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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS129-00658
Organism
Homo sapiens
Tissue/cell
MCF10A
Coordinate
chr1:27285580-27286840
Target genes
Number: 31
Name
Ensembl ID
UBXN11
ENSG00000158062
HMGN2
ENSG00000198830
RPS6KA1
ENSG00000117676
AL627313.1
ENSG00000243905
RP5
ENSG00000260063
ARID1A
ENSG00000117713
PIGV
ENSG00000060642
ZDHHC18
ENSG00000204160
SFN
ENSG00000175793
RP1
ENSG00000226698
GPN2
ENSG00000142751
NUDC
ENSG00000090273
GPATCH3
ENSG00000198746
NR0B2
ENSG00000131910
C1orf172
ENSG00000175707
RP11
ENSG00000172746
OSTCP2
ENSG00000225294
TRNP1
ENSG00000253368
FAM46B
ENSG00000158246
SLC9A1
ENSG00000090020
SNRPEP7
ENSG00000225990
WDTC1
ENSG00000142784
TMEM222
ENSG00000186501
U6
ENSG00000206888
SYTL1
ENSG00000142765
MAP3K6
ENSG00000142733
CD164L2
ENSG00000174950
GPR3
ENSG00000181773
WASF2
ENSG00000158195
AHDC1
ENSG00000126705
IFI6
ENSG00000126709
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr1
27286400
27286800
Enhancer Sequence
GTGAAGTGAC TGGCCCAGAG ACACCTAGCA AGAGAGGGCT GGAGTAAGAT TTGCACTGTG 60
GCCCGCCAGG CTCTGAAGCC TGCGTACTTT GTGTGTGCCA CACATCTCCA GCGGTGGTGG 120
GATGAGAAGA GAAGACCTGG GATAAGGACA ATGCCTGCCT CAGTTCCCCA CTTCCCTCCA 180
GCCATTGAAC CCTCCTGAAG TCAAACTCAG GCAGTTTCTT CCAGGCTGTA TCTCCCCGAC 240
CCTGCTGCCA CCGCCCCGCC ACCACCCCGC CCAATCCTAG GAACCTGGTC ACTTGGTTTA 300
GTGAGGGGAG ACTCCCTGTC CCTATTGTGG CTTGAGGCAA GATTCTTAAC CTCACTTTCC 360
TCATCTTTAA ATAAGGAGAG ACTAGTATCT TCATGCCCCG CCAATCCCGT GAGATTTAAA 420
TGAAATATTG AGTGCAGGGG GCTTCCCGCA GTGGCCTTGC CCATGGGAGG GGCTAGGTCA 480
CTAGGCGATC TAAGGCACCG CAAGGATGTT CCCGGGGGTC AGAGGGTCCC GGCCCGCCCT 540
CCCTGGATTT CTCGTTGATG CTTTCCTCTT CCCCCTTAGT CCCGCGAACA CACACACACA 600
CTCAAGGGTC TATGTACCGT CCCCTCCTCC GAGGGTCCCC AGGACAGGCC CGGCCGCACC 660
AGCCTCTGCC CCCAGCCCAG TGCCAAGCCT CGGACACCCG GCCGGGGAGG ACCACCCCAG 720
TCCTGCTCGA GAAACAGCCG TCGGCTCAGT GCACCCTCGG CCTCCTGCCC CAAAGGTGCA 780
GCCCGAGAGT CCCATATCCG CGGGCAGCTA GTCCTGGGGA CAAGGAAGAA CCAGATCCTG 840
GCACTGTCCC CCGGGCTACC ACAGCCCCTA CACCAACTCT GCCCTCGGGG CGAGCACTAC 900
CCTCTCCAGC TGCAAGGGCC CTACCCCGCG GGCGGACCCA GCCTCCCTCC CGTCCCGACG 960
CTGTTCCTCG GGGTGAGCAC CAGCGTTTGT CCCATCCCGA CGCTGCCCCC CGGTGAGTGC 1020
GGCCCCCGCA CCCAGCCAGT GCAGCCCTAA GGGCGAACGC GGCCCCTCAC CCCATTCTGC 1080
GCGCCCAGCC CGGGCGCCCG CTCAGGCCGC TCCCCAGCCC GGCCCGCGCA CCCCGGAAGT 1140
AGGAGGGTGG CCCCCGAGGA ACCGGGCCCG GGACCCTCTC CTGTCCGGGC TCAGCTTCGG 1200
GGGGCTCCCG ACACCGGCGC CGCCCTGGCT TGCGCCCCCC TGGGCCCGCG CCGGGCTTAC 1260