Variant report

Variant	rs162372
Chromosome Location	chr21:44928863-44928864
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:44926548..44929321-chr21:44932759..44934671,2	K562	blood:
2	chr21:44760744..44765599-chr21:44927861..44932973,6	MCF-7	breast:
3	chr21:44839515..44855046-chr21:44918803..44938582,70	MCF-7	breast:
4	chr21:44923096..44924889-chr21:44928271..44930094,2	K562	blood:
5	chr21:44928800..44930891-chr21:45050840..45052850,2	MCF-7	breast:
6	chr21:44928466..44930891-chr21:45052329..45054531,3	MCF-7	breast:
7	chr21:44926844..44929090-chr21:44929410..44931125,2	K562	blood:
8	chr21:44925704..44927836-chr21:44928810..44931005,2	K562	blood:
9	chr21:44926667..44929719-chr21:45029857..45032741,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000142178	Chromatin interaction

Extended variants
information (count: 164 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:145)

rs_ID	r²[population]
rs1003280	1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs1073522	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[YRI][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1122873	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[YRI][hapmap];0.93[ASN][1000 genomes]
rs11701518	0.87[CHB][hapmap]
rs11909064	0.80[JPT][hapmap]
rs12165286	0.85[YRI][hapmap]
rs12626757	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12627667	1.00[CHB][hapmap];0.93[JPT][hapmap];0.80[ASN][1000 genomes]
rs1378079	1.00[CHB][hapmap];0.82[JPT][hapmap];0.95[ASN][1000 genomes]
rs1378080	1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[YRI][hapmap];0.95[ASN][1000 genomes]
rs141521	1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs1454648	1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs1454650	1.00[CHB][hapmap];0.94[JPT][hapmap];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1454651	1.00[CHB][hapmap];0.94[JPT][hapmap];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1584917	1.00[CHB][hapmap];0.94[JPT][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1584918	1.00[CHB][hapmap];0.93[JPT][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1598206	1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs162343	0.86[CHB][hapmap];0.93[JPT][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs162344	1.00[CHB][hapmap];0.93[JPT][hapmap];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs162345	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs162366	1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs162367	0.86[CHB][hapmap];0.87[JPT][hapmap];0.95[ASN][1000 genomes]
rs162368	0.99[ASN][1000 genomes]
rs162369	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs162371	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs162373	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs162374	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs162375	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs162376	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs162377	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs162378	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs162380	0.86[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs162381	0.86[CHB][hapmap];0.93[JPT][hapmap];0.94[ASN][1000 genomes]
rs162388	1.00[CHB][hapmap];0.93[JPT][hapmap];0.96[ASN][1000 genomes]
rs162389	0.99[ASN][1000 genomes]
rs162390	0.86[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs162391	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs162392	0.86[EUR][1000 genomes]
rs162393	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs162394	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs162395	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs162396	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs162398	0.86[CHB][hapmap];0.93[JPT][hapmap];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs162399	0.86[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs162400	0.86[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs162402	0.97[ASN][1000 genomes]
rs162403	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs162404	0.95[ASN][1000 genomes]
rs167930	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1836856	0.87[CHB][hapmap]
rs189094	1.00[ASN][1000 genomes]
rs2051407	0.80[ASN][1000 genomes]
rs2155722	0.80[JPT][hapmap]
rs2236666	0.80[JPT][hapmap]
rs2246602	1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs2250773	0.80[JPT][hapmap]
rs2251253	0.80[JPT][hapmap]
rs229340	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs229357	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[YRI][hapmap];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2298561	0.80[JPT][hapmap]
rs230640	0.86[CHB][hapmap];0.93[JPT][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs230642	0.86[CHB][hapmap];0.93[JPT][hapmap];0.95[YRI][hapmap];0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs230643	0.97[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs230644	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs230645	0.86[CHB][hapmap];0.93[JPT][hapmap];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs230646	0.86[CHB][hapmap];0.93[JPT][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs230647	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2329442	1.00[CHB][hapmap];0.94[JPT][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2329443	0.82[ASN][1000 genomes]
rs2838316	1.00[CHB][hapmap];0.93[JPT][hapmap];0.95[YRI][hapmap];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2838317	1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs2838319	1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs2838320	0.86[CHB][hapmap];0.95[YRI][hapmap];0.89[EUR][1000 genomes]
rs2838321	1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs2838322	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2838323	1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs2838324	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[YRI][hapmap];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2838325	0.81[CHB][hapmap]
rs2838326	0.81[CHB][hapmap]
rs2838328	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs2838329	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2838330	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs2838331	1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2838336	1.00[CHB][hapmap];0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs2838337	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[YRI][hapmap];0.81[ASN][1000 genomes]
rs2838338	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs2838339	1.00[CHB][hapmap];0.88[JPT][hapmap];0.95[YRI][hapmap];0.80[ASN][1000 genomes]
rs2838340	0.81[CHB][hapmap]
rs2838341	1.00[CHB][hapmap];0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs2838343	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs2838344	0.80[JPT][hapmap]
rs2838348	0.80[JPT][hapmap]
rs2838350	0.80[JPT][hapmap]
rs2838351	0.80[JPT][hapmap]
rs28840140	0.93[ASN][1000 genomes]
rs35110281	0.80[ASN][1000 genomes]
rs3788062	1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs3819161	0.80[JPT][hapmap]
rs389278	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs463738	0.97[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs4818833	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4818843	0.94[ASN][1000 genomes]
rs4818850	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs4818856	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4818858	0.80[JPT][hapmap]
rs4819212	0.87[CHB][hapmap]
rs4819219	0.87[CHB][hapmap];0.91[YRI][hapmap]
rs4819264	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4819270	1.00[CHB][hapmap];0.94[JPT][hapmap];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4997353	0.88[ASN][1000 genomes]
rs58451308	0.80[ASN][1000 genomes]
rs6518301	1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs6518302	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6518309	1.00[CHB][hapmap];0.93[JPT][hapmap];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6518310	0.80[JPT][hapmap]
rs7275705	0.83[ASN][1000 genomes]
rs7276215	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[YRI][hapmap];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7276316	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7276633	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs7277539	0.86[CHB][hapmap];0.93[JPT][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7279958	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs7279959	0.86[CHB][hapmap];0.80[JPT][hapmap]
rs7279968	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs7282122	0.80[JPT][hapmap]
rs7282933	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7283362	0.87[CHB][hapmap]
rs762400	0.80[JPT][hapmap]
rs8131020	0.87[CHB][hapmap]
rs8133523	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[YRI][hapmap]
rs86138	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs86139	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs91424	0.86[CHB][hapmap];0.93[JPT][hapmap];0.94[ASN][1000 genomes]
rs9306159	1.00[CHB][hapmap];0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs9974710	0.82[ASN][1000 genomes]
rs9976441	1.00[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs9976443	0.80[ASN][1000 genomes]
rs9978811	1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs9978934	0.91[YRI][hapmap]
rs9979935	0.91[YRI][hapmap]
rs9980185	0.93[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs9981291	1.00[CHB][hapmap];0.94[JPT][hapmap];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9981790	1.00[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs9983752	0.95[YRI][hapmap]
rs9983763	1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9984002	0.94[JPT][hapmap];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv913831	chr21:44563995-44931821	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
2	nsv1057726	chr21:44711850-44957303	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	nsv544466	chr21:44711850-44957303	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
4	nsv913838	chr21:44740134-44931821	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
5	nsv913839	chr21:44750200-44931821	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
6	nsv913847	chr21:44792003-44931821	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
7	nsv913868	chr21:44835508-44954522	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Genic enhancers 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 miRNA target site	98 gene(s)	inside rSNPs	diseases
8	esv1839560	chr21:44864079-44973184	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases
9	nsv913873	chr21:44879869-45142427	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
10	nsv587689	chr21:44884252-44986050	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
11	nsv1061369	chr21:44886596-44931388	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS 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	26 gene(s)	inside rSNPs	diseases
12	nsv544468	chr21:44886596-44931388	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
13	nsv1059264	chr21:44895863-44944515	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
14	nsv1061539	chr21:44915533-45041824	Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
15	nsv1067171	chr21:44921187-45039471	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
16	nsv521700	chr21:44925334-45041790	Enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
17	nsv470903	chr21:44925334-45061501	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
18	nsv459289	chr21:44925334-45064600	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
19	nsv587690	chr21:44925334-45064600	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:44918800-44930200	Weak transcription	Fetal Kidney	kidney
2	chr21:44919800-44936800	Weak transcription	Fetal Brain Female	brain
3	chr21:44922800-44936000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr21:44923400-44929000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr21:44923400-44934000	Weak transcription	Gastric	stomach
6	chr21:44923400-44936600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr21:44923400-44936600	Weak transcription	Brain Germinal Matrix	brain
8	chr21:44924000-44930200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr21:44924200-44929800	Weak transcription	HMEC	breast
10	chr21:44924400-44929200	Weak transcription	A549	lung
11	chr21:44925400-44930000	Weak transcription	Right Atrium	heart
12	chr21:44926200-44929400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr21:44926400-44930000	Weak transcription	Left Ventricle	heart
14	chr21:44926600-44929200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr21:44926800-44938200	Enhancers	Fetal Thymus	thymus
16	chr21:44927000-44929200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr21:44927000-44929800	Weak transcription	Esophagus	oesophagus
18	chr21:44927000-44929800	Weak transcription	Thymus	Thymus
19	chr21:44927000-44930000	Weak transcription	Placenta	Placenta
20	chr21:44927000-44930000	Weak transcription	Psoas Muscle	Psoas
21	chr21:44927000-44930400	Weak transcription	HepG2	liver
22	chr21:44927000-44930600	Weak transcription	Stomach Mucosa	stomach
23	chr21:44927200-44930800	Weak transcription	Fetal Lung	lung
24	chr21:44927800-44929800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr21:44927800-44930200	Weak transcription	Fetal Intestine Small	intestine
26	chr21:44927800-44930200	Weak transcription	Pancreas	Pancrea
27	chr21:44928000-44929000	Weak transcription	NHEK	skin
28	chr21:44928000-44929200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr21:44928000-44929400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr21:44928000-44930400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr21:44928200-44929200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr21:44928200-44929200	Weak transcription	HSMMtube	muscle
33	chr21:44928200-44929800	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr21:44928200-44930200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr21:44928400-44929200	Weak transcription	HSMM	muscle
36	chr21:44928400-44929800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr21:44928400-44930600	Weak transcription	Ovary	ovary
38	chr21:44928600-44929000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr21:44928800-44929800	Weak transcription	Brain Cingulate Gyrus	brain
40	chr21:44928800-44941000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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