Variant report

Variant	esv3455556
Chromosome Location	chr21:46373636-46374754
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NFIC	chr21:46373430-46373853	ECC-1	luminal epithelium:	n/a	n/a
2	POLR2A	chr21:46374203-46374234	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr21:46373704-46374391	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:46374519-46374569	AG04449	skin:	fetal
2	chr21:46374519-46374569	RPTEC	kidney:	n/a
3	chr21:46374519-46374569	HPAEpiC	pulmonary alveolar:	n/a
4	chr21:46374519-46374569	MCF-7	breast:	n/a
5	chr21:46374519-46374569	AG04450	lung:	fetal
6	chr21:46374519-46374569	ProgFib	skin:	n/a
7	chr21:46374519-46374569	H1-hESC	embryonic stem cell:	embryo
8	chr21:46374519-46374569	Caco-2	colon:	n/a
9	chr21:46374519-46374569	HL-60	blood:	n/a
10	chr21:46374519-46374569	NB4	blood:	n/a
11	chr21:46374519-46374569	HRPEpiC	eye:	n/a
12	chr21:46374519-46374569	HEEpiC	esophagus:	n/a
13	chr21:46374519-46374569	SK-N-MC	brain:	n/a
14	chr21:46374519-46374569	Hepatocyte	liver:	n/a
15	chr21:46374519-46374569	GM12892	blood:	n/a
16	chr21:46374519-46374569	AG09319	gingival:	n/a
17	chr21:46374519-46374569	HCPEpiC	choroid plexus:	n/a
18	chr21:46374519-46374569	AoSMC	blood vessel:	n/a
19	chr21:46374519-46374569	HCT-116	colon:	n/a
20	chr21:46374519-46374569	BE2_C	brain:	n/a
21	chr21:46374519-46374569	U87	brain:	n/a
22	chr21:46374519-46374569	GM06990	blood:	n/a
23	chr21:46374519-46374569	PANC-1	pancreas:	n/a
24	chr21:46374519-46374569	ECC-1	luminal epithelium:	n/a
25	chr21:46374519-46374569	Hela-S3	cervix:	n/a
26	chr21:46374519-46374569	AG10803	skin:	n/a
27	chr21:46374519-46374569	HCM	heart:	n/a
28	chr21:46374519-46374569	NH-A	brain:	n/a
29	chr21:46374519-46374569	HNPCEpiC	eye:	n/a
30	chr21:46374519-46374569	PrEC	prostate:	n/a
31	chr21:46374519-46374569	T-47D	breast:	n/a
32	chr21:46374519-46374569	GM12878	blood:	n/a
33	chr21:46374519-46374569	PFSK-1	brain:	n/a
34	chr21:46374519-46374569	HCF	heart:	n/a
35	chr21:46374519-46374569	GM12891	blood:	n/a
36	chr21:46374519-46374569	HEK293	kidney:	embryo
37	chr21:46374519-46374569	HIPEpiC	eye:	n/a
38	chr21:46374519-46374569	HUVEC	blood vessel:	n/a
39	chr21:46374519-46374569	SKMC	muscle:	n/a
40	chr21:46374519-46374569	HMEC	breast:	n/a
41	chr21:46374519-46374569	HepG2	liver:	n/a
42	chr21:46374519-46374569	MCF10A-Er-Src	breast:	n/a
43	chr21:46374519-46374569	LNCaP	prostate:	n/a
44	chr21:46374519-46374569	AG09309	skin:	n/a
45	chr21:46374519-46374569	SK-N-SH_RA	brain:	n/a
46	chr21:46374519-46374569	SK-N-SH	brain:	n/a
47	chr21:46374519-46374569	ovcar-3	ovarian:	n/a
48	chr21:46374519-46374569	NT2-D1	testis:	n/a
49	chr21:46374519-46374569	IMR90	lung:	fetal
50	chr21:46374519-46374569	HAEpiC	amniotic membrane:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:46369744..46371483-chr21:46372356..46374168,2	MCF-7	breast:
2	chr21:46372736..46375420-chr21:46375819..46378170,2	MCF-7	breast:
3	chr21:46373821..46376741-chr21:46385880..46388857,2	MCF-7	breast:
4	chr21:46363747..46379047-chr21:46484156..46498795,67	K562	blood:
5	chr21:46374315..46377421-chr21:46386112..46389411,4	K562	blood:
6	chr21:46373591..46376395-chr21:46393601..46395111,2	MCF-7	breast:
7	chr21:46372382..46374637-chr21:46555803..46558629,2	K562	blood:
8	chr21:46348854..46378176-chr21:46489799..46500436,75	K562	blood:
9	chr21:46366778..46369466-chr21:46371570..46373998,2	MCF-7	breast:
10	chr21:46371607..46373687-chr21:46493241..46495203,2	MCF-7	breast:
11	chr21:46372175..46374627-chr21:46492552..46495748,3	MCF-7	breast:
12	chr21:46368229..46374115-chr21:46374495..46378460,7	MCF-7	breast:
13	chr21:46368791..46372085-chr21:46374524..46378071,4	MCF-7	breast:

No data

Variant related genes	Relation type
FAM207A	TF binding region
FAM207A	CpG island
ENSG00000160256	chromatin interactions
ENSG00000235374	chromatin interactions
ENSG00000268856	chromatin interactions
ENSG00000197381	chromatin interactions

Extended variants
information (count: 56 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:56 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190779756	chr21:46373658-46373659	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs545722064	chr21:46373668-46373669	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs563922966	chr21:46373704-46373705	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs531174385	chr21:46373738-46373739	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs549586833	chr21:46373760-46373761	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs554828332	chr21:46373771-46373772	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs372690996	chr21:46373776-46373777	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs561255404	chr21:46373823-46373824	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs529730513	chr21:46373849-46373850	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs528610462	chr21:46373867-46373868	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs546746844	chr21:46373876-46373877	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs140334389	chr21:46373908-46373909	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs538601670	chr21:46373982-46373983	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs59318141	chr21:46373986-46373987	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs73906974	chr21:46374034-46374035	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs201250794	chr21:46374038-46374039	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs555120511	chr21:46374044-46374045	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs117922796	chr21:46374051-46374052	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs114530819	chr21:46374059-46374060	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs552749859	chr21:46374076-46374077	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs73906975	chr21:46374077-46374078	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs532436397	chr21:46374086-46374087	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs17004718	chr21:46374124-46374125	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs575989339	chr21:46374136-46374137	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs543316714	chr21:46374147-46374148	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs558738465	chr21:46374188-46374189	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs182019750	chr21:46374191-46374192	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs528639235	chr21:46374192-46374193	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs149579259	chr21:46374204-46374205	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs142747793	chr21:46374221-46374222	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs11088973	chr21:46374229-46374230	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs532413259	chr21:46374238-46374239	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs112313545	chr21:46374257-46374258	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs550546764	chr21:46374311-46374312	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs569641828	chr21:46374318-46374319	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs536969848	chr21:46374323-46374324	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs546155836	chr21:46374371-46374372	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs186182756	chr21:46374385-46374386	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs534469605	chr21:46374393-46374394	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs553075808	chr21:46374398-46374399	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs11911762	chr21:46374453-46374454	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs189569778	chr21:46374457-46374458	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs147390547	chr21:46374488-46374489	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs575279751	chr21:46374499-46374500	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs529668034	chr21:46374501-46374502	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs148429725	chr21:46374559-46374560	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs142594601	chr21:46374560-46374561	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs7277529	chr21:46374598-46374599	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs528749446	chr21:46374602-46374603	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs73378607	chr21:46374612-46374613	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:102)

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
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
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
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
small cell lung cancer	17426248	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Congenital heart defects	20877625	CNVD
Aortic dissecting aneurysms	22263138	CNVD

Chromatin state (count:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46361000-46384200	Weak transcription	Fetal Kidney	kidney
2	chr21:46361400-46384600	Weak transcription	Small Intestine	intestine
3	chr21:46361600-46375600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr21:46361600-46378000	Weak transcription	Stomach Mucosa	stomach
5	chr21:46361600-46378200	Weak transcription	NHDF-Ad	bronchial
6	chr21:46361600-46389200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr21:46362000-46382800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr21:46362400-46383200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr21:46363000-46382400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
10	chr21:46363200-46373800	Strong transcription	Brain Germinal Matrix	brain
11	chr21:46363400-46377400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr21:46363600-46378000	Strong transcription	Fetal Intestine Large	intestine
13	chr21:46363600-46378000	Strong transcription	NHLF	lung
14	chr21:46363600-46378600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr21:46364200-46391400	Strong transcription	Dnd41	blood
16	chr21:46364400-46377200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr21:46364800-46380400	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr21:46365400-46375200	Weak transcription	Fetal Lung	lung
19	chr21:46365600-46378200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr21:46366200-46374600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr21:46366200-46375800	Enhancers	Left Ventricle	heart
22	chr21:46366600-46376600	Weak transcription	Osteobl	bone
23	chr21:46367600-46376400	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr21:46367600-46382200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr21:46367800-46375200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr21:46367800-46377600	Weak transcription	Ovary	ovary
27	chr21:46367800-46378000	Weak transcription	HUVEC	blood vessel
28	chr21:46368000-46373800	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr21:46368200-46376200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr21:46368800-46380600	Enhancers	Fetal Heart	heart
31	chr21:46368800-46382600	Genic enhancers	Fetal Muscle Leg	muscle
32	chr21:46369000-46383000	Genic enhancers	Fetal Muscle Trunk	muscle
33	chr21:46369600-46374200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr21:46369800-46377800	Strong transcription	Gastric	stomach
35	chr21:46370000-46376600	Weak transcription	Brain Hippocampus Middle	brain
36	chr21:46370000-46378400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr21:46370000-46378400	Weak transcription	Brain Substantia Nigra	brain
38	chr21:46370000-46380200	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr21:46370000-46384200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr21:46370000-46385000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr21:46370200-46373800	Weak transcription	HepG2	liver
42	chr21:46370200-46374400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr21:46370200-46374400	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr21:46370200-46375200	Weak transcription	NH-A	brain
45	chr21:46370200-46375800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr21:46370200-46378000	Strong transcription	Fetal Intestine Small	intestine
47	chr21:46370200-46380800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr21:46370200-46382600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr21:46370200-46383400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr21:46370200-46383600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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