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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS101-02911
Organism
Homo sapiens
Tissue/cell
HT29
Coordinate
chr1:156568900-156571200
Target genes
Number: 32
Name
Ensembl ID
GON4L
ENSG00000116580
SSR2
ENSG00000163479
UBQLN4
ENSG00000160803
LAMTOR2
ENSG00000116586
RAB25
ENSG00000132698
MEX3A
ENSG00000254726
LMNA
ENSG00000160789
SLC25A44
ENSG00000160785
RP11
ENSG00000260238
PMF1
ENSG00000160783
BGLAP
ENSG00000242252
PAQR6
ENSG00000160781
SMG5
ENSG00000198952
TMEM79
ENSG00000163472
C1orf85
ENSG00000198715
C1orf182
ENSG00000163467
CCT3
ENSG00000163468
C1orf61
ENSG00000125462
MEF2D
ENSG00000116604
IQGAP3
ENSG00000183856
APOA1BP
ENSG00000163382
GPATCH4
ENSG00000160818
BCAN
ENSG00000132692
NES
ENSG00000132688
CRABP2
ENSG00000143320
RRNAD1
ENSG00000143303
ISG20L2
ENSG00000143319
MRPL24
ENSG00000143314
PRCC
ENSG00000143294
HDGF
ENSG00000143321
SH2D2A
ENSG00000027869
PEAR1
ENSG00000187800
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3
Chromosome
Start
End
chr1
156569323
156569386
chr1
156569600
156569800
chr1
156569679
156569892
Enhancer Sequence
TAAGAAGAAA GTAGAAAGTG CCCAAACAGC CATCAGTTCC ATCCTGACTG CTTGTTAAGA 60
ATTCTCTGCT AGTTGGGTGC AGTGGCACAC ACCTGTAGTC CCAGCTACAT GGGAGGCTGA 120
GGCGGGATTG CTTGAGTCCA GCCTGGGCAG TATAGCAAGA CCCTCTCTCA TAAAAAGAAT 180
AAAGCGGCCA GGCACAGTGG TTCACATTTG TAATCCCAGC ACTTTGGAAG GCCAAGGTAG 240
AAGAATCACT TGAGCCCAGG AGTTCCAGAC CAGTGTGGGC AACGTAGTGA AACCCTGCCT 300
CTAGAAAAAA TAAAAAATTA AAAAGAAAGA AAAAAGAATT CTCTTTCCTG AGCCAGAGAC 360
AGAGGAAGGA GGTGGCCTGG TCTTTGGGGA GCTCCCTATC TGGCTACAGA AAGAGCATAT 420
AGAGAAGTCA AGGAGGAATG GTGTCAATTC TGATACCTAA GTTTATGGTG TGCTCACCAC 480
ATGCCAGGAT GTGCTAAGAC TTTACAAAGA TTATTTCATT TAATCTTCCC AGCCCATTCA 540
GGGAAATATT AGCCTATTTT ACAAATGAGT AAAGTAAGGC CTAAAAAGGT TAAGTGACTT 600
CAAGGTCACA CAGGTAACAT GTAGAATTCA AGCCCAGGCA GCTTGTCTGC AGAATCTGTA 660
CTGTACCACT ACATAGTATC TCCCAAAATA TATTACCTTG TAAACACAAA GCTAATGAGG 720
TGCTTATTAA CCTGAGTCAT AAGATAATGG TACTCGGTAG AGACCAGATC CTGTACTTAT 780
GCTTCAGCAT TTACACTGTC CTCTTGGTGT GGGGGCTACA CACTTCTCCC ACACCACTGC 840
AGTATTTCAG TCTGGCTGGA GTTCCCCTTT TGAAAGTGTC CAACTTAGGA AGGGCACTCC 900
TATTGAGCAC TTAATGCATA ACAGGTGGAT TACACATATT GCCACACTGT CATATTAACT 960
CAGTCAATCT TTTTTTTTTT TTTTTTTTTG AGACAGGGTT GCTCTGTCGC CCAGGCTGGA 1020
TGGAGTGGAG TGCAGTGGCA CGATCATGGC TCATTGCAGC CTCAAACTTC CAGGCTCAAG 1080
CAATCCTCCC ACCTCAGCCT CCCAAGTAGC TAGGACCACA GGCACATGCC ACCACGCCTG 1140
GCTAATTTTT GTATTTTTTT TTGTACAGAC AGGGTTTTGC CATGTTGCCC AGGCTGGTCT 1200
CTAACTCCTG GGCTCAAGCG ATCTGCCTAC CTCTGCTTTC CAAAATGCTG GGATTACAGG 1260
CGTGAGCCAC TATGTGTGGG CTTAACTCAT TTAATCTTGA TAGTCCTGTG AGATAGATAT 1320
TATTCTTATT TTACAAATGA AGAAAACAAG GCCTGGGTTT CTTGCCTAAG GTTACATGGC 1380
TAGTAAATGA TGGAGCTGGA ATTACATGAT GGAGGTGGAA TGAGCCCAAG TCGCCTGACT 1440
CCAAAGTGGT CCTCTGTCTT TCTTTTTTTT TTCTTTTTTG ATACGGAGTC TCACTCTGTC 1500
ACCCAGTCTG GAGTACAGTG GTGCGATCTT GGCTCACTGC AACCTCCACC TCCCAGCTTC 1560
AAGCGATTCT CCTGTCTCAG CCTCCGAGTA GCTGGGACTA CAAGGCTCAT GCCACCATGC 1620
CCGGCTAATT TTTGTATTTT TAGTAGAGAT AGGGTTTCCC CATATTGGCC AGGGGCTGGT 1680
CTCGAACTCC TGACCTCTGG TGATCCACCT GACTCGACCT ACCAAAGTGC TGGGATTACA 1740
GGCGTGAGCC AAGGCACCCG GCCAAAAACT GATGTTCTTC ATCACTACAC TCTTCAGTCT 1800
CTTACAGCTC TTTGTGCTTT CTCCTGTAAG ACCACACACA GCCTAACCCT TGTCGCAATA 1860
ATTGAAAACT ACATGCCCTG GAAGTTAAGA GACCGGCTTT ATTCCGCCAC TCCAGAGCAC 1920
GTAACGCGGC GCCAGAACTC AAGAATACAT TCAGTCGTTA TTTGTTGAAC TGAATGGCAT 1980
AGTTAGGAAT GGCTTTACCG GATTTTCAGT GGATAACTGG GTAGAAGCTG TGCGCCCCAG 2040
TCTTTCTGAA ACCTGTGATC ACACTTCGGG CACTGTCCCC TCTACAGTCA ATCTGTGTTT 2100
TCAGAAGTGG CCCCAGGTTC ACTCGTCTTA CAGCAGTCCT AAAGAGCCGG CTGCCCTTTC 2160
CCTAGGCTTC CTTGCTCTTG AGGGCTAAAT TCCAGCCCTC CTACCCCAGT GCCACTTGGG 2220
TAAAAATACT CTGCTCCTCT CACGTTTGCT AATAAGCCCG GGCTCCGACT ACCACCGTTC 2280
GGGGGAAGGG AGCCCCTTAC 2300