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

TagContent
EnhancerAtlas ID
HS146-06385 
Organism
Homo sapiens 
Tissue/cell
NHDF 
Coordinate
chr17:37035800-37038510 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr17:37035946-37035964CAAACCTTCCTTGCTTCC-6.13
EWSR1-FLI1MA0149.1chr17:37035950-37035968CCTTCCTTGCTTCCTTAC-8
Foxd3MA0041.1chr17:37037354-37037366AAACAAACAAAC-6.32
Foxd3MA0041.1chr17:37037358-37037370AAACAAACAAAC-6.32
Foxd3MA0041.1chr17:37037362-37037374AAACAAACAAAC-6.32
Nr2f6MA0677.1chr17:37036812-37036826TGACCTTTGGCCCA-6.12
RREB1MA0073.1chr17:37036254-37036274CCCCCTACCAACCCCTCCCA+7.08
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_01190chr17:37035895-37037190Adrenal_Gland
SE_01190chr17:37037633-37038469Adrenal_Gland
SE_01869chr17:37035678-37038474Aorta
SE_04550chr17:37037654-37038642Brain_Anterior_Caudate
SE_06121chr17:37035628-37039853Brain_Hippocampus_Middle
SE_08151chr17:37037139-37038973Brain_Inferior_Temporal_Lobe
SE_19419chr17:37035661-37036869CD4p_CD25-_Il17p_PMAstim_Th17
SE_19419chr17:37037562-37038411CD4p_CD25-_Il17p_PMAstim_Th17
SE_20407chr17:37037382-37038441CD56
SE_22571chr17:37035526-37037255CD8_primiary
SE_22571chr17:37037270-37038498CD8_primiary
SE_23506chr17:37035992-37037214Colon_Crypt_1
SE_24046chr17:37037688-37038133Colon_Crypt_2
SE_26978chr17:37035845-37037266Esophagus
SE_26978chr17:37037576-37038614Esophagus
SE_27795chr17:37035699-37038586Fetal_Intestine
SE_28678chr17:37035600-37038658Fetal_Intestine_Large
SE_30529chr17:37035598-37037236Fetal_Muscle
SE_31106chr17:37035651-37037195Fetal_Thymus
SE_31106chr17:37037458-37038519Fetal_Thymus
SE_31542chr17:37035806-37037252Gastric
SE_31542chr17:37037381-37038611Gastric
SE_42353chr17:37035784-37038629Lung
SE_47849chr17:37035811-37037123Pancreas
SE_48905chr17:37035789-37037336Right_Atrium
SE_48905chr17:37037450-37038623Right_Atrium
SE_50172chr17:37035751-37037342Sigmoid_Colon
SE_50172chr17:37037437-37038616Sigmoid_Colon
SE_52400chr17:37035787-37038605Small_Intestine
SE_53492chr17:37035744-37037201Spleen
SE_53492chr17:37037438-37038591Spleen
SE_56922chr17:37035801-37037166VACO_400
SE_59348chr17:37019329-37056453Ly3
SE_62887chr17:37023359-37058235Tonsil
SE_65628chr17:37035834-37037493Pancreatic_islets
SE_65628chr17:37037499-37038916Pancreatic_islets
SE_66745chr17:37036349-37037039Jurkat
SE_68729chr17:37035658-37038565H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr173703773137038463
Number: 1             
IDChromosomeStartEnd
GH17I038876chr173703283637043967
Enhancer Sequence
ATCTGACTTG AGTCCAGTTT TTTTTTTTTT TCTCTTAATT CTCAGTCAGG AGGCTCTTTG 60
CAGCTGAAGT TCACCCAGGG AAAAAAAAAT TTGGGACTTG TCTAAAAAGG GGGCTTAAAC 120
CTCCAGCCTT ACCCCTAACC TTACCCCAAA CCTTCCTTGC TTCCTTACCC CCTCCCGTTC 180
CCTGGCTAAG ACCACTCTTT CATCTTTTTA GGGGCTCGCT CATTCAGCAG ACATTTATTG 240
CCTGCCTGCT GCTATAATAC ATACTAACCT GCACCAGGTG CTGGGAAAAC AGATTCCTGA 300
TAAAAATCTC AAGCCCAAGA AGCAACATGA AGTTGTCCCT TCTGGAAGAA GGAGGGCACT 360
GGGCAGGTTA TCTGGGTAAA GGAAGGGTTG CAGCTCTGTC CTGGCCCCTC CTTCAGCTGC 420
CCCTTCTCTT CTATTAATTT CTACTGTTCC TCTTCCCCCT ACCAACCCCT CCCACCCCCA 480
CAAGGGAAAT GGGACATTCT TCGAATTCTT AAGGGCTCAC ACAAGCCCTG GTTCTCTGCC 540
ACTTCCTCCC TCCATTGGGT AGTGGGGTGG GGTTCAGAGA AGCCAGGGCA GTTAACCCCT 600
CCGTTGCTGG ACCACCTCAG GCTAGATTCT GAGCCTCCGC CCCAGCACGC AGAAGTCTGA 660
CCGAGCCTTG GAGCCCAGTG ACTCAAGCAG CCTAGAATTC AGTGAGCACT GGGAGCTGGA 720
GAAAAATCAG AGGCTTGTCC TTGTTTTCTC TGCGTTTTAT CAGCCTCATC CAAAGTTCCA 780
GCTTACTGTT TTTACTGTCT TCTTGGGAAG CTGCCACAAG GTTGGGTGGA GGGCTCCTGC 840
AGGGACTGGG GGAGCCAGAA GAGGCAGATC AAGGTTTCTT CTCTGGGTGA TGCTTCCAAC 900
TTGCAGAGGC AGAGGTTCCC CTGTCTCCCT CCTGGCCTCC AGCCAAAAGA AGCAGGTTGG 960
CCTCTCCATG TTTCCTCCAG CTTTTGTAGC CCTAGCCTCT GCCATGCCTC ATTGACCTTT 1020
GGCCCAGTTG GGATGTTTCC TGGGAAGGAG CCTAGTGAGA GAGACCTGGG GGCTTTGTGA 1080
CCCAGCTGTG TTTCACTTTA GCTGTAGTAG CACCTCCTCG CCCAAGGCAG TCATTCTCCC 1140
TCCCCTGCAT CCACTGGGCC AAGAAGTTAC CCGTGGGGAT TCTGGGATGA ACCAGGTGTG 1200
GCGCCCGCTT GCAAGGAGTG CTCTCTGGAC GTGTCTGAGC CTTGGTTTCC CCATGGTTAA 1260
AAATTCCTGC CCAGGAGGCC TGGCATAGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA 1320
GGCTGAAGCA GGTGGATCAC TTAAGGTCAG GAGTTCTATC AGCCTGGCCA ACATGGTGAA 1380
ACTCGTCTCT ACTAAAAATA CAAACATTAG CCAGATGTGG TGGTGGGCAC CTATAATCCC 1440
AGCTACTCAG GAGGCTGAGG CAGGAGAATT GCTTGAACCT GGGAGGCCAG GGCTGCAGTG 1500
AGCCAAGATT GCCTCTGCAC TTCAGTCTGA GCGACAGAGC GAGACTCCAT CTCAAAACAA 1560
ACAAACAAAC AAACTAAAGA TAAAAAAAAA TTCCTGCCCA GGGATGTTGG ACCCTAGACC 1620
AAAGAGGATT TATTGAGCTC TTGCTATGTG CCAGACGCTA GGCCGAGTGT TTGCTGTCAT 1680
TCCCTCCTGC TTTCTTACTT TTTTTGTTTT TATTTTGCTT TGGTTTTTTG GAGACAAGGT 1740
CTCCAAAAAA ACTTCGTCCT GCTCAGTCAC CCAGGCTGGA GTGCAGTGGA GTGATCATGG 1800
CTCACTGCAG CCTCCACCTC CTGGGTTTAA GTGATCCTCC TGCCTCAGCC TCCCTAGTAG 1860
CTGGGACCAC AGGCATGTGG CGCCATGCTA ATTTTTAAGT TTTTTGTAGA GAGGAGGGCT 1920
TGTCATACTC TTGGCCTCAG GTGATCTACC TGCTTTAGCC CAGCCTCCTC GTGTTTTCTT 1980
CCTGCCTCTG GTCTTATCCT TGAGTGACAT TCAGGTTCCT GAATCCTGGG TTTACCAGGG 2040
TACAGCTTTC TGCCATTTCT GTTCTGGTCT TGCTTTGTGG ACCACAGGCC TGGCTTCCTT 2100
CTCTGAAGCA TCACGTGCTC CATGCTGGGC CAAGCCCAGT GCAGGACCCG TAGGGGCACG 2160
TGGTTTCTTC TGGCACTTTG CCAGGGAGTT GGGCCCACCC AGTGAGTGTG TGAGTTTGGT 2220
GTGCAGGGAG GCCTCTATGT TCTGCCTGTC TCTGGCTAGT CTCTGAGGGG AGCTAGGATC 2280
TTGCAGGGGG CTGGTCAAGA AAGAAGAAAG CTATCTTTCC CTGTGGTTTC TCAAGATTCA 2340
GATTTAAGCT CTAGAAAGTG ACTGTAAAGT AGGCAGTGAA AAGGCCTCTT CTGTTTCTGT 2400
CCTTGCATCA GACTTGTTTG GGGGAGAGGC AGGGGAGAGA ACATAGGCCA GAGCTCACTG 2460
CCAGCCCACC TGGTGTGGCG GACCCCCACA TGCGTGCAGT TACACACATG CCTGGTGTGT 2520
AGGCAGACAC CCACGCCGGT GCTGGGGCGG GGGAGGAGGA CTTGGGAGCT GGACTGAATG 2580
GGCTGTGTTT GTGTTTCCAC CTTCAGGACT GCAGCCATGC AGCCAATGCT GTGGCAAGGT 2640
TGAGGGTGCA CTCCCGGCTT CTGCACAATA GCCAGTGGTG GAGGAAGAAC TGCTAATAGA 2700
ATTCTTTTTG 2710