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

TagContent
EnhancerAtlas ID
HS105-35927 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr17:75381130-75383920 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs73373322chr1775382039hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr17:75382536-75382551GCAGGTCAGAGGTCA+7.23
Nr2f6MA0677.1chr17:75382537-75382551CAGGTCAGAGGTCA+6.67
RxraMA0512.2chr17:75382537-75382551CAGGTCAGAGGTCA+6.27
ZfxMA0146.2chr17:75383297-75383311CCGGCCCAGGCCTC+6.38
Number of super-enhancer constituents: 30             
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
SE_68672chr17:75383506-75386490H9
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
TTTTAAAGTT CATGGGCTCG TGCCCGTAAT CCCAACACTC TGGGAGGCTG AGGCAGGAGG 60
ATTCCTTAAG CCCAGGAGTT TGAGACCAGC CTGGGCAACA TAGGGAGACC CCCACCTTTT 120
TTTTTTTTTT TTTTTGACAG AGTTTCACTG TGTCCCAGGC TGAAGTGGCG GTGGCACGTT 180
CTTGGTTCAC TGCAACCTCT GCCTCCCAGG TTCAGGTGAT TCTCATGCCT CAGCCTCCTG 240
AGTAGCTGGA TTACAGACAC TCATATTTGT AGGATTTGAG AATCCTACAA GAGGAAAGCC 300
TCCATTCGGA GGCTGCTGGG GACTTGGAGT TGCCAGCTCA CATATTTTTT AGTAGAGACA 360
GGGTTTCACC ATGTTGACCA GGCTGGTCTC AAACTCCTGT CCTCAAGTGA TCCATCCATC 420
TCGGCCTCCC AAGGTTCCAG GATTACAGGC GTGAGCCACT GCGCCCGGCC ATGGGAGACC 480
CCCTCTTAAA ACAAGAATAA AAATAAAAAT AAATAAAAGT TTACTGTCAA AAAGAAAAAC 540
ACATCACCCA ACCTAATCTC CCCCTAGGAT TGAGAGATGA GGAAGCAGAG GCCGGAAAGT 600
GTCACATTCC CTGGTCGCTG GCAGTCAGGG GACCTGAGGC CTGGGCTGGT TTTCTCGTGC 660
TCCAGGCCTG GGGTGTCAGG TGGAGCCCCT GCTTTGCCCA AAGGTCTAGG TGCCTCTGCC 720
AGCACTGCTT GCTTCTGCAT TTTTGGCCAC AAGGAATGTG GGCCAAAGGC AGGGTCCTTG 780
ACCTCTGCCC AGGAGGGTGA AGTGGGCTGG TCCTCCTTGT CCCTGCTCCA AGGCCCCTGC 840
GGCTGTGCCT TTGGAAACTG CTGGCCCGAG CTAGTGTGCG GAGCTGGGAC AGACCTCACC 900
GTGGCCCTCG TGGGGTCATT CCATGTCCGG GCTGGAAGGG ATCTTTCGGT CCAGCCCTTC 960
CTGTTCCTCA TCAGGAAACT GAGACCAGAG AGGTCATCTG CCTGGCCCGG GGTGGGGTGT 1020
AGATGGCGCT TGTGACTCCT GCATGCCACG TGCAGACAGT CCCTCAGCTG TGGGCTTCCC 1080
ACGCAAGCAG CCATGCTGGG GATAACTTGG CTGAAACCTG CGATTTAATG AAGAGAAGAA 1140
TGACTCCTCC TGCAGCCCTG TGCCCCACAG GCTCCCTCCT GCCCCCACCC CTCCTGCAGA 1200
GGGGCCTCAT GCTGGTGGGT GGGTCCCTGT TGCTGCAATG GGCCCAGGCA GTTTCTGGGC 1260
AGTGGAGGCT TGGCTGTCTT CCTGCCCAAT GTCCCCTGTA GCCCACGCTG TCCGGGAAGG 1320
GCGGGGAAGC ACTCAGCCAC TGGGGACTTC ACAAGATGGG TATCTGGGAG ATGCTGATTG 1380
GCAGGCCAGG CTCCCGTGGC CCACAGGCAG GTCAGAGGTC ACAGTGCTGA GCTGGGCTGA 1440
GTTGGCAGCT CAGGGCAGTG GGGGTGGGGG TACCTTGCTC AGCCATGGGC CTCTCTGGCA 1500
CAAGGGTTTG GAGTTTACTG TAAACAACTC CTTCAGTTTT TCCTTCTCTC ATAGGCCACC 1560
AGCAGAATTG AGGGGCCCTC TGTTGATGAG GTGTGGCCTG GGAGGGGCTA GTTGTCTGTC 1620
CACCTGATCC TTGCGGACAG GTGACCACAG GCTTCCTGCC CCAGGGGGCT GGGGGAAAGA 1680
TCGGGGAGGC CTCTCTGGCT TCCCCACTTG GAAGGAAAAT ACGGGCATAG GGGAGACACT 1740
TTACAGGGAC ACATTTCAGC CAGTACCCTC TGGCTGTGCT GGGGGCACAG TGCCTGCCCT 1800
GCCCACAAGA GGGGTCAGTT CTCTCCAGGA TTTAACTTCA GCCTTCAGTG CAGGGCAGAT 1860
GAGCACTCAG AGGCCCAGAG GACTCATATC ACGAGAGAGA AGCTGTGACC ACACAGGCAC 1920
TGAAGGTTAA GCAGAAGAGT GGGACACACG GGTGACCTGA AAGTCCCAGG GTCAGTGTGG 1980
TTAGCCCCAG ATAGCTGGGG AGCTTTGGGT ACCAGGCTTA GCAGGGGAGG AGGGCCCCCG 2040
TGACAGTTTG CTGGGGCTGC TGCAACAAAG CCCCACGAAC TTTGGGGGCT GAAGATGGTT 2100
CTAGAGGCCA GAAGTCCAAA ATCAAGGTGT CGACCAGGCT GATCCTTTGG GGCCTCTGCG 2160
GGAGGCTCCG GCCCAGGCCT CTCTCCCAGC TTCTGGTGGC TCCCGGGTGC TCCTGGGCAT 2220
GTAGATGCGT CACGCCACTC CCTGCTCCGT CTTCACATGG CCTTTTCTCT GTGTCTCTGT 2280
GTCTCGTAAG GATGCTTGTC ATTGCATTTA GAGCCCACCC TAAATCCAGG ATACTCTCCT 2340
CTTGAGATCC TTTATTGCAT CTGCAAAGAC CCTATTCCAA CTCCTGTCAC ATTCACAGGT 2400
CCGAGGGCTA GGGCTCTGGC ATGTCTTTTG GGGGTCACTA TTCAGTCCAC TGCGGCAGCT 2460
GATCTTAGGG GAAGCAGAAT GTTCTAAGCT TGGGGTGAGC GGAGGGAACG CTGCTGGGTG 2520
GGGAGTGGGA GACCAGGCTC GGAGACACCG CGGATCTCCT CTGTCTGATG AGGGCGTGAT 2580
GAGGTTCTCA TCTCAGGTCC TCTGAATGGC GGCTGCTTCT GAGGAGACCC TTTCCCCTGG 2640
ATCTGCCCCT CCAGAAACCT CCACTTAGGT CCAGGTCCCA AGGTGGATGG TAAGAGGCGG 2700
CTGTCCCTGC CACACTTGAT GGGTGAGTGT GTGAACGGGG CTGGGAGCAG GACACTTGTC 2760
ACTTCTGTGG ACAGATTCCA GAGGCTCATG 2790