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

TagContent
EnhancerAtlas ID
HS098-16752 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr13:114872050-114874200 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr13:114874181-114874192GGAGGGTGTGG-6.32
MyogMA0500.1chr13:114873663-114873674CCGCAGCTGTC-6.32
SREBF1MA0595.1chr13:114873941-114873951ATCACCCCAC+6.02
SREBF1MA0595.1chr13:114873997-114874007ATCACCCCAC+6.02
SREBF2MA0596.1chr13:114873792-114873802ATCACCCCAT-6.02
SREBF2MA0596.1chr13:114873983-114873993ATCACCCCAT-6.02
SREBF2MA0596.1chr13:114874011-114874021ATCACCCCAT-6.02
TBX21MA0690.1chr13:114874108-114874118TTCACACCTT-6.02
TBX2MA0688.1chr13:114874107-114874118ATTCACACCTT-6.02
ZBTB18MA0698.1chr13:114872537-114872550CCACATCTGGATC-6.34
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_02428chr13:114872731-114873928Astrocytes
SE_06573chr13:114872335-114874398Brain_Hippocampus_Middle
SE_14520chr13:114873694-114876925CD4_Memory_Primary_7pool
SE_15834chr13:114873773-114878002CD4_Naive_Primary_7pool
SE_17352chr13:114869676-114882291CD4p_CD25-_CD45RAp_Naive
SE_17971chr13:114872979-114878230CD4p_CD25-_CD45ROp_Memory
SE_18337chr13:114869903-114882128CD4p_CD25-_Il17-_PMAstim_Th
SE_19216chr13:114872434-114876766CD4p_CD25-_Il17p_PMAstim_Th17
SE_20430chr13:114872509-114876776CD56
SE_21920chr13:114872865-114877698CD8_Naive_8pool
SE_22425chr13:114869587-114879166CD8_primiary
SE_29941chr13:114872459-114873899Fetal_Muscle
SE_31056chr13:114873787-114879121Fetal_Thymus
SE_32435chr13:114873181-114873787Gastric
SE_32435chr13:114873860-114874532Gastric
SE_37803chr13:114871976-114874138HSMMtube
SE_38174chr13:114872340-114874997HUVEC
SE_38982chr13:114872436-114879177IMR90
SE_44466chr13:114872263-114874175NHDF-Ad
SE_44821chr13:114872178-114876775NHLF
SE_46527chr13:114871244-114874411Osteoblasts
SE_47322chr13:114872412-114879224Panc1
SE_48488chr13:114872396-114878962Psoas_Muscle
SE_50252chr13:114872403-114879191Sigmoid_Colon
SE_52117chr13:114872393-114873957Skeletal_Muscle_Myoblast
SE_54100chr13:114872722-114873505Spleen
SE_56179chr13:114872625-114873924u87
SE_63914chr13:114872393-114874006HSMM
SE_66755chr13:114873976-114876607Jurkat
SE_67713chr13:114872625-114873924u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr13114872330114873876
Number: 1             
IDChromosomeStartEnd
GH13I114104chr13114869826114879156
Enhancer Sequence
ATTTTACTTA GCGTAGGTGT AGAAATTCAC ACCCAAGTCC CACTTAGAAC ACGCTTCCCG 60
CTCCGGAGCA TAAGCCCCTG GCGTGGGGAG GGGTTGGGCT CTGTCTGAAC TGATCACCAC 120
CACTGCTTTA TTAATTGTTT TTGGCTTAAC ACCTGAACCA GCTGGGTGCA AACTATGACA 180
CACATTACAA AACCACCTGT CCATCCTCCA GGCACATGGA AGGCACACGG CCCACAGAAA 240
CCAAACTATA TGCTGCGTCC CATTTAGAAA GCTCTGCGTA TGTTTAAAAT TAAAAGTCTT 300
ATAAGGAAAC TATTTTTCTG TATTTTAAAA TGTTCTTAAT TACAAAGAAA TAGATATTCA 360
TTCTAGCCAG TTAAGTCTCC AGGTAGAAAA AGTTAACTCT TTTCCCTCCC TCAGCCAGGC 420
CCCCCCAGAG CCACATCTGG CAAGGACGGC TTGGTGTGCA CGCCCACACC TCCTCTCTCG 480
TGCACGGCCA CATCTGGATC AGATGTGCAG GCATTTCAAC ATGGCAGTCT CCATCCAGCC 540
ACGGTCTGCG GACAGCGTTC AGGCTCCAGC CTTGACCCTG GGCACCTTGA CCCTCACGGG 600
GTACGTGGCC TGTGTGTCTG CCTTTGTGTC CTGGTCCTCG CAGGGGACAG GCCTGTGTGT 660
CCCACGTTCG TGTCCTGGTC TTCGCAGGGG ATGTGGCCTG TGTGTCCCTC CTTCGTATCC 720
TGACCCTTGC GGGGGACGGG CCTGTGTGTC CCTCCTTCGT GTCCTGACCC TCGCGGGGGA 780
CGGGCCTGTG TGTCCTGCCT TCGTGCACCC TGACACCATG GGTCTGATTT TCCCACGCTG 840
GAGGTCTGCT TCTGAACAGC TGCATCTCCT CCTGCAGGGG AAGCTGTCTG TTCACCCAGG 900
TGCCTGTCCT GTCTGAGGGC TGGGCTCTTC CTACCCAAGG GTTGGGGGCT GGCCTGTCCC 960
TCATGACCCA GGCAGGCGGC CAGGGCTCCC CGGAACTCCA GGCTGCTGCG GGTGTCTGCT 1020
CTGCCCTGGG TGAGGCTCTA GAAGATTCCT GTGGAAGCGA CTGTGTCTAG GGGAGCCCAT 1080
TCCCCAGTTT AAAGGACGTC CCCCCCCATG GCTATCCACA TGCCCAGTCC TCTCAGGAAG 1140
TTCCAGGCTG CCAGGATCAG AGGAAGCAGA AGCCGCTGTC CTTCAGCAGG ACCCTGCAAA 1200
AGCAGGATGA ATCAGCGGGG CCATTCAGAA CAAGGTTCAA ATTACTGCTG CACTTTTCAG 1260
AATGGAGCCA GGCTCAGTGT TTCAGAACCA GAGGCTGACG CGGATCAGCT CGCACCCAGC 1320
CTGGGACCTG AGCCAGCCCC TGAGTGCCAC TCTCCACGGC CGCCTCAGAG GGTAAGCCTC 1380
TCCAAGCCTG CTTCCTCGCC GGCATGGTGG GGGTGGCCCT GCCATCCCCT AGGGGCTCTG 1440
CGGGATCCCC TGAACACTAC GAAAAACCTG AGCCCCACTC CTGGCCACTG GGTAAGGACC 1500
TCTCCGAGCC TTTCTCCTTC CCATTCACTC CCACCCCCAG GCAGGAGCGA CCAGTGCTGA 1560
GAAGTCCTAT CATCCCACAA CCCATCATCC TCCGTCATCC CCTGTCCGTC ACCCCGCAGC 1620
TGTCATCCCC CATCACCCCG TGTCTGTCAC CCCGCGTCTG TCACCCCATG TCTGTCACCC 1680
TGCATCCGTC ACCCCGTGTC TGTCATCCCC GTCCGTCACC CCATGTCTGT CACCCTGAAA 1740
CCATCACCCC ATCTGTCACC CCACATCCGT CATCCCGTGT CCATCACCCC GCGTCCATCA 1800
CCCCCATCCG TCACCCCATG TCCGTCACCC CATCCATCAC CCCGCGTCCA TCATCCCCCA 1860
TCCATCACCC CCCGTCCGTC ATCCTCCGTC CATCACCCCA CGTCCATGAT CCCCCGTCCG 1920
TCACCCCGCA TCCATCACCC CATGTCCATC ACCCCACGTC CATCACCCCA TGTCCATTAT 1980
CCCCTGTCTG TCACCCCGCG TCCGCCATCC ACATCCCATC ACCAGGTGCT GTTTTCTTGG 2040
TGCTAGAGCA AGGTGGGATT CACACCTTGT GTGCACAGCT TCTGAGTCAC TGGGCGGCTG 2100
GGCACAGCCT AACTCAGGAG CAGGGACCCA CGGAGGGTGT GGCGACGACA 2150