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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS184-13567
Organism
Homo sapiens
Tissue/cell
T47D
Coordinate
chr17:40858680-40859190
Target genes
Number: 26
Name
Ensembl ID
AC067852.1
ENSG00000256929
NAGLU
ENSG00000108784
HSD17B1
ENSG00000108786
COASY
ENSG00000068120
MLX
ENSG00000108788
PSMC3IP
ENSG00000131470
TUBG1
ENSG00000131462
FAM134C
ENSG00000141699
TUBG2
ENSG00000037042
PLEKHH3
ENSG00000068137
CCR10
ENSG00000184451
CNTNAP1
ENSG00000108797
CTD
ENSG00000239671
EZH1
ENSG00000108799
VPS25
ENSG00000131475
WNK4
ENSG00000126562
CCDC56
ENSG00000183978
CNTD1
ENSG00000176563
BECN1
ENSG00000126581
PSME3
ENSG00000131467
AOC2
ENSG00000131480
AOC3
ENSG00000131471
AC100793.2
ENSG00000213373
SNORA40
ENSG00000212149
Y
ENSG00000200127
VAT1
ENSG00000108828
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr17
40858811
40859116
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH17I042706
chr17
40858644
40859090
Enhancer Sequence
GAGCAACAGA GCTGAGATCC TGTCTCAAAA AAATTTAAAA AATGAAAAAA AAAGCAGGTA 60
TACTAATAAG AAGTGTCCCC TAGAGATTCC CCAACAATCC TCTCCCTCCC ACTGAGGTGG 120
AGAGTACCCC AGAGAATATG AAATCAGTGT GTTTCACTGG TAAATTGTCA CCATCAAAAC 180
AAGTATCATT TTGAGAACAG AATGCATCCG TTCTATGCCA TCCTTCTCCA CCCACTGCCC 240
AACCCAGCGC AACCACTTCT CTGCTGCGGC TAAGATCACT ATCTGCTATG GGTTAGGAGG 300
TATTTCCTCC AGCAAAACCG CCTGGGCACC AAGTTCTGCA AGCTGTGGGG ACTGCCATCA 360
AACTGCTCAG CTTTGAGTTG GGAAGGGCAT GGTGGGATAA GAAGTAAAAG ATAAGTACCC 420
GGATGTCTCT GCTGACATCC AGGCCCCTGT CTTCTACCTG ATATTAAAAC TCCAGCTATG 480
AAATGAAAAT AGACATACAC AGAATCACAA 510