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

TagContent
EnhancerAtlas ID
HS188-01122 
Organism
Homo sapiens 
Tissue/cell
Th2 
Coordinate
chr1:204421360-204423580 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EBF1MA0154.3chr1:204421660-204421674AATCCCAAGGGAAT-6.57
EBF1MA0154.3chr1:204421660-204421674AATCCCAAGGGAAT+7.04
ZNF263MA0528.1chr1:204422805-204422826GAAGAAGGGAGAGGATGAGAA+6.66
ZfxMA0146.2chr1:204423146-204423160CCCGCCTCGGCCTC+6.01
ZfxMA0146.2chr1:204423370-204423384GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_00064chr1:204417530-204422553Adipose_Nuclei
SE_00064chr1:204423204-204424583Adipose_Nuclei
SE_03975chr1:204421893-204422820Brain_Anterior_Caudate
SE_04850chr1:204421758-204422908Brain_Cingulate_Gyrus
SE_04850chr1:204423204-204428008Brain_Cingulate_Gyrus
SE_05834chr1:204414554-204422838Brain_Hippocampus_Middle
SE_05834chr1:204423062-204428058Brain_Hippocampus_Middle
SE_06778chr1:204419046-204422484Brain_Hippocampus_Middle_150
SE_07775chr1:204421681-204422937Brain_Inferior_Temporal_Lobe
SE_10255chr1:204419836-204423398CD19_Primary
SE_10905chr1:204414650-204438582CD20
SE_25125chr1:204417816-204422942Colon_Crypt_3
SE_28866chr1:204417158-204423024Fetal_Intestine_Large
SE_31610chr1:204417780-204422694Gastric
SE_34711chr1:204415846-204421729HeLa
SE_37407chr1:204418938-204421997HSMMtube
SE_40776chr1:204417564-204421617Left_Ventricle
SE_40776chr1:204421796-204423031Left_Ventricle
SE_42225chr1:204421747-204422546Lung
SE_48201chr1:204414946-204421702Psoas_Muscle
SE_49909chr1:204419158-204422984RPMI-8402
SE_50149chr1:204415315-204422829Sigmoid_Colon
SE_51536chr1:204417745-204423045Skeletal_Muscle
SE_52421chr1:204416678-204422949Small_Intestine
SE_58430chr1:204415099-204506026Ly1
SE_59794chr1:204415680-204491493Ly4
SE_62377chr1:204415291-204492168Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1204422070204422833
Number: 1             
IDChromosomeStartEnd
GH01I204445chr1204415101204423341
Enhancer Sequence
GGGTTTAAGG CCAATTTTTT AAAGTTCCTC CTGGGCCAGA ACACTGTGCA GCACCCTTTT 60
TTTTTTTTTT TTTTTTTTTT TGAGACAGGG TCTCGCTCTG TTGCCGAGGC TGGATACTCA 120
CTGCAGCCTT GACCTCCCAG GCTCAAGTGA TTCTCCCACC TCAGCCTCCT AAGTAGCTGG 180
AACCACAGGT GTATGCCACC ACACTTGGCT AATTTTTTGT ATTTTTTGTA GAGATTGGGT 240
CTCCCTTGTT GCCCAGGCTG GCACCCCTTC TCTTGACAGC AGCAGTAATT GTGACCAAAA 300
AATCCCAAGG GAATGGTGGA ACTCAAGGGC CATTTAATGC AGCTATCCTC TGCCTGCAAG 360
GAGTTTCTCC TGTCCTGGCA GTTGTTTGCT TGAGGACCTT TAATGCACAC CCCATGTCCT 420
TTTTTTTTTT TTTTTTTTTT AAGATAGGGT CTCACTCTGT TGCCCAGGCT ATAGTGCAGT 480
GGTGTGATCA TGGCTCACTG CAGCCTCGAC CTCCCAGGCT CAAGTGACTC TCCCACCTCA 540
GCCTCTTAAG TAGCTAGGAC TACAGATGCA CGCCACCACA CTCAGCTCAT TTAAAATAAT 600
TTTTTAGTAG AGATAAGGCC TCTTTGTGTT GCCCAGGCTG GTCTCAAATT CCTGATCTCA 660
AGTGATTATC CCGCCTTGTC CTCCCAAAGT ACGGTGAGAC TACAGGTGTG AGCCATCGTG 720
CCCAGCCATA TACACCTTTA TTGCTCTAAG AATTACCTAA GTGTGAAGGG CATGAGAAAG 780
GGTCCATTTT CCCAGTTGTC CATCTGTAAA AGGACCCACC TCTTCCAGCA TCTCCAGATT 840
CTTCATCTAC CTATTTTGCA TCCTCGGCCT CCCCAGGACC CTCCTCAGTC TCTTTAATCT 900
GTGCTACAAA TACTTAGCTT GCAGTGCTGC TCTGCAAATG AGGACTCTAA TATAGTCAGT 960
GTGGGGAAGC AAAGCCGGGG GCAGCAAACA GGGGATTTTC TGACTGACTG GAAGGAAGGT 1020
AGAGCATAGC ACAGATGAAG CACAGGGCAG GAAAACCCCT GCGGTGCCCC CATTCAAGCA 1080
AGGCACCCTC TCCTCCGTTT CCTTCCTGCT TTGCTTGGCT GACGCCTACC TTCCCGACAC 1140
CAAATTATTG TTTACATGTG GTGATTAATA TTACCTTGTG CTTTTGGTTT CATATTTATA 1200
TTTATAACCC ACCTATCTCA TCTCGACGCC ATAACTGCCT CTGAGTGAAA CCAATGTCCC 1260
CATTTCTCAG TTTGAAAAAA TGAGGCACAG AAAGAATAGA GAGAAAGTAG TATTCGAGAC 1320
AGAGCTAGAA ATAGAGGCTC ACTCCTGGGA ATCCAAGCTC AATATTCTTT CTCTAGACAA 1380
CCCTCCCTTC TCTATATATA AAGGGAAAAG CACAGTCTCC TCTCCATAGT CTACAGGAAC 1440
TGAGGGAAGA AGGGAGAGGA TGAGAAGCCC TCCAACTAGT TAAACTCTTT AAGGGAGACA 1500
AGATCAAAAA ATAAAGTATT ATTAAAATTA ACAACTAACA TTTAATTTTT TTTTTTTTGA 1560
GACAGAATTT CGCTCTTGTT GCCCAGGCTG GAGTGCAATG GCACGATCTC AGCTCACTAC 1620
AACCTCCACC TCCCGGGTTC AAGCGATTCT CCTGCCTCAG CCTCCCTAGT AGCTGGGATT 1680
ACAGGCATGC GCCACCATGC CCGGCTATTT TGTATTTTTT TTAGTAGAGA CGAGGTTTCT 1740
CCATGTTGGT CAGGCTGGTC TTGAACTCCC TGCCTCAGGT GATCCGCCCG CCTCGGCCTC 1800
CCAAAGCGCT GGGATTACAA GCGTAAGCCA CCGCGCCTGG TCAACAACTA AAATTTATAT 1860
GTTTTTTATG GTTTACAAAG AGCCTTTATA GATACTTCTC ATTGGATCCT CATGACAACT 1920
TGAGAAGTGG TAATTATACT TGGCTCCTTT AAGAGTCAGG GAAGTGGAGG CCAGGCGTGG 1980
TGGCTCACGC CTGTAATCCC AGCACTCTGG GAGGCCGAGG CGGGCAGATC ACGAGGTCAG 2040
GAGATCGAGA CTATCCTAGC TAACACATGG AAACCCCATC TCTGCTAAAA ATACAAAAAA 2100
TTAGCTGGGC GTGGTGGCGG GCGCCTGTAG TCCCAGCTAC TCGGGAGGCT GAGACAGAAG 2160
AATGGCGTGA ACCCAGGAGG CAGAGCTTGC AGTGAGCCGA GATCGCACCA CTGCACTCCA 2220