Variant report

Variant	esv3528069
Chromosome Location	chr21:45680724-45684322
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:305)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr21:45681498-45681620	HepG2	liver:	n/a	n/a
2	EGR1	chr21:45681705-45681972	K562	blood:	n/a	n/a
3	EGR1	chr21:45681580-45681947	K562	blood:	n/a	n/a
4	ELF1	chr21:45683096-45683404	GM12878	blood:	n/a	chr21:45683380-45683392
5	GABPA	chr21:45683381-45683602	H1-hESC	embryonic stem cell:	n/a	n/a
6	MAZ	chr21:45683341-45683375	K562	blood:	n/a	n/a
7	POLR2A	chr21:45681258-45681302	MCF-7	breast:	n/a	n/a
8	POLR2A	chr21:45681032-45681217	HepG2	liver:	n/a	n/a
9	THAP1	chr21:45681580-45681822	K562	blood:	n/a	n/a
10	USF1	chr21:45683349-45683657	H1-hESC	embryonic stem cell:	n/a	n/a
11	USF1	chr21:45683292-45683656	H1-hESC	embryonic stem cell:	n/a	n/a
12	USF2	chr21:45683401-45683536	H1-hESC	embryonic stem cell:	n/a	n/a
13	ZBTB7A	chr21:45683323-45683739	ECC-1	luminal epithelium:	n/a	n/a
14	ZBTB7A	chr21:45683090-45683659	K562	blood:	n/a	n/a
15	ZBTB7A	chr21:45681814-45681932	K562	blood:	n/a	n/a
16	ZBTB7A	chr21:45683266-45683648	ECC-1	luminal epithelium:	n/a	n/a
17	ZBTB7A	chr21:45683362-45683528	K562	blood:	n/a	n/a
18	ZBTB7A	chr21:45683861-45683993	K562	blood:	n/a	n/a
19	ZBTB7A	chr21:45683093-45683338	K562	blood:	n/a	n/a
20	ZNF384	chr21:45683671-45683677	K562	blood:	n/a	n/a
21	ZNF384	chr21:45683902-45684101	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45681834-45681884	ECC-1	luminal epithelium:	n/a
2	chr21:45683513-45683563	AG04449	skin:	fetal
3	chr21:45683513-45683563	GM06990	blood:	n/a
4	chr21:45683528-45683578	AG09309	skin:	n/a
5	chr21:45683513-45683563	PANC-1	pancreas:	n/a
6	chr21:45683302-45683352	T-47D	breast:	n/a
7	chr21:45683302-45683352	NH-A	brain:	n/a
8	chr21:45683146-45683196	PFSK-1	brain:	n/a
9	chr21:45683513-45683563	HRE	kidney:	n/a
10	chr21:45683146-45683196	NH-A	brain:	n/a
11	chr21:45681834-45681884	U87	brain:	n/a
12	chr21:45683302-45683352	HIPEpiC	eye:	n/a
13	chr21:45681834-45681884	NB4	blood:	n/a
14	chr21:45683146-45683196	Hepatocyte	liver:	n/a
15	chr21:45681834-45681884	ovcar-3	ovarian:	n/a
16	chr21:45681834-45681884	RPTEC	kidney:	n/a
17	chr21:45683146-45683196	HRCEpiC	kidney:	n/a
18	chr21:45683146-45683196	ovcar-3	ovarian:	n/a
19	chr21:45683513-45683563	MCF10A-Er-Src	breast:	n/a
20	chr21:45683302-45683352	CMK	blood:	n/a
21	chr21:45683528-45683578	Jurkat	blood:	n/a
22	chr21:45683528-45683578	HIPEpiC	eye:	n/a
23	chr21:45683302-45683352	IMR90	lung:	fetal
24	chr21:45681834-45681884	HCM	heart:	n/a
25	chr21:45681834-45681884	NT2-D1	testis:	n/a
26	chr21:45683146-45683196	GM12878	blood:	n/a
27	chr21:45683302-45683352	HepG2	liver:	n/a
28	chr21:45683302-45683352	Hela-S3	cervix:	n/a
29	chr21:45683146-45683196	Hela-S3	cervix:	n/a
30	chr21:45683302-45683352	SK-N-MC	brain:	n/a
31	chr21:45683528-45683578	AG04449	skin:	fetal
32	chr21:45683513-45683563	GM12892	blood:	n/a
33	chr21:45683528-45683578	SKMC	muscle:	n/a
34	chr21:45683528-45683578	AG04450	lung:	fetal
35	chr21:45681834-45681884	SAEC	small airway:	n/a
36	chr21:45681834-45681884	K562	blood:	n/a
37	chr21:45681834-45681884	AG04450	lung:	fetal
38	chr21:45683528-45683578	HUVEC	blood vessel:	n/a
39	chr21:45683528-45683578	A549	lung:	n/a
40	chr21:45683528-45683578	Caco-2	colon:	n/a
41	chr21:45683302-45683352	BE2_C	brain:	n/a
42	chr21:45683528-45683578	RPTEC	kidney:	n/a
43	chr21:45683513-45683563	HCPEpiC	choroid plexus:	n/a
44	chr21:45683528-45683578	HCM	heart:	n/a
45	chr21:45681834-45681884	GM06990	blood:	n/a
46	chr21:45683513-45683563	AG09319	gingival:	n/a
47	chr21:45683513-45683563	IMR90	lung:	fetal
48	chr21:45681834-45681884	LNCaP	prostate:	n/a
49	chr21:45683302-45683352	AG09319	gingival:	n/a
50	chr21:45681834-45681884	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr21:45657604..45660265-chr21:45683962..45685836,2	K562	blood:
2	chr21:45678302..45680831-chr21:45686072..45687676,2	MCF-7	breast:
3	chr21:45679421..45681484-chr21:45691729..45694649,2	MCF-7	breast:
4	chr21:45565598..45568910-chr21:45683665..45687558,4	MCF-7	breast:
5	chr21:45677174..45681552-chr21:45685520..45688325,5	K562	blood:
6	chr21:45680895..45685107-chr21:45717932..45721130,4	MCF-7	breast:

No data

Variant related genes	Relation type
DNMT3L	TF binding region
DNMT3L	CpG island
ENSG00000141959	chromatin interactions

Extended variants
information (count: 164 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:164 , 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	rs553210775	chr21:45680724-45680725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370267082	chr21:45680728-45680729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373680073	chr21:45680732-45680733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570957584	chr21:45680746-45680747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368717133	chr21:45680747-45680748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs72613643	chr21:45680782-45680783	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs114308751	chr21:45680808-45680809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570968707	chr21:45680849-45680850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537940811	chr21:45680860-45680861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189217451	chr21:45680878-45680879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573367235	chr21:45680879-45680880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368380199	chr21:45680891-45680892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540596019	chr21:45680900-45680901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371362613	chr21:45680926-45680927	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs141705594	chr21:45680928-45680929	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532590880	chr21:45680932-45680933	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs544577073	chr21:45680933-45680934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562971971	chr21:45680984-45680985	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs544896008	chr21:45680986-45680987	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs372284198	chr21:45681011-45681012	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs375758150	chr21:45681012-45681013	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs530108024	chr21:45681049-45681050	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs150520240	chr21:45681050-45681051	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368501877	chr21:45681058-45681059	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs567378551	chr21:45681085-45681086	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs528286200	chr21:45681093-45681094	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs75396112	chr21:45681109-45681110	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs376271029	chr21:45681110-45681111	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs369151415	chr21:45681114-45681115	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs373372632	chr21:45681122-45681123	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs150049925	chr21:45681137-45681138	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs2070565	chr21:45681153-45681154	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs112457300	chr21:45681163-45681164	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs77287369	chr21:45681165-45681166	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs556513516	chr21:45681186-45681187	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs535755434	chr21:45681194-45681195	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs535996041	chr21:45681202-45681203	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs554625850	chr21:45681215-45681216	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs573402251	chr21:45681223-45681224	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs540808794	chr21:45681259-45681260	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559302228	chr21:45681266-45681267	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs540732482	chr21:45681275-45681276	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs72613644	chr21:45681276-45681277	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs544638527	chr21:45681277-45681278	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs184062852	chr21:45681290-45681291	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146245304	chr21:45681304-45681305	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572366785	chr21:45681346-45681347	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542005929	chr21:45681352-45681353	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs369282528	chr21:45681368-45681369	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs79296121	chr21:45681376-45681377	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	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
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

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45662800-45705600	Weak transcription	Right Atrium	heart
2	chr21:45666200-45681000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr21:45671800-45681400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr21:45679600-45681000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr21:45681000-45681200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr21:45681000-45681600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr21:45681000-45681800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr21:45681000-45682600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr21:45681200-45681800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr21:45681400-45681800	Bivalent Enhancer	HepG2	liver
11	chr21:45681400-45682000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr21:45681600-45681800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr21:45681600-45683000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr21:45681800-45683000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr21:45681800-45683000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr21:45681800-45683200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr21:45682000-45682400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr21:45682400-45683800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr21:45682600-45683000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr21:45682600-45684600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr21:45682800-45684000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr21:45683000-45683200	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr21:45683000-45683400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr21:45683000-45683600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr21:45683000-45683600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr21:45683000-45683800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr21:45683000-45683800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr21:45683000-45683800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr21:45683000-45684000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr21:45683000-45684000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr21:45683000-45684000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr21:45683000-45684200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr21:45683200-45683400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr21:45683200-45683400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr21:45683200-45683400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr21:45683200-45683400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr21:45683200-45683400	Bivalent Enhancer	Fetal Stomach	stomach
38	chr21:45683200-45683600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr21:45683200-45683600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr21:45683200-45683600	Enhancers	Fetal Lung	lung
41	chr21:45683200-45683800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr21:45683200-45683800	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr21:45683200-45683800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr21:45683200-45683800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr21:45683200-45683800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr21:45683200-45683800	Enhancers	Fetal Muscle Leg	muscle
47	chr21:45683200-45684000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr21:45683200-45684000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr21:45683200-45684000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr21:45683200-45684000	Bivalent Enhancer	Fetal Muscle Trunk	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links