EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS045-28946 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr17:75381540-75383230 
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: 1             
ChromosomeStartEnd
chr177538177175383179
Number: 1             
IDChromosomeStartEnd
GH17I077379chr177537510975393825
Enhancer Sequence
TCCATCCATC TCGGCCTCCC AAGGTTCCAG GATTACAGGC GTGAGCCACT GCGCCCGGCC 60
ATGGGAGACC CCCTCTTAAA ACAAGAATAA AAATAAAAAT AAATAAAAGT TTACTGTCAA 120
AAAGAAAAAC ACATCACCCA ACCTAATCTC CCCCTAGGAT TGAGAGATGA GGAAGCAGAG 180
GCCGGAAAGT GTCACATTCC CTGGTCGCTG GCAGTCAGGG GACCTGAGGC CTGGGCTGGT 240
TTTCTCGTGC TCCAGGCCTG GGGTGTCAGG TGGAGCCCCT GCTTTGCCCA AAGGTCTAGG 300
TGCCTCTGCC AGCACTGCTT GCTTCTGCAT TTTTGGCCAC AAGGAATGTG GGCCAAAGGC 360
AGGGTCCTTG ACCTCTGCCC AGGAGGGTGA AGTGGGCTGG TCCTCCTTGT CCCTGCTCCA 420
AGGCCCCTGC GGCTGTGCCT TTGGAAACTG CTGGCCCGAG CTAGTGTGCG GAGCTGGGAC 480
AGACCTCACC GTGGCCCTCG TGGGGTCATT CCATGTCCGG GCTGGAAGGG ATCTTTCGGT 540
CCAGCCCTTC CTGTTCCTCA TCAGGAAACT GAGACCAGAG AGGTCATCTG CCTGGCCCGG 600
GGTGGGGTGT AGATGGCGCT TGTGACTCCT GCATGCCACG TGCAGACAGT CCCTCAGCTG 660
TGGGCTTCCC ACGCAAGCAG CCATGCTGGG GATAACTTGG CTGAAACCTG CGATTTAATG 720
AAGAGAAGAA TGACTCCTCC TGCAGCCCTG TGCCCCACAG GCTCCCTCCT GCCCCCACCC 780
CTCCTGCAGA GGGGCCTCAT GCTGGTGGGT GGGTCCCTGT TGCTGCAATG GGCCCAGGCA 840
GTTTCTGGGC AGTGGAGGCT TGGCTGTCTT CCTGCCCAAT GTCCCCTGTA GCCCACGCTG 900
TCCGGGAAGG GCGGGGAAGC ACTCAGCCAC TGGGGACTTC ACAAGATGGG TATCTGGGAG 960
ATGCTGATTG GCAGGCCAGG CTCCCGTGGC CCACAGGCAG GTCAGAGGTC ACAGTGCTGA 1020
GCTGGGCTGA GTTGGCAGCT CAGGGCAGTG GGGGTGGGGG TACCTTGCTC AGCCATGGGC 1080
CTCTCTGGCA CAAGGGTTTG GAGTTTACTG TAAACAACTC CTTCAGTTTT TCCTTCTCTC 1140
ATAGGCCACC AGCAGAATTG AGGGGCCCTC TGTTGATGAG GTGTGGCCTG GGAGGGGCTA 1200
GTTGTCTGTC CACCTGATCC TTGCGGACAG GTGACCACAG GCTTCCTGCC CCAGGGGGCT 1260
GGGGGAAAGA TCGGGGAGGC CTCTCTGGCT TCCCCACTTG GAAGGAAAAT ACGGGCATAG 1320
GGGAGACACT TTACAGGGAC ACATTTCAGC CAGTACCCTC TGGCTGTGCT GGGGGCACAG 1380
TGCCTGCCCT GCCCACAAGA GGGGTCAGTT CTCTCCAGGA TTTAACTTCA GCCTTCAGTG 1440
CAGGGCAGAT GAGCACTCAG AGGCCCAGAG GACTCATATC ACGAGAGAGA AGCTGTGACC 1500
ACACAGGCAC TGAAGGTTAA GCAGAAGAGT GGGACACACG GGTGACCTGA AAGTCCCAGG 1560
GTCAGTGTGG TTAGCCCCAG ATAGCTGGGG AGCTTTGGGT ACCAGGCTTA GCAGGGGAGG 1620
AGGGCCCCCG TGACAGTTTG CTGGGGCTGC TGCAACAAAG CCCCACGAAC TTTGGGGGCT 1680
GAAGATGGTT 1690