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

TagContent
EnhancerAtlas ID
HS076-10543 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr11:64682440-64684430 
Target genes
Number: 50             
NameEnsembl ID
STIP1ENSG00000168439
PLCB3ENSG00000149782
GPR137ENSG00000173264
TRMT112ENSG00000173113
PRDX5ENSG00000126432
SLC22A11ENSG00000168065
SLC22A12ENSG00000197891
AP001092.4ENSG00000237410
NRXN2ENSG00000110076
RASGRP2ENSG00000068831
PYGMENSG00000068976
SF1ENSG00000168066
MAP4K2ENSG00000168067
MEN1ENSG00000133895
AP001187.11ENSG00000230835
EHD1ENSG00000110047
AP001187.1ENSG00000203400
AP001187.9ENSG00000229719
ATG2AENSG00000110046
PPP2R5BENSG00000068971
GPHA2ENSG00000149735
C11orf85ENSG00000168070
BATF2ENSG00000168062
ARL2ENSG00000213465
SNX15ENSG00000110025
SAC3D1ENSG00000168061
NAALADL1ENSG00000168060
CDCA5ENSG00000146670
ZFPL1ENSG00000162300
C11orf2ENSG00000149823
AP003068.6ENSG00000187066
AP003068.9ENSG00000254501
TM7SF2ENSG00000149809
AP003068.12ENSG00000255173
ZNHIT2ENSG00000174276
MRPL49ENSG00000149792
FAUENSG00000149806
SYVN1ENSG00000162298
HIGD1AP10ENSG00000254455
U2ENSG00000222477
AP003068.18ENSG00000255200
CAPN1ENSG00000014216
AP003068.23ENSG00000254614
SLC22A20ENSG00000197847
POLA2ENSG00000014138
CDC42EP2ENSG00000149798
DPF2ENSG00000133884
FRMD8ENSG00000126391
MALAT1ENSG00000251562
SSSCA1ENSG00000173465
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
AATAAAGGGA GGGGGGATAG GCGCTGGTAG AAGGTGGTGT GTTGCAGGCA CAGGACAACA 60
TGGGCACATG TATGGCAGAG TCCAGAATAC CCATGTTCAC CCTGGATGAG CAGAGTTCAA 120
AGGGACAGTG TCCAAGAGAG GGGCTGACCT AATGCCAGAT GGGACCCCCC CCCCCCACCA 180
CCAACCCCAA ACACCTAGTG TAGCTGTGCC TCTCTGTGAG GCACAAGGCT GAGCCCCTGG 240
CTAAAATGTC CATGCTGGAG TTGTACCCCT GCCAACCTGG AAGCTCCTGG AGGGCTGTAC 300
CCCACCTGCC TCCCCCGTCA CCCCAGGTGC CACCCAGAAA GGGCCTCAGT AAACTGGTTG 360
GATCCAAGAA TAAAAAAGCA CATGGCAGAG CAGATGGGAG TCCAAATTCC TCACCCAGAG 420
ACCCACAGCT CGGGAAACTG AGGCCTAGAG ACAGGACTAA TCTAGTCACC CAGTATACAA 480
CAGGGACTGA GACTGGGATG CGGGCCTCTT TCTTTTCATG CCACTTCAGA GGCCCCAGAT 540
ACTCAGTTTC TTTGGGGGCC TTCAAGGCGG GGCCTGCAGG CTGAGCTGGG AGGGAGGAGG 600
GGCTGGTTAT CAAGAAAGCG CCTGCATTCC ACCAGGGCCC TAGAGAAGCC AATTCAATCC 660
CCAACAAGAG GGCAGGGAAC AGGAGTAGGG GCGTTTTCTG GAGCTGAAAG TAAAAAGGGG 720
AAGCCTAGGG CTGGGTATGG TGGTTCATGC CTATAATCTC AGCACTTTGG GAGGCTGAGG 780
TGGGAGGATC CCTTCAGGGG TTCAAGGCTA GCCTGGGCAA CATAGCGAAA TCCTGTCTCT 840
ATAAAAATAA AAAAGGGGCA GCCTAGAGAC GGCCTTAGAG GCTGAGGCTA AGGTTAGAGG 900
TCAGAGAGGG CTTCCTACAC CAGAATTCAC AGACAGCAGG CCACTGGGGG GTGCCCCCAG 960
TTCAGGGCCC ACGATTATCC TACCCCACAT TTGCTCACCA GGGCCTGGCC TACCCCCAAA 1020
GCCTAGCTCT TCTGCCCAGA TTAGCAGCCC CCTGAGTCCA GCCACAAAAC TGAGAAGTCC 1080
CTGCCTCCAT GCCCACCCCT GCTGCTCTGG ACCTGGTGGA TCGACCAGGA CGCGCCTCTA 1140
ATTGGTGGCT CCTTCAAAGC TCCCCAGGTC AGCTGAGCTG TGAGTCAGGG CTCCTCACCG 1200
TTCCCAGCCT CAAGCCTCTG ACCTTACACC TCTTGGCCTC CCTAGCATCT CCCTTGGCCT 1260
CCTCCCGGCT TGAAGCCAGA TCTCCCCACC TTTCCTCCAG GGCCTCCCTC CAGGCAGGGA 1320
CACTGAGCCG GGGGGGTCGG TGGGAGATGT AGGTGGGGGC CATCCAGTCC CTCCCTAGAC 1380
ACCCACTTGG CCCATCCCAC TCTCCCAAAA GCAGGAAGTA GGCAGCGACC CAGGCACACG 1440
AGGTGTTGAT CAACACTGGT ACTGACGTAC TGACGCGGTT GTTGACATAC ACATCCGGTG 1500
GTTTGTTGAT CCCACCTACG GGCTCAGGAC CGTGGGGTCA AGAGGTCAGG GCACATGATC 1560
CACAGGTGTC CTCGCCAGGG CTCCGGACCC CTACCAGCTT CCCCCACCAG CTGCGCAGGC 1620
CCAAGTCTGT CACTGCCCTG GCCCAGCTCA GTTCCTACGC TCCCTCCCCA GCCCCTCCTC 1680
AGCCCGAGAG CCAACCTCCT TAACTCAGCC CCCAAACTCG ACGAGTTTGT CTTGCATTCT 1740
CCAGACAGGT GATCTTGCCC TCTCCAGCCT CAGTTTCTCC TCCCGTGGAG ACAGAAACCC 1800
CTTCCCGCTC AGTTTCTGGC TCTGGTAAGG AACTGAAGAG GCCAGCCGGG GTGCCTCTGA 1860
CGCCTGGAGA GGGCAAGATT CCCCTGGCCT CTCTACGCCC GGTGCCTGAT CCCCCAGCCC 1920
GATCCTGCCG CAGGGAGCCT CAGGTCGCTG CGCTCCCACC CTCCGCACCT TCCTGGACTC 1980
GGGCCTGGCT 1990