr21:47343282-47343290
10	CTCF	chr21:47343260-47343410	GM12867	blood:	n/a	chr21:47343282-47343290
11	CTCF	chr21:47343156-47343444	ProgFib	skin:	n/a	chr21:47343282-47343290
12	CTCF	chr21:47343220-47343370	AG04450	lung:	n/a	chr21:47343282-47343290
13	CTCF	chr21:47343220-47343370	AoAF	blood vessel:	n/a	chr21:47343282-47343290
14	CTCF	chr21:47343159-47343442	Pancreas_OC	pancreas:	n/a	chr21:47343282-47343290
15	CTCF	chr21:47343140-47343290	GM12878	blood:	n/a	chr21:47343282-47343290
16	CTCF	chr21:47343160-47343450	HVMF	connective:	n/a	chr21:47343282-47343290
17	CTCF	chr21:47343174-47343413	Hela-S3	cervix:	n/a	chr21:47343282-47343290
18	CTCF	chr21:47343148-47343486	T-47D	breast:	n/a	chr21:47343282-47343290
19	CTCF	chr21:47343133-47343452	Gliobla	brain:	n/a	chr21:47343282-47343290
20	CTCF	chr21:47339116-47339267	K562	blood:	n/a	n/a
21	CTCF	chr21:47343034-47343412	A549	lung:	n/a	chr21:47343282-47343290
22	CTCF	chr21:47343240-47343390	GM12865	blood:	n/a	chr21:47343282-47343290
23	CTCF	chr21:47343240-47343390	GM12864	blood:	n/a	chr21:47343282-47343290
24	CTCF	chr21:47343220-47343370	AG09319	gingival:	n/a	chr21:47343282-47343290
25	CTCF	chr21:47343160-47343310	GM12873	blood:	n/a	chr21:47343282-47343290
26	CTCF	chr21:47343060-47343210	GM12865	blood:	n/a	n/a
27	CTCF	chr21:47343240-47343390	HBMEC	blood vessel:	n/a	chr21:47343282-47343290
28	CTCF	chr21:47343180-47343330	GM12871	blood:	n/a	chr21:47343282-47343290
29	CTCF	chr21:47343240-47343390	GM12872	blood:	n/a	chr21:47343282-47343290
30	CTCF	chr21:47343240-47343390	GM12869	blood:	n/a	chr21:47343282-47343290
31	CTCF	chr21:47343104-47343460	K562	blood:	n/a	chr21:47343282-47343290
32	CTCF	chr21:47343119-47343456	HepG2	liver:	n/a	chr21:47343282-47343290
33	CTCF	chr21:47343200-47343350	AG04450	lung:	n/a	chr21:47343282-47343290
34	CTCF	chr21:47343124-47343404	A549	lung:	n/a	chr21:47343282-47343290
35	CTCF	chr21:47343260-47343410	NHLF	lung:	n/a	chr21:47343282-47343290
36	CTCF	chr21:47343220-47343370	Hela-S3	cervix:	n/a	chr21:47343282-47343290
37	CTCF	chr21:47343113-47343463	K562	blood:	n/a	chr21:47343282-47343290
38	CTCF	chr21:47343140-47343290	GM12875	blood:	n/a	chr21:47343282-47343290
39	CTCF	chr21:47343240-47343390	HVMF	connective:	n/a	chr21:47343282-47343290
40	CTCF	chr21:47343129-47343496	MCF-7	breast:	n/a	chr21:47343282-47343290
41	CTCF	chr21:47341960-47342110	K562	blood:	n/a	n/a
42	CTCF	chr21:47343220-47343370	HMF	breast:	n/a	chr21:47343282-47343290
43	CTCF	chr21:47343129-47343362	SK-N-SH_RA	brain:	n/a	chr21:47343282-47343290
44	CTCF	chr21:47343184-47343416	K562	blood:	n/a	chr21:47343282-47343290
45	CTCF	chr21:47343260-47343410	HepG2	liver:	n/a	chr21:47343282-47343290
46	CTCF	chr21:47343260-47343410	GM12874	blood:	n/a	chr21:47343282-47343290
47	CTCF	chr21:47342800-47342950	HepG2	liver:	n/a	n/a
48	CTCF	chr21:47343215-47343350	GM20000	blood:	n/a	chr21:47343282-47343290
49	CTCF	chr21:47343200-47343350	SK-N-SH_RA	brain:	n/a	chr21:47343282-47343290
50	CTCF	chr21:47339080-47339230	HEK293	kidney:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47342677-47342727	RPTEC	kidney:	n/a
2	chr21:47317093-47317143	RPTEC	kidney:	n/a
3	chr21:47340130-47340180	HAEpiC	amniotic membrane:	n/a
4	chr21:47333731-47333781	SK-N-MC	brain:	n/a
5	chr21:47337825-47337875	AG04449	skin:	fetal
6	chr21:47340130-47340180	HCT-116	colon:	n/a
7	chr21:47334174-47334224	CMK	blood:	n/a
8	chr21:47322452-47322502	LNCaP	prostate:	n/a
9	chr21:47318899-47318949	HAEpiC	amniotic membrane:	n/a
10	chr21:47319304-47319354	Caco-2	colon:	n/a
11	chr21:47334448-47334498	GM12878	blood:	n/a
12	chr21:47340130-47340180	MCF-7	breast:	n/a
13	chr21:47340130-47340180	SK-N-SH	brain:	n/a
14	chr21:47334448-47334498	HRE	kidney:	n/a
15	chr21:47318899-47318949	CMK	blood:	n/a
16	chr21:47317093-47317143	NHBE	bronchial:	n/a
17	chr21:47319304-47319354	SK-N-MC	brain:	n/a
18	chr21:47322452-47322502	HNPCEpiC	eye:	n/a
19	chr21:47319304-47319354	HCPEpiC	choroid plexus:	n/a
20	chr21:47342677-47342727	PANC-1	pancreas:	n/a
21	chr21:47334174-47334224	NT2-D1	testis:	n/a
22	chr21:47340130-47340180	GM12892	blood:	n/a
23	chr21:47337825-47337875	U87	brain:	n/a
24	chr21:47318899-47318949	BJ	skin:	n/a
25	chr21:47335691-47335741	Hepatocyte	liver:	n/a
26	chr21:47319304-47319354	NT2-D1	testis:	n/a
27	chr21:47322452-47322502	HRE	kidney:	n/a
28	chr21:47334174-47334224	PANC-1	pancreas:	n/a
29	chr21:47330914-47330964	HIPEpiC	eye:	n/a
30	chr21:47319304-47319354	RPTEC	kidney:	n/a
31	chr21:47333731-47333781	ovcar-3	ovarian:	n/a
32	chr21:47334057-47334107	GM12891	blood:	n/a
33	chr21:47318899-47318949	SKMC	muscle:	n/a
34	chr21:47335691-47335741	PFSK-1	brain:	n/a
35	chr21:47334174-47334224	HL-60	blood:	n/a
36	chr21:47335691-47335741	HRE	kidney:	n/a
37	chr21:47334448-47334498	SK-N-SH	brain:	n/a
38	chr21:47333731-47333781	NHDF-neo	bronchial:	n/a
39	chr21:47322452-47322502	PrEC	prostate:	n/a
40	chr21:47335691-47335741	ECC-1	luminal epithelium:	n/a
41	chr21:47317093-47317143	NT2-D1	testis:	n/a
42	chr21:47333731-47333781	Jurkat	blood:	n/a
43	chr21:47333731-47333781	Caco-2	colon:	n/a
44	chr21:47342677-47342727	HEEpiC	esophagus:	n/a
45	chr21:47322452-47322502	HCT-116	colon:	n/a
46	chr21:47334174-47334224	HNPCEpiC	eye:	n/a
47	chr21:47334448-47334498	AG09309	skin:	n/a
48	chr21:47318899-47318949	AoSMC	blood vessel:	n/a
49	chr21:47319304-47319354	A549	lung:	n/a
50	chr21:47334448-47334498	NT2-D1	testis:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:47253579..47256281-chr21:47326370..47329354,2	K562	blood:
2	chr21:47267412..47269020-chr21:47335213..47337566,2	MCF-7	breast:
3	chr21:47329095..47331174-chr21:47334966..47337510,2	MCF-7	breast:
4	chr21:47326278..47326802-chr21:47335871..47336440,2	MCF-7	breast:
5	chr21:47338168..47340965-chr21:47341072..47342617,2	K562	blood:
6	chr21:46960597..46962517-chr21:47334850..47337245,2	MCF-7	breast:
7	chr21:47300090..47300627-chr21:47342032..47342538,2	MCF-7	breast:
8	chr21:47308842..47311490-chr21:47321844..47323697,2	MCF-7	breast:
9	chr21:47267694..47268408-chr21:47342147..47343416,5	MCF-7	breast:
10	chr21:47319454..47322116-chr21:47334445..47336417,2	MCF-7	breast:
11	chr21:47328644..47331016-chr21:47340908..47343121,3	MCF-7	breast:
12	chr21:47329285..47331470-chr21:47342066..47344987,2	MCF-7	breast:
13	chr21:47240324..47241096-chr21:47342788..47343697,3	MCF-7	breast:
14	chr21:47311846..47315136-chr21:47319001..47321928,3	K562	blood:
15	chr21:46976073..46976581-chr21:47342782..47343760,2	MCF-7	breast:
16	chr21:47312057..47314177-chr21:47322993..47325323,2	MCF-7	breast:
17	chr21:47336465..47338261-chr21:47339874..47342406,2	K562	blood:
18	chr21:47288031..47288840-chr21:47325915..47326785,5	MCF-7	breast:
19	chr21:47325287..47328224-chr21:47334114..47336660,2	MCF-7	breast:
20	chr21:47324736..47327193-chr21:47327348..47329802,3	K562	blood:
21	chr21:47267610..47268453-chr21:47342093..47343648,5	MCF-7	breast:
22	chr21:47338875..47340965-chr21:47341117..47343595,2	K562	blood:
23	chr21:47322615..47325568-chr21:47331282..47333525,2	K562	blood:
24	chr21:47326297..47326825-chr21:47620902..47621507,2	MCF-7	breast:
25	chr21:46960880..46963479-chr21:47338437..47340205,2	MCF-7	breast:
26	chr21:47336465..47338261-chr21:47339874..47342406,2	K562	blood:
27	chr21:47290679..47292853-chr21:47334808..47337713,2	MCF-7	breast:
28	chr21:47287743..47288527-chr21:47334754..47335348,2	MCF-7	breast:
29	chr21:47335161..47336863-chr21:47355343..47357271,2	MCF-7	breast:
30	chr21:47325937..47326745-chr21:47335899..47336761,2	MCF-7	breast:
31	chr21:47311846..47315136-chr21:47319001..47321928,3	K562	blood:
32	chr21:47242790..47243479-chr21:47342941..47343666,2	MCF-7	breast:
33	chr21:47322615..47325568-chr21:47331282..47333525,2	K562	blood:
34	chr21:47342692..47343850-chr21:47390349..47391235,3	MCF-7	breast:
35	chr21:46805769..46807395-chr21:47337287..47339395,2	MCF-7	breast:
36	chr21:47325937..47326745-chr21:47335899..47336761,2	MCF-7	breast:
37	chr21:47300119..47302715-chr21:47341992..47344397,3	MCF-7	breast:
38	chr21:47318888..47321827-chr21:47328391..47331106,3	MCF-7	breast:
39	chr21:47286639..47289783-chr21:47334819..47337166,3	MCF-7	breast:
40	chr21:47286434..47288542-chr21:47340592..47343360,3	MCF-7	breast:
41	chr21:47299971..47300594-chr21:47342907..47343695,3	MCF-7	breast:
42	chr21:47326278..47326802-chr21:47335871..47336440,2	MCF-7	breast:
43	chr21:47325287..47328224-chr21:47334114..47336660,2	MCF-7	breast:
44	chr21:47329285..47331470-chr21:47342066..47344987,2	MCF-7	breast:
45	chr21:47338875..47340965-chr21:47341117..47343595,2	K562	blood:
46	chr21:47188474..47189148-chr21:47343010..47343629,2	MCF-7	breast:
47	chr21:47329095..47331174-chr21:47334966..47337510,2	MCF-7	breast:
48	chr21:47324736..47327193-chr21:47327348..47329802,3	K562	blood:
49	chr21:47172572..47175558-chr21:47335784..47338015,2	MCF-7	breast:
50	chr21:47290546..47292380-chr21:47322273..47324632,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FTCD-6	chr21:47318001-47318626	NONHSAT082999
2	lnc-FTCD-6	chr21:47318759-47318789	NONHSAT082999

No data

Variant related genes	Relation type
PCBP3	TF binding region
PCBP3	CpG island
ENSG00000183570	chromatin interactions
ENSG00000173638	chromatin interactions

Extended variants
information (count: 1593 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567210157	chr21:47314900-47314901	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs534642376	chr21:47314918-47314919	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs191939109	chr21:47314932-47314933	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs368862142	chr21:47314936-47314937	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs144355569	chr21:47314946-47314947	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs116270017	chr21:47314953-47314954	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs183992243	chr21:47314954-47314955	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs530170557	chr21:47314955-47314956	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs570036224	chr21:47314991-47314992	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs537457950	chr21:47314992-47314993	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs555832331	chr21:47315024-47315025	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs8130202	chr21:47315045-47315046	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs189118820	chr21:47315080-47315081	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs553492622	chr21:47315085-47315086	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs181667132	chr21:47315111-47315112	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs57179897	chr21:47315186-47315187	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs545060648	chr21:47315187-47315188	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs73907906	chr21:47315205-47315206	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187298069	chr21:47315219-47315220	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs56303116	chr21:47315229-47315230	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374496689	chr21:47315237-47315238	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528379923	chr21:47315246-47315247	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546585525	chr21:47315265-47315266	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571372366	chr21:47315272-47315273	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532226400	chr21:47315318-47315319	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551861687	chr21:47315329-47315330	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190738795	chr21:47315333-47315334	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537570440	chr21:47315340-47315341	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547061034	chr21:47315362-47315363	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182024816	chr21:47315377-47315378	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141396368	chr21:47315414-47315415	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs550311455	chr21:47315415-47315416	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs9979000	chr21:47315422-47315423	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs553414250	chr21:47315435-47315436	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs114387718	chr21:47315439-47315440	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs7277666	chr21:47315454-47315455	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs367784851	chr21:47315505-47315506	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs532510980	chr21:47315521-47315522	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs35207744	chr21:47315542-47315543	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs114939234	chr21:47315545-47315546	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs7278917	chr21:47315552-47315553	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs182535427	chr21:47315569-47315570	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs552705817	chr21:47315626-47315627	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs143452972	chr21:47315662-47315663	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs540491567	chr21:47315670-47315671	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs565045441	chr21:47315704-47315705	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs9975891	chr21:47315709-47315710	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs570036204	chr21:47315711-47315712	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs550772826	chr21:47315765-47315766	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs569119009	chr21:47315817-47315818	Weak transcription Genic enhancers Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:36)

Disease	PMID	Source
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	17899364	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	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 adenocarcinoma	17086460	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

Chromatin state (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47308000-47343000	Weak transcription	Right Atrium	heart
2	chr21:47311000-47315400	Bivalent Enhancer	Fetal Stomach	stomach
3	chr21:47311400-47316200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr21:47311400-47316200	Enhancers	Fetal Thymus	thymus
5	chr21:47311600-47315200	Enhancers	Thymus	Thymus
6	chr21:47312600-47315200	Enhancers	HSMMtube	muscle
7	chr21:47313200-47315000	Enhancers	Placenta	Placenta
8	chr21:47313200-47315200	Enhancers	HSMM	muscle
9	chr21:47313200-47315800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr21:47313200-47335600	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr21:47313400-47321000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr21:47313600-47315000	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr21:47313600-47315000	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr21:47313600-47315000	Enhancers	NHDF-Ad	bronchial
15	chr21:47313600-47315200	Enhancers	Adipose Nuclei	Adipose
16	chr21:47313600-47316200	Enhancers	Fetal Muscle Leg	muscle
17	chr21:47313800-47315000	Enhancers	Osteobl	bone
18	chr21:47313800-47315200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr21:47313800-47315200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr21:47313800-47321600	Weak transcription	Primary T cells from cord blood	blood
21	chr21:47314000-47315000	Enhancers	NH-A	brain
22	chr21:47314200-47315600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr21:47314400-47315400	Weak transcription	Colonic Mucosa	Colon
24	chr21:47314400-47330200	Weak transcription	Brain Hippocampus Middle	brain
25	chr21:47314600-47315400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr21:47314600-47315600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr21:47314600-47315800	Weak transcription	Spleen	Spleen
28	chr21:47314600-47324600	Weak transcription	Rectal Smooth Muscle	rectum
29	chr21:47314600-47327400	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr21:47314600-47330200	Weak transcription	Brain Cingulate Gyrus	brain
31	chr21:47314800-47315200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr21:47314800-47315200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr21:47314800-47315200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr21:47314800-47315400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr21:47314800-47315400	Enhancers	Stomach Smooth Muscle	stomach
36	chr21:47314800-47317200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr21:47315000-47330200	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr21:47315200-47315400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr21:47315200-47315600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr21:47315200-47315600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr21:47315200-47316200	Genic enhancers	Thymus	Thymus
42	chr21:47315200-47323400	Weak transcription	HSMMtube	muscle
43	chr21:47315200-47330200	Weak transcription	Adipose Nuclei	Adipose
44	chr21:47315400-47315600	Enhancers	Colonic Mucosa	Colon
45	chr21:47315400-47316200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr21:47315400-47317400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr21:47315600-47315800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr21:47315600-47316600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr21:47315800-47317400	Strong transcription	Spleen	Spleen
50	chr21:47315800-47319600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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