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

TagContent
EnhancerAtlas ID
HS098-14920 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr12:124866030-124867700 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr12:124866574-124866595TTCCCCACTCCTTCCTTCTCT-6.03
ZNF263MA0528.1chr12:124866712-124866733AGGGGAGGGGCAGGAGGTGGA+6.22
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00866chr12:124862402-124868788Adrenal_Gland
SE_02192chr12:124863128-124867730Aorta
SE_02420chr12:124863547-124867814Astrocytes
SE_03150chr12:124865903-124867402Brain_Angular_Gyrus
SE_03868chr12:124863568-124867323Brain_Anterior_Caudate
SE_04770chr12:124863743-124867543Brain_Cingulate_Gyrus
SE_05769chr12:124862628-124885625Brain_Hippocampus_Middle
SE_06714chr12:124863625-124867720Brain_Hippocampus_Middle_150
SE_07720chr12:124863491-124868845Brain_Inferior_Temporal_Lobe
SE_08801chr12:124866182-124866408Brain_Mid_Frontal_Lobe
SE_09946chr12:124863833-124867909CD14
SE_23639chr12:124865346-124867530Colon_Crypt_1
SE_24091chr12:124865538-124867416Colon_Crypt_2
SE_25142chr12:124864557-124867508Colon_Crypt_3
SE_26654chr12:124863613-124867906Esophagus
SE_28184chr12:124863812-124867242Fetal_Intestine
SE_29418chr12:124863828-124867400Fetal_Intestine_Large
SE_29559chr12:124863018-124867193Fetal_Muscle
SE_31405chr12:124863080-124868665Gastric
SE_38211chr12:124862333-124878792HUVEC
SE_40749chr12:124862998-124868191Left_Ventricle
SE_41561chr12:124864204-124868495LNCaP
SE_42183chr12:124862482-124868314Lung
SE_44453chr12:124863057-124867983NHDF-Ad
SE_45099chr12:124863464-124867441NHLF
SE_46642chr12:124863397-124867568Ovary
SE_47406chr12:124863984-124868395Panc1
SE_47472chr12:124865532-124867415Pancreas
SE_48155chr12:124862220-124868165Psoas_Muscle
SE_48612chr12:124863545-124868056Right_Atrium
SE_50109chr12:124863333-124868082Sigmoid_Colon
SE_51247chr12:124862948-124878823Skeletal_Muscle
SE_52804chr12:124863121-124867997Small_Intestine
SE_54428chr12:124863582-124867631Spleen
SE_54615chr12:124862797-124867881Stomach_Smooth_Muscle
SE_65244chr12:124862101-124885693Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12124866398124866679
Enhancer Sequence
CTGGGATCTT TGTTCTCTGC TGTATTCCCA CCATACCTGG AACAGTGTCT AGCACAGAAC 60
AGACGCTCTG TAACTATGTC TTTAGATGAA TGAACCTGAT AGACAGTGAC AATGGCTCAG 120
AGAGGCAAAG ACACTTGCCC AAGACCACAC AGCTCATGAG TTGAGGAGCT CAGATTTGAA 180
TGCAGGCCAG CTTCAAACAT TTCGTGGCTG GACCATCTCT CTGCAGGCCT GTGCAGCCTC 240
AGGTAGAAGA GATTAACAGC AGAAAACAAG GCGGGGCTGG GCCAAGGCTG AGGCGGACAG 300
AGACTGAGGA ACGTGGAAGC CGAGCCCCAG GGGCCTGAAT TCACAGATGG GAGAAAAGGG 360
TAACCTTCGG CCATAAGGAG GGGGAGGGAA ACCTCGTAGA AGACACTGAT GCCAAGTGTT 420
ACATAACTCC GGGACATGCC CCGCCCGCCC GGCCGCCGGA TCCTGCTTCC TGCTGACGTC 480
GCCTGCGGCC ACACTCGGGC CAGACCTAGT GCAAGGCGGG AGGGGACACC CACTGACCCT 540
CTGCTTCCCC ACTCCTTCCT TCTCTGGCCA AGGGTGACAT GTCTTCCTGT ACTCCAGACA 600
GGGCTGGGCC AGCAGCCAGA GGTGGCTGAT ACTGCGTTAG GATTCACTGG GATATGCCCT 660
CCTCCCTGGG ACTGAAAGGC ACAGGGGAGG GGCAGGAGGT GGAGGTCACC AGGTTCAGCG 720
GCACCTCTCC TGGTGAGACC TGCTTGCTTA CTGCAGCGAT GGGGAGCTCA CCACTACACC 780
AAGAACGGCT ACTGTCAAGA CGGATGGCCT GGCCTGAGCC CCACTTCCTG TAGTGGGTCC 840
CTGCATCTGC TCCGCTTTCT CTGCAGCCCG CGATATGAGG GTGCTCCTTC AAGGTCGGCC 900
AGGAGCGAGA ACCAACCCCA CACTCCCAAA TCACTCATTC TCATCCAGGT CCCAACCTGG 960
ATCTCGGGGT CCCCTCCTGT CCACGCCTCC AGAGTCTTCA GCGTCAGGGG ACAGAAGGGC 1020
CACCTTCTTT ATCAGCTTTG ACTGTGTCAT TCGGATCAGA ATCACTTTCA TCGACACTAG 1080
GACGACCCAC TTTGAGTCCA GCCCTGGATG GGGGCTGTGT CTCAGCTCAG AATCCTTCAA 1140
TGCAGCCCCC ACTCCCTCCA CGGTCCACTA ACGAAGTGTT AGCTCCACAG CCCAGCAGGA 1200
AAACCCCATC CATGTCTCTG CCCTCAGGGC AGCTGCCATT GCTTCCCTGG GATACAGCAG 1260
GCGCTGAATA TGGGGCTGCT GAATGGACAG TGAGGATAAT ACTGAATGCT TATTGAGGGC 1320
TGACCAAGGA CCAGGCACCA CCCTTTACAA AAAGAAACAC ACTTGTTCTT CAACAGCCCT 1380
ACGACTGGGT CCCATTCTTA TCCCCATTTT ACAGAGGTGG AAACTGAAGC ACGGAGAGGT 1440
GAAGCCCAGT ATCCTTGGAC CCAGTCACTA AGCGGCAGAG CTGGGGTACA AAGCCACCAG 1500
CTCCAAAGCC CTGCTCTGCA CCATCCTTCT GGGATGCCTC TTTGAATGAA TGGATGAATG 1560
AATGAATGAA TCAATCAATC GTGAGTGTGC CACCACCAGC ACCATCACAG CTCTCACTAG 1620
CAGAGTGTCT GGGGCATACT AGGCCGCATT CCCAGCACTC TGCAGGCAGC 1670