EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS039-00743 
Organism
Homo sapiens 
Tissue/cell
ESC_NPC 
Coordinate
chr1:223913430-223914920 
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: 1             
ChromosomeStartEnd
chr1223914239223914747
Number: 1             
IDChromosomeStartEnd
GH01I223722chr1223910120223916233
Enhancer Sequence
TCACACAATG GTCATGGCCT CCTGATGTTT CCCACAAAGG GCCAGAGGCC CTTCAGTGCC 60
AAGGAACGTG GACTCTCTCC TATCCCAGCA CATACACGTG CTTCCAGTAC CTTGTGATCT 120
CTAGCCATAA GTTTCCACTC ACCCATCTGC GAAATGGGAA CAATGACGAT GTTTGCGTCC 180
TTTCTTTTTC TTTTCCTACA ATGCAGGGAA CTTTAAGACT ATGTGACAGA AAGGTGCCAC 240
TGGAACCCAG GGCCTCGTGG GTTTCCTCCG TCTCTCGGGA GACCAGGATC CGAGTGAGAA 300
AGTTTCCCAC GTTCATTCTT GTTGGGCCCA TTCTCAGGAT GATGTTTCTC CTGTATTTTG 360
CTACCCCAGC CCAAGCAAGA CTAGTAGTTC AGCTTTGTGA ATCCCCTCAG GAAGTCAGGA 420
AAATAGATAC TGTCTTTGGG CTTCCTCCAG GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA 480
GGAATTTAAG ACAGGAATTG GCAGCCGAGG GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT 540
GTGGGGTCTG TGATGAGAGC AGGGATGGGG AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG 600
GGGAGGGCAG CCATCAGGAA GGAGCAGCCA CCTCTGCTGG GGTACTGGAG ATAAAAACTC 660
TGATATTGAC TAGTGACCGT GGGGGCGATG GCCCAGGAGG GTCAGGGCTG CAGGGAACAG 720
GGACACAAAA ACGACAAAAC ATGCAACAGG TTATGTCCTT CTGGTCCAGG GCACGGCTGA 780
GACAGGCAAG GGACTAGAGA GAGGAAGAGT GAATGTCAAG CCCCAGCACC CTCGCCTCCC 840
TCCCATCCTC CCTTTTAGGG CCTCCCTTCT GGCAGATAGG GCAGGGAGAA GGGAAAGGAA 900
AGGCCTGGGA CACGTGGTTT GGATCACTGG CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG 960
TTTAGGGAAG GAGGCTGAAG ACTTCTTGTT AATAAGGGTG GGGCATGAGT AAAATGGAGG 1020
ATCTGCCCCC TCCCCTCCCA GCCCCTGATA CAAATGAAGG ATGATTGTAC ATGCATGGGG 1080
AATTCCACTT TGGGGGTATC CTTTTCTGGG CTGCTGCCAG ACTCTGAAAT GAGTAACAAA 1140
GGGATGGCCC AGGGTGACTC ATCAGCTACC CTCTCGCAGG CCTAGCACGC TGGCGGGGTG 1200
TGCATTTCCT CTAGAGAAGC CCCTCCCTGC CAGTTTCAGA GGGATGGCCC TGAATTGGCT 1260
TTTCAGAGGT TCCTTCTCCT CCCTTCCAAA GCGAAGACCC ACAGCTGCCT GAAAATGTGG 1320
CTCTCCGCCT TCTTGGGCTG CCTAGGACCT TGAGAGATGT GTCTCTCTGG GACAGGGTGT 1380
CAGGTCTGCT GGAGATTGTT AAAATGCTGT TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA 1440
GCAGTCTTCA GTAGCTTGGT CTGTTTATCG TGTATCTAGC TGTCAGCATG 1490