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

TagContent
EnhancerAtlas ID
HS193-14869 
Organism
Homo sapiens 
Tissue/cell
U87 
Coordinate
chr17:75381380-75383300 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs73373322chr1775382039hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr17:75382536-75382551GCAGGTCAGAGGTCA+7.23
Nr2f6MA0677.1chr17:75382537-75382551CAGGTCAGAGGTCA+6.67
RxraMA0512.2chr17:75382537-75382551CAGGTCAGAGGTCA+6.27
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00752chr17:75379427-75386768Adipose_Nuclei
SE_00855chr17:75381658-75386492Adrenal_Gland
SE_02895chr17:75381658-75382852Bladder
SE_02895chr17:75382962-75383465Bladder
SE_05840chr17:75381615-75389667Brain_Hippocampus_Middle
SE_14415chr17:75382058-75383438CD4_Memory_Primary_7pool
SE_17309chr17:75382056-75383624CD4p_CD25-_CD45RAp_Naive
SE_18261chr17:75382380-75383573CD4p_CD25-_Il17-_PMAstim_Th
SE_19099chr17:75381541-75383434CD4p_CD25-_Il17p_PMAstim_Th17
SE_22389chr17:75382025-75383434CD8_primiary
SE_25342chr17:75382053-75383383DND41
SE_26523chr17:75381117-75386501Esophagus
SE_31375chr17:75381198-75386381Gastric
SE_36938chr17:75378213-75383637HSMMtube
SE_40707chr17:75378294-75386541Left_Ventricle
SE_42146chr17:75378304-75383976Lung
SE_44144chr17:75379225-75383253NHDF-Ad
SE_44761chr17:75381422-75383184NHLF
SE_45597chr17:75381211-75383495Osteoblasts
SE_46677chr17:75381657-75382886Ovary
SE_47187chr17:75375489-75383559Panc1
SE_48637chr17:75381118-75386461Right_Atrium
SE_50053chr17:75381639-75383963Sigmoid_Colon
SE_52347chr17:75381276-75383382Small_Intestine
SE_53286chr17:75378270-75383520Spleen
SE_54499chr17:75381684-75389681Stomach_Smooth_Muscle
SE_62213chr17:75358289-75491858Tonsil
SE_65344chr17:75381637-75382916Pancreatic_islets
SE_68672chr17:75381609-75383265H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr177538138075381486
chr177538177175383179
Number: 1             
IDChromosomeStartEnd
GH17I077379chr177537510975393825
Enhancer Sequence
TTACAGACAC TCATATTTGT AGGATTTGAG AATCCTACAA GAGGAAAGCC TCCATTCGGA 60
GGCTGCTGGG GACTTGGAGT TGCCAGCTCA CATATTTTTT AGTAGAGACA GGGTTTCACC 120
ATGTTGACCA GGCTGGTCTC AAACTCCTGT CCTCAAGTGA TCCATCCATC TCGGCCTCCC 180
AAGGTTCCAG GATTACAGGC GTGAGCCACT GCGCCCGGCC ATGGGAGACC CCCTCTTAAA 240
ACAAGAATAA AAATAAAAAT AAATAAAAGT TTACTGTCAA AAAGAAAAAC ACATCACCCA 300
ACCTAATCTC CCCCTAGGAT TGAGAGATGA GGAAGCAGAG GCCGGAAAGT GTCACATTCC 360
CTGGTCGCTG GCAGTCAGGG GACCTGAGGC CTGGGCTGGT TTTCTCGTGC TCCAGGCCTG 420
GGGTGTCAGG TGGAGCCCCT GCTTTGCCCA AAGGTCTAGG TGCCTCTGCC AGCACTGCTT 480
GCTTCTGCAT TTTTGGCCAC AAGGAATGTG GGCCAAAGGC AGGGTCCTTG ACCTCTGCCC 540
AGGAGGGTGA AGTGGGCTGG TCCTCCTTGT CCCTGCTCCA AGGCCCCTGC GGCTGTGCCT 600
TTGGAAACTG CTGGCCCGAG CTAGTGTGCG GAGCTGGGAC AGACCTCACC GTGGCCCTCG 660
TGGGGTCATT CCATGTCCGG GCTGGAAGGG ATCTTTCGGT CCAGCCCTTC CTGTTCCTCA 720
TCAGGAAACT GAGACCAGAG AGGTCATCTG CCTGGCCCGG GGTGGGGTGT AGATGGCGCT 780
TGTGACTCCT GCATGCCACG TGCAGACAGT CCCTCAGCTG TGGGCTTCCC ACGCAAGCAG 840
CCATGCTGGG GATAACTTGG CTGAAACCTG CGATTTAATG AAGAGAAGAA TGACTCCTCC 900
TGCAGCCCTG TGCCCCACAG GCTCCCTCCT GCCCCCACCC CTCCTGCAGA GGGGCCTCAT 960
GCTGGTGGGT GGGTCCCTGT TGCTGCAATG GGCCCAGGCA GTTTCTGGGC AGTGGAGGCT 1020
TGGCTGTCTT CCTGCCCAAT GTCCCCTGTA GCCCACGCTG TCCGGGAAGG GCGGGGAAGC 1080
ACTCAGCCAC TGGGGACTTC ACAAGATGGG TATCTGGGAG ATGCTGATTG GCAGGCCAGG 1140
CTCCCGTGGC CCACAGGCAG GTCAGAGGTC ACAGTGCTGA GCTGGGCTGA GTTGGCAGCT 1200
CAGGGCAGTG GGGGTGGGGG TACCTTGCTC AGCCATGGGC CTCTCTGGCA CAAGGGTTTG 1260
GAGTTTACTG TAAACAACTC CTTCAGTTTT TCCTTCTCTC ATAGGCCACC AGCAGAATTG 1320
AGGGGCCCTC TGTTGATGAG GTGTGGCCTG GGAGGGGCTA GTTGTCTGTC CACCTGATCC 1380
TTGCGGACAG GTGACCACAG GCTTCCTGCC CCAGGGGGCT GGGGGAAAGA TCGGGGAGGC 1440
CTCTCTGGCT TCCCCACTTG GAAGGAAAAT ACGGGCATAG GGGAGACACT TTACAGGGAC 1500
ACATTTCAGC CAGTACCCTC TGGCTGTGCT GGGGGCACAG TGCCTGCCCT GCCCACAAGA 1560
GGGGTCAGTT CTCTCCAGGA TTTAACTTCA GCCTTCAGTG CAGGGCAGAT GAGCACTCAG 1620
AGGCCCAGAG GACTCATATC ACGAGAGAGA AGCTGTGACC ACACAGGCAC TGAAGGTTAA 1680
GCAGAAGAGT GGGACACACG GGTGACCTGA AAGTCCCAGG GTCAGTGTGG TTAGCCCCAG 1740
ATAGCTGGGG AGCTTTGGGT ACCAGGCTTA GCAGGGGAGG AGGGCCCCCG TGACAGTTTG 1800
CTGGGGCTGC TGCAACAAAG CCCCACGAAC TTTGGGGGCT GAAGATGGTT CTAGAGGCCA 1860
GAAGTCCAAA ATCAAGGTGT CGACCAGGCT GATCCTTTGG GGCCTCTGCG GGAGGCTCCG 1920