EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS141-02846 
Organism
Homo sapiens 
Tissue/cell
NB4 
Coordinate
chr10:105516910-105520090 
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: 3             
ChromosomeStartEnd
chr10105517207105518532
chr10105518533105518612
chr10105518614105519760
Number: 1             
IDChromosomeStartEnd
GH10I103756chr10105515876105520271
Enhancer Sequence
GGAAAGGATG TATTTCCAGG GGGAGGGAGT GGAGGGTAAA GGACAGGAGT GTCACCGAGC 60
CCTGAAATCA TGCCTGTCAC TTTCTGGTGA CTTTGCCAAC AAGCAAGGTG ATCCCTGATT 120
GCTCAAACTT AACTTCTTCA ATTTTGTGCC ATGGTGATTA GCATGGGGTG CACTAGAATC 180
CAGGACTCTG GAGACCCAGG CCCGGGTGCA TTTTCTGCGT CTTAGATGAC ACAGACTGAC 240
TGAGACCATG AGAAGAGACA GGCTTTTCGG CCCAGATCAG AAAGTTCCTG GGGAAGATAC 300
CTAGGATACA ATCCATCCAG GACGGAGGGT TGGGGGTAGG TGTTCAGGAG CTGATTCCCT 360
TCTAGAATGA TTGGGAAGGC ACATACCAAG TTGTAACAAG GTGGCCTGGC TCTTTTCCTG 420
GTCTTGGAAT GTGGGGATGT CGCGGGGGAA GGGCTTGGGA GACTGATCTA CATTTCAAAA 480
GTAAAAAAGC CCCTTGCGTG GCTGACCCCT GCAAAGCTTG TTACTCCCTG CAAGACCTGG 540
AGGGTCTGCA GCTCGGAGTC TGGAAGGTAG TGACAGTGAC ACTGCCATGT GATCAGAGGC 600
CGGATCCCCA CCTTTCATCC CAGATCAGCC ATCTGGGTCA TCTGCTCTTT AGAAACAAGC 660
TCCTTGCTGC TTTGCAAGTT ACCACAGGCC GGGAAAGAAC TGCAGGAAGT GAGGCTGTGC 720
CTGGGCTGCG GCCTGGGCTG CAGTGGGAAG AGCTGACTCA GCACAGAGTG GGGAGGGCAA 780
AGGAAATCCC ACATCTGTGT CCTGCGGCAA AGCCACCACG AGCACAGACA GGCTTGCGGC 840
ACCAGTCCTC TCCCGTTGCA CGCCACACAG CGCTTTCCAT GCATTAACTG CTTGCGATGT 900
CACCAAACCA TGATCAACCC ATTTGACAGA TGATGCTACA GAGCCTGGAG TCCGTGTGAC 960
TGGGCCAGAT GGCACAGCTC ACAAACACAC AGGTGGAGCC GCTCTGGAGT GTCTTGGCTC 1020
CACAAGTCCT GTCTGCCCAG CTGTCTCTGG GTGACTCAGC ACTCCTCACT GTTCCACACA 1080
CTTCTTACTG TTCTTCAAAC ATATACCGGT GGTCCGACTA AGGTTACTGT TCTTGCTGTC 1140
CCCCCAAGCC TGGCACCCCT GGGCCCTGAT GATCCAAACC TACTCAGTGG AGATGTCACC 1200
TCTGCAAAGA AGCCCTTTGT GACCATCTAA TTTCAGATGC CTTGAGCTGT AGCACCTGCC 1260
ACATGACCTG GTTATTTTTC CTTCTGGCAC TCATCACTCT TGGAAATTGC TCATCTATTT 1320
GTCTTCTGAC TCCCACACTG GAAGGTAAAC TTCCTGAGAA CCACAACCAG GCCTACTTTG 1380
TTCTCAGTCA TATCACCAGT GACCACAGCT GGCACACAGT ATGTGTTCAA TAAATATCTG 1440
TGATAGAAAG GAATGAATGT AGCTATTCCA CGCTGTGTTC AGAGTCAGCT GCTGACAGCA 1500
GGCCCTGAAA ACTGCCCGTC CAGATTACAG AGTAGGAGAC TGATTTTTGG GGATGGGAAG 1560
CAGTAATTAC ATCAAGAGAA GACAAAATAC CTCCAGTGGA GGTTGGAGGA AAGCTGTGTT 1620
TAAGATGGCA CACGGTGCCT CTCAGGCCTA TAATCTTGTT GACCTTTTTA AACCCCAGAA 1680
TTACCAACAG ACCCTATTTT TCCTTCTCCA TCACATAGTT TGGCTTTTCC TGACATCCCA 1740
GGTCACCTGT GGGACCCAGA AACTTCTCAA CCTCTCTTCC TTGGGGGTTG CAGTCTGGTG 1800
AAATCTCTGA GCCACAACCT CCCTCATAGC ATCCAGGGCC CTTCAGGAAG GGCTTTCTCA 1860
GCTGGTGCCT GGTGGAGACA CACACAGACA CCTATAGCCC AGGGAGCGGG CCACGGACCA 1920
GCTCTAGTTA AAGACATCCC TTCCCCCTGC TTCCTTCTAT GCTGGAACAA ATACCGGATC 1980
TTCTGCACAG GGCTCTGGGG GCTGGGAGAG GAAGGCCCCG GAGAACATGC TTGCAATTCA 2040
CCCAGCACCC TCTGCACTGT GGCTCCAAAC TGCCTCTTCA TTACAGGGCC GTTACGTAAA 2100
CTGGCGAGTC AGTACAAAAG AAGCAAGCAT GCCTGCTGAC TAAAAATATA CCTCTAAGCT 2160
CATAAGGTCA CAAGGCTGTC TGCAGGCTGG CAACGCCTAC CTTGATTATG GTTATAGATT 2220
CACTTTTCTC CCTAAGCAAT CTCACTTCTC CAGGACTCAT CAACCTGGGG ATATGGATAG 2280
CGATGCATGG GACTAACTCA GCTATTAGGA TGAAGGGCTT TCTGGAAGCC CAGAGGCCCA 2340
GTGCCAGCCA GTACAGAGAC ACAGATGGCT TGCTAGTGGG AGGGGACCTC GCACAGCCTT 2400
TGCAGAGGGA GTGCAGCTCT TTTTGCTCCA CTGCCTGGCT TCTGAAGTCC CTCAATCCCT 2460
GGCCACAGTT GTTTGCTTTT TACATCAGCA GCTACACACT CTACTTCATG TCGTAATGAC 2520
CATTTCCTCT CAGGGAGTCT CCTCAGGCCA GCAAACTCGG GATACACAGG AAATCTACTC 2580
CAATCCCAGG ATGGGCAACA GGAGATGGAT TTTCCACAGT CATCTTCTAA AACAAGGCAG 2640
AAAATTCCAA GTAAACAGTA GGCTGCCCTG AGAGGCTGGT GACCCCGCCA CGCTTGGCCC 2700
AATGTCCTAA GGAATTTGAT TTCTGCCCAC CCCTCCAAAA AGCAAGAGAC CTCAGAAAGC 2760
GCTAAGGCAC ACTTCTGAGC CAATTCTCCC TGGGCCTCCT GCTGTTGTAC ATGTCTTGTA 2820
AACAAGGCAC TAACTGCTTT TTGTTTTGGA TGATCTTTTC AAAGGTGCTT GCATAGCAAA 2880
CAGCCTTAGA AGACAGAGGT AGTGCCTTGC TCTGGGGCAT ACGGCAGGTT TGCATATAGT 2940
CTTGGACTAA GGATAGTGTC CATCTTGGGA GCAAAAGGGC AGGTTTGCTT ACCATCCATT 3000
ATAAAAAGAT GCAGGCTCCC CTCCTATAAA GTAACTCACT GCATATGCAG GCATTCATCT 3060
GAGCCCGTCT TGTCACACCT ACGGAACTTG GAGGAACAGG AGAAGTCCCA AAGTATAAAA 3120
ATATATGTAA ACCAGGTCAG GTGCAGTGGC TCACACCTGT AATCCCAACA CTTTGGGAAG 3180