Variant report

Variant	esv3372377
Chromosome Location	chr21:45172074-45174872
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:121)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:121 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr21:45173023-45173159	GM19239	blood:	n/a	n/a
2	MYC	chr21:45173022-45173197	MCF-7	breast:	n/a	n/a
3	MYC	chr21:45173029-45173183	MCF-7	breast:	n/a	n/a
4	NFATC1	chr21:45174830-45175440	GM12878	blood:	n/a	n/a
5	NFIC	chr21:45174587-45175085	ECC-1	luminal epithelium:	n/a	n/a
6	NFYA	chr21:45174590-45175517	K562	blood:	n/a	chr21:45175134-45175152 chr21:45175102-45175120 chr21:45175166-45175184
7	NFYA	chr21:45174775-45175516	Hela-S3	cervix:	n/a	chr21:45175134-45175152 chr21:45175102-45175120 chr21:45175166-45175184
8	NFYB	chr21:45174698-45175719	Hela-S3	cervix:	n/a	chr21:45175108-45175123 chr21:45175140-45175155 chr21:45175172-45175187
9	NFYB	chr21:45174514-45175979	K562	blood:	n/a	chr21:45175108-45175123 chr21:45175140-45175155 chr21:45175172-45175187
10	NFYB	chr21:45174761-45175512	GM12878	blood:	n/a	chr21:45175108-45175123 chr21:45175140-45175155 chr21:45175172-45175187
11	POLR2A	chr21:45172903-45172943	HepG2	liver:	n/a	n/a
12	POLR2A	chr21:45173838-45174069	A549	lung:	n/a	n/a
13	POLR2A	chr21:45171342-45175119	K562	blood:	n/a	n/a
14	POLR2A	chr21:45172460-45172505	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr21:45174280-45174317	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr21:45172283-45172439	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr21:45172569-45172579	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr21:45172258-45172322	HepG2	liver:	n/a	n/a
19	POLR2A	chr21:45172853-45173372	GM12891	blood:	n/a	n/a
20	POLR2A	chr21:45174536-45174659	HepG2	liver:	n/a	n/a
21	POLR2A	chr21:45172458-45172498	K562	blood:	n/a	n/a
22	POLR2A	chr21:45172553-45173320	MCF-7	breast:	n/a	n/a
23	POLR2A	chr21:45173277-45173428	A549	lung:	n/a	n/a
24	POLR2A	chr21:45172705-45173282	U87	brain:	n/a	n/a
25	POLR2A	chr21:45172873-45172914	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr21:45172577-45172843	U87	brain:	n/a	n/a
27	POLR2A	chr21:45174328-45174375	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr21:45174717-45174805	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr21:45172842-45173690	GM12892	blood:	n/a	n/a
30	POLR2A	chr21:45172899-45173166	ECC-1	luminal epithelium:	n/a	n/a
31	POLR2A	chr21:45172183-45172557	GM12878	blood:	n/a	n/a
32	POLR2A	chr21:45172184-45172613	HL-60	blood:	n/a	n/a
33	POLR2A	chr21:45172809-45174008	K562	blood:	n/a	n/a
34	POLR2A	chr21:45171789-45172540	A549	lung:	n/a	n/a
35	POLR2A	chr21:45172195-45172542	GM12891	blood:	n/a	n/a
36	POLR2A	chr21:45172523-45172538	K562	blood:	n/a	n/a
37	POLR2A	chr21:45174199-45174362	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr21:45173675-45173789	A549	lung:	n/a	n/a
39	POLR2A	chr21:45172967-45173233	GM12878	blood:	n/a	n/a
40	POLR2A	chr21:45172924-45173241	A549	lung:	n/a	n/a
41	POLR2A	chr21:45173444-45174461	K562	blood:	n/a	n/a
42	POLR2A	chr21:45171948-45174002	GM12878	blood:	n/a	n/a
43	POLR2A	chr21:45171900-45172496	A549	lung:	n/a	n/a
44	POLR2A	chr21:45174290-45174375	A549	lung:	n/a	n/a
45	POLR2A	chr21:45174685-45174749	K562	blood:	n/a	n/a
46	POLR2A	chr21:45173315-45173448	A549	lung:	n/a	n/a
47	POLR2A	chr21:45172274-45172456	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr21:45172656-45174239	K562	blood:	n/a	n/a
49	POLR2A	chr21:45172237-45173494	U87	brain:	n/a	n/a
50	POLR2A	chr21:45171573-45172332	K562	blood:	n/a	n/a

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45163023..45165790-chr21:45170856..45174314,3	K562	blood:
2	chr21:45173766..45177589-chr21:45178136..45181222,4	MCF-7	breast:
3	chr21:45173075..45175705-chr21:45194787..45196904,2	MCF-7	breast:
4	chr21:45156965..45158670-chr21:45174699..45176799,2	K562	blood:
5	chr21:45138491..45140784-chr21:45174555..45177027,2	MCF-7	breast:
6	chr21:45164290..45167394-chr21:45171722..45175273,3	K562	blood:
7	chr21:45154933..45157513-chr21:45174243..45177077,2	MCF-7	breast:
8	chr21:45174354..45177532-chr21:45180309..45182041,3	MCF-7	breast:
9	chr21:45154618..45156575-chr21:45170589..45173066,2	K562	blood:
10	chr21:45152139..45163298-chr21:45164540..45174522,16	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RRP1-2	chr21:45173464-45173600	NONHSAT082444

No data

Variant related genes	Relation type
PDXK	TF binding region
ENSG00000160213	chromatin interactions
ENSG00000160209	chromatin interactions

Extended variants
information (count: 162 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:162 , 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	rs557616186	chr21:45172074-45172075	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs140045281	chr21:45172082-45172083	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs185748463	chr21:45172153-45172154	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs112877959	chr21:45172154-45172155	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs577385880	chr21:45172157-45172158	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs545050204	chr21:45172160-45172161	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs146333648	chr21:45172168-45172169	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs368854934	chr21:45172178-45172179	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs540645593	chr21:45172179-45172180	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs190568230	chr21:45172200-45172201	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs533089310	chr21:45172239-45172240	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs544878475	chr21:45172245-45172246	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs183099726	chr21:45172250-45172251	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs373787070	chr21:45172258-45172259	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs530745822	chr21:45172284-45172285	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs372447371	chr21:45172304-45172305	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs548859573	chr21:45172326-45172327	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs553590476	chr21:45172346-45172347	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs372007377	chr21:45172349-45172350	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs139343607	chr21:45172362-45172363	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs374242465	chr21:45172369-45172370	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs187777467	chr21:45172370-45172371	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs202096648	chr21:45172378-45172379	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs8134507	chr21:45172379-45172380	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs557623579	chr21:45172384-45172385	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs368896821	chr21:45172389-45172390	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs369091058	chr21:45172429-45172430	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs372855286	chr21:45172431-45172432	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs117532045	chr21:45172452-45172453	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201509716	chr21:45172453-45172454	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs375933947	chr21:45172491-45172492	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs372754988	chr21:45172497-45172498	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs377024628	chr21:45172526-45172527	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs370120323	chr21:45172529-45172530	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs190780606	chr21:45172532-45172533	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs201445188	chr21:45172533-45172534	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs533441138	chr21:45172573-45172574	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs552574833	chr21:45172584-45172585	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs377726670	chr21:45172597-45172598	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs544567307	chr21:45172602-45172603	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs2010795	chr21:45172628-45172629	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs575421913	chr21:45172648-45172649	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs542825891	chr21:45172674-45172675	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs560911454	chr21:45172703-45172704	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150039772	chr21:45172710-45172711	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs145371029	chr21:45172756-45172757	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs565318425	chr21:45172777-45172778	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs530974500	chr21:45172794-45172795	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs549576641	chr21:45172800-45172801	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs532560027	chr21:45172822-45172823	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45149000-45194400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr21:45149400-45175400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr21:45149800-45175200	Weak transcription	HUVEC	blood vessel
4	chr21:45149800-45188200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr21:45150000-45173200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr21:45152200-45183400	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr21:45152400-45173200	Weak transcription	Psoas Muscle	Psoas
8	chr21:45154400-45184200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr21:45154800-45174600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr21:45158200-45173800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr21:45160600-45185600	Strong transcription	Fetal Intestine Small	intestine
12	chr21:45160800-45187200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr21:45161000-45174400	Weak transcription	Fetal Heart	heart
14	chr21:45161200-45177200	Strong transcription	HepG2	liver
15	chr21:45161200-45183600	Strong transcription	Fetal Intestine Large	intestine
16	chr21:45161400-45176400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr21:45161400-45182200	Strong transcription	Rectal Mucosa Donor 31	rectum
18	chr21:45161400-45183200	Strong transcription	Placenta Amnion	Placenta Amnion
19	chr21:45161400-45185400	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr21:45161600-45172400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr21:45161600-45174600	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr21:45161600-45176800	Strong transcription	Placenta	Placenta
23	chr21:45161600-45177000	Strong transcription	Osteobl	bone
24	chr21:45161600-45178000	Strong transcription	Duodenum Mucosa	Duodenum
25	chr21:45161600-45179000	Strong transcription	Primary T helper cells fromperipheralblood	blood
26	chr21:45161600-45179400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr21:45161600-45183000	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr21:45161800-45174400	Strong transcription	Spleen	Spleen
29	chr21:45161800-45184800	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr21:45162000-45176200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr21:45162000-45177200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr21:45162000-45178000	Strong transcription	Lung	lung
33	chr21:45162000-45180000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr21:45162000-45185200	Weak transcription	Thymus	Thymus
35	chr21:45162200-45181600	Strong transcription	NHEK	skin
36	chr21:45162400-45176600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr21:45162400-45177000	Strong transcription	Fetal Stomach	stomach
38	chr21:45162400-45177600	Strong transcription	Colonic Mucosa	Colon
39	chr21:45162800-45174600	Strong transcription	Ovary	ovary
40	chr21:45163200-45176800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr21:45163200-45183400	Strong transcription	NHLF	lung
42	chr21:45163400-45174400	Strong transcription	Fetal Muscle Trunk	muscle
43	chr21:45163400-45176600	Strong transcription	Liver	Liver
44	chr21:45163400-45177000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr21:45163400-45177200	Strong transcription	Skeletal Muscle Male	skeletal muscle
46	chr21:45163600-45173000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr21:45163600-45174400	Strong transcription	Fetal Muscle Leg	muscle
48	chr21:45163600-45176800	Strong transcription	Muscle Satellite Cultured Cells	--
49	chr21:45163600-45176800	Strong transcription	Fetal Brain Female	brain
50	chr21:45163600-45177000	Strong transcription	Duodenum Smooth Muscle	Duodenum

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