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

TagContent
EnhancerAtlas ID
HS091-07868 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr11:64682300-64684430 
Target genes
Number: 45             
NameEnsembl ID
GPR137ENSG00000173264
NRXN2ENSG00000110076
RASGRP2ENSG00000068831
PYGMENSG00000068976
SF1ENSG00000168066
MAP4K2ENSG00000168067
MEN1ENSG00000133895
CDC42BPGENSG00000171219
AP001187.11ENSG00000230835
EHD1ENSG00000110047
AP001187.1ENSG00000203400
MIR192ENSG00000207648
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
SPDYCENSG00000204710
PGAM1P8ENSG00000249251
AP003068.18ENSG00000255200
CAPN1ENSG00000014216
AP003068.23ENSG00000254614
POLA2ENSG00000014138
CDC42EP2ENSG00000149798
DPF2ENSG00000133884
NEAT1ENSG00000245532
MIR612ENSG00000207727
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
GCTCCAGCCA GGGACTCAGA GCAACTAGGA TGAAACTCAA GAGGTGAGCA GGTGCTTGGG 60
GGTGGTGAGG GGGCTGGTGG GGGGGCCGTG GGGAAGACGC CTAACCCAGC CTGGGCCGTC 120
AGAGGAGGGG CAAGCTGAAG AATAAAGGGA GGGGGGATAG GCGCTGGTAG AAGGTGGTGT 180
GTTGCAGGCA CAGGACAACA TGGGCACATG TATGGCAGAG TCCAGAATAC CCATGTTCAC 240
CCTGGATGAG CAGAGTTCAA AGGGACAGTG TCCAAGAGAG GGGCTGACCT AATGCCAGAT 300
GGGACCCCCC CCCCCCACCA CCAACCCCAA ACACCTAGTG TAGCTGTGCC TCTCTGTGAG 360
GCACAAGGCT GAGCCCCTGG CTAAAATGTC CATGCTGGAG TTGTACCCCT GCCAACCTGG 420
AAGCTCCTGG AGGGCTGTAC CCCACCTGCC TCCCCCGTCA CCCCAGGTGC CACCCAGAAA 480
GGGCCTCAGT AAACTGGTTG GATCCAAGAA TAAAAAAGCA CATGGCAGAG CAGATGGGAG 540
TCCAAATTCC TCACCCAGAG ACCCACAGCT CGGGAAACTG AGGCCTAGAG ACAGGACTAA 600
TCTAGTCACC CAGTATACAA CAGGGACTGA GACTGGGATG CGGGCCTCTT TCTTTTCATG 660
CCACTTCAGA GGCCCCAGAT ACTCAGTTTC TTTGGGGGCC TTCAAGGCGG GGCCTGCAGG 720
CTGAGCTGGG AGGGAGGAGG GGCTGGTTAT CAAGAAAGCG CCTGCATTCC ACCAGGGCCC 780
TAGAGAAGCC AATTCAATCC CCAACAAGAG GGCAGGGAAC AGGAGTAGGG GCGTTTTCTG 840
GAGCTGAAAG TAAAAAGGGG AAGCCTAGGG CTGGGTATGG TGGTTCATGC CTATAATCTC 900
AGCACTTTGG GAGGCTGAGG TGGGAGGATC CCTTCAGGGG TTCAAGGCTA GCCTGGGCAA 960
CATAGCGAAA TCCTGTCTCT ATAAAAATAA AAAAGGGGCA GCCTAGAGAC GGCCTTAGAG 1020
GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG CTTCCTACAC CAGAATTCAC AGACAGCAGG 1080
CCACTGGGGG GTGCCCCCAG TTCAGGGCCC ACGATTATCC TACCCCACAT TTGCTCACCA 1140
GGGCCTGGCC TACCCCCAAA GCCTAGCTCT TCTGCCCAGA TTAGCAGCCC CCTGAGTCCA 1200
GCCACAAAAC TGAGAAGTCC CTGCCTCCAT GCCCACCCCT GCTGCTCTGG ACCTGGTGGA 1260
TCGACCAGGA CGCGCCTCTA ATTGGTGGCT CCTTCAAAGC TCCCCAGGTC AGCTGAGCTG 1320
TGAGTCAGGG CTCCTCACCG TTCCCAGCCT CAAGCCTCTG ACCTTACACC TCTTGGCCTC 1380
CCTAGCATCT CCCTTGGCCT CCTCCCGGCT TGAAGCCAGA TCTCCCCACC TTTCCTCCAG 1440
GGCCTCCCTC CAGGCAGGGA CACTGAGCCG GGGGGGTCGG TGGGAGATGT AGGTGGGGGC 1500
CATCCAGTCC CTCCCTAGAC ACCCACTTGG CCCATCCCAC TCTCCCAAAA GCAGGAAGTA 1560
GGCAGCGACC CAGGCACACG AGGTGTTGAT CAACACTGGT ACTGACGTAC TGACGCGGTT 1620
GTTGACATAC ACATCCGGTG GTTTGTTGAT CCCACCTACG GGCTCAGGAC CGTGGGGTCA 1680
AGAGGTCAGG GCACATGATC CACAGGTGTC CTCGCCAGGG CTCCGGACCC CTACCAGCTT 1740
CCCCCACCAG CTGCGCAGGC CCAAGTCTGT CACTGCCCTG GCCCAGCTCA GTTCCTACGC 1800
TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG CCAACCTCCT TAACTCAGCC CCCAAACTCG 1860
ACGAGTTTGT CTTGCATTCT CCAGACAGGT GATCTTGCCC TCTCCAGCCT CAGTTTCTCC 1920
TCCCGTGGAG ACAGAAACCC CTTCCCGCTC AGTTTCTGGC TCTGGTAAGG AACTGAAGAG 1980
GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA GGGCAAGATT CCCCTGGCCT CTCTACGCCC 2040
GGTGCCTGAT CCCCCAGCCC GATCCTGCCG CAGGGAGCCT CAGGTCGCTG CGCTCCCACC 2100
CTCCGCACCT TCCTGGACTC GGGCCTGGCT 2130