EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-02895 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr1:223912930-223915930 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr1:223914582-223914593GGTGACTCATC+6.32
FOSL2MA0478.1chr1:223914581-223914592GGGTGACTCAT+6.14
JUNBMA0490.1chr1:223914581-223914592GGGTGACTCAT+6.32
JUNDMA0491.1chr1:223914582-223914593GGTGACTCATC+6.62
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00224chr1:223912311-223916909Adipose_Nuclei
SE_01908chr1:223913738-223914955Aorta
SE_02306chr1:223913344-223915961Astrocytes
SE_04026chr1:223913451-223915326Brain_Anterior_Caudate
SE_05036chr1:223913560-223915403Brain_Cingulate_Gyrus
SE_05972chr1:223913207-223916372Brain_Hippocampus_Middle
SE_07996chr1:223913125-223915466Brain_Inferior_Temporal_Lobe
SE_09681chr1:223912826-223918041CD14
SE_19702chr1:223913106-223916325CD4p_CD25-_Il17p_PMAstim_Th17
SE_24051chr1:223913880-223914466Colon_Crypt_2
SE_26209chr1:223912988-223915695Duodenum_Smooth_Muscle
SE_26925chr1:223913192-223915372Esophagus
SE_31491chr1:223913141-223916265Gastric
SE_34545chr1:223913070-223916058HCT-116
SE_34979chr1:223912930-223916086HeLa
SE_36294chr1:223913510-223915892HMEC
SE_37129chr1:223913319-223916436HSMMtube
SE_38254chr1:223913007-223915923HUVEC
SE_38957chr1:223913198-223916265IMR90
SE_41495chr1:223912854-223916323Left_Ventricle
SE_42269chr1:223912507-223916406Lung
SE_44530chr1:223913197-223916987NHDF-Ad
SE_44904chr1:223913680-223916262NHLF
SE_45872chr1:223913083-223917105Osteoblasts
SE_49408chr1:223912976-223915760Right_Atrium
SE_50365chr1:223913039-223916033Sigmoid_Colon
SE_51879chr1:223913896-223915223Skeletal_Muscle_Myoblast
SE_53249chr1:223913106-223915207Small_Intestine
SE_55958chr1:223913015-223914574u87
SE_55958chr1:223914578-223916004u87
SE_63671chr1:223913673-223915261HSMM
SE_64794chr1:223913313-223915321NHEK
SE_65644chr1:223913370-223915937Pancreatic_islets
SE_67677chr1:223913015-223914574u87
SE_67677chr1:223914578-223916004u87
SE_68376chr1:223892363-223922876TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1223914239223914747
chr1223913851223914937
chr1223913235223915200
Number: 1             
IDChromosomeStartEnd
GH01I223722chr1223910120223916233
Enhancer Sequence
AACAATTAGC CGGGCGTGGT GGCATGCACT TGTAGTCCCA GCTACTCAGG AGGCTGAGGC 60
AGGAGAATCG CTTGAACCTG AGAGGTGGAG GTTGCAGTGA GCCATGATCG CACCACTGCA 120
CTCCATCCTG GGCAATAGAG CGAGACTTCA TCTCAAAAAA AAAAAAATTG TGTCTACCTC 180
AGAGGACTGT AAAGATGAAA TGAAATAATA GACATATAAA GCTCAGAGCT CCAGAGGCTG 240
GTACATAGTA AAGGTTTAAT CCATGCAGAT TGCACGTTCT CTTTGGGGAC AGTACAGCTG 300
GAGGGGAGTA CTGTCAAATG AGGTCGCGTC GCTGAGGTGG AGACACATTG TGGCACATCT 360
TGAATACCCG ACTGGGTCCC AGCTTTAGCA CTTGACATTG GCGGCCACCT AAGTTTTGGA 420
GAGGGGTATG ACAGAGGAGG TGGTGTCCCA GGGGGAAGGT CCGGAAACTC AGAGGAGTTT 480
CCTGCTGTAA TTTTCTTTGG TCACACAATG GTCATGGCCT CCTGATGTTT CCCACAAAGG 540
GCCAGAGGCC CTTCAGTGCC AAGGAACGTG GACTCTCTCC TATCCCAGCA CATACACGTG 600
CTTCCAGTAC CTTGTGATCT CTAGCCATAA GTTTCCACTC ACCCATCTGC GAAATGGGAA 660
CAATGACGAT GTTTGCGTCC TTTCTTTTTC TTTTCCTACA ATGCAGGGAA CTTTAAGACT 720
ATGTGACAGA AAGGTGCCAC TGGAACCCAG GGCCTCGTGG GTTTCCTCCG TCTCTCGGGA 780
GACCAGGATC CGAGTGAGAA AGTTTCCCAC GTTCATTCTT GTTGGGCCCA TTCTCAGGAT 840
GATGTTTCTC CTGTATTTTG CTACCCCAGC CCAAGCAAGA CTAGTAGTTC AGCTTTGTGA 900
ATCCCCTCAG GAAGTCAGGA AAATAGATAC TGTCTTTGGG CTTCCTCCAG GAGCTAAGAA 960
AGGAGAGTTC CTGAAGAGCA GGAATTTAAG ACAGGAATTG GCAGCCGAGG GCAAGGTTCC 1020
ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG TGATGAGAGC AGGGATGGGG AGGAAGAGGG 1080
TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG CCATCAGGAA GGAGCAGCCA CCTCTGCTGG 1140
GGTACTGGAG ATAAAAACTC TGATATTGAC TAGTGACCGT GGGGGCGATG GCCCAGGAGG 1200
GTCAGGGCTG CAGGGAACAG GGACACAAAA ACGACAAAAC ATGCAACAGG TTATGTCCTT 1260
CTGGTCCAGG GCACGGCTGA GACAGGCAAG GGACTAGAGA GAGGAAGAGT GAATGTCAAG 1320
CCCCAGCACC CTCGCCTCCC TCCCATCCTC CCTTTTAGGG CCTCCCTTCT GGCAGATAGG 1380
GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA CACGTGGTTT GGATCACTGG CTGTGGCTCA 1440
CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG GAGGCTGAAG ACTTCTTGTT AATAAGGGTG 1500
GGGCATGAGT AAAATGGAGG ATCTGCCCCC TCCCCTCCCA GCCCCTGATA CAAATGAAGG 1560
ATGATTGTAC ATGCATGGGG AATTCCACTT TGGGGGTATC CTTTTCTGGG CTGCTGCCAG 1620
ACTCTGAAAT GAGTAACAAA GGGATGGCCC AGGGTGACTC ATCAGCTACC CTCTCGCAGG 1680
CCTAGCACGC TGGCGGGGTG TGCATTTCCT CTAGAGAAGC CCCTCCCTGC CAGTTTCAGA 1740
GGGATGGCCC TGAATTGGCT TTTCAGAGGT TCCTTCTCCT CCCTTCCAAA GCGAAGACCC 1800
ACAGCTGCCT GAAAATGTGG CTCTCCGCCT TCTTGGGCTG CCTAGGACCT TGAGAGATGT 1860
GTCTCTCTGG GACAGGGTGT CAGGTCTGCT GGAGATTGTT AAAATGCTGT TGTCTCAGGA 1920
AGGGTGAAAT TTAGCCAGGA GCAGTCTTCA GTAGCTTGGT CTGTTTATCG TGTATCTAGC 1980
TGTCAGCATG CAAAACAAAA GAACAAAAGG TCTAAAGAAA TATAACGCAA AACAGGTACG 2040
ATTTGAGATC CATCAGGGTT TCTCAACCTT GGCACAACTG ACTGGATAAT TGTTCATTGT 2100
AGGGGGCTGT CCTGTGAATT ATAGGATGTT TAGCTGCATC CTTGGCCTCT ACCCACACAC 2160
CCCCGTGTGC CACTCAAAAA TGTCTGCAGA CCTTGCCAAA TGTCCCCTGG GGGCTTGGCG 2220
GAGTTGGGGG GTGCATGGAA TGCCCCCAGT TGAGAACCAC TGGCAGAGCA GGAGTGAAGG 2280
GGGAGGTACT GTGGGGGTCA CTGGGCACAC AGAATGCCAT TTGGGGAGCC TGGTGCAAGG 2340
GAGTGGCCGG ATGGGAGGTA GGAATAGCAG TGGTAATCAG TAGGTGAGTT GCTGAAGACA 2400
AACTAAATAT TCTTTCCAGC ATTGCTTCAA TCTAATCCAG CCGCAAGTAT GAGTAAATAC 2460
TGTAGGAAAG GAGAAAACAT TGCATGTACG GGGTCAGGGC AGCATTGCTG GGATATTTGA 2520
GCCTGTGGGA GGGGAGCTTC AAGCTTCCCA CTAGCATTGG GAGGAACACA GCAAAGGAGG 2580
AGAAGGGCCC TCCCTGCTTC TTGGAGAATG GTTCCACTGG CAGGCCATTC CGTCTGCTCA 2640
GCTTCCTAGC TCAGGTGCCT TTCCAAACCA CACATCAGCA GGGAGACAGT GGGAACATCT 2700
CAGGTCCAGG GTACCTTGGG AACTGCAGAG CAGCTGGGTG GCCTGACACT GGCATTTCTC 2760
AGTGTTGGCT CCATTCTCTT GCTGGCACCC CCAGGTGGGA GACTCTGTTA GCAGGTGTAT 2820
CTTACTATCC CTGGCTCCCT GGTATGCGTT ACAGTTCAGA CTCCCAAGCA CAAGCTCCCT 2880
GTTTTGTCAC ACCTGTATCT AGTGTGTAAC AATCCACCCC AAAACAAATG GCTTGAAACA 2940
CAAGGCATTT TGTTCTCTCT CATGGTTCTG AAGGATGACG GGGCTGAGCT GGGCAACTCT 3000