Variant report

Variant	nsv459313
Chromosome Location	chr21:47964259-47982652
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:198)
CpG islands
(count:183)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:198 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr21:47971730-47971895	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr21:47979309-47979386	GM12878	blood:	n/a	n/a
3	BHLHE40	chr21:47979787-47979972	HepG2	liver:	n/a	n/a
4	BHLHE40	chr21:47974833-47975086	K562	blood:	n/a	n/a
5	BRCA1	chr21:47968213-47968319	GM12878	blood:	n/a	n/a
6	CTCF	chr21:47971720-47971870	GM06990	blood:	n/a	n/a
7	CTCF	chr21:47971740-47971890	GM12870	blood:	n/a	n/a
8	CTCF	chr21:47971700-47971850	GM12868	blood:	n/a	n/a
9	CTCF	chr21:47971676-47971792	Spleen_OC	spleen:	n/a	n/a
10	CTCF	chr21:47971680-47971830	HEK293	kidney:	n/a	n/a
11	CTCF	chr21:47974900-47975050	HepG2	liver:	n/a	chr21:47974967-47974985 chr21:47974989-47974998 chr21:47974985-47974998
12	CTCF	chr21:47971681-47971836	GM13977	blood:	n/a	n/a
13	CTCF	chr21:47971640-47971790	GM06990	blood:	n/a	n/a
14	CTCF	chr21:47971622-47971822	GM12878	blood:	n/a	n/a
15	CTCF	chr21:47971700-47971850	HL-60	blood:	n/a	n/a
16	CTCF	chr21:47971620-47971770	HepG2	liver:	n/a	n/a
17	CTCF	chr21:47971760-47971910	GM12867	blood:	n/a	n/a
18	CTCF	chr21:47964540-47964690	MCF-7	breast:	n/a	n/a
19	CTCF	chr21:47971657-47971828	MCF-7	breast:	n/a	n/a
20	CTCF	chr21:47964560-47964710	MCF-7	breast:	n/a	n/a
21	CTCF	chr21:47971560-47971710	GM12870	blood:	n/a	n/a
22	CTCF	chr21:47971640-47971790	GM12874	blood:	n/a	n/a
23	CTCF	chr21:47971620-47971770	GM12866	blood:	n/a	n/a
24	CTCF	chr21:47971642-47971799	GM10248	blood:	n/a	n/a
25	CTCF	chr21:47971700-47971850	MCF-7	breast:	n/a	n/a
26	CTCF	chr21:47971680-47971830	GM12873	blood:	n/a	n/a
27	CTCF	chr21:47964600-47964750	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr21:47971679-47971802	MCF-7	breast:	n/a	n/a
29	CTCF	chr21:47971660-47971810	GM12867	blood:	n/a	n/a
30	CTCF	chr21:47971660-47971810	GM12875	blood:	n/a	n/a
31	CTCF	chr21:47971680-47971830	GM12871	blood:	n/a	n/a
32	CTCF	chr21:47971625-47971812	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr21:47971660-47971910	GM12864	blood:	n/a	n/a
34	CTCF	chr21:47971660-47971810	GM12873	blood:	n/a	n/a
35	CTCF	chr21:47971700-47971850	GM12866	blood:	n/a	n/a
36	CTCF	chr21:47980700-47980850	HepG2	liver:	n/a	n/a
37	CTCF	chr21:47971640-47971790	GM12864	blood:	n/a	n/a
38	CTCF	chr21:47971660-47971810	NB4	blood:	n/a	n/a
39	CTCF	chr21:47971588-47971929	GM19238	blood:	n/a	n/a
40	CTCF	chr21:47971681-47971795	MCF-7	breast:	n/a	n/a
41	CTCF	chr21:47971570-47971909	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr21:47965620-47965770	HMEC	breast:	n/a	chr21:47965711-47965724 chr21:47965718-47965731
43	CTCF	chr21:47971620-47971770	GM12864	blood:	n/a	n/a
44	CTCF	chr21:47971589-47971888	GM12891	blood:	n/a	n/a
45	CTCF	chr21:47971740-47971890	GM12871	blood:	n/a	n/a
46	CTCF	chr21:47964600-47964750	HMEC	breast:	n/a	n/a
47	CTCF	chr21:47971724-47971809	GM12892	blood:	n/a	n/a
48	CTCF	chr21:47965400-47965550	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr21:47971660-47971810	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr21:47971622-47971853	GM19239	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47969887-47969937	SK-N-MC	brain:	n/a
2	chr21:47966967-47967017	AG09309	skin:	n/a
3	chr21:47965968-47966018	HCPEpiC	choroid plexus:	n/a
4	chr21:47966967-47967017	AG10803	skin:	n/a
5	chr21:47966967-47967017	H1-hESC	embryonic stem cell:	embryo
6	chr21:47969887-47969937	NB4	blood:	n/a
7	chr21:47966967-47967017	HCM	heart:	n/a
8	chr21:47969887-47969937	HL-60	blood:	n/a
9	chr21:47969887-47969937	ovcar-3	ovarian:	n/a
10	chr21:47966967-47967017	BJ	skin:	n/a
11	chr21:47966967-47967017	HRE	kidney:	n/a
12	chr21:47966967-47967017	GM12892	blood:	n/a
13	chr21:47966967-47967017	SAEC	small airway:	n/a
14	chr21:47969887-47969937	HIPEpiC	eye:	n/a
15	chr21:47966967-47967017	K562	blood:	n/a
16	chr21:47965968-47966018	U87	brain:	n/a
17	chr21:47969887-47969937	HPAEpiC	pulmonary alveolar:	n/a
18	chr21:47966967-47967017	HL-60	blood:	n/a
19	chr21:47965968-47966018	ECC-1	luminal epithelium:	n/a
20	chr21:47966967-47967017	ovcar-3	ovarian:	n/a
21	chr21:47965968-47966018	SK-N-MC	brain:	n/a
22	chr21:47966967-47967017	AoSMC	blood vessel:	n/a
23	chr21:47966967-47967017	HCPEpiC	choroid plexus:	n/a
24	chr21:47966967-47967017	HCT-116	colon:	n/a
25	chr21:47965968-47966018	K562	blood:	n/a
26	chr21:47965968-47966018	NHDF-neo	bronchial:	n/a
27	chr21:47969887-47969937	IMR90	lung:	fetal
28	chr21:47966967-47967017	HRPEpiC	eye:	n/a
29	chr21:47965968-47966018	ProgFib	skin:	n/a
30	chr21:47966967-47967017	Jurkat	blood:	n/a
31	chr21:47966967-47967017	NB4	blood:	n/a
32	chr21:47969887-47969937	T-47D	breast:	n/a
33	chr21:47965968-47966018	RPTEC	kidney:	n/a
34	chr21:47966967-47967017	PANC-1	pancreas:	n/a
35	chr21:47965968-47966018	HCM	heart:	n/a
36	chr21:47966967-47967017	MCF-7	breast:	n/a
37	chr21:47965968-47966018	IMR90	lung:	fetal
38	chr21:47965968-47966018	ovcar-3	ovarian:	n/a
39	chr21:47965968-47966018	HMEC	breast:	n/a
40	chr21:47969887-47969937	HRCEpiC	kidney:	n/a
41	chr21:47966967-47967017	NHBE	bronchial:	n/a
42	chr21:47966967-47967017	HIPEpiC	eye:	n/a
43	chr21:47969887-47969937	GM12891	blood:	n/a
44	chr21:47965968-47966018	CMK	blood:	n/a
45	chr21:47969887-47969937	BJ	skin:	n/a
46	chr21:47969887-47969937	HRPEpiC	eye:	n/a
47	chr21:47965968-47966018	LNCaP	prostate:	n/a
48	chr21:47965968-47966018	GM12892	blood:	n/a
49	chr21:47966967-47967017	SKMC	muscle:	n/a
50	chr21:47965968-47966018	GM12878	blood:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47972221..47973948-chr21:47980674..47982187,2	K562	blood:
2	chr21:47962897..47964618-chr21:47964925..47967563,2	K562	blood:
3	chr17:59415209..59417169-chr21:47966964..47969396,2	MCF-7	breast:
4	chr21:47974804..47979372-chr21:47979836..47984256,6	MCF-7	breast:
5	chr21:47962897..47964618-chr21:47964925..47967563,2	K562	blood:
6	chr21:47966167..47967910-chr21:47973256..47975447,2	MCF-7	breast:
7	chr21:47955962..47958891-chr21:47961483..47965848,4	MCF-7	breast:
8	chr21:47967795..47973717-chr21:47974569..47979109,7	K562	blood:
9	chr21:47976473..47979943-chr21:47981689..47985824,4	K562	blood:
10	chr21:47972251..47974231-chr21:48053496..48055796,2	K562	blood:
11	chr21:47964705..47967234-chr21:47968598..47971419,5	K562	blood:
12	chr21:47961062..47963795-chr21:47966527..47968756,2	MCF-7	breast:
13	chr21:47949927..47954811-chr21:47962745..47966393,6	K562	blood:
14	chr21:47975607..47978026-chr21:47981816..47984257,4	MCF-7	breast:
15	chr21:47876440..47878945-chr21:47970776..47973767,2	MCF-7	breast:
16	chr21:47966998..47969983-chr21:47970602..47975589,5	MCF-7	breast:
17	chr21:47967795..47973717-chr21:47974569..47979109,7	K562	blood:
18	chr21:47964705..47967234-chr21:47968598..47971419,5	K562	blood:
19	chr21:47971877..47975830-chr21:47983188..47986029,3	K562	blood:
20	chr21:47970600..47973376-chr21:47976429..47979323,2	MCF-7	breast:
21	chr21:47878343..47879844-chr21:47964827..47967163,2	MCF-7	breast:
22	chr21:47956156..47957836-chr21:47975877..47978282,2	K562	blood:
23	chr21:47974804..47979372-chr21:47979836..47984256,6	MCF-7	breast:
24	chr21:47972221..47973948-chr21:47980674..47982187,2	K562	blood:
25	chr21:47959900..47962353-chr21:47964256..47965869,2	K562	blood:
26	chr21:47964144..47967545-chr21:47972969..47977002,4	K562	blood:
27	chr21:47979855..47982153-chr21:48055162..48056734,2	MCF-7	breast:
28	chr21:47977884..47980372-chr21:47985950..47987706,2	K562	blood:

No data

Variant related genes	Relation type
DIP2A	TF binding region
DIP2A	CpG island
ENSG00000160310	chromatin interactions
ENSG00000160305	chromatin interactions

Extended variants
information (count: 872 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:872 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12483320	chr21:47964259-47964260	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
2	rs373965870	chr21:47964260-47964261	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs11089076	chr21:47964272-47964273	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs570938246	chr21:47964274-47964275	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537981443	chr21:47964317-47964318	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs555938219	chr21:47964329-47964330	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs574334168	chr21:47964420-47964421	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs535326568	chr21:47964441-47964442	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs78463142	chr21:47964481-47964482	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs370407263	chr21:47964547-47964548	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs725970	chr21:47964643-47964644	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs725969	chr21:47964669-47964670	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs112948552	chr21:47964676-47964677	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs562401550	chr21:47964697-47964698	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs373896416	chr21:47964771-47964772	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs558078964	chr21:47964785-47964786	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs563061434	chr21:47964797-47964798	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs530325108	chr21:47964807-47964808	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs542109910	chr21:47964809-47964810	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560861277	chr21:47964859-47964860	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs182663162	chr21:47964898-47964899	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143591571	chr21:47964940-47964941	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs148095889	chr21:47964964-47964965	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368109170	chr21:47964966-47964967	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531684513	chr21:47965001-47965002	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371741495	chr21:47965013-47965014	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187605083	chr21:47965014-47965015	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs369134421	chr21:47965020-47965021	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192869336	chr21:47965032-47965033	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs140943771	chr21:47965066-47965067	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs370091831	chr21:47965077-47965078	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs374354931	chr21:47965095-47965096	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs377659201	chr21:47965120-47965121	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553750795	chr21:47965121-47965122	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs565951201	chr21:47965135-47965136	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs200370702	chr21:47965143-47965144	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539382417	chr21:47965147-47965148	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373891540	chr21:47965152-47965153	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs34495896	chr21:47965155-47965156	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs377550062	chr21:47965171-47965172	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs150180949	chr21:47965205-47965206	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs374356816	chr21:47965210-47965211	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs138814032	chr21:47965255-47965256	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs71326332	chr21:47965275-47965276	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs143101170	chr21:47965287-47965288	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555502626	chr21:47965312-47965313	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575056753	chr21:47965343-47965344	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542423009	chr21:47965365-47965366	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs560556786	chr21:47965390-47965391	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs113309718	chr21:47965457-47965458	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 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:792 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47933000-47967200	Weak transcription	Fetal Kidney	kidney
2	chr21:47943600-47990600	Strong transcription	Fetal Stomach	stomach
3	chr21:47947200-47975200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr21:47947400-47965600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr21:47947600-47967200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr21:47947600-47989000	Strong transcription	Dnd41	blood
7	chr21:47947600-47991000	Strong transcription	Fetal Muscle Leg	muscle
8	chr21:47948000-47968400	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr21:47948400-47971600	Strong transcription	Fetal Muscle Trunk	muscle
10	chr21:47948400-47993600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr21:47948600-47968000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr21:47948600-47968000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr21:47948600-47971400	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr21:47948600-47993200	Strong transcription	Fetal Intestine Large	intestine
15	chr21:47948800-47969000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr21:47948800-47970400	Strong transcription	Placenta	Placenta
17	chr21:47948800-47979400	Strong transcription	Liver	Liver
18	chr21:47949000-47965000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr21:47949000-47965200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr21:47949000-47969000	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr21:47949000-47979000	Strong transcription	Adipose Nuclei	Adipose
22	chr21:47949000-47988200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr21:47949000-47993600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr21:47949600-47968600	Strong transcription	Primary neutrophils fromperipheralblood	blood
25	chr21:47949600-47970200	Strong transcription	Duodenum Mucosa	Duodenum
26	chr21:47949800-47967800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr21:47949800-47991800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr21:47950000-47965200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr21:47950000-47968800	Strong transcription	Duodenum Smooth Muscle	Duodenum
30	chr21:47950000-47989200	Strong transcription	Skeletal Muscle Female	skeletal muscle
31	chr21:47950000-47991000	Strong transcription	Sigmoid Colon	Sigmoid Colon
32	chr21:47950200-47993200	Strong transcription	Stomach Smooth Muscle	stomach
33	chr21:47950400-47971800	Strong transcription	Rectal Mucosa Donor 31	rectum
34	chr21:47950400-47974400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr21:47952000-47965200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr21:47952000-47978600	Strong transcription	Skeletal Muscle Male	skeletal muscle
37	chr21:47952200-47968200	Strong transcription	Fetal Brain Female	brain
38	chr21:47953000-47974800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr21:47953000-47988200	Strong transcription	Gastric	stomach
40	chr21:47953000-47988600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr21:47953200-47964600	Strong transcription	Esophagus	oesophagus
42	chr21:47953200-47965000	Strong transcription	NHEK	skin
43	chr21:47953200-47967000	Strong transcription	Brain Substantia Nigra	brain
44	chr21:47953200-47968400	Strong transcription	Lung	lung
45	chr21:47953200-47968400	Strong transcription	Spleen	Spleen
46	chr21:47953200-47968600	Strong transcription	Primary B cells from peripheral blood	blood
47	chr21:47953200-47968800	Strong transcription	Placenta Amnion	Placenta Amnion
48	chr21:47953200-47971800	Strong transcription	Thymus	Thymus
49	chr21:47953200-47972000	Strong transcription	Ovary	ovary
50	chr21:47953200-47983400	Strong transcription	Brain Inferior Temporal Lobe	brain

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