Variant report

Variant	nsv587980
Chromosome Location	chr21:47715296-47722530
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:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

No data

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47717352..47719126-chr21:47738602..47740767,2	MCF-7	breast:
2	chr21:47715232..47717039-chr21:47718960..47720713,2	MCF-7	breast:
3	chr21:47708141..47711504-chr21:47716399..47719423,3	K562	blood:
4	chr21:47706092..47709051-chr21:47718044..47720782,2	MCF-7	breast:
5	chr21:47705283..47707993-chr21:47713694..47717938,5	MCF-7	breast:
6	chr21:47713574..47717141-chr21:47740930..47745749,7	K562	blood:
7	chr21:47700722..47725192-chr21:47732201..47746452,77	K562	blood:
8	chr21:47714423..47717463-chr21:47743785..47745906,3	MCF-7	breast:
9	chr21:47721939..47724799-chr21:47732004..47733970,2	MCF-7	breast:
10	chr21:47714784..47717174-chr21:47723560..47726052,2	MCF-7	breast:
11	chr21:47716063..47717906-chr21:47723260..47724786,2	K562	blood:
12	chr21:47713494..47715322-chr21:47788049..47790112,2	K562	blood:
13	chr11:61128057..61129672-chr21:47713579..47716107,2	MCF-7	breast:
14	chr21:47715271..47717864-chr21:47741446..47743716,2	MCF-7	breast:
15	chr21:47647161..47649856-chr21:47719709..47722524,2	MCF-7	breast:
16	chr21:47708860..47711564-chr21:47715753..47717339,2	K562	blood:
17	chr21:47715739..47718156-chr21:47738100..47740706,2	K562	blood:
18	chr21:47715232..47717039-chr21:47718960..47720713,2	MCF-7	breast:
19	chr10:90639851..90640519-chr21:47714618..47715484,2	NB4	blood:
20	chr21:47713822..47715879-chr21:47788612..47790511,2	K562	blood:
21	chr21:47718241..47721111-chr21:47723406..47725990,2	K562	blood:
22	chr21:47713129..47716016-chr21:47743936..47746881,5	MCF-7	breast:
23	chr21:47705928..47708356-chr21:47720533..47726820,5	K562	blood:
24	chr21:47705312..47710550-chr21:47711386..47716259,4	K562	blood:
25	chr21:47695579..47697188-chr21:47713900..47716404,2	MCF-7	breast:
26	chr21:47716057..47717569-chr21:47742713..47744741,2	MCF-7	breast:
27	chr21:47705635..47707803-chr21:47716511..47719183,2	K562	blood:
28	chr21:47713705..47716420-chr21:47738596..47740217,2	MCF-7	breast:
29	chr21:47719443..47722298-chr21:47727196..47729251,2	MCF-7	breast:
30	chr21:47704377..47706136-chr21:47717916..47719656,3	MCF-7	breast:
31	chr21:47704395..47708420-chr21:47713514..47717582,8	K562	blood:
32	chr21:47704416..47706123-chr21:47722175..47724138,2	MCF-7	breast:
33	chr21:47718509..47724261-chr21:47732959..47738534,9	K562	blood:
34	chr21:47646455..47648066-chr21:47714633..47716764,2	MCF-7	breast:
35	chr21:47721776..47723554-chr21:47738747..47741577,2	MCF-7	breast:
36	chr21:47717404..47720722-chr21:47740886..47746438,5	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C21orf58	hsa-miR-149-5p	chr21:47721488-47721509
2	C21orf58	hsa-miR-149-5p	chr21:47721286-47721310

Variant related genes	Relation type
ENSG00000160299	chromatin interactions
ENSG00000162144	chromatin interactions
ENSG00000160294	chromatin interactions
ENSG00000149483	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000138134	chromatin interactions
ENSG00000160285	chromatin interactions
ENSG00000182362	chromatin interactions
ENSG00000160298	chromatin interactions

Extended variants
information (count: 380 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12626184	chr21:47715296-47715297	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570442877	chr21:47715299-47715300	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs537880371	chr21:47715307-47715308	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs555861625	chr21:47715317-47715318	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs552408280	chr21:47715358-47715359	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs568029200	chr21:47715365-47715366	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs113864793	chr21:47715385-47715386	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs535767367	chr21:47715387-47715388	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs143683373	chr21:47715402-47715403	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs554070662	chr21:47715410-47715411	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs572274534	chr21:47715434-47715435	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs545678147	chr21:47715442-47715443	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs73144798	chr21:47715483-47715484	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs577251839	chr21:47715539-47715540	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs10854481	chr21:47715563-47715564	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs2839201	chr21:47715594-47715595	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs374176214	chr21:47715618-47715619	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs529995885	chr21:47715634-47715635	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs147022726	chr21:47715639-47715640	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs67555917	chr21:47715640-47715641	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs34495570	chr21:47715641-47715642	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs542120753	chr21:47715675-47715676	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs560408689	chr21:47715715-47715716	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs56985872	chr21:47715776-47715777	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs193277621	chr21:47715796-47715797	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs570553872	chr21:47715818-47715819	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs11911263	chr21:47715863-47715864	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs549865531	chr21:47715870-47715871	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs568074646	chr21:47715877-47715878	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs535396229	chr21:47715886-47715887	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs145473660	chr21:47715891-47715892	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs565972455	chr21:47715893-47715894	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs539654390	chr21:47715901-47715902	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs374941046	chr21:47715907-47715908	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs143503711	chr21:47715951-47715952	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs576157817	chr21:47715980-47715981	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs534020943	chr21:47716000-47716001	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs562960312	chr21:47716023-47716024	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs368366625	chr21:47716042-47716043	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs184784240	chr21:47716052-47716053	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs376873198	chr21:47716055-47716056	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs369093335	chr21:47716069-47716070	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs556191167	chr21:47716090-47716091	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs373410701	chr21:47716107-47716108	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs144279527	chr21:47716126-47716127	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs376555710	chr21:47716152-47716153	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs188310781	chr21:47716155-47716156	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs200740539	chr21:47716156-47716157	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs199837524	chr21:47716161-47716162	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs572626632	chr21:47716180-47716181	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	4 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:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47707000-47717400	Weak transcription	Small Intestine	intestine
2	chr21:47707200-47715800	Weak transcription	Right Atrium	heart
3	chr21:47707200-47717400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr21:47707400-47715800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr21:47707400-47717200	Weak transcription	Psoas Muscle	Psoas
6	chr21:47708200-47715800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr21:47710000-47717400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr21:47710000-47727600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr21:47710200-47716000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr21:47710200-47720400	Weak transcription	Hela-S3	cervix
11	chr21:47711600-47717400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr21:47711600-47717400	Weak transcription	NHEK	skin
13	chr21:47711800-47717400	Weak transcription	HUVEC	blood vessel
14	chr21:47712000-47717200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr21:47712000-47719200	Weak transcription	A549	lung
16	chr21:47712200-47717200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr21:47712200-47717200	Weak transcription	Primary T cells from cord blood	blood
18	chr21:47712200-47717400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr21:47712200-47717400	Weak transcription	Brain Hippocampus Middle	brain
20	chr21:47712200-47717400	Weak transcription	HMEC	breast
21	chr21:47712200-47717600	Weak transcription	Aorta	Aorta
22	chr21:47712200-47717600	Weak transcription	Fetal Kidney	kidney
23	chr21:47712400-47715400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr21:47712400-47715800	Weak transcription	Primary B cells from cord blood	blood
25	chr21:47712400-47715800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr21:47712400-47716200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr21:47712400-47717200	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr21:47712400-47717200	Weak transcription	Brain Anterior Caudate	brain
29	chr21:47712400-47717200	Weak transcription	Esophagus	oesophagus
30	chr21:47712400-47717400	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr21:47712400-47717400	Weak transcription	Liver	Liver
32	chr21:47712400-47717400	Weak transcription	Brain Angular Gyrus	brain
33	chr21:47712400-47717400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr21:47712400-47717400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr21:47712400-47717400	Weak transcription	Brain Substantia Nigra	brain
36	chr21:47712400-47717400	Weak transcription	Gastric	stomach
37	chr21:47712400-47717400	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr21:47712400-47717600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr21:47712400-47719000	Weak transcription	Dnd41	blood
40	chr21:47713800-47715400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr21:47714600-47715400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr21:47714600-47715400	Enhancers	Pancreas	Pancrea
43	chr21:47714600-47715400	Enhancers	GM12878-XiMat	blood
44	chr21:47714600-47715600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr21:47714600-47715600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr21:47714600-47715600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr21:47714600-47715600	Enhancers	Stomach Mucosa	stomach
48	chr21:47714600-47716200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr21:47714600-47716200	Enhancers	Fetal Thymus	thymus
50	chr21:47714600-47716600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links