Variant report

Variant	nsv1064280
Chromosome Location	chr21:16664312-17049272
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2864)
CpG islands
(count:0)
Chromatin interactive
region (count:231)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2864 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:16964668-16964944	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:17000298-17000319	HepG2	liver:	n/a	n/a
3	ARID3A	chr21:16773271-16773461	HepG2	liver:	n/a	n/a
4	ARID3A	chr21:16915871-16916071	HepG2	liver:	n/a	n/a
5	ARID3A	chr21:16828186-16828544	HepG2	liver:	n/a	n/a
6	ARID3A	chr21:16964646-16964900	K562	blood:	n/a	n/a
7	ARID3A	chr21:16724367-16724605	HepG2	liver:	n/a	n/a
8	ARID3A	chr21:16696981-16697181	HepG2	liver:	n/a	n/a
9	ARID3A	chr21:16855594-16855756	K562	blood:	n/a	n/a
10	ARID3A	chr21:16813157-16814175	HepG2	liver:	n/a	n/a
11	ARID3A	chr21:16855480-16855834	HepG2	liver:	n/a	n/a
12	ARID3A	chr21:16886505-16887296	HepG2	liver:	n/a	n/a
13	ARID3A	chr21:16815869-16817310	HepG2	liver:	n/a	n/a
14	ARID3A	chr21:17032123-17032416	HepG2	liver:	n/a	n/a
15	ATF1	chr21:16673434-16673664	K562	blood:	n/a	n/a
16	ATF1	chr21:16665609-16665905	K562	blood:	n/a	n/a
17	ATF1	chr21:16930343-16930672	K562	blood:	n/a	n/a
18	ATF2	chr21:16780324-16780815	GM12878	blood:	n/a	n/a
19	ATF2	chr21:16780207-16780920	GM12878	blood:	n/a	n/a
20	ATF2	chr21:16886391-16887018	GM12878	blood:	n/a	n/a
21	ATF2	chr21:16810141-16810588	GM12878	blood:	n/a	n/a
22	ATF2	chr21:16817669-16818132	GM12878	blood:	n/a	n/a
23	ATF2	chr21:16817663-16818064	GM12878	blood:	n/a	n/a
24	ATF2	chr21:16810105-16810674	GM12878	blood:	n/a	n/a
25	ATF3	chr21:16816433-16817397	A549	lung:	n/a	n/a
26	ATF3	chr21:16816478-16817197	A549	lung:	n/a	n/a
27	ATF3	chr21:16665526-16665868	K562	blood:	n/a	n/a
28	BACH1	chr21:16738347-16738675	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr21:16816503-16816735	K562	blood:	n/a	n/a
30	BACH1	chr21:16715497-16715827	K562	blood:	n/a	n/a
31	BACH1	chr21:17001048-17001064	K562	blood:	n/a	n/a
32	BACH1	chr21:16884177-16884294	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr21:16673489-16673728	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr21:16715453-16715835	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr21:16816422-16817200	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr21:16673408-16673786	K562	blood:	n/a	n/a
37	BATF	chr21:16817678-16818010	GM12878	blood:	n/a	n/a
38	BATF	chr21:16794351-16794655	GM12878	blood:	n/a	chr21:16794491-16794502
39	BATF	chr21:16795072-16795322	GM12878	blood:	n/a	chr21:16795178-16795189 chr21:16795179-16795189 chr21:16795175-16795185
40	BATF	chr21:16810181-16810596	GM12878	blood:	n/a	chr21:16810356-16810367
41	BATF	chr21:16810169-16810645	GM12878	blood:	n/a	chr21:16810356-16810367
42	BATF	chr21:16817720-16817973	GM12878	blood:	n/a	n/a
43	BCL11A	chr21:16810144-16810663	GM12878	blood:	n/a	n/a
44	BCL11A	chr21:16817666-16817886	H1-hESC	embryonic stem cell:	n/a	n/a
45	BCL11A	chr21:16810249-16810537	GM12878	blood:	n/a	n/a
46	BCL11A	chr21:16780425-16780834	GM12878	blood:	n/a	n/a
47	BCL3	chr21:16733140-16733559	GM12878	blood:	n/a	n/a
48	BCL3	chr21:16816387-16817436	A549	lung:	n/a	n/a
49	BCL3	chr21:16858816-16859137	GM12878	blood:	n/a	n/a
50	BCL3	chr21:16997709-16997978	GM12878	blood:	n/a	n/a

No data

(count:231 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr21:16579850..16580693-chr21:16958976..16959754,3	MCF-7	breast:
2	chr21:16570442..16572661-chr21:16665803..16668621,2	MCF-7	breast:
3	chr21:16805980..16807840-chr21:16809511..16812685,3	K562	blood:
4	chr21:16989283..16990838-chr21:17003947..17006454,2	MCF-7	breast:
5	chr21:16732191..16734558-chr21:16742882..16744836,2	MCF-7	breast:
6	chr21:16663539..16666081-chr21:16712410..16715629,4	MCF-7	breast:
7	chr21:16436807..16439448-chr21:16663226..16666430,5	MCF-7	breast:
8	chr21:16779582..16781375-chr21:16786289..16788853,2	K562	blood:
9	chr21:16713454..16716441-chr21:16762500..16764229,2	MCF-7	breast:
10	chr21:16437453..16439202-chr21:16715691..16717267,2	MCF-7	breast:
11	chr21:16772297..16774137-chr21:16777440..16779221,2	K562	blood:
12	chr21:16435820..16438656-chr21:16711726..16715018,5	MCF-7	breast:
13	chr21:16804369..16806411-chr21:16810758..16812985,2	MCF-7	breast:
14	chr21:16925515..16927155-chr21:16928055..16930658,2	MCF-7	breast:
15	chr21:16959176..16959732-chr21:17011225..17011757,2	MCF-7	breast:
16	chr21:16582273..16583330-chr21:16919552..16920500,4	MCF-7	breast:
17	chr21:16668614..16670305-chr21:16854249..16855799,2	MCF-7	breast:
18	chr21:16704646..16706338-chr21:16708707..16710210,2	K562	blood:
19	chr21:16827722..16830026-chr21:16832130..16834284,2	K562	blood:
20	chr21:16236518..16237478-chr21:16855231..16856151,4	MCF-7	breast:
21	chr21:16925515..16927155-chr21:16928055..16930658,2	MCF-7	breast:
22	chr21:16663401..16665237-chr21:16852171..16854477,2	MCF-7	breast:
23	chr21:16584349..16587030-chr21:16664217..16666665,2	MCF-7	breast:
24	chr21:16713454..16716441-chr21:16762500..16764229,2	MCF-7	breast:
25	chr21:16662884..16665504-chr21:16853719..16855454,2	MCF-7	breast:
26	chr21:16581111..16587442-chr21:16661859..16666667,10	MCF-7	breast:
27	chr21:16435921..16437860-chr21:16878059..16879589,2	MCF-7	breast:
28	chr21:15755923..15757812-chr21:16863949..16865497,2	K562	blood:
29	chr21:17015627..17017680-chr21:17022587..17025053,2	K562	blood:
30	chr21:16743337..16743867-chr21:16816332..16817195,2	MCF-7	breast:
31	chr21:16919441..16920015-chr21:16959232..16959755,2	MCF-7	breast:
32	chr21:16436105..16438114-chr21:16663913..16667261,4	MCF-7	breast:
33	chr21:16827722..16830026-chr21:16832130..16834284,2	K562	blood:
34	chr21:16907370..16908917-chr21:16935643..16937758,2	K562	blood:
35	chr21:16375413..16376190-chr21:16714500..16715307,2	MCF-7	breast:
36	chr21:16714779..16715688-chr21:16816321..16817212,3	MCF-7	breast:
37	chr21:16235383..16236247-chr21:16959008..16959755,5	MCF-7	breast:
38	chr21:16668935..16671016-chr21:16674652..16676612,2	MCF-7	breast:
39	chr21:16742888..16745845-chr21:16814324..16816904,2	MCF-7	breast:
40	chr21:16582142..16583084-chr21:16919391..16920395,4	MCF-7	breast:
41	chr21:16714657..16715579-chr21:16959040..16959762,3	MCF-7	breast:
42	chr21:16899768..16901686-chr21:16905215..16907866,2	K562	blood:
43	chr21:16795224..16797113-chr21:16843935..16846229,2	MCF-7	breast:
44	chr21:16435856..16438455-chr21:16677252..16679908,2	MCF-7	breast:
45	chr21:16796146..16798117-chr21:16798542..16800941,2	MCF-7	breast:
46	chr21:17044032..17047282-chr21:17048018..17052321,5	K562	blood:
47	chr21:16919633..16920412-chr21:16959232..16959914,4	MCF-7	breast:
48	chr21:16582092..16583222-chr21:16714611..16715771,13	MCF-7	breast:
49	chr21:16772297..16774137-chr21:16777440..16779221,2	K562	blood:
50	chr21:16940802..16942430-chr21:16945970..16948560,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRIP1-6	chr21:16862849-16863086	NONHSAT081202
2	lnc-NRIP1-7	chr21:16943559-16943675	NONHSAT081206
3	lnc-NRIP1-7	chr21:16999365-16999459	NONHSAT081206
4	lnc-USP25-4	chr21:16934420-16934823	NONHSAT081204
5	lnc-USP25-5	chr21:16882816-16883306	l_2173_chr21:16882815-16883978_brain
6	lnc-USP25-6	chr21:16807725-16807828	NONHSAT081201
7	lnc-USP25-6	chr21:16806721-16807118	NONHSAT081201
8	lnc-NRIP1-7	chr21:16947589-16947729	NONHSAT081206
9	lnc-NRIP1-3	chr21:16866251-16867217	XLOC_014007
10	lnc-NRIP1-3	chr21:16868035-16868443	XLOC_014007
11	lnc-USP25-4	chr21:16925017-16925162	NONHSAT081204
12	lnc-USP25-4	chr21:16934420-16934873	NONHSAT081205
13	lnc-USP25-5	chr21:16883875-16883978	l_2173_chr21:16882815-16883978_brain
14	lnc-USP25-5	chr21:16883544-16883870	l_2173_chr21:16882815-16883978_brain
15	lnc-USP25-4	chr21:16925631-16925679	NONHSAT081205
16	lnc-NRIP1-9	chr21:17048709-17048960	NONHSAT081208
17	lnc-USP25-6	chr21:16808362-16809546	NONHSAT081201

No data

Variant related genes	Relation type
RNU6-1326P	TF binding region
CYCSP42	TF binding region
ENSG00000224247	TF binding region
ENSG00000229425	TF binding region
ENSG00000155313	chromatin interactions
ENSG00000180530	chromatin interactions
ENSG00000236471	chromatin interactions
ENSG00000085733	chromatin interactions
ENSG00000212564	chromatin interactions

Extended variants
information (count: 14621 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:14621 , 50 per page) page: 1 2 3 4 5 6 7 ... 293

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183571576	chr21:16664370-16664371	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs566227257	chr21:16664371-16664372	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs528998090	chr21:16664372-16664373	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs528797729	chr21:16664405-16664406	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs576737165	chr21:16664414-16664415	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs543596093	chr21:16664417-16664418	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs34479553	chr21:16664433-16664434	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs548466614	chr21:16664477-16664478	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs545791902	chr21:16664481-16664482	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs186872745	chr21:16664520-16664521	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs145313782	chr21:16664524-16664525	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373783595	chr21:16664540-16664541	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs556633400	chr21:16664556-16664557	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs570239867	chr21:16664612-16664613	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs556786595	chr21:16664626-16664627	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs116871389	chr21:16664647-16664648	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs148859880	chr21:16664680-16664681	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs143487594	chr21:16664751-16664752	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs2823209	chr21:16664777-16664778	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs555229385	chr21:16664859-16664860	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs370459009	chr21:16664866-16664867	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs575389282	chr21:16664908-16664909	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs192108464	chr21:16664913-16664914	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs183901083	chr21:16664929-16664930	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs532690887	chr21:16664944-16664945	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs548797032	chr21:16664945-16664946	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs79186154	chr21:16664952-16664953	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs528733409	chr21:16665002-16665003	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs528431905	chr21:16665008-16665009	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs548873442	chr21:16665011-16665012	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs568705186	chr21:16665032-16665033	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs530986750	chr21:16665050-16665051	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs550796166	chr21:16665051-16665052	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs140714367	chr21:16665072-16665073	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs541885596	chr21:16665077-16665078	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs539166631	chr21:16665163-16665164	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs548383088	chr21:16665174-16665175	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs566470866	chr21:16665176-16665177	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs113452197	chr21:16665194-16665195	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs535148056	chr21:16665199-16665200	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs186816335	chr21:16665204-16665205	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575479106	chr21:16665218-16665219	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs1474513	chr21:16665335-16665336	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs145716251	chr21:16665364-16665365	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs577384507	chr21:16665441-16665442	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs546323450	chr21:16665469-16665470	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs377547235	chr21:16665470-16665471	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs559448091	chr21:16665516-16665517	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs573185310	chr21:16665530-16665531	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs189745743	chr21:16665552-16665553	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Schizophrenia	23813976	CNVD
Type 2 diabetes	21526130	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Acute myeloid leukemia	20962326	CNVD
Autism	20841430	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1860 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16659000-16665000	Weak transcription	HSMMtube	muscle
2	chr21:16662000-16670200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr21:16662400-16665800	Enhancers	Placenta	Placenta
4	chr21:16662400-16666000	Enhancers	Fetal Intestine Large	intestine
5	chr21:16662600-16666000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr21:16662600-16666400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr21:16662800-16664400	Weak transcription	Esophagus	oesophagus
8	chr21:16662800-16666200	Enhancers	Stomach Mucosa	stomach
9	chr21:16663000-16666200	Enhancers	HMEC	breast
10	chr21:16663200-16665400	Weak transcription	Fetal Stomach	stomach
11	chr21:16663200-16665600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr21:16663200-16665800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr21:16663200-16665800	Enhancers	Fetal Intestine Small	intestine
14	chr21:16663200-16666200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr21:16663200-16674400	Weak transcription	Psoas Muscle	Psoas
16	chr21:16663400-16664800	Weak transcription	Fetal Kidney	kidney
17	chr21:16663400-16665000	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr21:16663400-16665200	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr21:16663400-16665400	Weak transcription	K562	blood
20	chr21:16663400-16666000	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr21:16663400-16676400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr21:16663600-16665000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr21:16663600-16665400	Enhancers	NHEK	skin
24	chr21:16663600-16666400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr21:16663600-16666400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr21:16663800-16664600	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr21:16663800-16664600	Enhancers	Pancreas	Pancrea
28	chr21:16663800-16664800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr21:16663800-16665000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr21:16663800-16665400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr21:16664000-16664600	Enhancers	Colonic Mucosa	Colon
32	chr21:16664000-16664600	Enhancers	Placenta Amnion	Placenta Amnion
33	chr21:16664000-16664600	Enhancers	Rectal Smooth Muscle	rectum
34	chr21:16664000-16665000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr21:16664000-16665400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr21:16664000-16665400	Enhancers	A549	lung
37	chr21:16664000-16665800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr21:16664000-16666000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr21:16664000-16666000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr21:16664200-16664600	Flanking Active TSS	HepG2	liver
41	chr21:16664400-16664600	Enhancers	Esophagus	oesophagus
42	chr21:16664400-16666200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr21:16664600-16665600	Weak transcription	Pancreas	Pancrea
44	chr21:16664600-16665600	Weak transcription	Rectal Smooth Muscle	rectum
45	chr21:16664600-16666000	Enhancers	HepG2	liver
46	chr21:16664800-16666000	Enhancers	Fetal Kidney	kidney
47	chr21:16664800-16673200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr21:16665000-16665800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr21:16665000-16665800	Enhancers	NHLF	lung
50	chr21:16665000-16666000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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