EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS016-00086 
Organism
Homo sapiens 
Tissue/cell
CD14+ 
Coordinate
chr1:223913790-223916640 
TF binding sites/motifs
Number: 5             
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
NKX2-5MA0063.2chr1:223915940-223915950CTCAAGTGGT-6.02
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: 2             
ChromosomeStartEnd
chr1223914239223914747
chr1223913851223914937
Number: 1             
IDChromosomeStartEnd
GH01I223722chr1223910120223916233
Enhancer Sequence
CTACCCCAGC CCAAGCAAGA CTAGTAGTTC AGCTTTGTGA ATCCCCTCAG GAAGTCAGGA 60
AAATAGATAC TGTCTTTGGG CTTCCTCCAG GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA 120
GGAATTTAAG ACAGGAATTG GCAGCCGAGG GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT 180
GTGGGGTCTG TGATGAGAGC AGGGATGGGG AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG 240
GGGAGGGCAG CCATCAGGAA GGAGCAGCCA CCTCTGCTGG GGTACTGGAG ATAAAAACTC 300
TGATATTGAC TAGTGACCGT GGGGGCGATG GCCCAGGAGG GTCAGGGCTG CAGGGAACAG 360
GGACACAAAA ACGACAAAAC ATGCAACAGG TTATGTCCTT CTGGTCCAGG GCACGGCTGA 420
GACAGGCAAG GGACTAGAGA GAGGAAGAGT GAATGTCAAG CCCCAGCACC CTCGCCTCCC 480
TCCCATCCTC CCTTTTAGGG CCTCCCTTCT GGCAGATAGG GCAGGGAGAA GGGAAAGGAA 540
AGGCCTGGGA CACGTGGTTT GGATCACTGG CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG 600
TTTAGGGAAG GAGGCTGAAG ACTTCTTGTT AATAAGGGTG GGGCATGAGT AAAATGGAGG 660
ATCTGCCCCC TCCCCTCCCA GCCCCTGATA CAAATGAAGG ATGATTGTAC ATGCATGGGG 720
AATTCCACTT TGGGGGTATC CTTTTCTGGG CTGCTGCCAG ACTCTGAAAT GAGTAACAAA 780
GGGATGGCCC AGGGTGACTC ATCAGCTACC CTCTCGCAGG CCTAGCACGC TGGCGGGGTG 840
TGCATTTCCT CTAGAGAAGC CCCTCCCTGC CAGTTTCAGA GGGATGGCCC TGAATTGGCT 900
TTTCAGAGGT TCCTTCTCCT CCCTTCCAAA GCGAAGACCC ACAGCTGCCT GAAAATGTGG 960
CTCTCCGCCT TCTTGGGCTG CCTAGGACCT TGAGAGATGT GTCTCTCTGG GACAGGGTGT 1020
CAGGTCTGCT GGAGATTGTT AAAATGCTGT TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA 1080
GCAGTCTTCA GTAGCTTGGT CTGTTTATCG TGTATCTAGC TGTCAGCATG CAAAACAAAA 1140
GAACAAAAGG TCTAAAGAAA TATAACGCAA AACAGGTACG ATTTGAGATC CATCAGGGTT 1200
TCTCAACCTT GGCACAACTG ACTGGATAAT TGTTCATTGT AGGGGGCTGT CCTGTGAATT 1260
ATAGGATGTT TAGCTGCATC CTTGGCCTCT ACCCACACAC CCCCGTGTGC CACTCAAAAA 1320
TGTCTGCAGA CCTTGCCAAA TGTCCCCTGG GGGCTTGGCG GAGTTGGGGG GTGCATGGAA 1380
TGCCCCCAGT TGAGAACCAC TGGCAGAGCA GGAGTGAAGG GGGAGGTACT GTGGGGGTCA 1440
CTGGGCACAC AGAATGCCAT TTGGGGAGCC TGGTGCAAGG GAGTGGCCGG ATGGGAGGTA 1500
GGAATAGCAG TGGTAATCAG TAGGTGAGTT GCTGAAGACA AACTAAATAT TCTTTCCAGC 1560
ATTGCTTCAA TCTAATCCAG CCGCAAGTAT GAGTAAATAC TGTAGGAAAG GAGAAAACAT 1620
TGCATGTACG GGGTCAGGGC AGCATTGCTG GGATATTTGA GCCTGTGGGA GGGGAGCTTC 1680
AAGCTTCCCA CTAGCATTGG GAGGAACACA GCAAAGGAGG AGAAGGGCCC TCCCTGCTTC 1740
TTGGAGAATG GTTCCACTGG CAGGCCATTC CGTCTGCTCA GCTTCCTAGC TCAGGTGCCT 1800
TTCCAAACCA CACATCAGCA GGGAGACAGT GGGAACATCT CAGGTCCAGG GTACCTTGGG 1860
AACTGCAGAG CAGCTGGGTG GCCTGACACT GGCATTTCTC AGTGTTGGCT CCATTCTCTT 1920
GCTGGCACCC CCAGGTGGGA GACTCTGTTA GCAGGTGTAT CTTACTATCC CTGGCTCCCT 1980
GGTATGCGTT ACAGTTCAGA CTCCCAAGCA CAAGCTCCCT GTTTTGTCAC ACCTGTATCT 2040
AGTGTGTAAC AATCCACCCC AAAACAAATG GCTTGAAACA CAAGGCATTT TGTTCTCTCT 2100
CATGGTTCTG AAGGATGACG GGGCTGAGCT GGGCAACTCT CTCCCGCTCT CTCAAGTGGT 2160
TGCAATCAGA TGGGGATGGG GACAGAGTCA TCTGTAGGCC CCCTCAACCA CATGTCTGGT 2220
GCCCGGGCTG AAGGGTGGAT CAGCAGGGGT CCAGGGATCT CTGTCTCTTT TGTGGTCTCC 2280
CCATCACAGG GACTTGAAGG TAGCTGAACA TCTTACAGCA GCTCATGTCC CAAGAGAAAG 2340
ACCTGGGAGC TGTCTCATCT TTACGACCTA GGCTTGGAAG TCACATAGCA TCACTTCTGC 2400
CATATCCTAT TCATTGAGAT CAATGAAGGC TCACCCAGGA TCAAAGAGAA GGGACATGGA 2460
GCCCACTTCT AGATGGAGAG TGGCAGGGTT CTGGAAGAAC ATGTGAAACC AGAAACATTG 2520
TTGCCACCAT TTTTGGAAGA CACCACGATT CCTCCCCTTT GAATAATGGC CTTCTTGTCC 2580
TTTACCAGTA ATAACCCAAG CTGCTTGGAC ATTAGCTCTT CATGGTTTGC GGGGTGGGGA 2640
GGATGTGTTT TCTGGGACTT CCCAAGGTAC ACAGTAGTGA AGGACTTCAC AAGCTGGGCT 2700
GATGTGCCAG CTTCAGGACT CCACTCACCC CCAAGCGTTC TGAGATGCCC ATGGGGCTCA 2760
GGAGCCCTGA CTTGCACAAG CCAGCAACTG CCTTTCTGCT TCCATTCAGC CAGCTTTACT 2820
GGGCATCTGT TATAGGAAGA GCAGTGGGCT 2850