EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS051-04742 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr11:64682450-64684430 
Target genes
Number: 46             
NameEnsembl ID
BADENSG00000002330
TRMT112ENSG00000173113
PRDX5ENSG00000126432
AP003774.5ENSG00000231492
AP005273.1ENSG00000232500
AP001092.4ENSG00000237410
NRXN2ENSG00000110076
RASGRP2ENSG00000068831
PYGMENSG00000068976
SF1ENSG00000168066
MAP4K2ENSG00000168067
MEN1ENSG00000133895
AP001187.11ENSG00000230835
EHD1ENSG00000110047
AP001187.1ENSG00000203400
MIR192ENSG00000207648
AP001187.9ENSG00000229719
ATG2AENSG00000110046
PPP2R5BENSG00000068971
GPHA2ENSG00000149735
C11orf85ENSG00000168070
ARL2ENSG00000213465
SNX15ENSG00000110025
SAC3D1ENSG00000168061
NAALADL1ENSG00000168060
CDCA5ENSG00000146670
ZFPL1ENSG00000162300
C11orf2ENSG00000149823
AP003068.6ENSG00000187066
AP003068.9ENSG00000254501
TM7SF2ENSG00000149809
AP003068.12ENSG00000255173
MRPL49ENSG00000149792
FAUENSG00000149806
SYVN1ENSG00000162298
HIGD1AP10ENSG00000254455
U2ENSG00000222477
AP003068.17ENSG00000255058
SPDYCENSG00000204710
PGAM1P8ENSG00000249251
AP003068.18ENSG00000255200
CAPN1ENSG00000014216
AP003068.23ENSG00000254614
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
GGGGGGATAG GCGCTGGTAG AAGGTGGTGT GTTGCAGGCA CAGGACAACA TGGGCACATG 60
TATGGCAGAG TCCAGAATAC CCATGTTCAC CCTGGATGAG CAGAGTTCAA AGGGACAGTG 120
TCCAAGAGAG GGGCTGACCT AATGCCAGAT GGGACCCCCC CCCCCCACCA CCAACCCCAA 180
ACACCTAGTG TAGCTGTGCC TCTCTGTGAG GCACAAGGCT GAGCCCCTGG CTAAAATGTC 240
CATGCTGGAG TTGTACCCCT GCCAACCTGG AAGCTCCTGG AGGGCTGTAC CCCACCTGCC 300
TCCCCCGTCA CCCCAGGTGC CACCCAGAAA GGGCCTCAGT AAACTGGTTG GATCCAAGAA 360
TAAAAAAGCA CATGGCAGAG CAGATGGGAG TCCAAATTCC TCACCCAGAG ACCCACAGCT 420
CGGGAAACTG AGGCCTAGAG ACAGGACTAA TCTAGTCACC CAGTATACAA CAGGGACTGA 480
GACTGGGATG CGGGCCTCTT TCTTTTCATG CCACTTCAGA GGCCCCAGAT ACTCAGTTTC 540
TTTGGGGGCC TTCAAGGCGG GGCCTGCAGG CTGAGCTGGG AGGGAGGAGG GGCTGGTTAT 600
CAAGAAAGCG CCTGCATTCC ACCAGGGCCC TAGAGAAGCC AATTCAATCC CCAACAAGAG 660
GGCAGGGAAC AGGAGTAGGG GCGTTTTCTG GAGCTGAAAG TAAAAAGGGG AAGCCTAGGG 720
CTGGGTATGG TGGTTCATGC CTATAATCTC AGCACTTTGG GAGGCTGAGG TGGGAGGATC 780
CCTTCAGGGG TTCAAGGCTA GCCTGGGCAA CATAGCGAAA TCCTGTCTCT ATAAAAATAA 840
AAAAGGGGCA GCCTAGAGAC GGCCTTAGAG GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG 900
CTTCCTACAC CAGAATTCAC AGACAGCAGG CCACTGGGGG GTGCCCCCAG TTCAGGGCCC 960
ACGATTATCC TACCCCACAT TTGCTCACCA GGGCCTGGCC TACCCCCAAA GCCTAGCTCT 1020
TCTGCCCAGA TTAGCAGCCC CCTGAGTCCA GCCACAAAAC TGAGAAGTCC CTGCCTCCAT 1080
GCCCACCCCT GCTGCTCTGG ACCTGGTGGA TCGACCAGGA CGCGCCTCTA ATTGGTGGCT 1140
CCTTCAAAGC TCCCCAGGTC AGCTGAGCTG TGAGTCAGGG CTCCTCACCG TTCCCAGCCT 1200
CAAGCCTCTG ACCTTACACC TCTTGGCCTC CCTAGCATCT CCCTTGGCCT CCTCCCGGCT 1260
TGAAGCCAGA TCTCCCCACC TTTCCTCCAG GGCCTCCCTC CAGGCAGGGA CACTGAGCCG 1320
GGGGGGTCGG TGGGAGATGT AGGTGGGGGC CATCCAGTCC CTCCCTAGAC ACCCACTTGG 1380
CCCATCCCAC TCTCCCAAAA GCAGGAAGTA GGCAGCGACC CAGGCACACG AGGTGTTGAT 1440
CAACACTGGT ACTGACGTAC TGACGCGGTT GTTGACATAC ACATCCGGTG GTTTGTTGAT 1500
CCCACCTACG GGCTCAGGAC CGTGGGGTCA AGAGGTCAGG GCACATGATC CACAGGTGTC 1560
CTCGCCAGGG CTCCGGACCC CTACCAGCTT CCCCCACCAG CTGCGCAGGC CCAAGTCTGT 1620
CACTGCCCTG GCCCAGCTCA GTTCCTACGC TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG 1680
CCAACCTCCT TAACTCAGCC CCCAAACTCG ACGAGTTTGT CTTGCATTCT CCAGACAGGT 1740
GATCTTGCCC TCTCCAGCCT CAGTTTCTCC TCCCGTGGAG ACAGAAACCC CTTCCCGCTC 1800
AGTTTCTGGC TCTGGTAAGG AACTGAAGAG GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA 1860
GGGCAAGATT CCCCTGGCCT CTCTACGCCC GGTGCCTGAT CCCCCAGCCC GATCCTGCCG 1920
CAGGGAGCCT CAGGTCGCTG CGCTCCCACC CTCCGCACCT TCCTGGACTC GGGCCTGGCT 1980