Variant report

Variant	esv3355743
Chromosome Location	chr21:47328549-47331397
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:16)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:16 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr21:47329478-47329550	Lung_OC	lung:	n/a	n/a
2	HDAC2	chr21:47330363-47330862	MCF-7	breast:	n/a	chr21:47330445-47330459
3	HMGN3	chr21:47328569-47328612	K562	blood:	n/a	n/a
4	MYC	chr21:47330617-47330699	MCF-7	breast:	n/a	n/a
5	MYC	chr21:47329030-47329114	MCF-7	breast:	n/a	n/a
6	MYC	chr21:47329186-47329188	MCF-7	breast:	n/a	n/a
7	MYC	chr21:47330898-47330903	MCF-7	breast:	n/a	n/a
8	MYC	chr21:47329200-47329262	MCF-7	breast:	n/a	n/a
9	NFIC	chr21:47330252-47330931	ECC-1	luminal epithelium:	n/a	chr21:47330583-47330599 chr21:47330581-47330597 chr21:47330581-47330598 chr21:47330582-47330599
10	NFIC	chr21:47330189-47330813	ECC-1	luminal epithelium:	n/a	chr21:47330583-47330599 chr21:47330581-47330597 chr21:47330581-47330598 chr21:47330582-47330599
11	NFIC	chr21:47330211-47330839	SK-N-SH	brain:	n/a	chr21:47330583-47330599 chr21:47330581-47330597 chr21:47330581-47330598 chr21:47330582-47330599
12	POLR2A	chr21:47328512-47328578	MCF-7	breast:	n/a	n/a
13	SRF	chr21:47330026-47330584	MCF-7	breast:	n/a	n/a
14	USF1	chr21:47330092-47330357	SK-N-SH_RA	brain:	n/a	n/a
15	USF1	chr21:47330098-47330276	SK-N-SH_RA	brain:	n/a	n/a
16	ZNF263	chr21:47330736-47330936	HEK293-T-REx	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47330914-47330964	MCF-7	breast:	n/a
2	chr21:47330914-47330964	HRE	kidney:	n/a
3	chr21:47330914-47330964	HEEpiC	esophagus:	n/a
4	chr21:47330914-47330964	Caco-2	colon:	n/a
5	chr21:47330914-47330964	AG09319	gingival:	n/a
6	chr21:47330914-47330964	MCF10A-Er-Src	breast:	n/a
7	chr21:47330914-47330964	HepG2	liver:	n/a
8	chr21:47330914-47330964	NT2-D1	testis:	n/a
9	chr21:47330914-47330964	GM12878	blood:	n/a
10	chr21:47330914-47330964	Hepatocyte	liver:	n/a
11	chr21:47330914-47330964	U87	brain:	n/a
12	chr21:47330914-47330964	NHBE	bronchial:	n/a
13	chr21:47330914-47330964	HMEC	breast:	n/a
14	chr21:47330914-47330964	ovcar-3	ovarian:	n/a
15	chr21:47330914-47330964	HCPEpiC	choroid plexus:	n/a
16	chr21:47330914-47330964	HRPEpiC	eye:	n/a
17	chr21:47330914-47330964	HNPCEpiC	eye:	n/a
18	chr21:47330914-47330964	GM12892	blood:	n/a
19	chr21:47330914-47330964	PANC-1	pancreas:	n/a
20	chr21:47330914-47330964	AG10803	skin:	n/a
21	chr21:47330914-47330964	RPTEC	kidney:	n/a
22	chr21:47330914-47330964	PFSK-1	brain:	n/a
23	chr21:47330914-47330964	NHDF-neo	bronchial:	n/a
24	chr21:47330914-47330964	PrEC	prostate:	n/a
25	chr21:47330914-47330964	HIPEpiC	eye:	n/a
26	chr21:47330914-47330964	HEK293	kidney:	embryo
27	chr21:47330914-47330964	HCF	heart:	n/a
28	chr21:47330914-47330964	GM06990	blood:	n/a
29	chr21:47330914-47330964	HAEpiC	amniotic membrane:	n/a
30	chr21:47330914-47330964	AG04450	lung:	fetal
31	chr21:47330914-47330964	AG04449	skin:	fetal
32	chr21:47330914-47330964	Hela-S3	cervix:	n/a
33	chr21:47330914-47330964	LNCaP	prostate:	n/a
34	chr21:47330914-47330964	NH-A	brain:	n/a
35	chr21:47330914-47330964	GM12891	blood:	n/a
36	chr21:47330914-47330964	NB4	blood:	n/a
37	chr21:47330914-47330964	T-47D	breast:	n/a
38	chr21:47330914-47330964	CMK	blood:	n/a
39	chr21:47330914-47330964	HRCEpiC	kidney:	n/a
40	chr21:47330914-47330964	HCT-116	colon:	n/a
41	chr21:47330914-47330964	HUVEC	blood vessel:	n/a
42	chr21:47330914-47330964	H1-hESC	embryonic stem cell:	embryo
43	chr21:47330914-47330964	SKMC	muscle:	n/a
44	chr21:47330914-47330964	K562	blood:	n/a
45	chr21:47330914-47330964	SAEC	small airway:	n/a
46	chr21:47330914-47330964	BJ	skin:	n/a
47	chr21:47330914-47330964	Jurkat	blood:	n/a
48	chr21:47330914-47330964	ECC-1	luminal epithelium:	n/a
49	chr21:47330914-47330964	GM19239	blood:	n/a
50	chr21:47330914-47330964	SK-N-SH_RA	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47329095..47331174-chr21:47334966..47337510,2	MCF-7	breast:
2	chr21:47322615..47325568-chr21:47331282..47333525,2	K562	blood:
3	chr21:47318888..47321827-chr21:47328391..47331106,3	MCF-7	breast:
4	chr21:47328644..47331016-chr21:47340908..47343121,3	MCF-7	breast:
5	chr21:47329285..47331470-chr21:47342066..47344987,2	MCF-7	breast:
6	chr21:47253579..47256281-chr21:47326370..47329354,2	K562	blood:
7	chr21:47324736..47327193-chr21:47327348..47329802,3	K562	blood:

No data

Variant related genes	Relation type
PCBP3	TF binding region
PCBP3	CpG island
ENSG00000183570	chromatin interactions

Extended variants
information (count: 170 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:170 , 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	rs530716242	chr21:47328579-47328580	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs542870217	chr21:47328585-47328586	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs562158545	chr21:47328595-47328596	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs529446366	chr21:47328620-47328621	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs542767013	chr21:47328625-47328626	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs547770232	chr21:47328654-47328655	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566066295	chr21:47328703-47328704	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs115637885	chr21:47328706-47328707	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs552069314	chr21:47328710-47328711	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs559300889	chr21:47328733-47328734	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs144576991	chr21:47328747-47328748	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs1124309	chr21:47328767-47328768	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs147903926	chr21:47328769-47328770	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567014003	chr21:47328831-47328832	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs530923772	chr21:47328836-47328837	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534422687	chr21:47328850-47328851	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552505580	chr21:47328851-47328852	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs577580428	chr21:47328863-47328864	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372661545	chr21:47328902-47328903	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550996819	chr21:47328982-47328983	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs9976042	chr21:47328990-47328991	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs148947541	chr21:47329006-47329007	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs370743127	chr21:47329021-47329022	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs142931137	chr21:47329022-47329023	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs151099076	chr21:47329023-47329024	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561069450	chr21:47329029-47329030	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529356776	chr21:47329038-47329039	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs374036633	chr21:47329039-47329040	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs541557427	chr21:47329044-47329045	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs117963482	chr21:47329063-47329064	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs74752882	chr21:47329064-47329065	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs551515068	chr21:47329074-47329075	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs570328940	chr21:47329101-47329102	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs112116908	chr21:47329103-47329104	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs549126303	chr21:47329146-47329147	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141032876	chr21:47329193-47329194	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs570035897	chr21:47329200-47329201	Strong transcription Weak transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs202124379	chr21:47329221-47329222	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs374320839	chr21:47329228-47329229	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs368321019	chr21:47329231-47329232	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs371743180	chr21:47329253-47329254	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs2277812	chr21:47329352-47329353	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs201330830	chr21:47329364-47329365	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs367782910	chr21:47329391-47329392	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs201370119	chr21:47329419-47329420	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371466860	chr21:47329420-47329421	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs538625178	chr21:47329423-47329424	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375755127	chr21:47329425-47329426	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556720525	chr21:47329426-47329427	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs200185743	chr21:47329427-47329428	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 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:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47308000-47343000	Weak transcription	Right Atrium	heart
2	chr21:47313200-47335600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr21:47314400-47330200	Weak transcription	Brain Hippocampus Middle	brain
4	chr21:47314600-47330200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr21:47315000-47330200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr21:47315200-47330200	Weak transcription	Adipose Nuclei	Adipose
7	chr21:47320200-47330200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr21:47321800-47333000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr21:47321800-47337800	Weak transcription	Primary T cells from cord blood	blood
10	chr21:47322200-47335200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr21:47322400-47330200	Weak transcription	Right Ventricle	heart
12	chr21:47325000-47331400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr21:47325600-47335600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr21:47326000-47330800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr21:47326200-47333000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr21:47327000-47335600	Weak transcription	Fetal Thymus	thymus
17	chr21:47327200-47331200	Enhancers	Fetal Heart	heart
18	chr21:47327600-47328800	Enhancers	Stomach Smooth Muscle	stomach
19	chr21:47328200-47328600	Strong transcription	Thymus	Thymus
20	chr21:47328400-47328800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr21:47328400-47329200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr21:47328400-47329600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr21:47328400-47330200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr21:47328400-47331200	Enhancers	Spleen	Spleen
25	chr21:47328600-47328800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr21:47328600-47329400	ZNF genes & repeats	Thymus	Thymus
27	chr21:47328800-47329000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
28	chr21:47328800-47329000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
29	chr21:47328800-47329600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr21:47328800-47330200	Weak transcription	Stomach Smooth Muscle	stomach
31	chr21:47329000-47329200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr21:47329000-47329600	Enhancers	Brain Germinal Matrix	brain
33	chr21:47329000-47330400	Enhancers	Esophagus	oesophagus
34	chr21:47329000-47331000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr21:47329200-47329600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr21:47329200-47329600	Enhancers	Brain Substantia Nigra	brain
37	chr21:47329200-47329800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr21:47329200-47330200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr21:47329200-47331200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr21:47329400-47334400	Strong transcription	Thymus	Thymus
41	chr21:47329600-47330000	Weak transcription	Brain Germinal Matrix	brain
42	chr21:47329600-47330000	Weak transcription	Brain Substantia Nigra	brain
43	chr21:47329600-47330200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr21:47329600-47330200	Enhancers	Fetal Muscle Trunk	muscle
45	chr21:47329600-47333400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr21:47330000-47330800	Enhancers	Brain Germinal Matrix	brain
47	chr21:47330000-47331000	Enhancers	Brain Substantia Nigra	brain
48	chr21:47330200-47330400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr21:47330200-47330400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr21:47330200-47330400	Flanking Active TSS	Fetal Muscle Trunk	muscle

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