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

TagContent
EnhancerAtlas ID
HS099-02081 
Organism
Homo sapiens 
Tissue/cell
HSMMtube 
Coordinate
chr1:223913620-223916050 
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
TTTTCCTACA ATGCAGGGAA CTTTAAGACT ATGTGACAGA AAGGTGCCAC TGGAACCCAG 60
GGCCTCGTGG GTTTCCTCCG TCTCTCGGGA GACCAGGATC CGAGTGAGAA AGTTTCCCAC 120
GTTCATTCTT GTTGGGCCCA TTCTCAGGAT GATGTTTCTC CTGTATTTTG CTACCCCAGC 180
CCAAGCAAGA CTAGTAGTTC AGCTTTGTGA ATCCCCTCAG GAAGTCAGGA AAATAGATAC 240
TGTCTTTGGG CTTCCTCCAG GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA GGAATTTAAG 300
ACAGGAATTG GCAGCCGAGG GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG 360
TGATGAGAGC AGGGATGGGG AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG 420
CCATCAGGAA GGAGCAGCCA CCTCTGCTGG GGTACTGGAG ATAAAAACTC TGATATTGAC 480
TAGTGACCGT GGGGGCGATG GCCCAGGAGG GTCAGGGCTG CAGGGAACAG GGACACAAAA 540
ACGACAAAAC ATGCAACAGG TTATGTCCTT CTGGTCCAGG GCACGGCTGA GACAGGCAAG 600
GGACTAGAGA GAGGAAGAGT GAATGTCAAG CCCCAGCACC CTCGCCTCCC TCCCATCCTC 660
CCTTTTAGGG CCTCCCTTCT GGCAGATAGG GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA 720
CACGTGGTTT GGATCACTGG CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG 780
GAGGCTGAAG ACTTCTTGTT AATAAGGGTG GGGCATGAGT AAAATGGAGG ATCTGCCCCC 840
TCCCCTCCCA GCCCCTGATA CAAATGAAGG ATGATTGTAC ATGCATGGGG AATTCCACTT 900
TGGGGGTATC CTTTTCTGGG CTGCTGCCAG ACTCTGAAAT GAGTAACAAA GGGATGGCCC 960
AGGGTGACTC ATCAGCTACC CTCTCGCAGG CCTAGCACGC TGGCGGGGTG TGCATTTCCT 1020
CTAGAGAAGC CCCTCCCTGC CAGTTTCAGA GGGATGGCCC TGAATTGGCT TTTCAGAGGT 1080
TCCTTCTCCT CCCTTCCAAA GCGAAGACCC ACAGCTGCCT GAAAATGTGG CTCTCCGCCT 1140
TCTTGGGCTG CCTAGGACCT TGAGAGATGT GTCTCTCTGG GACAGGGTGT CAGGTCTGCT 1200
GGAGATTGTT AAAATGCTGT TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA GCAGTCTTCA 1260
GTAGCTTGGT CTGTTTATCG TGTATCTAGC TGTCAGCATG CAAAACAAAA GAACAAAAGG 1320
TCTAAAGAAA TATAACGCAA AACAGGTACG ATTTGAGATC CATCAGGGTT TCTCAACCTT 1380
GGCACAACTG ACTGGATAAT TGTTCATTGT AGGGGGCTGT CCTGTGAATT ATAGGATGTT 1440
TAGCTGCATC CTTGGCCTCT ACCCACACAC CCCCGTGTGC CACTCAAAAA TGTCTGCAGA 1500
CCTTGCCAAA TGTCCCCTGG GGGCTTGGCG GAGTTGGGGG GTGCATGGAA TGCCCCCAGT 1560
TGAGAACCAC TGGCAGAGCA GGAGTGAAGG GGGAGGTACT GTGGGGGTCA CTGGGCACAC 1620
AGAATGCCAT TTGGGGAGCC TGGTGCAAGG GAGTGGCCGG ATGGGAGGTA GGAATAGCAG 1680
TGGTAATCAG TAGGTGAGTT GCTGAAGACA AACTAAATAT TCTTTCCAGC ATTGCTTCAA 1740
TCTAATCCAG CCGCAAGTAT GAGTAAATAC TGTAGGAAAG GAGAAAACAT TGCATGTACG 1800
GGGTCAGGGC AGCATTGCTG GGATATTTGA GCCTGTGGGA GGGGAGCTTC AAGCTTCCCA 1860
CTAGCATTGG GAGGAACACA GCAAAGGAGG AGAAGGGCCC TCCCTGCTTC TTGGAGAATG 1920
GTTCCACTGG CAGGCCATTC CGTCTGCTCA GCTTCCTAGC TCAGGTGCCT TTCCAAACCA 1980
CACATCAGCA GGGAGACAGT GGGAACATCT CAGGTCCAGG GTACCTTGGG AACTGCAGAG 2040
CAGCTGGGTG GCCTGACACT GGCATTTCTC AGTGTTGGCT CCATTCTCTT GCTGGCACCC 2100
CCAGGTGGGA GACTCTGTTA GCAGGTGTAT CTTACTATCC CTGGCTCCCT GGTATGCGTT 2160
ACAGTTCAGA CTCCCAAGCA CAAGCTCCCT GTTTTGTCAC ACCTGTATCT AGTGTGTAAC 2220
AATCCACCCC AAAACAAATG GCTTGAAACA CAAGGCATTT TGTTCTCTCT CATGGTTCTG 2280
AAGGATGACG GGGCTGAGCT GGGCAACTCT CTCCCGCTCT CTCAAGTGGT TGCAATCAGA 2340
TGGGGATGGG GACAGAGTCA TCTGTAGGCC CCCTCAACCA CATGTCTGGT GCCCGGGCTG 2400
AAGGGTGGAT CAGCAGGGGT CCAGGGATCT 2430