Variant report

Variant	nsv459291
Chromosome Location	chr21:45175958-45191139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:78)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

No data

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:45180929..45184497-chr21:45193980..45197167,4	MCF-7	breast:
2	chr21:45150500..45152044-chr21:45185669..45188271,2	MCF-7	breast:
3	chr21:45138109..45140029-chr21:45182845..45184770,2	MCF-7	breast:
4	chr21:45175067..45176952-chr21:45182703..45184647,2	MCF-7	breast:
5	chr21:45163956..45166849-chr21:45180813..45183270,2	K562	blood:
6	chr21:45177511..45180498-chr21:45193933..45196367,2	MCF-7	breast:
7	chr21:45154001..45156611-chr21:45177637..45180387,2	K562	blood:
8	chr21:45172031..45174493-chr21:45180363..45182490,3	K562	blood:
9	chr21:45136545..45138543-chr21:45189331..45190847,2	K562	blood:
10	chr21:45184800..45186919-chr21:45202076..45204506,2	MCF-7	breast:
11	chr21:45146947..45149079-chr21:45186898..45189138,2	MCF-7	breast:
12	chr21:45138824..45140737-chr21:45184086..45186856,2	MCF-7	breast:
13	chr21:45162810..45165204-chr21:45175505..45178426,2	K562	blood:
14	chr21:45162810..45165195-chr21:45176926..45179048,2	K562	blood:
15	chr21:45170373..45174526-chr21:45175102..45180278,8	K562	blood:
16	chr21:45187250..45190053-chr21:45278541..45281497,2	K562	blood:
17	chr21:45180145..45181960-chr21:45187482..45190363,2	MCF-7	breast:
18	chr21:45186409..45188413-chr21:45222813..45224847,2	MCF-7	breast:
19	chr21:45180883..45182749-chr21:45182963..45185452,2	K562	blood:
20	chr21:45147228..45149882-chr21:45188263..45191287,3	K562	blood:
21	chr21:45188150..45190644-chr21:45201210..45202764,2	MCF-7	breast:
22	chr21:45176316..45177949-chr21:46492855..46495309,2	K562	blood:
23	chr21:45077926..45080845-chr21:45188689..45190434,2	K562	blood:
24	chr21:45154933..45157513-chr21:45174243..45177077,2	MCF-7	breast:
25	chr21:45180145..45181960-chr21:45187482..45190363,2	MCF-7	breast:
26	chr21:45138604..45142209-chr21:45185832..45189641,4	K562	blood:
27	chr21:45177169..45178998-chr21:45188478..45190913,2	MCF-7	breast:
28	chr21:45188590..45190206-chr21:45212982..45214484,2	MCF-7	breast:
29	chr1:44115667..44116530-chr21:45187543..45188263,2	Hela-S3	cervix:
30	chr21:45176342..45178590-chr21:45192932..45195099,2	MCF-7	breast:
31	chr21:45175067..45176952-chr21:45182703..45184647,2	MCF-7	breast:
32	chr21:45176543..45179179-chr21:45179807..45182752,3	K562	blood:
33	chr21:45078322..45080845-chr21:45187869..45190189,2	K562	blood:
34	chr21:45172516..45176384-chr21:45184983..45188324,4	MCF-7	breast:
35	chr21:45147794..45149532-chr21:45185305..45188143,2	K562	blood:
36	chr21:45176365..45178705-chr21:45190387..45191910,2	MCF-7	breast:
37	chr21:45146831..45149878-chr21:45189453..45192393,3	K562	blood:
38	chr21:45175274..45178845-chr21:45192010..45195975,4	K562	blood:
39	chr21:45159505..45163027-chr21:45178422..45181506,3	MCF-7	breast:
40	chr21:45181077..45183120-chr21:45187370..45189689,2	K562	blood:
41	chr21:45186953..45189605-chr21:45526871..45528738,2	MCF-7	breast:
42	chr21:45174354..45177532-chr21:45180309..45182041,3	MCF-7	breast:
43	chr21:45156965..45158670-chr21:45174699..45176799,2	K562	blood:
44	chr21:45165588..45167444-chr21:45177367..45179445,2	MCF-7	breast:
45	chr21:45138491..45140784-chr21:45174555..45177027,2	MCF-7	breast:
46	chr21:45077798..45080390-chr21:45188444..45191047,2	MCF-7	breast:
47	chr21:45176919..45181577-chr21:45207690..45210859,4	MCF-7	breast:
48	chr21:45176491..45178777-chr21:45179789..45182236,2	K562	blood:
49	chr21:45173766..45177589-chr21:45178136..45181222,4	MCF-7	breast:
50	chr21:45172846..45174492-chr21:45176032..45177914,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RRP1-2	chr21:45175832-45176043	NONHSAT082444

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PDXK	hsa-miR-24-3p	chr21:45181006-45181013

Variant related genes	Relation type
ENSG00000197381	chromatin interactions
ENSG00000160214	chromatin interactions
ENSG00000241945	chromatin interactions
ENSG00000163041	chromatin interactions
ENSG00000268856	chromatin interactions
ENSG00000234030	chromatin interactions
ENSG00000160209	chromatin interactions
ENSG00000066135	chromatin interactions
ENSG00000160208	chromatin interactions
ENSG00000160213	chromatin interactions
ENSG00000160207	chromatin interactions
ENSG00000235374	chromatin interactions

Extended variants
information (count: 755 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:755 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7527	chr21:45175958-45175959	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562154224	chr21:45175959-45175960	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs377597960	chr21:45175975-45175976	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs114002037	chr21:45175976-45175977	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs529119792	chr21:45175977-45175978	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs148529944	chr21:45175989-45175990	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs565516422	chr21:45176021-45176022	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs533310449	chr21:45176059-45176060	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs551840250	chr21:45176069-45176070	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570009707	chr21:45176070-45176071	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs537455251	chr21:45176088-45176089	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141906527	chr21:45176105-45176106	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs567995922	chr21:45176116-45176117	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575838956	chr21:45176158-45176159	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374385244	chr21:45176160-45176161	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184901997	chr21:45176177-45176178	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573599993	chr21:45176190-45176191	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150665495	chr21:45176198-45176199	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs190786061	chr21:45176199-45176200	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543353139	chr21:45176220-45176221	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs576028855	chr21:45176255-45176256	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs543422859	chr21:45176267-45176268	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs8126928	chr21:45176268-45176269	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs529177313	chr21:45176303-45176304	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2070535	chr21:45176304-45176305	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs547234266	chr21:45176319-45176320	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs369675626	chr21:45176321-45176322	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs13051474	chr21:45176333-45176334	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs551238965	chr21:45176354-45176355	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs373823573	chr21:45176370-45176371	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs563824940	chr21:45176371-45176372	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs530872487	chr21:45176419-45176420	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs549428598	chr21:45176422-45176423	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs567664079	chr21:45176453-45176454	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs180797597	chr21:45176457-45176458	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs547329499	chr21:45176480-45176481	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs571922515	chr21:45176484-45176485	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs539244272	chr21:45176500-45176501	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs557239439	chr21:45176505-45176506	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs550980683	chr21:45176523-45176524	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs576123181	chr21:45176590-45176591	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs184582611	chr21:45176605-45176606	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs536723776	chr21:45176606-45176607	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs17004606	chr21:45176621-45176622	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs139922110	chr21:45176629-45176630	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs368833375	chr21:45176641-45176642	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs144883761	chr21:45176651-45176652	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs577829686	chr21:45176670-45176671	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs375819105	chr21:45176753-45176754	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs147957333	chr21:45176760-45176761	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
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 lymphoblastic leukemia	20435627	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
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	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
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Neuroblastoma	20406844	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	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 cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:811 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45149000-45194400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr21:45149800-45188200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr21:45152200-45183400	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr21:45154400-45184200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr21:45160600-45185600	Strong transcription	Fetal Intestine Small	intestine
6	chr21:45160800-45187200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr21:45161200-45177200	Strong transcription	HepG2	liver
8	chr21:45161200-45183600	Strong transcription	Fetal Intestine Large	intestine
9	chr21:45161400-45176400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr21:45161400-45182200	Strong transcription	Rectal Mucosa Donor 31	rectum
11	chr21:45161400-45183200	Strong transcription	Placenta Amnion	Placenta Amnion
12	chr21:45161400-45185400	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr21:45161600-45176800	Strong transcription	Placenta	Placenta
14	chr21:45161600-45177000	Strong transcription	Osteobl	bone
15	chr21:45161600-45178000	Strong transcription	Duodenum Mucosa	Duodenum
16	chr21:45161600-45179000	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr21:45161600-45179400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr21:45161600-45183000	Strong transcription	Sigmoid Colon	Sigmoid Colon
19	chr21:45161800-45184800	Strong transcription	Cortex derived primary cultured neurospheres	brain
20	chr21:45162000-45176200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr21:45162000-45177200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr21:45162000-45178000	Strong transcription	Lung	lung
23	chr21:45162000-45180000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr21:45162000-45185200	Weak transcription	Thymus	Thymus
25	chr21:45162200-45181600	Strong transcription	NHEK	skin
26	chr21:45162400-45176600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr21:45162400-45177000	Strong transcription	Fetal Stomach	stomach
28	chr21:45162400-45177600	Strong transcription	Colonic Mucosa	Colon
29	chr21:45163200-45176800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr21:45163200-45183400	Strong transcription	NHLF	lung
31	chr21:45163400-45176600	Strong transcription	Liver	Liver
32	chr21:45163400-45177000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr21:45163400-45177200	Strong transcription	Skeletal Muscle Male	skeletal muscle
34	chr21:45163600-45176800	Strong transcription	Muscle Satellite Cultured Cells	--
35	chr21:45163600-45176800	Strong transcription	Fetal Brain Female	brain
36	chr21:45163600-45177000	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr21:45163600-45177200	Strong transcription	Brain Cingulate Gyrus	brain
38	chr21:45163600-45177400	Strong transcription	Stomach Smooth Muscle	stomach
39	chr21:45163600-45179200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr21:45163600-45183600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr21:45163600-45184000	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr21:45163600-45184200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr21:45163600-45185000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr21:45163800-45177000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr21:45163800-45177400	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr21:45163800-45179600	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr21:45164200-45177000	Strong transcription	Brain Substantia Nigra	brain
48	chr21:45164400-45177000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr21:45165000-45176400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr21:45166400-45176200	Weak transcription	Fetal Brain Male	brain

The 2.0 version of rSNPBase

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