Variant report

Variant	nsv587701
Chromosome Location	chr21:45128190-45181446
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3252)
CpG islands
(count:2323)
Chromatin interactive
region (count:149)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3252 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:45148603-45148839	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:45148259-45148806	K562	blood:	n/a	n/a
3	ARID3A	chr21:45139049-45139374	HepG2	liver:	n/a	n/a
4	ATF1	chr21:45138761-45139394	K562	blood:	n/a	n/a
5	ATF1	chr21:45148262-45148872	K562	blood:	n/a	n/a
6	ATF1	chr21:45158438-45158813	K562	blood:	n/a	n/a
7	ATF2	chr21:45148518-45148902	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr21:45148245-45148490	GM12878	blood:	n/a	n/a
9	ATF2	chr21:45138605-45139005	GM12878	blood:	n/a	n/a
10	ATF2	chr21:45136426-45137111	GM12878	blood:	n/a	n/a
11	ATF2	chr21:45136479-45137042	GM12878	blood:	n/a	n/a
12	ATF2	chr21:45139110-45139649	GM12878	blood:	n/a	chr21:45139288-45139295
13	ATF2	chr21:45148223-45148920	GM12878	blood:	n/a	n/a
14	ATF2	chr21:45148457-45148916	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr21:45148520-45148802	GM12878	blood:	n/a	n/a
16	ATF3	chr21:45160710-45160988	A549	lung:	n/a	chr21:45160849-45160862
17	ATF3	chr21:45148027-45148828	K562	blood:	n/a	chr21:45148190-45148199
18	ATF3	chr21:45138711-45139487	K562	blood:	n/a	chr21:45138915-45138924
19	ATF3	chr21:45132027-45132855	A549	lung:	n/a	n/a
20	ATF3	chr21:45148175-45148679	A549	lung:	n/a	chr21:45148190-45148199
21	ATF3	chr21:45131986-45132677	A549	lung:	n/a	n/a
22	ATF3	chr21:45148013-45148760	K562	blood:	n/a	chr21:45148190-45148199
23	BACH1	chr21:45148326-45148831	K562	blood:	n/a	n/a
24	BACH1	chr21:45138412-45140005	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr21:45161393-45161618	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr21:45138660-45138850	K562	blood:	n/a	n/a
27	BACH1	chr21:45140213-45140388	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr21:45160396-45161112	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr21:45149047-45149169	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr21:45148278-45148817	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr21:45136466-45136752	GM12878	blood:	n/a	n/a
32	BATF	chr21:45144425-45144740	GM12878	blood:	n/a	n/a
33	BATF	chr21:45148256-45148467	GM12878	blood:	n/a	chr21:45148407-45148417
34	BATF	chr21:45136430-45137005	GM12878	blood:	n/a	n/a
35	BATF	chr21:45148259-45148908	GM12878	blood:	n/a	chr21:45148407-45148417
36	BATF	chr21:45144456-45144652	GM12878	blood:	n/a	n/a
37	BCL11A	chr21:45174931-45175334	GM12878	blood:	n/a	n/a
38	BCL11A	chr21:45136467-45137067	GM12878	blood:	n/a	n/a
39	BCL11A	chr21:45148279-45148902	GM12878	blood:	n/a	chr21:45148448-45148461
40	BCL11A	chr21:45136451-45137114	GM12878	blood:	n/a	n/a
41	BCL3	chr21:45148120-45148907	K562	blood:	n/a	chr21:45148448-45148461
42	BCL3	chr21:45132012-45132821	A549	lung:	n/a	n/a
43	BCL3	chr21:45148149-45148722	A549	lung:	n/a	chr21:45148448-45148461
44	BCL3	chr21:45174902-45175520	GM12878	blood:	n/a	n/a
45	BCL3	chr21:45174890-45175278	GM12878	blood:	n/a	n/a
46	BCL3	chr21:45164262-45164666	GM12878	blood:	n/a	n/a
47	BCL3	chr21:45159769-45160260	A549	lung:	n/a	chr21:45159789-45159802
48	BCL3	chr21:45164297-45164791	GM12878	blood:	n/a	n/a
49	BCL3	chr21:45131919-45132858	A549	lung:	n/a	n/a
50	BCL3	chr21:45148135-45148842	A549	lung:	n/a	chr21:45148448-45148461

(count:2323 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45140831-45140881	HL-60	blood:	n/a
2	chr21:45177538-45177588	HNPCEpiC	eye:	n/a
3	chr21:45139805-45139855	NT2-D1	testis:	n/a
4	chr21:45148332-45148382	HNPCEpiC	eye:	n/a
5	chr21:45153009-45153059	NB4	blood:	n/a
6	chr21:45140831-45140881	HL-60	blood:	n/a
7	chr21:45177538-45177588	HNPCEpiC	eye:	n/a
8	chr21:45139805-45139855	NT2-D1	testis:	n/a
9	chr21:45148332-45148382	HNPCEpiC	eye:	n/a
10	chr21:45153009-45153059	NB4	blood:	n/a
11	chr21:45149038-45149088	SK-N-SH_RA	brain:	n/a
12	chr21:45144343-45144393	Jurkat	blood:	n/a
13	chr21:45178331-45178381	ECC-1	luminal epithelium:	n/a
14	chr21:45148460-45148510	ECC-1	luminal epithelium:	n/a
15	chr21:45139379-45139429	HCPEpiC	choroid plexus:	n/a
16	chr21:45135999-45136049	AG09309	skin:	n/a
17	chr21:45176447-45176497	AG04449	skin:	fetal
18	chr21:45178331-45178381	SK-N-SH_RA	brain:	n/a
19	chr21:45149038-45149088	IMR90	lung:	fetal
20	chr21:45148460-45148510	SK-N-SH_RA	brain:	n/a
21	chr21:45138838-45138888	HMEC	breast:	n/a
22	chr21:45148864-45148914	CMK	blood:	n/a
23	chr21:45145759-45145809	PFSK-1	brain:	n/a
24	chr21:45177639-45177689	PANC-1	pancreas:	n/a
25	chr21:45139805-45139855	HCPEpiC	choroid plexus:	n/a
26	chr21:45178331-45178381	PrEC	prostate:	n/a
27	chr21:45161415-45161465	PrEC	prostate:	n/a
28	chr21:45138847-45138897	GM19239	blood:	n/a
29	chr21:45138838-45138888	GM19239	blood:	n/a
30	chr21:45138847-45138897	Caco-2	colon:	n/a
31	chr21:45139805-45139855	Hepatocyte	liver:	n/a
32	chr21:45179871-45179921	GM12878	blood:	n/a
33	chr21:45163611-45163661	SK-N-SH_RA	brain:	n/a
34	chr21:45139379-45139429	PANC-1	pancreas:	n/a
35	chr21:45137544-45137594	ProgFib	skin:	n/a
36	chr21:45139805-45139855	HNPCEpiC	eye:	n/a
37	chr21:45148460-45148510	NB4	blood:	n/a
38	chr21:45149038-45149088	MCF-7	breast:	n/a
39	chr21:45138294-45138344	SAEC	small airway:	n/a
40	chr21:45139805-45139855	HRPEpiC	eye:	n/a
41	chr21:45139805-45139855	HUVEC	blood vessel:	n/a
42	chr21:45148694-45148744	NH-A	brain:	n/a
43	chr21:45177538-45177588	NT2-D1	testis:	n/a
44	chr21:45139229-45139279	SAEC	small airway:	n/a
45	chr21:45177726-45177776	Hela-S3	cervix:	n/a
46	chr21:45138843-45138893	ProgFib	skin:	n/a
47	chr21:45140831-45140881	HCPEpiC	choroid plexus:	n/a
48	chr21:45149373-45149423	HRCEpiC	kidney:	n/a
49	chr21:45153009-45153059	MCF-7	breast:	n/a
50	chr21:45149398-45149448	GM12878	blood:	n/a

(count:149 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr21:45177511..45180498-chr21:45193933..45196367,2	MCF-7	breast:
2	chr21:45159250..45162021-chr21:45208113..45211544,3	MCF-7	breast:
3	chr21:33103919..33104588-chr21:45170107..45170783,2	Hela-S3	cervix:
4	chr21:45146427..45148749-chr21:45209148..45210811,2	K562	blood:
5	chr21:45164290..45167394-chr21:45171722..45175273,3	K562	blood:
6	chr21:45165363..45167088-chr21:45194223..45196266,2	MCF-7	breast:
7	chr21:45136006..45137816-chr21:45211885..45214018,2	MCF-7	breast:
8	chr21:45154001..45156611-chr21:45177637..45180387,2	K562	blood:
9	chr21:45147186..45147688-chr21:45160772..45161319,2	MCF-7	breast:
10	chr21:45165894..45167884-chr21:45171722..45174273,2	K562	blood:
11	chr21:45172031..45174493-chr21:45180363..45182490,3	K562	blood:
12	chr21:45180929..45184497-chr21:45193980..45197167,4	MCF-7	breast:
13	chr21:44527539..44529052-chr21:45138865..45141097,2	K562	blood:
14	chr21:45113016..45114535-chr21:45136348..45138090,2	MCF-7	breast:
15	chr21:45148918..45151033-chr21:45195012..45197870,3	MCF-7	breast:
16	chr21:45126696..45129955-chr21:45130404..45132264,4	MCF-7	breast:
17	chr21:45158524..45162841-chr21:45165683..45171048,8	K562	blood:
18	chr21:45176543..45179179-chr21:45179807..45182752,3	K562	blood:
19	chr21:45127579..45129189-chr21:45147237..45149838,2	K562	blood:
20	chr21:45152139..45155102-chr21:45167592..45169327,2	K562	blood:
21	chr21:44935152..44938727-chr21:45130277..45133903,3	MCF-7	breast:
22	chr21:45176316..45177949-chr21:46492855..46495309,2	K562	blood:
23	chr11:62432398..62433340-chr21:45138648..45139625,2	MCF-7	breast:
24	chr21:45146930..45150669-chr21:45163613..45169103,5	K562	blood:
25	chr21:45130889..45133239-chr21:45139686..45141208,2	K562	blood:
26	chr21:45176543..45179179-chr21:45179807..45182752,3	K562	blood:
27	chr21:44394729..44396277-chr21:45138959..45140606,2	MCF-7	breast:
28	chr21:45145345..45148604-chr21:45164623..45167520,3	MCF-7	breast:
29	chr21:45154933..45157513-chr21:45174243..45177077,2	MCF-7	breast:
30	chr21:45130889..45133239-chr21:45139686..45141208,2	K562	blood:
31	chr21:45138878..45139799-chr21:45148124..45149007,3	K562	blood:
32	chr21:45161547..45167086-chr21:45167365..45170424,6	MCF-7	breast:
33	chr21:45176491..45178777-chr21:45179789..45182236,2	K562	blood:
34	chr21:45156182..45158069-chr21:45230385..45232004,2	K562	blood:
35	chr21:45170139..45171974-chr21:45180747..45184494,3	K562	blood:
36	chr21:45164290..45167394-chr21:45171722..45175273,3	K562	blood:
37	chr21:44297829..44300678-chr21:45147311..45150231,2	K562	blood:
38	chr21:45154001..45156611-chr21:45177637..45180387,2	K562	blood:
39	chr21:45126696..45129955-chr21:45130404..45132264,4	MCF-7	breast:
40	chr21:45122068..45123972-chr21:45132668..45134422,2	K562	blood:
41	chr21:45078177..45082024-chr21:45131002..45134092,5	MCF-7	breast:
42	chr21:45073951..45077594-chr21:45129226..45132110,3	MCF-7	breast:
43	chr21:45120451..45123154-chr21:45126649..45128378,2	MCF-7	breast:
44	chr21:45172846..45174492-chr21:45176032..45177914,2	MCF-7	breast:
45	chr21:45131275..45134749-chr21:45135159..45139580,7	K562	blood:
46	chr21:45137445..45140588-chr21:45195005..45197401,3	K562	blood:
47	chr21:45141572..45144183-chr21:45194386..45198670,4	K562	blood:
48	chr21:45167914..45170036-chr21:45175029..45177838,2	K562	blood:
49	chr21:45154618..45156575-chr21:45170589..45173066,2	K562	blood:
50	chr21:45166127..45168190-chr21:45198985..45201869,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RRP1-2	chr21:45175358-45175645	NONHSAT082444
2	lnc-RRP1B-1	chr21:45152020-45152146	ENSG00000241238.1
3	lnc-RRP1-2	chr21:45173464-45173600	NONHSAT082444
4	lnc-RRP1-2	chr21:45175832-45176043	NONHSAT082444
5	lnc-RRP1B-1	chr21:45141573-45141787	ENSG00000241238.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PDXK	hsa-miR-193b-3p	chr21:45157285-45157305
2	PDXK	hsa-miR-24-3p	chr21:45181006-45181013

Variant related genes	Relation type
PDXK	TF binding region
PDXK	CpG island
ENSG00000173473	chromatin interactions
ENSG00000160214	chromatin interactions
ENSG00000160208	chromatin interactions
ENSG00000160199	chromatin interactions
ENSG00000197381	chromatin interactions
ENSG00000160218	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000160226	chromatin interactions
ENSG00000268856	chromatin interactions
ENSG00000258890	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000156304	chromatin interactions
ENSG00000160213	chromatin interactions
ENSG00000255432	chromatin interactions
ENSG00000160193	chromatin interactions
ENSG00000160207	chromatin interactions
ENSG00000160209	chromatin interactions
ENSG00000232969	chromatin interactions
ENSG00000162194	chromatin interactions
ENSG00000160194	chromatin interactions
ENSG00000214756	chromatin interactions
ENSG00000206597	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000160201	chromatin interactions
ENSG00000235374	chromatin interactions

Extended variants
information (count: 2658 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2658 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7279400	chr21:45128190-45128191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531282790	chr21:45128246-45128247	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs117748778	chr21:45128264-45128265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs115059979	chr21:45128270-45128271	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370186896	chr21:45128305-45128306	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs553783188	chr21:45128318-45128319	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565957660	chr21:45128319-45128320	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs539693329	chr21:45128331-45128332	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557963663	chr21:45128332-45128333	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs576646091	chr21:45128336-45128337	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs543950701	chr21:45128337-45128338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555804208	chr21:45128340-45128341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs576864019	chr21:45128341-45128342	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs573954196	chr21:45128346-45128347	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs371245886	chr21:45128376-45128377	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs559834861	chr21:45128377-45128378	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs533441284	chr21:45128406-45128407	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs545224131	chr21:45128412-45128413	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs563523517	chr21:45128438-45128439	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs376938944	chr21:45128446-45128447	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs79268608	chr21:45128449-45128450	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs3916995	chr21:45128454-45128455	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
23	rs568098387	chr21:45128458-45128459	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs182528914	chr21:45128504-45128505	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs547369181	chr21:45128528-45128529	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs374726413	chr21:45128540-45128541	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs539730132	chr21:45128548-45128549	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs558051735	chr21:45128563-45128564	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs113704750	chr21:45128612-45128613	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs386819066	chr21:45128618-45128619	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs114273828	chr21:45128619-45128620	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs187184400	chr21:45128630-45128631	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs534756129	chr21:45128632-45128633	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs115361362	chr21:45128633-45128634	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs143334612	chr21:45128637-45128638	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs116052758	chr21:45128657-45128658	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs367646749	chr21:45128677-45128678	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs113287775	chr21:45128738-45128739	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs138978673	chr21:45128766-45128767	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs543162944	chr21:45128767-45128768	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs370275309	chr21:45128768-45128769	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs553082129	chr21:45128769-45128770	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs374603491	chr21:45128781-45128782	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs142244651	chr21:45128782-45128783	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs116388724	chr21:45128796-45128797	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs528963705	chr21:45128810-45128811	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs145917791	chr21:45128811-45128812	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs559407722	chr21:45128812-45128813	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs532929235	chr21:45128823-45128824	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs111799720	chr21:45128827-45128828	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Neuroblastoma	20406844	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
Breast cancer	21364760	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3183 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45111000-45130600	Weak transcription	HSMM	muscle
2	chr21:45115000-45130800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr21:45115800-45131800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr21:45116600-45132200	Weak transcription	NHLF	lung
5	chr21:45123200-45138200	Weak transcription	Ovary	ovary
6	chr21:45123400-45131600	Weak transcription	NHEK	skin
7	chr21:45123600-45130400	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr21:45123600-45131200	Weak transcription	Stomach Mucosa	stomach
9	chr21:45123600-45132200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr21:45123600-45138400	Weak transcription	Right Atrium	heart
11	chr21:45123800-45130800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr21:45123800-45131000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr21:45123800-45131600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr21:45123800-45132000	Weak transcription	HSMMtube	muscle
15	chr21:45126600-45128600	Enhancers	A549	lung
16	chr21:45126800-45128600	Enhancers	HepG2	liver
17	chr21:45126800-45130400	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr21:45126800-45131400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr21:45127200-45128200	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr21:45127800-45128200	Weak transcription	Hela-S3	cervix
21	chr21:45128200-45128400	Enhancers	Primary T cells fromperipheralblood	blood
22	chr21:45128200-45129800	Enhancers	Hela-S3	cervix
23	chr21:45128600-45130400	Weak transcription	A549	lung
24	chr21:45129600-45129800	Enhancers	Fetal Intestine Large	intestine
25	chr21:45129800-45130600	Weak transcription	Hela-S3	cervix
26	chr21:45129800-45131000	Weak transcription	Fetal Intestine Large	intestine
27	chr21:45130200-45131400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr21:45130400-45130600	Enhancers	A549	lung
29	chr21:45130400-45131200	Weak transcription	Fetal Lung	lung
30	chr21:45130400-45131800	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr21:45130400-45131800	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr21:45130600-45130800	Enhancers	Adipose Nuclei	Adipose
33	chr21:45130600-45130800	Enhancers	Duodenum Mucosa	Duodenum
34	chr21:45130600-45130800	Enhancers	Fetal Muscle Leg	muscle
35	chr21:45130600-45130800	Enhancers	Fetal Thymus	thymus
36	chr21:45130600-45130800	Enhancers	HSMM	muscle
37	chr21:45130600-45131200	Enhancers	Colonic Mucosa	Colon
38	chr21:45130600-45131200	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr21:45130600-45131200	Bivalent Enhancer	HepG2	liver
40	chr21:45130600-45131400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr21:45130600-45131400	Flanking Active TSS	A549	lung
42	chr21:45130600-45133000	Flanking Active TSS	Hela-S3	cervix
43	chr21:45130800-45131200	Weak transcription	Duodenum Mucosa	Duodenum
44	chr21:45130800-45131400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr21:45130800-45131600	Weak transcription	Adipose Nuclei	Adipose
46	chr21:45130800-45131600	Weak transcription	HSMM	muscle
47	chr21:45130800-45131800	Enhancers	Fetal Intestine Small	intestine
48	chr21:45130800-45132200	Weak transcription	Fetal Muscle Leg	muscle
49	chr21:45130800-45132200	Weak transcription	Fetal Thymus	thymus
50	chr21:45130800-45132400	Enhancers	Placenta Amnion	Placenta Amnion

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