EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS092-38941 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr9:132113830-132116310 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs73621547chr9132113931hg19
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CrxMA0467.1chr9:132113867-132113878GAGAGGATTAG+6.02
KLF16MA0741.1chr9:132114584-132114595GCCCCGCCCCC+6.02
KLF5MA0599.1chr9:132114573-132114583GCCCCGCCCC+6.02
KLF5MA0599.1chr9:132114584-132114594GCCCCGCCCC+6.02
KLF5MA0599.1chr9:132114549-132114559GGGGCGGGGC-6.02
Myod1MA0499.1chr9:132115780-132115793GGGGACAGCTGCA-7.12
MyogMA0500.1chr9:132115783-132115794GACAGCTGCAG+6.62
SP2MA0516.2chr9:132114580-132114597CCCTGCCCCGCCCCCTC+6
Tcf12MA0521.1chr9:132115783-132115794GACAGCTGCAG+6.14
ZNF263MA0528.1chr9:132113920-132113941GGTGGAGGGGGTGAGGAAAGG+6.27
ZNF263MA0528.1chr9:132113956-132113977TGGGGAGGAAGATGAGGGGAG+6.57
ZNF263MA0528.1chr9:132113848-132113869AGGGGAGAAGGGGCAGGAGGA+6.69
ZNF263MA0528.1chr9:132113851-132113872GGAGAAGGGGCAGGAGGAGAG+6.95
ZNF263MA0528.1chr9:132114199-132114220TTCCCCTCCCCGCCTTCCTTC-7.05
ZNF263MA0528.1chr9:132113950-132113971GGAGGATGGGGAGGAAGATGA+7.23
ZNF263MA0528.1chr9:132113944-132113965AGGGGAGGAGGATGGGGAGGA+7.48
ZNF263MA0528.1chr9:132113947-132113968GGAGGAGGATGGGGAGGAAGA+9.76
Number of super-enhancer constituents: 14             
IDCoordinateTissue/cell
SE_04701chr9:132113139-132114634Brain_Anterior_Caudate
SE_06449chr9:132114142-132116676Brain_Hippocampus_Middle
SE_08526chr9:132114467-132116027Brain_Inferior_Temporal_Lobe
SE_09390chr9:132112910-132115292CD14
SE_27074chr9:132112820-132116466Esophagus
SE_29978chr9:132113093-132116939Fetal_Muscle
SE_31911chr9:132113968-132116545Gastric
SE_34442chr9:132114713-132116299HCT-116
SE_42813chr9:132114661-132116526Lung
SE_54065chr9:132114061-132114722Spleen
SE_54065chr9:132114968-132115860Spleen
SE_54065chr9:132116003-132116532Spleen
SE_65687chr9:132113402-132116095Pancreatic_islets
SE_68873chr9:132112292-132116082H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9132115135132115800
Number: 1             
IDChromosomeStartEnd
GH09I129350chr9132112561132116979
Enhancer Sequence
AGGGGAGAAG AGGGTAGGAG GGGAGAAGGG GCAGGAGGAG AGGATTAGGG AGGGAGATGA 60
GAGGGGAAGA GGAGGCTAGG GAGGGCGTGG GGTGGAGGGG GTGAGGAAAG GGCTAGGGGA 120
GGAGGATGGG GAGGAAGATG AGGGGAGCAC AGAAAAGAAC CCCCCCGCCC CCGCCTTGGT 180
GGCTCCCTAA GCAGATAGGA GATACATAAT TTACTACGGA AATGCAAAAA GAATTGGGAA 240
ACTCTCAATT TATAAATATT TATTTTTACA AGTTCGCCCC TCCCGGCTCC CCCTTGCTGG 300
CCCTGGTCTT TTCTCTCTGG GGCCCTCGGG GCGCAGGTCC CTCCTCTCCG GCTCCCACTC 360
TGGCCCCTCT TCCCCTCCCC GCCTTCCTTC TGCAGTCCCT TCCCCCTCGG GCGGTCTCTG 420
TCTCCCCCAG GTCCTCTCCT TCCTCTCTCC CGCCTGTGTC TCTCCCCCTA GTGCGTCTCT 480
GTCTCTGTCT CTCTTTGTGG CGGGACGGGG GCGATTTTTG AGTCTCCCCC GCCGTGGGTT 540
TCTGTCTCTC TGGCTGTCTC CCCCATCTCT CCATCTGCGT CCTCCCACTT GCCCCGCGCC 600
CCCCGTCTCT CACACCCGAG GACCCCAGCT CCCGCCAGAG GGTCCGGGGG CGGCAAGAGC 660
CCCCGTAGGC TCCCGGGGGA TGGGGGGAGG GGTCGTTTCC CTGGCAACAG CCGGTCGGCG 720
GGGCGGGGCG GGAATTGGGT TGAGCCCCGC CCCTGCCCCG CCCCCTCGCC CTGGCCGCGG 780
GTTGGGGGCG CCTGGGTGAG GCTTCCGAAG CACGTGGACC GGGCCGTGGG GGCGGGAGGG 840
GGCTCCCTGG GAGGCCGGCC CGGAGGAGGG GCGGGCAGGT AATCAGCCAA TCAGTTAATC 900
AATCGGCGGG TCAATCCATC AATCACAGGC CCCCAGAGCG GCTGGGGTTG AGCGCTCAGG 960
GTGTGGAAAG AGCTGAGTTC TAATCCCTGC TCGGCCTCTT CCTGGCCGTG TGGCCCCCAA 1020
GCCCGGAAGC CCCTGCACAG CGCCGAGCCT CGGGGTCCCC TCTGCGCAGT GGGGCTGTGG 1080
CAGCACCTGC CTGCGGGGCT GACAGTCCTT CCTGGTGGCC TGGTAGTCCC TGTCCACCCC 1140
TCCACCTCAC GGATGGGAAA CGGGAGCTGC TGAGAGGGGA AGTGGCCGGT GGGCACAGAA 1200
GGGATGGAGC GGGGAGGGGC ACCAGCCATT TCACAAGCTC GGCTGCATCT GCTGGCCCAG 1260
GCCGTTTTTT TTTTGTGAGC GGGGCCTGCG CTGTCCCCAT CCTTGGCAGC ACCTAGCTCA 1320
GTGCCCGACC TGCACAGGTC CTGGCTTCAG GTGGGAGAAC CCGAAATGCC CTTTTGATCG 1380
CTCCTCCCGG TCCCTCTCCC CTCCTGGGGT GGGGAACTGA GTCCGGGAGA GGCCAGATGG 1440
ATGCAGGGTT GCTTGGCTAG ACCCGTGCCG GCCCCTCCTC TTAAGCCATC CCTAGGCCTG 1500
ACACATGAGC TGGGGTGGGG CGGTTGTTTG TTAGTGAAGG AGGAGGCCTC AGGCAGCGTC 1560
TGCAGGGTCA GCAGCTGGAA GGGTCTCTAG ATGCTTCCTG CAACTCAAAG CCAGTTGTTT 1620
GTAACCAACA CGCAGGTCTG CTCAGCCTTC TAACCAGCAC CTCTCCCAGC CCTGTCCCTC 1680
CCTCCCTCCC AAGCGGGCTG GGGGCTGGAG TGGAGGCTGA TGAAGGGGCT GGTGGGAGGG 1740
CCCTCTCCAG GAGGGACTGG GGAGTCACAG GGAAGGTGGC TATTTATAAT TTCAGCAGCC 1800
CCTTTAAGCC CGGGCTCCAG GCCTGCTGCC AGGCCGGTTC TGTTTGAAGC TCCCAGCTCT 1860
AATCCTGCTG CAGTCCTGCT CTCAAATCCA GATCCTTTGG CTGCCTCCCA TGCAGGGAAC 1920
AAGCCCGGCC TGCGGAGCTC TCCCAAGGCT GGGGACAGCT GCAGGGCTAC TCCCTCACTG 1980
TCCCCAGCCT CCTATGCTGG GCAAGCACAT CACACACACA CACACACACA CACACACACA 2040
CACACACACA CACACACATT TCCCTGTGCT ACAAACAACA AATTCATCCT TTTTTATTTT 2100
TTTGTAGAGA CAGGGGTCTC ACTATGTTGC CCAGGCTGGT CTCAAACTCC TGGCCTCAAG 2160
CCATCCTACT GCCTTGGCCT CCCAGAGTGC TGGGATTGCA GGCATGAGCC AATGTGCCCG 2220
GCCTACAAAC GTGCTTTTCA TAGACTGGCA TTTCATGTCT GTGGCCTGTG GGCCCCAATC 2280
CCAAGGCCTG CCCTGCCCTC TGCGGGAAGG ATGTTTTCAG AACTTTGTGG CCCTCCCCAA 2340
AGGTTCTAGG TTCTATGCCC CACCTCCTTA GAGCCCCAGG GCCCCCAAGT GTGTTCAGAA 2400
CCCGAACCAG CCTAGGAACT GACAGGAAGA AAGAGTGGAA GTTGTGGTGG GGAGGGGTTG 2460
TCGGGTCTTG AAGGAGGGGA 2480