Variant report

Variant	esv3404140
Chromosome Location	chr21:47710824-47716522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:382)
CpG islands
(count:183)
Chromatin interactive
region (count:32)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:47714608-47714952	K562	blood:	n/a	n/a
2	ATF3	chr21:47714506-47714904	K562	blood:	n/a	n/a
3	ATF3	chr21:47716368-47716630	K562	blood:	n/a	n/a
4	BACH1	chr21:47714742-47714860	K562	blood:	n/a	n/a
5	BCL11A	chr21:47714374-47714531	GM12878	blood:	n/a	n/a
6	BCL11A	chr21:47712814-47713287	GM12878	blood:	n/a	n/a
7	BCL11A	chr21:47713919-47714085	GM12878	blood:	n/a	n/a
8	BCL11A	chr21:47712661-47713197	GM12878	blood:	n/a	n/a
9	BHLHE40	chr21:47713517-47713716	K562	blood:	n/a	n/a
10	BHLHE40	chr21:47716361-47716558	K562	blood:	n/a	chr21:47716441-47716457
11	BHLHE40	chr21:47714433-47715080	K562	blood:	n/a	n/a
12	CBX3	chr21:47714434-47715127	K562	blood:	n/a	n/a
13	CBX3	chr21:47716236-47716710	K562	blood:	n/a	n/a
14	CCNT2	chr21:47714529-47715500	K562	blood:	n/a	chr21:47715448-47715457
15	CEBPB	chr21:47714603-47715083	K562	blood:	n/a	n/a
16	CEBPB	chr21:47714867-47715148	K562	blood:	n/a	n/a
17	CEBPB	chr21:47714616-47714623	K562	blood:	n/a	n/a
18	CEBPD	chr21:47713465-47713932	K562	blood:	n/a	n/a
19	CEBPD	chr21:47714043-47714812	K562	blood:	n/a	n/a
20	CEBPD	chr21:47712489-47713029	K562	blood:	n/a	n/a
21	CEBPD	chr21:47715260-47715539	HepG2	liver:	n/a	n/a
22	CHD2	chr21:47715460-47715487	HepG2	liver:	n/a	n/a
23	CHD2	chr21:47714738-47714931	K562	blood:	n/a	n/a
24	CTCF	chr21:47713560-47713710	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr21:47714800-47714950	GM12875	blood:	n/a	n/a
26	CTCF	chr21:47714840-47714990	AG04450	lung:	n/a	n/a
27	CTCF	chr21:47714840-47714990	AG10803	skin:	n/a	n/a
28	CTCF	chr21:47714862-47714961	GM12878	blood:	n/a	n/a
29	CTCF	chr21:47714737-47715112	K562	blood:	n/a	n/a
30	CTCF	chr21:47714851-47714917	K562	blood:	n/a	n/a
31	CTCF	chr21:47714740-47714890	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr21:47714800-47714950	AG04449	skin:	n/a	n/a
33	CTCF	chr21:47714860-47715010	BJ	skin:	n/a	n/a
34	CTCFL	chr21:47714702-47714960	K562	blood:	n/a	n/a
35	CUX1	chr21:47714614-47715119	K562	blood:	n/a	n/a
36	E2F6	chr21:47716329-47716592	K562	blood:	n/a	n/a
37	E2F6	chr21:47716401-47716568	K562	blood:	n/a	n/a
38	E2F6	chr21:47714701-47714957	K562	blood:	n/a	n/a
39	E2F6	chr21:47716253-47716609	H1-hESC	embryonic stem cell:	n/a	n/a
40	E2F6	chr21:47716231-47716702	H1-hESC	embryonic stem cell:	n/a	n/a
41	EBF1	chr21:47715168-47715405	GM12878	blood:	n/a	chr21:47715311-47715320 chr21:47715309-47715322
42	EBF1	chr21:47714788-47714975	GM12878	blood:	n/a	n/a
43	EBF1	chr21:47714775-47715470	GM12878	blood:	n/a	chr21:47715311-47715320 chr21:47715309-47715322
44	EGR1	chr21:47715352-47715654	K562	blood:	n/a	chr21:47715538-47715549
45	EGR1	chr21:47714809-47715144	K562	blood:	n/a	chr21:47714947-47714956
46	EGR1	chr21:47715359-47715666	K562	blood:	n/a	chr21:47715538-47715549
47	EGR1	chr21:47714775-47715172	K562	blood:	n/a	chr21:47714947-47714956
48	EGR1	chr21:47716006-47716580	K562	blood:	n/a	chr21:47716545-47716554 chr21:47716233-47716246 chr21:47716234-47716243 chr21:47716234-47716244 chr21:47716232-47716247 chr21:47716234-47716244 chr21:47716439-47716452 chr21:47716233-47716246 chr21:47716234-47716245 chr21:47716232-47716246 chr21:47716233-47716246
49	EGR1	chr21:47715961-47716636	K562	blood:	n/a	chr21:47716545-47716554 chr21:47716233-47716246 chr21:47716234-47716243 chr21:47716234-47716244 chr21:47716232-47716247 chr21:47716234-47716244 chr21:47716439-47716452 chr21:47716233-47716246 chr21:47716234-47716245 chr21:47716232-47716246 chr21:47716233-47716246
50	ELF1	chr21:47716282-47716612	HepG2	liver:	n/a	chr21:47716442-47716454 chr21:47716441-47716450

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47716443-47716493	ovcar-3	ovarian:	n/a
2	chr21:47716443-47716493	GM12878	blood:	n/a
3	chr21:47715006-47715056	U87	brain:	n/a
4	chr21:47715006-47715056	NH-A	brain:	n/a
5	chr21:47711966-47712016	NB4	blood:	n/a
6	chr21:47716443-47716493	SK-N-SH_RA	brain:	n/a
7	chr21:47711966-47712016	U87	brain:	n/a
8	chr21:47711966-47712016	PrEC	prostate:	n/a
9	chr21:47711966-47712016	MCF10A-Er-Src	breast:	n/a
10	chr21:47715006-47715056	GM12878	blood:	n/a
11	chr21:47715006-47715056	BE2_C	brain:	n/a
12	chr21:47715006-47715056	Caco-2	colon:	n/a
13	chr21:47711966-47712016	HPAEpiC	pulmonary alveolar:	n/a
14	chr21:47716443-47716493	AG09309	skin:	n/a
15	chr21:47716443-47716493	SK-N-SH	brain:	n/a
16	chr21:47711966-47712016	HEEpiC	esophagus:	n/a
17	chr21:47715006-47715056	SK-N-SH_RA	brain:	n/a
18	chr21:47715006-47715056	ECC-1	luminal epithelium:	n/a
19	chr21:47716443-47716493	NH-A	brain:	n/a
20	chr21:47716443-47716493	Jurkat	blood:	n/a
21	chr21:47716443-47716493	HepG2	liver:	n/a
22	chr21:47715006-47715056	SAEC	small airway:	n/a
23	chr21:47716443-47716493	AG04450	lung:	fetal
24	chr21:47711966-47712016	CMK	blood:	n/a
25	chr21:47716443-47716493	T-47D	breast:	n/a
26	chr21:47711966-47712016	LNCaP	prostate:	n/a
27	chr21:47715006-47715056	AG10803	skin:	n/a
28	chr21:47711966-47712016	GM12878	blood:	n/a
29	chr21:47716443-47716493	H1-hESC	embryonic stem cell:	embryo
30	chr21:47711966-47712016	Caco-2	colon:	n/a
31	chr21:47716443-47716493	AG10803	skin:	n/a
32	chr21:47715006-47715056	HepG2	liver:	n/a
33	chr21:47716443-47716493	HRE	kidney:	n/a
34	chr21:47716443-47716493	NHDF-neo	bronchial:	n/a
35	chr21:47715006-47715056	HCT-116	colon:	n/a
36	chr21:47715006-47715056	AG04450	lung:	fetal
37	chr21:47711966-47712016	HCM	heart:	n/a
38	chr21:47715006-47715056	HNPCEpiC	eye:	n/a
39	chr21:47716443-47716493	HCPEpiC	choroid plexus:	n/a
40	chr21:47715006-47715056	Hepatocyte	liver:	n/a
41	chr21:47715006-47715056	HMEC	breast:	n/a
42	chr21:47711966-47712016	K562	blood:	n/a
43	chr21:47711966-47712016	HCT-116	colon:	n/a
44	chr21:47716443-47716493	HIPEpiC	eye:	n/a
45	chr21:47711966-47712016	HIPEpiC	eye:	n/a
46	chr21:47716443-47716493	K562	blood:	n/a
47	chr21:47715006-47715056	GM12892	blood:	n/a
48	chr21:47711966-47712016	GM12891	blood:	n/a
49	chr21:47715006-47715056	HCM	heart:	n/a
50	chr21:47716443-47716493	HEEpiC	esophagus:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47715271..47717864-chr21:47741446..47743716,2	MCF-7	breast:
2	chr21:47713129..47716016-chr21:47743936..47746881,5	MCF-7	breast:
3	chr21:47708860..47711564-chr21:47715753..47717339,2	K562	blood:
4	chr21:47704395..47708420-chr21:47713514..47717582,8	K562	blood:
5	chr21:47709790..47713110-chr21:47741267..47744584,4	MCF-7	breast:
6	chr21:47713822..47715879-chr21:47788612..47790511,2	K562	blood:
7	chr21:47714784..47717174-chr21:47723560..47726052,2	MCF-7	breast:
8	chr21:47646455..47648066-chr21:47714633..47716764,2	MCF-7	breast:
9	chr21:47702524..47712328-chr21:47732975..47746274,46	K562	blood:
10	chr21:47708860..47711564-chr21:47715753..47717339,2	K562	blood:
11	chr21:47713705..47716420-chr21:47738596..47740217,2	MCF-7	breast:
12	chr21:47713494..47715322-chr21:47788049..47790112,2	K562	blood:
13	chr21:47703549..47712907-chr21:47732716..47739888,14	MCF-7	breast:
14	chr21:47715232..47717039-chr21:47718960..47720713,2	MCF-7	breast:
15	chr21:47714423..47717463-chr21:47743785..47745906,3	MCF-7	breast:
16	chr21:47700722..47725192-chr21:47732201..47746452,77	K562	blood:
17	chr21:47705635..47707803-chr21:47716511..47719183,2	K562	blood:
18	chr21:47706415..47708286-chr21:47708333..47712836,4	K562	blood:
19	chr21:47716063..47717906-chr21:47723260..47724786,2	K562	blood:
20	chr21:47705068..47711362-chr21:47735611..47740059,7	MCF-7	breast:
21	chr21:47716057..47717569-chr21:47742713..47744741,2	MCF-7	breast:
22	chr21:47708141..47711504-chr21:47716399..47719423,3	K562	blood:
23	chr21:47695579..47697188-chr21:47713900..47716404,2	MCF-7	breast:
24	chr11:61128057..61129672-chr21:47713579..47716107,2	MCF-7	breast:
25	chr10:90639851..90640519-chr21:47714618..47715484,2	NB4	blood:
26	chr21:47713574..47717141-chr21:47740930..47745749,7	K562	blood:
27	chr21:47705283..47707993-chr21:47713694..47717938,5	MCF-7	breast:
28	chr21:47712217..47713877-chr21:47743379..47745476,2	MCF-7	breast:
29	chr21:47714401..47714998-chr21:47744184..47744759,2	MCF-7	breast:
30	chr21:47715739..47718156-chr21:47738100..47740706,2	K562	blood:
31	chr21:47708141..47711504-chr21:47716399..47719423,3	K562	blood:
32	chr21:47705312..47710550-chr21:47711386..47716259,4	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCNT-2	chr21:47712679-47713546	NONHSAT083055
2	lnc-PCNT-2	chr21:47714455-47714711	NONHSAT083057
3	lnc-PCNT-2	chr21:47712922-47714711	NONHSAT083056
4	lnc-PCNT-2	chr21:47712922-47713491	NONHSAT083057

No data

Variant related genes	Relation type
MCM3AP	TF binding region
MCM3AP	CpG island
ENSG00000162144	chromatin interactions
ENSG00000160294	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000138134	chromatin interactions
ENSG00000149483	chromatin interactions
ENSG00000182362	chromatin interactions

Extended variants
information (count: 401 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:401 , 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	rs13050740	chr21:47710828-47710829	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs61067282	chr21:47710839-47710840	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs13051590	chr21:47710842-47710843	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs13052101	chr21:47710884-47710885	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs13050850	chr21:47710891-47710892	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs188184549	chr21:47710917-47710918	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs9978468	chr21:47710928-47710929	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs528025616	chr21:47710932-47710933	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs35202939	chr21:47710933-47710934	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
10	rs551073656	chr21:47710945-47710946	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs35552596	chr21:47710949-47710950	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs185532811	chr21:47710978-47710979	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs13052226	chr21:47711026-47711027	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs376870450	chr21:47711036-47711037	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs556012219	chr21:47711043-47711044	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs534461680	chr21:47711055-47711056	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs368510695	chr21:47711066-47711067	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs553891902	chr21:47711067-47711068	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs144572662	chr21:47711068-47711069	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs552834518	chr21:47711092-47711093	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs539485146	chr21:47711095-47711096	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs557848211	chr21:47711107-47711108	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs386394893	chr21:47711112-47711113	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs576359341	chr21:47711126-47711127	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs371481603	chr21:47711130-47711131	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs111640590	chr21:47711138-47711139	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs113732411	chr21:47711140-47711141	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs150862012	chr21:47711179-47711180	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs374018800	chr21:47711202-47711203	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs367922546	chr21:47711223-47711224	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs2276257	chr21:47711229-47711230	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs373666382	chr21:47711231-47711232	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs541640705	chr21:47711241-47711242	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs145267170	chr21:47711256-47711257	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs533037690	chr21:47711332-47711333	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs79395473	chr21:47711344-47711345	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs140433074	chr21:47711368-47711369	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs368758593	chr21:47711382-47711383	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs200576225	chr21:47711383-47711384	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs553720951	chr21:47711386-47711387	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs115622469	chr21:47711409-47711410	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs139297921	chr21:47711411-47711412	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs567218067	chr21:47711413-47711414	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs576724657	chr21:47711460-47711461	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs368108388	chr21:47711469-47711470	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs534545278	chr21:47711477-47711478	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs150042906	chr21:47711525-47711526	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs368616121	chr21:47711552-47711553	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs79887423	chr21:47711573-47711574	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs372702834	chr21:47711611-47711612	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	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:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47707000-47711200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr21:47707000-47711400	Weak transcription	Esophagus	oesophagus
3	chr21:47707000-47711400	Weak transcription	Left Ventricle	heart
4	chr21:47707000-47711400	Weak transcription	Ovary	ovary
5	chr21:47707000-47711400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr21:47707000-47715200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr21:47707000-47717400	Weak transcription	Small Intestine	intestine
8	chr21:47707200-47711000	Weak transcription	Primary T cells from cord blood	blood
9	chr21:47707200-47711200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr21:47707200-47711200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr21:47707200-47711200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr21:47707200-47711200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr21:47707200-47711200	Weak transcription	Fetal Thymus	thymus
14	chr21:47707200-47711200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr21:47707200-47711200	Weak transcription	K562	blood
16	chr21:47707200-47711400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr21:47707200-47711400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr21:47707200-47711400	Weak transcription	Aorta	Aorta
19	chr21:47707200-47711400	Weak transcription	Brain Angular Gyrus	brain
20	chr21:47707200-47711400	Weak transcription	Brain Substantia Nigra	brain
21	chr21:47707200-47711400	Weak transcription	Thymus	Thymus
22	chr21:47707200-47714800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr21:47707200-47715000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr21:47707200-47715800	Weak transcription	Right Atrium	heart
25	chr21:47707200-47717400	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr21:47707400-47711000	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr21:47707400-47711200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr21:47707400-47711200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr21:47707400-47711200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr21:47707400-47711200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr21:47707400-47711200	Weak transcription	Adipose Nuclei	Adipose
32	chr21:47707400-47711200	Weak transcription	Liver	Liver
33	chr21:47707400-47711200	Weak transcription	Fetal Intestine Large	intestine
34	chr21:47707400-47711200	Weak transcription	A549	lung
35	chr21:47707400-47711200	Weak transcription	HSMM	muscle
36	chr21:47707400-47711400	Weak transcription	Brain Anterior Caudate	brain
37	chr21:47707400-47711400	Weak transcription	Brain Cingulate Gyrus	brain
38	chr21:47707400-47711400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr21:47707400-47711400	Weak transcription	Rectal Smooth Muscle	rectum
40	chr21:47707400-47711400	Weak transcription	HUVEC	blood vessel
41	chr21:47707400-47711400	Weak transcription	NHDF-Ad	bronchial
42	chr21:47707400-47711600	Weak transcription	Fetal Lung	lung
43	chr21:47707400-47711800	Weak transcription	Placenta	Placenta
44	chr21:47707400-47714600	Weak transcription	Stomach Mucosa	stomach
45	chr21:47707400-47715800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr21:47707400-47717200	Weak transcription	Psoas Muscle	Psoas
47	chr21:47707600-47711200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr21:47707600-47711200	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr21:47707600-47711200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr21:47707600-47711200	Weak transcription	Muscle Satellite Cultured Cells	--

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