EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-13174 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr17:21178610-21179700 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr17:21179211-21179225TGGGGGGCGTGGCT-6.26
KLF16MA0741.1chr17:21179213-21179224GGGGGCGTGGC-6.62
Klf12MA0742.1chr17:21179223-21179238CTGGAGGGCGTGGCC-6.16
NFYAMA0060.3chr17:21179174-21179185AGCCAATCAGA+6.32
NKX2-3MA0672.1chr17:21178643-21178653ACCACTTGAA+6.02
RREB1MA0073.1chr17:21179559-21179579CCACCCGCCACCCCCACCCG+6.13
SP1MA0079.4chr17:21179212-21179227GGGGGGCGTGGCTGG-6.27
SP3MA0746.2chr17:21179212-21179225GGGGGGCGTGGCT-6.74
SP8MA0747.1chr17:21179212-21179224GGGGGGCGTGGC-6.44
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_10839chr17:21178719-21180066CD19_Primary
SE_12406chr17:21178953-21180042CD3
SE_18098chr17:21178375-21180651CD4p_CD25-_CD45ROp_Memory
SE_19017chr17:21178448-21180171CD4p_CD25-_Il17-_PMAstim_Th
SE_19511chr17:21178481-21180011CD4p_CD25-_Il17p_PMAstim_Th17
SE_20528chr17:21178474-21180192CD56
SE_22813chr17:21178431-21179952CD8_primiary
SE_23898chr17:21178691-21179218Colon_Crypt_2
SE_23898chr17:21179250-21179741Colon_Crypt_2
SE_25244chr17:21178581-21179903Colon_Crypt_3
SE_27120chr17:21178642-21179696Esophagus
SE_31667chr17:21178677-21179722Gastric
SE_41043chr17:21178140-21179815Left_Ventricle
SE_41861chr17:21178592-21179801LNCaP
SE_42495chr17:21178575-21179836Lung
SE_47630chr17:21178994-21179563Pancreas
SE_48170chr17:21177698-21180005Psoas_Muscle
SE_49589chr17:21178701-21179228Right_Ventricle
SE_50520chr17:21178624-21179779Sigmoid_Colon
SE_51538chr17:21177951-21180065Skeletal_Muscle
SE_52785chr17:21178711-21179735Small_Intestine
SE_53759chr17:21178517-21179883Spleen
SE_58432chr17:21170318-21277177Ly1
SE_61419chr17:21170524-21296554Toledo
SE_65398chr17:21178443-21180096Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr172117910021179414
Number: 1             
IDChromosomeStartEnd
GH17I021274chr172117825321180112
Enhancer Sequence
TGCAATCCTT CGGATGGCAG TTTTCCAAGA CCGACCACTT GAATGTCCTC TCTACCCTCA 60
TAAAAGCAAG ACCTGTTCCT TGCTGGGAAA GCATGGGGTG GGTGATCGTC TTCAACCTTT 120
AAAGGGCTGG ACCCGTAGCT GCTGCACCCG GGGGCACAGC TGACGGGAGA GGAGAAGCGG 180
CCTCTTCTCA GCATGGGGAT GTGGGGAGCC GCTCAGGGAG AGAAAACGAG GCCTTTACAG 240
CACCGGTTTA ACAGCCTCGG CCACGCATCT GCCCGCACAG ATCTAAGGCT TGGCTTCGGG 300
TCCGGCTCCA CGCCTGCCCC ATGTCCCCAC GGTCCGCGGC CCTCGGGAGG CCCGGCCCTG 360
GGGGCTGAGC TCTGCCCTGG GACCGAAGGC CACTCTCCCA GCCAAGGCCG GAGGGCTCTG 420
CCCTGGGCAC ATGCGCCCCA TCCGCCTGCC CTGAGCTGAC CCCGCCGCTC CACACCACCC 480
CACTCGCGGC TGAAAAGCTG AAGGCAGCCG CACACTCGCC CTTGCAGCTT GCCCTGCAGC 540
CCGCGCGGCC ATGTGAGCAA GCGCAGCCAA TCAGAGGCTC GCCCTGGACT CCGTCCCGGG 600
CTGGGGGGCG TGGCTGGAGG GCGTGGCCGG GCGGTACCCG CGGCGTCTCT GCGCTGCCGC 660
CTTTGCTTGC GCGGCTGTGT AGGGGGTTGT GGCGGGCCGG AGAGTCCCCG AGTGACTTAA 720
CATTCTCTAA AAATACCCCA TTTTTGAACT TCGACGACCT GGGTTGGCCT GCTCACTCTG 780
TGTCCCTGCG CTCCTCTGCT TCTCTGCTCC TTCGGTCTTG TGTGCTGGGG ACACGTGGGC 840
CTTTCCAGTT CCCTGCAGCC ACCTTTGGTC TGTAGGAAGG CAGTGGCGCA GGGAGCGGTG 900
GGAGCCCGGG TCTGCAGGGC TCAAGGTGGC GACGGCGAAG CGGTCTGCCC CACCCGCCAC 960
CCCCACCCGC AGGATGCGCA TCGCCAGTGC AGCCCGGGTC GTGGCCCCCC AACAGACCCA 1020
GTCCCGCCGC GACACGGCAG CAGCACCTCT TCGCCGCGAC ACGGCAGCAG CACCTCTTCG 1080
GCCCTTTGAG 1090