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

TagContent
EnhancerAtlas ID
HS187-04941 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr11:114053090-114054870 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:114054143-114054161CCTGGCCTCCTTCCTTTC-6.17
EWSR1-FLI1MA0149.1chr11:114054139-114054157CCTACCTGGCCTCCTTCC-6.45
RARA(var.2)MA0730.1chr11:114054703-114054720GGGACACCCAGAGGTCA+6.26
ZNF143MA0088.2chr11:114053481-114053497TAATGCATTTTGGGAA-6.13
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00146chr11:114048829-114054998Adipose_Nuclei
SE_00894chr11:114053054-114054555Adrenal_Gland
SE_01539chr11:114050406-114054998Aorta
SE_02904chr11:114053516-114054037Bladder
SE_03142chr11:114053118-114054249Brain_Angular_Gyrus
SE_04786chr11:114023147-114054779Brain_Cingulate_Gyrus
SE_05774chr11:114020992-114055319Brain_Hippocampus_Middle
SE_07716chr11:114019371-114055249Brain_Inferior_Temporal_Lobe
SE_08782chr11:114053298-114053483Brain_Mid_Frontal_Lobe
SE_08782chr11:114053500-114053727Brain_Mid_Frontal_Lobe
SE_08782chr11:114053814-114054248Brain_Mid_Frontal_Lobe
SE_11536chr11:114052651-114060438CD20
SE_25795chr11:114048102-114054794Duodenum_Smooth_Muscle
SE_26631chr11:114052974-114054830Esophagus
SE_31457chr11:114045387-114054817Gastric
SE_40584chr11:114019219-114058700Left_Ventricle
SE_41565chr11:114053606-114054428LNCaP
SE_42095chr11:114019339-114055053Lung
SE_46633chr11:114053599-114054154Ovary
SE_48046chr11:114017688-114058762Psoas_Muscle
SE_48553chr11:114033903-114055025Right_Atrium
SE_50118chr11:114053066-114054857Sigmoid_Colon
SE_51074chr11:114023148-114058772Skeletal_Muscle
SE_52371chr11:114052963-114054909Small_Intestine
SE_53400chr11:114053456-114054708Spleen
SE_54491chr11:114023084-114055304Stomach_Smooth_Muscle
SE_55213chr11:114053713-114054829Thymus
SE_59771chr11:114027337-114069797Ly4
SE_62067chr11:114028949-114059278Toledo
SE_62758chr11:114028370-114069174Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11114053936114054155
Number: 1             
IDChromosomeStartEnd
GH11I114174chr11114045493114059176
Enhancer Sequence
CTCTTTTTAT CACTTATCAC CACCTGGCCT GTTTTGTATT TACTCGCTCT TTAAAAATCT 60
GCCCTCCCAT CTTGAACATA AACTCCCTGA GGGCAGGGAT TTCGTCTCTT TTGTTTATTT 120
CCTGTAATCC ACCTCTCGGC ATATAGCTAC TGGACATTCA AAAACCAGCC CCCGTGTGTA 180
GGAAGGATAT GGCAAGTCAT GGCCATCCCA GAGCTGTGTC CCTGGAGTTC TCCCTACTCC 240
AGGTTGAGCC CCAGGAAATT TTGTGGGTGT AAATGCTGCT GCTAGGTCCA TGCGCACCCG 300
CTGTGTTCAG CTGGCGTGAC CTTCTTCCCT CCCACTTCGC CCCCTCCCAT TGATGCTTTA 360
TAAATGTATT AGTGGCTGCA TGATGTCACC GTAATGCATT TTGGGAATAG CCATGTGGTT 420
TATACACACT TGAGTTGCTT TGAATGCAAA CCTGACATCA TACTGAAGGC AGCAGTGAAC 480
AACATATGCA CAGTAAACAG GCAGAGACTG TCTTATTGAT TAACAGATGA GGCCTCTATT 540
ATCGATCAAA GCTTGGCGAG GAAATTTATC ACTTTTAATT TCAGGGCTGC CAAATATTTC 600
TGCCTCTGAG CCAGCCATTA CAGAGACCAT TTAAAGGCAC AAGCCTCCTC AGGAGAGAGG 660
ATTTTGTCTG TCTCGCTCGG CTCCGCTCAC GTGTCCATGG AACTGCCTGT CTTTGCTCTC 720
ACCCTGGAGA GCTGGGGGGG AAGTCAGAGC CTGTCCGGGT GGGCGTGGGA GTACTGGGGC 780
TTCGTGAGTG GGGGCTAGCA ATGGGAGCTG ACGTTTGTGT TATCCACGTG TAAGGAGGGA 840
CCTGGCCCAG AGTCACTGAG GACAGGGGCT TTCACATGCT CAGCTCAGTG TCGTGACTTC 900
AGCGAGGTGG GGGTGGAGTG GCGGGACTTT GAAGGCAAGC AGATGTGGTC AGGCTTGGGC 960
CGAGGCAGCC GCCTTTACTG ATCATGTGTG CTTATCTGTC TTCATCTTCC TCTGCACTTG 1020
TCTGATGGTA CACATCCGGC CCTTTATTTC CTACCTGGCC TCCTTCCTTT CTCTCTGCTT 1080
CTCAGTCATT AAAGCGAGAA GCTCCTCTAG CCCACAGTGA TGGCTGTTTT CTAAGAACCC 1140
TCCGCGCCAC ATCCCTTGGA AGCCTGTGGC ATGGTGGGCT TCTCGCCGAT TGGAGTGCCC 1200
TCCCCTTCCC AGCTGGTGCT TCCCTCCTCG GGCCTTTGCT TCCCCTTTCT CCTTTAGGGA 1260
GCTGTGAGAG CGGATAGAAC CCAAGGAAGA AATACAATTA AAATCAGATT CCTTACAGAT 1320
CCACAGAAAA TCATTGATGG CTGATGATTT GGGACTGGGG GCAGTTTCTA ATTGTGAGGG 1380
AGCTGTGACT TCATCCAGCC GCAGCTTTCC CATCCAGGCC CACTCTGCTC TTGGAGGTGC 1440
TTTCTGCATT TCCAGTGTAA ATGGATGAAA GGTAGTCTTG GCTGCTACCC CTGTGAACAC 1500
ATGTCATGAC TGCTTTGCTG TCACTGGGGG CTAGAAGTTT TCTTGGCTCT TTCTTCAAAG 1560
CTCTCTTAAG CCGTGTACCA GGTGCTTGGC CTGAGGATGC CCTGTGGCGT GAAGGGACAC 1620
CCAGAGGTCA CCATGGGATT CTCCCTGCCT CCAGGTGAAA TTCAACCCCA GCCACCTAAG 1680
GCAAATGACA ATATTTATTT TTAAAGCTCT TCAGTAAAAG TGAGTTCATA TCTTCCATGG 1740
GGTACTTTAT CACCCACTTA TCCAGCCAGT CGACTCACAT 1780