Variant report

Variant	nsv1063385
Chromosome Location	chr21:16521617-16926212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3632)
CpG islands
(count:0)
Chromatin interactive
region (count:419)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3632 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:16813157-16814175	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:16773271-16773461	HepG2	liver:	n/a	n/a
3	ARID3A	chr21:16915871-16916071	HepG2	liver:	n/a	n/a
4	ARID3A	chr21:16582490-16582932	HepG2	liver:	n/a	n/a
5	ARID3A	chr21:16583235-16584758	HepG2	liver:	n/a	n/a
6	ARID3A	chr21:16886505-16887296	HepG2	liver:	n/a	n/a
7	ARID3A	chr21:16545316-16545864	HepG2	liver:	n/a	n/a
8	ARID3A	chr21:16568071-16568620	HepG2	liver:	n/a	n/a
9	ARID3A	chr21:16855594-16855756	K562	blood:	n/a	n/a
10	ARID3A	chr21:16593912-16594775	HepG2	liver:	n/a	n/a
11	ARID3A	chr21:16696981-16697181	HepG2	liver:	n/a	n/a
12	ARID3A	chr21:16815869-16817310	HepG2	liver:	n/a	n/a
13	ARID3A	chr21:16828186-16828544	HepG2	liver:	n/a	n/a
14	ARID3A	chr21:16522130-16522466	HepG2	liver:	n/a	n/a
15	ARID3A	chr21:16724367-16724605	HepG2	liver:	n/a	n/a
16	ARID3A	chr21:16855480-16855834	HepG2	liver:	n/a	n/a
17	ATF1	chr21:16673434-16673664	K562	blood:	n/a	n/a
18	ATF1	chr21:16577187-16577529	K562	blood:	n/a	n/a
19	ATF1	chr21:16521733-16521933	K562	blood:	n/a	n/a
20	ATF1	chr21:16625066-16625256	K562	blood:	n/a	n/a
21	ATF1	chr21:16621743-16622076	K562	blood:	n/a	n/a
22	ATF1	chr21:16665609-16665905	K562	blood:	n/a	n/a
23	ATF2	chr21:16554987-16555417	GM12878	blood:	n/a	n/a
24	ATF2	chr21:16594941-16595475	GM12878	blood:	n/a	n/a
25	ATF2	chr21:16886391-16887018	GM12878	blood:	n/a	n/a
26	ATF2	chr21:16578766-16579268	GM12878	blood:	n/a	n/a
27	ATF2	chr21:16780207-16780920	GM12878	blood:	n/a	n/a
28	ATF2	chr21:16817669-16818132	GM12878	blood:	n/a	n/a
29	ATF2	chr21:16780324-16780815	GM12878	blood:	n/a	n/a
30	ATF2	chr21:16810105-16810674	GM12878	blood:	n/a	n/a
31	ATF2	chr21:16531755-16532311	GM12878	blood:	n/a	n/a
32	ATF2	chr21:16810141-16810588	GM12878	blood:	n/a	n/a
33	ATF2	chr21:16817663-16818064	GM12878	blood:	n/a	n/a
34	ATF3	chr21:16816478-16817197	A549	lung:	n/a	n/a
35	ATF3	chr21:16531777-16531984	K562	blood:	n/a	n/a
36	ATF3	chr21:16536959-16537232	K562	blood:	n/a	n/a
37	ATF3	chr21:16816433-16817397	A549	lung:	n/a	n/a
38	ATF3	chr21:16582503-16582887	A549	lung:	n/a	n/a
39	ATF3	chr21:16665526-16665868	K562	blood:	n/a	n/a
40	BACH1	chr21:16715453-16715835	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr21:16673489-16673728	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr21:16738347-16738675	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr21:16582862-16582975	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr21:16715497-16715827	K562	blood:	n/a	n/a
45	BACH1	chr21:16673408-16673786	K562	blood:	n/a	n/a
46	BACH1	chr21:16884177-16884294	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr21:16816503-16816735	K562	blood:	n/a	n/a
48	BACH1	chr21:16816422-16817200	H1-hESC	embryonic stem cell:	n/a	n/a
49	BATF	chr21:16578873-16579186	GM12878	blood:	n/a	n/a
50	BATF	chr21:16794351-16794655	GM12878	blood:	n/a	chr21:16794491-16794502

No data

(count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Distal block	Cell Line	Cell type
1	chr21:16235915..16238127-chr21:16662847..16665093,2	MCF-7	breast:
2	chr21:16235506..16236268-chr21:16582287..16582963,3	MCF-7	breast:
3	chr21:16559200..16562028-chr21:16613543..16615271,2	MCF-7	breast:
4	chr21:16779582..16781375-chr21:16786289..16788853,2	K562	blood:
5	chr21:16796146..16798117-chr21:16798542..16800941,2	MCF-7	breast:
6	chr21:16796146..16798117-chr21:16798542..16800941,2	MCF-7	breast:
7	chr21:16545087..16546235-chr21:16571540..16572822,5	MCF-7	breast:
8	chr21:16743337..16743867-chr21:16816332..16817195,2	MCF-7	breast:
9	chr21:16827722..16830026-chr21:16832130..16834284,2	K562	blood:
10	chr21:16544983..16547085-chr21:16581063..16583747,4	MCF-7	breast:
11	chr21:16235506..16236232-chr21:16582287..16582804,2	MCF-7	breast:
12	chr21:16528404..16530433-chr21:16531935..16534391,2	K562	blood:
13	chr21:16543825..16546494-chr21:16577749..16579512,2	MCF-7	breast:
14	chr21:16637346..16640353-chr21:16642715..16647121,4	MCF-7	breast:
15	chr14:99603512..99604012-chr21:16582594..16583180,2	MCF-7	breast:
16	chr21:16864702..16867275-chr21:16868651..16870885,2	MCF-7	breast:
17	chr21:16545350..16545973-chr21:16571500..16572040,2	MCF-7	breast:
18	chr21:16714501..16715255-chr21:16742984..16743509,2	MCF-7	breast:
19	chr21:16582142..16583084-chr21:16919391..16920395,4	MCF-7	breast:
20	chr21:16671940..16673950-chr21:16682197..16684550,2	K562	blood:
21	chr21:16545040..16546076-chr21:16582206..16583228,5	MCF-7	breast:
22	chr21:16235013..16237732-chr21:16570965..16574658,5	MCF-7	breast:
23	chr21:16624090..16626111-chr21:16855588..16857234,2	MCF-7	breast:
24	chr21:16918481..16920234-chr21:16923318..16925112,2	MCF-7	breast:
25	chr21:16545090..16545903-chr21:16564214..16564994,2	MCF-7	breast:
26	chr21:16864646..16867573-chr21:16872741..16874702,2	K562	blood:
27	chr21:16773347..16773877-chr21:16816611..16817237,2	MCF-7	breast:
28	chr21:16880501..16882055-chr21:16883399..16885226,2	MCF-7	breast:
29	chr21:16375351..16376357-chr21:16571993..16572634,4	MCF-7	breast:
30	chr21:16545028..16546143-chr21:16581995..16583350,24	MCF-7	breast:
31	chr21:16516359..16518250-chr21:16523848..16526042,2	K562	blood:
32	chr21:16545028..16546143-chr21:16581995..16583350,24	MCF-7	breast:
33	chr21:16864227..16867131-chr21:16888537..16890334,2	MCF-7	breast:
34	chr21:16441312..16443585-chr21:16535126..16536830,2	MCF-7	breast:
35	chr21:16580777..16584780-chr21:16852967..16856651,5	MCF-7	breast:
36	chr21:16534393..16538479-chr21:16576836..16579884,4	MCF-7	breast:
37	chr21:16662853..16665318-chr21:16789620..16791689,2	MCF-7	breast:
38	chr21:16578858..16581806-chr21:16778065..16780066,2	MCF-7	breast:
39	chr21:16899768..16901686-chr21:16905215..16907866,2	K562	blood:
40	chr21:16235351..16235999-chr21:16582483..16583245,2	MCF-7	breast:
41	chr21:16545419..16546006-chr21:16714667..16715382,3	MCF-7	breast:
42	chr21:16714493..16715731-chr21:16816300..16817254,11	MCF-7	breast:
43	chr21:16435793..16439229-chr21:16922155..16925068,5	MCF-7	breast:
44	chr21:16575825..16576340-chr21:16714614..16715418,2	MCF-7	breast:
45	chr21:16434791..16438927-chr21:16592548..16596753,6	MCF-7	breast:
46	chr21:16899768..16901686-chr21:16905215..16907866,2	K562	blood:
47	chr21:16433429..16438088-chr21:16628669..16632555,5	MCF-7	breast:
48	chr21:16912535..16914166-chr21:16914818..16917552,2	MCF-7	breast:
49	chr21:16568438..16570001-chr21:16571756..16574334,2	MCF-7	breast:
50	chr21:16472331..16474791-chr21:16561734..16563675,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRIP1-5	chr21:16582725-16583011	NONHSAT081196
2	lnc-USP25-6	chr21:16806721-16807118	NONHSAT081201
3	lnc-USP25-6	chr21:16807725-16807828	NONHSAT081201
4	lnc-USP25-6	chr21:16808362-16809546	NONHSAT081201
5	lnc-NRIP1-6	chr21:16862849-16863086	NONHSAT081202
6	lnc-NRIP1-3	chr21:16868035-16868443	XLOC_014007
7	lnc-NRIP1-5	chr21:16588147-16588197	NONHSAT081196
8	lnc-USP25-4	chr21:16925631-16925679	NONHSAT081205
9	lnc-USP25-5	chr21:16883544-16883870	l_2173_chr21:16882815-16883978_brain
10	lnc-USP25-5	chr21:16882816-16883306	l_2173_chr21:16882815-16883978_brain
11	lnc-USP25-4	chr21:16925017-16925162	NONHSAT081204
12	lnc-NRIP1-3	chr21:16866251-16867217	XLOC_014007
13	lnc-USP25-5	chr21:16883875-16883978	l_2173_chr21:16882815-16883978_brain

No data

Variant related genes	Relation type
CYCSP42	TF binding region
ENSG00000224247	TF binding region
ENSG00000229425	TF binding region
ENSG00000235609	chromatin interactions
ENSG00000236471	chromatin interactions
ENSG00000180530	chromatin interactions
ENSG00000136813	chromatin interactions

Extended variants
information (count: 16137 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:16137 , 50 per page) page: 1 2 3 4 5 6 7 ... 323

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9979508	chr21:16521617-16521618	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140927197	chr21:16521650-16521651	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs202043016	chr21:16521679-16521680	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs397961593	chr21:16521685-16521686	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs543985867	chr21:16521721-16521722	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs539269241	chr21:16521766-16521767	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs557234993	chr21:16521770-16521771	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs577617257	chr21:16521772-16521773	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs150278346	chr21:16521792-16521793	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs193081598	chr21:16521814-16521815	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs528080515	chr21:16521851-16521852	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs573831455	chr21:16521920-16521921	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs138939147	chr21:16521970-16521971	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs185626593	chr21:16522008-16522009	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs550753465	chr21:16522034-16522035	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs570523851	chr21:16522053-16522054	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs2823096	chr21:16522082-16522083	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs542984690	chr21:16522087-16522088	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs546471819	chr21:16522105-16522106	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs565764415	chr21:16522181-16522182	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs534693626	chr21:16522190-16522191	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs113064857	chr21:16522195-16522196	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568549559	chr21:16522212-16522213	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537105239	chr21:16522213-16522214	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs557554149	chr21:16522217-16522218	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs373454868	chr21:16522219-16522220	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs199787197	chr21:16522231-16522232	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs192334501	chr21:16522256-16522257	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs375983821	chr21:16522264-16522265	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs183637372	chr21:16522279-16522280	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs2014048	chr21:16522346-16522347	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs188254841	chr21:16522377-16522378	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs181430042	chr21:16522393-16522394	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs149420076	chr21:16522411-16522412	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs530649176	chr21:16522418-16522419	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs543935427	chr21:16522423-16522424	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs73891998	chr21:16522431-16522432	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs73892000	chr21:16522432-16522433	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs2403881	chr21:16522512-16522513	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs181697871	chr21:16522528-16522529	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs529110371	chr21:16522544-16522545	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs540115573	chr21:16522571-16522572	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs146365845	chr21:16522609-16522610	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs568336152	chr21:16522638-16522639	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs187189664	chr21:16522643-16522644	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs550781415	chr21:16522680-16522681	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs553687855	chr21:16522685-16522686	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs540038422	chr21:16522698-16522699	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs553746050	chr21:16522710-16522711	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs373752813	chr21:16522714-16522715	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
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 myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	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
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
Epilepsy	20502679	CNVD
22q11.2 microdeletion syndrome	19750312	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Type 2 diabetes	21526130	CNVD
early-passage human iPS cells	21368824	CNVD
Acute myeloid leukemia	20962326	CNVD

Chromatin state (count:2549 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16514600-16529600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr21:16516800-16521800	Weak transcription	Liver	Liver
3	chr21:16517200-16526800	Weak transcription	Pancreas	Pancrea
4	chr21:16520800-16522000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr21:16521400-16522000	Enhancers	Fetal Intestine Small	intestine
6	chr21:16521400-16522200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr21:16521400-16522200	Enhancers	Fetal Intestine Large	intestine
8	chr21:16521400-16529600	Weak transcription	Adipose Nuclei	Adipose
9	chr21:16521600-16522000	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr21:16521600-16525600	Enhancers	HepG2	liver
11	chr21:16521800-16524800	Enhancers	Liver	Liver
12	chr21:16523600-16524800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr21:16524600-16525400	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr21:16525000-16525400	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr21:16525600-16527800	Weak transcription	HepG2	liver
16	chr21:16526800-16528200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr21:16526800-16528200	Enhancers	Pancreas	Pancrea
18	chr21:16527000-16528200	Enhancers	Left Ventricle	heart
19	chr21:16527400-16528600	Enhancers	Fetal Intestine Small	intestine
20	chr21:16527400-16528800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr21:16527400-16528800	Enhancers	Fetal Intestine Large	intestine
22	chr21:16527800-16528000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr21:16527800-16528200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr21:16527800-16528200	Enhancers	Fetal Heart	heart
25	chr21:16527800-16528200	Enhancers	Gastric	stomach
26	chr21:16527800-16528200	Enhancers	HepG2	liver
27	chr21:16527800-16528200	Enhancers	K562	blood
28	chr21:16528000-16536600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr21:16528200-16529600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr21:16528200-16530400	Weak transcription	Pancreas	Pancrea
31	chr21:16528200-16536800	Weak transcription	Fetal Heart	heart
32	chr21:16528800-16531600	Weak transcription	Fetal Intestine Large	intestine
33	chr21:16529600-16530000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr21:16529600-16530400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
35	chr21:16529600-16531000	Enhancers	Adipose Nuclei	Adipose
36	chr21:16530000-16535400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr21:16530200-16531000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr21:16530400-16530600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
39	chr21:16530400-16531000	Enhancers	Pancreas	Pancrea
40	chr21:16531000-16533400	Weak transcription	Pancreas	Pancrea
41	chr21:16531200-16531400	Weak transcription	Primary hematopoietic stem cells	blood
42	chr21:16531200-16533400	Enhancers	Primary B cells from peripheral blood	blood
43	chr21:16531400-16531600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr21:16531400-16531600	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr21:16531400-16532200	Enhancers	Primary hematopoietic stem cells	blood
46	chr21:16531400-16532200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr21:16531400-16533400	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr21:16531400-16533600	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr21:16531400-16533600	Enhancers	Primary B cells from cord blood	blood
50	chr21:16531600-16532000	Enhancers	Fetal Intestine Large	intestine

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