EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS045-09486 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr10:105517160-105520060 
TF binding sites/motifs
Number: 12             
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
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: 3             
ChromosomeStartEnd
chr10105517207105518532
chr10105518533105518612
chr10105518614105519760
Number: 1             
IDChromosomeStartEnd
GH10I103756chr10105515876105520271
Enhancer Sequence
AGAAGAGACA GGCTTTTCGG CCCAGATCAG AAAGTTCCTG GGGAAGATAC CTAGGATACA 60
ATCCATCCAG GACGGAGGGT TGGGGGTAGG TGTTCAGGAG CTGATTCCCT TCTAGAATGA 120
TTGGGAAGGC ACATACCAAG TTGTAACAAG GTGGCCTGGC TCTTTTCCTG GTCTTGGAAT 180
GTGGGGATGT CGCGGGGGAA GGGCTTGGGA GACTGATCTA CATTTCAAAA GTAAAAAAGC 240
CCCTTGCGTG GCTGACCCCT GCAAAGCTTG TTACTCCCTG CAAGACCTGG AGGGTCTGCA 300
GCTCGGAGTC TGGAAGGTAG TGACAGTGAC ACTGCCATGT GATCAGAGGC CGGATCCCCA 360
CCTTTCATCC CAGATCAGCC ATCTGGGTCA TCTGCTCTTT AGAAACAAGC TCCTTGCTGC 420
TTTGCAAGTT ACCACAGGCC GGGAAAGAAC TGCAGGAAGT GAGGCTGTGC CTGGGCTGCG 480
GCCTGGGCTG CAGTGGGAAG AGCTGACTCA GCACAGAGTG GGGAGGGCAA AGGAAATCCC 540
ACATCTGTGT CCTGCGGCAA AGCCACCACG AGCACAGACA GGCTTGCGGC ACCAGTCCTC 600
TCCCGTTGCA CGCCACACAG CGCTTTCCAT GCATTAACTG CTTGCGATGT CACCAAACCA 660
TGATCAACCC ATTTGACAGA TGATGCTACA GAGCCTGGAG TCCGTGTGAC TGGGCCAGAT 720
GGCACAGCTC ACAAACACAC AGGTGGAGCC GCTCTGGAGT GTCTTGGCTC CACAAGTCCT 780
GTCTGCCCAG CTGTCTCTGG GTGACTCAGC ACTCCTCACT GTTCCACACA CTTCTTACTG 840
TTCTTCAAAC ATATACCGGT GGTCCGACTA AGGTTACTGT TCTTGCTGTC CCCCCAAGCC 900
TGGCACCCCT GGGCCCTGAT GATCCAAACC TACTCAGTGG AGATGTCACC TCTGCAAAGA 960
AGCCCTTTGT GACCATCTAA TTTCAGATGC CTTGAGCTGT AGCACCTGCC ACATGACCTG 1020
GTTATTTTTC CTTCTGGCAC TCATCACTCT TGGAAATTGC TCATCTATTT GTCTTCTGAC 1080
TCCCACACTG GAAGGTAAAC TTCCTGAGAA CCACAACCAG GCCTACTTTG TTCTCAGTCA 1140
TATCACCAGT GACCACAGCT GGCACACAGT ATGTGTTCAA TAAATATCTG TGATAGAAAG 1200
GAATGAATGT AGCTATTCCA CGCTGTGTTC AGAGTCAGCT GCTGACAGCA GGCCCTGAAA 1260
ACTGCCCGTC CAGATTACAG AGTAGGAGAC TGATTTTTGG GGATGGGAAG CAGTAATTAC 1320
ATCAAGAGAA GACAAAATAC CTCCAGTGGA GGTTGGAGGA AAGCTGTGTT TAAGATGGCA 1380
CACGGTGCCT CTCAGGCCTA TAATCTTGTT GACCTTTTTA AACCCCAGAA TTACCAACAG 1440
ACCCTATTTT TCCTTCTCCA TCACATAGTT TGGCTTTTCC TGACATCCCA GGTCACCTGT 1500
GGGACCCAGA AACTTCTCAA CCTCTCTTCC TTGGGGGTTG CAGTCTGGTG AAATCTCTGA 1560
GCCACAACCT CCCTCATAGC ATCCAGGGCC CTTCAGGAAG GGCTTTCTCA GCTGGTGCCT 1620
GGTGGAGACA CACACAGACA CCTATAGCCC AGGGAGCGGG CCACGGACCA GCTCTAGTTA 1680
AAGACATCCC TTCCCCCTGC TTCCTTCTAT GCTGGAACAA ATACCGGATC TTCTGCACAG 1740
GGCTCTGGGG GCTGGGAGAG GAAGGCCCCG GAGAACATGC TTGCAATTCA CCCAGCACCC 1800
TCTGCACTGT GGCTCCAAAC TGCCTCTTCA TTACAGGGCC GTTACGTAAA CTGGCGAGTC 1860
AGTACAAAAG AAGCAAGCAT GCCTGCTGAC TAAAAATATA CCTCTAAGCT CATAAGGTCA 1920
CAAGGCTGTC TGCAGGCTGG CAACGCCTAC CTTGATTATG GTTATAGATT CACTTTTCTC 1980
CCTAAGCAAT CTCACTTCTC CAGGACTCAT CAACCTGGGG ATATGGATAG CGATGCATGG 2040
GACTAACTCA GCTATTAGGA TGAAGGGCTT TCTGGAAGCC CAGAGGCCCA GTGCCAGCCA 2100
GTACAGAGAC ACAGATGGCT TGCTAGTGGG AGGGGACCTC GCACAGCCTT TGCAGAGGGA 2160
GTGCAGCTCT TTTTGCTCCA CTGCCTGGCT TCTGAAGTCC CTCAATCCCT GGCCACAGTT 2220
GTTTGCTTTT TACATCAGCA GCTACACACT CTACTTCATG TCGTAATGAC CATTTCCTCT 2280
CAGGGAGTCT CCTCAGGCCA GCAAACTCGG GATACACAGG AAATCTACTC CAATCCCAGG 2340
ATGGGCAACA GGAGATGGAT TTTCCACAGT CATCTTCTAA AACAAGGCAG AAAATTCCAA 2400
GTAAACAGTA GGCTGCCCTG AGAGGCTGGT GACCCCGCCA CGCTTGGCCC AATGTCCTAA 2460
GGAATTTGAT TTCTGCCCAC CCCTCCAAAA AGCAAGAGAC CTCAGAAAGC GCTAAGGCAC 2520
ACTTCTGAGC CAATTCTCCC TGGGCCTCCT GCTGTTGTAC ATGTCTTGTA AACAAGGCAC 2580
TAACTGCTTT TTGTTTTGGA TGATCTTTTC AAAGGTGCTT GCATAGCAAA CAGCCTTAGA 2640
AGACAGAGGT AGTGCCTTGC TCTGGGGCAT ACGGCAGGTT TGCATATAGT CTTGGACTAA 2700
GGATAGTGTC CATCTTGGGA GCAAAAGGGC AGGTTTGCTT ACCATCCATT ATAAAAAGAT 2760
GCAGGCTCCC CTCCTATAAA GTAACTCACT GCATATGCAG GCATTCATCT GAGCCCGTCT 2820
TGTCACACCT ACGGAACTTG GAGGAACAGG AGAAGTCCCA AAGTATAAAA ATATATGTAA 2880
ACCAGGTCAG GTGCAGTGGC 2900