Variant report

Variant	esv3339878
Chromosome Location	chr21:45745574-45748372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:193)
CpG islands
(count:62)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:193 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr21:45748243-45748554	GM12878	blood:	n/a	n/a
2	BCL3	chr21:45748102-45750488	GM12878	blood:	n/a	chr21:45748793-45748802
3	BCL3	chr21:45748117-45748457	GM12878	blood:	n/a	n/a
4	CHD2	chr21:45748158-45748171	HepG2	liver:	n/a	n/a
5	CTCF	chr21:45746860-45747010	BE2_C	brain:	n/a	n/a
6	CTCF	chr21:45746960-45747110	HRPEpiC	eye:	n/a	n/a
7	CTCF	chr21:45746920-45747070	GM12878	blood:	n/a	n/a
8	CTCF	chr21:45746900-45747050	GM12865	blood:	n/a	n/a
9	CTCF	chr21:45746880-45747030	SAEC	small airway:	n/a	n/a
10	CTCF	chr21:45746997-45747043	MCF-7	breast:	n/a	n/a
11	CTCF	chr21:45746982-45746994	MCF-7	breast:	n/a	n/a
12	CTCF	chr21:45746960-45747110	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr21:45746978-45747082	MCF-7	breast:	n/a	n/a
14	CTCF	chr21:45747080-45747230	BE2_C	brain:	n/a	n/a
15	CTCF	chr21:45746920-45747070	HEK293	kidney:	n/a	n/a
16	CTCF	chr21:45746960-45747110	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr21:45747024-45747070	GM19240	blood:	n/a	n/a
18	CTCF	chr21:45746900-45747050	HA-sp	spinal cord:	n/a	n/a
19	CTCF	chr21:45746940-45747090	NB4	blood:	n/a	n/a
20	CTCF	chr21:45747540-45747690	HEK293	kidney:	n/a	chr21:45747614-45747623
21	CTCF	chr21:45746940-45747090	HMF	breast:	n/a	n/a
22	CTCF	chr21:45746000-45746150	GM12865	blood:	n/a	n/a
23	CTCF	chr21:45746992-45747072	GM12891	blood:	n/a	n/a
24	CTCF	chr21:45746985-45747089	GM12892	blood:	n/a	n/a
25	CTCF	chr21:45747520-45747670	NB4	blood:	n/a	chr21:45747614-45747623 chr21:45747524-45747537 chr21:45747522-45747530
26	CTCF	chr21:45746913-45747105	GM12878	blood:	n/a	n/a
27	CTCF	chr21:45747520-45747670	SAEC	small airway:	n/a	chr21:45747614-45747623 chr21:45747524-45747537 chr21:45747522-45747530
28	CTCF	chr21:45747640-45747790	GM12865	blood:	n/a	n/a
29	CTCF	chr21:45746940-45747090	AG09309	skin:	n/a	n/a
30	EBF1	chr21:45747588-45747897	GM12878	blood:	n/a	chr21:45747802-45747812
31	ELF1	chr21:45748316-45749860	MCF-7	breast:	n/a	n/a
32	ELF1	chr21:45745358-45745615	K562	blood:	n/a	n/a
33	FOSL2	chr21:45747301-45751180	HepG2	liver:	n/a	chr21:45748315-45748326 chr21:45747628-45747639
34	HMGN3	chr21:45747704-45747775	K562	blood:	n/a	n/a
35	MAX	chr21:45748293-45748310	NB4	blood:	n/a	n/a
36	MAX	chr21:45747037-45747922	NB4	blood:	n/a	n/a
37	MAZ	chr21:45747727-45747733	Hela-S3	cervix:	n/a	n/a
38	MTA3	chr21:45747728-45750894	GM12878	blood:	n/a	n/a
39	MYC	chr21:45747479-45747938	NB4	blood:	n/a	n/a
40	NFATC1	chr21:45748031-45750468	GM12878	blood:	n/a	n/a
41	PML	chr21:45747382-45748425	GM12878	blood:	n/a	n/a
42	PML	chr21:45748270-45748662	K562	blood:	n/a	n/a
43	PML	chr21:45747532-45747778	K562	blood:	n/a	n/a
44	POLR2A	chr21:45745409-45746280	U87	brain:	n/a	n/a
45	POLR2A	chr21:45745520-45746481	GM12878	blood:	n/a	n/a
46	POLR2A	chr21:45746238-45746269	HepG2	liver:	n/a	n/a
47	POLR2A	chr21:45747663-45752616	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr21:45747061-45747257	K562	blood:	n/a	n/a
49	POLR2A	chr21:45747576-45747768	A549	lung:	n/a	n/a
50	POLR2A	chr21:45748152-45748864	A549	lung:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45746856-45746906	HRCEpiC	kidney:	n/a
2	chr21:45746856-45746906	HRCEpiC	kidney:	n/a
3	chr21:45746856-45746906	Hepatocyte	liver:	n/a
4	chr21:45746856-45746906	ovcar-3	ovarian:	n/a
5	chr21:45746856-45746906	IMR90	lung:	fetal
6	chr21:45746856-45746906	HIPEpiC	eye:	n/a
7	chr21:45746856-45746906	AG09309	skin:	n/a
8	chr21:45746856-45746906	HRPEpiC	eye:	n/a
9	chr21:45746856-45746906	SK-N-SH_RA	brain:	n/a
10	chr21:45746856-45746906	HEEpiC	esophagus:	n/a
11	chr21:45746856-45746906	H1-hESC	embryonic stem cell:	embryo
12	chr21:45746856-45746906	SKMC	muscle:	n/a
13	chr21:45746856-45746906	GM06990	blood:	n/a
14	chr21:45746856-45746906	NHBE	bronchial:	n/a
15	chr21:45746856-45746906	CMK	blood:	n/a
16	chr21:45746856-45746906	GM12892	blood:	n/a
17	chr21:45746856-45746906	HCPEpiC	choroid plexus:	n/a
18	chr21:45746856-45746906	MCF10A-Er-Src	breast:	n/a
19	chr21:45746856-45746906	GM19239	blood:	n/a
20	chr21:45746856-45746906	BE2_C	brain:	n/a
21	chr21:45746856-45746906	Hela-S3	cervix:	n/a
22	chr21:45746856-45746906	AG09319	gingival:	n/a
23	chr21:45746856-45746906	HUVEC	blood vessel:	n/a
24	chr21:45746856-45746906	A549	lung:	n/a
25	chr21:45746856-45746906	PFSK-1	brain:	n/a
26	chr21:45746856-45746906	PrEC	prostate:	n/a
27	chr21:45746856-45746906	HNPCEpiC	eye:	n/a
28	chr21:45746856-45746906	LNCaP	prostate:	n/a
29	chr21:45746856-45746906	HMEC	breast:	n/a
30	chr21:45746856-45746906	HEK293	kidney:	embryo
31	chr21:45746856-45746906	AoSMC	blood vessel:	n/a
32	chr21:45746856-45746906	K562	blood:	n/a
33	chr21:45746856-45746906	GM12878	blood:	n/a
34	chr21:45746856-45746906	NB4	blood:	n/a
35	chr21:45746856-45746906	NHDF-neo	bronchial:	n/a
36	chr21:45746856-45746906	RPTEC	kidney:	n/a
37	chr21:45746856-45746906	AG10803	skin:	n/a
38	chr21:45746856-45746906	HPAEpiC	pulmonary alveolar:	n/a
39	chr21:45746856-45746906	SK-N-MC	brain:	n/a
40	chr21:45746856-45746906	PANC-1	pancreas:	n/a
41	chr21:45746856-45746906	HCF	heart:	n/a
42	chr21:45746856-45746906	T-47D	breast:	n/a
43	chr21:45746856-45746906	HRE	kidney:	n/a
44	chr21:45746856-45746906	ECC-1	luminal epithelium:	n/a
45	chr21:45746856-45746906	HCM	heart:	n/a
46	chr21:45746856-45746906	Jurkat	blood:	n/a
47	chr21:45746856-45746906	GM12891	blood:	n/a
48	chr21:45746856-45746906	HAEpiC	amniotic membrane:	n/a
49	chr21:45746856-45746906	AG04449	skin:	fetal
50	chr21:45746856-45746906	SK-N-SH	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45744755..45747310-chr21:45770895..45772522,2	K562	blood:
2	chr21:45561393..45564285-chr21:45746908..45749087,3	K562	blood:
3	chr21:45721842..45725498-chr21:45743836..45746079,3	MCF-7	breast:
4	chr21:45561454..45564242-chr21:45746295..45748408,3	K562	blood:
5	chr21:45566230..45568537-chr21:45744712..45747553,2	K562	blood:
6	chr21:45747059..45748898-chr21:45852124..45853647,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000184441	TF binding region
ENSG00000255902	TF binding region
ENSG00000184441	CpG island
ENSG00000255902	CpG island
ENSG00000141959	chromatin interactions

Extended variants
information (count: 183 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:183 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549232523	chr21:45745574-45745575	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs560957733	chr21:45745581-45745582	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs528440321	chr21:45745583-45745584	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546272266	chr21:45745617-45745618	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571705534	chr21:45745625-45745626	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs539289372	chr21:45745629-45745630	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551530157	chr21:45745635-45745636	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142515786	chr21:45745688-45745689	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562140670	chr21:45745692-45745693	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs150140560	chr21:45745702-45745703	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs558274549	chr21:45745708-45745709	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs138641261	chr21:45745716-45745717	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs534606030	chr21:45745748-45745749	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs552829519	chr21:45745798-45745799	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572778439	chr21:45745802-45745803	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs375804472	chr21:45745818-45745819	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs370017152	chr21:45745824-45745825	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373156682	chr21:45745912-45745913	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs139092292	chr21:45745917-45745918	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs563558193	chr21:45745924-45745925	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs575394602	chr21:45745926-45745927	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs373752195	chr21:45745927-45745928	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149471945	chr21:45745930-45745931	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370159883	chr21:45745931-45745932	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374183792	chr21:45745937-45745938	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs147169525	chr21:45745940-45745941	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368732092	chr21:45745958-45745959	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371368298	chr21:45745963-45745964	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs376813964	chr21:45745964-45745965	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs374308622	chr21:45745976-45745977	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs199607979	chr21:45745985-45745986	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs370841161	chr21:45745991-45745992	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs114995452	chr21:45746025-45746026	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34330261	chr21:45746030-45746031	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs367795946	chr21:45746044-45746045	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532660507	chr21:45746045-45746046	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs140263235	chr21:45746058-45746059	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs144669255	chr21:45746067-45746068	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs569873029	chr21:45746070-45746071	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs530675453	chr21:45746083-45746084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549342348	chr21:45746095-45746096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567538766	chr21:45746096-45746097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371443517	chr21:45746099-45746100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201494001	chr21:45746100-45746101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs17850433	chr21:45746102-45746103	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs148807445	chr21:45746115-45746116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375721190	chr21:45746116-45746117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142401488	chr21:45746125-45746126	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs11558848	chr21:45746132-45746133	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs200303857	chr21:45746140-45746141	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
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
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
small cell lung cancer	17426248	CNVD
Ependymoma	20639864	CNVD
Breast cancer	21364760	CNVD
Down syndrome	21154855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Williams-beuren syndrome	16826523	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45721000-45757600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr21:45724800-45748400	Strong transcription	Dnd41	blood
3	chr21:45725000-45758000	Weak transcription	Right Atrium	heart
4	chr21:45725400-45747800	Strong transcription	Sigmoid Colon	Sigmoid Colon
5	chr21:45725400-45748000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr21:45725600-45747600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr21:45725600-45748000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr21:45725600-45752800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr21:45725800-45757400	Strong transcription	Thymus	Thymus
10	chr21:45726000-45747800	Strong transcription	Stomach Smooth Muscle	stomach
11	chr21:45726000-45749200	Strong transcription	NHLF	lung
12	chr21:45726200-45747000	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr21:45726200-45747600	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr21:45726200-45747600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr21:45726200-45747600	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr21:45726200-45748000	Strong transcription	Colonic Mucosa	Colon
17	chr21:45726200-45748200	Strong transcription	Rectal Mucosa Donor 29	rectum
18	chr21:45726200-45753200	Strong transcription	Fetal Stomach	stomach
19	chr21:45726400-45747600	Strong transcription	Duodenum Smooth Muscle	Duodenum
20	chr21:45726400-45747800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr21:45726400-45748400	Strong transcription	Adipose Nuclei	Adipose
22	chr21:45726400-45751600	Strong transcription	Fetal Muscle Leg	muscle
23	chr21:45726600-45746400	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr21:45726600-45747600	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr21:45726600-45747800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr21:45726600-45747800	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr21:45726600-45747800	Strong transcription	Duodenum Mucosa	Duodenum
28	chr21:45726600-45748200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr21:45726600-45748400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr21:45726600-45748600	Strong transcription	Liver	Liver
31	chr21:45726600-45749000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr21:45726600-45749400	Strong transcription	Brain Germinal Matrix	brain
33	chr21:45726600-45749400	Strong transcription	Fetal Intestine Large	intestine
34	chr21:45726600-45753200	Strong transcription	Gastric	stomach
35	chr21:45726600-45757200	Strong transcription	Fetal Intestine Small	intestine
36	chr21:45726800-45748400	Strong transcription	Right Ventricle	heart
37	chr21:45727000-45750600	Strong transcription	Fetal Brain Female	brain
38	chr21:45727200-45748400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr21:45727400-45747600	Strong transcription	Primary T cells fromperipheralblood	blood
40	chr21:45727600-45750200	Weak transcription	NHDF-Ad	bronchial
41	chr21:45727600-45751200	Strong transcription	Fetal Muscle Trunk	muscle
42	chr21:45727800-45751800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr21:45728800-45747800	Strong transcription	Placenta Amnion	Placenta Amnion
44	chr21:45729000-45747600	Strong transcription	Primary B cells from peripheral blood	blood
45	chr21:45729200-45747800	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr21:45729400-45747400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr21:45729400-45752800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr21:45729800-45747800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr21:45729800-45748000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
50	chr21:45729800-45748000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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