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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS101-10384
Organism
Homo sapiens
Tissue/cell
HT29
Coordinate
chr12:52711760-52712930
Target genes
Number: 20
Name
Ensembl ID
RP11
ENSG00000257851
ACVR1B
ENSG00000135503
GRASP
ENSG00000161835
NR4A1
ENSG00000123358
C12orf44
ENSG00000123395
KRT80
ENSG00000167767
KRT7
ENSG00000135480
RP3
ENSG00000257671
AC021066.1
ENSG00000170442
KRT121P
ENSG00000135477
KRT81
ENSG00000205426
KRT85
ENSG00000135443
KRT18
ENSG00000111057
KRT8
ENSG00000170421
EIF4B
ENSG00000063046
SPRYD3
ENSG00000167778
ITGB7
ENSG00000139626
RARG
ENSG00000172819
PFDN5
ENSG00000123349
C12orf10
ENSG00000139637
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3
Chromosome
Start
End
chr12
52712741
52712805
chr12
52712475
52712525
chr12
52712325
52712399
Enhancer Sequence
TGAGCAGGGA GAACAGGACC TTGTCTGAAC AGCTCTTGAT CTTGGCCATG AGCATATATG 60
CAAAGGAGTC TCTTTCCTAG ACCTCCCCCT GCTTGTCTCC TGCCCCCAAG TGAAATGGGT 120
GGGGCTCTGC AGGAACCAGG CTGCTGGCCT GGGTACTACT GGGATGCACT GGAGAAATGA 180
AGTGCCTACT CCCCTGTTTT TTTTTGTTTT TGTTTTTGAG ATGGAGTCTC GCTCTGTCGC 240
CCAGGTTGGA GCACAGTGGC GCGGTCTCGG CTCACTGCAA GCTCCGCCTC CCAGGTTCAT 300
GCCATTCTCC CCTCTCAGCC TCCCGAGTAG CTGGGACTAC AGGTGCCCAC CACCACGCCT 360
GGCTAATTCA CTCCCCTGTT TTGGTGGAGG TTGGGAGAGC AGGATCTGGA AGCTGAGTGT 420
GTGAATGTGT GTGGTTGGGG AGTGGGAGGT GCTGTTTTTC TCGCCTAGGT CTCCATCTTT 480
TCTTCCTTCG AGCCCTCCCC TGCCCCCACT CAGCTGCAGG TGGTGGGATC CTCGCTCTGT 540
CTCTCCCCTC CTGGCCTGAG CTGTGGGAGG CAGCTCAGAG ACAGGGAGGG AGGGGTATGC 600
TGGGCCTGGG GAGTCCATGG AGAGAATGTT ACTGAAGGAA GCTGGCCACC CCTCAAAAGC 660
AGATTCCTTC TGAGGATCCA GTGCGTATTC TTCATACCAT ATATCACACT TTGTAGCTGA 720
AGGGCTAGAT CTGTGGCTCT GTCATGACTG CCTTCCAGCA GACTGCAGGC TCCACAAGAA 780
CCCGCACTGT GTGGCTTGCG TGGCCCTGTG TCACTATCAC CAGCACAGCG TGCTGCATGT 840
GGTAGGTGAT CAGATAGTGT TAGCTGAGTG AGAGAGCAAA CTTAGGAAGA CACATGTCCA 900
GGACTTTGAG ATCTGGTCTC AAAGGGACCC AGGAATACAA GTTTTTGTGA AAAATGGATG 960
GAGAAAGGGA GAGAGCATTG TTTCCCTGAT CTGCTGGTGG AAAGACAAGC TGAGCCTCCA 1020
TCCCCCACAC CCAAGGGACC CCTGTGTCTC AAACAGGGGG TACAGGTTCT TCTCCACTCT 1080
CAGGCAGAGA TGCCAGCTGC AGACTGGATA CTCCTCCGGG CTCAGGGAGC TGCCACCATG 1140
CTATTTCCTG TGCCCAGAAC CCCTCCTGCC 1170