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

TagContent
EnhancerAtlas ID
HS118-04900 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr12:113683290-113685680 
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
AGCTACTCGG GAGGCTGAGG CAGGAGAATG GCGTGAGCCC GGGAGGCGGA GCTTGCAGTG 60
AGCCGAGATC GCGCCACTGC ACTCCAGCCT GGGCGACAGA GCAAGACTCC GTCTCAAAAA 120
AAAAAAAAAA AAAAAAGAAA AGAAAAGGGG TAGGCCCCTC AGTATCACCC TTCCTGAGAA 180
CAGTCATTCT CTGCTTTTTC TGATCAGAGC TCCCTCCCAG GAGGGGCCCT TTTATCCAAA 240
GCGATCTCTG GCCCAGGCAC CAAAGAAAGG CCCCAGTGGT TTACGCAGCC GGGCTGCCCC 300
CTGCGCCTGC TGGGTGAGGG GTGGGTCGTG GAAGCCTTCC CCTCCTGCCT GTTCTTTCCT 360
GCTCCTCCCC AGTGCATCTT TATAGCTGGC ATATGGAAAC TGTTTCTATT TATCTGGCAC 420
CACCAGGACG CTGCTGCATG CTGTGCTCCA GCAAACAGAA ACCTTGGATT CCCTGCAGGG 480
TCATTTCCGA TGTGGCGTGC AAAGCAGCCA GCTGTTTCGA GGGAGCGTCT GGGCCCTGTG 540
ACATCAGCAT GTGGGAGTGT TACCGTGTGT GCAAACAGGT CATTCTGGTT TGTCTGCCTG 600
TCCTCTGCAC CGGGATGTCT CTCCTGCTTC GAGTCAGAGT TTGCGTTGTT GTTTTGTATT 660
CTCATGCCTG TCAGTTCAGC TGTTTCTTTC CACTCCTTCC CGTCCTCTGA GTGGTTTTAC 720
GTTCTCTCCT CCGGGCTGAT TGCCAGGATT CAGGGAGGGA GGTTAAGGGG CTGGTGCCAC 780
ATAAATCTTT AGTGGCCAAA GTCTGCAGGC CTGCAAGGCT GCGCCTGTCC TCTTGGTCTG 840
GTTTTCCCAA GAGAGCTGTC TGCCCAGGGC ACCAGAAGGG CAGGACAAAA TGTTTCCCTT 900
CGTGGAACTT TCCCCAGAGG CCCAGAACAG AGATGCAGAA TACAGTCTTC CTGGTTGCCA 960
AGAGTGTTCC TGGTCAGCCT CCTCTGGTCC TTTCTGAAAC CTGCATGTGG AGCTTGCTGG 1020
CTGTGGGAGC CAGGGAGACT GCAAATCCTG CCCGCCTGCC CACGCTGCTG CTCATCTCCC 1080
TCCCTCCTAT GTCCGGCCCG GTTGCCTCCC AGGAAAGGTA AACATGCAGA GGCAAGGGCT 1140
AGCTGCCGGC CTTCTGGAGG AGGCAGTGGA GGGCCAGCTT CCTGACAGCC CCGTGGTGAG 1200
GTCGTCCTGT CTTCTCAAGC TGGGCCCCTG CGACGTGCCC CAGTTCCTGC CTTTCCAGCT 1260
GGCCTGGAAG AACCCGTTCT GCTCTGGGCA AGAACAGTGC CAAGGTCAGA GGCCAAAGGT 1320
GTTGCTTCTT CCGTGGTCCG TAATGAGCAC CAGTTGGAGA GGGCCAGCCC CGGCACACAG 1380
AGGAAGGGGC TGGACTGGGG TGATGCGGGG TGAGCCTGCC CGGTCACTTT GTTGGCTAGG 1440
ATGCTTCCTG TGCTTTCTGT GCCTGGTACT CCAAAGATGC GAGTGCCAGT CATTGACCTG 1500
GAGGTTCTGC CCAGGGTCTG TGGGCAGTAG GAGGTCAGAA CAAGGCACCA GGCCACTAGA 1560
GCAGGTGGGT GTAAACAACT GTTGGCATTC GAGGCTGCCC AGGTAGAGGT CCTGGAGTGA 1620
ACCCAGTGGG CACGATGGGC TTCAGTGGGG CAGAGTGTCC TCTAGCTTCA CACACAGTGC 1680
TGATGACTCA GGCCAGCTGG GGGCCCCTGC ACATGCTCTT AGTTCCCACG TGGAGGGTAT 1740
TCATTTTGAG GAAGCTGGGC CTGCCGGGAT TGGTTCCCCA GCAAGCAGGG GCTCATTCTC 1800
CCAGAAACCA CTCCATCTGC ACTCACACCC TGACTCACCA GGCTCACATC CTGACTTACC 1860
AGGACTTGGC TATCAGCCTG TCCCCTTTGA TCTGCCCCTT CTGCCCCCTG CCTTCCCGCT 1920
TTCTGGGCCT GAAATGTCCT CCTCAGAAAG CTGCCGAGCC TTCGAGCATA CCTTCTGCGG 1980
GAACAACGCA GCACTCGGAG TGGGAGCATA TCCATTGTCC CTTCAGCCAC TTCTGCAACC 2040
TCTTAAGTGG GGAAGAGGGT TAGACAGCAG ACAGGGCAGG GGATTAGCAC TCCACGAGGT 2100
GGCCCAGCCC CACCCGGCCC CTGCCGTGCC CTCGTCTTGG CTGGTACAGC TGCACTGCTG 2160
CGTGAAGGCC ACGTACAAAA GGAACAGAAT GGAACTGTGG CTCCTCGCCT TCCATTTGCA 2220
CCCTTTCTAT AATCCCTAAA TATGTAGCCC AGTTGCTCGT GCCTTGATGT GAAGGAGGCC 2280
CTTTGCGATC ACCTGTGGCT TTCTTGAAAA GTCCCTGAGT GGCCAGTGTC ACCCCAGGCC 2340
TTCCATCCCT CTCTCCGTGT GGAGAAATGA GCGATCATGC TTTGCCTTTT 2390