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

TagContent
EnhancerAtlas ID
HS187-02184 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr1:204430040-204432740 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr1:204430535-204430556AGAGGAGGGGCAGAGGGAGAA+6.85
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00064chr1:204429083-204439520Adipose_Nuclei
SE_01898chr1:204432147-204436806Aorta
SE_03188chr1:204430961-204431525Brain_Angular_Gyrus
SE_03188chr1:204432108-204432739Brain_Angular_Gyrus
SE_03975chr1:204428687-204432015Brain_Anterior_Caudate
SE_03975chr1:204432055-204439410Brain_Anterior_Caudate
SE_04850chr1:204428109-204440381Brain_Cingulate_Gyrus
SE_05834chr1:204428180-204440061Brain_Hippocampus_Middle
SE_06778chr1:204428166-204440350Brain_Hippocampus_Middle_150
SE_07775chr1:204428249-204440457Brain_Inferior_Temporal_Lobe
SE_10255chr1:204428606-204432650CD19_Primary
SE_10905chr1:204414650-204438582CD20
SE_26688chr1:204429951-204431942Esophagus
SE_26688chr1:204432283-204434113Esophagus
SE_30246chr1:204429678-204437104Fetal_Muscle
SE_31610chr1:204430030-204431806Gastric
SE_31610chr1:204432232-204434041Gastric
SE_40776chr1:204428531-204437031Left_Ventricle
SE_42225chr1:204428390-204439096Lung
SE_48746chr1:204429089-204432007Right_Atrium
SE_48746chr1:204432136-204436808Right_Atrium
SE_49909chr1:204428267-204431997RPMI-8402
SE_49909chr1:204432030-204436617RPMI-8402
SE_50149chr1:204429244-204432000Sigmoid_Colon
SE_50149chr1:204432208-204434072Sigmoid_Colon
SE_51536chr1:204429613-204432149Skeletal_Muscle
SE_52421chr1:204429319-204432028Small_Intestine
SE_58430chr1:204415099-204506026Ly1
SE_59794chr1:204415680-204491493Ly4
SE_61475chr1:204430067-204500813Toledo
SE_62377chr1:204415291-204492168Tonsil
SE_65868chr1:204430139-204431482Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr1204430292204431282
chr1204430759204431008
chr1204432329204432499
chr1204432124204432239
chr1204432250204432649
Number: 1             
IDChromosomeStartEnd
GH01I204460chr1204429650204437135
Enhancer Sequence
TTATTACCCG TGTGGTAATC ACTGGTTCAC TCCAGGGCTG GGAACTGTTG GAGAGAGCGG 60
GGAAACAGAG GCACATCACA GGGAGCAGTT GCTGAAGCCC TATCTTCTGG GCCTCTGTAT 120
AGGGGACAAC CAGGAAGAGA CATGTTGGAG TCCACCTGTG CTCAGGCTCC AGGGTGGGAG 180
CTCAGCGAGA GACCCCTCTT CCAATGCTAC CAACTAGGGT GCTGAGGCCA AAAAAACTTG 240
GGGCAAGCCT ACCAAGCCTC CAGATCAGTG TCCCCACCCA ACTTCTTTTT CTGCCTTCCA 300
TCTGTTGGCC CTGCCTGCTT GTGAATAACC TTACAAATTT CTATGACTTC TTGAAAAGTC 360
CCAAATGCAT GCCAGTCCCA CCTGCTCAAG CACCCATGTG TGAGACTCCC CCTTTCAGAG 420
AGAAGGCCTA GGAGCCCTCG GCGATCCAAC CTCTTCCTCT CTCCCAAATC ACACCTTCAA 480
CAGCAAGGAA ACCCAAGAGG AGGGGCAGAG GGAGAACTAC CTCCAGGCCA GCACTGCAGG 540
CCTGGGCCTG GCCTCAGCAG CTGGGTAACA GAAGCCGGAA AAGGACTTCC TTCCTCAGCA 600
GAGCTGGGAA TCTAGGCCAG AAATGGAGAG GAGAGGACAG GAGCATAAGG GGGGCAGTAT 660
ATGTAAAAGC TGGCGGAGGT GCAGGGCCCA GGGTCGTCTA GGTCCCATGA GGGCTCGAGT 720
GAGGGGTTCT CCACATCCTG AGAGGACCAA ATCTCCGATC TAGACCCTCT CAGATCTAAG 780
ACTGAAGTGC AGCCAAAACC TGGAGGTGGT GAGGCTGGGC TGTGGGGCTG GGCCTGGTGG 840
GAGAGCCTGG GAGGAAGGAA GAGTGTGGTG GGGCTGGGGG AGGTGGCAGG AAACCCAACC 900
CTCCCACGGG ACTGCCTCAA GGTTCTTATC TGAGAGCAGC CTGCATCCTG AACCCACTCA 960
CCCCCTCAGT ATCAGCCCCT CCTGCCAGGC AGGGGTAGAA AATCTCAGGG CTTCCTTGGG 1020
AACTAGCAGA TTTCTGGAAC CCCCGGAGCG TCCTTTCCAC CCCCATCCCA GGCAGTTGTC 1080
ATGTGTTGGG GGTCTGGGGG CTGGGCCAGG AGACAGCATT GTGCTTTTCT GTTGGGTGGG 1140
AGTGGGGCTC CTAGGCCAGG AGTCATGCAC ACAGGTCCCC TGGGGACTTG CTTGATCTTC 1200
TCTGTGGAAG GCCTTCCTCT CTGTGCATTC AAGTGAGAGT ATGAGGGGTG TGATCTGAGG 1260
ACCGCTGACC CTGTCCCACC TCACTAAGAA TATTTCACCT GAGTCTTAGC AGGAAGGTAG 1320
AACTTGACAG CTCCCACTAC CTCCGGACCC AGGGGCTCCA GGATTTGGGG TGCTGCAAGG 1380
GAAATGGCAG TATCTGTGCA GCCCAGAGCC CTAGGACTTC TCTCCGTGGG CTGCTCCTTC 1440
CCTGCTGGTA TTTACTGATT GCTCACAGGT CATTCTCACA TTTCACCCTC ACTGCAGCTT 1500
ACAGAGGGCC CTGAGCATCA ATCAGCCTTC ACAACTAGTA AGTGGCAAGT CCGAATTCAA 1560
ACCTGTGTAA TGGCGTCAGC AGGAGCTCCA ACTTATCCAC TATGTCCCCT TTTTCCCTTC 1620
TAACAGTGGC AGGCCACCTG GCACTCTCTC TGCCAGGCAA CCCTGAGTCT AGGACCCCTC 1680
CTGTTCCTCT AGGGGAAAAG TGTGTACATA AGTGAGTTTA AAGGTGGGGC ACATTTGAAG 1740
GGTACCCTGG AGTTGTACCA TACAGAACCC TGCCTCTTTC CTTTCCCTTA GCTTCGAGAT 1800
GAGGAGGCAG AGGCCAGAAA GGACCCCACA ATATCCTTAA ATTTGAAATA AGCCCAGATA 1860
GCTGGGCACA GTGGCTCACA CCTGTAATCC CAGCACTTTG GGAGGCCAAG GCGGGCAGAT 1920
CACCCGAGGT CAGGAGTTCG AGACCAGCCT GGCCAACATG GTGAAACCCA GTCTCTATTA 1980
AAAAATACAA AAATTAGCCG GGCGTGGTGG TGCTTATGCC TGTAATCCCA GCTACTCAGG 2040
AGGCTGAGGC ATGAGAATCG CTTGAGCCTG GGAGACGGAG GTTGCAGTGA GCTGAGTGAG 2100
ATGGCGCCAC AGCACTCCAG CCTGCACGAC AGAGTGAGAC TCTGTCTCAA AAAAAGAAAG 2160
AAGTCCAGAA ATGAATCTTC CATCCTGACT GCCAAATCTT ATGCTCTAGA CATAGATCAA 2220
CCATCCTTGC ATCTAGACCT GAATGTAAGA GAGAGAAAAA GCAAGCAGTG GCACTTATAG 2280
GGCACTCCTA AGAAGTGAGA CACAGGTCTC TCCTTTCTCT ATTCCCAAAA CGTGCTTCCT 2340
CCAAGTGGAC AGAGACTGGG GGCAGGAGCG GCTCTGAAGC CTAAGAGAGG AAAGCAGATC 2400
TTATCTGTCT GCTGTCACAC AGCTGTACCA TCTGAGAAGT GATAACCTTG CCCCTGCCTC 2460
TCTTCCACTG CAGCCCTCCA GAGCCCAGGG TAGTGGAAAG GGGGTTGCCT CAGCTGGTCC 2520
ACATCAGACT TTCCAGGGAG GCTGCTTTCC AGAGAGGGCA CTGGATGGAG AGGAGCTGGA 2580
GGCACGCCTT TGGGAGGAGG ATAACTAGCT GCACGGGCCA GCTGGGGAAA AGACTTGTTG 2640
GCAGGAGAAT GGGGAGAGAC AGTAATTGTA ATTTCTCCCC TGGGCTCCAC AAGGGAACTT 2700