Variant report

Variant	nsv587996
Chromosome Location	chr21:47846760-47858248
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:89)
CpG islands
(count:977)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:89 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr21:47855134-47855161	K562	blood:	n/a	n/a
2	CHD2	chr21:47854192-47854246	Hela-S3	cervix:	n/a	n/a
3	CTCF	chr21:47855984-47856177	H1-hESC	embryonic stem cell:	n/a	chr21:47856071-47856087
4	CTCF	chr21:47852040-47852190	HL-60	blood:	n/a	chr21:47852134-47852147 chr21:47852137-47852150
5	ELF1	chr21:47858028-47858469	GM12878	blood:	n/a	n/a
6	HMGN3	chr21:47850589-47850651	K562	blood:	n/a	n/a
7	HMGN3	chr21:47856590-47856745	K562	blood:	n/a	n/a
8	HMGN3	chr21:47849026-47849146	K562	blood:	n/a	n/a
9	MAFF	chr21:47855770-47855908	HepG2	liver:	n/a	chr21:47855860-47855878
10	MAFK	chr21:47855747-47855881	HepG2	liver:	n/a	n/a
11	MAFK	chr21:47855748-47855975	HepG2	liver:	n/a	n/a
12	MAFK	chr21:47855821-47855893	IMR90	lung:	n/a	n/a
13	MXI1	chr21:47856869-47856889	Hela-S3	cervix:	n/a	n/a
14	MYC	chr21:47857215-47857288	GM12878	blood:	n/a	n/a
15	MYC	chr21:47857214-47857372	MCF-7	breast:	n/a	n/a
16	POLR2A	chr21:47850575-47850587	MCF-7	breast:	n/a	n/a
17	POLR2A	chr21:47857203-47857582	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr21:47847048-47847097	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr21:47857068-47857121	MCF-7	breast:	n/a	n/a
20	POLR2A	chr21:47854194-47854847	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr21:47846182-47847518	K562	blood:	n/a	n/a
22	POLR2A	chr21:47849840-47849878	K562	blood:	n/a	n/a
23	POLR2A	chr21:47851055-47851078	K562	blood:	n/a	n/a
24	POLR2A	chr21:47851379-47852303	K562	blood:	n/a	n/a
25	POLR2A	chr21:47849421-47849494	HUVEC	blood vessel:	n/a	n/a
26	POLR2A	chr21:47848223-47849089	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr21:47857252-47857316	MCF-7	breast:	n/a	n/a
28	POLR2A	chr21:47851402-47851720	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr21:47848866-47849278	K562	blood:	n/a	n/a
30	POLR2A	chr21:47857775-47857812	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr21:47857262-47857327	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr21:47854645-47854732	MCF-7	breast:	n/a	n/a
33	POLR2A	chr21:47857189-47857430	MCF-7	breast:	n/a	n/a
34	POLR2A	chr21:47856577-47856841	K562	blood:	n/a	n/a
35	POLR2A	chr21:47857159-47857163	MCF-7	breast:	n/a	n/a
36	POLR2A	chr21:47857841-47858474	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr21:47855022-47855032	K562	blood:	n/a	n/a
38	POLR2A	chr21:47854600-47854646	HepG2	liver:	n/a	n/a
39	POLR2A	chr21:47858181-47858240	K562	blood:	n/a	n/a
40	POLR2A	chr21:47857156-47857385	MCF-7	breast:	n/a	n/a
41	POLR2A	chr21:47855798-47856289	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr21:47847118-47847689	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr21:47857166-47857262	ProgFib	skin:	n/a	n/a
44	POLR2A	chr21:47848622-47848705	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr21:47857580-47857763	K562	blood:	n/a	n/a
46	POLR2A	chr21:47857583-47857622	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr21:47855901-47856035	K562	blood:	n/a	n/a
48	POLR2A	chr21:47848064-47848099	GM12878	blood:	n/a	n/a
49	POLR2A	chr21:47848826-47849259	K562	blood:	n/a	n/a
50	POLR2A	chr21:47852430-47852539	Hela-S3	cervix:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47855049-47855099	HL-60	blood:	n/a
2	chr21:47855049-47855099	HL-60	blood:	n/a
3	chr21:47856140-47856190	HCF	heart:	n/a
4	chr21:47851470-47851520	Hepatocyte	liver:	n/a
5	chr21:47851742-47851792	NHBE	bronchial:	n/a
6	chr21:47851621-47851671	SK-N-SH	brain:	n/a
7	chr21:47856140-47856190	PFSK-1	brain:	n/a
8	chr21:47851941-47851991	NHDF-neo	bronchial:	n/a
9	chr21:47847919-47847969	HCM	heart:	n/a
10	chr21:47855893-47855943	HepG2	liver:	n/a
11	chr21:47849050-47849100	HCPEpiC	choroid plexus:	n/a
12	chr21:47855049-47855099	AG09309	skin:	n/a
13	chr21:47851545-47851595	LNCaP	prostate:	n/a
14	chr21:47849050-47849100	AG09309	skin:	n/a
15	chr21:47849174-47849224	ovcar-3	ovarian:	n/a
16	chr21:47847919-47847969	Jurkat	blood:	n/a
17	chr21:47851470-47851520	SAEC	small airway:	n/a
18	chr21:47850317-47850367	GM12891	blood:	n/a
19	chr21:47851742-47851792	HMEC	breast:	n/a
20	chr21:47847919-47847969	RPTEC	kidney:	n/a
21	chr21:47851545-47851595	HRE	kidney:	n/a
22	chr21:47855916-47855966	IMR90	lung:	fetal
23	chr21:47851941-47851991	HAEpiC	amniotic membrane:	n/a
24	chr21:47856215-47856265	LNCaP	prostate:	n/a
25	chr21:47851545-47851595	Caco-2	colon:	n/a
26	chr21:47856140-47856190	ECC-1	luminal epithelium:	n/a
27	chr21:47851470-47851520	AG09309	skin:	n/a
28	chr21:47856215-47856265	Hela-S3	cervix:	n/a
29	chr21:47851621-47851671	A549	lung:	n/a
30	chr21:47855893-47855943	SKMC	muscle:	n/a
31	chr21:47847919-47847969	GM12878	blood:	n/a
32	chr21:47856215-47856265	PANC-1	pancreas:	n/a
33	chr21:47856020-47856070	H1-hESC	embryonic stem cell:	embryo
34	chr21:47851545-47851595	ProgFib	skin:	n/a
35	chr21:47851545-47851595	PFSK-1	brain:	n/a
36	chr21:47848216-47848266	BJ	skin:	n/a
37	chr21:47849050-47849100	HRPEpiC	eye:	n/a
38	chr21:47851545-47851595	HL-60	blood:	n/a
39	chr21:47851941-47851991	HCT-116	colon:	n/a
40	chr21:47848216-47848266	SK-N-MC	brain:	n/a
41	chr21:47856020-47856070	HIPEpiC	eye:	n/a
42	chr21:47851941-47851991	PrEC	prostate:	n/a
43	chr21:47847919-47847969	AG04450	lung:	fetal
44	chr21:47851941-47851991	LNCaP	prostate:	n/a
45	chr21:47847919-47847969	K562	blood:	n/a
46	chr21:47856020-47856070	LNCaP	prostate:	n/a
47	chr21:47856215-47856265	HRPEpiC	eye:	n/a
48	chr21:47855893-47855943	AoSMC	blood vessel:	n/a
49	chr21:47855049-47855099	BE2_C	brain:	n/a
50	chr21:47855049-47855099	U87	brain:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47857607..47860157-chr21:47877897..47880411,2	MCF-7	breast:
2	chr21:47836799..47839696-chr21:47847990..47849925,2	K562	blood:
3	chr21:47842082..47844141-chr21:47845967..47848443,2	K562	blood:
4	chr21:47841259..47843546-chr21:47843811..47847040,4	K562	blood:
5	chr21:47844449..47847171-chr21:47854131..47855917,2	K562	blood:
6	chr21:47848467..47851272-chr21:47852866..47855440,2	K562	blood:
7	chr21:47843264..47847636-chr21:47874814..47878644,6	K562	blood:
8	chr21:47857792..47859466-chr21:47861182..47863133,2	MCF-7	breast:
9	chr21:47847865..47850685-chr21:47852500..47855672,4	K562	blood:
10	chr21:47746558..47749011-chr21:47851647..47853522,2	K562	blood:
11	chr21:47853352..47856633-chr21:47878140..47880096,4	MCF-7	breast:
12	chr21:47857857..47859725-chr21:47876652..47878543,2	MCF-7	breast:
13	chr21:47851003..47853080-chr21:47856086..47858235,2	K562	blood:
14	chr21:47742209..47744590-chr21:47846184..47848146,2	MCF-7	breast:
15	chr21:47649218..47651291-chr21:47846633..47848855,2	K562	blood:
16	chr21:47792720..47794427-chr21:47846612..47849567,2	K562	blood:
17	chr21:47845265..47847081-chr21:47878915..47881102,2	K562	blood:
18	chr21:47851003..47853080-chr21:47856086..47858235,2	K562	blood:
19	chr21:47847865..47850685-chr21:47852500..47855672,4	K562	blood:
20	chr21:47854363..47856833-chr21:47869358..47873122,3	MCF-7	breast:
21	chr21:47854459..47856094-chr21:47859695..47861438,2	K562	blood:
22	chr21:47856507..47858157-chr21:47860635..47863396,2	MCF-7	breast:
23	chr21:47844449..47847171-chr21:47854131..47855917,2	K562	blood:
24	chr21:47843582..47848242-chr21:47854131..47857783,6	K562	blood:
25	chr21:47856273..47858659-chr21:47860032..47862884,2	K562	blood:
26	chr21:47839389..47841162-chr21:47847458..47849832,2	MCF-7	breast:

No data

Variant related genes	Relation type
PCNT	TF binding region
PCNT	CpG island
ENSG00000160299	chromatin interactions
ENSG00000160305	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000225043	chromatin interactions

Extended variants
information (count: 699 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:699 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs915578	chr21:47846760-47846761	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571999618	chr21:47846804-47846805	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs527923986	chr21:47846809-47846810	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs58228841	chr21:47846813-47846814	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs570915218	chr21:47846888-47846889	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs537960491	chr21:47846961-47846962	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs58468580	chr21:47846974-47846975	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs374277831	chr21:47847089-47847090	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs532569862	chr21:47847101-47847102	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs141896742	chr21:47847136-47847137	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs535067614	chr21:47847169-47847170	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs553691976	chr21:47847199-47847200	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs572303862	chr21:47847206-47847207	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs539309923	chr21:47847264-47847265	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs557944474	chr21:47847270-47847271	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs74752283	chr21:47847318-47847319	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs78685576	chr21:47847341-47847342	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs562953200	chr21:47847352-47847353	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs574924656	chr21:47847379-47847380	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs543293043	chr21:47847391-47847392	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs542239908	chr21:47847394-47847395	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs560478483	chr21:47847395-47847396	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs527996429	chr21:47847428-47847429	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs552560061	chr21:47847438-47847439	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs556868553	chr21:47847459-47847460	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs146272442	chr21:47847470-47847471	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs537730055	chr21:47847473-47847474	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs557732449	chr21:47847476-47847477	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs2839254	chr21:47847498-47847499	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs199892286	chr21:47847509-47847510	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs538606043	chr21:47847514-47847515	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs535126420	chr21:47847515-47847516	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs150882711	chr21:47847547-47847548	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs140044774	chr21:47847550-47847551	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs199778396	chr21:47847560-47847561	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs61735816	chr21:47847568-47847569	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs576217371	chr21:47847571-47847572	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs186973307	chr21:47847586-47847587	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs114739559	chr21:47847613-47847614	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs77075366	chr21:47847619-47847620	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs191561981	chr21:47847628-47847629	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs149779006	chr21:47847639-47847640	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs371278609	chr21:47847649-47847650	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs144662431	chr21:47847662-47847663	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs201185279	chr21:47847674-47847675	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs572321857	chr21:47847679-47847680	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs148485670	chr21:47847680-47847681	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs61735817	chr21:47847700-47847701	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs200022982	chr21:47847726-47847727	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs564609095	chr21:47847728-47847729	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 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:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47775600-47857600	Weak transcription	Stomach Mucosa	stomach
2	chr21:47803200-47872400	Weak transcription	Fetal Kidney	kidney
3	chr21:47814400-47861000	Weak transcription	Fetal Brain Male	brain
4	chr21:47818400-47850200	Weak transcription	Small Intestine	intestine
5	chr21:47820400-47851200	Weak transcription	NH-A	brain
6	chr21:47823200-47850200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr21:47827400-47866600	Strong transcription	Fetal Stomach	stomach
8	chr21:47828000-47863200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr21:47828600-47872400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr21:47829400-47862600	Strong transcription	Skeletal Muscle Female	skeletal muscle
11	chr21:47829400-47867800	Strong transcription	Cortex derived primary cultured neurospheres	brain
12	chr21:47829600-47862800	Strong transcription	Skeletal Muscle Male	skeletal muscle
13	chr21:47829600-47864000	Strong transcription	Fetal Intestine Small	intestine
14	chr21:47830200-47862800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr21:47830400-47862800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr21:47831000-47857600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr21:47832800-47847000	Weak transcription	Fetal Lung	lung
18	chr21:47833400-47863400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr21:47834000-47868200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr21:47834200-47868200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr21:47836800-47872400	Weak transcription	Right Atrium	heart
22	chr21:47837200-47847000	Weak transcription	NHDF-Ad	bronchial
23	chr21:47837800-47854800	Weak transcription	K562	blood
24	chr21:47838000-47853600	Strong transcription	Lung	lung
25	chr21:47838400-47849800	Weak transcription	Osteobl	bone
26	chr21:47838400-47852200	Strong transcription	NHLF	lung
27	chr21:47838600-47847400	Weak transcription	HUVEC	blood vessel
28	chr21:47838800-47846800	Weak transcription	HMEC	breast
29	chr21:47838800-47862800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr21:47840000-47847600	Weak transcription	Primary hematopoietic stem cells	blood
31	chr21:47840000-47850200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr21:47841000-47847200	Weak transcription	Hela-S3	cervix
33	chr21:47841000-47847400	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr21:47841200-47849800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr21:47841200-47852400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr21:47841400-47848600	Weak transcription	Rectal Smooth Muscle	rectum
37	chr21:47842000-47847800	Genic enhancers	Fetal Thymus	thymus
38	chr21:47842200-47850200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr21:47842400-47848400	Weak transcription	Psoas Muscle	Psoas
40	chr21:47842800-47846800	Weak transcription	Fetal Intestine Large	intestine
41	chr21:47842800-47847200	Weak transcription	Ovary	ovary
42	chr21:47842800-47848200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr21:47842800-47855800	Weak transcription	A549	lung
44	chr21:47843000-47846800	Weak transcription	Brain Anterior Caudate	brain
45	chr21:47843000-47847000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr21:47843000-47847000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr21:47843000-47847000	Weak transcription	Liver	Liver
48	chr21:47843000-47847000	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr21:47843000-47847000	Weak transcription	HSMMtube	muscle
50	chr21:47843000-47847200	Weak transcription	Muscle Satellite Cultured Cells	--

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