EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS191-16145 
Organism
Homo sapiens 
Tissue/cell
Trophoblast 
Coordinate
chr17:38707350-38708990 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr17:38707692-38707703CCACACCCTCC+6.32
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_00517chr17:38704041-38711605Adipose_Nuclei
SE_01363chr17:38707380-38711401Adrenal_Gland
SE_02998chr17:38707691-38711204Bladder
SE_03777chr17:38707372-38707888Brain_Angular_Gyrus
SE_03777chr17:38707928-38711600Brain_Angular_Gyrus
SE_06594chr17:38703241-38712085Brain_Hippocampus_Middle
SE_08685chr17:38707023-38711875Brain_Inferior_Temporal_Lobe
SE_09113chr17:38708445-38708781Brain_Mid_Frontal_Lobe
SE_10389chr17:38707133-38711422CD19_Primary
SE_10931chr17:38702970-38725331CD20
SE_17295chr17:38703039-38725883CD4p_CD25-_CD45RAp_Naive
SE_17919chr17:38708678-38711930CD4p_CD25-_CD45ROp_Memory
SE_18283chr17:38706851-38724489CD4p_CD25-_Il17-_PMAstim_Th
SE_25403chr17:38702928-38718860DND41
SE_25943chr17:38703327-38711335Duodenum_Smooth_Muscle
SE_26577chr17:38703197-38711655Esophagus
SE_29882chr17:38703163-38711198Fetal_Muscle
SE_32359chr17:38704623-38707593Gastric
SE_32359chr17:38707613-38711719Gastric
SE_33816chr17:38703114-38708920HCC1954
SE_37372chr17:38703086-38711540HSMMtube
SE_38887chr17:38703213-38711458IMR90
SE_41480chr17:38704694-38712276Left_Ventricle
SE_42403chr17:38703320-38712269Lung
SE_44181chr17:38703751-38712177NHDF-Ad
SE_44928chr17:38704505-38711023NHLF
SE_45551chr17:38703094-38718321Osteoblasts
SE_46930chr17:38707317-38709406Ovary
SE_47885chr17:38707924-38708280Pancreas
SE_47885chr17:38708474-38708922Pancreas
SE_48754chr17:38704793-38717455Right_Atrium
SE_50356chr17:38704638-38712329Sigmoid_Colon
SE_51567chr17:38703835-38711470Skeletal_Muscle
SE_51937chr17:38703234-38711019Skeletal_Muscle_Myoblast
SE_52624chr17:38703812-38712069Small_Intestine
SE_53520chr17:38704586-38719298Spleen
SE_54860chr17:38703054-38711418Stomach_Smooth_Muscle
SE_56221chr17:38703802-38710170u87
SE_58835chr17:38672665-38782311Ly3
SE_61067chr17:38687460-38781557HBL1
SE_61495chr17:38672564-38757231Toledo
SE_62232chr17:38671160-38782171Tonsil
SE_63720chr17:38703221-38711093HSMM
SE_67770chr17:38703802-38710170u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr173870749538707811
Enhancer Sequence
TTACATATAT GGATTCGTTG CCTTCCACAA CAATCCTAGG ACATAGGTAC CATTAGTATC 60
CCCATTATAC AGATTAAGAA ACTGAGGTAC AGGGAGGCTA AGTAACCAGC CCAGGCAGTG 120
GAGCCGGGGT TCAAACCAGG CAGTCTGGCT GCAAAGTCCC TCTTCCTCAC CACCACACTC 180
AACATTCCAG GCACTGTGCT AACTGTTTAC ACAAATCCTC TCCATTTTGC AGTTGAGAAA 240
CCCAAGACTC AGACCAGTTG GGCAACAGCT GAAGGTCACA TAGCTGGGAA GCAGTAGAGA 300
TGAGATTCAA AGTCGGCAGA GCTCCAGAGT CTCTGCTCTC CCCCACACCC TCCTGCAACC 360
CTGCCAGACG CTCAGGCTTC CAAAGCAAGT TTAACCAATA TCCCTGCATT GCCACGCCTC 420
TTCAGGCAAG TCAGCTTCTC CCCGCTGGGC CTCAGTTTCA CCATCTAGAA AATGACTGGG 480
GGATTGGCCC AGCTGATCTT TGAGGTCCCT TGGAGCTCTG TGAGTCTGTG ATGAGAAAGG 540
TGTGGTGCTT CTAGCTGAAA GGGAAGACCT GTGGCCTGGG AATACCTTGG GCTTGGCTTG 600
GGGTTGCAGC CAGCAAGGAT GAGGGAGATG AGGGCCTGGG GATGAAATGA AAAGGAAATT 660
TCAGGTGACT GGAGAAGGCT TATTGGCTGT GAACCTGGGA AGAGGGTTCA GATGTATGAA 720
GCAGGTAAGA AAAGAAGAGA GAAGCCCTGG GTGGGCCTCC CAGGGGGCCT TTTCCTTCTT 780
CCCAGGGGTC ACCCCAAGCT CAAGATGGGC ACATGAGAGC CTCGGGCAAG GGAGCAGGGA 840
TCAGGCCAGC ACTGAACCGA GGTCAGAACT TCTGAGACAC AGCAGTTCGA GGGAATTGAC 900
ATTGCTGGGG GTTTTGTTTT CTCTGTAAAT ATTTGGAGAT GTCCAGTTAT TCTAGAAAAA 960
TGTATCTGCA GCTGAGGGGG CGCATTTGTG CGGCTGGCCT GGCTGCCTTT TGCATGACTG 1020
CTCTGTTACA TTCTTCCCCT TCAGGAACCG AGGGTTGTTT TCCCATCTGT AACCTCATTA 1080
GGATGTCCAC ACCAGCGGGC TCCACACGCA CATGCGCTCC GGCAGGTTCC CCTCGGGGAC 1140
ACACACGCAC ACTGGCATTG CCCCCTGGCC ACACGCTCAC GCACACAGTC GCAGCTGTGC 1200
CTTTTAATAT TTAATGCCAT TGCTGCAAAC GCCGCTCCAC GCTGACTGCA TCCGTGCCAG 1260
GCTCATTCCT CTCAGGGCGC CAATTCCCGG CTTGGAGACC AGCTGACAAA TCTTGTTAAA 1320
AACCTTCCAG CCCAGTGCAT CTCTCGGAGG AGGGTAATGT CACGTGCTTG CGAGATGAGC 1380
GAATGGGTGT CATTACCAGG CAGCTCCATT TTCAACGAGG CTCTTTCCAC TTGGGGAAAT 1440
GGATGGAATC ACCTATTGCG TGAGTGCCTC AGCCCTCCCT CTAGCTCCCC ACGGCCCAGA 1500
GCTATTGCAG CTCTGGGTCC TTCAGACCCC TCTTGACGCA TTGTAGGTTG GACTGACCTG 1560
CTCTCTGGCT TGCAGAAGTC ACGGCTCTGG GTGGCACCAA GGCACGAAAT GACACGGACA 1620
CCTGGCCTGT GTGGGGGCCT 1640