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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS139-09767
Organism
Homo sapiens
Tissue/cell
Myotube
Coordinate
chr11:65789350-65790310
Target genes
Number: 38
Name
Ensembl ID
SCYL1
ENSG00000142186
SSSCA1
ENSG00000173465
FAM89B
ENSG00000176973
EHBP1L1
ENSG00000173442
MAP3K11
ENSG00000173327
PCNXL3
ENSG00000197136
SIPA1
ENSG00000213445
RELA
ENSG00000173039
KAT5
ENSG00000172977
RNASEH2C
ENSG00000172922
KRT8P26
ENSG00000214659
AP001266.1
ENSG00000175827
AP5B1
ENSG00000254470
SNX32
ENSG00000172803
MUS81
ENSG00000172732
CFL1
ENSG00000172757
EFEMP2
ENSG00000172638
CTSW
ENSG00000172543
FIBP
ENSG00000172500
CCDC85B
ENSG00000175602
C11orf68
ENSG00000175573
DRAP1
ENSG00000175550
SART1
ENSG00000175467
BANF1
ENSG00000175334
EIF1AD
ENSG00000175376
CST6
ENSG00000175315
CATSPER1
ENSG00000175294
GAL3ST3
ENSG00000175229
SF3B2
ENSG00000087365
RP11
ENSG00000255038
PACS1
ENSG00000175115
KLC2
ENSG00000174996
RAB1B
ENSG00000174903
YIF1A
ENSG00000174851
CD248
ENSG00000174807
RIN1
ENSG00000174791
BRMS1
ENSG00000174744
B3GNT1
ENSG00000174684
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr11
65789725
65789997
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH11I066020
chr11
65787514
65790547
Enhancer Sequence
CTGCAGGAAC ACAGGGGTGC ACTCAGAGCT GTCCCCAGCA CCCAGTGCCC TCTCTCTCCT 60
CAGCATTAGC CTCACACAAG CCCAGATTCC CAGGCTCTCC CCGGCTCTGC GTAAGCAGCT 120
GCGCGACTTC ACTACTGCTG TGTCTCAGTT TTCTTGTCTT TAAAATGGGG ATAATTGTGT 180
CCAGGAGCAG TGGCTCACAC CTGTAATCCC AGCACATTGG GAGGTTGAGG CGGGCGCATC 240
ACTGGAGGTC AGGAGTTCGA GACCAGCCTG GCCAACATGG TGAAACCCTG TTTCTACCAA 300
AAATACAAAA ATTAGCTGGG CATGGTGGTG GGCACCTGTA GTCCCAGCTA CTTGGGAGGC 360
TGAGGCAGGA GAATCACTTG AACCCGGGAG GCGGAGGTTG CAGTGAGATC GCGCCACTGC 420
ACTCCAGCCT GGGTGACAGA GCCAGACTCC GTCTAAAATA AAATAAAATA AAATGGGGAT 480
AATTGAAGTC CACTTGATAG AGTTGTGAGC GTTAAATGCA TGAACACAAG CGAAGTGCTT 540
AGAATGGAGC CTGAGACAGC GAGCCGGGCA GCTCCTGTCC TTCACCCTGC TCCACGGCGT 600
TGGAGGGCCC AGCCTTCCCC GACCTTACAT CCTCGCCCCT CCAGGGCCTT CTCGGGCTCC 660
CGGCCCTTCC GCGAAGCTCG GGCTCCAGGC GCCCGCCCGC CCTCAGCCGC ACATTTGGAG 720
CAGATGCGCT CCCTAGTGGC TGCGGCGCGA ACAGCACCGC CTCCCGCCTA GCGGGTCCTT 780
CTGTCTCGGG CCGGCCTCAG CGGGGTCTTT CTGAGACGCT CTCTAATACT GGGTAAGGCC 840
ATCTACTTCC CAGGGGTGAG GATCAAGTGA GCTGAGTCCT ATAAACCGCC CGGCACTGGA 900
TCAGGCCCAC GGAGGTCCTG GAAGAGCATC GGTGGCTTCT CCATGGGAAC AGGACTCCCT 960