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

TagContent
EnhancerAtlas ID
HS101-06029 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr10:105516720-105519860 
TF binding sites/motifs
Number: 14             
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
NR2C2MA0504.1chr10:105516738-105516753TGCCCTCTCACCTCT-6.44
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: 3             
ChromosomeStartEnd
chr10105517207105518532
chr10105518533105518612
chr10105518614105519760
Number: 1             
IDChromosomeStartEnd
GH10I103756chr10105515876105520271
Enhancer Sequence
TAGCCTCAGC TGCCCACTTG CCCTCTCACC TCTATCAACC CTGGTCTCAG TAACCATCCA 60
GTCTGCCATC TACGCTGGAG TATGAGTTGG CTGGAAGCAC CAACCCTGGG GACACCAGGG 120
TATAACTGTA CTCTCTCAGC ATGGAGGGAA AGGATCCAAC CTTGTAAAAG GACATTTAGG 180
CATCAGGTAA GGAAAGGATG TATTTCCAGG GGGAGGGAGT GGAGGGTAAA GGACAGGAGT 240
GTCACCGAGC CCTGAAATCA TGCCTGTCAC TTTCTGGTGA CTTTGCCAAC AAGCAAGGTG 300
ATCCCTGATT GCTCAAACTT AACTTCTTCA ATTTTGTGCC ATGGTGATTA GCATGGGGTG 360
CACTAGAATC CAGGACTCTG GAGACCCAGG CCCGGGTGCA TTTTCTGCGT CTTAGATGAC 420
ACAGACTGAC TGAGACCATG AGAAGAGACA GGCTTTTCGG CCCAGATCAG AAAGTTCCTG 480
GGGAAGATAC CTAGGATACA ATCCATCCAG GACGGAGGGT TGGGGGTAGG TGTTCAGGAG 540
CTGATTCCCT TCTAGAATGA TTGGGAAGGC ACATACCAAG TTGTAACAAG GTGGCCTGGC 600
TCTTTTCCTG GTCTTGGAAT GTGGGGATGT CGCGGGGGAA GGGCTTGGGA GACTGATCTA 660
CATTTCAAAA GTAAAAAAGC CCCTTGCGTG GCTGACCCCT GCAAAGCTTG TTACTCCCTG 720
CAAGACCTGG AGGGTCTGCA GCTCGGAGTC TGGAAGGTAG TGACAGTGAC ACTGCCATGT 780
GATCAGAGGC CGGATCCCCA CCTTTCATCC CAGATCAGCC ATCTGGGTCA TCTGCTCTTT 840
AGAAACAAGC TCCTTGCTGC TTTGCAAGTT ACCACAGGCC GGGAAAGAAC TGCAGGAAGT 900
GAGGCTGTGC CTGGGCTGCG GCCTGGGCTG CAGTGGGAAG AGCTGACTCA GCACAGAGTG 960
GGGAGGGCAA AGGAAATCCC ACATCTGTGT CCTGCGGCAA AGCCACCACG AGCACAGACA 1020
GGCTTGCGGC ACCAGTCCTC TCCCGTTGCA CGCCACACAG CGCTTTCCAT GCATTAACTG 1080
CTTGCGATGT CACCAAACCA TGATCAACCC ATTTGACAGA TGATGCTACA GAGCCTGGAG 1140
TCCGTGTGAC TGGGCCAGAT GGCACAGCTC ACAAACACAC AGGTGGAGCC GCTCTGGAGT 1200
GTCTTGGCTC CACAAGTCCT GTCTGCCCAG CTGTCTCTGG GTGACTCAGC ACTCCTCACT 1260
GTTCCACACA CTTCTTACTG TTCTTCAAAC ATATACCGGT GGTCCGACTA AGGTTACTGT 1320
TCTTGCTGTC CCCCCAAGCC TGGCACCCCT GGGCCCTGAT GATCCAAACC TACTCAGTGG 1380
AGATGTCACC TCTGCAAAGA AGCCCTTTGT GACCATCTAA TTTCAGATGC CTTGAGCTGT 1440
AGCACCTGCC ACATGACCTG GTTATTTTTC CTTCTGGCAC TCATCACTCT TGGAAATTGC 1500
TCATCTATTT GTCTTCTGAC TCCCACACTG GAAGGTAAAC TTCCTGAGAA CCACAACCAG 1560
GCCTACTTTG TTCTCAGTCA TATCACCAGT GACCACAGCT GGCACACAGT ATGTGTTCAA 1620
TAAATATCTG TGATAGAAAG GAATGAATGT AGCTATTCCA CGCTGTGTTC AGAGTCAGCT 1680
GCTGACAGCA GGCCCTGAAA ACTGCCCGTC CAGATTACAG AGTAGGAGAC TGATTTTTGG 1740
GGATGGGAAG CAGTAATTAC ATCAAGAGAA GACAAAATAC CTCCAGTGGA GGTTGGAGGA 1800
AAGCTGTGTT TAAGATGGCA CACGGTGCCT CTCAGGCCTA TAATCTTGTT GACCTTTTTA 1860
AACCCCAGAA TTACCAACAG ACCCTATTTT TCCTTCTCCA TCACATAGTT TGGCTTTTCC 1920
TGACATCCCA GGTCACCTGT GGGACCCAGA AACTTCTCAA CCTCTCTTCC TTGGGGGTTG 1980
CAGTCTGGTG AAATCTCTGA GCCACAACCT CCCTCATAGC ATCCAGGGCC CTTCAGGAAG 2040
GGCTTTCTCA GCTGGTGCCT GGTGGAGACA CACACAGACA CCTATAGCCC AGGGAGCGGG 2100
CCACGGACCA GCTCTAGTTA AAGACATCCC TTCCCCCTGC TTCCTTCTAT GCTGGAACAA 2160
ATACCGGATC TTCTGCACAG GGCTCTGGGG GCTGGGAGAG GAAGGCCCCG GAGAACATGC 2220
TTGCAATTCA CCCAGCACCC TCTGCACTGT GGCTCCAAAC TGCCTCTTCA TTACAGGGCC 2280
GTTACGTAAA CTGGCGAGTC AGTACAAAAG AAGCAAGCAT GCCTGCTGAC TAAAAATATA 2340
CCTCTAAGCT CATAAGGTCA CAAGGCTGTC TGCAGGCTGG CAACGCCTAC CTTGATTATG 2400
GTTATAGATT CACTTTTCTC CCTAAGCAAT CTCACTTCTC CAGGACTCAT CAACCTGGGG 2460
ATATGGATAG CGATGCATGG GACTAACTCA GCTATTAGGA TGAAGGGCTT TCTGGAAGCC 2520
CAGAGGCCCA GTGCCAGCCA GTACAGAGAC ACAGATGGCT TGCTAGTGGG AGGGGACCTC 2580
GCACAGCCTT TGCAGAGGGA GTGCAGCTCT TTTTGCTCCA CTGCCTGGCT TCTGAAGTCC 2640
CTCAATCCCT GGCCACAGTT GTTTGCTTTT TACATCAGCA GCTACACACT CTACTTCATG 2700
TCGTAATGAC CATTTCCTCT CAGGGAGTCT CCTCAGGCCA GCAAACTCGG GATACACAGG 2760
AAATCTACTC CAATCCCAGG ATGGGCAACA GGAGATGGAT TTTCCACAGT CATCTTCTAA 2820
AACAAGGCAG AAAATTCCAA GTAAACAGTA GGCTGCCCTG AGAGGCTGGT GACCCCGCCA 2880
CGCTTGGCCC AATGTCCTAA GGAATTTGAT TTCTGCCCAC CCCTCCAAAA AGCAAGAGAC 2940
CTCAGAAAGC GCTAAGGCAC ACTTCTGAGC CAATTCTCCC TGGGCCTCCT GCTGTTGTAC 3000
ATGTCTTGTA AACAAGGCAC TAACTGCTTT TTGTTTTGGA TGATCTTTTC AAAGGTGCTT 3060
GCATAGCAAA CAGCCTTAGA AGACAGAGGT AGTGCCTTGC TCTGGGGCAT ACGGCAGGTT 3120
TGCATATAGT CTTGGACTAA 3140