EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-04142 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr11:64681970-64684430 
Target genes
Number: 46             
NameEnsembl ID
MACROD1ENSG00000133315
STIP1ENSG00000168439
PPP1R14BENSG00000173457
GPR137ENSG00000173264
BADENSG00000002330
TRMT112ENSG00000173113
PRDX5ENSG00000126432
RPS6KA4ENSG00000162302
SLC22A11ENSG00000168065
NRXN2ENSG00000110076
RASGRP2ENSG00000068831
PYGMENSG00000068976
SF1ENSG00000168066
MAP4K2ENSG00000168067
MEN1ENSG00000133895
CDC42BPGENSG00000171219
EHD1ENSG00000110047
AP001187.1ENSG00000203400
MIR192ENSG00000207648
AP001187.9ENSG00000229719
ATG2AENSG00000110046
PPP2R5BENSG00000068971
GPHA2ENSG00000149735
C11orf85ENSG00000168070
ARL2ENSG00000213465
SNX15ENSG00000110025
SAC3D1ENSG00000168061
CDCA5ENSG00000146670
ZFPL1ENSG00000162300
C11orf2ENSG00000149823
AP003068.6ENSG00000187066
AP003068.9ENSG00000254501
TM7SF2ENSG00000149809
AP003068.12ENSG00000255173
ZNHIT2ENSG00000174276
MRPL49ENSG00000149792
FAUENSG00000149806
SYVN1ENSG00000162298
HIGD1AP10ENSG00000254455
U2ENSG00000222477
AP003068.17ENSG00000255058
SPDYCENSG00000204710
AP003068.18ENSG00000255200
SLC22A20ENSG00000197847
POLA2ENSG00000014138
CDC42EP2ENSG00000149798
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs188954228chr1164682925hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr11:64683973-64683988GGGGTCAAGAGGTCA+8.07
Nr2f6MA0677.1chr11:64683329-64683343AAGGTTAGAGGTCA+6.06
RARAMA0729.1chr11:64683973-64683991GGGGTCAAGAGGTCAGGG+6.56
RREB1MA0073.1chr11:64682613-64682633CCCACCACCAACCCCAAACA+6.16
RREB1MA0073.1chr11:64682610-64682630CCCCCCACCACCAACCCCAA+6.93
RREB1MA0073.1chr11:64682607-64682627CCCCCCCCCACCACCAACCC+7.34
TCF7L2MA0523.1chr11:64682551-64682565AGAGTTCAAAGGGA+6.28
ZNF740MA0753.2chr11:64682605-64682618CCCCCCCCCCCAC+6.92
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr116468287064682981
chr116468286364683400
chr116468340064683600
Enhancer Sequence
GACTGGGAGC AAGCAAGAGA CAAAACCAGC TCAGGGAAAC CCCAAATCCC ACAGGCTGGC 60
ACAGCCTTAT CTGGCCATAG TGCCTTGGAG AGCACCCTTG GCTTGCCCTG TCCCTCCACG 120
TGTTATCTAC AAGGTCCCAC CTATGCTCAT GCTGTCCCCT ACTACAGGCC AGCCCCCCTA 180
CCCCGTCACC CAAAGGTGCC TAATCCTTCA AGCCAGAGCA GATGTTTCCC TCACCACTTA 240
ATTCAAGATA ATATTTACCG AGCACTTTCT ACATGCTGAC ACTGAGACTA GATGGGTAAA 300
TAAAATGTCT TCATTCCCCA GCCAAGCTAG GCTCCAGCCA GGGACTCAGA GCAACTAGGA 360
TGAAACTCAA GAGGTGAGCA GGTGCTTGGG GGTGGTGAGG GGGCTGGTGG GGGGGCCGTG 420
GGGAAGACGC CTAACCCAGC CTGGGCCGTC AGAGGAGGGG CAAGCTGAAG AATAAAGGGA 480
GGGGGGATAG GCGCTGGTAG AAGGTGGTGT GTTGCAGGCA CAGGACAACA TGGGCACATG 540
TATGGCAGAG TCCAGAATAC CCATGTTCAC CCTGGATGAG CAGAGTTCAA AGGGACAGTG 600
TCCAAGAGAG GGGCTGACCT AATGCCAGAT GGGACCCCCC CCCCCCACCA CCAACCCCAA 660
ACACCTAGTG TAGCTGTGCC TCTCTGTGAG GCACAAGGCT GAGCCCCTGG CTAAAATGTC 720
CATGCTGGAG TTGTACCCCT GCCAACCTGG AAGCTCCTGG AGGGCTGTAC CCCACCTGCC 780
TCCCCCGTCA CCCCAGGTGC CACCCAGAAA GGGCCTCAGT AAACTGGTTG GATCCAAGAA 840
TAAAAAAGCA CATGGCAGAG CAGATGGGAG TCCAAATTCC TCACCCAGAG ACCCACAGCT 900
CGGGAAACTG AGGCCTAGAG ACAGGACTAA TCTAGTCACC CAGTATACAA CAGGGACTGA 960
GACTGGGATG CGGGCCTCTT TCTTTTCATG CCACTTCAGA GGCCCCAGAT ACTCAGTTTC 1020
TTTGGGGGCC TTCAAGGCGG GGCCTGCAGG CTGAGCTGGG AGGGAGGAGG GGCTGGTTAT 1080
CAAGAAAGCG CCTGCATTCC ACCAGGGCCC TAGAGAAGCC AATTCAATCC CCAACAAGAG 1140
GGCAGGGAAC AGGAGTAGGG GCGTTTTCTG GAGCTGAAAG TAAAAAGGGG AAGCCTAGGG 1200
CTGGGTATGG TGGTTCATGC CTATAATCTC AGCACTTTGG GAGGCTGAGG TGGGAGGATC 1260
CCTTCAGGGG TTCAAGGCTA GCCTGGGCAA CATAGCGAAA TCCTGTCTCT ATAAAAATAA 1320
AAAAGGGGCA GCCTAGAGAC GGCCTTAGAG GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG 1380
CTTCCTACAC CAGAATTCAC AGACAGCAGG CCACTGGGGG GTGCCCCCAG TTCAGGGCCC 1440
ACGATTATCC TACCCCACAT TTGCTCACCA GGGCCTGGCC TACCCCCAAA GCCTAGCTCT 1500
TCTGCCCAGA TTAGCAGCCC CCTGAGTCCA GCCACAAAAC TGAGAAGTCC CTGCCTCCAT 1560
GCCCACCCCT GCTGCTCTGG ACCTGGTGGA TCGACCAGGA CGCGCCTCTA ATTGGTGGCT 1620
CCTTCAAAGC TCCCCAGGTC AGCTGAGCTG TGAGTCAGGG CTCCTCACCG TTCCCAGCCT 1680
CAAGCCTCTG ACCTTACACC TCTTGGCCTC CCTAGCATCT CCCTTGGCCT CCTCCCGGCT 1740
TGAAGCCAGA TCTCCCCACC TTTCCTCCAG GGCCTCCCTC CAGGCAGGGA CACTGAGCCG 1800
GGGGGGTCGG TGGGAGATGT AGGTGGGGGC CATCCAGTCC CTCCCTAGAC ACCCACTTGG 1860
CCCATCCCAC TCTCCCAAAA GCAGGAAGTA GGCAGCGACC CAGGCACACG AGGTGTTGAT 1920
CAACACTGGT ACTGACGTAC TGACGCGGTT GTTGACATAC ACATCCGGTG GTTTGTTGAT 1980
CCCACCTACG GGCTCAGGAC CGTGGGGTCA AGAGGTCAGG GCACATGATC CACAGGTGTC 2040
CTCGCCAGGG CTCCGGACCC CTACCAGCTT CCCCCACCAG CTGCGCAGGC CCAAGTCTGT 2100
CACTGCCCTG GCCCAGCTCA GTTCCTACGC TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG 2160
CCAACCTCCT TAACTCAGCC CCCAAACTCG ACGAGTTTGT CTTGCATTCT CCAGACAGGT 2220
GATCTTGCCC TCTCCAGCCT CAGTTTCTCC TCCCGTGGAG ACAGAAACCC CTTCCCGCTC 2280
AGTTTCTGGC TCTGGTAAGG AACTGAAGAG GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA 2340
GGGCAAGATT CCCCTGGCCT CTCTACGCCC GGTGCCTGAT CCCCCAGCCC GATCCTGCCG 2400
CAGGGAGCCT CAGGTCGCTG CGCTCCCACC CTCCGCACCT TCCTGGACTC GGGCCTGGCT 2460