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

TagContent
EnhancerAtlas ID
HS023-02205 
Organism
Homo sapiens 
Tissue/cell
CD8+ 
Coordinate
chr1:204429940-204432740 
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: 6             
ChromosomeStartEnd
chr1204430000204431924
chr1204430292204431282
chr1204430759204431008
chr1204432329204432499
chr1204432124204432239
chr1204432250204432649
Number: 1             
IDChromosomeStartEnd
GH01I204460chr1204429650204437135
Enhancer Sequence
ACACGGTAGA GCTTAGGAGA AGGAACAGAG GTCTATCTAA ACAAAAGCCA CCTAATATAC 60
TTAATCCTTG GCCGGTATAA ATATTGACTC TCTTAGATAT TTATTACCCG TGTGGTAATC 120
ACTGGTTCAC TCCAGGGCTG GGAACTGTTG GAGAGAGCGG GGAAACAGAG GCACATCACA 180
GGGAGCAGTT GCTGAAGCCC TATCTTCTGG GCCTCTGTAT AGGGGACAAC CAGGAAGAGA 240
CATGTTGGAG TCCACCTGTG CTCAGGCTCC AGGGTGGGAG CTCAGCGAGA GACCCCTCTT 300
CCAATGCTAC CAACTAGGGT GCTGAGGCCA AAAAAACTTG GGGCAAGCCT ACCAAGCCTC 360
CAGATCAGTG TCCCCACCCA ACTTCTTTTT CTGCCTTCCA TCTGTTGGCC CTGCCTGCTT 420
GTGAATAACC TTACAAATTT CTATGACTTC TTGAAAAGTC CCAAATGCAT GCCAGTCCCA 480
CCTGCTCAAG CACCCATGTG TGAGACTCCC CCTTTCAGAG AGAAGGCCTA GGAGCCCTCG 540
GCGATCCAAC CTCTTCCTCT CTCCCAAATC ACACCTTCAA CAGCAAGGAA ACCCAAGAGG 600
AGGGGCAGAG GGAGAACTAC CTCCAGGCCA GCACTGCAGG CCTGGGCCTG GCCTCAGCAG 660
CTGGGTAACA GAAGCCGGAA AAGGACTTCC TTCCTCAGCA GAGCTGGGAA TCTAGGCCAG 720
AAATGGAGAG GAGAGGACAG GAGCATAAGG GGGGCAGTAT ATGTAAAAGC TGGCGGAGGT 780
GCAGGGCCCA GGGTCGTCTA GGTCCCATGA GGGCTCGAGT GAGGGGTTCT CCACATCCTG 840
AGAGGACCAA ATCTCCGATC TAGACCCTCT CAGATCTAAG ACTGAAGTGC AGCCAAAACC 900
TGGAGGTGGT GAGGCTGGGC TGTGGGGCTG GGCCTGGTGG GAGAGCCTGG GAGGAAGGAA 960
GAGTGTGGTG GGGCTGGGGG AGGTGGCAGG AAACCCAACC CTCCCACGGG ACTGCCTCAA 1020
GGTTCTTATC TGAGAGCAGC CTGCATCCTG AACCCACTCA CCCCCTCAGT ATCAGCCCCT 1080
CCTGCCAGGC AGGGGTAGAA AATCTCAGGG CTTCCTTGGG AACTAGCAGA TTTCTGGAAC 1140
CCCCGGAGCG TCCTTTCCAC CCCCATCCCA GGCAGTTGTC ATGTGTTGGG GGTCTGGGGG 1200
CTGGGCCAGG AGACAGCATT GTGCTTTTCT GTTGGGTGGG AGTGGGGCTC CTAGGCCAGG 1260
AGTCATGCAC ACAGGTCCCC TGGGGACTTG CTTGATCTTC TCTGTGGAAG GCCTTCCTCT 1320
CTGTGCATTC AAGTGAGAGT ATGAGGGGTG TGATCTGAGG ACCGCTGACC CTGTCCCACC 1380
TCACTAAGAA TATTTCACCT GAGTCTTAGC AGGAAGGTAG AACTTGACAG CTCCCACTAC 1440
CTCCGGACCC AGGGGCTCCA GGATTTGGGG TGCTGCAAGG GAAATGGCAG TATCTGTGCA 1500
GCCCAGAGCC CTAGGACTTC TCTCCGTGGG CTGCTCCTTC CCTGCTGGTA TTTACTGATT 1560
GCTCACAGGT CATTCTCACA TTTCACCCTC ACTGCAGCTT ACAGAGGGCC CTGAGCATCA 1620
ATCAGCCTTC ACAACTAGTA AGTGGCAAGT CCGAATTCAA ACCTGTGTAA TGGCGTCAGC 1680
AGGAGCTCCA ACTTATCCAC TATGTCCCCT TTTTCCCTTC TAACAGTGGC AGGCCACCTG 1740
GCACTCTCTC TGCCAGGCAA CCCTGAGTCT AGGACCCCTC CTGTTCCTCT AGGGGAAAAG 1800
TGTGTACATA AGTGAGTTTA AAGGTGGGGC ACATTTGAAG GGTACCCTGG AGTTGTACCA 1860
TACAGAACCC TGCCTCTTTC CTTTCCCTTA GCTTCGAGAT GAGGAGGCAG AGGCCAGAAA 1920
GGACCCCACA ATATCCTTAA ATTTGAAATA AGCCCAGATA GCTGGGCACA GTGGCTCACA 1980
CCTGTAATCC CAGCACTTTG GGAGGCCAAG GCGGGCAGAT CACCCGAGGT CAGGAGTTCG 2040
AGACCAGCCT GGCCAACATG GTGAAACCCA GTCTCTATTA AAAAATACAA AAATTAGCCG 2100
GGCGTGGTGG TGCTTATGCC TGTAATCCCA GCTACTCAGG AGGCTGAGGC ATGAGAATCG 2160
CTTGAGCCTG GGAGACGGAG GTTGCAGTGA GCTGAGTGAG ATGGCGCCAC AGCACTCCAG 2220
CCTGCACGAC AGAGTGAGAC TCTGTCTCAA AAAAAGAAAG AAGTCCAGAA ATGAATCTTC 2280
CATCCTGACT GCCAAATCTT ATGCTCTAGA CATAGATCAA CCATCCTTGC ATCTAGACCT 2340
GAATGTAAGA GAGAGAAAAA GCAAGCAGTG GCACTTATAG GGCACTCCTA AGAAGTGAGA 2400
CACAGGTCTC TCCTTTCTCT ATTCCCAAAA CGTGCTTCCT CCAAGTGGAC AGAGACTGGG 2460
GGCAGGAGCG GCTCTGAAGC CTAAGAGAGG AAAGCAGATC TTATCTGTCT GCTGTCACAC 2520
AGCTGTACCA TCTGAGAAGT GATAACCTTG CCCCTGCCTC TCTTCCACTG CAGCCCTCCA 2580
GAGCCCAGGG TAGTGGAAAG GGGGTTGCCT CAGCTGGTCC ACATCAGACT TTCCAGGGAG 2640
GCTGCTTTCC AGAGAGGGCA CTGGATGGAG AGGAGCTGGA GGCACGCCTT TGGGAGGAGG 2700
ATAACTAGCT GCACGGGCCA GCTGGGGAAA AGACTTGTTG GCAGGAGAAT GGGGAGAGAC 2760
AGTAATTGTA ATTTCTCCCC TGGGCTCCAC AAGGGAACTT 2800