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

TagContent
EnhancerAtlas ID
HS095-04074 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr10:81027520-81030150 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr10:81029206-81029226CCCCCCAACACACACACACA+6.69
RREB1MA0073.1chr10:81029208-81029228CCCCAACACACACACACACA+7.29
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00967chr10:81027238-81028746Adrenal_Gland
SE_00967chr10:81029282-81031256Adrenal_Gland
SE_03471chr10:81027754-81028786Brain_Angular_Gyrus
SE_03471chr10:81029265-81030614Brain_Angular_Gyrus
SE_04037chr10:81023957-81031899Brain_Anterior_Caudate
SE_04933chr10:81023858-81031819Brain_Cingulate_Gyrus
SE_05772chr10:81019645-81038182Brain_Hippocampus_Middle
SE_06946chr10:81023686-81031620Brain_Hippocampus_Middle_150
SE_07838chr10:81024857-81031892Brain_Inferior_Temporal_Lobe
SE_09148chr10:81023879-81031947CD14
SE_11725chr10:81024446-81028976CD20
SE_13540chr10:81025139-81027888CD34_Primary_RO01536
SE_13540chr10:81029466-81030423CD34_Primary_RO01536
SE_26661chr10:81019581-81029059Esophagus
SE_26661chr10:81029244-81031856Esophagus
SE_31588chr10:81027266-81028807Gastric
SE_37872chr10:81025005-81031082HSMMtube
SE_40721chr10:81023665-81031388Left_Ventricle
SE_42200chr10:81022481-81031862Lung
SE_44361chr10:81024138-81029166NHDF-Ad
SE_44361chr10:81029267-81031446NHDF-Ad
SE_45787chr10:81020615-81030652Osteoblasts
SE_48707chr10:81027257-81029217Right_Atrium
SE_50353chr10:81023745-81031471Sigmoid_Colon
SE_52824chr10:81024807-81028601Small_Intestine
SE_54038chr10:81024390-81029280Spleen
SE_54038chr10:81029386-81031222Spleen
SE_54575chr10:81025293-81028541Stomach_Smooth_Muscle
SE_62376chr10:81000995-81055642Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr108102757581027693
chr108102867681029041
chr108102797381028590
chr108102956881029668
Number: 1             
IDChromosomeStartEnd
GH10I079263chr108102303081031541
Enhancer Sequence
TTGACAAAGG GGCCCTTCCT TCACCTCATG GTTCCTCACA CCAGGCCAGT GAGCAGGAGA 60
GGTTCCTCTT AGTGTCTGTC CATTTTAGAG ATTTGATGAG GAGTCCAGGC CCGTGTTGAC 120
TCAAACCCCT GTGTCTGCTG CACTCTCCCG CCCCTCCCAA GCCCTCACCA CCACTTCTTT 180
TCTGTGCATG GCTATAGAAC TTGGGGTCCC AGGGATATTC AGGAGACCCC ATTGCCTTGA 240
ACTCCCAGGC TTCCCCGGTC CCAGGACCCT GTGTTTGGGA GCTGAAAGAG GAGGATCAGA 300
GGGTAGGGGA GCACGGCCTG GGCCCAGGAG CAGAAGGAGC AGCACTATCT CCAGGGAGCC 360
CTGGGTGAGA TGCTGGGAAC ATCTCACTAA CATGAACAGC AGCGCCGGCC CCTGAGCAGA 420
GGACGACCAG GGCTGTGGCT GGCCCCCACG CTGTATGAAC TGTTGCTGCT GTGAACTGCT 480
TGCCTCCTGT TCCCCGTGAC TGGGGTGGCT GTGCATGTCA TGAAACATGT GTCATGTGAC 540
TCAGTTGTAG GTTTTATTTG AGGACAGCAC CAGTCTCTGG ACACATTCGT GATGAGATTC 600
CTTTCAGAAC CCTGTTTCTG AAGCTGGTTT CCTGCCCCCA GGAATGGGGA GCTGCTGGTA 660
GGTTTAAAGG CCGCTGAGCG CCTGGTCACA GATGCTGCTC CAGTTGTCCG GGTCTCAGTG 720
TCTGTCCTTC CTTCCCAGTC GTCTCAGCAT ATTGGGTTAT TTCTAGCTGT GATTCATGTC 780
AGTGTGTTAG TCATCTGTTG GCTGCATAGC ATGTGCTAAA CGCCGTGCTG GGTGCCAGGG 840
TTGTAGAAGT GAAGCCCCCA AATCCGATCG TGGCCCCAGG GGCTCATGCT GTCGCTACGG 900
AGCACCATGG CATTCCCCTG GGTAGTGTGG CCCAAGATTC GTGTCTGCAT CCATCAAGCA 960
ACTGCCATCT ACCAGGCCCT GTGCAGCCTC TGGGGATACA GATTGGAAAG AGGTAATCAG 1020
AATGCATGGG TGGAAGAAGT CCTCTGACCG CGTTGCAGAG GGCAGGTTGG CAGGAGGCAG 1080
GTTTGGAGAT GGAGAGGAAT GACAGGATGC TGTTGTCATA ATTCAGAGGA GAACCGGCAG 1140
GGCTGCAGAA GGTGATTGGA TTGGAGCAGG CAAGGAGCAA AGGGAACAGA CTGCAAAGAT 1200
CATCAGGATG TGGTGACCAG CGGGTGGGAC AGGGAGGGGC CCGTCTTCCT GAGGCAGCTC 1260
GAGGTGCTCC CTGGGATTCT AGTGGATGTG GGAGCAGGAA CTTGCGACAT GTCAGAGGGG 1320
AGAGTGTGAG GACCAGTGTG GGGGCCTGGC TCTCCTGCCC CTGACTCAAC AGGCAAGCCC 1380
CTGCAGCTCC CATGCCCAGT CTCCCCCGCT GCGGAGTGGC GCCACTCTCA CTGCTGCTGC 1440
TACTTCAGAG GGTCTTGTGT GGCCTTTTGT AAGCTCATGG GATGGAAGCA TCTGAAAATG 1500
TATCATTCAT ATTTTTATTG GAATCATGAA TCCCACTTGC CACCTGCCAG GGCATGGTTT 1560
GAGGATGAGA GGGCCCTGCT TCAAGATGCT GCTGCCATTG CTTCGCAGGC CTCTTCCTGG 1620
GCCCCTCTGA GTGCTGCCCC ATCCCTGGGG GTCTCCTGGG TCTCAGAAGC ACCCCTCCCA 1680
ACACCTCCCC CCAACACACA CACACACACA CACACACACA CACACACTTT CTCTGTTCTC 1740
CAGCAGCCTT TTAGCTGCTA AGATGCTCTT TGATACTTAG GCCTTTGTTT CATTTTGCGT 1800
GTGGCTTCCC CAGGCTGCAG TGTGTTCGAT GACTCTCCCG CCCAGCCATA CATCCAGGCT 1860
TCTGTTCCCT TCTCCAGATG GCCTTTCATC CCTCCCAGCC TCCCCCTGCA CCCCACTGCT 1920
GCTGTCATCC ATTCCTGACC GCCAGATCTT ACCAGGAGCA AGCATCCCAG GCTTCTCACT 1980
GTCCGCACCT CCCCTTGCCT GGCTCCATCA GGAGCGCCTC TTTCCCTATG GCTGCTGTGG 2040
CTGCCTCTGC TTTCTTGCTC CTTTTCAAGC CAAGTGCAGC CTGGCGAGGA AGCCTTTCCC 2100
AGGTGCCCAG GTGAGCGTAC CTGCTCCCCG TGACACCCGA CCCGATCGAT GCTAACAAAG 2160
GCTGGTCACT CGGCCTGTCT GAACAGTACA TGTAGATCCA CCCTCCTCAC CTGGCACTCA 2220
GGCGATTCCT GAACTAGGGC TGCACTCCTC TGCCTCTCAC CTCCTCATTT GGTCAGCCAG 2280
TCCTGGGCGT CTGTGCTGCT AGGAGCTACA GGTACAGGGG CAAATACAGG GCCTGTCACT 2340
GCCCCTGGGG AGGGCACGCC TGAGCAAGCC AGGACCAGCT GCCCCGGCAT CCTCACTCAG 2400
GCCTGCCTCA CCCGACATCT GGTTTCATTT TTTCCCCCTA ACGGACAGAC AGTATGGGGG 2460
CTGCTGGCTA CAGGGGAGTT GCTGGAAAGG TCTTGGGGAA GCAGATGTTG GGAAGCTGGC 2520
TCTTCCTCGG TGCCTTCCTG CCTGGTCCCC TTCTGATCCT CAGAGCCAGT GCTTGTTCAC 2580
TCCCTTTTCT GTTTTAGATG AGTGACCACA GGGTCACTGG CTAGTGTTGG 2630