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

TagContent
EnhancerAtlas ID
HS127-08096 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr12:113683350-113685560 
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
AGCCGAGATC GCGCCACTGC ACTCCAGCCT GGGCGACAGA GCAAGACTCC GTCTCAAAAA 60
AAAAAAAAAA AAAAAAGAAA AGAAAAGGGG TAGGCCCCTC AGTATCACCC TTCCTGAGAA 120
CAGTCATTCT CTGCTTTTTC TGATCAGAGC TCCCTCCCAG GAGGGGCCCT TTTATCCAAA 180
GCGATCTCTG GCCCAGGCAC CAAAGAAAGG CCCCAGTGGT TTACGCAGCC GGGCTGCCCC 240
CTGCGCCTGC TGGGTGAGGG GTGGGTCGTG GAAGCCTTCC CCTCCTGCCT GTTCTTTCCT 300
GCTCCTCCCC AGTGCATCTT TATAGCTGGC ATATGGAAAC TGTTTCTATT TATCTGGCAC 360
CACCAGGACG CTGCTGCATG CTGTGCTCCA GCAAACAGAA ACCTTGGATT CCCTGCAGGG 420
TCATTTCCGA TGTGGCGTGC AAAGCAGCCA GCTGTTTCGA GGGAGCGTCT GGGCCCTGTG 480
ACATCAGCAT GTGGGAGTGT TACCGTGTGT GCAAACAGGT CATTCTGGTT TGTCTGCCTG 540
TCCTCTGCAC CGGGATGTCT CTCCTGCTTC GAGTCAGAGT TTGCGTTGTT GTTTTGTATT 600
CTCATGCCTG TCAGTTCAGC TGTTTCTTTC CACTCCTTCC CGTCCTCTGA GTGGTTTTAC 660
GTTCTCTCCT CCGGGCTGAT TGCCAGGATT CAGGGAGGGA GGTTAAGGGG CTGGTGCCAC 720
ATAAATCTTT AGTGGCCAAA GTCTGCAGGC CTGCAAGGCT GCGCCTGTCC TCTTGGTCTG 780
GTTTTCCCAA GAGAGCTGTC TGCCCAGGGC ACCAGAAGGG CAGGACAAAA TGTTTCCCTT 840
CGTGGAACTT TCCCCAGAGG CCCAGAACAG AGATGCAGAA TACAGTCTTC CTGGTTGCCA 900
AGAGTGTTCC TGGTCAGCCT CCTCTGGTCC TTTCTGAAAC CTGCATGTGG AGCTTGCTGG 960
CTGTGGGAGC CAGGGAGACT GCAAATCCTG CCCGCCTGCC CACGCTGCTG CTCATCTCCC 1020
TCCCTCCTAT GTCCGGCCCG GTTGCCTCCC AGGAAAGGTA AACATGCAGA GGCAAGGGCT 1080
AGCTGCCGGC CTTCTGGAGG AGGCAGTGGA GGGCCAGCTT CCTGACAGCC CCGTGGTGAG 1140
GTCGTCCTGT CTTCTCAAGC TGGGCCCCTG CGACGTGCCC CAGTTCCTGC CTTTCCAGCT 1200
GGCCTGGAAG AACCCGTTCT GCTCTGGGCA AGAACAGTGC CAAGGTCAGA GGCCAAAGGT 1260
GTTGCTTCTT CCGTGGTCCG TAATGAGCAC CAGTTGGAGA GGGCCAGCCC CGGCACACAG 1320
AGGAAGGGGC TGGACTGGGG TGATGCGGGG TGAGCCTGCC CGGTCACTTT GTTGGCTAGG 1380
ATGCTTCCTG TGCTTTCTGT GCCTGGTACT CCAAAGATGC GAGTGCCAGT CATTGACCTG 1440
GAGGTTCTGC CCAGGGTCTG TGGGCAGTAG GAGGTCAGAA CAAGGCACCA GGCCACTAGA 1500
GCAGGTGGGT GTAAACAACT GTTGGCATTC GAGGCTGCCC AGGTAGAGGT CCTGGAGTGA 1560
ACCCAGTGGG CACGATGGGC TTCAGTGGGG CAGAGTGTCC TCTAGCTTCA CACACAGTGC 1620
TGATGACTCA GGCCAGCTGG GGGCCCCTGC ACATGCTCTT AGTTCCCACG TGGAGGGTAT 1680
TCATTTTGAG GAAGCTGGGC CTGCCGGGAT TGGTTCCCCA GCAAGCAGGG GCTCATTCTC 1740
CCAGAAACCA CTCCATCTGC ACTCACACCC TGACTCACCA GGCTCACATC CTGACTTACC 1800
AGGACTTGGC TATCAGCCTG TCCCCTTTGA TCTGCCCCTT CTGCCCCCTG CCTTCCCGCT 1860
TTCTGGGCCT GAAATGTCCT CCTCAGAAAG CTGCCGAGCC TTCGAGCATA CCTTCTGCGG 1920
GAACAACGCA GCACTCGGAG TGGGAGCATA TCCATTGTCC CTTCAGCCAC TTCTGCAACC 1980
TCTTAAGTGG GGAAGAGGGT TAGACAGCAG ACAGGGCAGG GGATTAGCAC TCCACGAGGT 2040
GGCCCAGCCC CACCCGGCCC CTGCCGTGCC CTCGTCTTGG CTGGTACAGC TGCACTGCTG 2100
CGTGAAGGCC ACGTACAAAA GGAACAGAAT GGAACTGTGG CTCCTCGCCT TCCATTTGCA 2160
CCCTTTCTAT AATCCCTAAA TATGTAGCCC AGTTGCTCGT GCCTTGATGT 2210