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

TagContent
EnhancerAtlas ID
HS059-03834 
Organism
Homo sapiens 
Tissue/cell
GM12878 
Coordinate
chr1:204430010-204432730 
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
GCCGGTATAA ATATTGACTC TCTTAGATAT TTATTACCCG TGTGGTAATC ACTGGTTCAC 60
TCCAGGGCTG GGAACTGTTG GAGAGAGCGG GGAAACAGAG GCACATCACA GGGAGCAGTT 120
GCTGAAGCCC TATCTTCTGG GCCTCTGTAT AGGGGACAAC CAGGAAGAGA CATGTTGGAG 180
TCCACCTGTG CTCAGGCTCC AGGGTGGGAG CTCAGCGAGA GACCCCTCTT CCAATGCTAC 240
CAACTAGGGT GCTGAGGCCA AAAAAACTTG GGGCAAGCCT ACCAAGCCTC CAGATCAGTG 300
TCCCCACCCA ACTTCTTTTT CTGCCTTCCA TCTGTTGGCC CTGCCTGCTT GTGAATAACC 360
TTACAAATTT CTATGACTTC TTGAAAAGTC CCAAATGCAT GCCAGTCCCA CCTGCTCAAG 420
CACCCATGTG TGAGACTCCC CCTTTCAGAG AGAAGGCCTA GGAGCCCTCG GCGATCCAAC 480
CTCTTCCTCT CTCCCAAATC ACACCTTCAA CAGCAAGGAA ACCCAAGAGG AGGGGCAGAG 540
GGAGAACTAC CTCCAGGCCA GCACTGCAGG CCTGGGCCTG GCCTCAGCAG CTGGGTAACA 600
GAAGCCGGAA AAGGACTTCC TTCCTCAGCA GAGCTGGGAA TCTAGGCCAG AAATGGAGAG 660
GAGAGGACAG GAGCATAAGG GGGGCAGTAT ATGTAAAAGC TGGCGGAGGT GCAGGGCCCA 720
GGGTCGTCTA GGTCCCATGA GGGCTCGAGT GAGGGGTTCT CCACATCCTG AGAGGACCAA 780
ATCTCCGATC TAGACCCTCT CAGATCTAAG ACTGAAGTGC AGCCAAAACC TGGAGGTGGT 840
GAGGCTGGGC TGTGGGGCTG GGCCTGGTGG GAGAGCCTGG GAGGAAGGAA GAGTGTGGTG 900
GGGCTGGGGG AGGTGGCAGG AAACCCAACC CTCCCACGGG ACTGCCTCAA GGTTCTTATC 960
TGAGAGCAGC CTGCATCCTG AACCCACTCA CCCCCTCAGT ATCAGCCCCT CCTGCCAGGC 1020
AGGGGTAGAA AATCTCAGGG CTTCCTTGGG AACTAGCAGA TTTCTGGAAC CCCCGGAGCG 1080
TCCTTTCCAC CCCCATCCCA GGCAGTTGTC ATGTGTTGGG GGTCTGGGGG CTGGGCCAGG 1140
AGACAGCATT GTGCTTTTCT GTTGGGTGGG AGTGGGGCTC CTAGGCCAGG AGTCATGCAC 1200
ACAGGTCCCC TGGGGACTTG CTTGATCTTC TCTGTGGAAG GCCTTCCTCT CTGTGCATTC 1260
AAGTGAGAGT ATGAGGGGTG TGATCTGAGG ACCGCTGACC CTGTCCCACC TCACTAAGAA 1320
TATTTCACCT GAGTCTTAGC AGGAAGGTAG AACTTGACAG CTCCCACTAC CTCCGGACCC 1380
AGGGGCTCCA GGATTTGGGG TGCTGCAAGG GAAATGGCAG TATCTGTGCA GCCCAGAGCC 1440
CTAGGACTTC TCTCCGTGGG CTGCTCCTTC CCTGCTGGTA TTTACTGATT GCTCACAGGT 1500
CATTCTCACA TTTCACCCTC ACTGCAGCTT ACAGAGGGCC CTGAGCATCA ATCAGCCTTC 1560
ACAACTAGTA AGTGGCAAGT CCGAATTCAA ACCTGTGTAA TGGCGTCAGC AGGAGCTCCA 1620
ACTTATCCAC TATGTCCCCT TTTTCCCTTC TAACAGTGGC AGGCCACCTG GCACTCTCTC 1680
TGCCAGGCAA CCCTGAGTCT AGGACCCCTC CTGTTCCTCT AGGGGAAAAG TGTGTACATA 1740
AGTGAGTTTA AAGGTGGGGC ACATTTGAAG GGTACCCTGG AGTTGTACCA TACAGAACCC 1800
TGCCTCTTTC CTTTCCCTTA GCTTCGAGAT GAGGAGGCAG AGGCCAGAAA GGACCCCACA 1860
ATATCCTTAA ATTTGAAATA AGCCCAGATA GCTGGGCACA GTGGCTCACA CCTGTAATCC 1920
CAGCACTTTG GGAGGCCAAG GCGGGCAGAT CACCCGAGGT CAGGAGTTCG AGACCAGCCT 1980
GGCCAACATG GTGAAACCCA GTCTCTATTA AAAAATACAA AAATTAGCCG GGCGTGGTGG 2040
TGCTTATGCC TGTAATCCCA GCTACTCAGG AGGCTGAGGC ATGAGAATCG CTTGAGCCTG 2100
GGAGACGGAG GTTGCAGTGA GCTGAGTGAG ATGGCGCCAC AGCACTCCAG CCTGCACGAC 2160
AGAGTGAGAC TCTGTCTCAA AAAAAGAAAG AAGTCCAGAA ATGAATCTTC CATCCTGACT 2220
GCCAAATCTT ATGCTCTAGA CATAGATCAA CCATCCTTGC ATCTAGACCT GAATGTAAGA 2280
GAGAGAAAAA GCAAGCAGTG GCACTTATAG GGCACTCCTA AGAAGTGAGA CACAGGTCTC 2340
TCCTTTCTCT ATTCCCAAAA CGTGCTTCCT CCAAGTGGAC AGAGACTGGG GGCAGGAGCG 2400
GCTCTGAAGC CTAAGAGAGG AAAGCAGATC TTATCTGTCT GCTGTCACAC AGCTGTACCA 2460
TCTGAGAAGT GATAACCTTG CCCCTGCCTC TCTTCCACTG CAGCCCTCCA GAGCCCAGGG 2520
TAGTGGAAAG GGGGTTGCCT CAGCTGGTCC ACATCAGACT TTCCAGGGAG GCTGCTTTCC 2580
AGAGAGGGCA CTGGATGGAG AGGAGCTGGA GGCACGCCTT TGGGAGGAGG ATAACTAGCT 2640
GCACGGGCCA GCTGGGGAAA AGACTTGTTG GCAGGAGAAT GGGGAGAGAC AGTAATTGTA 2700
ATTTCTCCCC TGGGCTCCAC 2720