Variant report

Variant	nsv587976
Chromosome Location	chr21:47676711-47687144
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:218)
CpG islands
(count:0)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:218 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr21:47684765-47684960	K562	blood:	n/a	n/a
2	CEBPB	chr21:47677859-47678201	MCF-7	breast:	n/a	n/a
3	CEBPB	chr21:47681581-47681605	IMR90	lung:	n/a	n/a
4	CEBPB	chr21:47681545-47681741	K562	blood:	n/a	chr21:47681597-47681608
5	CEBPB	chr21:47680308-47680569	K562	blood:	n/a	chr21:47680410-47680421 chr21:47680409-47680420 chr21:47680409-47680422
6	CEBPB	chr21:47681527-47681698	HepG2	liver:	n/a	chr21:47681597-47681608
7	CEBPB	chr21:47681563-47681747	A549	lung:	n/a	chr21:47681597-47681608
8	CEBPB	chr21:47677857-47678214	K562	blood:	n/a	n/a
9	CEBPB	chr21:47680318-47680512	IMR90	lung:	n/a	chr21:47680410-47680421 chr21:47680409-47680420 chr21:47680409-47680422
10	CEBPB	chr21:47677947-47678157	IMR90	lung:	n/a	n/a
11	CEBPB	chr21:47680352-47680501	HepG2	liver:	n/a	chr21:47680410-47680421 chr21:47680409-47680420 chr21:47680409-47680422
12	CEBPB	chr21:47677902-47678198	HepG2	liver:	n/a	n/a
13	CEBPB	chr21:47677892-47678242	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr21:47684740-47684791	K562	blood:	n/a	n/a
15	CHD2	chr21:47685077-47685494	K562	blood:	n/a	n/a
16	CTCF	chr21:47684868-47685026	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr21:47684760-47684910	SAEC	small airway:	n/a	n/a
18	CTCF	chr21:47684874-47684961	GM12891	blood:	n/a	n/a
19	CTCF	chr21:47684911-47684928	MCF-7	breast:	n/a	n/a
20	CTCF	chr21:47676720-47676870	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr21:47676779-47676864	K562	blood:	n/a	n/a
22	CTCF	chr21:47684714-47685243	K562	blood:	n/a	n/a
23	CTCF	chr21:47684840-47684990	HepG2	liver:	n/a	n/a
24	CTCF	chr21:47684930-47684977	GM19238	blood:	n/a	n/a
25	CTCF	chr21:47684916-47684943	Gliobla	brain:	n/a	n/a
26	CTCF	chr21:47676759-47676876	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr21:47684892-47684937	GM12878	blood:	n/a	n/a
28	CTCF	chr21:47684880-47685030	HEK293	kidney:	n/a	n/a
29	CTCF	chr21:47687104-47687192	MCF-7	breast:	n/a	n/a
30	CTCF	chr21:47684865-47684975	MCF-7	breast:	n/a	n/a
31	CTCF	chr21:47684860-47685010	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr21:47684776-47685058	K562	blood:	n/a	n/a
33	CTCF	chr21:47684911-47684966	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr21:47687137-47687236	K562	blood:	n/a	n/a
35	CTCF	chr21:47687116-47687224	MCF-7	breast:	n/a	n/a
36	CTCF	chr21:47687104-47687225	MCF-7	breast:	n/a	n/a
37	CTCF	chr21:47687121-47687198	GM12878	blood:	n/a	n/a
38	CTCF	chr21:47686300-47686450	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr21:47684860-47685010	K562	blood:	n/a	n/a
40	CTCF	chr21:47684900-47685050	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr21:47684820-47684970	K562	blood:	n/a	n/a
42	CTCF	chr21:47684907-47684995	MCF-7	breast:	n/a	n/a
43	CTCF	chr21:47676660-47676810	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr21:47684900-47685050	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr21:47687144-47687166	K562	blood:	n/a	n/a
46	CTCF	chr21:47687080-47687230	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr21:47684900-47685050	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr21:47684792-47685065	K562	blood:	n/a	n/a
49	CTCF	chr21:47684789-47685109	K562	blood:	n/a	n/a
50	CTCF	chr21:47676680-47676830	HEK293	kidney:	n/a	n/a

No data

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47679222..47682491-chr21:47688426..47691032,3	K562	blood:
2	chr21:47673462..47676957-chr21:47743809..47746402,3	MCF-7	breast:
3	chr21:47647891..47649801-chr21:47679065..47680838,2	K562	blood:
4	chr21:47665373..47666953-chr21:47675647..47678386,2	K562	blood:
5	chr21:47677887..47680451-chr21:47703023..47707250,4	MCF-7	breast:
6	chr21:47680435..47682223-chr21:47691504..47693900,2	K562	blood:
7	chr21:47680616..47682212-chr21:47682299..47683872,2	MCF-7	breast:
8	chr21:47674767..47676764-chr21:47876863..47879561,2	K562	blood:
9	chr21:47656119..47658355-chr21:47680181..47682317,2	K562	blood:
10	chr21:47670941..47674537-chr21:47676599..47680173,5	K562	blood:
11	chr21:47679763..47682789-chr21:47682949..47685079,3	K562	blood:
12	chr21:47680616..47682212-chr21:47682299..47683872,2	MCF-7	breast:
13	chr21:47670803..47673759-chr21:47680950..47683663,2	K562	blood:
14	chr21:47681311..47683636-chr21:47742237..47744496,2	K562	blood:
15	chr21:47685582..47687708-chr21:47742870..47745120,2	K562	blood:
16	chr21:47684294..47686629-chr21:47687169..47689868,2	MCF-7	breast:
17	chr21:47675606..47678213-chr21:47678769..47680314,2	K562	blood:
18	chr21:47678521..47681263-chr21:47682949..47685748,2	K562	blood:
19	chr21:47685253..47687082-chr21:47738865..47741678,2	K562	blood:
20	chr21:47681818..47684216-chr21:47689100..47690855,2	K562	blood:
21	chr21:47684242..47686410-chr21:47704277..47706154,2	MCF-7	breast:
22	chr21:47676348..47678546-chr21:47704213..47706057,2	K562	blood:
23	chr21:47679763..47682789-chr21:47682949..47685079,3	K562	blood:
24	chr21:47681971..47687315-chr21:47701766..47706280,5	K562	blood:
25	chr21:47668808..47671436-chr21:47681970..47684489,2	K562	blood:
26	chr21:47648381..47651139-chr21:47684651..47687035,3	MCF-7	breast:
27	chr21:47673957..47677589-chr21:47684900..47687101,3	MCF-7	breast:
28	chr21:47673957..47677589-chr21:47684900..47687101,3	MCF-7	breast:
29	chr21:47672405..47674929-chr21:47676682..47680003,3	MCF-7	breast:
30	chr21:47675606..47678213-chr21:47678769..47680314,2	K562	blood:
31	chr21:47674756..47677469-chr21:47692219..47695037,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-YBEY-2	chr21:47678838-47679304	ENSG00000215424.5

No data

Variant related genes	Relation type
ENSG00000239415	TF binding region
MCM3AP	TF binding region
ENSG00000239415	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000228137	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000160285	chromatin interactions
ENSG00000160294	chromatin interactions
ENSG00000182362	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000160305	chromatin interactions

Extended variants
information (count: 570 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2839173	chr21:47676711-47676712	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145449243	chr21:47676766-47676767	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs137961032	chr21:47676769-47676770	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs142441939	chr21:47676775-47676776	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs369418309	chr21:47676780-47676781	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs373406587	chr21:47676791-47676792	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs535949676	chr21:47676796-47676797	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs143889139	chr21:47676801-47676802	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs376354711	chr21:47676802-47676803	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs199914820	chr21:47676809-47676810	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs17183017	chr21:47676837-47676838	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs370439179	chr21:47676838-47676839	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs7279894	chr21:47676840-47676841	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs150680624	chr21:47676853-47676854	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs372593235	chr21:47676862-47676863	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs576312688	chr21:47676878-47676879	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs377767113	chr21:47676883-47676884	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs371194956	chr21:47676903-47676904	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs17176625	chr21:47676920-47676921	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs138613682	chr21:47676930-47676931	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs2839174	chr21:47676934-47676935	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs17176611	chr21:47676948-47676949	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs532911726	chr21:47676952-47676953	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs551069520	chr21:47676959-47676960	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs570001068	chr21:47676983-47676984	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs537334261	chr21:47677000-47677001	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs17176604	chr21:47677001-47677002	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs567424617	chr21:47677003-47677004	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs535588828	chr21:47677028-47677029	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs554206936	chr21:47677033-47677034	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs75817575	chr21:47677052-47677053	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs141609917	chr21:47677064-47677065	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs192440658	chr21:47677079-47677080	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs576372323	chr21:47677080-47677081	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs7275223	chr21:47677102-47677103	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs555549583	chr21:47677105-47677106	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs573861006	chr21:47677108-47677109	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs184786084	chr21:47677159-47677160	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs17183004	chr21:47677163-47677164	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs144480124	chr21:47677164-47677165	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs532871815	chr21:47677230-47677231	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs570378544	chr21:47677262-47677263	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs188345406	chr21:47677268-47677269	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs539270643	chr21:47677278-47677279	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs374266275	chr21:47677289-47677290	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs530831994	chr21:47677316-47677317	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs549260688	chr21:47677337-47677338	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs567486440	chr21:47677344-47677345	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs1811078	chr21:47677361-47677362	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
50	rs2330354	chr21:47677365-47677366	Strong transcription Weak transcription	Chromatin interactive region	3 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:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47649800-47701600	Weak transcription	Right Atrium	heart
2	chr21:47650000-47705200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr21:47650800-47701000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr21:47650800-47701400	Strong transcription	Fetal Muscle Leg	muscle
5	chr21:47650800-47701600	Strong transcription	Fetal Stomach	stomach
6	chr21:47651000-47703200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr21:47651200-47701400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr21:47651600-47679000	Strong transcription	HSMM	muscle
9	chr21:47651600-47703000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr21:47651600-47703200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr21:47651800-47681000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr21:47651800-47701400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr21:47651800-47702600	Strong transcription	Osteobl	bone
14	chr21:47652000-47701000	Strong transcription	Duodenum Mucosa	Duodenum
15	chr21:47652000-47703000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr21:47652200-47701600	Strong transcription	Fetal Thymus	thymus
17	chr21:47652400-47685200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr21:47652400-47702000	Strong transcription	H9 Cell Line	embryonic stem cell
19	chr21:47652800-47678000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr21:47652800-47702200	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr21:47653000-47701600	Strong transcription	H1 Cell Line	embryonic stem cell
22	chr21:47653200-47696000	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr21:47653200-47702000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr21:47653400-47686000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr21:47653600-47701800	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr21:47653600-47702400	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr21:47658200-47681400	Strong transcription	Brain Hippocampus Middle	brain
28	chr21:47658200-47702200	Strong transcription	Skeletal Muscle Female	skeletal muscle
29	chr21:47658400-47702800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr21:47658600-47681400	Strong transcription	NHEK	skin
31	chr21:47658600-47682400	Strong transcription	Fetal Brain Female	brain
32	chr21:47658600-47696000	Strong transcription	Duodenum Smooth Muscle	Duodenum
33	chr21:47658600-47696000	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr21:47658600-47701400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr21:47658600-47702600	Strong transcription	Fetal Muscle Trunk	muscle
36	chr21:47658600-47703000	Strong transcription	Placenta	Placenta
37	chr21:47658600-47703200	Strong transcription	HUES48 Cell Line	embryonic stem cell
38	chr21:47658600-47703600	Strong transcription	Fetal Intestine Large	intestine
39	chr21:47658800-47677000	Strong transcription	HSMMtube	muscle
40	chr21:47658800-47677200	Strong transcription	Hela-S3	cervix
41	chr21:47658800-47679000	Strong transcription	HUVEC	blood vessel
42	chr21:47658800-47679200	Strong transcription	NHLF	lung
43	chr21:47658800-47681600	Strong transcription	Colonic Mucosa	Colon
44	chr21:47658800-47681600	Strong transcription	Placenta Amnion	Placenta Amnion
45	chr21:47658800-47682400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
46	chr21:47658800-47695800	Strong transcription	Sigmoid Colon	Sigmoid Colon
47	chr21:47658800-47696000	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr21:47658800-47699800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr21:47658800-47700600	Strong transcription	Stomach Smooth Muscle	stomach
50	chr21:47661800-47682400	Strong transcription	Colon Smooth Muscle	Colon

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