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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS101-27074
Organism
Homo sapiens
Tissue/cell
HT29
Coordinate
chr20:33280940-33281730
Target genes
Number: 31
Name
Ensembl ID
PXMP4
ENSG00000101417
ZNF341
ENSG00000131061
RP5
ENSG00000228265
RP1
ENSG00000229472
EIF2S2
ENSG00000125977
RPS2P1
ENSG00000225246
ASIP
ENSG00000101440
XPOTP1
ENSG00000214185
RP4
ENSG00000236456
AHCY
ENSG00000101444
ITCH
ENSG00000078747
CDC42P1
ENSG00000234933
FDX1P1
ENSG00000181741
DYNLRB1
ENSG00000125971
MAP1LC3A
ENSG00000101460
TP53INP2
ENSG00000078804
GGT7
ENSG00000131067
GSS
ENSG00000100983
MYH7B
ENSG00000078814
TRPC4AP
ENSG00000100991
PROCR
ENSG00000101000
MMP24
ENSG00000125966
EDEM2
ENSG00000088298
MT1P3
ENSG00000126005
EIF6
ENSG00000242372
UQCC
ENSG00000101019
CEP250
ENSG00000126001
FER1L4
ENSG00000088340
SPAG4
ENSG00000061656
7SK
ENSG00000222460
RBM12
ENSG00000244462
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr20
33281221
33281600
Enhancer Sequence
AGCTCTGTTG CCCAGGCTGG AGTGCAGTGG CACGATCTCG GCTCGTTGCA ACCTCTGCCT 60
CCTGGGTTCA AGTGATTCTC CTGCCTCAGC CTCCCGAGTA GCTGAGATCA CAGGCACCTG 120
CCACTACACC CAGCTAATAT TTGTATTTTT AGTAGAGATG GGGTTTTGCC ATGTTGGCCA 180
GGCAGCTGGC TGGTTTCAAA CTCCTGACCT CAAGTGATTT GCCCACCTCG GCCTCCCAAA 240
CTGCTGGGAT TACAGGCGTG AGCCACAGTG CCCAGCCTGT TACATCATTT AAAATCCATT 300
TTAATCTTTA AAAGTAGGCT TCAGGTGGAT GGAACACAAC CACAGCCTGG CAAAGGAATG 360
AGGCTGACTC TCCTCCTTCT GAGGGAAGTA TTCATGTTGT GCTCTTTGTC CCACTGCCTT 420
CCCCAAGGAC AGCCTGGCTC AGTGGAGGCA CCGGGGCTAC TCCTGGCATC ATTCCAGAGA 480
GCCTCTCTTG TCACCTCTTA CCCACTTGGC TCCCTGTCAC CAGTGTTCTG GGCTGGGCTG 540
AGAAGCAGCA CAGATTAACT ATTGGGTTGT ATCTCCAGAA GCCCCATCGA TGTCAGGTTG 600
GGCAGAGCCA GCCCAGGAAA CATGGAACAT CTGCCTCTGG CCTCTCACCT CTTTGTTCTC 660
CTACGAAGCC CGGCTTTTTT TTCTTTTTTT GAGACGGAGT CTGCTCTGTC ACCCAGGCTG 720
GAGTGCAGTG GCGCGGTCTC AGCTCACTGC AAGCTCCGCC TCCCAGGTTC ACCCCATTCT 780
CCTGCTTCAG 790