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

TagContent
EnhancerAtlas ID
HS092-37935 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr9:33130510-33133870 
Target genes
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MecomMA0029.1chr9:33132142-33132156TTGACAAGATAAGA+6.06
ZNF263MA0528.1chr9:33132221-33132242GGAAGAGGAGGGAGGGAGGGA+6.87
ZNF263MA0528.1chr9:33132224-33132245AGAGGAGGGAGGGAGGGAGGA+8.55
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_00330chr9:33131315-33133010Adipose_Nuclei
SE_00992chr9:33132242-33132769Adrenal_Gland
SE_09459chr9:33129171-33132533CD14
SE_10229chr9:33127769-33131935CD19_Primary
SE_10912chr9:33119344-33169982CD20
SE_12090chr9:33130620-33131585CD3
SE_18665chr9:33129793-33132844CD4p_CD25-_Il17-_PMAstim_Th
SE_19329chr9:33130392-33131632CD4p_CD25-_Il17p_PMAstim_Th17
SE_19329chr9:33131921-33132804CD4p_CD25-_Il17p_PMAstim_Th17
SE_20045chr9:33128349-33132443CD56
SE_22416chr9:33128783-33132526CD8_primiary
SE_26031chr9:33129309-33132935Duodenum_Smooth_Muscle
SE_26859chr9:33129122-33131571Esophagus
SE_27770chr9:33128137-33132419Fetal_Intestine
SE_27770chr9:33133434-33136209Fetal_Intestine
SE_28724chr9:33128066-33132484Fetal_Intestine_Large
SE_28724chr9:33133427-33136185Fetal_Intestine_Large
SE_31534chr9:33128891-33131746Gastric
SE_31534chr9:33132180-33132827Gastric
SE_32659chr9:33129028-33131615GM12878
SE_35029chr9:33130436-33131878HeLa
SE_40894chr9:33128725-33131858Left_Ventricle
SE_40894chr9:33132104-33132852Left_Ventricle
SE_41831chr9:33130578-33131658LNCaP
SE_41831chr9:33132179-33132815LNCaP
SE_42236chr9:33128546-33131800Lung
SE_42236chr9:33132132-33132898Lung
SE_42236chr9:33133177-33134351Lung
SE_44340chr9:33130634-33131475NHDF-Ad
SE_44340chr9:33131613-33132990NHDF-Ad
SE_45447chr9:33132176-33132836NHLF
SE_45731chr9:33130368-33132932Osteoblasts
SE_48426chr9:33133123-33134192Psoas_Muscle
SE_48738chr9:33130653-33131691Right_Atrium
SE_48738chr9:33132163-33132855Right_Atrium
SE_50176chr9:33128355-33131838Sigmoid_Colon
SE_50176chr9:33132062-33132876Sigmoid_Colon
SE_52621chr9:33128937-33131899Small_Intestine
SE_52621chr9:33132123-33132884Small_Intestine
SE_53402chr9:33129123-33131619Spleen
SE_58985chr9:33124740-33168862Ly3
SE_62118chr9:33106994-33169093Toledo
SE_62346chr9:33106942-33169226Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 6             
ChromosomeStartEnd
chr93313218733132686
chr93313278233132857
chr93313203033132096
chr93313328033133507
chr93313373033133860
chr93313130133131811
Number: 2             
IDChromosomeStartEnd
GH09I033127chr93312796433132882
GH09I033133chr93313369733146567
Enhancer Sequence
TATATCTCAA CCAGGAAAGC CTCTCCCGGC TCATTCCTTC AATATCCTTA TTTTAAGATA 60
TAAGTTAGTA CAATAATTAC AGAGGCATAA GCCAAATGGG AGTGGTTAAC AGCTTACTAT 120
AGACAGAGTA TGAGTCATAA CAACTTGTGA AAGTTCACTC CTGTGTGTAA AGCTTGATAC 180
GTGGCCCTAT TTTGAAGAGG CTTATAGGCC CGGGATGGCC TCTGAGATTC TGCCACCTGG 240
CTCACTCCAC TATCCATTAC CCTCTGACTC CAAGGAGTTC AAACCAATAG GAGGAAGGGT 300
CCTGATGCGG GCCCTGAGTG GGGGTGCAGC AGGAGGCGGT GGGAGCCATG AAGAATTCAC 360
CACCACAGAA GCAGGCAGAG GAAGCAGGCA GAGGAAACAG GCAGGATGAA TGGAGAGTGG 420
AGAGGCAGGA GTGGACCCTC CTAGTAACGG CTGGTATTTA CTGAAGGTTT ACCATGAGAA 480
GGATGCCTCA TAACCCTCCC CACCAAGGAG GAAACTGAGG CCTGCAGAGC TTAAGTAACC 540
TGCCTGAGGT CACTGACTGT AAAGTGGCAG TGCCAGGACT GAACCCAGGC AGTCTGAGCA 600
CACAGCACAC TCTCAGCCCT GGATACCAGA CTGTGAGCAA CACTGGGGGC ACCCTGGCCA 660
TGAGGAGTGT CACTGATGCC CTGAGAAGGC ACTAAACCTG GAGTCAGACG CTGGGGTTTG 720
AGCCGCAGCC CTACTGTTGT CTATGTGACT TTCGGAGCCT GTCCCTCTCT GAGCCTGTTT 780
CCTCACCTGT GACATGGAGC AGAAGTTTCT ACATTGTCTG GCCTCAGGGG TCTAGGCAAA 840
TCCTAGCAGT GACTGAATGG GAAGCCAAGG AAGTGGAAAT GGGACATGGC CCCTACTTCA 900
AGTAGAATGA AACCCTTGTG ACCTGCTGTA AGCGGAAGGT TGTGTAGCAT TTCAATGGGG 960
CAGAAAGAAA TCTGATACTG AAAAGCCTGT TTGGGAACCC TTGGACTAAA TGTCTCAGAA 1020
GCCACTCCAT TTTGAGCATT ACTTCTGTCT AATCTTAAAT GGTATGTGTG TGTGTGTACA 1080
TGTGTGTGCA TGTGTATGTG TGTGTGGGAA TGAAAAGTCA AAATGACAGC AGGGTGTCTG 1140
GGCCAGGGAT AAGCTGAGAG GCTATAAAGA GGGCTAACAG CCCATAAGGT TTATTTGCTC 1200
AACAAACAGT GCAGAAAGGT CAAAACCAGG TGCTACAAAA TCCCTTTCTT CTTCTAGAAT 1260
ATAACCATAA AACAGATAAC ACAGGCAGTT CCTAATTTGT AGACAGGATG TGCTCCAAAT 1320
GTTTCTCCTT CCACCTCTTT TTTTTCAGGG TTCAGGTTTC CCATTACCAT TTTATTATTT 1380
ATTAGGTAAT ATTCTTTACT GGAAAGGTAT GGCAGAGTTT AAGCATTTCT CAACTTAGTT 1440
ATCTGGACTC TGACCATATT TTCCCAAAAT GATCAATTAG GGTGAGATTG GAGCAGATGA 1500
TAAGAGAGTA GCTGGGGAAG TGGGAGAAAA AGCAGAAAAG ATTCTCCTAA GGTGGAAAGT 1560
TAACCCTTGG AGAAGGAAAG GATGAAGAGA AAAAAAAGTA TGAGGAAAAG CAAAGAAAAA 1620
AAAAAGATGA TATTGACAAG ATAAGAAAAA AGGAGGTATA TATGTTTGAA AAACCAAAAC 1680
TAAAATATTC CTGATGCTAA GTTGTGAAGT GGGAAGAGGA GGGAGGGAGG GAGGACGGGC 1740
AGTTCCTAGT GTTCCAGGGA AAGCAGGGAG GCAGCTGGGA GGAGATGCTA ACTTAGGCCC 1800
GCTTTCCCCA AAGTGTGACT CACAAAACAC TCATCACTTG AGACGGTTCT TGGAAAAGTT 1860
GTCTCGTCAG GCAAGCTCAG GAAACACTTC TGGGGTTACA GTGTACACCG GGGTACCAAA 1920
GGCTCTGCGG GAATGAGACC TGCTTTACAT GGTTCAACCC AACATTCCTC AAGCGTATTT 1980
CGCTCCATTT GGGGAAGCAC ACTTTTGGAG AAGCACTCTC TTAGGTGGTG CCCAGTGTTA 2040
GCCAGCACAG CTGTGCCACC GGTCTGAGCT GGCTTGGTTA GTTGTTCCAT CTACTCGGAT 2100
TGAGGTGGGC AGGAGCATGT AGCTGGCAGA GGACATTCAG AAATCTACTG TGTTGAGCCT 2160
GGGGAGTATG TAAATTGTAT CATAGGAATT TAAGCTGATG GCTAGATTTT ACTGGTCCAA 2220
TATTTGACTT CAAAACAGGG AAGTCTCACA TTCACCTAAA CTGCAACATA TCTAGACGTA 2280
GCATCCCACC CTCCAGTCTT CCTTGAAAAC AGCCACCTCA GTTCAAAAAT TCAGCATCAT 2340
CGCTAACTCT TTTATCCTCT TTACCCAAGT ATATATTTTA TTTATTTATT TATTTATTTT 2400
ATTTTTTTGA GACAGAGTCT CACTCTGTTG CCCAGGCTGG AGTGCAGTGG CATGATCTCG 2460
GCTCACTGCA ACCTCTGCCT CCTGGGTTCA AGAGATTCTC CTGCCTCAGC CTCCCGAGTA 2520
GCTGGGATTA CAGCCGCCCA CCACTATGTC CAGCTAATTT TTGTATTTTT AGTAGAGACG 2580
GGGTTTCGCC ATGTTGGCCA GGCTGGTCTT GAACTCCTGA CTTCAAGTGA TCCGCCTGCC 2640
TTGGCCTCCC AAAGTGCTGG GATTACAGGC ATGAGCCACT GCGCCTAGGC CCAAATATAT 2700
ATTTTAACCT ACCTATATGG CACCCAGACC ACAGCTGTCT GTCTTCTACT CAGGCAGATT 2760
TGTGGGATGC TATCAGATGC CCTGCTGAAT AAGATATGAC AGCATTGTAT CCACAGTACA 2820
TCCCTCATCT ACTGGCATAG CAACTGTCAA GAGAGAAACG AGATGCAGCT GGCACGGCTT 2880
ATTAGTCATC CCTGCTGGCT CCTGGTGATG GTGGCCGCCT CTTCCAGGTG CTCGCTGCCA 2940
CTGCTTTAAT AACAGGCTCC TGAATCTTGC CGTCATTGGT ATGTGCTAAC TGGCATCAGA 3000
CAAATGTTTC TCAATCACAG AGCTTTTCTT AAATGAATAT GTGTTGGGTT AAAGTGACCC 3060
GCATTTTGCA GGACATTTAC CTGTTCTCTC TTGCATTCTC CAATATTCTT CCAAGGTGAC 3120
CCACAACTGC GTGGCTGTCT TGCTTGCAGG TGTTCATAGG GCCCTGGTCT GTACCTCACT 3180
TGGCCGAAGA ATTCAAACAG CCTCAAGGGG TTTGCCCACC ACCTGCTCTC CTGCTTCAGT 3240
TTCCTTGTAA CAGGGCTTGT TCTGCTCTCT CCTGCCTCAC AGGCTTAACT CTGACACCTG 3300
GTCCCAGAGC TTCTGGTGCT TTCCTACCCC AGTGGGCATC TCAATTTCCA GGAACATGCA 3360