Variant report

Variant	rs45621438
Chromosome Location	chr21:45790238-45790239
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:45783291..45785038-chr21:45790105..45792428,2	MCF-7	breast:
2	chr21:45789259..45790797-chr21:45809641..45812634,2	MCF-7	breast:
3	chr21:45757587..45760440-chr21:45787714..45792009,6	MCF-7	breast:
4	chr21:45789103..45790840-chr21:45794560..45797280,2	K562	blood:
5	chr21:45759142..45761625-chr21:45788983..45791784,2	MCF-7	breast:
6	chr21:45758998..45760559-chr21:45788952..45791849,2	K562	blood:

Variant related genes	Relation type
ENSG00000160226	Chromatin interaction
ENSG00000232969	Chromatin interaction

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs11088949	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11700418	0.91[EUR][1000 genomes]
rs11702292	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11702323	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11908957	0.91[EUR][1000 genomes]
rs11908983	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11911248	0.97[EUR][1000 genomes]
rs11911332	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12626312	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12626318	0.81[EUR][1000 genomes]
rs12627182	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13313851	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1556314	0.96[EUR][1000 genomes]
rs2226686	0.97[EUR][1000 genomes]
rs2276252	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2838553	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2838554	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2838555	0.93[EUR][1000 genomes]
rs2838556	0.96[EUR][1000 genomes]
rs2838557	0.93[EUR][1000 genomes]
rs28532655	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28636732	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28688635	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28709583	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28752243	0.97[EUR][1000 genomes]
rs4169	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs45457102	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs45590835	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4818713	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4818714	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4818715	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4818716	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4818910	0.91[EUR][1000 genomes]
rs4818911	0.91[EUR][1000 genomes]
rs4818912	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4818913	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4818915	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4818917	0.94[EUR][1000 genomes]
rs55712486	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56195574	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62218764	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62218765	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62218767	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62218769	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7277517	0.99[EUR][1000 genomes]
rs7278527	0.96[EUR][1000 genomes]
rs73231283	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs762426	0.93[EUR][1000 genomes]
rs9974187	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9974189	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9974813	0.92[EUR][1000 genomes]
rs9975269	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9977290	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9980508	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9982831	0.93[EUR][1000 genomes]
rs9984977	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33817	chr21:45169412-46031810	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv1064420	chr21:45460089-45814986	Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	nsv544472	chr21:45460089-45814986	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
4	nsv913898	chr21:45555079-45941566	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	74 gene(s)	inside rSNPs	diseases
5	nsv428042	chr21:45560437-45848190	Enhancers Active TSS Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
6	nsv459295	chr21:45629565-45849864	Genic enhancers Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
7	nsv587740	chr21:45629565-45849864	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
8	nsv913906	chr21:45657970-45818609	Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
9	esv3361489	chr21:45669073-46013747	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	69 gene(s)	inside rSNPs	diseases
10	nsv913911	chr21:45681153-45893907	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
11	nsv913918	chr21:45697755-45941566	Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	60 gene(s)	inside rSNPs	diseases
12	nsv913920	chr21:45699404-45824792	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
13	nsv913921	chr21:45699404-45854431	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
14	nsv913922	chr21:45699404-45893907	Genic enhancers Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
15	nsv913928	chr21:45700641-45811343	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
16	nsv913929	chr21:45700641-45860912	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
17	nsv913930	chr21:45700641-45893907	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
18	nsv913933	chr21:45703660-45811343	ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
19	nsv913936	chr21:45709153-45811343	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
20	nsv913937	chr21:45709153-45865167	Genic enhancers Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
21	nsv913939	chr21:45712588-45818609	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
22	nsv913940	chr21:45712588-45893907	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
23	nsv913941	chr21:45722442-45885589	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
24	nsv1058359	chr21:45724055-45941566	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
25	nsv1065203	chr21:45731690-45941566	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
26	nsv544473	chr21:45731690-45941566	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
27	nsv913942	chr21:45740823-45941566	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
28	nsv913943	chr21:45740823-46031810	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
29	nsv1059107	chr21:45749304-45813036	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
30	nsv1067264	chr21:45757599-45941566	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
31	nsv544474	chr21:45757599-45941566	Bivalent/Poised TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
32	nsv913944	chr21:45757905-45941566	Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
33	nsv587781	chr21:45764397-45867471	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
34	esv1837121	chr21:45768598-45829570	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
35	esv3442899	chr21:45787949-45790697	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45771200-45795800	Weak transcription	Brain Angular Gyrus	brain
2	chr21:45776600-45794600	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr21:45780200-45793600	Weak transcription	Primary T cells from cord blood	blood
4	chr21:45780400-45795000	Weak transcription	Thymus	Thymus
5	chr21:45783200-45792600	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr21:45783600-45794400	Weak transcription	Primary B cells from peripheral blood	blood
7	chr21:45783800-45794600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr21:45784200-45793800	Weak transcription	Primary B cells from cord blood	blood
9	chr21:45784400-45795600	Weak transcription	Right Atrium	heart
10	chr21:45788200-45793200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr21:45788800-45790400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
12	chr21:45788800-45790400	Enhancers	Esophagus	oesophagus
13	chr21:45788800-45790600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
14	chr21:45788800-45790600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr21:45788800-45791000	Enhancers	Pancreas	Pancrea
16	chr21:45788800-45791200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr21:45789200-45790400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr21:45789200-45790600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
19	chr21:45789200-45790600	Enhancers	Liver	Liver
20	chr21:45789400-45790400	Weak transcription	Spleen	Spleen
21	chr21:45789400-45790600	Enhancers	HMEC	breast
22	chr21:45789400-45790800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr21:45789800-45790400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
24	chr21:45789800-45790400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr21:45789800-45790400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr21:45789800-45790400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
27	chr21:45789800-45790400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
28	chr21:45789800-45790400	Bivalent Enhancer	Fetal Stomach	stomach
29	chr21:45789800-45790400	Bivalent Enhancer	K562	blood
30	chr21:45789800-45790600	Bivalent Enhancer	Colonic Mucosa	Colon
31	chr21:45789800-45790800	Flanking Active TSS	HepG2	liver
32	chr21:45790000-45790400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
33	chr21:45790000-45790400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr21:45790000-45790400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr21:45790000-45790400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr21:45790000-45790400	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr21:45790000-45790400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
38	chr21:45790000-45790400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
39	chr21:45790000-45790400	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr21:45790000-45790400	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
41	chr21:45790000-45790400	Active TSS	Right Ventricle	heart
42	chr21:45790000-45790400	Flanking Active TSS	Hela-S3	cervix
43	chr21:45790000-45790400	Enhancers	HSMM	muscle
44	chr21:45790000-45790400	Active TSS	Monocytes-CD14+_RO01746	blood
45	chr21:45790000-45790600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr21:45790000-45790600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr21:45790000-45790600	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
48	chr21:45790000-45790600	Flanking Active TSS	Ovary	ovary
49	chr21:45790000-45790600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
50	chr21:45790000-45790800	Bivalent Enhancer	Fetal Intestine Large	intestine

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