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

TagContent
EnhancerAtlas ID
HS172-04826 
Organism
Homo sapiens 
Tissue/cell
SGBS_adipocyte 
Coordinate
chr17:75381430-75383980 
Target genes
Number: 5             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs73373322chr1775382039hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr17:75382536-75382551GCAGGTCAGAGGTCA+7.23
Nr2f6MA0677.1chr17:75382537-75382551CAGGTCAGAGGTCA+6.67
RxraMA0512.2chr17:75382537-75382551CAGGTCAGAGGTCA+6.27
ZNF263MA0528.1chr17:75383956-75383977CCCTCCACCCCCACCTCCCCC-7.21
ZfxMA0146.2chr17:75383297-75383311CCGGCCCAGGCCTC+6.38
Number of super-enhancer constituents: 31             
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_65344chr17:75383665-75387609Pancreatic_islets
SE_68672chr17:75381609-75383265H9
SE_68672chr17:75383506-75386490H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177538177175383179
Number: 1             
IDChromosomeStartEnd
GH17I077379chr177537510975393825
Enhancer Sequence
TCCATTCGGA GGCTGCTGGG GACTTGGAGT TGCCAGCTCA CATATTTTTT AGTAGAGACA 60
GGGTTTCACC ATGTTGACCA GGCTGGTCTC AAACTCCTGT CCTCAAGTGA TCCATCCATC 120
TCGGCCTCCC AAGGTTCCAG GATTACAGGC GTGAGCCACT GCGCCCGGCC ATGGGAGACC 180
CCCTCTTAAA ACAAGAATAA AAATAAAAAT AAATAAAAGT TTACTGTCAA AAAGAAAAAC 240
ACATCACCCA ACCTAATCTC CCCCTAGGAT TGAGAGATGA GGAAGCAGAG GCCGGAAAGT 300
GTCACATTCC CTGGTCGCTG GCAGTCAGGG GACCTGAGGC CTGGGCTGGT TTTCTCGTGC 360
TCCAGGCCTG GGGTGTCAGG TGGAGCCCCT GCTTTGCCCA AAGGTCTAGG TGCCTCTGCC 420
AGCACTGCTT GCTTCTGCAT TTTTGGCCAC AAGGAATGTG GGCCAAAGGC AGGGTCCTTG 480
ACCTCTGCCC AGGAGGGTGA AGTGGGCTGG TCCTCCTTGT CCCTGCTCCA AGGCCCCTGC 540
GGCTGTGCCT TTGGAAACTG CTGGCCCGAG CTAGTGTGCG GAGCTGGGAC AGACCTCACC 600
GTGGCCCTCG TGGGGTCATT CCATGTCCGG GCTGGAAGGG ATCTTTCGGT CCAGCCCTTC 660
CTGTTCCTCA TCAGGAAACT GAGACCAGAG AGGTCATCTG CCTGGCCCGG GGTGGGGTGT 720
AGATGGCGCT TGTGACTCCT GCATGCCACG TGCAGACAGT CCCTCAGCTG TGGGCTTCCC 780
ACGCAAGCAG CCATGCTGGG GATAACTTGG CTGAAACCTG CGATTTAATG AAGAGAAGAA 840
TGACTCCTCC TGCAGCCCTG TGCCCCACAG GCTCCCTCCT GCCCCCACCC CTCCTGCAGA 900
GGGGCCTCAT GCTGGTGGGT GGGTCCCTGT TGCTGCAATG GGCCCAGGCA GTTTCTGGGC 960
AGTGGAGGCT TGGCTGTCTT CCTGCCCAAT GTCCCCTGTA GCCCACGCTG TCCGGGAAGG 1020
GCGGGGAAGC ACTCAGCCAC TGGGGACTTC ACAAGATGGG TATCTGGGAG ATGCTGATTG 1080
GCAGGCCAGG CTCCCGTGGC CCACAGGCAG GTCAGAGGTC ACAGTGCTGA GCTGGGCTGA 1140
GTTGGCAGCT CAGGGCAGTG GGGGTGGGGG TACCTTGCTC AGCCATGGGC CTCTCTGGCA 1200
CAAGGGTTTG GAGTTTACTG TAAACAACTC CTTCAGTTTT TCCTTCTCTC ATAGGCCACC 1260
AGCAGAATTG AGGGGCCCTC TGTTGATGAG GTGTGGCCTG GGAGGGGCTA GTTGTCTGTC 1320
CACCTGATCC TTGCGGACAG GTGACCACAG GCTTCCTGCC CCAGGGGGCT GGGGGAAAGA 1380
TCGGGGAGGC CTCTCTGGCT TCCCCACTTG GAAGGAAAAT ACGGGCATAG GGGAGACACT 1440
TTACAGGGAC ACATTTCAGC CAGTACCCTC TGGCTGTGCT GGGGGCACAG TGCCTGCCCT 1500
GCCCACAAGA GGGGTCAGTT CTCTCCAGGA TTTAACTTCA GCCTTCAGTG CAGGGCAGAT 1560
GAGCACTCAG AGGCCCAGAG GACTCATATC ACGAGAGAGA AGCTGTGACC ACACAGGCAC 1620
TGAAGGTTAA GCAGAAGAGT GGGACACACG GGTGACCTGA AAGTCCCAGG GTCAGTGTGG 1680
TTAGCCCCAG ATAGCTGGGG AGCTTTGGGT ACCAGGCTTA GCAGGGGAGG AGGGCCCCCG 1740
TGACAGTTTG CTGGGGCTGC TGCAACAAAG CCCCACGAAC TTTGGGGGCT GAAGATGGTT 1800
CTAGAGGCCA GAAGTCCAAA ATCAAGGTGT CGACCAGGCT GATCCTTTGG GGCCTCTGCG 1860
GGAGGCTCCG GCCCAGGCCT CTCTCCCAGC TTCTGGTGGC TCCCGGGTGC TCCTGGGCAT 1920
GTAGATGCGT CACGCCACTC CCTGCTCCGT CTTCACATGG CCTTTTCTCT GTGTCTCTGT 1980
GTCTCGTAAG GATGCTTGTC ATTGCATTTA GAGCCCACCC TAAATCCAGG ATACTCTCCT 2040
CTTGAGATCC TTTATTGCAT CTGCAAAGAC CCTATTCCAA CTCCTGTCAC ATTCACAGGT 2100
CCGAGGGCTA GGGCTCTGGC ATGTCTTTTG GGGGTCACTA TTCAGTCCAC TGCGGCAGCT 2160
GATCTTAGGG GAAGCAGAAT GTTCTAAGCT TGGGGTGAGC GGAGGGAACG CTGCTGGGTG 2220
GGGAGTGGGA GACCAGGCTC GGAGACACCG CGGATCTCCT CTGTCTGATG AGGGCGTGAT 2280
GAGGTTCTCA TCTCAGGTCC TCTGAATGGC GGCTGCTTCT GAGGAGACCC TTTCCCCTGG 2340
ATCTGCCCCT CCAGAAACCT CCACTTAGGT CCAGGTCCCA AGGTGGATGG TAAGAGGCGG 2400
CTGTCCCTGC CACACTTGAT GGGTGAGTGT GTGAACGGGG CTGGGAGCAG GACACTTGTC 2460
ACTTCTGTGG ACAGATTCCA GAGGCTCATG AATCTGCTGC TGGGGAAGGT GCCTGATCTA 2520
GCCTGACCCT CCACCCCCAC CTCCCCCTTC 2550