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

TagContent
EnhancerAtlas ID
HS076-04113 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr1:156643320-156645000 
Target genes
Number: 47             
NameEnsembl ID
RIT1ENSG00000143622
KIAA0907ENSG00000132680
ARHGEF2ENSG00000116584
SSR2ENSG00000163479
UBQLN4ENSG00000160803
LAMTOR2ENSG00000116586
RAB25ENSG00000132698
AL355388.1ENSG00000222611
MEX3AENSG00000254726
LMNAENSG00000160789
SEMA4AENSG00000196189
SLC25A44ENSG00000160785
PMF1ENSG00000160783
BGLAPENSG00000242252
PAQR6ENSG00000160781
SMG5ENSG00000198952
TMEM79ENSG00000163472
C1orf85ENSG00000198715
VHLLENSG00000189030
AL589685.1ENSG00000228155
C1orf182ENSG00000163467
CCT3ENSG00000163468
RHBGENSG00000132677
RP11ENSG00000237390
C1orf61ENSG00000125462
MEF2DENSG00000116604
IQGAP3ENSG00000183856
TTC24ENSG00000187862
APOA1BPENSG00000163382
GPATCH4ENSG00000160818
HAPLN2ENSG00000132702
BCANENSG00000132692
NESENSG00000132688
CRABP2ENSG00000143320
RRNAD1ENSG00000143303
ISG20L2ENSG00000143319
MRPL24ENSG00000143314
PRCCENSG00000143294
HDGFENSG00000143321
NTRK1ENSG00000198400
SH2D2AENSG00000027869
INSRRENSG00000027644
PEAR1ENSG00000187800
LRRC71ENSG00000160838
MIR765ENSG00000211581
ARHGEF11ENSG00000132694
KRT8P45ENSG00000224520
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUNMA0488.1chr1:156643647-156643660ATGACCTCATCCT-6.23
JUND(var.2)MA0492.1chr1:156643646-156643661AATGACCTCATCCTC-6.09
Myod1MA0499.1chr1:156644078-156644091AGCAGCTGCTCCT+6.11
RELMA0101.1chr1:156644782-156644792GGGGATTTCC+6.02
STAT3MA0144.2chr1:156644352-156644363TTTCCCAGAAG-6.62
ZNF263MA0528.1chr1:156644205-156644226CTCTCCTCCACGTCCTCCCCA-6.22
ZNF263MA0528.1chr1:156644202-156644223CCCCTCTCCTCCACGTCCTCC-6.54
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_29621chr1:156629384-156648365Fetal_Muscle
SE_37066chr1:156627097-156648542HSMMtube
SE_40945chr1:156642205-156648314Left_Ventricle
SE_42863chr1:156642204-156648249Lung
SE_48663chr1:156642130-156648223Right_Atrium
SE_51411chr1:156642526-156648415Skeletal_Muscle
SE_54003chr1:156642286-156648271Spleen
SE_64001chr1:156643058-156647960HSMM
SE_68702chr1:156642289-156647729H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1156643426156643791
Enhancer Sequence
TGGAGAGGAC AGAGGGAAAG TGGGGTCAGC CCTCTGCCCC CAGGCCTGCA GGCAGCAAGC 60
CAGCTGGGGA CAACTCAGGC TGAGCTTGCA CCATCCAGGC CCTGCAGGCT TCCTCTTCAT 120
TTGACACTGT CACACAAAAG CCACACTCAG GGTGAAATCA CACAGTCACA TACCCACAGA 180
CATCACACAC TTGGTCACAC AAAGTCACAC TGTATTTGGG ATACACAGCA GAGCTCAGAC 240
ATAGAAGCAG ATTCCCACAC AGTCGGACAT TGCCCTACAC ACACCCACAC AAGGCTTAGG 300
CTAGCCTCCT CCTCCCACCC CAGGCCAATG ACCTCATCCT CTGTGTGGGG GACCGATTCT 360
CATGCTAATT GCTGCCATTG TCCAAGCCAC CATCTGGAGG GTCTGAGAAG GAGAGGATTC 420
TGGGGAAGTG GGAATTCTCA GGCCGTTCCC ATGGGATGGG CTCCCTCCTC CTTCCCCGGT 480
GGCCCCCAGA GCTAGCGACA GACAAAAGCA AATGAATTCA GCTCCCCCTC TCCAAATCCT 540
TTTCATGCCT CAAAAAATAG CAGTTAAATT CCTCGGGGCC CACCAGACCC TTCCCCTTGG 600
TGGCTTCACT GGGGGTCAGG GCCCTCATCT CAGGATCTCT AAGCACTCTG GATCCCAAGC 660
TCTTCGGGGC ACAGAGGTCT TTGTGTCCAG GCCCCTTCCT CAGCGCCCCT TGAACCAAAG 720
AGGGGAGCAG GGACCAATCA ATTCAATAAC TTAGGATGAG CAGCTGCTCC TCTCTGCTTT 780
GCTCCATGAT CTCTGAGTCT GGTTAGCACT CGCTGTAGCC TCACCTCTGT CCTTGCCAGT 840
GCTGCGGCCT TCCTTCTGGG CTTCTCTTCC CTGGCGGTGG AGCCCCTCTC CTCCACGTCC 900
TCCCCAGAGC CTCACTGACC TTCCATCTCT GGGCCTTGCC TCTCCTCCTT TCCTGGATCT 960
CATGTGGCCC CTCACCAGCC ACAGAGCCCC TTCCTCAGGC CCCATCAATG GCCCCTCAGC 1020
CAACAGGACC AGTTTCCCAG AAGAGACTGC GGGCTTTGCC CAAGGCCACA TAGCAAGTGA 1080
GAAGCCACCC CTCCTTGGTC TCAGCCATTT CTAGGATAAC AGAAAATGTG GACAATGAAA 1140
GGCTGGGCAG GACCAAGGGC ACTAGGGGCA TCAGAGGAGT CTCGCCCCAT GACATCCAGG 1200
CTAGAAGAGG CCTTGGAAGT CCCCCAGCCC AGCCCTCAGC CCCTAGACGA GGCTGAGGCC 1260
CAGGTCAGGT GGCAAGTCAG TGCAGCCACC CCATGCCTGC AATGCCTCCT TTCCGTGGCT 1320
GCCAAAGGAC ATGACCCCCT GGGTGCGGGC ACACATAGAG TTGGAGCTTT GCCCCTTGGG 1380
GGAAGGGTCT GGATGCAGTT GCCCCACACG GGCCCAGCCC CTCTCCAGAG GCTGTCCCGC 1440
TCGGCAATAT CATCTCTCCT GGGGGGATTT CCTGGGCACA GGACATTGCT CAGGTCTCCA 1500
GCCTATGGGG GAGCAGACGG TTTCAGGCAG GACATGTTCC GGTGTGGAAG TGACCAGCCT 1560
AGAGTCACAG AACCCAGTGG CAGCAGAGTT GCCATCACCT ACACCTCTGG TCCCCTTCAG 1620
CCACGTAGTC TGCCCCAGCA TGTGTGTGTG CCTCTGTGTG CCTGGGTGGA CAGGGCTCGT 1680