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

TagContent
EnhancerAtlas ID
HS086-03010 
Organism
Homo sapiens 
Tissue/cell
HEK293 
Coordinate
chr12:113683310-113685490 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GSCMA0648.1chr12:113685368-113685378GGGGATTAGC-6.02
NR2C2MA0504.1chr12:113684590-113684605CAAGGTCAGAGGCCA+6.24
Stat6MA0520.1chr12:113683457-113683472CCCTTCCTGAGAACA+6.01
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00883chr12:113683342-113686698Adrenal_Gland
SE_01635chr12:113683327-113688666Aorta
SE_03074chr12:113683375-113685473Bladder
SE_03506chr12:113684410-113685192Brain_Angular_Gyrus
SE_04226chr12:113683249-113686805Brain_Anterior_Caudate
SE_05290chr12:113676945-113688044Brain_Cingulate_Gyrus
SE_06123chr12:113676787-113688773Brain_Hippocampus_Middle
SE_07164chr12:113681229-113687363Brain_Hippocampus_Middle_150
SE_08283chr12:113683213-113686051Brain_Inferior_Temporal_Lobe
SE_09132chr12:113683621-113684005Brain_Mid_Frontal_Lobe
SE_09132chr12:113684557-113684823Brain_Mid_Frontal_Lobe
SE_23178chr12:113683354-113685924Colon_Crypt_1
SE_24018chr12:113683410-113685761Colon_Crypt_2
SE_26345chr12:113681599-113685097Duodenum_Smooth_Muscle
SE_26677chr12:113683335-113686993Esophagus
SE_27860chr12:113683294-113686963Fetal_Intestine
SE_28798chr12:113681446-113686701Fetal_Intestine_Large
SE_29890chr12:113683290-113685679Fetal_Muscle
SE_37095chr12:113677131-113685805HSMMtube
SE_40725chr12:113683293-113688763Left_Ventricle
SE_41860chr12:113683440-113685760LNCaP
SE_42290chr12:113683300-113687155Lung
SE_44290chr12:113683293-113685251NHDF-Ad
SE_46894chr12:113683424-113685786Ovary
SE_47597chr12:113683411-113685798Pancreas
SE_48084chr12:113673313-113688344Psoas_Muscle
SE_48792chr12:113683328-113687025Right_Atrium
SE_49644chr12:113683419-113685464Right_Ventricle
SE_50157chr12:113683349-113685797Sigmoid_Colon
SE_51183chr12:113681221-113686478Skeletal_Muscle
SE_52527chr12:113683325-113686155Small_Intestine
SE_53751chr12:113683299-113685810Spleen
SE_57125chr12:113683422-113683782VACO_400
SE_57125chr12:113683897-113685375VACO_400
SE_57981chr12:113683423-113683883VACO_9m
SE_57981chr12:113683893-113685652VACO_9m
SE_64197chr12:113683297-113685238HSMM
SE_65505chr12:113677296-113687345Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12113683425113685477
Number: 1             
IDChromosomeStartEnd
GH12I113235chr12113673514113686887
Enhancer Sequence
CAGGAGAATG GCGTGAGCCC GGGAGGCGGA GCTTGCAGTG AGCCGAGATC GCGCCACTGC 60
ACTCCAGCCT GGGCGACAGA GCAAGACTCC GTCTCAAAAA AAAAAAAAAA AAAAAAGAAA 120
AGAAAAGGGG TAGGCCCCTC AGTATCACCC TTCCTGAGAA CAGTCATTCT CTGCTTTTTC 180
TGATCAGAGC TCCCTCCCAG GAGGGGCCCT TTTATCCAAA GCGATCTCTG GCCCAGGCAC 240
CAAAGAAAGG CCCCAGTGGT TTACGCAGCC GGGCTGCCCC CTGCGCCTGC TGGGTGAGGG 300
GTGGGTCGTG GAAGCCTTCC CCTCCTGCCT GTTCTTTCCT GCTCCTCCCC AGTGCATCTT 360
TATAGCTGGC ATATGGAAAC TGTTTCTATT TATCTGGCAC CACCAGGACG CTGCTGCATG 420
CTGTGCTCCA GCAAACAGAA ACCTTGGATT CCCTGCAGGG TCATTTCCGA TGTGGCGTGC 480
AAAGCAGCCA GCTGTTTCGA GGGAGCGTCT GGGCCCTGTG ACATCAGCAT GTGGGAGTGT 540
TACCGTGTGT GCAAACAGGT CATTCTGGTT TGTCTGCCTG TCCTCTGCAC CGGGATGTCT 600
CTCCTGCTTC GAGTCAGAGT TTGCGTTGTT GTTTTGTATT CTCATGCCTG TCAGTTCAGC 660
TGTTTCTTTC CACTCCTTCC CGTCCTCTGA GTGGTTTTAC GTTCTCTCCT CCGGGCTGAT 720
TGCCAGGATT CAGGGAGGGA GGTTAAGGGG CTGGTGCCAC ATAAATCTTT AGTGGCCAAA 780
GTCTGCAGGC CTGCAAGGCT GCGCCTGTCC TCTTGGTCTG GTTTTCCCAA GAGAGCTGTC 840
TGCCCAGGGC ACCAGAAGGG CAGGACAAAA TGTTTCCCTT CGTGGAACTT TCCCCAGAGG 900
CCCAGAACAG AGATGCAGAA TACAGTCTTC CTGGTTGCCA AGAGTGTTCC TGGTCAGCCT 960
CCTCTGGTCC TTTCTGAAAC CTGCATGTGG AGCTTGCTGG CTGTGGGAGC CAGGGAGACT 1020
GCAAATCCTG CCCGCCTGCC CACGCTGCTG CTCATCTCCC TCCCTCCTAT GTCCGGCCCG 1080
GTTGCCTCCC AGGAAAGGTA AACATGCAGA GGCAAGGGCT AGCTGCCGGC CTTCTGGAGG 1140
AGGCAGTGGA GGGCCAGCTT CCTGACAGCC CCGTGGTGAG GTCGTCCTGT CTTCTCAAGC 1200
TGGGCCCCTG CGACGTGCCC CAGTTCCTGC CTTTCCAGCT GGCCTGGAAG AACCCGTTCT 1260
GCTCTGGGCA AGAACAGTGC CAAGGTCAGA GGCCAAAGGT GTTGCTTCTT CCGTGGTCCG 1320
TAATGAGCAC CAGTTGGAGA GGGCCAGCCC CGGCACACAG AGGAAGGGGC TGGACTGGGG 1380
TGATGCGGGG TGAGCCTGCC CGGTCACTTT GTTGGCTAGG ATGCTTCCTG TGCTTTCTGT 1440
GCCTGGTACT CCAAAGATGC GAGTGCCAGT CATTGACCTG GAGGTTCTGC CCAGGGTCTG 1500
TGGGCAGTAG GAGGTCAGAA CAAGGCACCA GGCCACTAGA GCAGGTGGGT GTAAACAACT 1560
GTTGGCATTC GAGGCTGCCC AGGTAGAGGT CCTGGAGTGA ACCCAGTGGG CACGATGGGC 1620
TTCAGTGGGG CAGAGTGTCC TCTAGCTTCA CACACAGTGC TGATGACTCA GGCCAGCTGG 1680
GGGCCCCTGC ACATGCTCTT AGTTCCCACG TGGAGGGTAT TCATTTTGAG GAAGCTGGGC 1740
CTGCCGGGAT TGGTTCCCCA GCAAGCAGGG GCTCATTCTC CCAGAAACCA CTCCATCTGC 1800
ACTCACACCC TGACTCACCA GGCTCACATC CTGACTTACC AGGACTTGGC TATCAGCCTG 1860
TCCCCTTTGA TCTGCCCCTT CTGCCCCCTG CCTTCCCGCT TTCTGGGCCT GAAATGTCCT 1920
CCTCAGAAAG CTGCCGAGCC TTCGAGCATA CCTTCTGCGG GAACAACGCA GCACTCGGAG 1980
TGGGAGCATA TCCATTGTCC CTTCAGCCAC TTCTGCAACC TCTTAAGTGG GGAAGAGGGT 2040
TAGACAGCAG ACAGGGCAGG GGATTAGCAC TCCACGAGGT GGCCCAGCCC CACCCGGCCC 2100
CTGCCGTGCC CTCGTCTTGG CTGGTACAGC TGCACTGCTG CGTGAAGGCC ACGTACAAAA 2160
GGAACAGAAT GGAACTGTGG 2180