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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS101-18610
Organism
Homo sapiens
Tissue/cell
HT29
Coordinate
chr17:40260130-40260740
Target genes
Number: 22
Name
Ensembl ID
KRT19
ENSG00000171345
KRT17
ENSG00000128422
EIF1
ENSG00000173812
HAP1
ENSG00000173805
JUP
ENSG00000173801
FKBP10
ENSG00000141756
RP11
ENSG00000259623
KLHL11
ENSG00000178502
CNP
ENSG00000173786
NKIRAS2
ENSG00000168256
DNAJC7
ENSG00000168259
DHX58
ENSG00000108771
KAT2A
ENSG00000108773
HSPB9
ENSG00000197723
RAB5C
ENSG00000108774
KCNH4
ENSG00000089558
GHDC
ENSG00000167925
STAT5B
ENSG00000173757
STAT3
ENSG00000168610
PTRF
ENSG00000177469
TUBG1
ENSG00000131462
HMGN2P42
ENSG00000214578
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr17
40260269
40260400
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH17I042107
chr17
40259219
40260904
Enhancer Sequence
GCAAGAGGAG AGTTGGAGGG GATTCCCATA CACGTTGGAG GATGGGCACC CAGTGGGGGT 60
GCTGACCCCG GCGTGTAGCA CACCGCGACT GCCTCACCCA TCTGTCTTAG CTGTGGTGTG 120
AGCTCCAGAG GGAGGCCGGC TAGGGTGTGG GGGAGTCCTG CCCTGTCTCA CCCGCGATGT 180
GCTCTTACCC TTTGGCCTGG GCACGGTGAT GCCTAGTGTA AGGCACATGG ACGTGCTTTG 240
GTCAAGGAAT AGGCCGAGGC GGACATCCGG GCCAGAGTGA CTCAGCGAGT TTGGGGGGCA 300
GGCACGTACT CCACTTGCTA TATAACCTGT TTGTGTAAGT TCATACTGGA CTCTACTGTC 360
AGTAGAAGGT AAAACTGCCC TGCTGACGCT GTTCACGGAG CTTGGTTCAG CTCGGCACGG 420
CAGGGCACGC TTGCTCGCCC AGAGAGAGAA TAATGCTACT AACCCCTGCA AGGGACAGCC 480
GGTCGCCTTG AAGGTGGGCA GTGGGGAGCC AGGAACCCGC TTGTGCCCAG AGGGAAAGAG 540
TTAAGCTGCT GACCCTGACA GAGCTGGCCT TGCCGGCCAG GGAGAGCAGC TGCAGGCGTG 600
GGGGCAGCAG 610