EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-03759 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr10:105516960-105519930 
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
GTCACCGAGC CCTGAAATCA TGCCTGTCAC TTTCTGGTGA CTTTGCCAAC AAGCAAGGTG 60
ATCCCTGATT GCTCAAACTT AACTTCTTCA ATTTTGTGCC ATGGTGATTA GCATGGGGTG 120
CACTAGAATC CAGGACTCTG GAGACCCAGG CCCGGGTGCA TTTTCTGCGT CTTAGATGAC 180
ACAGACTGAC TGAGACCATG AGAAGAGACA GGCTTTTCGG CCCAGATCAG AAAGTTCCTG 240
GGGAAGATAC CTAGGATACA ATCCATCCAG GACGGAGGGT TGGGGGTAGG TGTTCAGGAG 300
CTGATTCCCT TCTAGAATGA TTGGGAAGGC ACATACCAAG TTGTAACAAG GTGGCCTGGC 360
TCTTTTCCTG GTCTTGGAAT GTGGGGATGT CGCGGGGGAA GGGCTTGGGA GACTGATCTA 420
CATTTCAAAA GTAAAAAAGC CCCTTGCGTG GCTGACCCCT GCAAAGCTTG TTACTCCCTG 480
CAAGACCTGG AGGGTCTGCA GCTCGGAGTC TGGAAGGTAG TGACAGTGAC ACTGCCATGT 540
GATCAGAGGC CGGATCCCCA CCTTTCATCC CAGATCAGCC ATCTGGGTCA TCTGCTCTTT 600
AGAAACAAGC TCCTTGCTGC TTTGCAAGTT ACCACAGGCC GGGAAAGAAC TGCAGGAAGT 660
GAGGCTGTGC CTGGGCTGCG GCCTGGGCTG CAGTGGGAAG AGCTGACTCA GCACAGAGTG 720
GGGAGGGCAA AGGAAATCCC ACATCTGTGT CCTGCGGCAA AGCCACCACG AGCACAGACA 780
GGCTTGCGGC ACCAGTCCTC TCCCGTTGCA CGCCACACAG CGCTTTCCAT GCATTAACTG 840
CTTGCGATGT CACCAAACCA TGATCAACCC ATTTGACAGA TGATGCTACA GAGCCTGGAG 900
TCCGTGTGAC TGGGCCAGAT GGCACAGCTC ACAAACACAC AGGTGGAGCC GCTCTGGAGT 960
GTCTTGGCTC CACAAGTCCT GTCTGCCCAG CTGTCTCTGG GTGACTCAGC ACTCCTCACT 1020
GTTCCACACA CTTCTTACTG TTCTTCAAAC ATATACCGGT GGTCCGACTA AGGTTACTGT 1080
TCTTGCTGTC CCCCCAAGCC TGGCACCCCT GGGCCCTGAT GATCCAAACC TACTCAGTGG 1140
AGATGTCACC TCTGCAAAGA AGCCCTTTGT GACCATCTAA TTTCAGATGC CTTGAGCTGT 1200
AGCACCTGCC ACATGACCTG GTTATTTTTC CTTCTGGCAC TCATCACTCT TGGAAATTGC 1260
TCATCTATTT GTCTTCTGAC TCCCACACTG GAAGGTAAAC TTCCTGAGAA CCACAACCAG 1320
GCCTACTTTG TTCTCAGTCA TATCACCAGT GACCACAGCT GGCACACAGT ATGTGTTCAA 1380
TAAATATCTG TGATAGAAAG GAATGAATGT AGCTATTCCA CGCTGTGTTC AGAGTCAGCT 1440
GCTGACAGCA GGCCCTGAAA ACTGCCCGTC CAGATTACAG AGTAGGAGAC TGATTTTTGG 1500
GGATGGGAAG CAGTAATTAC ATCAAGAGAA GACAAAATAC CTCCAGTGGA GGTTGGAGGA 1560
AAGCTGTGTT TAAGATGGCA CACGGTGCCT CTCAGGCCTA TAATCTTGTT GACCTTTTTA 1620
AACCCCAGAA TTACCAACAG ACCCTATTTT TCCTTCTCCA TCACATAGTT TGGCTTTTCC 1680
TGACATCCCA GGTCACCTGT GGGACCCAGA AACTTCTCAA CCTCTCTTCC TTGGGGGTTG 1740
CAGTCTGGTG AAATCTCTGA GCCACAACCT CCCTCATAGC ATCCAGGGCC CTTCAGGAAG 1800
GGCTTTCTCA GCTGGTGCCT GGTGGAGACA CACACAGACA CCTATAGCCC AGGGAGCGGG 1860
CCACGGACCA GCTCTAGTTA AAGACATCCC TTCCCCCTGC TTCCTTCTAT GCTGGAACAA 1920
ATACCGGATC TTCTGCACAG GGCTCTGGGG GCTGGGAGAG GAAGGCCCCG GAGAACATGC 1980
TTGCAATTCA CCCAGCACCC TCTGCACTGT GGCTCCAAAC TGCCTCTTCA TTACAGGGCC 2040
GTTACGTAAA CTGGCGAGTC AGTACAAAAG AAGCAAGCAT GCCTGCTGAC TAAAAATATA 2100
CCTCTAAGCT CATAAGGTCA CAAGGCTGTC TGCAGGCTGG CAACGCCTAC CTTGATTATG 2160
GTTATAGATT CACTTTTCTC CCTAAGCAAT CTCACTTCTC CAGGACTCAT CAACCTGGGG 2220
ATATGGATAG CGATGCATGG GACTAACTCA GCTATTAGGA TGAAGGGCTT TCTGGAAGCC 2280
CAGAGGCCCA GTGCCAGCCA GTACAGAGAC ACAGATGGCT TGCTAGTGGG AGGGGACCTC 2340
GCACAGCCTT TGCAGAGGGA GTGCAGCTCT TTTTGCTCCA CTGCCTGGCT TCTGAAGTCC 2400
CTCAATCCCT GGCCACAGTT GTTTGCTTTT TACATCAGCA GCTACACACT CTACTTCATG 2460
TCGTAATGAC CATTTCCTCT CAGGGAGTCT CCTCAGGCCA GCAAACTCGG GATACACAGG 2520
AAATCTACTC CAATCCCAGG ATGGGCAACA GGAGATGGAT TTTCCACAGT CATCTTCTAA 2580
AACAAGGCAG AAAATTCCAA GTAAACAGTA GGCTGCCCTG AGAGGCTGGT GACCCCGCCA 2640
CGCTTGGCCC AATGTCCTAA GGAATTTGAT TTCTGCCCAC CCCTCCAAAA AGCAAGAGAC 2700
CTCAGAAAGC GCTAAGGCAC ACTTCTGAGC CAATTCTCCC TGGGCCTCCT GCTGTTGTAC 2760
ATGTCTTGTA AACAAGGCAC TAACTGCTTT TTGTTTTGGA TGATCTTTTC AAAGGTGCTT 2820
GCATAGCAAA CAGCCTTAGA AGACAGAGGT AGTGCCTTGC TCTGGGGCAT ACGGCAGGTT 2880
TGCATATAGT CTTGGACTAA GGATAGTGTC CATCTTGGGA GCAAAAGGGC AGGTTTGCTT 2940
ACCATCCATT ATAAAAAGAT GCAGGCTCCC 2970