EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS138-16230 
Organism
Homo sapiens 
Tissue/cell
MSC_BM 
Coordinate
chr17:16913790-16915040 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr17:16914069-16914080GGTGACTCATG+6.62
FOSL2MA0478.1chr17:16914068-16914079GGGTGACTCAT+6.14
JUN(var.2)MA0489.1chr17:16914065-16914079GAGGGGTGACTCAT+6.1
JUNBMA0490.1chr17:16914068-16914079GGGTGACTCAT+6.32
JUNDMA0491.1chr17:16914069-16914080GGTGACTCATG+6.02
ZNF263MA0528.1chr17:16914367-16914388TGAGGAGGGCGAGCAGGAAGG+6.84
ZNF263MA0528.1chr17:16914690-16914711CTCCCACCCCTTCCGTCCTCC-6
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_03884chr17:16913012-16915519Brain_Anterior_Caudate
SE_04928chr17:16912965-16915433Brain_Cingulate_Gyrus
SE_05858chr17:16910885-16915644Brain_Hippocampus_Middle
SE_23636chr17:16913280-16915489Colon_Crypt_1
SE_24609chr17:16913349-16915236Colon_Crypt_2
SE_26997chr17:16913232-16915454Esophagus
SE_27670chr17:16913014-16915514Fetal_Intestine
SE_28856chr17:16912988-16915594Fetal_Intestine_Large
SE_31426chr17:16911294-16915533Gastric
SE_34197chr17:16913015-16915492HCC1954
SE_34341chr17:16910923-16915870HCT-116
SE_34638chr17:16911053-16916556HeLa
SE_35971chr17:16912952-16915524HMEC
SE_37027chr17:16912540-16915700HSMMtube
SE_41253chr17:16913151-16915400Left_Ventricle
SE_42192chr17:16913006-16915550Lung
SE_46284chr17:16912929-16915506Osteoblasts
SE_47491chr17:16913333-16915163Pancreas
SE_52055chr17:16913231-16915357Skeletal_Muscle_Myoblast
SE_55953chr17:16912112-16915638u87
SE_57371chr17:16913179-16914126VACO_503
SE_57371chr17:16914183-16915422VACO_503
SE_58168chr17:16913504-16914813VACO_9m
SE_58168chr17:16914820-16915158VACO_9m
SE_63843chr17:16913199-16915461HSMM
SE_65457chr17:16912950-16915516Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr171691443316914621
Number: 1             
IDChromosomeStartEnd
GH17I017009chr171691326216915113
Enhancer Sequence
GTTTTTAAAC ATGGGAAGGG CTTCTAAAAA GTCACACAGC TGGTTAATGT TTGAACCAGG 60
GTGGCACAGG TTTGTGCGAA GCAGTGAGTG GAGCTGTCTG AATGCCAGGA GGAGGGTCAC 120
CCTGGAGGCG GGTGACACAG GGGTCAGTGC AGGTCAGAGG CAGAGGCTGG GCCCAGATGC 180
CATGCGAGCT CCAGGCCACT TTCCCAGAGA AGTGAGCGGC GGCCAGGCTG CCGGAGGCTG 240
TGTGGCCTCT TCAGGCCCTC ACTGGTCCTG ATTTTGAGGG GTGACTCATG CCGGCTTGGA 300
CATCCACTTC TGGCTCAAGT TGCTCTGGGT TCCTCCACAC AGACCAGAGG GATTCCTGCG 360
TCACAGGAAT CCAGGAAGGG GTGGGGGGAG TTGCAGGTTG AGAAGACAGA GGTGAGTGGC 420
CCCCGGGCCC CTCCCCTGTT GAGTCACGGG AAGGGAATGG AAATAGTGTG TGCTGAAGCT 480
GAGTCAGGGC CCAGCCTCAC CTTCTCGGGA CCTCATATGG GCTCTGAGGC GAGAGGCCCA 540
CCTGTCCCCC CCTCCTTGCT GCCTCCTCTC CCAAGCATGA GGAGGGCGAG CAGGAAGGAT 600
TTAGGTTAGC TCTCAAGAAG GACTTCCTGA ATCGCGCCAG GCGACACTGA GAGGCATCTC 660
TCAAAGGAAG TTGTGAAATC TTCCTTGGGA CCAATTTGAG GTTTGGTCTG GGTCCAACCA 720
GGACTATCTT TATGGCTCTA GAATATTTTC AAGTGTTAGA CATTCCTTCC TCGACATGAC 780
TCAGGGAGCA TCCGATGTGT GCCAGGCCTG GTGGCAGGAG CAGGGCCAGC TGAGTGTGGG 840
ACATGCCCCA CTCTGGGGGT CTTCTCTAGG TCAGCATTAC AGCAGCCTTG GAGAAGACGG 900
CTCCCACCCC TTCCGTCCTC CCCTCTCCTG GCTCCCTTGG GCAGCCTGCT CTGCCAGCCA 960
CACCACACTC CACTTTCGGA TTCCGGAAGG AAACTATGGG TAATAAATAG GACAAAGGGT 1020
CAATTTCCTT CCTGTGCAAA TCCCAGTAGC ATTTGCAGAG TGCCAAGCAT GGGAGGGCGC 1080
CCTCCTAAGT GCTTTACCTG CCTTCACTCC ACCACAGCCC TGTGAGGAAG GTGCTCCCCT 1140
TTCACAGAGA AGGAAACTGA GGCTCAGTGA GGTGAGCAGC CTGGCTACAG TGGCACTGCC 1200
AGTGAGCAGC TGACCCAGCC TGTGACCTGG GCTGTGGCAC AGCAAACAGC 1250