EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-03791 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr1:223913400-223915190 
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: 2             
ChromosomeStartEnd
chr1223914239223914747
chr1223913851223914937
Number: 1             
IDChromosomeStartEnd
GH01I223722chr1223910120223916233
Enhancer Sequence
AGAGGAGTTT CCTGCTGTAA TTTTCTTTGG TCACACAATG GTCATGGCCT CCTGATGTTT 60
CCCACAAAGG GCCAGAGGCC CTTCAGTGCC AAGGAACGTG GACTCTCTCC TATCCCAGCA 120
CATACACGTG CTTCCAGTAC CTTGTGATCT CTAGCCATAA GTTTCCACTC ACCCATCTGC 180
GAAATGGGAA CAATGACGAT GTTTGCGTCC TTTCTTTTTC TTTTCCTACA ATGCAGGGAA 240
CTTTAAGACT ATGTGACAGA AAGGTGCCAC TGGAACCCAG GGCCTCGTGG GTTTCCTCCG 300
TCTCTCGGGA GACCAGGATC CGAGTGAGAA AGTTTCCCAC GTTCATTCTT GTTGGGCCCA 360
TTCTCAGGAT GATGTTTCTC CTGTATTTTG CTACCCCAGC CCAAGCAAGA CTAGTAGTTC 420
AGCTTTGTGA ATCCCCTCAG GAAGTCAGGA AAATAGATAC TGTCTTTGGG CTTCCTCCAG 480
GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA GGAATTTAAG ACAGGAATTG GCAGCCGAGG 540
GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG TGATGAGAGC AGGGATGGGG 600
AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG CCATCAGGAA GGAGCAGCCA 660
CCTCTGCTGG GGTACTGGAG ATAAAAACTC TGATATTGAC TAGTGACCGT GGGGGCGATG 720
GCCCAGGAGG GTCAGGGCTG CAGGGAACAG GGACACAAAA ACGACAAAAC ATGCAACAGG 780
TTATGTCCTT CTGGTCCAGG GCACGGCTGA GACAGGCAAG GGACTAGAGA GAGGAAGAGT 840
GAATGTCAAG CCCCAGCACC CTCGCCTCCC TCCCATCCTC CCTTTTAGGG CCTCCCTTCT 900
GGCAGATAGG GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA CACGTGGTTT GGATCACTGG 960
CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG GAGGCTGAAG ACTTCTTGTT 1020
AATAAGGGTG GGGCATGAGT AAAATGGAGG ATCTGCCCCC TCCCCTCCCA GCCCCTGATA 1080
CAAATGAAGG ATGATTGTAC ATGCATGGGG AATTCCACTT TGGGGGTATC CTTTTCTGGG 1140
CTGCTGCCAG ACTCTGAAAT GAGTAACAAA GGGATGGCCC AGGGTGACTC ATCAGCTACC 1200
CTCTCGCAGG CCTAGCACGC TGGCGGGGTG TGCATTTCCT CTAGAGAAGC CCCTCCCTGC 1260
CAGTTTCAGA GGGATGGCCC TGAATTGGCT TTTCAGAGGT TCCTTCTCCT CCCTTCCAAA 1320
GCGAAGACCC ACAGCTGCCT GAAAATGTGG CTCTCCGCCT TCTTGGGCTG CCTAGGACCT 1380
TGAGAGATGT GTCTCTCTGG GACAGGGTGT CAGGTCTGCT GGAGATTGTT AAAATGCTGT 1440
TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA GCAGTCTTCA GTAGCTTGGT CTGTTTATCG 1500
TGTATCTAGC TGTCAGCATG CAAAACAAAA GAACAAAAGG TCTAAAGAAA TATAACGCAA 1560
AACAGGTACG ATTTGAGATC CATCAGGGTT TCTCAACCTT GGCACAACTG ACTGGATAAT 1620
TGTTCATTGT AGGGGGCTGT CCTGTGAATT ATAGGATGTT TAGCTGCATC CTTGGCCTCT 1680
ACCCACACAC CCCCGTGTGC CACTCAAAAA TGTCTGCAGA CCTTGCCAAA TGTCCCCTGG 1740
GGGCTTGGCG GAGTTGGGGG GTGCATGGAA TGCCCCCAGT TGAGAACCAC 1790