EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS154-03094 
Organism
Homo sapiens 
Tissue/cell
Osteoblast 
Coordinate
chr10:105516760-105519980 
TF binding sites/motifs
Number: 13             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr10:105517958-105517969GGGTGACTCAG+6.02
FOXP1MA0481.2chr10:105519558-105519570AAGTAAACAGTA+6.18
JUNBMA0490.1chr10:105517958-105517969GGGTGACTCAG+6.02
MAFFMA0495.3chr10:105517659-105517674GAGCTGACTCAGCAC+6.55
MAFFMA0495.3chr10:105517659-105517674GAGCTGACTCAGCAC-6.63
MAFGMA0659.1chr10:105517656-105517677GAAGAGCTGACTCAGCACAGA-6.16
MAFGMA0659.1chr10:105517656-105517677GAAGAGCTGACTCAGCACAGA+6.36
MAFKMA0496.2chr10:105517657-105517676AAGAGCTGACTCAGCACAG+6.29
MAFKMA0496.2chr10:105517657-105517676AAGAGCTGACTCAGCACAG-6.64
NFE2L1MA0089.2chr10:105517958-105517973GGGTGACTCAGCACT+6.67
Nfe2l2MA0150.2chr10:105517956-105517971CTGGGTGACTCAGCA+6.53
Stat6MA0520.1chr10:105518257-105518272AACTTCCTGAGAACC+6.11
ZNF263MA0528.1chr10:105516928-105516949GGGGGAGGGAGTGGAGGGTAA+6.37
Number of super-enhancer constituents: 15             
IDCoordinateTissue/cell
SE_23068chr10:105517553-105519967Colon_Crypt_1
SE_23830chr10:105518603-105519105Colon_Crypt_2
SE_23830chr10:105519137-105519471Colon_Crypt_2
SE_25254chr10:105518110-105519057Colon_Crypt_3
SE_25254chr10:105519117-105519915Colon_Crypt_3
SE_26541chr10:105515035-105520069Esophagus
SE_27893chr10:105518101-105520176Fetal_Intestine
SE_32316chr10:105517119-105519921Gastric
SE_35962chr10:105516443-105520023HMEC
SE_43235chr10:105515418-105520185Lung
SE_50087chr10:105516979-105520122Sigmoid_Colon
SE_51690chr10:105515419-105520378Skeletal_Muscle
SE_56459chr10:105516981-105519876u87
SE_64487chr10:105516561-105520142NHEK
SE_65384chr10:105517045-105519857Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr10105517207105518532
chr10105518533105518612
chr10105518614105519760
chr10105516800105519919
Number: 1             
IDChromosomeStartEnd
GH10I103756chr10105515876105520271
Enhancer Sequence
CTGGTCTCAG TAACCATCCA GTCTGCCATC TACGCTGGAG TATGAGTTGG CTGGAAGCAC 60
CAACCCTGGG GACACCAGGG TATAACTGTA CTCTCTCAGC ATGGAGGGAA AGGATCCAAC 120
CTTGTAAAAG GACATTTAGG CATCAGGTAA GGAAAGGATG TATTTCCAGG GGGAGGGAGT 180
GGAGGGTAAA GGACAGGAGT GTCACCGAGC CCTGAAATCA TGCCTGTCAC TTTCTGGTGA 240
CTTTGCCAAC AAGCAAGGTG ATCCCTGATT GCTCAAACTT AACTTCTTCA ATTTTGTGCC 300
ATGGTGATTA GCATGGGGTG CACTAGAATC CAGGACTCTG GAGACCCAGG CCCGGGTGCA 360
TTTTCTGCGT CTTAGATGAC ACAGACTGAC TGAGACCATG AGAAGAGACA GGCTTTTCGG 420
CCCAGATCAG AAAGTTCCTG GGGAAGATAC CTAGGATACA ATCCATCCAG GACGGAGGGT 480
TGGGGGTAGG TGTTCAGGAG CTGATTCCCT TCTAGAATGA TTGGGAAGGC ACATACCAAG 540
TTGTAACAAG GTGGCCTGGC TCTTTTCCTG GTCTTGGAAT GTGGGGATGT CGCGGGGGAA 600
GGGCTTGGGA GACTGATCTA CATTTCAAAA GTAAAAAAGC CCCTTGCGTG GCTGACCCCT 660
GCAAAGCTTG TTACTCCCTG CAAGACCTGG AGGGTCTGCA GCTCGGAGTC TGGAAGGTAG 720
TGACAGTGAC ACTGCCATGT GATCAGAGGC CGGATCCCCA CCTTTCATCC CAGATCAGCC 780
ATCTGGGTCA TCTGCTCTTT AGAAACAAGC TCCTTGCTGC TTTGCAAGTT ACCACAGGCC 840
GGGAAAGAAC TGCAGGAAGT GAGGCTGTGC CTGGGCTGCG GCCTGGGCTG CAGTGGGAAG 900
AGCTGACTCA GCACAGAGTG GGGAGGGCAA AGGAAATCCC ACATCTGTGT CCTGCGGCAA 960
AGCCACCACG AGCACAGACA GGCTTGCGGC ACCAGTCCTC TCCCGTTGCA CGCCACACAG 1020
CGCTTTCCAT GCATTAACTG CTTGCGATGT CACCAAACCA TGATCAACCC ATTTGACAGA 1080
TGATGCTACA GAGCCTGGAG TCCGTGTGAC TGGGCCAGAT GGCACAGCTC ACAAACACAC 1140
AGGTGGAGCC GCTCTGGAGT GTCTTGGCTC CACAAGTCCT GTCTGCCCAG CTGTCTCTGG 1200
GTGACTCAGC ACTCCTCACT GTTCCACACA CTTCTTACTG TTCTTCAAAC ATATACCGGT 1260
GGTCCGACTA AGGTTACTGT TCTTGCTGTC CCCCCAAGCC TGGCACCCCT GGGCCCTGAT 1320
GATCCAAACC TACTCAGTGG AGATGTCACC TCTGCAAAGA AGCCCTTTGT GACCATCTAA 1380
TTTCAGATGC CTTGAGCTGT AGCACCTGCC ACATGACCTG GTTATTTTTC CTTCTGGCAC 1440
TCATCACTCT TGGAAATTGC TCATCTATTT GTCTTCTGAC TCCCACACTG GAAGGTAAAC 1500
TTCCTGAGAA CCACAACCAG GCCTACTTTG TTCTCAGTCA TATCACCAGT GACCACAGCT 1560
GGCACACAGT ATGTGTTCAA TAAATATCTG TGATAGAAAG GAATGAATGT AGCTATTCCA 1620
CGCTGTGTTC AGAGTCAGCT GCTGACAGCA GGCCCTGAAA ACTGCCCGTC CAGATTACAG 1680
AGTAGGAGAC TGATTTTTGG GGATGGGAAG CAGTAATTAC ATCAAGAGAA GACAAAATAC 1740
CTCCAGTGGA GGTTGGAGGA AAGCTGTGTT TAAGATGGCA CACGGTGCCT CTCAGGCCTA 1800
TAATCTTGTT GACCTTTTTA AACCCCAGAA TTACCAACAG ACCCTATTTT TCCTTCTCCA 1860
TCACATAGTT TGGCTTTTCC TGACATCCCA GGTCACCTGT GGGACCCAGA AACTTCTCAA 1920
CCTCTCTTCC TTGGGGGTTG CAGTCTGGTG AAATCTCTGA GCCACAACCT CCCTCATAGC 1980
ATCCAGGGCC CTTCAGGAAG GGCTTTCTCA GCTGGTGCCT GGTGGAGACA CACACAGACA 2040
CCTATAGCCC AGGGAGCGGG CCACGGACCA GCTCTAGTTA AAGACATCCC TTCCCCCTGC 2100
TTCCTTCTAT GCTGGAACAA ATACCGGATC TTCTGCACAG GGCTCTGGGG GCTGGGAGAG 2160
GAAGGCCCCG GAGAACATGC TTGCAATTCA CCCAGCACCC TCTGCACTGT GGCTCCAAAC 2220
TGCCTCTTCA TTACAGGGCC GTTACGTAAA CTGGCGAGTC AGTACAAAAG AAGCAAGCAT 2280
GCCTGCTGAC TAAAAATATA CCTCTAAGCT CATAAGGTCA CAAGGCTGTC TGCAGGCTGG 2340
CAACGCCTAC CTTGATTATG GTTATAGATT CACTTTTCTC CCTAAGCAAT CTCACTTCTC 2400
CAGGACTCAT CAACCTGGGG ATATGGATAG CGATGCATGG GACTAACTCA GCTATTAGGA 2460
TGAAGGGCTT TCTGGAAGCC CAGAGGCCCA GTGCCAGCCA GTACAGAGAC ACAGATGGCT 2520
TGCTAGTGGG AGGGGACCTC GCACAGCCTT TGCAGAGGGA GTGCAGCTCT TTTTGCTCCA 2580
CTGCCTGGCT TCTGAAGTCC CTCAATCCCT GGCCACAGTT GTTTGCTTTT TACATCAGCA 2640
GCTACACACT CTACTTCATG TCGTAATGAC CATTTCCTCT CAGGGAGTCT CCTCAGGCCA 2700
GCAAACTCGG GATACACAGG AAATCTACTC CAATCCCAGG ATGGGCAACA GGAGATGGAT 2760
TTTCCACAGT CATCTTCTAA AACAAGGCAG AAAATTCCAA GTAAACAGTA GGCTGCCCTG 2820
AGAGGCTGGT GACCCCGCCA CGCTTGGCCC AATGTCCTAA GGAATTTGAT TTCTGCCCAC 2880
CCCTCCAAAA AGCAAGAGAC CTCAGAAAGC GCTAAGGCAC ACTTCTGAGC CAATTCTCCC 2940
TGGGCCTCCT GCTGTTGTAC ATGTCTTGTA AACAAGGCAC TAACTGCTTT TTGTTTTGGA 3000
TGATCTTTTC AAAGGTGCTT GCATAGCAAA CAGCCTTAGA AGACAGAGGT AGTGCCTTGC 3060
TCTGGGGCAT ACGGCAGGTT TGCATATAGT CTTGGACTAA GGATAGTGTC CATCTTGGGA 3120
GCAAAAGGGC AGGTTTGCTT ACCATCCATT ATAAAAAGAT GCAGGCTCCC CTCCTATAAA 3180
GTAACTCACT GCATATGCAG GCATTCATCT GAGCCCGTCT 3220