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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS098-20976
Organism
Homo sapiens
Tissue/cell
HSMM
Coordinate
chr16:2346540-2347300
Target genes
Number: 25
Name
Ensembl ID
RP11
ENSG00000259933
PKD1
ENSG00000008710
RAB26
ENSG00000167964
TRAF7
ENSG00000131653
CASKIN1
ENSG00000167971
MLST8
ENSG00000167965
C16orf79
ENSG00000182685
PGP
ENSG00000184207
E4F1
ENSG00000167967
ECI1
ENSG00000167969
AC009065.1
ENSG00000167970
RNPS1
ENSG00000205937
ABCA17P
ENSG00000238098
ABCA3
ENSG00000167972
ATP6V0C
ENSG00000185883
AMDHD2
ENSG00000162066
CEMP1
ENSG00000205923
PDPK1
ENSG00000140992
CTD
ENSG00000261093
AC141586.5
ENSG00000215154
PDPK2
ENSG00000205918
KCTD5
ENSG00000167977
SRRM2
ENSG00000167978
TCEB2
ENSG00000103363
FLYWCH2
ENSG00000162076
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr16
2346808
2347135
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH16I002296
chr16
2346261
2347412
Enhancer Sequence
GTCCTCTTTA GAGACAAGGA TGCCAGGCCC AGGAAGAACA ATGGCTCTGC CAACTGGGCA 60
GTGGGGCAGG AAGTGGCTAG TGAAACTCTC AGAGGCCGTG GTGGATGGTT CCTCATCTCC 120
TAACGCCTGC TGTCCTCCCT CTTGGTAACA AAACCCTGGT ATCTTGGCTG AGCATGTGGC 180
TGCCCAGGAC AAAGGCCATC CCCTCCAGCC TACTGCTGAC CACACTGGGT TGCCACTCAG 240
TCACTAGGGG GCAGAAGTGG GACGTGAACT TGGGGGGTGT CCTGAGGGGA GGAGGGCTCC 300
TATGTCTTTG CTCCACCCCG TTGGAATGTG GGGGACGCTG GCACACCCAG ATCGTGCTGG 360
ACCAGGAGGT GACCTTGAAA GGGAAGCCGT AGTTGCACAG TACAGTCAGA GGTCTGGGCC 420
CAGATCCTGT CAGCCCCTGC TGGCCCTGGC CATGCTGTGA GCTGCTCTCA CGTGGGAGCT 480
GCCATGTTGG TGCGTGTGTT GGCCTCTCCA AGGGCAGTGC TGCTCCTAGT GGCACTAGGC 540
TTGGCCTCTG TTCTTCTGGT CATGGCTGAA CCACATCCTA ACCAAATTGA GACTTTCAGC 600
TCCATTTCCT GCCTCTTCCC TCTCACAAGC CCCCCTGCCT GGTTGGGCTC TCCACCCAGA 660
GGCAACAGAC AGGAAGTCTA GAAAAGGCCA CCCCTGCCTG ATCTGAGGGC CCTTCATGAA 720
GGTAGCAGCC ATTCCCTCAG CACGGCAGCC AGGACACCGA 760