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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS101-02898
Organism
Homo sapiens
Tissue/cell
HT29
Coordinate
chr1:156367900-156368630
Target genes
Number: 31
Name
Ensembl ID
RXFP4
ENSG00000173080
RP11
ENSG00000224276
ARHGEF2
ENSG00000116584
SSR2
ENSG00000163479
UBQLN4
ENSG00000160803
LAMTOR2
ENSG00000116586
RAB25
ENSG00000132698
MEX3A
ENSG00000254726
LMNA
ENSG00000160789
SEMA4A
ENSG00000196189
SLC25A44
ENSG00000160785
PMF1
ENSG00000160783
BGLAP
ENSG00000242252
PAQR6
ENSG00000160781
SMG5
ENSG00000198952
TMEM79
ENSG00000163472
C1orf85
ENSG00000198715
C1orf182
ENSG00000163467
CCT3
ENSG00000163468
MEF2D
ENSG00000116604
IQGAP3
ENSG00000183856
APOA1BP
ENSG00000163382
GPATCH4
ENSG00000160818
BCAN
ENSG00000132692
CRABP2
ENSG00000143320
RRNAD1
ENSG00000143303
ISG20L2
ENSG00000143319
MRPL24
ENSG00000143314
PRCC
ENSG00000143294
HDGF
ENSG00000143321
SH2D2A
ENSG00000027869
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr1
156368207
156368504
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH01I156398
chr1
156367929
156368970
Enhancer Sequence
CTGACCTGGT GATCCGCCTG CCTCAGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA 60
CTGCACCTGG CTTATTTATT TTTTGAGACG GAGTTTTGCT CTTGTTACCC AGGCTGAAGT 120
GCAATAGCGC CATCTCTGCT CACTGCAATC TCCACCTCCT GGGTTCAAGC GATTCTCATG 180
CCTCAGCCTC CTGAGTAGCT GGGATTACAG GCGTGTTCCA CCACACCTGG CTAATTTTGT 240
ATATTTAGTA GAGATGGGGT TTCTCCATGT TGGTCAGGCT GGTCTGGAAC TCCCCACATC 300
AGGTGATCTT CCCGCCTTGG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACAGCAC 360
CCGGCCTTGT TCTCCATTTT AAAGTTTAAC TTCCTCATTC TTTGTCTCCT TGCCCCTAGT 420
CTCAGTAAAC AACTCCCTCC TAGCCTCTAT CACCTGCTCT GTCCTTAGTA ACCTGCTTTG 480
TCCTTAGTCA TCCTTAGTCA CCTGCTCTGT CCTTAGTCAT CCTTAGTCAC CTGCTCTGTA 540
ACCGTCCTTC CCGCCAAAAC TACTCACCCC ACCACTCCGG CTCCTACCCT CGCTCTCTTT 600
TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTTTGTG AGACGGAGTC TCGCTCTGTC 660
GCCCAGGCCG GACTGCAGAC TGCAGTGGCG CAATCTCGGC TCACTGCAAG CTCCGCCTCC 720
CGGGTTCACG 730