EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-05250 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr1:223913870-223915800 
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
CTTCCTCCAG GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA GGAATTTAAG ACAGGAATTG 60
GCAGCCGAGG GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG TGATGAGAGC 120
AGGGATGGGG AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG CCATCAGGAA 180
GGAGCAGCCA CCTCTGCTGG GGTACTGGAG ATAAAAACTC TGATATTGAC TAGTGACCGT 240
GGGGGCGATG GCCCAGGAGG GTCAGGGCTG CAGGGAACAG GGACACAAAA ACGACAAAAC 300
ATGCAACAGG TTATGTCCTT CTGGTCCAGG GCACGGCTGA GACAGGCAAG GGACTAGAGA 360
GAGGAAGAGT GAATGTCAAG CCCCAGCACC CTCGCCTCCC TCCCATCCTC CCTTTTAGGG 420
CCTCCCTTCT GGCAGATAGG GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA CACGTGGTTT 480
GGATCACTGG CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG GAGGCTGAAG 540
ACTTCTTGTT AATAAGGGTG GGGCATGAGT AAAATGGAGG ATCTGCCCCC TCCCCTCCCA 600
GCCCCTGATA CAAATGAAGG ATGATTGTAC ATGCATGGGG AATTCCACTT TGGGGGTATC 660
CTTTTCTGGG CTGCTGCCAG ACTCTGAAAT GAGTAACAAA GGGATGGCCC AGGGTGACTC 720
ATCAGCTACC CTCTCGCAGG CCTAGCACGC TGGCGGGGTG TGCATTTCCT CTAGAGAAGC 780
CCCTCCCTGC CAGTTTCAGA GGGATGGCCC TGAATTGGCT TTTCAGAGGT TCCTTCTCCT 840
CCCTTCCAAA GCGAAGACCC ACAGCTGCCT GAAAATGTGG CTCTCCGCCT TCTTGGGCTG 900
CCTAGGACCT TGAGAGATGT GTCTCTCTGG GACAGGGTGT CAGGTCTGCT GGAGATTGTT 960
AAAATGCTGT TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA GCAGTCTTCA GTAGCTTGGT 1020
CTGTTTATCG TGTATCTAGC TGTCAGCATG CAAAACAAAA GAACAAAAGG TCTAAAGAAA 1080
TATAACGCAA AACAGGTACG ATTTGAGATC CATCAGGGTT TCTCAACCTT GGCACAACTG 1140
ACTGGATAAT TGTTCATTGT AGGGGGCTGT CCTGTGAATT ATAGGATGTT TAGCTGCATC 1200
CTTGGCCTCT ACCCACACAC CCCCGTGTGC CACTCAAAAA TGTCTGCAGA CCTTGCCAAA 1260
TGTCCCCTGG GGGCTTGGCG GAGTTGGGGG GTGCATGGAA TGCCCCCAGT TGAGAACCAC 1320
TGGCAGAGCA GGAGTGAAGG GGGAGGTACT GTGGGGGTCA CTGGGCACAC AGAATGCCAT 1380
TTGGGGAGCC TGGTGCAAGG GAGTGGCCGG ATGGGAGGTA GGAATAGCAG TGGTAATCAG 1440
TAGGTGAGTT GCTGAAGACA AACTAAATAT TCTTTCCAGC ATTGCTTCAA TCTAATCCAG 1500
CCGCAAGTAT GAGTAAATAC TGTAGGAAAG GAGAAAACAT TGCATGTACG GGGTCAGGGC 1560
AGCATTGCTG GGATATTTGA GCCTGTGGGA GGGGAGCTTC AAGCTTCCCA CTAGCATTGG 1620
GAGGAACACA GCAAAGGAGG AGAAGGGCCC TCCCTGCTTC TTGGAGAATG GTTCCACTGG 1680
CAGGCCATTC CGTCTGCTCA GCTTCCTAGC TCAGGTGCCT TTCCAAACCA CACATCAGCA 1740
GGGAGACAGT GGGAACATCT CAGGTCCAGG GTACCTTGGG AACTGCAGAG CAGCTGGGTG 1800
GCCTGACACT GGCATTTCTC AGTGTTGGCT CCATTCTCTT GCTGGCACCC CCAGGTGGGA 1860
GACTCTGTTA GCAGGTGTAT CTTACTATCC CTGGCTCCCT GGTATGCGTT ACAGTTCAGA 1920
CTCCCAAGCA 1930