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

TagContent
EnhancerAtlas ID
HS038-05271 
Organism
Homo sapiens 
Tissue/cell
ESC_neuron 
Coordinate
chr12:120700830-120703410 
Target genes
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TFAP4MA0691.1chr12:120701006-120701016AACAGCTGAT+6.02
ZNF263MA0528.1chr12:120703380-120703401CCTCTCGCCTCCTCCTCCCTC-6.65
ZfxMA0146.2chr12:120703305-120703319GAGGCCGGGGCCGC-6.15
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_00357chr12:120699026-120704024Adipose_Nuclei
SE_00942chr12:120699479-120703632Adrenal_Gland
SE_06253chr12:120699039-120704699Brain_Hippocampus_Middle
SE_09726chr12:120699180-120703605CD14
SE_14823chr12:120699448-120703942CD4_Memory_Primary_7pool
SE_18785chr12:120698968-120703994CD4p_CD25-_Il17-_PMAstim_Th
SE_20423chr12:120699127-120703580CD56
SE_25945chr12:120699371-120703569Duodenum_Smooth_Muscle
SE_27013chr12:120699505-120703604Esophagus
SE_27737chr12:120699245-120703575Fetal_Intestine
SE_28646chr12:120699139-120704554Fetal_Intestine_Large
SE_29635chr12:120699245-120703562Fetal_Muscle
SE_31816chr12:120699564-120703746Gastric
SE_34374chr12:120699385-120703966HCT-116
SE_34701chr12:120698855-120704407HeLa
SE_35936chr12:120699195-120703620HMEC
SE_36961chr12:120697194-120703989HSMMtube
SE_37987chr12:120699436-120703922HUVEC
SE_40794chr12:120699180-120703598Left_Ventricle
SE_41766chr12:120700775-120701475LNCaP
SE_42203chr12:120699160-120704680Lung
SE_44237chr12:120699237-120703630NHDF-Ad
SE_44983chr12:120699514-120703556NHLF
SE_46156chr12:120699436-120703572Osteoblasts
SE_47284chr12:120682425-120704730Panc1
SE_48117chr12:120699189-120704354Psoas_Muscle
SE_48648chr12:120699182-120703574Right_Atrium
SE_50261chr12:120699273-120704268Sigmoid_Colon
SE_51208chr12:120699282-120704912Skeletal_Muscle
SE_51764chr12:120699388-120703117Skeletal_Muscle_Myoblast
SE_52496chr12:120699196-120703571Small_Intestine
SE_53419chr12:120699464-120703847Spleen
SE_54833chr12:120699258-120703558Stomach_Smooth_Muscle
SE_55411chr12:120701523-120703566Thymus
SE_55760chr12:120699235-120703604u87
SE_63549chr12:120699388-120703603HSMM
SE_64693chr12:120699279-120703553NHEK
SE_65557chr12:120700557-120701655Pancreatic_islets
SE_67501chr12:120699235-120703604u87
SE_68119chr12:120694476-120731991TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12120701000120701400
Enhancer Sequence
AAAGTCACAG AGGAGGTGAT GCACCCTCTG GCCTTGCTAC CGGACACACC ATAAACTCTC 60
CCCTGTGTTA GGGACCAGGA GGCACACGGC TGAGAGCACG CTCAGGAGAA AAATAAAAAC 120
AAGAGGTCTG GGCTTTGTGT CCACCCTAAG GAAAACAGCT GAGCCACCCT AAGGAAAACA 180
GCTGATGGCA GTGTGCTGAG CCGCCATCCA GACAGCTGAC GGGGCCCCAG TGCAAAGGCA 240
AATTCCTCTC CCCTCCTGCA CACCCCATTC CTCCCACCCC AGGCTCCGGT CAGTCAGGCG 300
TGGCTTGCCC CTTGGGAGCT CAGGCCAAGG AAGTCGGGCA GCCCGGATGT AAGCAACTGG 360
GAGTCTATGG TAGAAAGCAG TAGAAGTTAC AGGTGATCGC CATCACCCAG TGGCAACCCC 420
TCCTTCAAGT GCCCTTGCCT CCTCCCCAGG AAAAAAAGTC TTCTCGGTAT ACAAGAGCCA 480
CAGATCTGGG AGCTAGGAAT TGGGCTTCCA GTTATGGTTT TGTCATTTCA TGGCTGTGCA 540
GCCTTGGGCA AGAGAATCAG CCTCTCTTCG TCTCGGCTTT CTCAATCTGT AAAAAGGCAG 600
GTGGTCATGA CAGCATTGGC TTTAAGGTGG AATCTGATAA AAGGGTTGTT GTGAGGATAT 660
CACAAATCGA GGTAGAGGGA AGTACTCCAC AAACAGCAAT TTAAATCCCT ACAATCCCCT 720
CTCCCGTATA CAGTACTCTC TTTCCTTTCA GAACTCAGTT TCCTGGCCCT AAATGGAAGA 780
CTGTCAGAAG ACAGGAATTC CAGATTTCGA TGGCGAGCTC TACAAAGACT TTCTCAGTCC 840
TTGAAACAGC ACGGGGACTG CCGAGAAGCA ACAGAACTGC ACCAGCACTT TAGAAACTGT 900
AACTTTGCTC CCAGTTCCCA CTGGGAAAGC ACTCAGACTC TTAGATCCTG GTTCAAAGAA 960
CATCCCCCAG CCTCCTTCCA GCTGAGCTAT TTTTATGTGA AAAAAAAAAA TACCTGCCTG 1020
GAAGCCATGC CAACCTTGAG CACACTGGAA AAATGGGTGC CAAGCCTGAC CCAAAGGCAG 1080
AACCACGCTT GGCAGCCATC TCACTCTGCA AAACAGGCAG GACCCTACAC CAACCCCAGC 1140
TCCAGGATCT CAGGGGCACC CTGATCCCAA AAGGAAGCTG GAGGGAAGCA GTCAAGTCCA 1200
GCACCTACAA ATAGCCAGTC TTAACTTAGT GCCCGGCGCT GCTTGGTAGA GGTCCATCAG 1260
TCCTGTCTGC TGAATCTACT CCTCAGAGCC TGGGACAGAG GAAGCATCAG TGGTCACACA 1320
AGCCACCCAC AGTCCAGAGA GGAAAGACAA GGCTCCTGCA GAGAAGAAAC GTTGCCCCCC 1380
TCCTCACCTC CCAAGCTCAG GGCCCTCCAG CTACAGGCGT GAAGGGGAGG GAGAGACAGC 1440
GAATCCTCCC ACTCCTGCGT TCACGCCACC CAAGGCATTC CTAGAACCCT GGCACCAACC 1500
CCCTTGGGTT TAGAGTCGGC TTCCAGGAGA TACTTTCTTT CCCCTAACAC CAGATCAAGA 1560
CTGGACTGAA AAGAGTAGCC TTGGGGCTCC AATAACAGGA AAACAGTAAA ACTCTGTTCT 1620
GGGCATCCTG TCCTCTTTCA CCTGCGTGGC TTCCAGCAGG GCCTGACGCA GAGAGGGTGG 1680
AGGGGACTCT GCTAGCCAGG ACACGTTCAG GGATGGTCAT ACCTTGGGGC CCACCTTCCA 1740
CCTCATTCCC CTGGCATTTC ACCAGAATCT AGGGGTGGGG AGAGAATCAG GACTCCCAAA 1800
TTACCGTTCT AGACTTAGAT ACCATGGTAG ACGGACTGGT CTGTGAATTG AGGGGCTGGT 1860
CCACAGAGCG GGGAGGTCAG TGAGAGAAAA TGAGTGATGG GTCCTTGAAA CGGGGTGACC 1920
AGATTTGAAG TGGGGGGTCA GAAGAGCAGG CAGACTGGGA AACTTGTCTT TGAAATGGGG 1980
GTGTGGTCAT CACACGCTCA TCTCTAGCTT TTGCATCTGA CTTGTGAAAT GAAAGGGGTG 2040
GGCTCCGAGG GGTTATCCCT GAAGGGGGGT GCTAGTCTGT GAAGTGGGGG GCGGCCCTGG 2100
AGGGACGGGG AGCAGGTCGA GGAAATGAGG GAGCAGCCCA TGAGATCGGG CAGCTGCTCC 2160
CCGAGTTGGG CGGTCGATCT GTGAGGTGGG GGTGGGGAGA GGTCTGCGAG GTGAGGGTCC 2220
CGTAGCTGAC GAGGTGGTCT GCCGCAGGAA GTCTCGTCCC TGCAGCGGAC GGGGTGGGTC 2280
CCTGAGGGGC GGGCTGGTCC CTGGGGCCCT TCTGGGAGAT GGTGATGGGT CCCCGAGGTC 2340
GGGGGTCCAG AGGTGAAGCC GTCCCAGACG GGGGGTCGCT GCTGTGCGGT CGGTGCCGGG 2400
GCCGGCCTGG CCCGAGACTA AGGCCCGGTT AGGGATCCCA GCCCCGCGGA GCCCCGGCCG 2460
GCAGGGACAG GAGCTGAGGC CGGGGCCGCC GAGGGTGGGA TCCCGCGGCC CCTGCCGCTC 2520
GCTGGCGCCC TCCTGGCCCC AAGCTGCGCG CCTCTCGCCT CCTCCTCCCT CGGCCTCCCG 2580